RU2004122480A - Производные гетероарил-замещенного аминоциклодекана - Google Patents
Производные гетероарил-замещенного аминоциклодекана Download PDFInfo
- Publication number
- RU2004122480A RU2004122480A RU2004122480/04A RU2004122480A RU2004122480A RU 2004122480 A RU2004122480 A RU 2004122480A RU 2004122480/04 A RU2004122480/04 A RU 2004122480/04A RU 2004122480 A RU2004122480 A RU 2004122480A RU 2004122480 A RU2004122480 A RU 2004122480A
- Authority
- RU
- Russia
- Prior art keywords
- ness
- alkyl
- compounds
- compound according
- trans
- Prior art date
Links
- TXGVDTJWMZUNMP-UHFFFAOYSA-N cyclodecanamine Chemical class NC1CCCCCCCCC1 TXGVDTJWMZUNMP-UHFFFAOYSA-N 0.000 title 1
- 150000001875 compounds Chemical class 0.000 claims 41
- 125000000217 alkyl group Chemical group 0.000 claims 18
- -1 carboxy, carboxy Chemical group 0.000 claims 14
- 125000003545 alkoxy group Chemical group 0.000 claims 7
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims 6
- 229910052739 hydrogen Inorganic materials 0.000 claims 6
- 239000001257 hydrogen Substances 0.000 claims 6
- 125000003342 alkenyl group Chemical group 0.000 claims 5
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 claims 4
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 4
- 229910052760 oxygen Inorganic materials 0.000 claims 4
- 230000002265 prevention Effects 0.000 claims 4
- 125000004076 pyridyl group Chemical group 0.000 claims 4
- 229910052717 sulfur Inorganic materials 0.000 claims 4
- 206010003210 Arteriosclerosis Diseases 0.000 claims 3
- 208000002705 Glucose Intolerance Diseases 0.000 claims 3
- 208000035150 Hypercholesterolemia Diseases 0.000 claims 3
- AFVFQIVMOAPDHO-UHFFFAOYSA-N Methanesulfonic acid Chemical group CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 claims 3
- 208000031888 Mycoses Diseases 0.000 claims 3
- 206010028980 Neoplasm Diseases 0.000 claims 3
- 208000030852 Parasitic disease Diseases 0.000 claims 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 claims 3
- 208000011775 arteriosclerosis disease Diseases 0.000 claims 3
- 229910052794 bromium Inorganic materials 0.000 claims 3
- 229910052801 chlorine Inorganic materials 0.000 claims 3
- 201000001883 cholelithiasis Diseases 0.000 claims 3
- 125000000753 cycloalkyl group Chemical group 0.000 claims 3
- 206010012601 diabetes mellitus Diseases 0.000 claims 3
- 230000006806 disease prevention Effects 0.000 claims 3
- 201000005577 familial hyperlipidemia Diseases 0.000 claims 3
- 239000003574 free electron Substances 0.000 claims 3
- 229910052736 halogen Inorganic materials 0.000 claims 3
- 150000002367 halogens Chemical class 0.000 claims 3
- 230000003463 hyperproliferative effect Effects 0.000 claims 3
- 229910052740 iodine Inorganic materials 0.000 claims 3
- 238000000034 method Methods 0.000 claims 3
- 201000009104 prediabetes syndrome Diseases 0.000 claims 3
- 125000002098 pyridazinyl group Chemical group 0.000 claims 3
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 3
- 150000003839 salts Chemical class 0.000 claims 3
- 125000001424 substituent group Chemical group 0.000 claims 3
- JOXIMZWYDAKGHI-UHFFFAOYSA-N toluene-4-sulfonic acid Chemical group CC1=CC=C(S(O)(=O)=O)C=C1 JOXIMZWYDAKGHI-UHFFFAOYSA-N 0.000 claims 3
- ITMCEJHCFYSIIV-UHFFFAOYSA-M triflate Chemical group [O-]S(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-M 0.000 claims 3
- 208000019553 vascular disease Diseases 0.000 claims 3
- 125000002947 alkylene group Chemical group 0.000 claims 2
- 125000003118 aryl group Chemical group 0.000 claims 2
- 239000003814 drug Substances 0.000 claims 2
