JP2010265258A - Pharmaceutical composition containing a pyrimidylindoline compound - Google Patents

Abstract

Disclosed is a pharmaceutical composition comprising a pyrimidylindoline compound having a structure different from that of a compound used as an active ingredient of a conventional oral hypoglycemic agent and having an excellent hypoglycemic action.
General formula (I):
[Chemical 1]

Or a pharmaceutically acceptable salt thereof.
[Selection figure] None

Description

  The present invention relates to a pharmaceutical composition containing a novel pyrimidylindoline compound having a hypoglycemic action or a pharmaceutically acceptable salt thereof as an active ingredient.

  Diabetes is a metabolic disease mainly characterized by a chronic hyperglycemic state due to insufficient insulin action. For the treatment of diabetes, drug therapy is generally administered together with diet therapy and exercise therapy. Oral hypoglycemic agents that are a type of anti-diabetic agent include biguanides or thiazolidinediones that improve insulin resistance, sulfonylureas or glinides that promote insulin secretion from pancreatic β cells, and α that inhibit sugar absorption -Glucosidase inhibitors are used.

  However, biguanides have side effects such as lactic acidosis, thiazolidinedione has weight gain and edema, sulfonylureas and glinides have secondary effects due to hypoglycemia and long-term use, and α-glucosidase inhibitors have diarrhea. It has been reported. Therefore, development of an oral hypoglycemic agent that solves such problems is desired.

  In recent years, pyrimidine compounds, piperidine-1-carboxylate compounds and the like have been developed as oral hypoglycemic agents having a new structure (see, for example, Patent Documents 1 to 4).

International Publication No. 05/7647 Pamphlet International Publication No. 05/121121 Pamphlet US Patent Application Publication No. 2007/167473 International Publication No. 07/3962 Pamphlet

  Accordingly, the present invention provides a pyrimidylindoline compound having a structure different from that of a compound used as an active ingredient of a conventional oral hypoglycemic agent and having an excellent hypoglycemic action, or a pharmaceutically acceptable salt thereof. As an active ingredient, and such a pharmaceutical composition comprising type 1 diabetes, type 2 diabetes, gestational diabetes, hyperglycemia due to other factors, impaired glucose tolerance (IGT), Diabetes-related diseases (eg, obesity, hyperlipidemia, hypercholesterolemia, dyslipidemia, hypertension, fatty liver, metabolic syndrome, edema, heart failure, angina, myocardial infarction, arteriosclerosis, hyperuricemia , Gout), or diabetic complications (eg, retinopathy, nephropathy, neuropathy, cataract, foot gangrene, infection, ketosis) An object of the present invention is to provide a pharmaceutical composition.

The present invention
(1) General formula (I):

[Where,
p is 1 or 2,
R ¹ has ¹ to 3 substituents selected from the substituent group α, may have 1 to 3 substituents selected from the substituent group α, and has 1 to 3 substituents selected from the substituent group β. A C3-C7 cycloalkyl group, a C2-C6 alkynyl group which may have 1 to 3 substituents selected from the substituent group β, and a substituent selected from the substituent group β A C2-C6 alkenyl group, an amino group or a mono- or di (C1-C6 alkyl) amino group which may have
The substituent group α is a halogen atom, a hydroxyl group, a C1-C6 alkoxy group, a C3-C7 cycloalkyl group which may have 1 to 3 substituents selected from the substituent group β, an amino group, a mono group Or a di (C1-C6 alkyl) amino group, an aryl group optionally having 1 to 3 substituents selected from the substituent group β, and 1 to 3 substituents selected from the substituent group β A group of heteroaryl groups that may have
Substituent group β is a group consisting of a halogen atom, a hydroxyl group, a C1-C6 alkyl group and a C1-C6 alkoxy group,
m is an integer from 0 to 3,
R ² is the same or different and is a halogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group or a C1-C6 alkoxy C1-C6 alkyl group,
n is an integer from 0 to 4,
R ³ is the same or different and is a halogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group or a C1-C6 alkoxy C1-C6 alkyl group,
R ⁴ and R ⁵ are each independently a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group or a C1-C6 alkoxy C1-C6 alkyl group,
R ⁶ is -C (O) OR ^6a , -C (O) -R ^6b or -S (O) ₂ -R ^6c ,
R ^6a has a C1 to C6 alkyl group optionally having 1 to 3 substituents selected from the substituent group α, and 1 to 3 substituents selected from the substituent group β. A C3-C7 cycloalkyl group, a C2-C6 alkynyl group which may have 1 to 3 substituents selected from the substituent group β, and a substituent selected from the substituent group β A C2-C6 alkenyl group optionally having 1 to 3 aryl groups optionally having 1 to 3 substituents selected from the substituent group β, and 1 to 3 substituents selected from the substituent group β. A heteroaryl group which may have three,
R ^6b has a hydrogen atom, a C1-C6 alkyl group optionally having 1 to 3 substituents selected from the substituent group α, and 1 to 3 substituents selected from the substituent group β. A C3-C7 cycloalkyl group which may optionally be substituted, a C2-C6 alkynyl group which may have 1 to 3 substituents selected from the substituent group β, and a substituent selected from the substituent group β. 1 to 3 optionally having 1 to 3 substituents selected from C2-C6 alkenyl group, amino group, mono- or di (C1-C6 alkyl) amino group, substituent group β A heteroaryl group that may have 1 to 3 substituents selected from the substituent group β,
R ^6c is a C1-C6 alkyl group,
R ⁷ is a hydrogen atom, a halogen atom or a C1-C6 alkyl group.
Or a pharmaceutical composition containing a pharmaceutically acceptable salt thereof;

(2) R ¹ has ¹ to 3 substituents selected from the substituent group β, optionally having 1 to 3 substituents selected from the substituent group α, and C1 to C6 alkyl groups. The pharmaceutical composition according to the above (1), which may be a C3-C7 cycloalkyl group, an amino group, or a mono- or di (C1-C6 alkyl) amino group;

(3) R ¹ has ¹ to 3 substituents selected from the C1-C6 alkyl group or substituent group β which may have 1 to 3 substituents selected from the substituent group α. The pharmaceutical composition according to the above (1) or (2), which is a C3-C7 cycloalkyl group which may optionally be present;

(4) The pharmaceutical composition according to any one of (1) to (3), wherein m is 0;

(5) The pharmaceutical composition according to any one of (1) to (3), wherein m is 1 and R ² is a halogen atom;

(6) The pharmaceutical composition according to any one of (1) to (5), wherein n is 0;

(7) The pharmaceutical composition according to any one of (1) to (5), wherein n is 1 and R ³ is a halogen atom;

(8) The pharmaceutical composition according to any one of (1) to (7), wherein R ⁴ is a hydrogen atom;

(9) The pharmaceutical composition according to any one of (1) to (8), wherein R ⁵ is a hydrogen atom, a C1-C6 alkyl group or a C1-C6 alkoxy group;

(10) The pharmaceutical composition according to any one of (1) to (9), wherein R ⁵ is a hydrogen atom or a C1-C6 alkoxy group;

(11) The pharmaceutical composition according to any one of (1) to (10), wherein R ⁶ is —C (O) OR ^6a ;

(12) R ^6a may have 1 to 3 substituents selected from the substituent group α and may have 1 to 3 substituents selected from the substituent group β. An optionally substituted C3-C7 cycloalkyl group, an aryl group which may have 1 to 3 substituents selected from the substituent group β, or a substituent selected from the substituent group β The pharmaceutical composition according to any one of the above (1) to (11), which is a heteroaryl group which may be present individually;

(13) The pharmaceutical composition according to any one of (1) to (10), wherein R ⁶ is —C (O) —R ^6b ;

(14) R ^6b has 1 to 3 substituents selected from the C1-C6 alkyl group or substituent group β which may have 1 to 3 substituents selected from the substituent group α. The pharmaceutical composition according to any one of (1) to (10) or (13) above, which is an aryl group which may be:

(15) Any one of the above (1) to (10), wherein R ^6b is a C1 to C6 alkyl group optionally having 1 to 3 substituents selected from the substituent group α (13) or the pharmaceutical composition according to (14);

(16) The pharmaceutical composition according to any one of (1) to (10), wherein R ⁶ is —S (O) ₂ —R ^6c ;

(17) The pharmaceutical composition according to any one of (1) to (10) or (16), wherein R ^6c is a C1-C4 alkyl group;

(18) The pharmaceutical composition according to any one of (1) to (17), wherein R ⁷ is a hydrogen atom, a fluorine atom, or a C1-C3 alkyl group;

(19) General formula (II):

[Where,
R ¹ has ¹ to 3 substituents selected from the substituent group α, may have 1 to 3 substituents selected from the substituent group α, and has 1 to 3 substituents selected from the substituent group β. A C3-C7 cycloalkyl group, a C2-C6 alkynyl group which may have 1 to 3 substituents selected from the substituent group β, and a substituent selected from the substituent group β A C2-C6 alkenyl group, an amino group or a mono- or di (C1-C6 alkyl) amino group which may have
The substituent group α is a halogen atom, a hydroxyl group, a C1-C6 alkoxy group, a C3-C7 cycloalkyl group which may have 1 to 3 substituents selected from the substituent group β, an amino group, a mono group Or a di (C1-C6 alkyl) amino group, an aryl group optionally having 1 to 3 substituents selected from the substituent group β, and 1 to 3 substituents selected from the substituent group β A group of heteroaryl groups that may have
Substituent group β is a group consisting of a halogen atom, a hydroxyl group, a C1-C6 alkyl group and a C1-C6 alkoxy group,
m is an integer from 0 to 3,
R ² is the same or different and is a halogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group or a C1-C6 alkoxy C1-C6 alkyl group,
n is an integer from 0 to 4,
R ³ is the same or different and is a halogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group or a C1-C6 alkoxy C1-C6 alkyl group,
R ⁴ and R ⁵ are each independently a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group or a C1-C6 alkoxy C1-C6 alkyl group,
R ^6a has a C1 to C6 alkyl group optionally having 1 to 3 substituents selected from the substituent group α, and 1 to 3 substituents selected from the substituent group β. A C3-C7 cycloalkyl group, a C2-C6 alkynyl group which may have 1 to 3 substituents selected from the substituent group β, and a substituent selected from the substituent group β A C2-C6 alkenyl group optionally having 1 to 3 aryl groups optionally having 1 to 3 substituents selected from the substituent group β, and 1 to 3 substituents selected from the substituent group β. A heteroaryl group which may have three,
R ⁷ is a hydrogen atom, a halogen atom or a C1-C6 alkyl group.
Or a pharmaceutical composition containing a pharmaceutically acceptable salt thereof;

(20) A pharmaceutical composition comprising one compound selected from the group consisting of:
Isopropyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Isobutyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
tert-butyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Cyclobutyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Cyclopentyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
1-ethylpropyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Cyclopropylmethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
3-furylmethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
1-cyclopropylethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2-fluoroethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2,2-difluoroethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2,2,2-trifluoroethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
1- (6-{[1- (3-methylbutanoyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (methylsulfonyl) indoline;
Isopropyl 4-({5-methoxy-6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
tert-butyl 4-({5-methoxy-6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Isopropyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Isobutyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
sec-butyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Cyclobutyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Cyclopropylmethyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2,2-difluoroethyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2,2,2-trifluoroethyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
tert-butyl 4-[(6- {5-[(2-fluoroethyl) sulfonyl] indoline-1-yl} pyrimidin-4-yl) oxy] piperidine-1-carboxylate;
tert-butyl 4-({6- [5- (propylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2,2,2-trifluoroethyl 4-({6- [5- (propylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
tert-butyl 4-({6- [5- (cyclobutylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
tert-butyl 4-({6- [5- (methylsulfinyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2,2,2-trifluoroethyl 4-({6- [5- (methylsulfinyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate; and isopropyl cis-3-fluoro -4- [6- (5-methanesulfonyl-2,3-dihydro-indol-1-yl) -pyrimidin-4-yloxy] -piperidine-1-carboxylate;

(21) The pharmaceutical composition according to any one of (1) to (20) above for treating and / or preventing type 1 diabetes, type 2 diabetes or diabetes-related disease; and

(22) The pharmaceutical composition according to any one of (1) to (21) above, for treating and / or preventing obesity.

  According to the present invention, a pharmaceutical composition containing, as an active ingredient, a pyrimidylindoline compound having an excellent hypoglycemic effect or a pharmaceutically acceptable salt thereof, and such a pharmaceutical composition comprising type 1 diabetes, Type 2 diabetes, gestational diabetes, hyperglycemia due to other factors, impaired glucose tolerance (IGT), diabetes related diseases (eg obesity, hyperlipidemia, hypercholesterolemia, dyslipidemia, hypertension) , Fatty liver, metabolic syndrome, edema, heart failure, angina, myocardial infarction, arteriosclerosis, hyperuricemia, gout, etc. or diabetic complications (eg retinopathy, nephropathy, neuropathy, cataract, foot gangrene) , Infectious diseases, ketosis, etc.), and a pharmaceutical composition having an excellent therapeutic effect and / or preventive effect.

In the present specification, “p” in S (O) _p represents the number of oxygen atoms bonded to a sulfur atom.

  In the present specification, the “C1-C6 alkyl group” means a linear or branched alkyl group having 1 to 6 carbon atoms, such as a methyl group, an ethyl group, a propyl group, an isopropyl group, a butyl group. , Isobutyl, sec-butyl, tert-butyl, pentyl, isopentyl, 2-methylbutyl, neopentyl, 1-ethylpropyl, hexyl, isohexyl, 4-methylpentyl, 3-methylpentyl Group, 2-methylpentyl group, 1-methylpentyl group, 3,3-dimethylbutyl group, 2,2-dimethylbutyl group, 1,1-dimethylbutyl group, 1,2-dimethylbutyl group, 1,3- Examples thereof include a dimethylbutyl group, a 2,3-dimethylbutyl group, and a 2-ethylbutyl group.

  In the present specification, the “C3 to C7 cycloalkyl group” means a saturated cyclic hydrocarbon group having 3 to 7 carbon atoms, and examples thereof include a cyclopropyl group, a cyclobutyl group, a cyclopentyl group, a cyclohexyl group, and a cycloheptyl group. .

  In the present specification, the “C2 to C6 alkynyl group” refers to a linear or branched alkynyl group having 2 to 6 carbon atoms, such as ethynyl group, 2-propynyl group, 1-methyl-2- Propinyl group, 2-ethyl-2-propynyl group, 2-butynyl group, 1-methyl-2-butynyl group, 3-butynyl group, 2-pentynyl group, 1-methyl-2-pentynyl group, 2-hexynyl group, etc. Is mentioned.

  In the present specification, the “C2 to C6 alkenyl group” refers to a linear or branched alkenyl group having 2 to 6 carbon atoms, such as an ethenyl group, a 1-propenyl group, a 2-propenyl group, 1 -Methyl-2-propenyl group, 1-methyl-1-propenyl group, 2-methyl-1-propenyl group, 2-methyl-2-propenyl group, 2-ethyl-2-propenyl group, 1-butenyl group, 2 -Butenyl group, 1-methyl-2-butenyl group, 1-methyl-1-butenyl group, 1-ethyl-3-butenyl group, 1-pentenyl group, 1-hexenyl group and the like can be mentioned.

  In the present specification, the “mono or di (C1-C6 alkyl) amino group” refers to a group in which one or two of the “C1-C6 alkyl groups” are bonded to an amino group. Examples of mono (C1-C6 alkyl) amino groups include, for example, methylamino group, ethylamino group, propylamino group, isopropylamino group, butylamino group, isobutylamino group, sec-butylamino group, tert-butylamino group, Pentylamino group, isopentylamino group, 2-methylbutylamino group, neopentylamino group, 1-ethylpropylamino group, hexylamino group, isohexylamino group, 4-methylpentylamino group, 3-methylpentylamino group , 2-methylpentylamino group, 1-methylpentylamino group and the like, and as di (C1-C6 alkyl) amino group, for example, dimethylamino group, diethylamino group, N-ethyl-N-methylamino group, Examples include a dipropylamino group, a dibutylamino group, a dipentylamino group, a dihexylamino group, and the like.

  In the present specification, the “halogen atom” refers to a fluorine atom, a chlorine atom, a bromine atom or an iodine atom.

  In the present specification, the “C1-C6 alkoxy group” refers to a group in which the “C1-C6 alkyl group” is bonded to an oxygen atom, for example, a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, a butoxy group. , Isobutoxy group, sec-butoxy group, tert-butoxy group, pentoxy group, isopentoxy group, 2-methylbutoxy group, neopentoxy group, hexyloxy group, 4-methylpentoxy group, 3-methylpentoxy group, 2-methyl Examples include a pentoxy group.

  In the present specification, the “aryl group” refers to an aromatic hydrocarbon group having 5 to 14 carbon atoms, and examples thereof include a phenyl group, an indenyl group, a naphthyl group, a phenanthrenyl group, and an anthracenyl group.

  In the present specification, the “heteroaryl group” refers to a 5- to 8-membered aromatic heterocycle containing 1 to 5 of the same or different heteroatoms selected from the group consisting of oxygen atom, sulfur atom and nitrogen atom. For example, furanyl group, thienyl group, pyrrolyl group, oxazolyl group, isoxazolyl group, thiazolyl group, thianyl group, pyridyl group, pyridazinyl group, pyrimidinyl group, pyrazolyl group, imidazolyl group, triazinyl group, thiadiazolyl group, imidazolothiazolyl group Benzoisoxazolyl group, chromenyl group, quinolyl group, benzothianyl group, quinoxalinyl group, benzotriazinyl group and the like.

  In the present specification, the “C1-C6 alkoxy C1-C6 alkyl group” refers to a group in which the “C1-C6 alkoxy group” is substituted with the “C1-C6 alkyl group”. Examples include an ethyl group, a methoxypropyl group, a methoxybutyl group, an ethoxymethyl group, an ethoxyethyl group, an ethoxypropyl group, an ethoxybutyl group, a butoxymethyl group, a butoxyethyl group, a butoxypropyl group, and a butoxybutyl group.

  “Pharmaceutically acceptable salt” refers to a salt formed by reacting a compound represented by formula (I) or (II) with an acid or a base.

  Examples of the salt include hydrohalides such as hydrofluoride, hydrochloride, hydrobromide, hydroiodide; hydrochloride, nitrate, perchlorate, sulfate, phosphate, etc. Inorganic acid salts; lower alkane sulfonates such as methane sulfonate, trifluoromethane sulfonate and ethane sulfonate; aryl sulfonates such as benzene sulfonate and p-toluene sulfonate; acetate and malic acid Organic salts such as salts, fumarate, succinate, citrate, ascorbate, tartrate, oxalate, maleate; alkali metal salts such as sodium salt, potassium salt, lithium salt; calcium salt Alkaline earth metal salts such as magnesium salts; metal salts such as aluminum salts and iron salts; inorganic salts such as ammonium salts; t-octylamine salts, dibenzylamine salts, morpho Phosphorus salt, glucosamine salt, phenylglycine alkyl ester salt, ethylenediamine salt, N-methylglucamine salt, guanidine salt, diethylamine salt, triethylamine salt, dicyclohexylamine salt, N, N'-dibenzylethylenediamine salt, chloroprocaine salt, procaine Salts, diethanolamine salts, N-benzylphenethylamine salts, piperazine salts, tetramethylammonium salts, amine salts such as organic salts such as tris (hydroxymethyl) aminomethane salts; glycine salts, lysine salts, arginine salts, ornithine salts, glutamate salts And amino acid salts such as aspartate.

  When the compound represented by the general formula (I) or (II) is left in the air or recrystallized, it absorbs moisture and attaches adsorbed water, which may become a hydrate. Such hydrates are also included in the salts referred to in the present invention.

  Since the compound represented by the general formula (I) or (II) may have an asymmetric carbon atom in the molecule, an optical isomer exists. These isomers and mixtures of these isomers are all represented by a single formula, ie, general formula (I) or (II). Therefore, the compound represented by the general formula (I) or (II) includes all optical isomers and mixtures of optical isomers in an arbitrary ratio.

R ¹ in the general formula (I) or (II) is preferably selected from a C1-C6 alkyl group optionally having 1 to 3 substituents selected from the substituent group α, and a substituent group β A C3-C7 cycloalkyl group, amino group or mono (C1-C6 alkyl) amino group which may have 1 to 3 substituents, more preferably a substituent selected from the substituent group α A C1 to C6 alkyl group optionally having 1 to 3 groups or a C3 to C7 cycloalkyl group optionally having 1 to 3 substituents selected from the substituent group β, and more A methyl group, an ethyl group, a propyl group, an isobutyl group, a 2-fluoroethyl group or a cyclobutyl group is preferable.

  M in the general formula (I) or (II) is preferably 0 or 1, more preferably 0.

R ² in the general formula (I) or (II) is the same or different and is preferably a halogen atom.

  N in the general formula (I) or (II) is preferably 0 or 1, more preferably 0.

R ³ in the general formula (I) or (II) is the same or different and is preferably a halogen atom.

R ⁴ in the general formula (I) or (II) is preferably a hydrogen atom.

R ⁵ in the general formula (I) or (II) is preferably a hydrogen atom, a C1-C6 alkyl group or a C1-C6 alkoxy group, more preferably a hydrogen atom or a C1-C6 alkoxy group, More preferably, they are a hydrogen atom or a methoxy group.

R ^6a in formula (I) or (II) is preferably selected from a C1-C6 alkyl group optionally having 1 to 3 substituents selected from substituent group α, and substituent group β C3-C7 cycloalkyl group optionally having 1 to 3 substituents, aryl group optionally having 1 to 3 substituents selected from substituent group β or substituent group β A heteroaryl group optionally having 1 to 3 substituents selected from, more preferably C1 to optionally having 1 to 3 substituents selected from the substituent group α. 1 to 3 substituents selected from C3 to C7 cycloalkyl groups or substituent group β which may have 1 to 3 substituents selected from C6 alkyl group and substituent group β A heteroaryl group that may be, even more preferably, isopropyl, isobutyl, sec-butyl, tert-butyl, 1-ethylpropylene. Group, 2-fluoroethyl group, 2,2-difluoroethyl group, 2,2,2-trifluoroethyl group, cyclopentylmethyl group, 1-cyclopropylethyl group, cyclopentyl group, cyclobutyl group or 3-furylmethyl group is there.

R ^6b in the general formula (I) is preferably a C1-C6 alkyl group which may have 1 to 3 substituents selected from the substituent group α or a substituent selected from substituent group β. Is an aryl group optionally having 1 to 3, more preferably a C1 to C6 alkyl group optionally having 1 to 3 substituents selected from the substituent group α, More preferably, it is an isobutyl group.

R ^6c in the general formula (I) is preferably a C1-C4 alkyl group, and more preferably a butyl group.

R ⁷ in the general formula (I) or (II) is preferably a hydrogen atom, a fluorine atom or a C1-C3 alkyl group, more preferably a hydrogen atom or a methyl group.

Specific examples of the compound represented by the general formula (I) include, for example, compounds described in Table 1 below, but are not limited to these compounds. In Table 1 below, the following abbreviations are used.

Aly: Allyl group
Bn: benzyl group
Bu: Butyl group
cBu: Cyclobutyl group
cHp: cycloheptyl group
cHx: cyclohexyl group
cPn: cyclopentyl group
cPr: cyclopropyl group
Et: Ethyl group
Ety: Ethynyl group
Fur: Furyl group
Hx: n-hexyl group
iBu: Isobutyl group
iPr: Isopropyl group
Me: Methyl group
NPn: 2,2-dimethyl-1-propyl group
Ph: Phenyl group
Pn: n-pentyl group
Prpe: propenyl group
Pyr: Pyridyl group
sBu: sec-butyl group
tBu: tert-butyl group
In the R ² column, “-” indicates that m is 0, and in the R ³ column, “-” indicates that n is 0.

  Among the above exemplified compounds, 4, 6, 8, 9, 11, 13, 19, 26, 28, 34, 53, 54, 69, 262, 264, 305, 307, 308, 310, 313, 325, 326 , 355, 391, 396, 503 or 617 are preferred, and compounds of 4, 8, 19, 34, 53, 54, 69, 262, 264, 305, 313 or 617 are more preferred.

  The compound represented by the general formula (I) can be produced, for example, by the method described later. Indoline intermediates, piperidine intermediates, and pyrimidine intermediates in the following production methods are, for example, J. Med. Chem, 41, 1998, 1598-1612, Bioorg. Med. Chem. Lett., 2002, 12 , 3105-3110, Chem. Pharm. Bull., 1993, 41, 529-538, J. Org. Chem., 53, (1988), 2947-2052, WO2003 / 47586, WO2006 / 76243, etc. can do. In addition, commercially available indoline derivatives, piperidine derivatives, and pyrimidine derivatives may be used as the intermediates.

In the method described later, R ¹ , R ² , R ³ , R ⁴ , R ⁵ , R ⁶ , R ^6a , R ^6b , R ^6c , R ⁷ , m, n, and p are the same as defined in general formula (I) R ^{6 ′} is a group obtained by removing the —C (O) O-tert-butyl group from the definition of R ⁶ , and R ^a is 1 to 3 substituents selected from the substituent group β. An optionally substituted C1-C6 alkyl group, Boc represents a tert-butoxycarbonyl group, and tBu represents a tert-butyl group.

  In the reaction of each step of the method described later, when a compound serving as a reaction substrate has a group that inhibits the target reaction (for example, an amino group, a hydroxyl group, a carboxyl group, etc.) You may introduce | transduce a protective group and remove the introduced protective group. These protecting groups are not particularly limited as long as they are commonly used protecting groups. For example, TH Greene, PG Wuts, Protective Groups in Organic Synthesis. Third Edition, 1999, John Wiley & Sons, Inc. Protected protecting groups. The reaction for introducing these protecting groups and the reaction for removing the protecting groups can be carried out according to conventional methods such as the methods described in the above-mentioned documents.

  The solvent used in the reaction in each step of the method described later is not particularly limited as long as it does not inhibit the reaction and dissolves the starting materials to some extent. For example, fat such as hexane, pentane, petroleum ether, cyclohexane, etc. Aromatic hydrocarbons such as benzene, toluene, xylene; halogenated hydrocarbons such as dichloromethane, chloroform, carbon tetrachloride, dichloroethane, chlorobenzene, dichlorobenzene; diethyl ether, diisopropyl ether, tetrahydrofuran, dioxane, Ethers such as dimethoxyethane and diethylene glycol dimethyl ether; ketones such as acetone, methyl ethyl ketone, methyl isobutyl ketone and cyclohexanone; esters such as ethyl acetate, propyl acetate and butyl acetate; Nitriles such as cetonitrile, propionitrile, butyronitrile, isobutyronitrile; carboxylic acids such as acetic acid and propionic acid; methanol, ethanol, 1-propanol, 2-propanol, 1-butanol, 2-butanol, 2-methyl- Alcohols such as 1-propanol and 2-methyl-2-propanol; Amides such as formamide, dimethylformamide, dimethylacetamide, N-methyl-2-pyrrolidone and hexamethylphosphorotriamide; Sulfoxides such as dimethyl sulfoxide and sulfolane Water; and a mixture thereof.

  The reaction temperature in the reaction of each step of the method described later varies depending on the solvent, starting material, reagent, and the like, and the reaction time varies depending on the solvent, starting material, reagent, reaction temperature, and the like.

  In the reaction in each step of the method described later, after completion of the reaction, the target compound in each step is isolated from the reaction mixture according to a conventional method. For the target compound, for example, (i) if necessary, insoluble matters such as a catalyst are removed by filtration, and (ii) water and a solvent immiscible with water (for example, dichloromethane, diethyl ether, ethyl acetate, etc.) are added to the reaction mixture. The target compound is extracted, (iii) the organic layer is washed with water, dried using a desiccant such as anhydrous magnesium sulfate, and (iv) the solvent is distilled off. The obtained target compound can be further purified by a conventional method such as recrystallization, reprecipitation, silica gel column chromatography and the like, if necessary. Alternatively, the target compound in each step can be directly used in the next reaction without purification.

The A method will be described.
[Method A]

(Process A-1)
Step A-1 is a step for producing compound (3) by reacting compound (1) with compound (2) in the presence of a base.

  Examples of the base used include tert-butoxy sodium, tert-butoxy potassium, sodium hydride, potassium hydride and the like, preferably tert-butoxy potassium or sodium hydride, more preferably tert-butoxy potassium. is there.

  Examples of the solvent used include tetrahydrofuran, dioxane, cyclopentylmethyl ether, dimethylformamide, dimethylacetamide, and the like, preferably tetrahydrofuran or dimethylformamide, more preferably tetrahydrofuran.

  The reaction temperature is 0 to 120 ° C, preferably 0 to 60 ° C. The reaction time is 10 minutes to 12 hours, preferably 30 minutes to 6 hours.

(Process A-2)
In step A-2, compound (3) obtained in step A-1 is reacted with compound (4) by a Buchwald-Hartwig reaction using a palladium catalyst to obtain a compound represented by general formula (I). It is a manufacturing process.

  The palladium catalyst, ligand, base and reaction conditions to be used are not particularly limited as long as they are reagents and conditions usually used for the Buchwald-Hartwig reaction. For example, AR Muci, SL Buchwald, Top. Curr. Chem. 2002 Year, 219, p.131.

  A preferred palladium catalyst is palladium (II) acetate or palladium (0) dibenzylideneacetone, more preferably palladium (II) acetate.

  Preferred ligands are tricyclohexylphosphine, 1,3-bis (phenylphosphono) propane, 2,2'-bis (diphenylphosphanyl) -1,1'-binaphthyl, 2- (dicyclohexylphosphono) biphenyl or 2- Dicyclohexylphosphino-2 ′-(N, N-dimethylamino) biphenyl is preferred, and 2-dicyclohexylphosphino-2 ′-(N, N-dimethylamino) biphenyl is more preferred.

  Preferred bases are sodium carbonate, potassium carbonate, cesium carbonate, tert-butoxy sodium or tert-butoxy potassium, more preferably potassium carbonate.

  A preferred solvent is toluene or dioxane, more preferably 1,4-dioxane.

  The reaction temperature is preferably 20 to 150 ° C. The reaction time is preferably 30 minutes to 12 hours.

A compound in which p in general formula (I) is 2 can also be produced by the following method B.
[Method B]

(Process B-1)
In step B-1, compound (5) is reacted with compound (1) in the presence of an acid, and then oxidized in the presence of an oxidizing agent to produce compound (6).

  Examples of the acid used include hydrochloric acid, hydrobromic acid, sulfuric acid, methanesulfonic acid, trifluoromethanesulfonic acid and the like, and concentrated hydrochloric acid is preferable.

  Examples of the oxidizing agent used in the oxidation include hydrogen peroxide, peracetic acid, pertrifluoroacetic acid, dimethyldioxirane, oxone (trade name), m-chloroperbenzoic acid, bis (peroxyphthalic acid) magnesium hexa Hydrates, potassium permanganate, chromium (VI) oxide and the like can be mentioned, and m-chloroperbenzoic acid is preferred.

  Examples of the solvent used in the reaction with the compound (1) include acetone, methyl ethyl ketone, tetrahydrofuran, dioxane, a mixture of cyclopentyl methyl ether and water, and preferably a mixture of acetone and water.

  Examples of the solvent used in the oxidation include dichloromethane, dichloroethane, chloroform and the like, preferably dichloromethane.

  The reaction temperature in the reaction with the compound (1) is 0 to 150 ° C, preferably 0 to 100 ° C. The reaction time in the reaction with the compound (1) is 15 minutes to 24 hours, preferably 30 minutes to 12 hours.

  The reaction temperature in the oxidation is -30 to 50 ° C, preferably -10 to 30 ° C. The reaction time in the oxidation is 5 minutes to 10 hours, preferably 10 minutes to 5 hours.

(Process B-2)
Step B-2 is a step of producing compound (7) by reacting compound (6) obtained in step B-1 with compound (2) in the presence of a base.

  Examples of the base used include sodium hydride and potassium hydride, and sodium hydride is preferable.

  Examples of the solvent to be used include tetrahydrofuran, dioxane, dimethylformamide, dimethylacetamide, and the like, preferably tetrahydrofuran.

  The reaction temperature is 0 to 120 ° C, preferably 0 to 80 ° C.

  The reaction time is 10 minutes to 24 hours, preferably 30 minutes to 6 hours.

A compound in which R ⁶ in general formula (I) is not Boc can also be produced by the following method C using a compound in which R ⁶ in general formula (I) is Boc as an intermediate.
[Method C]

  Method C is a method for producing the compound (10) by removing the Boc group from the compound (8) and then reacting with the compound (9) in the presence of a base.

  The reagent used for removing the Boc group in the compound (8) is described in, for example, TH Greene, PG Wuts, Protective Groups in Organic Synthesis. Third Edition, 1999, John Wiley & Sons, Inc. Examples thereof include a reagent capable of removing the Boc group, preferably trifluoroacetic acid or hydrochloric acid-ethyl acetate.

  Examples of the solvent used for removing the Boc group include dichloromethane, chloroform, ethyl acetate, dioxane and the like, and preferably dichloromethane or ethyl acetate.

  The reaction temperature for removing the Boc group is 0 to 100 ° C, preferably 0 to 50 ° C.

  The reaction time for removing the Boc group is 5 minutes to 24 hours, preferably 10 minutes to 6 hours.

  Examples of the base used include triethylamine, diisopropylethylamine, pyridine, 4-dimethylaminopyridine (DMAP), 2,6-lutidine, 1,4-diazabicyclo [2.2.2] octane (DABCO), and the like. Triethylamine or diisopropylethylamine is preferable, and diisopropylethylamine is more preferable.

  Examples of the solvent used in the reaction with the compound (9) include dichloromethane, dichloroethane, chloroform, tetrahydrofuran, toluene and the like, preferably dichloromethane or tetrahydrofuran, and more preferably dichloromethane.

  The reaction temperature in the reaction with the compound (9) is −30 to 100 ° C., preferably −20 to 50 ° C.

The reaction time in the reaction with the compound (9) is 5 minutes to 24 hours, preferably 10 minutes to 12 hours.
[Method D]

  Method D is a method for producing the compound (12) by removing the Boc group from the compound (8) and then reacting with the compound (11) in the presence of a condensing agent and a base.

Removal of the Boc group can be carried out in the same manner as the removal of the Boc group in Method C.
The condensing agent to be used is not particularly limited as long as it is used for the amidation reaction. The condensing agent described in RC Larock, Comprehensive Organic Transformations. Second Edition, 1999, John Wiley & Sons, Inc. It can be. As a specific example,
(I) a combination of a phosphate ester such as diethyl phosphoryl cyanide and the following base;
(Ii) carbodiimides such as 1,3-dicyclohexylcarbodiimide, 1,3-diisopropylcarbodiimide, 1-ethyl-3- (3-dimethylaminopropyl) carbodiimide (WSC); combinations of these carbodiimides and the following bases; Combinations of these carbodiimides with N-hydroxy compounds such as N-hydroxysuccinimide;
(Iii) Imidazoles such as 1,1′-carbonyldiimidazole (CDI);
(Iv) 4- (4,6-dimethoxy-1,3,5-triazin-2-yl) -4-methylmorpholinium chloride (DMT-MM); and (v) O- (7-azabenzotriazole -1-yl) -N, N, N ', N'-tetramethyluronium hexafluorophosphate (HATU), O-benzotriazol-1-yl-N, N, N', N'-tetramethyluronium Phosphates such as hexafluorophosphate (HBTU);
DMT-MM is preferable.

  Examples of the base used include triethylamine, diisopropylethylamine, pyridine, DMAP, 2,6-lutidine, DABCO, and the like, and preferably diisopropylethylamine.

  Examples of the solvent used in the reaction with the compound (11) include alcohols, tetrahydrofuran, dioxane, dimethylformamide, dimethylacetamide, etc., preferably alcohols or dimethylformamide, more preferably dimethylformamide. is there.

  The reaction temperature in the reaction with the compound (11) is 0 to 100 ° C, preferably 0 to 50 ° C.

The reaction time in the reaction with the compound (11) is 30 minutes to 96 hours, preferably 1 to 12 hours.
[Method E]

  Method E is a method for producing compound (14) by removing the Boc group from compound (8) and then reacting with compound (13) that can be produced with reference to WO2006 / 4142 and the like.

  Removal of the Boc group can be carried out in the same manner as the removal of the Boc group in Method C.

  Examples of the base used include triethylamine, diisopropylethylamine, pyridine, DMAP, 2,6-lutidine, DABCO, sodium carbonate, potassium carbonate, cesium carbonate and the like, and potassium carbonate is preferable.

  Examples of the solvent used in the reaction with the compound (13) include tetrahydrofuran, dioxane, cyclopentylmethyl ether, dimethylformamide, dimethylacetamide, toluene and the like, and preferably 1,4-dioxane.

  The reaction temperature in the reaction with the compound (13) is 0 to 150 ° C, preferably 10 to 100 ° C.

The reaction time in the reaction with the compound (13) is 30 minutes to 24 hours, preferably 1 to 12 hours.
[F method]

  Another method for producing the compound (14) is Method F. Method F was obtained in steps F-1 and F-1 in which the Boc group in compound (8) was removed and then reacted with 1,1′-carbonyldiimidazole to produce compound (15). This is a method comprising F-2 step of producing compound (14) by reacting compound (15) with compound (16).

(F-1 process)
Removal of the Boc group can be carried out in the same manner as the removal of the Boc group in Method C.

  Examples of the solvent used in the reaction with 1,1′-carbonyldiimidazole include dichloromethane, dichloroethane, chloroform, tetrahydrofuran, dioxane, cyclopentylmethyl ether, toluene, and preferably tetrahydrofuran.

  The reaction temperature in the reaction with 1,1′-carbonyldiimidazole is 0 to 100 ° C., preferably 10 to 50 ° C.

  The reaction time in the reaction with 1,1′-carbonyldiimidazole is 10 minutes to 12 hours, preferably 30 minutes to 6 hours.

(Process F-2)
Examples of the solvent used include dichloromethane, dichloroethane, chloroform, tetrahydrofuran, dioxane, cyclopentyl methyl ether, toluene, and the like, and preferably tetrahydrofuran.

  The reaction temperature is −20 to 100 ° C., preferably 0 to 50 ° C.

  The reaction time is 10 minutes to 12 hours, preferably 30 minutes to 6 hours.

[G method]

  Method G is a method for producing the compound (18) by removing the Boc group from the compound (8) and then reacting with the compound (17).

  Removal of the Boc group can be carried out in the same manner as the removal of the Boc group in Method C.

  Examples of the solvent used in the reaction with the compound (17) include dichloromethane, dichloroethane, chloroform, toluene and the like, preferably dichloromethane.

  The reaction temperature in the reaction with the compound (17) is −10 to 60 ° C., preferably 0 to 40 ° C.

  The reaction time in the reaction with the compound (17) is 10 minutes to 12 hours, preferably 20 minutes to 6 hours.

  The compound represented by the general formula (I) or (II) obtained by the above method, or a pharmaceutically acceptable salt thereof is type 1 diabetes, type 2 diabetes, gestational diabetes, hyperglycemia due to other factors, glucose tolerance Impaired glucose tolerance (IGT), diabetes related diseases (eg obesity, hyperlipidemia, hypercholesterolemia, dyslipidemia, hypertension, fatty liver, metabolic syndrome, edema, heart failure, angina, myocardium Used for the treatment and / or prevention of infarction, arteriosclerosis, hyperuricemia, gout etc.) or diabetic complications (eg retinopathy, nephropathy, neuropathy, cataract, foot gangrene, infection, ketosis, etc.) It is useful as an active ingredient of the obtained pharmaceutical composition.

  When administered to a mammal (eg, human, horse, cow, pig, etc., preferably human), the pharmaceutical composition of the present invention may be administered systemically or locally, orally or parenterally.

  The pharmaceutical composition of the present invention can be prepared by selecting an appropriate form according to the administration method and preparing various preparations that are usually used.

  Examples of the form of the oral pharmaceutical composition include tablets, pills, powders, granules, capsules, solutions, suspensions, emulsions, syrups, elixirs and the like. The preparation of such a pharmaceutical composition includes excipients, binders, disintegrants, lubricants, swelling agents, swelling aids, coating agents, plasticizers, stabilizers, antiseptics, anti-fouling agents, ordinarily used as additives. An oxidizing agent, a coloring agent, a solubilizing agent, a suspending agent, an emulsifying agent, a sweetening agent, a preservative, a buffering agent, a diluent, a wetting agent and the like are appropriately selected as necessary, and can be produced according to a conventional method.

  The forms of parenteral pharmaceutical compositions include injections, ointments, gels, creams, poultices, patches, sprays, inhalants, sprays, eye drops, nasal drops, suppositories, and inhalations. Agents and the like. Preparation of the pharmaceutical composition in such a form involves the use of stabilizers, preservatives, solubilizers, moisturizers, preservatives, antioxidants, flavoring agents, gelling agents, neutralizing agents, dissolution, which are usually used as additives. Adjuvants, buffers, isotonic agents, surfactants, colorants, buffering agents, thickeners, wetting agents, fillers, absorption enhancers, suspending agents, binders, etc. are selected as necessary. However, it can be produced according to a conventional method.

  The dosage of the pharmaceutical composition of the present invention varies depending on symptoms, age, body weight, etc., but in the case of oral administration, one to several times a day, once for each adult, the general formula (I) or (II) Or a pharmaceutically acceptable salt equivalent amount thereof represented by 1 to 2000 mg, preferably 1 to 400 mg. In the case of parenteral administration, 1 to several times a day, once per adult, The compound represented by the general formula (I) or (II) or a pharmaceutically acceptable salt equivalent thereof is 0.01 to 500 mg, preferably 0.1 to 300 mg.

  Hereinafter, although a reference example, a manufacture example, an Example, and a test example are given and this invention is demonstrated further in detail, the scope of the present invention is not limited to these.

  In the following, hexane represents n-hexane, THF represents tetrahydrofuran, and DMF represents dimethylformamide.

Reference Example 1 5- (isobutylthio) indoline Sodium sulfide nonahydrate (1.84 g, 7.66 mmol) in water (2.8 mL) was added to indoline-5-yl thiocyanate (reference J. Med. Chem., 1998, Vol. 41, p. 1598, 1.33 g, 7.55 mmol) in ethanol (14 mL) was added, and the mixture was stirred at 50 ° C. for 2 hours. A solution of isobutyl iodide (1.2 mL, 10.4 mmol) in ethanol (2.4 mL) was added to the reaction mixture, and the mixture was stirred at 50 ° C. for 2 hr. Water was added to the reaction mixture, and the mixture was extracted 3 times with ether. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 90: 10 → 80: 20 → 55: 45, v / v) to give the title brown oily compound (0.65 g, yield: 41%). Obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 7.20 (1H, s), 7.12-7.10 (1H, m), 6.55 (1H, d, J = 8Hz), 3.80 (1H, brs), 3.57 (2H, t, J = 8Hz), 3.01 (2H, t, J = 8Hz), 2.66 (2H, d, J = 7Hz), 1.82-1.72 (1H, m), 0.99 (6H, d, J = 7Hz).

(Reference Example 2) 5- (Ethylthio) indoline In place of isobutyl iodide of the method described in Reference Example 1, the same reaction was carried out using iodoethane, and the title brown oily compound (125 mg, yield: 61%) Got.
¹ H-NMR (400 MHz, DMSO-d ₆ ) δ ppm: 7.08 (1H, s), 6.97 (1H, d, J = 8 Hz), 6.43 (1H, s), 5.63 (1H, s), 3.42 (2H, td, J = 8Hz, 1Hz), 2.89 (2H, t, J = 8Hz), 2.71 (2H, q, J = 7Hz), 1.12 (3H, t, J = 7Hz).

(Reference Example 3) 5- (Isopropylthio) indoline Instead of isobutyl iodide in the method described in Reference Example 1, 2-iodopropane was used in the same reaction to give the title brown oily compound (109 mg, yield). : 50%).
¹ H-NMR (400 MHz, DMSO-d ₆ ) δ ppm: 7.08 (1H, s), 6.99 (1H, d, J = 8 Hz), 6.43 (1H, d, J = 8 Hz), 5.69 (1H, brs), 3.42 (2H, t, J = 9Hz), 3.05 (1H, sept, J = 6Hz), 2.89 (2H, t, J = 8Hz), 1.14 (6H, d, J = 6Hz).

(Reference Example 4) 5- (Propylthio) indoline In place of isobutyl iodide in the method described in Reference Example 1, 1-iodopropane (122 μL, 1.25 mmol) was used in the same reaction to give the title brown oily compound (151 mg, yield: 69%) was obtained.
¹ H-NMR (400 MHz, DMSO-d ₆ ) δ ppm: 7.07 (1H, s), 6.97 (1H, d, J = 8 Hz), 6.42 (1H, d, J = 8 Hz), 5.62 (1H, brs), 3.42 (2H, t, J = 8Hz), 2.88 (2H, t, J = 8Hz), 2.68 (2H, t, J = 7Hz), 1.47 (2H, dt, J = 14Hz, 7Hz), 0.92 (3H, t, J = 7Hz).

Reference Example 5 5-[(3-Chloropropyl) thio] indoline Instead of isobutyl iodide in the method described in Reference Example 1, 1-chloro-3-iodopropane (344 μL, 3.20 mmol) was used. The reaction was conducted in the same manner to obtain the title pale yellow oily compound (51.3 mg, yield: 28%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 7.20 (1H, m), 7.12 (1H, m), 6.56 (1H, d, J = 8Hz), 3.65 (2H, t, J = 6Hz), 3.58 ( 2H, t, J = 8Hz), 3.02 (2H, t, J = 9Hz), 2.89 (2H, t, J = 7Hz), 1.99 (2H, m, J = 6Hz).

(Reference Example 6) 5- (Cyclopentylthio) indoline In place of isobutyl iodide in the method described in Reference Example 1, iodocyclopentane (457 μL, 3.95 mmol) was used for the same reaction to give the title colorless oily compound (311 mg, yield: 40%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 7.35-7.06 (2H, m), 6.54 (1H, m), 3.82 (1H, brs), 3.57 (2H, m), 3.01 (2H, m), 2.76 (1H, m), 2.00-1.16 (8H, m).

(Reference Example 7) 5-{[2- (Benzyloxy) ethyl] thio} indoline Instead of isobutyl iodide in the method described in Reference Example 1, benzyl (2-iodoethyl) ether (literature Tetrahedron Lett., 1987) The same reaction was carried out using the compound described in Y., 28, p. 3091, 962 mg, 3.67 mmol) to obtain the title light green oily compound (338 mg, yield: 48%).
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 7.36-7.25 (5H, m), 7.20 (1H, m), 7.12 (1H, m), 6.53 (1H, d, J = 8Hz), 4.51 (2H, s), 3.80 (1H, brs), 3.64-3.53 (4H, m), 3.03-2.93 (4H, m).

(Reference Example 8) 5- (cyclobutylthio) indoline and 5-[(cyclopropylmethyl) thio] indoline In place of isobutyl iodide in the method described in Reference Example 1, the reaction was similarly carried out using bromocyclobutane. To obtain a crude product. The obtained crude product was purified by preparative HPLC (Inertsil ODS-3 (30 mmi.d. × 250 mm); GL Science, water: acetonitrile = 95: 5 → 0: 100 (gradient)) to give a colorless oil 5-[(Cyclopropylmethyl) thio] indoline as a compound (less polar, 81.4 mg: 13% yield) and 5- (cyclobutylthio) indoline as a colorless oily compound (polar, 62.9 mg, yield: 10) %).
5-[(Cyclopropylmethyl) thio] indoline
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 7.24 (1H, s), 7.16 (1H, d, J = 8Hz), 6.57 (1H, d, J = 8Hz), 3.58 (2H, t, J = 8Hz ), 3.02 (2H, t, J = 8Hz), 2.70 (2H, d, J = 7Hz), 1.04-0.95 (1H, m), 0.55-0.50 (2H, m), 0.20-0.16 (2H, m) .
5- (Cyclobutylthio) indoline
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 7.16 (1H, s), 7.08 (1H, d, J = 8 Hz), 6.57 (1H, d, J = 8 Hz), 3.86 (1H, brs), 3.69- 3.56 (3H, m), 3.02 (2H, t, J = 8Hz), 2.32-2.24 (2H, m), 2.07-1.97 (2H, m), 1.91-1.87 (2H, m).

Reference Example 9 6-Fluoro-5- (methylthio) indoline
To a solution of 6-fluoroindoline (600 mg, 4.37 mmol) and potassium thiocyanate (1.28 g, 13.1 mmol) in methanol (13.2 mL) at 0 ° C. with bromine (235 μL, 9.19 mmol) in saturated sodium bromide-methanol ( 3.0 mL) solution was added and stirred for 1.5 hours. Water was added to the reaction solution at 0 ° C., neutralized with sodium carbonate, and extracted three times with ethanol. The organic layer was washed with water and dried over anhydrous sodium sulfate, and then the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 19: 1 → 4: 1, v / v) to give a colorless oily compound.

Using the obtained compound, the same reaction was carried out using iodomethane in place of isobutyl iodide in the method described in Reference Example 1 to obtain the title brown oily compound (472 mg, yield: 59%). .
¹ H-NMR (400 MHz, DMSO-d ₆ ) δppm: 7.07 (1H, s), 6.28 (1H, d, J = 11 Hz), 5.91 (1H, brs), 3.49-3.43 (2H, m), 2.87 ( 2H, t, J = 8Hz), 2.29 (3H, s).

Reference Example 10 6-Methoxy-5- (methylthio) indoline
Using 6-methoxyindoline (compound described in J. Med. Chem., 2004, 47, p.5451, 1.29 g, 8.65 mmol), the reaction was carried out in the same manner as described in Reference Example 9. To obtain the title white foamy compound (535 mg, yield: 32%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 6.93 (1H, s), 6.20 (1H, s), 5.56 (1H, brs), 3.71 (3H, s), 3.41 (2H, t, J = 8Hz), 2.83 (2H, t, J = 8Hz), 2.22 (3H, s).

(Reference Example 11) 5- (isobutylsulfonyl) indoline hydrochloride Di (tert-butyl) dicarbonate (790 μL, 3.44 mmol) in a solution of the compound obtained in Reference Example 1 (0.65 g, 3.13 mmol) in dichloromethane (5 mL) And triethylamine (620 μL, 4.44 mmol) were added and stirred at room temperature for 18 hours. Saturated aqueous sodium hydrogen carbonate was added to the reaction mixture, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 90: 10 → 80: 20, v / v) to obtain a pale yellow oily compound.

  To a solution of the obtained compound in dichloromethane (20 mL), m-chloroperbenzoic acid (ca. 65%, 1.69 g, 6.37 mmol) was added at 0 ° C. and stirred for 1 hour. A 10% aqueous sodium sulfite solution was added to the reaction mixture, and the mixture was extracted 3 times with dichloromethane. The resulting organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Left. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 80: 20 → 60: 40, v / v) to obtain a white powdery compound.

A 4N hydrochloric acid-ethyl acetate solution (10 mL) was added to a suspension of the obtained compound in ethyl acetate (10 mL), and the mixture was stirred at room temperature for 1.5 hours and left for 14 hours. The reaction solution was filtered, and the resulting crude product was washed with a mixed solvent of ethyl acetate and diisopropyl ether to obtain the title light red powdery compound (445 mg, yield: 52%).
¹ H-NMR (400 MHz, DMSO-d ₆ ) δppm: 7.43-7.40 (2H, m), 6.71-6.57 (1H, m), 3.59-3.55 (1H, m), 3.04-3.00 (4H, m), 2.00-1.90 (1H, m), 0.95 (6H, d, J = 7Hz).

(Reference Example 12) 5- (Cyclopentylsulfonyl) indoline Using the compound (311 mg, 1.42 mmol) obtained in Reference Example 6, the reaction was carried out in the same manner as described in Reference Example 11, and N-Boc indoline intermediate Got the body.

Trifluoroacetic acid (5 mL) was added to a dichloromethane (20 mL) solution of the obtained compound, and the mixture was stirred at room temperature for 1 hour. The solvent was distilled off from the reaction solution under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane: ethyl acetate = 70: 30 → 50: 50, v / v) to give the title colorless oily compound (208 mg Yield: 58%).
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 7.55-7.50 (2H, m), 6.60 (1H, d, J = 9 Hz), 4.41 (1H, s), 3.70 (2H, t, J = 9 Hz), 3.44 (1H, m), 3.09 (2H, t, J = 9Hz), 2.02 (2H, m), 1.88 (2H, m), 1.74 (2H, m), 1.58 (2H, m).

(Reference Example 13) 5-{[2- (Benzyloxy) ethyl] sulfonyl} indoline Using the compound (338 mg, 1.18 mmol) obtained in Reference Example 7, the reaction was carried out in the same manner as described in Reference Example 12. The title white powdery compound (316 mg, yield: 65%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 7.54-5.48 (2H, m), 7.34-7.17 (5H, m), 6.57 (1H, d, J = 7Hz), 4.54 (1H, s), 4.42 ( 2H, s), 3.82 (2H, t, J = 6Hz), 3.64 (2H, t, J = 9Hz), 3.38 (2H, t, J = 6Hz), 3.00 (2H, t, J = 9Hz).

Reference Example 14 5-[(3-Chloropropyl) sulfonyl] indoline To a solution of the compound obtained in Reference Example 5 (230 mg, 1.01 mmol) in dichloromethane (10 mL) was added triethylamine (283 μL, 2.02 mmol), dicarbonate dicarbonate. (Tert-Butyl) (331 mg, 1.52 mmol) was added and stirred at room temperature for 40 minutes. Dimethylaminopyridine (25 mg, 0.245 mmol) was added to the reaction solution, and the mixture was stirred at room temperature for 1.5 hours. Di (tert-butyl) dicarbonate (110 mg, 0.504 mmol) was added to the reaction solution, and the mixture was stirred at room temperature for 30 minutes. A saturated aqueous ammonium chloride solution was added to the reaction solution, and the mixture was extracted twice with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 49: 1 → 4: 1, v / v) to give a colorless oily compound.

M-Chloroperbenzoic acid (428 mg, 2.48 mmol) was added to a dichloromethane (10 mL) solution of the obtained compound at 0 ° C., and the mixture was stirred at 0 ° C. for 1 hour. A saturated aqueous sodium sulfite solution was added to the reaction solution, followed by extraction three times with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 9: 1 → 1: 1, v / v) to obtain the title white powdery compound (193 mg).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 7.97 (1H, brs), 7.71 (1H, dd, J = 7Hz, 1Hz), 7.64 (1H, d, J = 1Hz), 4.07 (2H, t, J = 9Hz), 3.62 (2H, t, J = 6Hz), 3.23 (2H, t, J = 7Hz), 3.17 (2H, t, J = 9Hz), 2.19 (2H, m), 1.58 (9H, s) .

Reference Example 15 5- (Cyclopropylsulfonyl) indoline To a solution of the compound obtained in Reference Example 5 (80.2 mg, 0.223 mmol) in THF (5 mL) at −78 ° C., potassium hexamethyldisilazide (0.5M Toluene solution, 892 μL, 0.446 mmol) was added, and the mixture was stirred for 1 hour while warming to room temperature. Saturated aqueous ammonium chloride solution was added to the reaction solution, followed by extraction three times with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 7: 3, v / v) to obtain a white powdery compound.

Trifluoroacetic acid (1 mL) was added to a dichloromethane (4 mL) solution of the obtained compound, and the mixture was stirred at room temperature for 1 hour. The solvent was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane: ethyl acetate = 3: 2, v / v) to give the title white powdery compound (20.8 mg, yield). Rate: 42%).
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 7.58-7.50 (2H, m), 6.61 (1H, m), 4.16 (1H, s), 3.70 (2H, t, J = 8Hz), 3.09 (2H, t, J = 7Hz), 2.42 (1H, m), 1.28 (2H, m), 0.98 (2H, m).

Reference Example 16 5-[(Cyclopropylmethyl) sulfonyl] indoline Using the compound obtained in Reference Example 8 (81.4 mg, 0.396 mmol), the reaction was carried out in the same manner as in Reference Example 11, and the title white powdery compound (57 mg, yield: 59%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 7.51 (1H, brs), 7.42 (1H, s), 7.41 (1H, d, J = 9 Hz), 6.57 (1H, d, J = 8 Hz), 3.57 (2H, t, J = 8Hz), 3.04 (2H, d, J = 7Hz), 3.01 (2H, t, J = 9Hz), 0.86-0.77 (1H, m), 0.45-0.42 (2H, m) , 0.12-0.09 (2H, m).