- 229940079593 drug Drugs 0.000 claims 2
- 125000000623 heterocyclic group Chemical group 0.000 claims 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims 2
- 230000003993 interaction Effects 0.000 claims 2
- 238000004519 manufacturing process Methods 0.000 claims 2
- 125000003373 pyrazinyl group Chemical group 0.000 claims 2
- 125000000446 sulfanediyl group Chemical group *S* 0.000 claims 2
- 125000000954 2-hydroxyethyl group Chemical group [H]C([*])([H])C([H])([H])O[H] 0.000 claims 1
- KNEXQXLCAKXIAG-CTYIDZIISA-N BrC=1C=NC(=NC1)N(C)[C@@H]1CC[C@H](CC1)C#CCN(C)C Chemical compound BrC=1C=NC(=NC1)N(C)[C@@H]1CC[C@H](CC1)C#CCN(C)C KNEXQXLCAKXIAG-CTYIDZIISA-N 0.000 claims 1
- XDYOVZCKJLZVGM-QAQDUYKDSA-N BrC=1C=NC(=NC=1)CNC[C@@H]1CC[C@H](CC1)C#CCN(CCO)CC Chemical compound BrC=1C=NC(=NC=1)CNC[C@@H]1CC[C@H](CC1)C#CCN(CCO)CC XDYOVZCKJLZVGM-QAQDUYKDSA-N 0.000 claims 1
- VAUDEWFFICAZKC-MXVIHJGJSA-N C(C)N(CCO)CC#C[C@@H]1CC[C@H](CC1)CNCC1=NC=C(C=N1)CC Chemical compound C(C)N(CCO)CC#C[C@@H]1CC[C@H](CC1)CNCC1=NC=C(C=N1)CC VAUDEWFFICAZKC-MXVIHJGJSA-N 0.000 claims 1
- FKVZFXCPXAFTSW-SHTZXODSSA-N CN(C)CC#C[C@H]1CC[C@H](CN(C)c2ncc(Br)cn2)CC1 Chemical compound CN(C)CC#C[C@H]1CC[C@H](CN(C)c2ncc(Br)cn2)CC1 FKVZFXCPXAFTSW-SHTZXODSSA-N 0.000 claims 1
- SQQULBWNBXEAMQ-QAQDUYKDSA-N CN(CC#C[C@@H]1CC[C@H](CC1)N(C)C1=NC=C(C=N1)CC)C Chemical compound CN(CC#C[C@@H]1CC[C@H](CC1)N(C)C1=NC=C(C=N1)CC)C SQQULBWNBXEAMQ-QAQDUYKDSA-N 0.000 claims 1
- NCNMIXHELVOCFY-HDJSIYSDSA-N ClC1=CC=C(N=N1)N(C)[C@@H]1CC[C@H](CC1)C#CCN(C)C Chemical compound ClC1=CC=C(N=N1)N(C)[C@@H]1CC[C@H](CC1)C#CCN(C)C NCNMIXHELVOCFY-HDJSIYSDSA-N 0.000 claims 1
- VTCXBGBFOZBMOV-CTYIDZIISA-N ClC=1C=NC(=NC1)N(C)[C@@H]1CC[C@H](CC1)C#CCN(C)C Chemical compound ClC=1C=NC(=NC1)N(C)[C@@H]1CC[C@H](CC1)C#CCN(C)C VTCXBGBFOZBMOV-CTYIDZIISA-N 0.000 claims 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N EtOH Substances CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims 1
- 229910052770 Uranium Inorganic materials 0.000 claims 1
- 239000013543 active substance Substances 0.000 claims 1
- 239000002671 adjuvant Substances 0.000 claims 1
- 125000004450 alkenylene group Chemical group 0.000 claims 1
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims 1
- 125000000304 alkynyl group Chemical group 0.000 claims 1
- 125000004104 aryloxy group Chemical group 0.000 claims 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 claims 1
- 229910052799 carbon Inorganic materials 0.000 claims 1
- 125000004432 carbon atom Chemical group C* 0.000 claims 1
- QOGRQXGQKOEKKF-QAQDUYKDSA-N chembl165381 Chemical compound C1C[C@@H](CCN(CCC)CCC)CC[C@@H]1NC1=NC=CC=N1 QOGRQXGQKOEKKF-QAQDUYKDSA-N 0.000 claims 1
- 125000004663 dialkyl amino group Chemical group 0.000 claims 1
- 201000010099 disease Diseases 0.000 claims 1
- 239000003937 drug carrier Substances 0.000 claims 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 claims 1
- 125000000031 ethylamino group Chemical group [H]C([H])([H])C([H])([H])N([H])[*] 0.000 claims 1
- 125000001072 heteroaryl group Chemical group 0.000 claims 1
- 125000000250 methylamino group Chemical group [H]N(*)C([H])([H])[H] 0.000 claims 1
- 229910052757 nitrogen Inorganic materials 0.000 claims 1
- 239000008194 pharmaceutical composition Substances 0.000 claims 1
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 claims 1
- 125000001544 thienyl group Chemical group 0.000 claims 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 claims 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/72—Nitrogen atoms