Reference Example 17 5- (Cyclobutylsulfonyl) indoline Using the compound obtained in Reference Example 8 (62.9 mg, 0.306 mmol), the reaction was carried out in the same manner as in Reference Example 11, and the title white powdery compound (57.0 mg Yield: 69%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 7.37 (1H, s), 7.36 (1H, d, J = 7 Hz), 6.55 (1H, d, J = 8 Hz), 6.42 (1H, brs), 3.87 (1H, quint, J = 8Hz), 3.56 (2H, t, J = 8Hz), 3.00 (2H, t, J = 9Hz), 2.29-2.21 (2H, m), 2.11-2.04 (2H, m) , 1.92-1.77 (2H, m).

Reference Example 18 1-acetyl-N, N-dibenzylindoline-5-sulfonamide
Dibenzylamine (302 μL, 1.57 mmol) was added to a solution of 1-acetylindoline-5-sulfonyl chloride (273 mg, 1.05 mmol) in dichloromethane (10 mL), and the mixture was stirred at room temperature for 1 hour. Triethylamine (441 μL, 3.15 mmol) was added to the reaction solution, and the mixture was stirred at room temperature for 20 minutes. Triethylamine (147 μL, 1.05 mmol) and dibenzylamine (100 μL, 0.521 mmol) were added to the reaction solution, and the mixture was stirred overnight at room temperature. Water was added to the reaction solution, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography ((i) hexane: ethyl acetate = 1: 1, v / v; (ii) ethyl acetate) to obtain a white powdery compound.

To a solution of the obtained compound in methanol (10 mL) was added potassium hydroxide (277 mg, 4.94 mmol), and the mixture was stirred for 12.5 hours while heating under reflux. Saturated ammonium chloride was added to the reaction solution, followed by extraction three times with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 3: 2, v / v) to obtain the title white powdery compound (386 mg, yield: 100%).
¹ H-NMR (500 MHz, CDCl ₃ ) δ ppm: 7.54 (1H, d, J = 8 Hz), 7.49 (1H, s), 7.25-7.18 (6H, m), 7.13-7.05 (4H, m), 6.58 ( 1H, dd, J = 8Hz, 1Hz), 4.28 (4H, s), 4.18 (1H, brs), 3.69 (2H, td, J = 8Hz, 1Hz), 3.06 (2H, t, J = 8Hz).

Reference Example 19 1- (6-Chloropyrimidin-4-yl) -5- (methylsulfonyl) indoline
2,4-dichloropyrimidine (1.22 g, 8.19 mmol) and 5-methylthioindoline (compound described in literature J. Med. Chem., 1998, 41, p. 1598, 1.63 g, 9.86 mmol), Concentrated hydrochloric acid (810 μL, 9.86 mmol) was added to a mixed solution of acetone (12 mL) and water (3 mL), and the mixture was stirred at 80 ° C. for 1.5 hours. Saturated aqueous sodium hydrogen carbonate was added to the reaction solution, the precipitate was collected by filtration, and the resulting crude product was washed with water and diisopropyl ether to obtain a yellow powdery compound.

To a solution of the obtained compound in dichloromethane (95 mL), m-chloroperbenzoic acid (ca. 65%, 3.96 g, 14.9 mmol) was added at 0 ° C. and stirred for 2 hours. A 10% aqueous sodium sulfite solution was added to the reaction mixture, and the mixture was extracted 3 times with dichloromethane. The resulting organic layer was washed with saturated aqueous sodium hydrogen carbonate and saturated brine, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. Left. The obtained residue was washed with diisopropyl ether and a mixed solvent of ethyl acetate to obtain the title white powdery compound (2.18 g, yield: 86%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.67 (1H, s), 8.63 (1H, d, J = 9 Hz), 7.83 (1H, dd, J = 9 Hz, 2 Hz), 7.77 (1H, m), 6.68 (1H, s), 4.13 (2H, t, J = 9Hz), 3.37 (2H, t, J = 9Hz), 3.06 (3H, s).

Reference Example 20 1- (6-Chloropyrimidin-4-yl) -5- (ethylsulfonyl) indoline The compound obtained in Reference Example 2 (120 mg, 0.669 mmol) was used to describe in Reference Example 19. The reaction was performed in the same manner as in the method to obtain the title white powdery compound (122 mg, yield: 56%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.69 (1H, s), 8.59 (1H, d, J = 9 Hz), 7.74 (2H, brs), 7.11 (1H, s), 4.17 (2H, t, J = 9Hz), 3.32 (2H, t, J = 9Hz), 3.23 (2H, q, J = 7Hz), 1.10 (3H, t, J = 7Hz).

Reference Example 21 1- (6-Chloropyrimidin-4-yl) -5- (propylsulfonyl) indoline The compound obtained in Reference Example 4 (148 mg, 0.766 mmol) was used to describe in Reference Example 19. The reaction was performed in the same manner as in the method to obtain the title white foamy compound (125 mg, yield: 49%).
¹ H-NMR (400 MHz, DMSO-d ₆ ) δ ppm: 8.69 (1H, s), 8.59 (1H, d, J = 9 Hz), 7.76-7.73 (2H, m), 7.11 (1H, s), 4.17 ( 2H, t, J = 9Hz), 3.34-3.30 (2H, m), 3.24-3.20 (2H, m), 1.61-1.51 (2H, m), 0.91 (3H, t, J = 7Hz).

Reference Example 22 1- (6-Chloropyrimidin-4-yl) -5- (isopropylsulfonyl) indoline Using 5- (isopropylthio) indoline (100 mg, 0.517 mmol) prepared in Reference Example 3, The reaction was conducted in the same manner as described in Example 19 to obtain the title white powdery compound (63 mg, yield: 38%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.69 (1H, s), 8.60 (1H, d, J = 9 Hz), 7.71 (1H, d, J = 9 Hz), 7.70 (1H, s), 7.11 (1H, s), 4.18 (2H, t, J = 9Hz), 3.37-3.31 (3H, m), 1.16 (6H, d, J = 7Hz).

Reference Example 23 1- (6-Chloropyrimidin-4-yl) -6-fluoro-5- (methylsulfonyl) indoline Using the compound obtained in Reference Example 9 (250 mg, 1.36 mmol), Reference Example 19 To give the title white foamy compound (289 mg, yield: 65%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.73 (1H, s), 8.40 (1H, d, J = 13 Hz), 7.68 (1H, d, J = 7 Hz), 7.16 (1H, s), 4.20 (2H, t, J = 9Hz), 3.32 (3H, s), 3.32-3.26 (2H, m).

Reference Example 24 6-Chloro-1- (6-chloropyrimidin-4-yl) -5- (methylsulfonyl) indoline
It was described in Reference Example 19 using 6-chloro-5- (methylthio) indoline (compound described in literature J. Med. Chem., 1997, 40, p. 3494, 380 mg, 1.90 mmol). The reaction was conducted in the same manner as in the method to obtain the title white powdery compound (454 mg, yield: 69%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.76 (1H, s), 8.67 (1H, s), 7.89 (1H, s), 7.15 (1H, s), 4.19 (2H, t, J = 9Hz), 3.32 (3H, s), 3.31-3.29 (2H, m).

Reference Example 25 1- (6-Chloropyrimidin-4-yl) -6-methoxy-5- (methylsulfonyl) indoline Using the compound obtained in Reference Example 10 (532 mg, 2.72 mmol), Reference Example 19 To give the title white powdery compound (421 mg, yield: 43%).
¹ H-NMR (400 MHz, DMSO-d ₆ ) δ ppm: 8.70 (1H, s), 8.40 (1H, s), 7.63 (1H, s), 7.10 (1H, s), 4.16 (2H, t, J = 9Hz), 3.97 (3H, s), 3.21 (2H, t, J = 9Hz), 3.19 (3H, s).

Reference Example 26 1- (6-Chloro-2-methylpyrimidin-4-yl) -5- (methylsulfonyl) indoline
5-methylthioindoline (compound described in J. Med. Chem., 1998, 41, p. 1598, 454 mg, 2.75 mmol) and 4,6-dichloro-2-methylpyrimidine (672 mg, 4.12 mmol) Was used in the same manner as described in Reference Example 19 to obtain the title white powdery compound (223 mg, yield: 25%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.64 (1H, d, J = 9 Hz), 7.83 (1H, d, J = 9 Hz), 7.76 (1H, s), 6.51 (1H, s), 4.11 ( 2H, t, J = 9Hz), 3.35 (2H, t, J = 9Hz), 3.05 (3H, s), 2.66 (3H, s).

Reference Example 27 5- (Methylsulfonyl) -1- [6- (piperidin-4-yloxy) pyrimidin-4-yl] indoline hydrochloride Acetic acid of the compound obtained in Production Example 1 (1.04 g, 2.19 mmol) A 4N hydrochloric acid-ethyl acetate solution (20 mL) was added to the ethyl (10 mL) suspension, and the mixture was stirred at room temperature for 1 hour. The reaction solution was filtered, and the resulting crude product was washed with ethyl acetate to obtain the title white powdery compound (898 mg, yield: equivalent).
¹ H-NMR (400 MHz, DMSO-d ₆ ) δ ppm: 8.96 (2H, brs), 8.56-8.53 (2H, m), 7.75-7.73 (2H, m), 6.28 (1H, s), 5.36-5.31 ( 1H, m), 6.28 (1H, s), 5.36-5.31 (1H, m), 4.10 (2H, t, J = 9Hz), 3.29 (2H, t, J = 9Hz), 3.27-3.23 (2H, m ), 3.15 (3H, s), 3.15-3.10 (2H, m), 2.19-2.14 (2H, m), 1.95-1.87 (2H, m).

Reference Example 28 5- (Methylsulfonyl) -1- [6- (piperidin-4-yloxy) pyrimidin-4-yl] indoline Ethyl acetate (3.15) of the compound obtained in Production Example 1 (630 mg, 1.33 mmol) To the suspension was added 4N hydrochloric acid-ethyl acetate solution (9.45 mL) at 0 ° C., and the mixture was stirred for 1 hour. The solvent was distilled off under reduced pressure. To the obtained residue was added 1N aqueous sodium hydroxide solution (20 mL), and the precipitate was collected by filtration and washed with water to give the title white powdery compound (489 mg, yield: 99%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.54 (1H, d, J = 9 Hz), 8.52 (1H, s), 7.73 (2H, s), 6.20 (1H, s), 5.15-5.10 ( 1H, m), 4.09 (2H, t, J = 9Hz), 3.28 (2H, t, J = 9Hz), 3.14 (3H, s), 2.97-2.94 (2H, m), 2.56 (2H, t, J = 10Hz), 1.95-1.93 (2H, m), 1.53-1.45 (2H, m).

Reference Example 29 1- (6-{[1- (1H-imidazol-1-ylcarbonyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (methylsulfonyl) indoline In Reference Example 28 1,1′-carbonyldiimidazole (67.0 mg, 0.413 mmol) was added to a THF (2.06 mL) solution of the obtained compound (103 mg, 0.275 mmol), and the mixture was stirred at room temperature for 1 hour. The solvent of the reaction solution was distilled off under reduced pressure, and water was added to the residue and stirred. The precipitate was collected by filtration and washed with water to give the title white powdery compound (105 mg, yield: 82%) Got.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, s), 8.55 (1H, d, J = 9 Hz), 8.05 (1H, s), 7.74 (1H, s), 7.73 (1H, d, J = 7Hz), 7.49 (1H, s), 7.04 (1H, s), 6.25 (1H, s), 5.39-5.35 (1H, m), 4.10 (2H, t, J = 9Hz), 3.79- 3.74 (2H, m), 3.49-3.44 (2H, m), 3.30-3.27 (2H, m), 3.15 (3H, s), 2.13-2.07 (2H, m), 1.83-1.75 (2H, m).

Reference Example 30 5- (Ethylsulfonyl) -1- [6- (piperidin-4-yloxy) pyrimidin-4-yl] indoline Reference using the compound (2.58 g, 5.58 mmol) obtained in Production Example 30 The reaction was conducted in the same manner as described in Example 28 to obtain the title white powdery compound (1.72 g, yield: 79%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, d, J = 9 Hz), 8.52 (1H, s), 7.69 (1H, d, J = 9 Hz), 7.68 (1H, s), 6.21 (1H, s), 5.15-5.10 (1H, m), 4.09 (2H, t, J = 9Hz), 3.30-3.26 (3H, m), 3.22 (2H, q, J = 7Hz), 2.96 (2H , dt, J = 13Hz, 4Hz), 2.57 (2H, td, J = 11Hz, 1Hz), 1.97-1.94 (2H, m), 1.49 (2H, t, J = 9Hz, 4Hz), 1.10 (3H, t , J = 7Hz).

Reference Example 31 5- (Ethylsulfonyl) -1- (6-{[1- (1H-imidazol-1-ylcarbonyl) piperidin-4-yl] oxy} pyrimidin-4-yl) indoline In Reference Example 30 The obtained compound (1.96 g, 5.05 mmol) was used for reaction in the same manner as described in Reference Example 29 to obtain the title white powdery compound (1.98 g, yield: 81%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, d, J = 9 Hz), 8.56 (1H, s), 8.05 (1H, s), 7.69 (1H, d, J = 7 Hz), 7.68 (1H, s), 7.49 (1H, s), 7.04 (1H, s), 6.25 (1H, s), 5.40-5.35 (1H, m), 4.10 (2H, t, J = 9Hz), 3.79- 3.74 (2H, m), 3.49-3.44 (2H, m), 3.29 (2H, t, J = 9Hz), 3.21 (2H, q, J = 7Hz), 2.13-2.08 (2H, m), 1.83-1.75 (2H, m), 1.10 (3H, t, J = 7Hz).

Reference Example 32 1- [6- (Piperidin-4-yloxy) pyrimidin-4-yl] -5- (propylsulfonyl) indoline hydrochloride Using the compound (1.19 g, 2.37 mmol) obtained in Production Example 36 Then, the reaction was carried out in the same manner as described in Reference Example 27 to obtain the title white powdery compound (1.07 g, yield: equivalent).
¹ H-NMR (400 MHz, DMSO-d ₆ ) δ ppm: 8.96 (2H, brs), 8.56-8.54 (2H, m), 7.71-7.68 (2H, m), 6.28 (1H, s), 5.36-5.30 ( 1H, m), 6.28 (1H, s), 5.36-5.30 (1H, m), 4.10 (2H, t, J = 9Hz), 3.31-3.08 (8H, m), 2.19-2.14 (2H, m), 1.99-1.87 (2H, m), 1.60-1.50 (2H, m), 0.91 (3H, t, J = 7Hz).

Reference Example 33 1- (6-{[1- (1H-imidazol-1-ylcarbonyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (propylsulfonyl) indoline In Reference Example 32 Triethylamine (286 μL, 2.05 mmol) and 1,1′-carbonyldiimidazole (249 mg, 1.54 mmol) were added to a THF (9.00 mL) solution of the obtained compound (450 mg, 1.03 mmol), and the mixture was stirred at room temperature for 3 hours. . The solvent of the reaction solution was distilled off under reduced pressure, water was added to the residue and stirred. The precipitate was collected by filtration and washed with water to give the title white powdery compound (291 mg, yield: 57%). Obtained.
¹ H-NMR (400 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, s), 8.55 (1H, d, J = 9 Hz), 8.05 (1H, s), 7.69 (1H, d, J = 7 Hz), 7.68 (1H, s), 7.49 (1H, s), 7.05 (1H, s), 6.25 (1H, s), 5.40-5.34 (1H, m), 4.10 (2H, t, J = 9Hz), 3.80- 3.74 (2H, m), 3.49-3.43 (2H, m), 3.31-3.27 (2H, m), 3.21-3.18 (2H, m), 2.14-2.07 (2H, m), 1.84-1.76 (2H, m ), 1.60-1.51 (2H, m), 0.91 (3H, t, J = 7Hz).

Reference Example 34 1- [6- (piperidin-4-yloxy) pyrimidin-4-yl] -5- (propylsulfonyl) indoline Compound (180 mg, 0.363 mmol) of ethylene glycol (3.6 To the solution, 2N aqueous sodium hydroxide solution (363 mL, 0.726 mmol) was added and stirred at 100 ° C. for 2.5 hours. Water was added to the reaction solution and extracted three times with ethyl acetate. The obtained organic layer was washed with water, dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure to give the title white powdery compound (106 mg, yield: 73%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.54 (1H, d, J = 9 Hz), 8.53 (1H, s,), 7.69 (1H, d, J = 6 Hz), 7.68 (1H, s) , 6.21 (1H, s), 5.18-5.11 (1H, m), 4.09 (2H, t, J = 9Hz), 3.21-3.17 (4H, m), 2.99 (2H, dt, J = 13Hz, 5Hz), 2.67-2.60 (2H, m), 2.00-1.95 (2H, m), 1.60-1.49 (4H, m), 0.91 (3H, t, J = 7Hz).

Reference Example 35 1- (6-{[1- (1H-imidazol-1-ylcarbonyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (isopropylsulfonyl) indoline In Production Example 32 Using the obtained compound (272 mg, 0.541 mmol), the reaction was carried out in the same manner as described in Reference Example 28 to obtain a white powdery compound.

The obtained compound was used in the same manner as in the method described in Reference Example 33 to obtain the title white powdery compound (240 mg, yield: 91%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.57 (1H, d, J = 9 Hz), 8.56 (1H, s), 8.05 (1H, s), 7.66 (1H, d, J = 8 Hz), 7.65 (1H, s), 7.49 (1H, s), 7.04 (1H, s), 6.25 (1H, s), 5.40-5.35 (1H, m), 4.10 (2H, t, J = 9Hz), 3.79- 3.74 (2H, m), 3.49-3.44 (2H, m), 3.31-3.28 (3H, m), 2.13-2.07 (2H, m), 1.83-1.75 (2H, m), 1.16 (6H, d, J = 7Hz).

Reference Example 36 5- (isobutylsulfonyl) -1- [6- (piperidin-4-yloxy) pyrimidin-4-yl] indoline Using the compound obtained in Production Example 25 (2.08 g, 4.03 mmol), The reaction was performed in the same manner as described in Reference Example 30 to obtain the title white powdery compound (1.60 g, yield: 95%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.54 (1H, d, J = 9 Hz), 8.52 (1H, s), 7.70-7.69 (2H, m), 6.20 (1H, s), 5.15- 5.10 (1H, m), 4.09 (2H, t, J = 9Hz), 3.28 (2H, t, J = 9Hz), 3.13 (2H, d, J = 7Hz), 2.98-2.94 (2H, m), 2.59 -2.54 (2H, m), 2.03-1.93 (3H, m), 1.53-1.45 (2H, m), 0.97 (6H, d, J = 6Hz).

Reference Example 37 1- (6-{[1- (1H-imidazol-1-ylcarbonyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (isobutylsulfonyl) indoline In Reference Example 36 The obtained compound (900 mg, 2.16 mmol) was used in the same manner as in the method described in Reference Example 33 to obtain the title white powdery compound (965 mg, yield: 88%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, s), 8.55 (1H, d, J = 9 Hz), 8.05 (1H, s), 7.71 (1H, d, J = 9 Hz), 7.70 (1H, s), 7.49 (1H, s), 7.04 (1H, s), 6.25 (1H, s), 5.40-5.35 (1H, m), 4.10 (2H, t, J = 9Hz), 3.79- 3.74 (2H, m), 3.49-3.44 (2H, m), 3.31-3.27 (2H, m), 3.13 (2H, d, J = 6Hz), 2.13-2.07 (2H, m), 2.03-1.95 (1H , m), 1.83-1.77 (2H, m), 0.96 (6H, d, J = 7Hz).

Reference Example 38 5-[(Cyclopropylmethyl) sulfonyl] -1- [6- (piperidin-4-yloxy) pyrimidin-4-yl] indoline Compound obtained in Production Example 56 (1.36 g, 2.64 mmol) Was used in the same manner as described in Reference Example 30 to obtain a white powdery compound (621 mg, yield: 57%).
¹ H-NMR (400 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, d, J = 9 Hz), 8.52 (1H, s,), 7.69 (1H, d, J = 8 Hz), 7.68 (1H, s) , 6.20 (1H, s), 5.16-5.09 (1H, m), 4.09 (2H, t, J = 9Hz), 3.28 (2H, t, J = 9Hz), 3.17 (2H, d, J = 7Hz), 2.96 (2H, dt, J = 13Hz, 4Hz), 2.60-2.54 (2H, m), 1.98-1.92 (2H, m), 1.54-1.45 (2H, m), 0.88-0.79 (1H, m), 0.47 -0.43 (2H, m), 0.13-0.09 (2H, m).

Reference Example 39 5-[(Cyclopropylmethyl) sulfonyl] -1- (6-{[1- (1H-imidazol-1-ylcarbonyl) piperidin-4-yl] oxy} pyrimidin-4-yl) indoline Using the compound (122 mg, 0.293 mmol) obtained in Reference Example 38, the reaction was carried out in the same manner as described in Reference Example 33 to obtain the title white powdery compound (121 mg, yield: 81%). .
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, s), 8.55 (1H, d, J = 9 Hz), 8.05 (1H, s), 7.70 (1H, d, J = 8 Hz), 7.69 (1H, s), 7.49 (1H, s), 7.04 (1H, s), 6.25 (1H, s), 5.40-5.35 (1H, m), 4.11 (2H, t, J = 9Hz), 3.79- 3.74 (2H, m), 3.49-3.44 (2H, m), 3.31-3.27 (2H, m), 3.18 (2H, d, J = 7Hz), 2.12-2.08 (2H, m), 1.83-1.77 (2H , m), 0.87-0.80 (1H, m), 0.47-0.43 (2H, m), 0.13-0.10 (2H, m).

Reference Example 40 tert-Butyl 4-[(6-chloro-5-methylpyrimidin-4-yl) oxy] piperidine-1-carboxylate
To a solution of 2,4-dichloro-3-methylpyrimidine (1.60 g, 9.82 mmol) in THF (20 mL) was added tert-butyl 4-hydroxypiperidine-1-carboxylate (2.47 g, 12.3 mmol) and tert-butoxypotassium ( 1.42 g, 12.7 mmol) was added and stirred for 2 hours. Water was added to the reaction mixture, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was washed with saturated brine, dried over anhydrous sodium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 80: 20 → 60: 40, v / v) to obtain the title colorless oily compound (3.07 g, yield: 95%).
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.39 (1H, s), 5.36-5.31 (1H, m), 3.75-3.69 (2H, m), 3.75-3.69 (2H, m), 3.39-3.33 ( 2H, m), 2.23 (3H, s), 2.02-1.95 (2H, m), 1.80-1.72 (2H, m), 1.48 (9H, s).

Reference Example 41 tert-butyl 4-[(6-chloropyrimidin-4-yl) oxy] piperidine-1-carboxylate
The reaction was carried out in the same manner as described in Reference Example 40 using 2,4-dichloropyrimidine (3.14 g, 15.6 mmol) to obtain the title white powdery compound (3.22 g, yield: 66%). .
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.55 (1H, s), 6.76 (1H, s), 5.34-5.28 (1H, m), 3.79-3.75 (2H, m), 3.32-3.26 (2H, m), 2.02-1.96 (2H, m), 1.78-1.69 (2H, m), 1.48 (9H, s).

Reference Example 42 Isopropyl 4-[(6-chloropyrimidin-4-yl) oxy] piperidine-1-carboxylate
Using 2,4-dichloropyrimidine (4.19 g, 28.1 mmol) instead of tert-butyl 4-hydroxypiperidine-1-carboxylate in the method described in Reference Example 40, isopropyl 4-hydroxypiperidine-1- The same reaction was carried out using carboxylate (5.25 g, 28.1 mmol) to obtain the title white powdery compound (5.88 g, yield: 70%).
¹ H-NMR (500 MHz, CDCl ₃ ) δ ppm: 8.55 (1H, s), 6.76 (1H, s), 5.35-5.31 (1H, m), 4.93 (1H, sept, J = 6Hz), 3.81-3.79 ( 2H, m), 3.36-3.31 (2H, m), 2.01-1.96 (2H, m), 1.78-1.72 (2H, m), 1.26 (6H, d, J = 6Hz).

Reference Example 43 tert-butyl 4-[(6-chloro-5-methoxypyrimidin-4-yl) oxy] piperidine-1-carboxylate
Using 2,4-dichloro-5-methoxypyrimidine (302 mg, 1.50 mmol) in the same manner as in the method described in Reference Example 40, the title white powdery compound (357 mg, yield: 69%) was obtained. Obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.27 (1H, s), 5.40-5.34 (1H, m), 3.91 (3H, s), 3.78-3.72 (2H, m), 3.39-3.33 (2H, m), 2.04-1.97 (2H, m), 1.48 (9H, s).

(Reference Example 44) tert-butyl 4-{[6- (5-{[2- (benzyloxy) ethyl] sulfonyl} indoline-1-yl) pyrimidin-4-yl] oxy} piperidine-1-carboxylate Reference Using the compound obtained in Example 41 (397 mg, 1.27 mmol) instead of 5-[(cyclopropylmethyl) sulfonyl] indoline of the method described in Preparation Example 56, the compound obtained in Reference Example 13 ( The same reaction was carried out using 316 mg (0.998 mmol) to obtain the title pale yellow oily compound (486 mg, yield: 82%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.53 (1H, d, J = 9Hz), 8.51 (1H, d, J = 1Hz), 7.74 (1H, dd, J = 9Hz, 2Hz), 7.63 (1H , m), 7.27-7.21 (3H, m), 7.18-7.13 (2H, m), 5.98 (1H, d, J = 1Hz), 5.32 (1H, m), 4.40 (2H, s), 3.99 (2H , t, J = 9Hz), 3.85 (2H, t, J = 6Hz), 3.81 (2H, m), 3.42 (2H, t, J = 6Hz), 3.28 (2H, m), 3.16 (2H, t, J = 9Hz), 2.01 (2H, m), 1.73 (2H, m), 1.48 (9H, s).

Reference Example 45 tert-Butyl 4-[(6- {5-[(dibenzylamino) sulfonyl] indoline-1-yl} pyrimidin-4-yl) oxy] piperidine-1-carboxylate Obtained in Reference Example 41 Using the obtained compound (185 mg, 0.591 mmol) instead of 5-[(cyclopropylmethyl) sulfonyl] indoline of the method described in Preparation 56, the compound obtained in Reference Example 18 (187 mg, 0.493 mmol) ) To give the title colorless oily compound (269 mg, yield: 83%).
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.52 (1H, d, J = 8 Hz), 8.51 (1H, s), 7.74 (1H, dd, J = 9 Hz, 2 Hz), 7.57 (1H, s), 7.25-7.20 (6H, m), 7.12-7.07 (4H, m), 5.98 (1H, s), 5.32 (1H, m), 4.31 (4H, s), 4.05 (2H, t, J = 9Hz), 3.81 (2H, m), 3.33-3.22 (4H, m), 2.01 (2H, m), 1.73 (2H, m), 1.48 (9H, s).

(Production Example 1) tert-butyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 8)
To a suspension of sodium hydride (mineral oil 63% dispersion, hereinafter referred to as sodium hydride (63%), 281 mg, 7.38 mmol) in THF (15 mL) at 0 ° C. in tert-butyl 4-hydroxypiperidine-1-carboxyl Lat (1.24 g, 6.16 mmol) was added and stirred at room temperature for 1 hour. To the reaction solution, the compound obtained in Reference Example 19 (1.87 g, 6.04 mmol) and THF (5 mL) were added and stirred at 70 ° C. for 4 hours. Saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography ((i) hexane: ethyl acetate = 50: 50, v / v; (ii) ethyl acetate), and the resulting crude product was washed with water and diisopropyl ether. The title white powdery compound (2.03 g, yield: 71%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, d, J = 1 Hz), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H , d, J = 2Hz), 5.98 (1H, d, J = 1Hz), 5.35-5.29 (1H, m), 4.07 (2H, t, J = 9Hz), 3.83-3.77 (2H, m), 3.33- 3.25 (4H, m), 3.04 (3H, s), 2.03-1.97 (2H, m), 1.77-1.69 (2H, m), 1.48 (9H, s);
MS (ESI) m / z: 475 [M + H] ⁺ .

(Production Example 2) Isopropyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 4)
Trifluoroacetic acid (1 mL) was added to a solution of the compound obtained in Production Example 1 (188 mg, 0.396 mmol) in dichloromethane (1 mL), and the mixture was stirred at room temperature for 2 hours. The reaction solution was evaporated under reduced pressure, and to a solution of the obtained residue in dichloromethane (2.5 mL) at 0 ° C. was added isopropyl chloroformate (68 μL, 0.60 mmol) and triethylamine (276 μL, 1.98 mmol) at room temperature. And stirred. After 1.5 hours, isopropyl chloroformate (100 μL, 0.878 mmol) and triethylamine (410 μL, 2.94 mmol) were added to the reaction solution, and the mixture was further stirred for 1 hour. Water was added to the reaction mixture, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography ((i) hexane: ethyl acetate = 70: 30 → 50: 50, v / v; (ii) ethyl acetate) to give the title white powdery compound (82.8 mg, Yield: 45%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.57 (1H, d, J = 9Hz), 8.51 (1H, d, J = 1Hz), 7.79 (1H, dd, J = 9Hz, 2Hz), 7.72 (1H , d, J = 2Hz), 5.98 (1H, d, J = 1Hz), 5.36-5.30 (1H, m), 4.94 (1H, sept, J = 6Hz), 4.07 (2H, t, J = 9Hz), 3.87-3.80 (2H, m), 3.36-3.29 (4H, m), 3.06 (3H, s), 2.03-1.98 (2H, m), 1.78-1.70 (2H, m), 1.26 (6H, d, J = 6Hz);
MS (ESI) m / z: 461 [M + H] ⁺ .

Production Example 3 2-Fluoroethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 34)
To a suspension of the compound obtained in Reference Example 27 (188 mg, 0.396 mmol) in dichloromethane (2 mL) was added diisopropylethylamine (178 μL, 0.997 mmol) and chloroformic acid (2-fluoroethyl) (33 μL, 0.350 mmol) at 0 ° C. And stirred at room temperature for 80 minutes. Water was added to the reaction mixture, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was subjected to silica gel column chromatography ((i) hexane: dichloromethane = 1: 1, v / v; (ii) hexane: ethyl acetate: dichloromethane = 2: 1: 2 → 1: 1: 1 → 2: 2 : 1, v / v; (iii) ethyl acetate: dichloromethane = 1: 1, v / v) to obtain the title white powdery compound (58.8 mg, yield: 38%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, d, J = 1 Hz), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H , d, J = 2Hz), 5.99 (1H, d, J = 1Hz), 5.38-5.35 (1H, m), 4.70-4.68 (1H, m), 4.58-4.56 (1H, m), 4.40-4.38 ( 1H, m), 4.33-4.31 (1H, m), 4.07 (2H, t, J = 9Hz), 3.88-3.82 (2H, m), 3.44-3.38 (2H, m), 3.32 (2H, t, J = 9Hz), 3.04 (3H, s), 2.06-2.00 (2H, m), 1.82-1.74 (2H, m);
MS (ESI) m / z: 465 [M + H] ⁺ .

(Production Example 4) 4- [4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidin-1-yl] -4-oxobutan-2-ol ( Exemplary compound number: 97)
To a suspension of the compound (224 mg, 0.545 mmol) obtained in Reference Example 27 in ethanol (3 mL), 3-hydroxybutanoic acid (61 μL, 0.66 mmol), diisopropylethylamine (102 μL, 0.571 mmol) and 4- (dimethoxy chloride) were added. -1,3,5-Triazin-2-yl) -4-methylmorpholinium (235 mg, 0.849 mmol) was added, and the mixture was stirred at room temperature for 3 days. Water was added to the reaction mixture, and the mixture was extracted 3 times with dichloromethane. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by thin layer silica gel chromatography (dichloromethane: methanol = 1: 1, v / v), and the resulting crude product was washed with diisopropyl ether to give the title off-white foam compound (174 mg, yield). Rate: 69%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.57 (1H, d, J = 9 Hz), 8.51 (1H, brs), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H, d, J = 2Hz), 5.99 (1H, brs), 5.42-5.37 (1H, m), 4.24-3.30 (9H, m), 3.04 (3H, s), 2.55-2.31 (2H, m), 2.08-2.00 (2H , m), 1.84-1.76 (2H, m), 1.24 (3H, d, J = 7Hz);
MS (FAB) m / z: 461 [M + H] ⁺ .

(Production Example 5) Benzyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 49)
To a solution of the compound obtained in Reference Example 28 (100 mg, 0.267 mmol) in dichloromethane (5 mL) was added diisopropylethylamine (93 μL, 0.53 mmol) and benzyl chloroformate (57 μL, 0.40 mmol) at 0 ° C. for 1 hour at room temperature. Stir. Water was added to the reaction solution, followed by extraction with dichloromethane three times. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 5: 1 → 1: 1, v / v), and the resulting crude product was washed with diisopropyl ether to give the title white powdery compound (67.3 mg, yield: 50%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, d, J = 1 Hz), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H , brs), 7.38-7.37 (5H, m), 5.98 (1H, d, J = 1Hz), 5.37-5.31 (1H, m), 5.15 (2H, m), 4.07 (2H, t, J = 9Hz) , 3.89-3.82 (2H, m), 3.43-3.37 (2H, m), 3.31 (2H, t, J = 9Hz), 3.04 (3H, s), 2.05-1.98 (2H, m), 1.80-1.72 ( 2H, m);
MS (CI) m / z: 509 [M + H] ⁺ .

(Production Example 6) Butyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary compound number: 5)
To a solution of the compound obtained in Reference Example 28 (100 mg, 0.267 mmol) in dichloromethane (5 mL) was added diisopropylethylamine (186 μL, 1.07 mmol) and butyl chloroformate (51 μL, 0.40 mmol) at 0 ° C. Stir. Water was added to the reaction solution, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 5: 1 → 1: 2, v / v) to obtain the title white powdery compound (53.9 mg, yield: 43%). .
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, d, J = 1 Hz), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H , brs), 5.98 (1H, d, J = 1Hz), 5.36-5.31 (1H, m), 4.10 (2H, t, J = 7Hz), 4.07 (2H, t, J = 9Hz), 3.87-3.80 ( 2H, m), 3.38-3.29 (4H, m), 3.04 (3H, s), 2.05-1.98 (2H, m), 1.79-1.71 (2H, m), 1.67-1.60 (2H, m), 1.45- 1.35 (2H, m), 0.95 (3H, t, J = 7Hz);
MS (CI) m / z: 475 [M + H] ⁺ .

Production Example 7 Propyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 3)
Using the compound (100 mg, 0.267 mmol) obtained in Reference Example 28, the same reaction was carried out using propyl chloroformate (45 μL, 0.40 mmol) instead of butyl chloroformate of the method described in Preparation Example 6. The title white powdery compound (58.6 mg, yield: 48%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9Hz), 8.52 (1H, d, J = 1Hz), 7.79 (1H, dd, J = 9Hz, 2Hz), 7.72 (1H , brs), 5.99 (1H, s), 5.37-5.32 (1H, m), 4.10-4.05 (4H, m), 3.05 (3H, s), 2.05-1.98 (2H, m), 1.80-1.63 (4H , m), 0.96 (3H, t, J = 7Hz);
MS (CI) m / z: 461 [M + H] ⁺ .

(Production Example 8) 2-methoxyethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 40)
Using the compound (100 mg, 0.267 mmol) obtained in Reference Example 28, the reaction was similarly carried out using methoxyethyl chloroformate (46 μL, 0.40 mmol) instead of butyl chloroformate in the method described in Preparation Example 6. The title white powdery compound (79.6 mg, yield: 63%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, brs), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H, brs), 5.99 (1H, s), 5.37-5.31 (1H, m), 4.28-4.25 (2H, m), 4.07 (2H, t, J = 9Hz), 3.88-3.82 (2H, m), 3.64-3.61 (2H , m), 3.41-3.30 (4H, m), 3.41 (3H, s), 3.05 (3H, s), 2.05-1.98 (2H, m), 1.81-1.72 (4H, m);
MS (CI) m / z: 477 [M + H] ⁺ .

(Production Example 9) sec-butyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 7)
To a solution of 2-butanol (86 mg, 0.93 mmol) in THF (3.5 mL) was added tert-butoxypotassium (174 mg, 1.55 mmol), and the mixture was stirred at room temperature for 30 minutes, and then the compound (150 mg, 0.311 mmol) in THF (3 mL) was added, and the mixture was stirred at room temperature for 2 hours. Saturated aqueous ammonium chloride solution and water were added to the reaction solution, followed by extraction three times with ethyl acetate. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. . The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 5: 1 → 1: 2, v / v) to obtain the title white foam compound (20.0 mg, yield: 14%). .
¹ H-NMR (500 MHz, CDCl ₃ ) δ ppm: 8.59 (1H, d, J = 9 Hz), 8.52 (1H, s), 7.80 (1H, dd, J = 9 Hz, 2 Hz), 7.73 (1H, d, J = 2Hz), 5.99 (1H, d, J = 1Hz), 5.37-5.32 (1H, m), 4.80-4.76 (1H, m), 4.08 (2H, t, J = 9Hz), 3.87-3.82 (2H, m), 3.37-3.30 (4H, m), 3.05 (3H, s), 2.04-1.99 (2H, m), 1.79-1.71 (2H, m), 1.55 (2H, s), 1.24 (3H, d, J = 6Hz), 0.93 (3H, t, J = 7Hz);
MS (CI) m / z: 475 [M + H] ⁺ .

(Production Example 10) 2-Cyclopropylethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 30)
Using the compound obtained in Reference Example 29 (150 mg, 0.311 mmol) and the method described in Preparation Example 9 in the same manner using 2-cyclopropylethanol (56 μL, 0.93 mmol) instead of 2-butanol Reaction was performed to obtain the title white powdery compound (44.7 mg, yield: 30%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.73-7.72 (1H, m ), 5.99 (1H, s), 5.37-5.31 (1H, m), 4.18 (2H, t, J = 7Hz), 4.07 (2H, t, J = 9Hz), 3.88-3.81 (2H, m), 3.40 -3.30 (4H, m), 3.05 (3H, s), 2.06-1.99 (2H, m), 1.80-1.73 (2H, m), 1.58-1.53 (2H, m), 0.76-0.70 (1H, m) , 0.49-0.45 (2H, m), 0.11-0.07 (2H, m);
MS (CI) m / z: 487 [M + H] ⁺ .

(Production Example 11) (1-Methylcyclopropyl) methyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. : 24)
Using the compound obtained in Reference Example 29 (150 mg, 0.311 mmol), (1-methylcyclopropyl) methanol (91 μL, 0.93 mmol) was used instead of 2-butanol in the method described in Preparation Example 9. In the same manner, the title white powdery compound (50.3 mg, yield: 33%) was obtained.
¹ H-NMR (500 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9 Hz), 8.52 (1H, d, J = 1 Hz), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H , brs), 5.99 (1H, d, J = 1Hz), 5.38-5.32 (1H, m), 4.07 (2H, t, J = 9Hz), 3.90 (2H, s), 3.90-3.83 (2H, m) , 3.41-3.29 (4H, m), 3.04 (3H, s), 2.06-2.00 (2H, m), 1.81-1.72 (2H, m), 1.14 (3H, s), 0.51-0.48 (2H, m) , 0.37-0.34 (2H, m);
MS (CI) m / z: 487 [M + H] ⁺ .

Production Example 12 2,2-Difluoroethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 53 )
Using the compound obtained in Reference Example 29 (150 mg, 0.311 mmol) and using 2,2-difluoroethanol (76.5 mg, 0.933 mmol) instead of 2-butanol in the method described in Preparation Example 9 The title white powdery compound (105 mg, yield: 70%) was obtained.
¹ H-NMR (500 MHz, CDCl ₃ ) δ ppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H, brs), 5.99 (1H, s), 5.97 (1H, tt, J = 55Hz, 4Hz), 5.38-5.34 (1H, m), 4.30 (2H, td, J = 14Hz, 4Hz), 4.07 (2H, t, J = 9Hz), 3.85-3.79 (2H, m), 3.45-3.40 (2H, m), 3.32 (2H, t, J = 9Hz), 3.04 (3H, s), 2.06-1.99 (2H, m), 1.82- 1.75 (2H, m);
MS (CI) m / z: 483 [M + H] ⁺ .

(Production Example 13) Cycloheptyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary compound number: 23)
Using the compound obtained in Reference Example 29 (150 mg, 0.311 mmol), the same reaction was carried out using cycloheptanol (149 μL, 1.24 mmol) instead of 2-butanol in the method described in Preparation Example 9. The crude product was obtained. The obtained crude product was purified by preparative HPLC (Inertsil ODS-3 (30 mmi.d. × 250 mm), GL Science, water: acetonitrile = 95: 5 → 0: 100 (gradient)), and the title white A powdery compound (18.0 mg, yield: 8%) was obtained.
¹ H-NMR (500 MHz, CDCl ₃ ) δ ppm: 8.58 (1H, d, J = 9 Hz), 8.52 (1H, s), 7.80 (1H, dd, J = 9 Hz, 2 Hz), 7.73 (1H, brs), 5.99 (1H, s), 5.36-5.32 (1H, m), 4.90-4.85 (1H, m), 4.07 (2H, t, J = 9Hz), 3.87-3.83 (2H, m), 3.37-3.30 (4H , m), 3.05 (3H, s), 2.03-2.00 (2H, m), 1.95-1.89 (2H, m), 1.75-1.45 (12H, m);
MS (CI) m / z: 515 [M + H] ⁺ .

(Production Example 14) Cyclohexyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 22)
Using the compound obtained in Reference Example 29 (150 mg, 0.311 mmol), the same reaction was carried out using cyclohexanol (131 μL, 1.24 mmol) instead of 2-butanol in the method described in Preparation Example 9, A crude product was obtained. The obtained crude product was purified by preparative HPLC (Inertsil ODS-3 (30 mmi.d. × 250 mm), GL Science, water: acetonitrile = 95: 5 → 0: 100 (gradient)), and the title white A powdery compound (22.2 mg, yield: 11%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, d, J = 1 Hz), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H , d, J = 2Hz), 5.98 (1H, d, J = 1Hz), 5.36-5.31 (1H, m), 4.73-4.67 (1H, m), 4.07 (2H, t, J = 9Hz), 3.87- 3.81 (2H, m), 3.37-3.29 (4H, m), 3.04 (3H, s), 2.05-1.98 (2H, m), 1.90-1.84 (2H, m), 1.79-1.68 (4H, m), 1.55-1.25 (6H, m);
MS (FAB) m / z: 501 [M + H] ⁺ .

Production Example 15 1-Cyclopropylethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 28)
Using the compound obtained in Reference Example 29 (150 mg, 0.311 mmol) and using the method described in Preparation Example 9 in the same manner using 1-cyclopropylethanol (90 μL, 0.93 mmol) instead of 2-butanol. Reaction was performed to obtain the title white foamy compound (56.1 mg, yield: 37%).
¹ H-NMR (500 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, d, J = 1 Hz), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H , d, J = 2Hz), 5.98 (1H, d, J = 1Hz), 5.37-5.31 (1H, m), 4.09 (2H, t, J = 9Hz), 3.88-3.82 (2H, m), 3.38- 3.29 (4H, m), 3.04 (3H, s), 2.05-1.98 (2H, m), 1.79-1.71 (2H, m), 1.32 (3H, d, J = 6Hz), 1.02-0.94 (1H, m ), 0.54-0.39 (3H, m), 0.27-0.22 (1H, m);
MS (CI) m / z: 487 [M + H] ⁺ .

Production Example 16 2-Furylmethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 25)
Using the compound (150 mg, 0.311 mmol) obtained in Reference Example 29 and reacting in the same manner using 2-furylmethanol (81 μL, 0.93 mmol) instead of 2-butanol in the method described in Preparation Example 9. To obtain the title white foamy compound (18.0 mg, yield: 2%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.57 (1H, d, J = 9 Hz), 8.50 (1H, d, J = 1 Hz), 7.78 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H , brs), 6.42-6.36 (2H, m), 5.97 (1H, d, J = 1Hz), 5.36-5.30 (1H, m), 5.09 (2H, s), 4.06 (2H, t, J = 9Hz) , 3.86-3.77 (2H, m), 3.40-3.29 (4H, m), 3.04 (3H, s), 2.05-1.86 (2H, m), 1.80-1.70 (2H, m);
MS (CI) m / z: 499 [M + H] ⁺ .

(Production Example 17) Dicyclopropylmethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplified compound number: 29)
Using the compound (150 mg, 0.311 mmol) obtained in Reference Example 29 and reacting in the same manner using dicyclopropylmethanol (72 μL, 0.93 mmol) instead of 2-butanol in the method described in Preparation Example 9. The title white powdery compound (45.7 mg, yield: 29%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, d, J = 1 Hz), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H , brs), 5.99 (1H, s), 5.37-5.32 (1H, m), 4.07 (2H, t, J = 9Hz), 3.91-3.83 (3H, m), 3.38-3.29 (4H, m), 3.04 (3H, s), 2.05-1.99 (2H, m), 1.80-1.71 (2H, m), 1.11-1.04 (2H, m), 0.58-0.41 (6H, m), 0.36-0.30 (2H, m) ;
MS (FAB) m / z: 513 [M + H] ⁺ .

Production Example 18 1-Phenylethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 52)
Using the compound (150 mg, 0.311 mmol) obtained in Reference Example 29, and using DL-1-phenylethanol (113 μL, 0.933 mmol) instead of 2-butanol in the method described in Preparation Example 9 in the same manner Reaction was performed to obtain the title white powdery compound (60.5 mg, yield: 37%).
¹ H-NMR (500 MHz, CDCl ₃ ) δ ppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.73 (1H, brs), 7.37-7.36 (5H, m), 5.98 (1H, s), 5.84 (1H, q, J = 6Hz), 5.36-5.32 (1H, m), 4.07 (2H, t, J = 9Hz), 3.90-3.83 (2H, m), 3.44-3.30 (4H, m), 3.05 (3H, s), 2.04-1.99 (2H, m), 1.80-1.72 (2H, m), 1.56 (3H, d, J = 6Hz) ;
MS (CI) m / z: 523 [M + H] ⁺ .

Production Example 19 3-Furylmethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 26)
Using the compound obtained in Reference Example 29 (150 mg, 0.311 mmol), the same reaction was carried out using 3-furylmethanol (81 μL, 0.93 mmol) instead of 2-butanol in the method described in Preparation Example 9. The title white foamy compound (11.6 mg, yield: 7%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9Hz), 8.50 (1H, d, J = 1Hz), 7.79 (1H, dd, J = 9Hz, 2Hz), 7.72 (1H , brs), 7.48 (1H, brs), 7.41-7.40 (1H, m), 6.45 (1H, brs), 5.98 (1H, s), 5.36-5.31 (1H, m), 5.02 (2H, s), 4.06 (2H, t, J = 9Hz), 3.86-3.78 (2H, m), 3.40-3.29 (4H, m), 3.04 (3H, s), 2.05-1.97 (2H, m), 1.79-1.71 (2H , m);
MS (FAB) m / z: 499 [M + H] ⁺ .

Production Example 20 Cyclopentylmethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 21)
Using the compound obtained in Reference Example 29 (150 mg, 0.311 mmol), the same procedure as described in Preparation Example 9 was performed using cyclopentylmethanol (101 μL, 0.933 mmol) instead of 2-butanol. The title white powdery compound (36.8 mg, yield: 24%) was obtained.
¹ H-NMR (500 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9Hz), 8.50 (1H, d, J = 1Hz), 7.78 (1H, dd, J = 9Hz, 2Hz), 7.72 (1H , d, J = 2Hz), 5.98 (1H, s), 5.36-5.31 (1H, m), 4.07 (2H, t, J = 9Hz), 3.98 (2H, d, J = 7Hz), 3.86-3.81 ( 2H, m), 3.38-3.29 (4H, m), 3.04 (3H, s), 2.22 (1H, quintet, J = 7Hz), 2.05-1.98 (2H, m), 1.79-1.64 (8H, m), 1.32-1.25 (2H, m);
MS (CI) m / z: 501 [M + H] ⁺ .

Production Example 21 2-Fluoro-1- (fluoromethyl) ethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate ( Exemplary compound number: 55)
Using the compound obtained in Reference Example 29 (150 mg, 0.311 mmol), 1,3-difluoropropan-2-ol (72 μL, 0.93 mmol) instead of 2-butanol in the method described in Preparation Example 9 The title white powdery compound (65.8 mg, yield: 43%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9Hz), 8.51 (1H, d, J = 1Hz), 7.79 (1H, dd, J = 9Hz, 2Hz), 7.73 (1H , d, J = 2Hz), 5.98 (1H, s), 5.39-5.33 (1H, m), 5.15 (1H, tt, J = 20Hz, 5Hz), 4.70-4.57 (4H, m), 4.07 (2H, t, J = 9Hz), 3.86-3.80 (2H, m), 3.45-3.39 (2H, m), 3.32 (2H, t, J = 9Hz), 3.04 (3H, s), 2.06-2.00 (2H, m ), 1.83-1.76 (2H, m);
MS (CI) m / z: 497 [M + H] ⁺ .

(Production Example 22) Isobutyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 307)
Using the compound (154 mg, 0.315 mmol) obtained in Preparation Example 30, instead of isopropyl chloroformate and triethylamine of the method described in Preparation Example 2, and isobutyl chloroformate (130 μL, 1.00 mmol), and Reaction was similarly performed using diisopropylethylamine (560 μL, 3.14 mmol) to obtain the title grayish white powdery compound (94.2 mg, yield: 61%).
¹ H-NMR (500 MHz, CDCl ₃ ) δppm: 8.57 (1H, d, J = 9 Hz), 8.51 (1H, d, J = 1 Hz), 7.75 (1H, dd, J = 8 Hz, 2 Hz), 7.68 (1H , d, J = 2Hz), 5.98 (1H, d, J = 1Hz), 5.36-5.32 (1H, m), 4.07 (2H, t, J = 9Hz), 3.88 (2H, d, J = 6Hz), 3.88-3.82 (2H, m), 3.39-3.30 (4H, m), 3.10 (2H, q, J = 7Hz), 2.05-1.99 (2H, m), 1.95 (1H, sept, J = 7Hz), 1.79 -1.72 (2H, m), 1.28 (3H, t, J = 7Hz), 0.95 (6H, d, J = 7Hz);
MS (ESI) m / z: 489 [M + H] ⁺ .

(Production Example 23) Cyclobutyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 310)
To a suspension of the compound obtained in Reference Example 31 (109 mg, 0.226 mmol) in THF (2.5 mL) was added cyclobutanol (90 μL, 1.15 mmol) and tert-butoxypotassium (50 mg, 0.446 mmol) at room temperature. For 1 hour. Water was added to the reaction mixture, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography ((i) hexane: ethyl acetate = 50: 50, v / v; (ii) ethyl acetate), and the resulting crude product was washed with diisopropyl ether. The title white powdery compound (34.6 mg, yield: 32%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9Hz), 8.51 (1H, d, J = 1Hz), 7.75 (1H, dd, J = 9Hz, 2Hz), 7.68 (1H , d, J = 2Hz), 5.98 (1H, d, J = 1Hz), 5.36-5.30 (1H, m), 4.98-4.91 (1H, m), 4.07 (2H, t, J = 9Hz), 3.85- 3.80 (2H, m), 3.38-3.29 (4H, m), 3.10 (2H, q, J = 7Hz), 2.39-2.31 (2H, m), 2.12-1.98 (4H, m), 1.81-1.55 (4H , m), 1.28 (3H, t, J = 7Hz);
MS (ESI) m / z: 487 [M + H] ⁺ .

(Production Example 24) sec-Butyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 308)
Using the compound obtained in Reference Example 31 (179 mg, 0.371 mmol), the same reaction was carried out using 2-butanol (170 μL, 1.85 mmol) instead of cyclobutanol of the method described in Preparation Example 23. The title white foam compound (55.1 mg, yield: 30%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9Hz), 8.51 (1H, d, J = 1Hz), 7.75 (1H, dd, J = 9Hz, 2Hz), 7.68 (1H , d, J = 2Hz), 5.98 (1H, d, J = 1Hz), 5.37-5.31 (1H, m), 4.77 (1H, sext, J = 6Hz), 4.07 (2H, t, J = 9Hz), 3.87-3.82 (2H, m), 3.37-3.25 (4H, m), 3.10 (2H, q, J = 7Hz), 2.04-1.99 (2H, m), 1.79-1.73 (2H, m), 1.66-1.52 (2H, m), 1.28 (3H, t, J = 7Hz), 1.23 (3H, d, J = 6Hz), 0.92 (3H, t, J = 7Hz);
MS (ESI) m / z: 489 [M + H] ⁺ .

Production Example 25 tert-Butyl 4-({6- [5- (isobutylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 481)
To a solution of 2-dicyclohexylphosphino-2 '-(N, N-dimethylamino) biphenyl (37.2 mg, 0.0945 mmol) in 1,4-dioxane (7.5 mL), palladium acetate (11.3 mg, 0.0503 mmol) was added, The solution stirred at room temperature for 10 minutes was mixed with tert-butyl 4-[(6-chloro-5-methylpyrimidin-4-yl) oxy] piperidine-1-carboxylate (143 mg, 0.456 mmol) prepared in Reference Example 41. In addition, a suspension of the compound obtained in Reference Example 11 (123 mg, 0.446 mmol) and potassium carbonate (1.12 g, 8.10 mmol) in 1,4-dioxane (7.5 mL) was added at 100 ° C. for 1 hour, 120 ° C. For 1 hour. The reaction solution was filtered through Celite (trade name), and the filtrate was washed with 10% hydrochloric acid, water and saturated brine, dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was subjected to silica gel column chromatography ((i) hexane: ethyl acetate = 50: 50, v / v; (ii) ethyl acetate) and thin layer silica gel chromatography (hexane: ethyl acetate = 1: 1, v / v). Purification by v) gave the title white powdery compound (12.6 mg, yield: 5%).
^{1 H-NMR (400MHz, CDCl} 3) δppm: 8.57 (1H, d, J = 9Hz), 8.51 (1H, d, J = 1Hz), 7.75 (1H, dd, J = 9Hz, 2Hz), 7.68 (1H , d, J = 2Hz), 5.98 (1H, d, J = 1Hz), 5.35-5.28 (1H, m), 4.06 (2H, t, J = 9Hz), 3.82-3.77 (2H, m), 3.33- 3.25 (4H, m), 2.97 (2J, d, J = 6Hz), 2.25-2.17 (1H, m), 2.03-1.97 (2H, m), 1.77-1.69 (2H, m), 1.48 (9H, s ), 1.05 (6H, d, J = 7Hz);
MS (ESI) m / z: 517 [M + H] ⁺ .

(Production Example 26) tert-butyl 4-({5-methyl-6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary compound number: 202)
Using the compound obtained in Reference Example 40 (291 mg, 0.888 mmol) and 5-methanesulfonylindoline (162 mg, 0.821 mmol), the reaction was carried out in the same manner as described in Production Example 25, and the title white powder A compound (365 mg, yield: 91%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.43 (1H, s), 7.71-7.67 (2H, m), 6.70 (1H, d, J = 8Hz), 5.40-5.34 (1H, m), 4.20 ( 2H, t, J = 9Hz), 3.78-3.72 (2H, m), 3.42-3.35 (2H, m), 3.22 (2H, t, J = 8Hz), 3.03 (3H, s), 2.05 (3H, s ), 2.05-1.99 (2H, m), 1.84-1.76 (2H, m), 1.49 (9H, s);
MS (ESI) m / z: 489 [M + H] ⁺ .

Production Example 27 Isobutyl 4-({6- [5- (propylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 390)
Using the compound obtained in Reference Example 32 (199 mg, 0.453 mmol), the same reaction was carried out using isobutyl chloroformate instead of butyl chloroformate in the method described in Preparation Example 6, and the title white foamy compound ( 193 mg, yield: 85%).
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.57 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.75 (1H, dd, J = 9 Hz, 2 Hz), 7.68 (1H, s), 5.98 (1H, s), 5.37-5.31 (1H, m), 4.06 (2H, t, J = 9Hz), 3.88 (2H, d, J = 7Hz), 3.88-3.81 (2H, m), 3.39-3.29 (4H, m), 3.07-3.03 (2H, m), 2.05-1.90 (3H, m), 1.80-1.69 (4H, m), 0.99 (3H, t, J = 7Hz), 0.95 (6H, d, J = 7Hz);
MS (ESI) m / z: 503 [M + H] ⁺ .