- C07D213/74—Amino or imino radicals substituted by hydrocarbon or substituted hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/10—Antimycotics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/84—Nitriles
- C07D213/85—Nitriles in position 3
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D237/20—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D237/00—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings
- C07D237/02—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings
- C07D237/06—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members
- C07D237/10—Heterocyclic compounds containing 1,2-diazine or hydrogenated 1,2-diazine rings not condensed with other rings having three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D237/22—Nitrogen and oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/30—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/32—One oxygen, sulfur or nitrogen atom
- C07D239/42—One nitrogen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Endocrinology (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Emergency Medicine (AREA)
- Gastroenterology & Hepatology (AREA)
- Tropical Medicine & Parasitology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pyridine Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Claims (32)
1. Соединения формулы (I)
где U означает О или свободную электронную пару,
V означает простую связь, О, S, -СН=СН-СН2-O-, -СН=СН- или -С≡С-,
m и n независимо друг от друга равны 0-7 и m+n равно 0-7, при условии, что m не равно 0, если V означает О или S,
о равно 0-2,
А1 означает водород, (низш.)алкил, гидрокси(низш.)алкил или (низш.)алкенил,
А2 означает (низш.)алкил, циклоалкил, циклоалкил(низш.)алкил или
(низш.)алкенил, необязательно замещенный R1, или
А1 и А2 связаны друг с другом с образованием цикла и -А1-А2 - означает (низш.)алкилен или (низш.)алкенилен, необязательно замещенный R1, в котором одна из -СН2- групп в составе -А1-А2 - необязательно замещена группой NR2, S или О,
А3 и А4 независимо друг от друга означают водород или (низш.)алкил, или А3 и А4 связаны друг с другом и вместе с атомом углерода, к которому они присоединены, образуют цикл, а -А3-А4 - означает -(СН2)2-5-,
А5 означает водород, (низш.)алкил или (низш.)алкенил,
А6 означает пиридинил, пиридазинил, пиримидинил или пиразинил, необязательно замещенный одним или двумя заместителями, независимо выбранными из группы, включающей (низш.)алкил, (низш.)алкилциклоалкил, тио(низш.)алкокси, циклоалкил, карбамоил, карбокси, карбокси(низш.)алкил, циано, амино, моно- и диалкиламино, (низш.)алкокси, (низш.)алкокси(низш.)алкил, (низш.)алкоксикарбонил, (низш.)алкоксикарбонил(низш.)алкил, (низш.)алкенил, (низш.)алкинил, арил, арил(низш.)алкил, арилокси, галоген, гетероарил, гетероциклил, гетероциклил(низш.)алкил и трифторметил,
R1 означает гидрокси, гидрокси(низш.)алкил, (низш.)алкокси, (низш.)алкоксикарбонил, галоген, CN, N(R3,R4) или тио(низш.)алкокси, R2, R3 и R4 независимо друг от друга означают водород или (низш.)алкил, и их фармацевтически приемлемые соли, при условии, что соединение формулы (I) не означает транс-[4-(2-дипропиламиноэтил)циклогексил]пиримидин-2-иламин.
2. Соединения по п.1, где U означает свободную электронную пару.
3. Соединения по п.1, где V означает простую связь, О, -СН=СН-СН2-O-или -С≡С-.
4. Соединения по п.1, где V означает -С≡С-.
5. Соединения по п.1, где m равно 0-3.
6. Соединения по п.1, где m равно 0.
7. Соединения по п.1, где n равно 0-1.
8. Соединения по п.1, где n равно 0.
9. Соединения по п.1, где о равно 0 или 1.
10. Соединения по п.1, где А1 означает (низш.)алкил.