Production Example 28 Isopropyl 4-({5-methyl-6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 200)
Using the compound obtained in Preparation Example 26 (208 mg, 0.426 mmol), the same reaction was carried out using diisopropylethylamine (380 μL, 2.13 mmol) instead of triethylamine in the method described in Preparation Example 2. A white foamy compound (177 mg, yield: 88%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.43 (1H, s), 7.71-7.67 (2H, m), 6.70 (1H, d, J = 8Hz), 5.42-5.36 (1H, m), 4.95 ( 1H, sept, J = 6Hz), 4.19 (2H, t, J = 8Hz), 3.81-3.76 (2H, m), 3.46-3.40 (2H, m), 3.22 (2H, t, J = 8Hz), 3.03 (3H, s), 2.06-2.00 (2H, m), 2.05 (3H, s), 1.85-1.77 (2H, m), 1.27 (6H, d, J = 6Hz);
MS (FAB) m / z: 475 [M + H] ⁺ .

(Production Example 29) 2,2,2-trifluoroethyl 4-({6- [5- (isobutylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 486)
Using the compound (260 mg, 0.509 mmol) obtained in Reference Example 37 and using 2,2,2-trifluoroethanol (185 μL, 2.54 mmol) instead of cyclobutanol in the method described in Preparation Example 23 The reaction was conducted in the same manner to obtain the title white powdery compound (217 mg, yield: 79%).
^{1 H-NMR (400MHz, CDCl} 3) δppm: 8.57 (1H, d, J = 9Hz), 8.51 (1H, s), 7.75 (1H, dd, J = 9Hz, 2Hz), 7.69 (1H, s), 5.99 (1H, s), 5.40-5.34 (1H, m), 4.54-4.47 (2H, m), 4.07 (2H, t, J = 8Hz), 3.86-3.80 (2H, m), 3.48-3.42 (2H , m), 3.31 (2H, t, J = 9Hz), 2.97 (2H, d, J = 7Hz), 2.26-2.16 (1H, m), 2.06-2.01 (2H, m), 1.84-1.77 (2H, m), 1.05 (6H, d, J = 7Hz);
MS (ESI) m / z: 543 [M + H] ⁺ .

Production Example 30 tert-Butyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 309)
Using the compound obtained in Reference Example 20 (114 mg, 0.551 mmol), the reaction was carried out in the same manner as described in Production Example 1 to obtain the title white powdery compound (79.0 mg, yield: 35%). It was.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, d, J = 9 Hz), 8.54 (1H, s), 7.69 (1H, d, J = 9 Hz), 7.68 (1H, s), 6.23 (1H, s), 5.29-5.24 (1H, m), 4.09 (2H, t, J = 9Hz), 4.03 (2H, q, J = 7Hz), 3.71 (2H, dt, J = 14Hz, 5Hz) , 3.28 (2H, t, J = 9Hz), 3.21 (2H, q, J = 7Hz), 1.99-1.95 (2H, m), 1.60-1.53 (2H, m), 1.41 (9H, s), 1.10 ( 3H, t, J = 7Hz);
MS (ESI) m / z: 489 [M + H] ⁺ .

Production Example 31 Isopropyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 305)
Using the compound obtained in Reference Example 30 (56.0 mg, 0.143 mmol) in the same manner using isopropyl chloroformate (20.0 mg, 0.158 mmol) instead of butyl chloroformate in the method described in Preparation Example 6. Reaction was performed to obtain the title white foamy compound (65.0 mg, yield: 96%).
¹ H-NMR (400 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, d, J = 9 Hz), 8.54 (1H, s), 7.69 (1H, d, J = 9 Hz), 7.68 (1H, s), 6.23 (1H, s), 5.31-5.25 (1H, m), 4.78 (1H, sept, J = 6Hz), 4.09 (2H, t, J = 9Hz), 3.74 (2H, dt, J = 14Hz, 6Hz) , 3.30-3.18 (6H, m), 2.01-1.94 (2H, m), 1.62-1.54 (2H, m), 1.20 (6H, d, J = 6Hz), 1.10 (3H, t, J = 7Hz);
MS (FAB) m / z: 475 [M + H] ⁺ .

Production Example 32 tert-Butyl 4-({6- [5- (isopropylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 414)
Using the compound obtained in Reference Example 22 (60.0 mg, 0.178 mmol), the reaction was carried out in the same manner as in Production Example 1 to obtain the title white powdery compound (84.0 mg, yield: 94%). It was.
¹ H-NMR (400 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, d, J = 9 Hz), 8.54 (1H, s), 7.65 (1H, d, J = 9 Hz), 7.64 (1H, s), 6.24 (1H, s), 5.30-5.24 (1H, m), 4.09 (2H, t, J = 9Hz), 3.75-3.69 (2H, m), 3.41-3.25 (3H, m), 3.19-3.14 (2H , m), 1.99-1.95 (2H, m), 1.60-1.53 (2H, m), 1.41 (9H, s), 1.15 (6H, d, J = 7Hz);
MS (ESI) m / z: 503 [M + H] ⁺ .

Production Example 33 Isopropyl 4-({6- [5- (isopropylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 412)
The reaction was carried out in the same manner as in Production Example 28 using the compound obtained in Production Example 32 (80.0 mg, 0.159 mmol) to give the title white foamy compound (64.0 mg, yield: 82%). It was.
¹ H-NMR (400 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, d, J = 9 Hz), 8.55 (1H, s), 7.66 (1H, d, J = 9 Hz), 7.65 (1H, s), 6.24 (1H, s), 5.31-5.25 (1H, m), 4.78 (1H, sept, J = 6Hz), 4.10 (2H, t, J = 9Hz), 3.78-3.72 (2H, m), 3.38-3.19 (5H, m), 2.01-1.96 (2H, m), 1.63-1.54 (2H, m), 1.20 (6H, d, J = 6Hz), 1.16 (6H, d, J = 7Hz);
MS (FAB) m / z: 488 [M + H] ⁺ .

(Production Example 34) tert-butyl 4-({6- [6-fluoro-5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary compound number: 133)
Using the compound obtained in Reference Example 23 (286 mg, 0.873 mmol), a reaction was carried out in the same manner as described in Production Example 1 to obtain the title white foam compound (141 mg, yield: 33%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.58 (1H, s), 8.38 (1H, d, J = 13H), 7.62 (1H, d, J = 8 Hz), 6.28 (1H, s), 5.30-5.25 (1H, m), 4.12 (2H, t, J = 9Hz), 3.73-3.69 (2H, m), 3.27-3.14 (7H, m), 1.99-1.95 (2H, m), 1.69-1.64 (2H, m), 1.38 (9H, s);
MS (ESI) m / z: 492 [M + H] ⁺ .

(Production Example 35) Isopropyl 4-({6- [6-fluoro-5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 131)
Reaction was carried out in the same manner as in Production Example 28 using the compound obtained in Production Example 34 (86.0 mg, 0.175 mmol) to give the title white powdery compound (56.0 mg, yield: 68%). It was.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 8.58 (1H, s), 8.37 (1H, d, J = 13H), 7.62 (1H, d, J = 7 Hz), 6.28 (1H, s), 5.31-5.26 (1H, m), 4.78 (1H, sept, J = 6Hz), 4.12 (2H, t, J = 9Hz), 3.74 (2H, dt, J = 14Hz, 5Hz), 3.28 (2H, t, J = 9Hz), 3.25 (3H, s), 3.21-3.13 (2H, m), 2.00-1.94 (2H, m), 1.61-1.50 (2H, m), 1.41 (6H, d, J = 6Hz);
MS (FAB) m / z: 479 [M + H] ⁺ .

Production Example 36 tert-Butyl 4-({6- [5- (propylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 391)
Using the compound obtained in Reference Example 21 (122 mg, 0.542 mmol), the reaction was carried out in the same manner as described in Production Example 1 to obtain the title white powdery compound (84.0 mg, yield: 46%). .
¹ H-NMR (400 MHz, DMSO-d ₆ ) δppm: 8.55 (1H, d, J = 9 Hz), 8.54 (1H, s), 7.69 (1H, d, J = 9 Hz), 7.68 (1H, s), 6.23 (1H, s), 5.27 (1H, sept, J = 4Hz), 4.09 (2H, t, J = 9Hz), 3.72 (2H, dt, J = 14Hz, 5Hz), 3.28 (2H, t, J = 9Hz), 3.21-3.13 (4H, m), 2.00-1.94 (2H, m), 1.61-1.50 (4H, m), 1.41 (9H, s), 0.91 (3H, t, J = 7Hz);
MS (ESI) m / z: 503 [M + H] ⁺ .

(Production Example 37) 2,2-Dimethylpropyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 18) )
Using the compound obtained in Reference Example 28 (45.0 mg, 0.151 mmol), the same reaction was carried out using neopentyl chloroformate (26 mg, 0.17 mmol) instead of butyl chloroformate in the method described in Preparation Example 6. The title white powdery compound (32.0 mg, yield: 54%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.54 (1H, s), 8.54 (1H, d, J = 9 Hz), 7.74 (1H, s), 7.73 (1H, d, J = 9 Hz), 6.24 (1H, s), 5.32-5.27 (1H, m), 4.09 (2H, t, J = 9Hz), 3.77 (2H, brs), 3.72 (2H, s), 3.30-3.22 (4H, m), 3.15 (3H, s), 2.02-1.99 (2H, m), 1.63-1.57 (2H, m), 0.91 (9H, s);
MS (ESI) m / z: 489 [M + H] ⁺ .

(Production Example 38) Phenyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 46)
Using the compound (49.0 mg, 0.162 mmol) obtained in Reference Example 28, the reaction was similarly carried out using phenyl chloroformate (28 mg, 0.18 mmol) instead of butyl chloroformate in the method described in Preparation Example 6. The title white powdery compound (23.0 mg, yield: 36%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 8.56 (1H, s), 8.55 (1H, d, J = 9 Hz), 7.74 (1H, s), 7.73 (1H, d, J = 9 Hz), 7.39 (2H, t, J = 7Hz), 7.23 (1H, t, J = 8Hz), 7.14 (2H, d, J = 8Hz), 6.27 (1H, s), 5.38-5.33 (1H, m), 4.11 (2H, t, J = 9Hz), 3.95 (1H, brs), 3.81 (1H, brs), 3.50 (1H, brs), 3.37-3.27 (3H, m), 3.15 (3H, s), 2.09 (2H , brs), 1.73 (2H, brs);
MS (ESI) m / z: 495 [M + H] ⁺ .

(Production Example 39) Isobutyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary compound number: 6)
Using the compound obtained in Reference Example 28 (47.0 mg, 0.154 mmol), the same reaction was carried out using isobutyl chloroformate (23 mg, 0.17 mmol) instead of butyl chloroformate in the method described in Preparation Example 6. The title white powdery compound (30.0 mg, yield: 51%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.54 (1H, s), 8.54 (1H, d, J = 9 Hz), 7.73 (1H, s), 7.72 (1H, d, J = 9 Hz), 6.24 (1H, s), 5.31-5.26 (1H, m), 4.09 (2H, t, J = 9Hz), 3.79 (2H, d, J = 6Hz), 3.79-3.74 (2H, m), 3.29-3.21 (4H, m), 3.15 (3H, s), 2.02-1.97 (2H, m), 1.87 (1H, sept, J = 6Hz), 1.63-1.56 (2H, m), 0.90 (6H, d, J = 6Hz);
MS (ESI) m / z: 475 [M + H] ⁺ .

(Production Example 40) Isopropyl 4-({6- [5- (propylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 389)
Using the compound obtained in Production Example 36 (65.0 mg, 0.129 mmol), the reaction was carried out in the same manner as in Production Example 28, and the title white powdery compound (42.0 mg, yield: 66%) was obtained. Obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, d, J = 8 Hz), 8.54 (1H, s), 7.69 (1H, d, J = 8 Hz), 7.68 (1H, s), 6.23 (1H, s), 5.30-5.26 (1H, m), 4.78 (1H, sept, J = 6Hz), 4.09 (2H, t, J = 9Hz), 3.77-3.72 (2H, m), 3.32-3.18 (6H, m), 2.00-1.95 (2H, m), 1.62-1.51 (4H, m), 1.19 (6H, d, J = 6Hz), 0.91 (3H, t, J = 8Hz);
MS (ESI) m / z: 489 [M + H] ⁺ .

Production Example 41 5- (Methylsulfonyl) -1- (6-{[1- (3,3,3-trifluoropropanoyl) piperidin-4-yl] oxy} pyrimidin-4-yl) indoline (exemplified) Compound number: 81)
To a solution of 3,3,3-trifluoropropionic acid (63 mg, 0.50 mmol) in dichloromethane (1.9 mL) at 0 ° C. was added oxalyl chloride (65 μL, 0.74 mmol) and 1 drop of DMF for 3.5 hours at room temperature. After stirring, the solvent of the reaction solution was distilled off. The obtained residue is referred to as an acid chloride compound.

To a solution of the compound obtained in Production Example 1 (469 mg, 0.988 mmol) in dichloromethane (9.38 mL) was added trifluoroacetic acid (2.35 mL) at 0 ° C. and stirred at room temperature for 1 hour, and then the solvent of the reaction solution was distilled. Left. To a part of the obtained residue (150 mg) and diisopropylethylamine (431 μL, 2.48 mmol) in THF (450 μL), a solution of the acid chloride compound prepared above at 0 ° C. in THF (3.0 mL) was added at room temperature. Stir for 3 hours. A saturated aqueous ammonium chloride solution and water were added to the reaction solution, followed by extraction three times with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by preparative thin layer silica gel chromatography (hexane: ethyl acetate = 1: 2, v / v) to obtain the title white foam compound (13 mg, yield: 11%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, s), 8.55 (1H, d, J = 9 Hz), 7.74 (1H, s), 7.73 (1H, d, J = 9 Hz), 6.25 (1H, s), 5.35-5.31 (1H, m), 4.09 (2H, t, J = 9Hz), 3.95-3.90 (1H, m), 3.74-3.66 (3H, m), 3.40-3.35 (1H , m), 3.30-3.25 (3H, m), 3.15 (3H, s), 2.06-1.96 (2H, m), 1.72-1.65 (1H, m), 1.61-1.54 (1H, m);
MS (FAB) m / z: 485 [M + H] ⁺ .

Production Example 42 1- (6-{[1- (Butylsulfonyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (methylsulfonyl) indoline (Exemplary Compound No. 126)
To a solution of the compound (145 mg, 0.306 mmol) obtained in Production Example 1 in dichloromethane (2.90 mL) was added trifluoroacetic acid (727 μL) at 0 ° C., and the mixture was stirred at room temperature for 1 hour. The solvent was distilled off under reduced pressure, and the obtained residue and a solution of diisopropylethylamine (1.07 mL, 6.14 mmol) in dichloromethane (3.70 mL) were added to 1-butanesulfonic acid chloride (72.0 mg, 0.461) at 0 ° C. mmol) in dichloromethane (1.85 mL) was added, and the mixture was stirred at 0 ° C for 1 hour, and then stirred at 80 ° C for 3 hours. The solvent was distilled off under reduced pressure, methanol was added, the precipitate was collected by filtration, and the resulting crude product was washed with methanol to give the title white powdery compound (125 mg, yield: 82%). It was.
¹ H-NMR (400MHz, DMSO-d ₆ ) δppm: 8.55 (1H, s), 8.54 (1H, d, J = 9Hz), 7.74 (1H, s), 7.73 (1H, d, J = 9Hz), 6.25 (1H, s), 5.29-5.22 (1H, m), 4.10 (2H, t, J = 9Hz), 3.49-3.43 (2H, m), 3.28 (2H, t, J = 9Hz), 3.21-3.15 (2H, m), 3.15 (3H, s), 3.08-3.04 (2H, m), 2.10-2.03 (2H, m), 1.78-1.62 (4H, m), 1.46-1.37 (2H, m), 0.91 (3H, t, J = 7Hz);
MS (FAB) m / z: 495 [M + H] ⁺ .

(Production Example 43) Isopropyl 4-({6- [6-chloro-5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 155)
Using the compound (353 mg, 1.03 mmol) obtained in Reference Example 24, instead of tert-butyl 4-hydroxypiperidine-1-carboxylate in the method described in Preparation Example 1, isopropyl 4-hydroxypiperidine-1 -Carboxylate (288 mg, 1.54 mmol) was used for the same reaction to obtain the title white powdery compound (446 mg, yield: 88%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 8.65 (1H, s), 8.60 (1H, s), 7.83 (1H, s), 6.27 (1H, s), 5.31-5.26 (1H, m) , 4.78 (1H, sept, J = 6Hz), 4.11 (2H, t, J = 9Hz), 3.74 (2H, dt, J = 13Hz, 5Hz), 3.30 (3H, s), 3.29-3.18 (4H, m ), 2.00-1.96 (2H, m), 1.61-1.55 (2H, m), 1.20 (6H, d, J = 6Hz);
MS (FAB) m / z: 495 [M + H] ⁺ .

(Production Example 44) Cyclopropylmethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 19)
Using the compound obtained in Reference Example 29 (102 mg, 0.218 mmol), cyclopropylmethanol (26 μL, 0.33 mmol) was used in the same manner instead of 2-butanol of the method described in Preparation Example 9. The title white powdery compound (49.0 mg, yield: 48%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 8.55 (1H, s), 8.54 (1H, d, J = 9 Hz), 7.74-7.72 (2H, m), 6.24 (1H, s), 5.31- 5.26 (1H, m), 4.09 (2H, t, J = 9Hz), 3.86 (2H, d, J = 7Hz), 3.76 (2H, dt, J = 14Hz, 5Hz), 3.33-3.20 (4H, m) , 3.15 (3H, s), 2.01-1.98 (2H, m), 1.64-1.57 (2H, m), 1.14-1.06 (1H, m), 0.52-0.48 (2H, m), 0.28-0.25 (2H, m);
MS (ESI) m / z: 473 [M + H] ⁺ .

Production Example 45 1- {6-[(1-Benzoylpiperidin-4-yl) oxy] pyrimidin-4-yl} -5- (methylsulfonyl) indoline (Exemplary Compound No. 84)
Using the compound obtained in Reference Example 28 (50.0 mg, 0.134 mmol), the same reaction was carried out using benzoyl chloride (19 μL, 0.16 mmol) instead of butyl chloroformate in the method described in Preparation Example 6. The title white powdery compound (24.0 mg, yield: 38%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 8.55 (1H, s), 8.54 (1H, d, J = 9 Hz), 7.74 (1H, s), 7.73 (1H, d, J = 7 Hz), 7.46-7.45 (3H, m), 7.43-7.40 (2H, m), 6.24 (1H, s), 5.39-5.34 (1H, m), 4.09 (2H, t, J = 9Hz), 4.06 (1H, brs ), 3.56 (1H, brs), 3.41 (1H, brs), 3.30-3.25 (3H, m), 3.15 (3H, s), 2.08 (1H, brs), 1.99 (1H, brs), 1.68 (2H, brs);
MS (ESI) m / z: 479 [M + H] ⁺ .

(Production Example 46) Ethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary compound number: 2)
Using the compound (90.0 mg, 0.240 mmol) obtained in Reference Example 28, the same reaction was carried out using ethyl chloroformate (34 μL, 0.36 mmol) instead of butyl chloroformate in the method described in Preparation Example 6. The title white powdery compound (75.0 mg, yield: 70%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.54 (1H, s), 8.54 (1H, d, J = 9 Hz), 7.74 (1H, s), 7.73 (1H, d, J = 7 Hz), 6.24 (1H, s), 5.30-5.25 (1H, m), 4.09 (2H, t, J = 8Hz), 4.05 (2H, q, J = 7Hz), 3.75 (2H, dt, J = 14Hz, 5Hz) , 3.28 (2H, t, J = 9Hz), 3.24 (2H, brs), 3.15 (3H, s), 2.01-1.96 (2H, m), 1.63-1.56 (2H, m), 1.19 (3H, t, J = 7Hz);
MS (ESI) m / z: 447 [M + H] ⁺ .

Production Example 47 2-Chloroethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 36)
Using the compound obtained in Reference Example 28 (250 mg, 0.668 mmol) in the same manner using 2-chloroethyl chloroformate (103 μL, 1.00 mmol) instead of butyl chloroformate in the method described in Preparation Example 6. Reaction was performed to obtain the title white powdery compound (229 mg, yield: 71%).
¹ H-NMR (400 MHz, DMSO-d ₆ ) δppm: 8.54 (1H, s), 8.54 (1H, d, J = 9 Hz), 7.73-7.72 (2H, m), 6.24 (1H, s), 5.33- 5.27 (1H, m), 4.27 (2H, t, J = 5Hz), 4.09 (2H, t, J = 9Hz), 3.82 (2H, dd, J = 6Hz, 5Hz), 3.80-3.74 (2H, m) , 3.31-3.24 (4H, m), 3.15 (3H, s), 2.03-1.95 (2H, m), 1.66-1.57 (2H, m);
MS (ESI) m / z: 481 [M + H] ⁺ .

Production Example 48 1- (6-{[1- (Cyclopropylacetyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (methylsulfonyl) indoline (Exemplary Compound No. 78)
To a DMF (4.20 mL) solution of the compound obtained in Reference Example 28 (70.0 mg, 0.187 mmol) and cyclopropylacetic acid (28.0 mg, 0.280 mmol) at room temperature, 4- (4,4-dimethoxy-1, 3,5-Triazin-2-yl) -4-methylmorpholinium (72 mg, 0.262 mmol) was added, and the mixture was stirred at room temperature for 6 hours. Water was added to the reaction solution, followed by extraction three times with ethyl acetate. The obtained organic layer was washed with water and dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography ((i) hexane: ethyl acetate = 9: 1, v / v; (ii) ethyl acetate) to give the title white foam compound (71.0 mg, yield: 84). %).
¹ H-NMR (500MHz, DMSO-d ₆ ) δppm: 8.55 (1H, s), 8.54 (1H, d, J = 9Hz), 7.74-7.72 (2H, m), 6.24 (1H, s), 5.34- 5.29 (1H, m), 4.09 (2H, t, J = 9Hz), 3.98-3.94 (1H, m), 3.75-3.70 (1H, m), 3.36-3.26 (3H, m), 3.22-3.17 (1H , m), 3.15 (3H, s), 2.28 (2H, d, J = 7Hz), 2.04-1.95 (2H, m), 1.67-1.51 (2H, m), 1.00-0.92 (1H, m), 0.47 -0.43 (2H, m), 0.13-0.11 (2H, m);
MS (FAB) m / z: 457 [M + H] ⁺ .

Production Example 49 Cyclopentyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 11)
Using the compound obtained in Reference Example 29 (162 mg, 0.346 mmol), cyclopentanol (94 μL, 1.04 mmol) was used in the same manner instead of 2-butanol in the method described in Preparation Example 9. The title white powdery compound (104 mg, yield: 62%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.54 (1H, s), 8.54 (1H, d, J = 9 Hz), 7.74-7.72 (2H, m), 6.23 (1H, s), 5.30- 5.25 (1H, m), 5.01-4.98 (1H, m), 4.09 (2H, t, J = 9Hz), 3.75-3.70 (2H, m), 3.28 (2H, t, J = 9Hz), 3.24-3.18 (2H, m), 3.15 (3H, s), 1.99-1.95 (2H, m), 1.82-1.77 (2H, m), 1.67-1.53 (8H, m);
MS (ESI) m / z: 487 [M + H] ⁺ .

Production Example 50 1- (6-{[1- (Cyclopropylcarbonyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (methylsulfonyl) indoline (Exemplary Compound No. 67)
Using the compound obtained in Reference Example 28 (100 mg, 0.267 mmol), a similar reaction was performed using cyclopropanecarboxylic acid (32 μL, 0.40 mmol) instead of cyclopropylacetic acid in the method described in Preparation Example 48. The title white powdery compound (61.0 mg, yield: 52%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 8.55 (1H, s), 8.55 (1H, d, J = 9 Hz), 7.74-7.72 (2H, m), 6.24 (1H, s), 5.36- 5.31 (1H, m), 4.09 (2H, t, J = 9Hz), 4.06-3.95 (2H, m), 3.52 (1H, brs), 3.28 (2H, t, J = 9Hz), 3.21 (1H, brs ), 3.15 (3H, s), 2.09-1.96 (3H, m), 1.66 (1H, brs), 1.54 (1H, brs), 0.73-0.69 (4H, m);
MS (ESI) m / z: 443 [M + H] ⁺ .

Production Example 51 1- (6-{[1- (Isobutylsulfonyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (methylsulfonyl) indoline (Exemplary Compound No. 127)
Using the compound obtained in Reference Example 28 (100 mg, 0.267 mmol), and isobutanesulfonic acid chloride (54 μL, 0.40 mmol) instead of 1-butanesulfonic acid chloride of the method described in Preparation Example 42 The reaction was conducted in the same manner to obtain the title white powdery compound (117 mg, yield: 89%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 8.55 (1H, s), 8.55 (1H, d, J = 9Hz), 7.74-7.72 (2H, m), 6.25 (1H, s), 5.28- 5.23 (1H, m), 4.09 (2H, t, J = 9Hz), 3.46-3.42 (2H, m), 3.28 (2H, t, J = 9Hz), 3.18-3.14 (2H, m), 3.15 (3H , s), 2.93 (2H, d, J = 7Hz), 2.17-2.03 (3H, m), 1.78-1.72 (2H, m), 1.05 (6H, d, J = 7Hz);
MS (ESI) m / z: 495 [M + H] ⁺ .

(Production Example 52) Cyclobutyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 9)
Using the compound obtained in Reference Example 29 (170 mg, 0.363 mmol), the same reaction was carried out using cyclobutanol (86 μL, 1.1 mmol) instead of 2-butanol of the method described in Preparation Example 9. The title white powdery compound (109 mg, yield: 64%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 8.55 (1H, s), 8.55 (1H, d, J = 9 Hz), 7.74 (1H, s), 7.73 (1H, d, J = 6 Hz), 6.24 (1H, s), 5.30-5.25 (1H, m), 4.86-4.80 (1H, m), 4.09 (2H, t, J = 9Hz), 3.76-3.73 (2H, m), 3.28 (2H, t , J = 9Hz), 3.23 (2H, brs), 3.15 (3H, s), 2.27-2.22 (2H, m), 2.03-1.95 (4H, m), 1.71 (1H, q, J = 10Hz), 1.63 -1.51 (3H, m);
MS (FAB) m / z: 473 [M + H] ⁺ .

Production Example 53 1-Ethylpropyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 13)
Using the compound obtained in Reference Example 29 (176 mg, 0.376 mmol), the same reaction was carried out using 3-pentanol (122 μL, 1.13 mmol) instead of 2-butanol in the method described in Preparation Example 9. To obtain the title white foamy compound (93.0 mg, yield: 51%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.54 (1H, s), 8.54 (1H, d, J = 9 Hz), 7.74 (1H, s), 7.73 (1H, d, J = 5 Hz), 6.24 (1H, s), 5.32-5.27 (1H, m), 4.56-4.51 (1H, m), 4.09 (2H, t, J = 9Hz), 3.79-3.76 (2H, m), 3.28 (2H, t , J = 9Hz), 3.24 (2H, brs), 3.15 (3H, s), 2.01-1.97 (2H, m), 1.61-1.46 (6H, m), 0.85 (3H, d, J = 7Hz), 0.84 (3H, d, J = 7Hz);
MS (FAB) m / z: 489 [M + H] ⁺ .

Production Example 54 1- (6-{[1- (Ethylsulfonyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (methylsulfonyl) indoline (Exemplary Compound No. 122)
Using the compound obtained in Reference Example 28 (100 mg, 0.267 mmol) and using ethanesulfonic acid chloride (38 μL, 0.40 mmol) instead of 1-butanesulfonic acid chloride in the method described in Preparation Example 42 The reaction was conducted in the same manner to obtain the title white powdery compound (102 mg, yield: 82%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 8.55 (1H, s), 8.55 (1H, d, J = 9 Hz), 7.74 (1H, s), 7.73 (1H, d, J = 7 Hz), 6.26 (1H, s), 5.28-5.24 (1H, m), 4.09 (2H, t, J = 8Hz), 3.49-3.45 (2H, m), 3.28 (2H, t, J = 9Hz), 3.21-3.16 (2H, m), 3.15 (3H, s), 3.09 (2H, q, J = 7Hz), 2.08-2.03 (2H, m), 1.77-1.70 (2H, m), 1.23 (3H, t, J = 6Hz);
MS (FAB m / z: 467 [M + H] ⁺ .

Production Example 55 Cyclobutylmethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 20)
Using the compound obtained in Reference Example 29 (176 mg, 0.376 mmol), the same reaction was carried out using cyclobutylmethanol (107 μL, 1.13 mmol) instead of 2-butanol in the method described in Preparation Example 9. The title white powdery compound (136 mg, yield: 74%) was obtained.
¹ H-NMR (400 MHz, DMSO-d ₆ ) δppm: 8.54 (1H, s), 8.54 (1H, d, J = 9 Hz), 7.74-7.71 (2H, m), 6.24 (1H, s), 5.31- 5.25 (1H, m), 4.09 (2H, t, J = 9Hz), 3.98 (2H, d, J = 7Hz), 3.76 (2H, dt, J = 14Hz, 5Hz), 3.28 (2H, t, J = 9Hz), 3.24 (2H, brs), 3.15 (3H, s), 2.62-2.50 (1H, m), 2.03-1.96 (4H, m), 1.92-1.69 (4H, m), 1.63-1.54 (2H, m);
MS (FAB) m / z: 487 [M + H] ⁺ .

(Production Example 56) tert-butyl 4-[(6- {5-[(cyclopropylmethyl) sulfonyl] -indoline-1-yl} pyrimidin-4-yl] oxy) piperidine-1-carboxylate (Exemplary Compound No. : 537)
The compound obtained in Reference Example 16 (55.0 mg, 0.201 mmol), the compound obtained in Reference Example 41 (76.0 mg, 0.241 mmol), potassium carbonate (555 mg, 4.02 mmol), 2-dicyclohexylphosphino-2′- To a suspension of (N, N-dimethylamino) biphenyl (16.0 mg, 0.040 mmol) in 1,4-dioxane (10.0 mL), palladium acetate (5.0 mg, 0.020 mmol) is added, and heated under a nitrogen atmosphere for 1 hour. Refluxed. The reaction solution was filtered, an aqueous ammonium chloride solution was added to the filtrate, and the mixture was extracted 3 times with acetic acid. The organic layer was dried over anhydrous sodium sulfate and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 9: 1 → 3: 2, v / v) to obtain the title white powdery compound (102 mg, yield: 99%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, d, J = 9 Hz), 8.54 (1H, s), 7.70 (1H, d, J = 8 Hz), 7.69 (1H, s), 6.23 (1H, s), 5.29-5.24 (1H, m), 4.09 (2H, t, J = 9Hz), 3.75-3.70 (2H, m), 3.28 (2H, t, J = 9Hz), 3.17 (2H , d, J = 7Hz), 3.17 (2H, brs), 2.00-1.95 (2H, m), 1.60-1.53 (2H, m), 1.41 (9H, s), 0.87-0.80 (1H, m), 0.47 -0.43 (2H, m), 0.13-0.10 (2H, m);
MS (FAB) m / z: 515 [M + H] ⁺ .

(Production Example 57) tert-butyl 4-({6- [5- (cyclobutylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplified Compound No .: 503)
Using the compound obtained in Reference Example 17 (55.0 mg, 0.208 mmol), the reaction was carried out in the same manner as in Production Example 56 to obtain the title white powdery compound (73.0 mg, yield: 71%). It was.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, d, J = 9 Hz), 8.54 (1H, s), 7.66 (1H, d, J = 9 Hz), 7.65 (1H, s), 6.23 (1H, s), 5.29-5.24 (1H, m), 4.09 (2H, t, J = 9Hz), 4.04-3.97 (1H, m), 3.75-3.70 (2H, m), 3.28 (2H, t , J = 9Hz), 3.17 (2H, brs), 2.35-2.27 (2H, m), 2.15-2.08 (2H, m), 2.00-1.81 (4H, m), 1.60-1.53 (2H, m), 1.41 (9H, s);
MS (FAB) m / z: 515 [M + H] ⁺ .

(Production Example 58) tert-butyl 4-({6- [6-methoxy-5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary compound number: 251)
Reaction was carried out in the same manner as in the method described in Production Example 1 using the compound (200 mg, 0.589 mmol) obtained in Reference Example 25 to obtain the title white powdery compound (184 mg, yield: 62%).
¹ H-NMR (400 MHz, DMSO-d ₆ ) δppm: 8.55 (1H, s), 8.38 (1H, s), 7.58 (1H, s), 6.23 (1H, s), 5.30-5.24 (1H, m) , 4.07 (2H, t, J = 9Hz), 3.95 (3H, s), 3.72 (2H, dt, J = 14Hz, 5Hz), 3.22-3.12 (4H, m), 3.17 (3H, s), 2.00- 1.94 (2H, m), 1.61-1.52 (2H, m), 1.41 (9H, s);
MS (FAB) m / z: 505 [M + H] ⁺ .

(Production Example 59) Isopropyl 4-({6- [6-methoxy-5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 249)
Using the compound obtained in Production Example 58 (153 mg, 0.303 mmol), the reaction was carried out in the same manner as in the method described in Reference Example 28 to obtain a white powdery compound. Using the obtained compound, the reaction was carried out in the same manner as described in Production Example 31 to obtain the title white powdery compound (120 mg, yield: 82%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 8.55 (1H, s), 8.38 (1H, s), 7.58 (1H, s), 6.23 (1H, s), 5.31-5.26 (1H, m) , 4.78 (1H, sept, J = 6Hz), 4.07 (2H, t, J = 9Hz), 3.95 (3H, s), 3.74 (2H, dt, J = 14Hz, 5Hz), 3.26-3.16 (4H, m ), 3.17 (3H, s), 2.01-1.94 (2H, m), 1.61-1.54 (2H, m), 1.19 (6H, d, J = 6Hz);
MS (FAB) m / z: 491 [M + H] ⁺ .

(Production Example 60) 2,2-difluoroethyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 325) )
Using the compound obtained in Reference Example 31 (300 mg, 0.622 mmol), the reaction was carried out in the same manner as described in Production Example 12 to obtain the title white powdery compound (233 mg, yield: 76%). .
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 8.56 (1H, d, J = 9 Hz), 8.55 (1H, s), 7.69 (1H, d, J = 6 Hz), 7.68 (1H, s), 6.25 (1H, tt, J = 55Hz, 3Hz), 6.24 (1H, s), 5.33-5.28 (1H, m), 4.31 (2H, td, J = 16Hz, 3Hz), 4.09 (2H, t, J = 9Hz), 3.76 (2H, dt, J = 14Hz, 5Hz), 3.34-3.27 (4H, m), 3.21 (2H, q, J = 7Hz), 2.03-1.99 (2H, m), 1.66-1.59 (2H , m), 1.10 (3H, t, J = 7Hz);
MS (ESI) m / z: 497 [M + H] ⁺ .

(Production Example 61) 2,2,2-trifluoroethyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 326)
Using the compound (300 mg, 0.622 mmol) obtained in Reference Example 31, 2,2,2-trifluoroethanol (187 mg, 1.87 mmol) was used instead of 2-butanol in the method described in Preparation Example 9. And the same reaction was carried out to obtain the title white powdery compound (233 mg, yield: 58%).
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, d, J = 9 Hz), 8.55 (1H, s), 7.69 (1H, d, J = 7 Hz), 7.68 (1H, s), 6.25 (1H, s), 5.34-5.29 (1H, m), 4.72 (2H, q, J = 9Hz), 4.09 (2H, t, J = 9Hz), 3.76 (2H, dt, J = 14Hz, 5Hz) , 3.34-3.27 (4H, m), 3.21 (2H, q, J = 7Hz), 2.04-1.99 (2H, m), 1.67-1.60 (2H, m), 1.10 (3H, t, J = 7Hz);
MS (ESI) m / z: 515 [M + H] ⁺ .

(Production Example 62) 3-Furylmethyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 315)
Using the compound (200 mg, 0.414 mmol) obtained in Reference Example 31, the reaction was carried out in the same manner as described in Production Example 19 to obtain the title white foam compound (107 mg, yield: 50%). .
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, d, J = 9 Hz), 8.54 (1H, s), 7.73 (1H, s), 7.69 (1H, d, J = 7 Hz), 7.68 (1H, s), 7.65 (1H, s), 6.53 (1H, s), 6.23 (1H, s), 5.30-5.25 (1H, m), 4.94 (2H, m), 4.09 (2H, t, J = 9Hz), 3.77-3.74 (2H, m), 3.30-3.19 (6H, m), 1.99-1.97 (2H, m), 1.62-1.56 (2H, m), 1.10 (3H, t, J = 7Hz );
MS (ESI) m / z: 513 [M + H] ⁺ .

Production Example 63 5- (Ethylsulfonyl) -1- (6-{[1- (3-methylbutanoyl) piperidin-4-yl] oxy} pyrimidin-4-yl) indoline (Exemplary Compound Number: 328)
Using the compound obtained in Reference Example 30 (200 mg, 0.515 mmol), the same reaction was carried out using isovaleric acid chloride (69 μL, 0.57 mmol) instead of butyl chloroformate in the method described in Preparation Example 6. The title white powdery compound (195 mg, yield: 80%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, d, J = 9 Hz), 8.55 (1H, s), 7.69 (1H, d, J = 7 Hz), 7.68 (1H, s), 6.24 (1H, s), 5.34-5.29 (1H, m), 4.09 (2H, t, J = 9Hz), 4.00-3.95 (1H, m), 3.79-3.74 (1H, m), 3.37-3.16 (6H , m), 2.22 (2H, d, J = 7Hz), 2.04-1.95 (3H, m), 1.65-1.49 (2H, m), 1.10 (3H, t, J = 7Hz), 0.91 (6H, d, J = 7Hz);
MS (ESI) m / z: 473 [M + H] ⁺ .

(Production Example 64) 2,2,2-trifluoroethyl 4-({6- [5- (propylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 396)
Using the compound obtained in Reference Example 33 (140 mg, 0.282 mmol), the reaction was carried out in the same manner as described in Production Example 61 to obtain the title white powdery compound (89.0 mg, yield: 60%). It was.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, d, J = 9 Hz), 8.55 (1H, s), 7.69 (1H, d, J = 7 Hz), 7.68 (1H, s), 6.24 (1H, s), 5.33-5.29 (1H, m), 4.72 (2H, q, J = 9Hz), 4.09 (2H, t, J = 9Hz), 3.76 (2H, dt, J = 14Hz, 5Hz) , 3.36-3.26 (4H, m), 3.19 (2H, t, J = 8Hz), 2.04-2.00 (2H, m), 1.67-1.60 (2H, m), 1.59-1.51 (2H, m), 0.91 ( 3H, t, J = 7Hz);
MS (ESI) m / z: 529 [M + H] ⁺ .

Production Example 65 1- (6-{[1- (3-Methylbutanoyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (propylsulfonyl) indoline (Exemplary Compound No. 397)
Using the compound (200 mg, 0.456 mmol) obtained in Reference Example 32, the reaction was carried out in the same manner as described in Production Example 63 to obtain the title white powdery compound (107 mg, yield: 48%). .
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, d, J = 9 Hz), 8.55 (1H, s), 7.69 (1H, d, J = 7 Hz), 7.68 (1H, s), 6.24 (1H, s), 5.34-5.29 (1H, m), 4.09 (2H, t, J = 9Hz), 4.00-3.95 (1H, m), 3.79-3.74 (1H, m), 3.37-3.26 (3H , m), 3.21-3.16 (3H, m), 2.22 (2H, d, J = 7Hz), 2.04-1.95 (3H, m), 1.65-1.49 (4H, m), 0.91 (3H, t, J = 6Hz), 0.90 (6H, d, J = 6Hz);
MS (ESI) m / z: 487 [M + H] ⁺ .

(Production Example 66) 2,2,2-trifluoroethyl 4-({6- [5- (isopropylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 419)
Using the compound obtained in Reference Example 35 (140 mg, 0.282 mmol), the reaction was carried out in the same manner as described in Production Example 61 to obtain the title white powdery compound (136 mg, yield: 91%). .
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, d, J = 9 Hz), 8.55 (1H, s), 7.65 (1H, d, J = 7 Hz), 7.64 (1H, s), 6.25 (1H, s), 5.33-5.29 (1H, m), 4.72 (2H, q, J = 9Hz), 4.09 (2H, t, J = 9Hz), 3.76 (2H, dt, J = 14Hz, 5Hz) , 3.37-3.27 (5H, m), 2.05-2.00 (2H, m), 1.67-1.60 (2H, m), 1.16 (6H, d, J = 6Hz);
MS (ESI) m / z: 529 [M + H] ⁺ .

Production Example 67 1- (6-{[1- (3,3-Dimethylbutanoyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (methylsulfonyl) indoline (Exemplary compound number: 73)
Using the compound obtained in Reference Example 27 (150 mg, 0.365 mmol), tert-butylacetyl chloride (76 μL, 0.55 mmol) instead of chloroformic acid (2-fluoroethyl) in the method described in Preparation Example 3 The title white foam compound (149 mg, yield: 86%) was obtained in the same manner as above.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, d, J = 9 Hz), 8.55 (1H, s), 7.74 (1H, s), 7.73 (1H, d, J = 7 Hz), 6.24 (1H, s), 5.34-5.29 (1H, m), 4.09 (2H, t, J = 9Hz), 4.02-3.97 (1H, m), 3.85-3.80 (1H, m), 3.41-3.36 (1H , m), 3.29 (2H, t, J = 9Hz), 3.22-3.17 (1H, m), 3.15 (3H, s), 2.26 (2H, s), 2.05-1.94 (2H, m), 1.66-1.50 (2H, m), 1.00 (9H, s);
MS (ESI) m / z: 473 [M + H] ⁺ .

Production Example 68 Cyclopropylmethyl 4-({6- [5- (propylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 392)
Using the compound obtained in Reference Example 33 (205 mg, 0.413 mmol), the reaction was carried out in the same manner as described in Production Example 44 to obtain the title white foam compound (145 mg, yield: 70%). .
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, d, J = 9 Hz), 8.55 (1H, s), 7.69 (1H, d, J = 7 Hz), 7.68 (1H, s), 6.24 (1H, s), 5.31-5.26 (1H, m), 4.09 (2H, t, J = 9Hz), 3.86 (2H, d, J = 7Hz), 3.79-3.75 (2H, m), 3.30-3.18 (6H, m), 2.01-1.98 (2H, m), 1.64-1.51 (4H, m), 1.14-1.06 (1H, m), 0.91 (3H, t, J = 7Hz), 0.52-0.48 (2H, m), 0.28-0.25 (2H, m);
MS (ESI) m / z: 501 [M + H] ⁺ .

Production Example 69 Cyclopropylmethyl 4-({6- [5- (isopropylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 415)
Using the compound obtained in Reference Example 35 (184 mg, 0.371 mmol), the reaction was carried out in the same manner as described in Production Example 44 to obtain the title white foam compound (72.0 mg, yield: 39%). It was.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, d, J = 9 Hz), 8.54 (1H, s), 7.65 (1H, d, J = 7 Hz), 7.64 (1H, s), 6.24 (1H, s), 5.31-5.26 (1H, m), 4.09 (2H, t, J = 9Hz), 3.85 (2H, d, J = 7Hz), 3.79-3.75 (2H, m), 3.34-3.22 (5H, m), 2.01-1.98 (2H, m), 1.64-1.56 (2H, m), 1.15 (6H, d, J = 7Hz), 1.13-1.06 (1H, m), 0.52-0.48 (2H, m), 0.28-0.25 (2H, m);
MS (ESI) m / z: 501 [M + H] ⁺ .

Production Example 70 2-Fluoroethyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 317)
Using the compound (101 mg, 0.260 mmol) obtained in Reference Example 30 and using chloroformate (2-fluoroethyl) (28 μL, 0.29 mmol) instead of butyl chloroformate in the method described in Preparation Example 6. In the same manner, the title white foamy compound (108 mg, yield: 87%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.56 (1H, d, J = 9 Hz), 8.55 (1H, s), 7.69 (1H, d, J = 7 Hz), 7.68 (1H, s), 6.24 (1H, s), 5.32-5.27 (1H, m), 4.61 (2H, dt, J = 48Hz, 4Hz), 4.26 (2H, dt, J = 30Hz, 4Hz), 4.09 (2H, t, J = 9Hz), 3.77 (2H, dt, J = 14Hz, 5Hz), 3.30-3.19 (6H, m), 2.03-1.97 (2H, m), 1,65-1.58 (2H, m), 1.10 (3H, t , J = 7Hz);
MS (ESI) m / z: 479 [M + H] ⁺ .

(Production Example 71) 2-Fluoroethyl 4-({6- [5- (propylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 393)
Using the compound obtained in Reference Example 34 (103 mg, 0.256 mmol), the reaction was carried out in the same manner as described in Production Example 70 to obtain the title white foam compound (61.0 mg, yield: 48%). It was.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 8.55 (1H, d, J = 9 Hz), 8.54 (1H, s), 7.69 (1H, d, J = 7 Hz), 7.68 (1H, s), 6.24 (1H, s), 5.32-5.27 (1H, m), 4.61 (2H, dt, J = 48Hz, 4Hz), 4.26 (2H, dt, J = 30Hz, 4Hz), 4.09 (2H, t, J = 9Hz), 3.77 (2H, dt, J = 14Hz, 5Hz), 3.31-3.18 (6H, m), 2.02-1.99 (2H, m), 1,65-1.51 (4H, m), 0.91 (3H, t , J = 7Hz);
MS (ESI) m / z: 493 [M + H] ⁺ .

(Production Example 72) 2-Fluoroethyl 4-({6- [5- (isobutylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 483)
Using the compound obtained in Reference Example 36 (101 mg, 0.242 mmol), the reaction was carried out in the same manner as described in Production Example 70 to obtain the title white foam compound (113 mg, yield: 92%). .
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, d, J = 9 Hz), 8.55 (1H, s), 7.71 (1H, d, J = 6 Hz), 7.70 (1H, s), 6.24 (1H, s), 5.32-5.27 (1H, m), 4.61 (2H, dt, J = 48Hz, 4Hz), 4.26 (2H, dt, J = 30Hz, 4Hz), 4.09 (2H, t, J = 9Hz), 3.80-3.75 (2H, m), 3.30-3.26 (4H, m), 3.12 (2H, d, J = 6Hz), 2.03-1.95 (3H, m), 1.65-1.58 (2H, m), 0.97 (6H, d, J = 7Hz);
MS (ESI) m / z: 507 [M + H] ⁺ .

(Production Example 73) Isopropyl 4-({6- [5- (isobutylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 479)
Using the compound (100 mg, 0.240 mmol) obtained in Reference Example 36, the reaction was carried out in the same manner as described in Production Example 31 to obtain the title white foam compound (119 mg, yield: 99%). .
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.54 (1H, d, J = 9 Hz), 8.54 (1H, s), 7.71 (1H, d, J = 7 Hz), 7.70 (1H, s), 6.23 (1H, s), 5.30-5.25 (1H, m), 4.78 (1H, sept, J = 6Hz), 4.09 (2H, t, J = 9Hz), 3.74 (2H, dt, J = 14Hz, 5Hz) , 3.30-3.20 (4H, m), 3.12 (2H, d, J = 6Hz), 2.03-1.94 (3H, m), 1.62-1.55 (2H, m), 1.19 (6H, d, J = 6Hz), 0.97 (6H, d, J = 6Hz);
MS (ESI) m / z: 503 [M + H] ⁺ .

Production Example 74 Isopropyl 4-[(6- {5-[(cyclopropylmethyl) sulfonyl] -indoline-1-yl} pyrimidin-4-yl] oxy) piperidine-1-carboxylate (Exemplary Compound No. 535) )
Using the compound obtained in Reference Example 38 (150 mg, 0.360 mmol), the reaction was carried out in the same manner as described in Production Example 31 to obtain the title white foam compound (177 mg, yield: 98%). .
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, d, J = 7 Hz), 8.54 (1H, s), 7.70 (1H, d, J = 8 Hz), 7.69 (1H, s), 6.23 (1H, s), 5.31-5.26 (1H, m), 4.78 (1H, sept, J = 6Hz), 4.10 (2H, t, J = 9Hz), 3.74 (2H, dt, J = 14Hz, 5Hz) , 3.30-3.26 (2H, m), 3.24-3.20 (2H, m), 3.17 (2H, d, J = 7Hz), 2.01-1.95 (2H, m), 1.62-1.55 (2H, m), 1.19 ( 6H, d, J = 6Hz), 0.87-0.85 (1H, m), 0.47-0.43 (2H, m), 0.13-0.10 (2H, m);
MS (ESI) m / z: 501 [M + H] ⁺ .

Production Example 75 2-Fluoroethyl 4-[(6- {5-[(cyclopropylmethyl) sulfonyl] -indoline-1-yl} pyrimidin-4-yl] oxy) piperidine-1-carboxylate (Exemplary Compound Number: 539)
Using the compound obtained in Reference Example 38 (150 mg, 0.360 mmol), the reaction was carried out in the same manner as described in Production Example 70 to obtain the title white foam compound (182 mg, yield: 92%). .
¹ H-NMR (500 MHz, DMSO-d ₆ ) δppm: 8.56 (1H, d, J = 6 Hz), 8.55 (1H, s), 7.70 (1H, d, J = 8 Hz), 7.69 (1H, s), 6.24 (1H, s), 5.32-5.27 (1H, m), 4.61 (2H, dt, J = 48Hz, 4Hz), 4.26 (2H, dt, J = 30Hz, 4Hz), 4.10 (2H, t, J = 9Hz), 3.79-3.75 (2H, m), 3.30-3.26 (4H, m), 3.17 (2H, d, J = 7Hz), 2.03-1.98 (2H, m), 1,65-1.58 (2H, m ), 0.87-0.85 (1H, m), 0.47-0.43 (2H, m), 0.13-0.10 (2H, m);
MS (ESI) m / z: 505 [M + H] ⁺ .

(Production Example 76) 2,2,2-trifluoroethyl 4-[(6- {5-[(cyclopropylmethyl) sulfonyl] -indoline-1-yl} pyrimidin-4-yl] oxy) piperidine-1- Carboxylate (Exemplary Compound Number: 542)
The compound obtained in Reference Example 39 (70.0 mg, 0.696 mmol) was used in the same manner as in the method described in Preparation Example 61 to give the title white foamy compound (99.0 mg, yield: 79%). Obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, d, J = 9 Hz), 8.55 (1H, s), 7.70 (1H, d, J = 8 Hz), 7.69 (1H, s), 6.24 (1H, s), 5.34-5.29 (1H, m), 4.72 (2H, q, J = 9Hz), 4.10 (2H, t, J = 9Hz), 3.76 (2H, dt, J = 14Hz, 4Hz) , 3.30-3.26 (4H, m), 3.17 (2H, d, J = 7Hz), 2.04-2.00 (2H, m), 1.67-1.60 (2H, m), 0.87-0.85 (1H, m), 0.47- 0.43 (2H, m), 0.13-0.10 (2H, m);
MS (ESI) m / z: 541 [M + H] ⁺ .

Production Example 77 1- (6-{[1- (Methoxyacetyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (methylsulfonyl) indoline (Exemplary Compound No. 98)
Using the compound obtained in Reference Example 28 (114 mg, 0.304 mmol), methoxyacetyl chloride (32 μL, 0.34 mmol) was used in the same manner instead of butyl chloroformate as described in Preparation Example 6. The title white foamy compound (108 mg, yield: 79%) was obtained.
¹ H-NMR (500 MHz, DMSO-d ₆ ) δ ppm: 8.55 (1H, s), 8.55 (1H, d, J = 9 Hz), 7.74 (1H, s), 7.73 (1H, d, J = 7 Hz), 6.24 (1H, s), 5.35-5.30 (1H, m), 4.11-4.08 (4H, m), 3.95-3.90 (1H, m), 3.69-3.65 (1H, m), 3.29 (3H, s), 3.29-3.26 (4H, m), 3.15 (3H, s), 2.04-1.96 (2H, m), 1.69-1.52 (2H, m);
MS (ESI) m / z: 469 [M + H] ⁺ .

Production Example 78 tert-Butyl 4-({6- [5- (cyclopropylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 437)
Reaction was carried out in the same manner as in Production Example 56 using the compound obtained in Reference Example 15 (30.3 mg, 0.136 mmol) to obtain the title white powdery compound (63.2 mg, yield: 93%). It was.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.56 (1H, d, J = 9 Hz), 8.50 (1H, s), 7.74 (1H, dd, J = 9 Hz, 2 Hz), 7.67 (1H, s), 5.98 (1H, s), 5.31 (1H, m), 4.06 (2H, t, J = 8Hz), 3.80 (2H, m), 3.31 (2H, t, J = 8Hz), 3.28 (2H, m), 2.45 (1H, m), 2.00 (2H, m), 1.73 (2H, m), 1.47 (9H, s), 1.33 (2H, m), 1.00 (2H, m);
MS (ESI) m / z: 501 [M + H] ⁺ .

Production Example 79 tert-Butyl 4-({6- [5- (cyclopentylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 526)
Using the compound obtained in Reference Example 12 (102 mg, 0.406 mmol), the reaction was carried out in the same manner as described in Production Example 56 to obtain the title white powdery compound (189 mg, yield: 88%). .
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.56 (1H, d, J = 9 Hz), 8.50 (1H, s), 7.73 (1H, d, J = 9 Hz), 7.67 (1H, s), 5.98 ( 1H, s), 5.31 (1H, m), 4.06 (2H, t, J = 9Hz), 3.80 (2H, m), 3.47 (1H, m), 3.34-3.23 (4H, m), 2.11-1.95 ( 4H, m), 1.88 (2H, m), 1.81-1.66 (4H, m), 1.60 (2H, m), 1.48 (9H, s);
MS (ESI) m / z: 528 [M + H] ⁺ .

Production Example 80 tert-Butyl 4-({6- [5- (methylsulfinyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 617)
Using 5-methylsulfinylindoline (116 mg, 0.641 mmol), the reaction was carried out in the same manner as described in Production Example 56 to obtain the title white powdery compound (146 mg, yield: 50%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.48 (1H, d, J = 9 Hz), 8.43 (1H, s), 7.50 (1H, s), 7.37 (1H, dd, J = 9 Hz, 1 Hz), 5.89 (1H, s), 5.26 (1H, m), 3.98 (2H, t, J = 9Hz), 3.75 (2H, m), 3.28-3.18 (4H, m), 2.66 (3H, s), 1.95 ( 2H, m), 1.68 (2H, m), 1.43 (9H, s);
MS (ESI) m / z: 459 [M + H] ⁺ .

(Production Example 81) Isopropyl 4-({6- [5- (methylsulfinyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 615)
Using 5-methylsulfinylindoline (329 mg, 1.79 mmol) instead of tert-butyl 4-hydroxypiperidine-1-carboxylate of the method described in Preparation 56, the compound obtained in Reference Example 42 (535 mg , 1.79 mmol) to give the title white powdery compound (467 mg, yield: 59%).
¹ H-NMR (400MHz, CDCl ₃ ) δppm: 8.42 (1H, d, J = 9Hz), 8.36 (1H, s), 7.42 (1H, s), 7.31 (1H, dd, J = 9Hz, 1Hz), 5.83 (1H, s), 5.22 (1H, m), 4.83 (1H, m), 3.90 (2H, t, J = 9Hz), 3.73 (2H, m), 3.24 (2H, m), 3.17 (2H, t, J = 9Hz), 2.60 (3H, s), 1.91 (2H, m), 1.64 (2H, m), 1.16 (6H, d, J = 6Hz);
MS (ESI) m / z: 445 [M + H] ⁺ .

(Production Example 82) tert-butyl 4-({5-methoxy-6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary compound number: 264)
Using 5-methylsulfonylindoline (199 mg, 1.01 mmol) instead of tert-butyl 4-hydroxypiperidine-1-carboxylate of the method described in Preparation 56, the compound obtained in Reference Example 43 (347 mg 1.01 mmol), and the title grayish white foam compound (431 mg, yield: 85%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.23 (1H, s), 7.73-7.70 (3H, m), 5.38 (1H, m), 4.34 (2H, t, J = 8Hz), 3.79 (2H, m), 3.77 (3H, s), 3.36 (2H, m), 3.24 (2H, t, J = 9Hz), 3.03 (3H, s), 2.04 (2H, m), 1.83 (2H, m), 1.48 (9H, s);
MS (ESI) m / z: 505 [M + H] ⁺ .