11. Соединения по п.1, где А1 означает метил или этил.
12. Соединения по п.1, где А2 означает (низш.)алкенил или (низш.)алкил, необязательно замещенный группой R2, причем R2 означает гидрокси или (низш.)алкокси.
13. Соединения по п.1, где А2 означает метил, пропил или 2-гидроксиэтил.
14. Соединения по п.1, где А1 и А2 связаны друг с другом с образованием цикла, а -А1-А2 - означает (низш.)алкилен.
15. Соединения по п.14, где -А1-А2 - означают -(СН2)5-.
16. Соединения по п.1, где А3 и А4 означают водород.
17. Соединения по п.1, где А5 означает водород или (низш.)алкил.
18. Соединения по п.1, где А5 означает метил.
19. Соединения по п.1, где А6 означает пиридинил, пиридазинил, пиримидинил или пиразинил, необязательно замещенный 1 или 2 заместителями, независимо выбранными из группы, включающей (низш.)алкил, (низш.)алкокси, галоген, пиридил и тиенил.
20. Соединения по п.1, где А6 означает пиридазинил или пиримидинил, необязательно замещенный 1 или 2 заместителями, независимо выбранными из группы, включающей бром, хлор, этил и пиридил.
21. Соединения по п.1, где А6 означает 5-бромпиримидин-2-ил, 6-хлорпиридазин-3-ил, 5-хлорпиримидин-2-ил, 5-пиридин-4-илпиримидин-2-ил, 5-этилпиримидин-2-ил.
22. Соединение по п.1, выбранное из группы, включающей
транс-(5-бромпиримидин-2-ил)метил-{4-[3-(метилпропиламино)проп-1-инил]циклогексил}амин,
транс-(5-бромпиримидин-2-ил)[4-(3-диметиламинопроп-1-инил)циклогексил]метиламин,
транс-(6-хлорпиридазин-3-ил)[4-(3-диметиламинопроп-1-инил)циклогексил]метиламин,
транс-(5-хлорпиримидин-2-ил)[4-(3-диметиламинопроп-1-инил)циклогексил]метиламин,
транс-[(5-бромпиримидин-2-ил)метил[4-(3-пиперидин-1-илпроп-1-инил)циклогексил]амин],
транс-[4-(3-диметиламинопроп-1-инил)циклогексил]метил(5-пиридин-4-илпиримидин-2-ил)амин,
транс-[4-(3-диметиламинопроп-1-инил)циклогексил](5-этилпиримидин-2-ил)метиламин,
транс-(5-бромпиримидин-2-ил)[4-(3-диметиламинопроп-1-инил)циклогексилметил]метиламин,
транс-2-{[3-(4-{[(5-бромпиримидин-2-ил)метиламино]метил}циклогексил)проп-2-инил]этиламино}этанол,
транс-2-{этил[3-(4-{[(5-этилпиримидин-2-ил)метиламино]метил}циклогексил)проп-2-инил]амино}этанол,
транс-(5-этилпиримидин-2-ил)метил[4-(3-пиперидин-1-илпроп-1-инил)циклогексилметил]амин и
транс-2-{[3-(4-{[(6-хлорпиридазин-3-ил)метиламино]метил}циклогксил)проп-2-инил]этиламино}этанол,
и их фармацевтически приемлемые соли.
23. Способ получения соединений по любому из пп.1-22, включающий а) взаимодействие соединения формулы (II)
с соединением (А1,А2,U)N-C(A3,А4)-(СН2)m-М, где V означает О или S, М означает мезилат, тозилат, трифлат, Cl, Br или I, а U, А1, А2, А3, A4, A5, A6, m, n и о имеют значения, указанные в п.1, или где HV означает мезилат, тозилат, трифлат, Cl, Br или I, a M означает ОН или SH, или
б) взаимодействие соединения формулы (III)
с соединением NHA1А2, где М означает мезилат, тозилат, трифлат, Cl, Br или I, a А1, А2, А3, А4, А5, А6, V, m, n и о имеют значения, указанные в п.1, и необязательно превращение соединения по любому из пп.1-22 в его фармацевтически приемлемую соль,
и необязательно превращение соединения по любому из пп.1-22, где U означает свободную электронную пару, в соответствующее соединение, где U означает О.
24. Соединения по п.1, полученные способом по п.23.