(Production Example 83) Isopropyl 4-({5-methoxy-6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 262)
The reaction was carried out in the same manner as in Production Example 28 using the compound obtained in Production Example 82 (369 mg, 0.731 mmol) to obtain the title white foamy compound (209 mg, yield: 58%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.23 (1H, s), 7.73-7.71 (3H, m), 5.39 (1H, m), 4.94 (1H, m), 4.34 (2H, t, J = 8Hz), 3.83 (2H, m), 3.77 (3H, s), 3.40 (2H, m), 3.24 (2H, t, J = 9Hz), 3.03 (3H, s), 2.05 (2H, m), 1.84 (2H, m), 1.27 (6H, d, J = 6Hz);
MS (ESI) m / z: 491 [M + H] ⁺ .

(Production Example 84) tert-butyl 4-[(6- {5-[(2-hydroxyethyl) sulfonyl] indoline-1-yl} pyrimidin-4-yl) oxy] piperidine-1-carboxylate (Exemplary Compound No. : 373)
Palladium hydroxide (100 mg) was added to a mixed solution of the compound obtained in Reference Example 44 (486 mg, 0.817 mmol) in methanol (10 mL) and ethyl acetate (10 mL), and the mixture was stirred in a hydrogen atmosphere for 19.5 hours. The reaction solution was filtered through Celite (trade name), and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 3: 2 → 4: 1, v / v) to obtain the title white foam compound (330 mg, yield: 80%).
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.61 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.76 (1H, dd, J = 9 Hz, 2 Hz), 7.70 (1H, s), 5.99 (1H, s), 5.32 (1H, m), 4.07 (2H, t, J = 9Hz), 3.99 (2H, m), 3.80 (2H, m), 3.36-3.23 (6H, m), 2.85 ( 1H, t, J = 6Hz), 2.00 (2H, m), 1.73 (2H, m), 1.48 (9H, s);
MS (ESI) m / z: 505 [M + H] ⁺ .

(Production Example 85) tert-butyl 4-[(6- {5-[(2-fluoroethyl) sulfonyl] indoline-1-yl} pyrimidin-4-yl) oxy] piperidine-1-carboxylate (Exemplary Compound No. : 355)
(Diethylamino) sulfur trifluoride (DAST, 34 μL, 0.260 mmol) was added to a solution of the compound obtained in Production Example 84 (43.1 mg, 0.0855 mmol) in dichloromethane (5 mL) at −78 ° C., and then at −78 ° C. for 1 hour. The mixture was further stirred for 30 minutes while raising the temperature to 0 ° C. A saturated aqueous sodium hydrogen carbonate solution was added to the reaction solution, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 4: 1 → 7: 3, v / v) to obtain the title white foam compound (17.0 mg, yield: 39%). .
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.59 (1H, d, J = 8Hz), 8.51 (1H, d, J = 1Hz), 7.77 (1H, d, J = 9Hz, 2Hz), 7.70 (1H , s), 5.98 (1H, s), 5.32 (1H, m), 4.81 (2H, dt, J = 47Hz, 5Hz), 4.07 (2H, t, J = 9Hz), 3.80 (2H, m), 3.50 (2H, dt, J = 22Hz, 5Hz), 3.35-3.23 (4H, m), 2.00 (2H, m), 1.73 (2H, m), 1.48 (9H, s);
MS (ESI) m / z: 507 [M + H] ⁺ .

Production Example 86 tert-Butyl 4-[(6- {5-[(2-chloroethyl) sulfonyl] indoline-1-yl} pyrimidin-4-yl) oxy] piperidine-1-carboxylate (Exemplary Compound Number: 364)
Carbon tetrachloride (58 μL, 0.601 mmol) and triphenylphosphine (52 mg, 0.198 mmol) were added to a solution of the compound obtained in Production Example 84 (49.9 mg, 0.0990 mmol) in dichloromethane (5 mL), and the mixture was stirred at room temperature overnight. . The solvent of the reaction solution was distilled off under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane: ethyl acetate = 9: 1 → 7: 3, v / v) to give the title white foam The compound (32.3 mg, yield: 62%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.60 (1H, d, J = 9Hz), 8.51 (1H, s), 7.74 (1H, dd, J = 9Hz, 2Hz), 7.67 (1H, s), 5.99 (1H, s), 5.32 (1H, m), 4.08 (2H, t, J = 9Hz), 3.80 (2H, m), 3.74 (2H, t, J = 7Hz), 3.51 (2H, t, J = 7Hz), 3.36-3.23 (4H, m), 2.00 (2H, m), 1.73 (2H, m), 1.48 (9H, s);
MS (ESI) m / z: 524 [M + H] ⁺ .

(Production Example 87) tert-butyl 4-({6- [5- (aminosulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplified Compound No .: 562)
A concentrated sulfuric acid (5 mL) solution of the compound (269 mg, 0.410 mmol) obtained in Reference Example 45 was stirred at room temperature overnight. To the reaction solution, 2N aqueous sodium hydroxide solution and di (tert-butyl) dicarbonate (1.1 g, 5.0 mmol) were added at 0 ° C., and the mixture was stirred at room temperature. After 3 hours, THF (100 mL) and di (tert-butyl) dicarbonate (1.1 g, 5.0 mmol) were added, and the mixture was stirred at room temperature for 30 minutes. The reaction solution was extracted three times with ethyl acetate, the obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 1: 1, v / v) to obtain the title white powdery compound (151 mg, yield: 77%).
¹ H-NMR (400MHz, CDCl ₃ ) δppm: 8.53 (1H, d, J = 9Hz), 8.51 (1H, d, J = 1Hz), 7.78 (1H, dd, J = 9Hz, 2Hz), 7.72 (1H , s), 5.97 (1H, d, J = 1Hz), 5.31 (1H, m), 4.72 (2H, s), 4.05 (2H, t, J = 8Hz), 3.80 (2H, m), 3.33-3.24 (4H, m), 2.00 (2H, m), 1.73 (2H, m), 1.48 (9H, s);
MS (ESI) m / z: 476 [M + H] ⁺ .

(Production Example 88) Isopropyl 4-[(6- {5-[(dimethylamino) sulfonyl] indoline-1-yl} pyrimidin-4-yl) oxy] piperidine-1-carboxylate (Exemplary Compound Number: 604)
To a mixed solution of N, N-dimethylindoline-5-sulfonamide (120 mg, 0.531 mmol) and the compound obtained in Reference Example 42 (79.6 mg, 0.266 mmol) in acetone (8 mL) and water (2 mL) Concentrated hydrochloric acid (235 μL, 2.66 mmol) was added, and the mixture was stirred at 80 ° C. for 15 hours. A saturated aqueous sodium hydrogen carbonate solution was added to the reaction solution, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 4: 1 → 1: 1, v / v) to obtain the title pale yellow powdery compound (77.2 mg, yield: 59%). It was.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.55 (1H, d, J = 9 Hz), 8.50 (1H, s), 7.63 (1H, dd, J = 9 Hz, 2 Hz), 7.57 (1H, s), 5.97 (1H, s), 5.33 (1H, m), 4.94 (1H, m), 4.05 (2H, t, J = 9Hz), 3.83 (2H, m), 3.38-3.26 (4H, m), 2.70 ( 6H, s), 2.01 (2H, m), 1.74 (2H, m), 1.26 (6H, d, J = 6Hz);
MS (ESI) m / z: 490 [M + H] ⁺ .

Production Example 89 Isopropyl 4-({6- [5- (aminosulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 560)
Using the compound (239 mg, 0.800 mmol) obtained in Reference Example 42, instead of N, N-dimethylindoline-5-sulfonamide in the method described in Preparation Example 88, indoline-5-sulfonamide (106 mg , 0.533 mmol) to give the title white powdery compound (17.0 mg, yield: 7%).
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.53 (1H, d, J = 9 Hz), 8.50 (1H, s), 7.78 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H, s), 5.97 (1H, s), 5.33 (1H, m), 4.94 (1H, m), 4.72 (2H, s), 4.05 (2H, t, J = 9Hz), 3.83 (2H, m), 3.33 (2H, m), 3.30 (2H, t, J = 9Hz), 2.01 (2H, m), 1.74 (2H, m), 1.26 (6H, d, J = 6Hz);
MS (ESI) m / z: 462 [M + H] ⁺ .

(Production Example 90) Isopropyl 4-[(6- {5-[(methylamino) sulfonyl] indoline-1-yl} pyrimidin-4-yl) oxy] piperidine-1-carboxylate (Exemplary Compound Number: 583)
Using the compound (214 mg, 0.714 mmol) obtained in Reference Example 42, N-methylindoline-5-sulfonamide instead of N, N-dimethylindoline-5-sulfonamide in the method described in Preparation Example 88 (101 mg, 0.476 mmol) was used in the same manner to obtain the title white powdery compound (20.0 mg, yield: 9%).
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.55 (1H, d, J = 8 Hz), 8.51 (1H, s), 7.73 (1H, d, J = 8 Hz), 7.64 (1H, s), 5.98 ( 1H, s), 5.37 (1H, m), 4.94 (1H, m), 4.37 (1H, m), 4.06 (2H, t, J = 8Hz), 3.83 (2H, m), 3.38-3.28 (4H, m), 2.66 (3H, d, J = 5Hz), 2.03 (2H, m), 1.76 (2H, m), 1.24 (6H, d, J = 7Hz);
MS (ESI) m / z: 476 [M + H] ⁺ .

(Production Example 91) tert-butyl 4-({2-methyl-6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary compound number: 193)
Using the compound obtained in Reference Example 26 (67.3 mg, 0.203 mmol), the reaction was carried out in the same manner as described in Production Example 1 to obtain the title white powdery compound (49.1 mg, yield: 72%). Obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.60 (1H, d, J = 9 Hz), 7.78 (1H, dd, J = 9 Hz, 2 Hz), 7.70 (1H, s), 5.79 (1H, s), 5.34 (1H, m), 4.04 (2H, t, J = 9Hz), 3.77 (2H, m), 3.34-3.24 (4H, m), 3.03 (3H, m), 2.56 (3H, s), 1.98 ( 2H, m), 1.72 (2H, m), 1.48 (9H, s);
MS (ESI) m / z: 489 [M + H] ⁺ .

Production Example 92 1- (6-{[1- (3-Methylbutanoyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (methylsulfonyl) indoline (Exemplary Compound No. 69)
Using the compound obtained in Reference Example 28 (843 mg, 2.25 mmol), the reaction was carried out in the same manner as described in Production Example 63 to obtain the title white powdery compound (961 mg, yield: 93%). .
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.57 (1H, d, J = 9 Hz), 8.50 (1H, s), 7.76 (1H, d, J = 9 Hz), 7.70 (1H, s), 5.98 ( 1H, s), 5.38 (1H, m), 4.06 (2H, t, J = 9Hz), 4.04 (1H, m), 3.76 (1H, m), 3.43 (2H, m), 3.30 (2H, t, J = 9Hz), 3.04 (3H, s), 2.25 (2H, d, J = 7Hz), 2.13 (1H, m), 2.05 (2H, m), 1.76 (2H, m), 0.99 (6H, d, J = 7Hz);
MS (ESI) m / z: 459 [M + H] ⁺ .

(Production Example 93) 4-Fluorophenyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. 47)
Using the compound obtained in Reference Example 28 (133 mg, 0.356 mmol) and using 4-fluorophenyl chloroformate (55 μL, 0.430 mmol) instead of butyl chloroformate in the method described in Preparation Example 6, the same procedure was performed. The title white powdery compound (150 mg, yield: 82%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.59 (1H, d, J = 9 Hz), 8.52 (1H, s), 7.79 (1H, d, J = 9 Hz), 7.73 (1H, s), 7.12- 7.01 (4H, m), 6.01 (1H, s), 5.41 (1H, m), 4.08 (2H, t, J = 9Hz), 4.03-3.84 (2H, m), 3.64-3.43 (2H, m), 3.32 (2H, t, J = 9Hz), 3.04 (3H, s), 2.10 (2H, m), 1.88 (2H, m);
MS (ESI) m / z: 513 [M + H] ⁺ .

(Production Example 94) 4-Methoxyphenyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 48)
Using the compound obtained in Reference Example 28 (135 mg, 0.361 mmol), and using 4-methoxyphenyl chloroformate (65 μL, 0.437 mmol) instead of butyl chloroformate in the method described in Preparation Example 6 The title white powdery compound (166 mg, yield: 88%) was obtained.
¹ H-NMR (500 MHz, CDCl ₃ ) δ ppm: 8.58 (1H, d, J = 9 Hz), 8.52 (1H, s), 7.79 (1H, d, J = 9 Hz), 7.73 (1H, s), 7.03 ( 2H, d, J = 9Hz), 6.88 (2H, d, J = 9Hz), 6.01 (1H, s), 5.41 (1H, m), 4.08 (2H, t, J = 9Hz), 4.03-3.85 (2H , m), 3.80 (3H, s), 3.63-3.43 (2H, m), 3.32 (2H, t, J = 9Hz), 3.04 (3H, s), 2.09 (2H, m), 1.86 (2H, m );
MS (ESI) m / z: 525 [M + H] ⁺ .

(Production Example 95) N, N-dimethyl-4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxamide (Exemplary Compound No. 114)
Using the compound obtained in Reference Example 28 (63.3 mg, 0.169 mmol), using dimethylcarbamic acid chloride (19 μL, 0.206 mmol) instead of butyl chloroformate in the method described in Preparation Example 6 in the same manner. Reaction was performed to obtain the title white powdery compound (66.1 mg, yield: 88%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.78 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H, m), 5.98 (1H, s), 5.32 (1H, m), 4.06 (2H, t, J = 9Hz), 3.55 (2H, m), 3.31 (2H, t, J = 9Hz), 3.13 (2H, m), 3.04 (3H, s), 2.85 (6H, s), 2.05 (2H, m), 1.79 (2H, m);
MS (ESI) m / z: 446 [M + H] ⁺ .

Production Example 96 5- (Methylsulfonyl) -1- (6-{[1- (3-phenylpropanoyl) piperidin-4-yl] oxy} pyrimidin-4-yl) indoline (Exemplary Compound No. 93)
Using the compound obtained in Reference Example 28 (118 mg, 0.316 mmol) and using 3-phenylpropionic acid (90 mg, 0.602 mmol) instead of cyclopropylacetic acid according to the method described in Preparation 48 Reaction was performed to obtain the title white powdery compound (150 mg, yield: 94%).
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.57 (1H, d, J = 9 Hz), 8.49 (1H, s), 7.77 (1H, dd, J = 9 Hz, 2 Hz), 7.70 (1H, s), 7.34-7.18 (5H, m), 5.97 (1H, s), 5.34 (1H, m), 4.05 (2H, t, J = 9Hz), 3.98 (1H, m), 3.66 (1H, m), 3.49 ( 1H, m), 3.33 (1H, m), 3.29 (2H, t, J = 9Hz), 3.04 (3H, s), 2.99 (2H, t, J = 8Hz), 2.67 (2H, t, J = 7Hz ), 2.03-1.87 (2H, m), 1.81-1.61 (2H, m);
MS (ESI) m / z: 507 [M + H] ⁺ .

Production Example 97 1- [6-({1- [3- (4-Methoxyphenyl) propanoyl] piperidin-4-yl} oxy) pyrimidin-4-yl] -5- (methylsulfonyl) indoline (Exemplary Compound Number: 95)
Using the compound (148 mg, 0.396 mmol) obtained in Reference Example 28, 3- (4-methoxyphenyl) propionic acid (107 mg, 0.594 mmol) instead of cyclopropylacetic acid according to the method described in Preparation Example 48 Was used in the same manner to obtain the title white powdery compound (178 mg, yield: 84%).
¹ H-NMR (400MHz, CDCl ₃ ) δppm: 8.57 (1H, d, J = 9Hz), 8.50 (1H, s), 7.78 (1H, dd, J = 9Hz, 2Hz), 7.72 (1H, s), 7.15 (2H, d, J = 9Hz), 6.84 (2H, d, J = 9Hz), 5.98 (1H, s), 5.35 (1H, m), 4.06 (2H, t, J = 9Hz), 4.00 (1H , m), 3.79 (3H, s), 3.66 (1H, m), 3.47 (1H, m), 3.38-3.26 (3H, m), 3.04 (3H, s), 2.93 (2H, t, J = 8Hz ), 2.63 (2H, t, J = 7Hz), 2.04-1.89 (2H, m), 1.81-1.61 (2H, m);
MS (ESI) m / z: 537 [M + H] ⁺ .

Production Example 98 1- [6-({1- [3- (4-Fluorophenyl) propanoyl] piperidin-4-yl} oxy) pyrimidin-4-yl] -5- (methylsulfonyl) indoline (Exemplary Compound Number: 94)
Using the compound obtained in Reference Example 28 (179 mg, 0.479 mmol), 3- (4-fluorophenyl) propionic acid (121 mg, 0.720 mmol) instead of cyclopropylacetic acid in the method described in Preparation Example 48 Was used in the same manner to obtain the title white powdery compound (183 mg, yield: 73%).
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.57 (1H, d, J = 9 Hz), 8.49 (1H, s), 7.78 (1H, dd, J = 9 Hz, 2 Hz), 7.71 (1H, s), 7.19 (2H, m), 6.98 (2H, m), 5.98 (1H, s), 5.36 (1H, m), 4.06 (2H, t, J = 9Hz), 4.00 (1H, m), 3.66 (1H, m), 3.48 (1H, m), 3.39-3.26 (3H, m), 3.04 (3H, s), 2.96 (2H, t, J = 7Hz), 2.64 (2H, t, J = 7Hz), 2.04- 1.85 (2H, m), 1.81-1.62 (2H, m);
MS (ESI) m / z: 525 [M + H] ⁺ .

Production Example 99 1- (6-{[1- (3-Cyclopropylpropanoyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (methylsulfonyl) indoline (Exemplary Compound No. 79 )
Using the compound obtained in Reference Example 28 (112 mg, 0.299 mmol) and using 3-cyclopropylpropionic acid (209 mg, 1.83 mmol) instead of cyclopropylacetic acid in the method described in Preparation Example 48 The title white powdery compound (62.9 mg, yield: 44%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H, s), 5.99 (1H, s), 5.38 (1H, m), 4.07 (2H, t, J = 9Hz), 4.03 (1H, m), 3.77 (1H, m), 3.50-3.38 (2H, m), 3.31 ( 2H, t, J = 9Hz), 3.04 (3H, s), 2.48 (2H, t, J = 8Hz), 2.12-1.96 (2H, m), 1.85-1.68 (2H, m), 1.56 (2H, m ), 0.74 (1H, m), 0.45 (2H, m), 0.08 (2H, m);
MS (ESI) m / z: 471 [M + H] ⁺ .

(Production Example 100) 5- (Methylsulfonyl) -1- (6-{[1- (4,4,4-trifluorobutanoyl) piperidin-4-yl] oxy} pyrimidin-4-yl) indoline (exemplified) Compound number: 82)
Using the compound (220 mg, 0.588 mmol) obtained in Reference Example 28, 4,4,4-trifluorobutanoic acid (107 mg, 0.754 mmol) instead of cyclopropylacetic acid in the method described in Preparation Example 48 The title white powdery compound (135 mg, yield: 46%) was obtained in the same manner.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.73 (1H, s), 5.99 (1H, s), 5.40 (1H, m), 4.07 (2H, t, J = 9Hz), 3.98 (1H, m), 3.73 (1H, m), 3.52 (1H, m), 3.43 (1H, m), 3.32 (2H, t, J = 9Hz), 3.04 (3H, s), 2.65-2.46 (4H, m), 2.13-1.97 (2H, m), 1.88-1.73 (2H, m);
MS (ESI) m / z: 499 [M + H] ⁺ .

(Production Example 101) N-isopropyl-4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxamide (Exemplary Compound No. 106)
Isopropyl isocyanate (31 μL, 0.315 mmol) was added to a solution of the compound obtained in Reference Example 28 (78.1 mg, 0.209 mmol) in dichloromethane (5 mL), and the mixture was stirred at room temperature for 30 minutes. Water was added to the reaction solution, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (ethyl acetate) to obtain the title white powdery compound (87.3 mg, yield: 91%).
^{1 H-NMR (400MHz, CDCl} 3) δppm: 8.57 (1H, d, J = 9Hz), 8.50 (1H, s), 7.78 (1H, dd, J = 9Hz, 2Hz), 7.71 (1H, s), 5.98 (1H, s), 5.33 (1H, m), 4.31 (1H, d, J = 7Hz), 4.06 (2H, t, J = 9Hz), 3.99 (1H, m), 3.70 (2H, m), 3.31 (2H, t, J = 9Hz), 3.25 (2H, m), 3.04 (3H, s), 2.03 (2H, m), 1.77 (2H, m), 1.17 (6H, d, J = 6Hz);
MS (ESI) m / z: 460 [M + H] ⁺ .

(Production Example 102) 1-methylcyclopentyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 16)
1,1'-carbonyldiimidazole (1.09 g, 6.70 mmol) was added to a toluene (30 mL) solution of 1-methylcyclopentanol (671 mg, 6.70 mmol), and the mixture was stirred at room temperature for 4.5 hours. The solvent was distilled off from the reaction solution under reduced pressure, and the resulting residue was purified by silica gel column chromatography (hexane: ethyl acetate = 4: 1, v / v) to obtain a colorless oily compound (417 mg). Hereinafter, this compound is referred to as an imidazole compound.

To a dioxane (10 mL) solution of the compound obtained in Reference Example 28 (82.9 mg, 0.222 mmol) were added potassium carbonate (153 mg, 1.11 mmol) and an imidazole compound (129 mg, 0.665 mmol), and the mixture was heated to reflux for 8 hours. A saturated aqueous ammonium chloride solution was added to the reaction solution, and the mixture was extracted with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 4: 1 → 3: 2, v / v) to obtain the title white powdery compound (46.8 mg, yield: 42%). .
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.57 (1H, d, J = 9 Hz), 8.50 (1H, s), 7.78 (1H, dd, J = 9 Hz, 2 Hz), 7.71 (1H, s), 5.98 (1H, s), 5.32 (1H, m), 4.06 (2H, t, J = 9Hz), 3.80 (2H, m), 3.34-3.24 (4H, m), 3.04 (3H, s), 2.14 ( 2H, m), 2.00 (2H, m), 1.79-1.60 (8H, m), 1.59 (3H, s);
MS (ESI) m / z: 501 [M + H] ⁺ .

(Production Example 103) 2-Fluoro-1-methylethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound No. : 56)
Using the compound (47.7 mg, 0.128 mmol) obtained in Reference Example 28, using 1-fluoro-2-propanol instead of 1-methylcyclopentanol in the method described in Preparation Example 102, the same manner Reaction was performed to obtain the title white powdery compound (27.8 mg, yield: 45%).
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H, s), 5.98 (1H, s), 5.35 (1H, m), 5.06 (1H, m), 4.44 (2H, m), 4.07 (2H, t, J = 9Hz), 3.84 (2H, m), 3.38 (2H, m), 3.31 (2H, d, J = 9Hz), 3.04 (3H, s), 2.02 (2H, m), 1.77 (2H, m), 1.31 (3H, d, J = 7Hz);
MS (ESI) m / z: 479 [M + H] ⁺ .

(Production Example 104) 2,2,2-trifluoroethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 54)
Using the compound obtained in Reference Example 29 (300 mg, 0.640 mmol), the reaction was carried out in the same manner as described in Production Example 61 to obtain the title white foam compound (217 mg, yield: 68%). .
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.78 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H, s), 5.99 (1H, s), 5.37 (1H, m), 4.52 (2H, qd, J = 9Hz, 2Hz), 4.06 (2H, t, J = 9Hz), 3.83 (2H, m), 3.46 (2H, m ), 3.31 (2H, t, J = 9Hz), 3.04 (3H, s), 2.03 (2H, m), 1.81 (2H, m);
MS (ESI) m / z: 501 [M + H] ⁺ .

(Production Example 105) 1,1-dimethylpropyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 14) )
Trifluoroacetic acid (2 mL) was added to a solution of the compound obtained in Production Example 1 (430 mg, 0.881 mmol) in dichloromethane (10 mL), and the mixture was stirred at room temperature for 2 hours. Using a part of the residue obtained by distilling off the solvent under reduced pressure (201 mg), 2-methyl-2-butanol was used instead of 1-methylcyclopentanol in the method described in Preparation Example 102. The title white powdery compound (50.4 mg, yield: 19%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.78 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H, s), 5.98 (1H, s), 5.32 (1H, m), 4.07 (2H, t, J = 9Hz), 3.80 (2H, m), 3.31 (2H, d, J = 9Hz), 3.29 (2H, m), 3.04 (3H, s), 2.00 (2H, m), 1.80 (2H, q, J = 7Hz), 1.73 (2H, m), 1.45 (6H, s), 0.91 (3H, t, J = 7Hz);
MS (ESI) m / z: 489 [M + H] ⁺ .

Production Example 106 1-Methylcyclohexyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 17)
Using the compound (430 mg, 0.881 mmol) obtained in Production Example 1, the same reaction was carried out using 1-methylcyclohexanol instead of 2-methyl-2-butanol in the method described in Production Example 105. The title white powdery compound (78.5 mg, yield: 34%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H, s), 5.98 (1H, s), 5.33 (1H, m), 4.07 (2H, t, J = 9Hz), 3.84 (2H, m), 3.36-3.26 (4H, m), 3.04 (3H, s), 2.19 ( 2H, m), 2.02 (2H, m), 1.74 (2H, m), 1.62-1.23 (8H, m), 1.50 (3H, s);
MS (ESI) m / z: 515 [M + H] ⁺ .

(Production Example 107) 4-Methoxybenzyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 51)
Using the compound obtained in Reference Example 29 (180 mg, 1.60 mmol) in the same manner using 4-methoxybenzyl alcohol (100 μL, 0.802 mmol) instead of 2-butanol in the method described in Preparation Example 9. Reaction was performed to obtain the title white powdery compound (167 mg, yield: 81%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.57 (1H, d, J = 9Hz), 8.50 (1H, d, J = 1Hz), 7.78 (1H, dd, J = 9Hz, 2Hz), 7.71 (1H , s), 7.32 (2H, m), 6.88 (2H, m), 5.97 (1H, s), 5.33 (1H, m), 5.08 (2H, s), 4.06 (2H, t, J = 9Hz), 3.84 (2H, m), 3.81 (3H, s), 3.37 (2H, m), 3.30 (2H, t, J = 9Hz), 3.04 (3H, s), 2.00 (2H, m), 1.75 (2H, m);
MS (ESI) m / z: 539 [M + H] ⁺ .

Production Example 108 4-Fluorobenzyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 50)
Using the compound (170 mg, 0.363 mmol) obtained in Reference Example 29 in the same manner using 4-fluorobenzyl alcohol (100 μL, 0.917 mmol) instead of 2-butanol in the method described in Preparation Example 9. Reaction was performed to obtain the title white foamy compound (50.4 mg, yield: 26%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.57 (1H, d, J = 9Hz), 8.50 (1H, d, J = 1Hz), 7.79 (1H, dd, J = 9Hz, 2Hz), 7.72 (1H , m), 7.36 (2H, m), 7.05 (2H, m), 5.99 (1H, d, J = 1Hz), 5.34 (1H, m), 5.11 (2H, s), 4.06 (2H, t, J = 9Hz), 3.84 (2H, m), 3.39 (2H, m), 3.31 (2H, t, J = 9Hz), 3.04 (3H, s), 2.02 (2H, m), 1.76 (2H, m);
MS (ESI) m / z: 527 [M + H] ⁺ .

(Preparation Example 109) (2,2-Difluorocyclopropyl) methyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary) Compound number: 57)
Using the compound obtained in Reference Example 29 (240 mg, 0.513 mmol), 2,2-difluorocyclopropylmethanol (199 mg, 1.84 mmol) was used instead of 2-butanol in the method described in Preparation Example 9. In the same manner, the title white powdery compound (194 mg, yield: 74%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9Hz), 8.51 (1H, d, J-1Hz), 7.78 (1H, dd, J = 9Hz, 2Hz), 7.72 (1H , m), 5.99 (1H, d, J = 1Hz), 5.35 (1H, m), 4.28 (1H, m), 4.10-4.02 (3H, m), 3.83 (2H, m), 3.39 (2H, m ), 3.31 (2H, t, J = 9Hz), 3.04 (3H, s), 2.08-1.95 (3H, m), 1.77 (2H, m), 1.52 (1H, m), 1.23 (1H, m);
MS (ESI) m / z: 509 [M + H] ⁺ .

(Production Example 110) Cyclopropylmethyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 313)
Using the compound obtained in Reference Example 31 (97.9 mg, 0.203 mmol), the same operation as in the method described in Preparation Example 44 was performed, and the title white powdery compound (44.1 mg, yield: 45%) was obtained. Obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.74 (1H, dd, J = 9 Hz, 2 Hz), 7.68 (1H, s), 5.99 (1H, s), 5.34 (1H, m), 4.07 (2H, t, J = 9Hz), 3.93 (2H, d, J = 7Hz), 3.86 (2H, m), 3.37 (2H, m), 3.31 (2H, t, J = 9Hz), 3.10 (2H, q, J = 7Hz), 2.03 (2H, m), 1.76 (2H, m), 1.28 (3H, t, J = 7Hz), 1.15 (1H , m), 0.57 (2H, m), 0.29 (2H, m);
MS (ESI) m / z: 487 [M + H] ⁺ .

(Production Example 111) Cyclopentyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 312)
Using the compound obtained in Reference Example 31 (130 mg, 0.269 mmol), the reaction was carried out in the same manner as in Production Example 49 to obtain the title white powdery compound (85.6 mg, yield: 64%). It was.
¹ H-NMR (400 MHz, CDCl ₃ ) δ ppm: 8.57 (1H, d, J = 9 Hz), 8.50 (1H, s), 7.74 (1H, dd, J = 9 Hz, 2 Hz), 7.67 (1H, s), 5.98 (1H, s), 5.33 (1H, m), 5.12 (1H, m), 4.06 (2H, t, J = 9Hz), 3.81 (2H, m), 3.37-3.27 (4H, m), 3.10 ( 2H, q, J = 7Hz), 2.01 (2H, m), 1.86 (2H, m), 1.79-1.66 (6H, m), 1.60 (2H, m), 1.27 (3H, t, J = 7Hz);
MS (ESI) m / z: 501 [M + H] ⁺ .

(Production Example 112) Benzyl rac-cis-2-methyl-4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 299)
Benzyl rac-cis-4-hydroxy-2-methylpiperidine-1-carboxylate (compound described in J. Chem. Soc., Perkin Trans. 1, 1998, 20, p. 3365, 152 mg, 0.610 mmol) in THF (10 mL) was added sodium hydride (63%) (49 mg, 1.23 mmol) and stirred at room temperature for 30 minutes. To the reaction solution, 1- (6-chloropyrimidin-4-yl) -5- (methylsulfonyl) indoline (227 mg, 0.733 mmol) produced in Reference Example 19 was added and stirred for 10.5 hours. Saturated aqueous ammonium chloride solution was added to the reaction solution, followed by extraction three times with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 7: 3 → 3: 2, v / v) to obtain the title white powdery compound (271 mg, yield: 85%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.78 (1H, dd, J = 9 Hz, 2 Hz), 7.71 (1H, m), 7.39-7.27 (5H, m), 5.96 (1H, s), 5.50 (1H, m), 5.15 (2H, d, J = 2Hz), 4.49 (1H, m), 4.13-3.99 (3H, m), 3.39-3.25 (3H, m), 3.03 (3H, s), 2.05-1.95 (2H, m), 1.87-1.76 (2H, m) 1.33 (3H, d, J = 7Hz);
MS (ESI) m / z: 523 [M + H] ⁺ .

(Preparation Example 113) Isopropyl rac-cis-2-methyl-4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 295)
To a mixed solution of the compound obtained in Production Example 112 (271 mg, 0.519 mmol) in methanol (5 mL) and ethyl acetate (5 mL) was added palladium hydroxide (300 mg), and the mixture was stirred under a hydrogen atmosphere for 2 hours. The reaction solution was filtered through Celite (trade name), and the solvent was distilled off under reduced pressure. To a solution of the obtained residue in dichloromethane (10 mL) were added diisopropylethylamine (447 μL, 2.63 mmol) and isopropyl chloroformate (218 μL, 1.56 mmol) at 0 ° C., and the mixture was stirred for 30 minutes while warming to room temperature. Saturated aqueous ammonium chloride solution was added to the reaction solution, followed by extraction three times with ethyl acetate. The obtained organic layer was dried over anhydrous sodium sulfate, and the solvent was distilled off under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 7: 3-3: 2, v / v) to obtain the title white powdery compound (39.8 mg, yield: 16%). .
¹ H-NMR (400MHz, CDCl ₃ ) δppm: 8.59 (1H, d, J = 9Hz), 8.52 (1H, s), 7.79 (1H, dd, J = 9Hz, 2Hz), 7.73 (1H, m), 5.97 (1H, s), 5.50 (1H, m), 4.95 (1H, m), 4.43 (1H, m), 4.09 (2H, t, J = 9Hz), 3.99 (1H, m), 3.35-3.24 ( 3H, m), 3.04 (3H, s), 2.02-1.94 (3H, m), 1.87-1.76 (1H, m), 1.30 (3H, d, J = 7Hz), 1.26 (6H, dd, J = 6Hz , 1Hz);
MS (ESI) m / z: 475 [M + H] ⁺ .

(Production Example 114) Allyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 31)
Using the compound obtained in Reference Example 28 (518 mg, 1.39 mmol), the same reaction was carried out using allyl chloroformate (220 μL, 2.08 mmol) instead of butyl chloroformate in the method described in Preparation Example 6. The title white powdery compound (522 mg, yield: 82%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.57 (1H, d, J = 9Hz), 8.50 (1H, d, J = 1Hz), 7.77 (1H, dd, J = 9Hz, 2Hz), 7.71 (1H , s), 5.99 (1H, s), 5.96 (1H, m), 5.34 (1H, m), 5.32 (1H, m), 5.22 (1H, m), 4.62 (2H, m), 4.06 (2H, t, J = 9Hz), 3.85 (2H, m), 3.39 (2H, ddd, J = 13Hz, 9Hz, 4Hz), 3.31 (2H, t, J = 9Hz), 3.04 (3H, s), 2.02 (2H , m), 1.77 (2H, m);
MS (ESI) m / z: 459 [M + H] ⁺ .

Production Example 115 Prop-2-yn-1-yl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 33)
Using the compound obtained in Reference Example 28 (408 mg, 1.09 mmol), the reaction was similarly carried out using propargyl chloroformate (159 μL, 1.63 mmol) instead of butyl chloroformate in the method described in Preparation Example 6. The title pale yellow powdery compound (338 mg, yield: 68%) was obtained.
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.58 (1H, d, J = 9 Hz), 8.51 (1H, s), 7.79 (1H, dd, J = 9 Hz, 2 Hz), 7.72 (1H, d, J = 1Hz), 5.99 (1H, s), 5.96 (1H, m), 5.35 (1H, m), 4.73 (1H, d, J = 2Hz), 4.07 (2H, t, J = 9Hz), 3.83 (2H , m), 3.42 (2H, ddd, J = 13Hz, 9Hz, 4Hz), 3.31 (2H, t, J = 9Hz), 3.04 (3H, s), 2.48 (1H, t, J = 2Hz), 2.02 ( 2H, m), 1.78 (2H, m);
MS (ESI) m / z: 457 [M + H] ⁺ .

(Production Example 116) 2,2,2-trifluoroethyl 4-({6- [5- (methylsulfinyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 626)
The compound obtained in Production Example 80 (604 mg, 1.32 mmol) was used for reaction in the same manner as described in Reference Example 32 to obtain a yellow oily compound (511 mg). A part of the obtained oily compound (293 mg) was used to carry out a reaction similar to the method described in Production Example 61 to obtain the title white powdery compound (103 mg, yield: 28%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.53 (1H, d, J = 9 Hz), 8.49 (1H, s), 7.57 (1H, s), 7.43 (1H, d, J = 9 Hz), 5.96 ( 1H, s), 5.39-5.34 (1H, m), 4.54-4.47 (2H, m), 4.04 (2H, t, J = 9Hz), 3.85-3.79 (2H, m), 3.48-3.42 (2H, m ), 3.31 (2H, t, J = 9Hz), 2.71 (3H, s), 2.06-1.99 (2H, m), 1.85-1.75 (2H, m);
MS (ESI) m / z: 485 [M + H] ⁺ .

Production Example 117 Isopropyl cis-3-fluoro-4- [6- (5-methanesulfonyl-2,3-dihydro-indol-1-yl) -pyrimidin-4-yloxy] -piperidine-1-carboxylate ( Exemplary compound number: 665)
(117a) tert-butyl cis-3-fluoro-4- [6- (5-methanesulfonyl-2,3-dihydro-indol-1-yl) -pyrimidin-4-yloxy] -piperidine-1-carboxylate

  Sodium hydride was added to a solution of tert-butyl cis-3-fluoro-4-hydroxy-piperidine-1-carboxylate (315 mg, 1.43 mmol) and the compound obtained in Reference Example 19 (296 mg, 0.956 mmol) in THF (12 mL). (109 mg, 2.87 mmol) was added, and the mixture was heated to reflux for 2 hours 30 minutes under a nitrogen atmosphere. Saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was washed with diethyl ether and ethyl acetate to obtain the title yellow powdery compound (326.8 mg, yield: 70%).

(117b) Isopropyl cis-3-fluoro-4- [6- (5-methanesulfonyl-2,3-dihydro-indol-1-yl) -pyrimidin-4-yloxy] -piperidine-1-carboxylate 4N hydrochloric acid solution (10 ml) was added to the compound obtained in (311 mg, 0.632 mmol) and stirred at room temperature for 45 minutes. The precipitated solid was collected by filtration and washed with ethyl acetate to obtain a compound (364.9 mg). N, N-diisopropylethylamine (108 μL, 1.13 mmol) and isopropyl chloroformate (38 μL, 0.338 mmol) were added to a suspension of the obtained compound (130 mg) in dichloromethane (2 mL), and the mixture was stirred at room temperature. Saturated aqueous ammonium chloride solution was added to the reaction mixture, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (hexane: ethyl acetate = 1: 2 to 2: 1, v / v), and the resulting crude product was washed with methanol to give the title white powdery compound (85.7 mg, yield: 80%).
¹ H-NMR (400MHz, CDCl ₃ ) δppm: 8.59 (1H, d, J = 8.6Hz), 8.50 (1H, s), 7.79 (1H, d, J = 8.6Hz), 7.73 (1H, s), 6.08 (1H, s), 5.45-5.34 (1H, m), 4.95 (1H, qu, J = 5.9Hz), 4.91 (1H, d, J = 47.7Hz), 4.33 (1H, brs), 4.18-4.07 (1H, m), 4.07 (2H, t, J = 8.8Hz), 3.37-3.26 (1H, m), 3.32 (2H, t, J = 8.8Hz), 3.15 (1H, brs), 3.05 (3H, s), 2.17-2.06 (1H, m), 1.96-1.88 (1H, m), 1.27 (6H, d, J = 5.9Hz).

(Production Example 118) Cyclopropylmethyl 4-({6- [5- (methylsulfinyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 620)
Using the compound obtained in Production Example 80 (604 mg, 1.32 mmol), a reaction was carried out in the same manner as in the method described in Reference Example 32 to obtain a yellow foamy compound (511 mg). Using a part (214 mg) of the obtained foamy compound, the reaction was carried out in the same manner as in the method described in Production Example 44 to obtain the title white powdery compound (19.3 mg, yield: 8%).
¹ H-NMR (500 MHz, CDCl ₃ ) δ ppm: 8.53 (1H, d, J = 9 Hz), 8.49 (1H, s), 7.57 (1H, s), 7.43 (1H, d, J = 8 Hz), 5.95 ( 1H, s), 5.36-5.31 (1H, m), 4.04 (2H, t, J = 9Hz), 3.93 (2H, d, J = 7Hz), 3.88-3.83 (2H, m), 3.39-3.34 (2H , m), 3.31 (2H, t, J = 9Hz), 2.71 (3H, s), 2.04-1.99 (2H, m), 1.79-1.73 (2H, m), 1.17-1.11 (1H, m), 0.57 -0.54 (2H, m), 0.30-0.27 (2H, m);
MS (ESI) m / z: 457 [M + H] ⁺ .

(Production Example 119) Isopropyl 4-({5-methoxy-6- [5- (methylsulfinyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (Exemplary Compound Number: 637)
(119a) tert-butyl 4-({5-methoxy-6- [5- (methylsulfinyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate
Instead of tert-butyl 4-[(6-chloropyrimidin-4-yl) oxy] piperidine-1-carboxylate of the method described in Preparation 56 using 5-methylsulfinylindoline (276 mg, 1.52 mmol) The same reaction was carried out using the compound (576 mg, 1.68 mmol) obtained in Reference Example 43 to obtain a yellow oily compound.

Acetyl chloride (125 μL, 1.76 mmol) and diisopropylethylamine (630 μL, 3.53 mmol) were added to a solution of the obtained oily compound in dichloromethane (7.5 mL) at 0 ° C., and the mixture was stirred at room temperature for 2.5 hours. Water was added to the reaction mixture, and the mixture was extracted 3 times with ethyl acetate. The obtained organic layer was washed with water and saturated brine, dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography ((i) ethyl acetate; (ii) ethyl acetate: methanol = 98: 2 → 96: 4 → 93: 7 → 90: 10, v / v). Was used in the same manner as in Production Example 61 to obtain the title yellow oily compound (283 mg, yield: 38%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.21 (1H, s), 7.77 (1H, d, J = 9Hz), 7.55 (1H, s), 7.39 (1H, J = 9Hz), 5.39-5.33 ( 1H, m), 4.32 (2H, t, J = 9Hz), 3.81-3.74 (2H, m), 3.76 (3H, s), 3.39-3.32 (2H, m), 3.23 (2H, t, J = 9Hz ), 2.71 (3H, s), 2.07-2.02 (2H, m), 1.87-1.79 (2H, m), 1.48 (9H, s);
MS (ESI) m / z: 489 [M + H] ⁺ .

(119b) Isopropyl 4-({5-methoxy-6- [5- (methylsulfinyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate (119a) 108 mg, 0.221 mmol) was used in the same manner as described in Production Example 28 to obtain the title white powdery compound (80.1 mg, yield: 76%).
¹ H-NMR (400 MHz, CDCl ₃ ) δppm: 8.21 (1H, s), 7.77 (1H, d, J = 9 Hz), 7.55 (1H, s), 7.39 (1H, d, J = 9 Hz), 5.40- 5.35 (1H, m), 4.94 (1H, sept, J = 6Hz), 4.32 (2H, t, J = 9Hz), 3.86-3.80 (2H, m), 3.76 (3H, s), 3.43-3.36 (2H , m), 3.24 (2H, t, J = 9Hz), 2.71 (3H, s), 2.08-2.02 (2H, m), 1.88-1.80 (2H, m), 1.27 (6H, d, J = 6Hz) ;
MS (ESI) m / z: 475 [M + H] ⁺ .

(Example)
A compound is obtained by mixing 5 g of the compound obtained in Production Example, 90 g of lactose, 34 g of corn starch, 20 g of crystalline cellulose and 1 g of magnesium stearate with a blender, and then tableting with a tableting machine.

(Test Example 1) Mouse oGTT (oral glucose tolerance test) test
After weighing 2.0-8.0 mg of the test compound, it was put in an agate mortar, and while pulverizing the compound, a 0.5% methylcellulose solution was added to prepare a 1 mg / ml suspension. Mice C57 / BL6J (male, 6-8 weeks old) were purchased from Japan Charles River, reared until 9-13 weeks of age with a gauge, and fasted at 17-18 hours the day before the test. On the day of the test day, blood was collected from the tail vein, and the previously prepared suspension was orally administered. 30 minutes after administration, blood was further collected from the tail vein (the plasma blood glucose level at this time was pre-valued), and a 20-30% glucose solution was orally administered at a dose of 10 ml / kg to perform glucose loading. After glucose loading, blood was collected from the tail vein at 15, 30, 60 and 120 minutes. The collected blood was centrifuged to separate the plasma. The plasma blood glucose level at 15, 30, 60 and 120 minutes after glucose loading was measured with Glucoloader GXT (Sinotest Co., Ltd.), and the AUC reduction rate (%) of blood glucose level for the vehicle administration group was calculated. For the vehicle administration group, 0.5% methylcellulose solution was administered instead of the compound suspension.

(Test Example 2) Rat blood compound concentration measurement test
After weighing 20 to 50 mg of the test compound, it is placed in an agate mortar, and while pulverizing the compound, a 0.5% methylcellulose solution is added to prepare a 2.5 mg / ml suspension. F344 rats (male, 5-7 weeks old) are purchased from Japan Charles River and fasted from 17 to 18:00 the day before the test. After measuring the body weight of the rat on the day of the test, the test compound is orally administered at a dose of 10 mg / kg, and blood is collected from the tail vein 0.5, 1, 2, 4, 6, 24 hours after administration. The collected blood is centrifuged to separate the plasma. After deproteinizing the plasma, it is subjected to a liquid chromatography / mass spectrometer to calculate the concentration of the compound in the plasma.

(Test Example 3) Rat oGTT (oral glucose tolerance test) test
After weighing 200 mg of the test compound, it is put in an agate mortar, and 0.5% methylcellulose solution is added while pulverizing the compound to prepare a suspension of 7.5 mg / ml. When preparing another dose of the suspension, the suspension prepared above is sequentially diluted with a 0.5% methylcellulose solution to prepare the desired suspension. Zucker fatty rats and Zucker Diabetic Fatty rats (male, 8-12 weeks old) are purchased from Japan Charles River, and the groups are adjusted so that the basal blood glucose level and body weight between the administered groups are the same level before the test. Rats are fasted at 15-18 o'clock the day before the test. After the blood is collected from the tail vein on the day of the test, the previously prepared suspension is orally administered. 30 minutes after administration, blood was further collected from the tail vein (the plasma blood glucose level at this time was pre-valued), and then a 20% glucose solution was orally administered at a dose of 4 ml / kg to perform glucose loading. Blood is collected from the tail vein at 30 minutes, 1, 2 and 4 hours after glucose loading. The collected blood is centrifuged to separate the plasma. The plasma blood glucose level at 30 minutes, 1, 2, and 4 hours after glucose loading is measured with Glucoloader GXT (Sinotest Co., Ltd.), and the AUC reduction rate (%) of blood glucose level for the vehicle administration group is calculated. For the vehicle administration group, 0.5% methylcellulose solution is administered instead of the compound suspension.

The pharmaceutical composition of the present invention treats and / or treats type 1 diabetes, type 2 diabetes, gestational diabetes, hyperglycemia due to other factors, impaired glucose tolerance (IGT), diabetes related diseases, diabetic complications, and the like. Or useful for prevention.

Claims (22)

Formula (I):

[Where,
p is 1 or 2,
R ¹ has ¹ to 3 substituents selected from the substituent group β, and a C1-C6 alkyl group that may have 1 to 3 substituents selected from the substituent group α. A C3-C7 cycloalkyl group, a C2-C6 alkynyl group optionally having 1 to 3 substituents selected from the substituent group β, and a substituent selected from 1 to 3 substituents β. A C2-C6 alkenyl group, an amino group or a mono- or di (C1-C6 alkyl) amino group which may have
Substituent group α is a halogen atom, hydroxyl group, C1-C6 alkoxy group, C3-C7 cycloalkyl group optionally having 1 to 3 substituents selected from substituent group β, amino group, mono group Or 1 to 3 substituents selected from a di (C1-C6 alkyl) amino group, an aryl group which may have 1 to 3 substituents selected from substituent group β, and substituent group β A group of heteroaryl groups that may have
Substituent group β is a group consisting of a halogen atom, a hydroxyl group, a C1-C6 alkyl group and a C1-C6 alkoxy group,
m is an integer from 0 to 3,
R ² is the same or different and is a halogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group or a C1-C6 alkoxy C1-C6 alkyl group,
n is an integer from 0 to 4,
R ³ is the same or different and is a halogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group or a C1-C6 alkoxy C1-C6 alkyl group,
R ⁴ and R ⁵ are each independently a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group or a C1-C6 alkoxy C1-C6 alkyl group,
R ⁶ is -C (O) OR ^6a , -C (O) -R ^6b or -S (O) ₂ -R ^6c ,
R ^6a has 1 to 3 substituents selected from the C1-C6 alkyl group which may have 1 to 3 substituents selected from the substituent group α, and substituent group β. A C3-C7 cycloalkyl group, a C2-C6 alkynyl group optionally having 1 to 3 substituents selected from the substituent group β, and a substituent selected from 1 to 3 substituents β. A C2-C6 alkenyl group optionally having 1 to 3 aryl groups optionally having 1 to 3 substituents selected from the substituent group β, 1 to 1 substituents selected from the substituent group β. A heteroaryl group which may have three,
R ^6b has 1 to 3 substituents selected from a hydrogen atom, a C1-C6 alkyl group optionally having 1 to 3 substituents selected from the substituent group α, and a substituent group β. A C3-C7 cycloalkyl group which may optionally be substituted, a C2-C6 alkynyl group which may have 1 to 3 substituents selected from the substituent group β, and a substituent selected from the substituent group β. 1 to 3 substituents selected from a C2-C6 alkenyl group, an amino group, a mono- or di (C1-C6 alkyl) amino group, and a substituent group β, which may have 1 to 3 Or a heteroaryl group which may have 1 to 3 substituents selected from the substituent group β.
R ^6c is a C1-C6 alkyl group,
R ⁷ is a hydrogen atom, a halogen atom or a C1-C6 alkyl group.
Or a pharmaceutically acceptable salt thereof. R ¹ has ¹ to 3 substituents selected from the substituent group β, a C1-C6 alkyl group that may have 1 to 3 substituents selected from the substituent group α; The pharmaceutical composition according to claim 1, which may be a C3-C7 cycloalkyl group, an amino group, or a mono- or di (C1-C6 alkyl) amino group. R ¹ has ¹ to 3 substituents selected from the C1-C6 alkyl group or substituent group β which may have 1 to 3 substituents selected from the substituent group α. The pharmaceutical composition according to claim 1 or 2, which is a C3-C7 cycloalkyl group.   The pharmaceutical composition according to any one of claims 1 to 3, wherein m is 0. The pharmaceutical composition according to any one of claims 1 to 3, wherein m is 1 and R ² is a halogen atom.   The pharmaceutical composition according to any one of claims 1 to 5, wherein n is 0. n is 1, R ³ is a halogen atom, a pharmaceutical composition according to any one of claims 1 to 5. The pharmaceutical composition according to any one of claims 1 to 7, wherein R ⁴ is a hydrogen atom. R ⁵ is a hydrogen atom, a C1~C6 alkyl group or C1~C6 alkoxy group, a pharmaceutical composition according to any one of claims 1-8. R ⁵ is hydrogen atom or a C1~C6 alkoxy group, a pharmaceutical composition according to any one of claims 1 to 9. The pharmaceutical composition according to any one of claims 1 to 10, wherein R ⁶ is -C (O) OR ^6a . R ^6a has 1 to 3 substituents selected from the C1-C6 alkyl group which may have 1 to 3 substituents selected from the substituent group α, and substituent group β. A C3-C7 cycloalkyl group, an aryl group which may have 1 to 3 substituents selected from the substituent group β, or 1 to 3 substituents selected from the substituent group β. The pharmaceutical composition according to any one of claims 1 to 11, which is a heteroaryl group which may be present. The pharmaceutical composition according to any one of claims 1 to 10, wherein R ⁶ is -C (O) -R ^6b . R ^6b has 1 to 3 substituents selected from the C1-C6 alkyl group or substituent group β which may have 1 to 3 substituents selected from the substituent group α. 14. The pharmaceutical composition according to any one of claims 1 to 10 or claim 13, which is a good aryl group. The R ^6b is a C1-C6 alkyl group which may have 1 to 3 substituents selected from the substituent group α, or any one of claims 1 to 10, or claim 13 or 14. Pharmaceutical composition. The pharmaceutical composition according to any one of claims 1 to 10, wherein R ⁶ is -S (O) ₂ -R ^6c . The pharmaceutical composition according to any one of claims 1 to 10, wherein R ^6c is a C1 to C4 alkyl group. The pharmaceutical composition according to any one of claims 1 to 17, wherein R ⁷ is a hydrogen atom, a fluorine atom or a C1-C3 alkyl group. Formula (II):

[Where,
R ¹ has ¹ to 3 substituents selected from the substituent group β, and a C1-C6 alkyl group that may have 1 to 3 substituents selected from the substituent group α. A C3-C7 cycloalkyl group, a C2-C6 alkynyl group optionally having 1 to 3 substituents selected from the substituent group β, and a substituent selected from 1 to 3 substituents β. A C2-C6 alkenyl group, an amino group or a mono- or di (C1-C6 alkyl) amino group which may have
Substituent group α is a halogen atom, hydroxyl group, C1-C6 alkoxy group, C3-C7 cycloalkyl group optionally having 1 to 3 substituents selected from substituent group β, amino group, mono group Or 1 to 3 substituents selected from a di (C1-C6 alkyl) amino group, an aryl group which may have 1 to 3 substituents selected from substituent group β, and substituent group β A group of heteroaryl groups that may have
Substituent group β is a group consisting of a halogen atom, a hydroxyl group, a C1-C6 alkyl group and a C1-C6 alkoxy group,
m is an integer from 0 to 3,
R ² is the same or different and is a halogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group or a C1-C6 alkoxy C1-C6 alkyl group,
n is an integer from 0 to 4,
R ³ is the same or different and is a halogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group or a C1-C6 alkoxy C1-C6 alkyl group,
R ⁴ and R ⁵ are each independently a hydrogen atom, a halogen atom, a C1-C6 alkyl group, a C1-C6 alkoxy group or a C1-C6 alkoxy C1-C6 alkyl group,
R ^6a has 1 to 3 substituents selected from the C1-C6 alkyl group which may have 1 to 3 substituents selected from the substituent group α, and substituent group β. A C3-C7 cycloalkyl group, a C2-C6 alkynyl group optionally having 1 to 3 substituents selected from the substituent group β, and a substituent selected from 1 to 3 substituents β. A C2-C6 alkenyl group optionally having 1 to 3 aryl groups optionally having 1 to 3 substituents selected from the substituent group β, 1 to 1 substituents selected from the substituent group β. A heteroaryl group which may have three,
R ⁷ is a hydrogen atom, a halogen atom or a C1-C6 alkyl group.
Or a pharmaceutically acceptable salt thereof. A pharmaceutical composition comprising one compound selected from the group consisting of:
Isopropyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Isobutyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
tert-butyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Cyclobutyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Cyclopentyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
1-ethylpropyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Cyclopropylmethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
3-furylmethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
1-cyclopropylethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2-fluoroethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2,2-difluoroethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2,2,2-trifluoroethyl 4-({6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
1- (6-{[1- (3-methylbutanoyl) piperidin-4-yl] oxy} pyrimidin-4-yl) -5- (methylsulfonyl) indoline;
Isopropyl 4-({5-methoxy-6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
tert-butyl 4-({5-methoxy-6- [5- (methylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Isopropyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Isobutyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
sec-butyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Cyclobutyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Cyclopropylmethyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2,2-difluoroethyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2,2,2-trifluoroethyl 4-({6- [5- (ethylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
tert-butyl 4-[(6- {5-[(2-fluoroethyl) sulfonyl] indoline-1-yl} pyrimidin-4-yl) oxy] piperidine-1-carboxylate;
tert-butyl 4-({6- [5- (propylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2,2,2-trifluoroethyl 4-({6- [5- (propylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
tert-butyl 4-({6- [5- (cyclobutylsulfonyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
tert-butyl 4-({6- [5- (methylsulfinyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
2,2,2-trifluoroethyl 4-({6- [5- (methylsulfinyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate;
Isopropyl cis-3-fluoro-4- [6- (5-methanesulfonyl-2,3-dihydro-indol-1-yl) -pyrimidin-4-yloxy] -piperidine-1-carboxylate;
Cyclopropylmethyl 4-({6- [5- (methylsulfinyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate; and isopropyl 4-({5-methoxy-6- [ 5- (Methylsulfinyl) indoline-1-yl] pyrimidin-4-yl} oxy) piperidine-1-carboxylate.   21. The pharmaceutical composition according to any one of claims 1 to 20, for treating and / or preventing type 1 diabetes, type 2 diabetes or diabetes related diseases.   21. A pharmaceutical composition according to any one of claims 1 to 20 for treating and / or preventing obesity.