25. Фармацевтические композиции, включающие соединение по любому из пп.1-22 и фармацевтически приемлемы носитель и/или адъювант.
26. Соединения по п.1 для применения в качестве терапевтически активных субстанций.
27. Соединения по п.1 для применения в качестве терапевтически активных соединений при лечении и/или профилактике заболеваний, ассоциированных с OSC.
28. Способ лечения и/или профилактики заболеваний, ассоциированных с OSC, таких, как гиперхолестеринемия, гиперлипемия, артериосклероз, сосудистые заболевания, микозы, паразитарные инфекции, желчнокаменная болезнь, опухоли и/или гиперпролиферативные нарушения, и/или лечения и/или профилактики нарушенной толерантности к глюкозе и диабета, включающий введение соединения по любому из пп.1-22 человеку или животному.
29. Применение соединений по любому из пп.1-22 для лечения и/или профилактики заболеваний, ассоциированных с OSC.
30. Применение соединений по любому из пп.1-22 для лечения и/или профилактики гиперхолестеринемии, гиперлипемии, артериосклероза, сосудистых заболеваний, микозов, паразитарных инфекций, желчнокаменной болезни, опухолей и/или гиперпролиферативных нарушений, и/или лечения и/или профилактики нарушенной толерантности к глюкозе и диабета.
31. Применение соединений по любому из пп.1-22 для получения лекарственных средств, предназначенных для лечения и/или профилактики заболеваний, ассоциированных с OSC.
32. Применение соединений по любому из пп.1-22 для получения лекарственных средств, предназначенных для лечения и/или профилактики гиперхолестеринемии, гиперлипемии, артериосклероза, сосудистых заболеваний, микозов, паразитарных инфекций, желчнокаменной болезни, опухолей и/или гиперпролиферативных нарушений, и/или лечения и/или профилактики нарушенной толерантности к глюкозе и диабета.
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01130284.1 | 2001-12-20 | ||
EP01130284 | 2001-12-20 |
Publications (2)
Publication Number | Publication Date |
---|---|
RU2004122480A true RU2004122480A (ru) | 2005-08-10 |
RU2286987C2 RU2286987C2 (ru) | 2006-11-10 |
Family
ID=8179606
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
RU2004122480/04A RU2286987C2 (ru) | 2001-12-20 | 2002-12-11 | Производные гетероарилзамещенного аминоциклогексана, способ их получения, фармацевтическая композиция и применение |
Country Status (16)
Country | Link |
---|---|
US (1) | US7012077B2 (ru) |
EP (1) | EP1458683B1 (ru) |
JP (1) | JP4316384B2 (ru) |
KR (1) | KR20040075905A (ru) |
CN (1) | CN1296357C (ru) |
AR (1) | AR038549A1 (ru) |
AT (1) | ATE346045T1 (ru) |
AU (1) | AU2002366732B2 (ru) |
BR (1) | BR0215257A (ru) |
CA (1) | CA2469380C (ru) |
DE (1) | DE60216319T2 (ru) |
ES (1) | ES2275939T3 (ru) |
MX (1) | MXPA04005907A (ru) |
PL (1) | PL370713A1 (ru) |
RU (1) | RU2286987C2 (ru) |
WO (1) | WO2003053933A1 (ru) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
BR0113408A (pt) * | 2000-08-16 | 2003-06-17 | Hoffmann La Roche | Derivados de aminociclohexano |
CN101475528A (zh) * | 2003-03-31 | 2009-07-08 | 大正制药株式会社 | 新的喹啉、四氢喹唑啉和嘧啶衍生物以及与其应用有关的治疗方法 |
US20050197350A1 (en) * | 2003-03-31 | 2005-09-08 | Taisho Pharmaceutical Co., Ltd. | Novel quinoline, tetrahydroquinazoline, and pyrimidine derivatives and methods of treatment related to the use thereof |
WO2005049574A1 (en) * | 2003-11-20 | 2005-06-02 | Warner-Lambert Company Llc | Androgen receptor modulators |
ITMI20110666A1 (it) * | 2011-04-19 | 2012-10-20 | Dipharma Francis Srl | Procedimento per la preparazione di (r) ed (s) pramipexolo e suoi intermedi |
US9156831B2 (en) | 2013-01-23 | 2015-10-13 | Astrazeneca Ab | Chemical compounds |
CA3026149A1 (en) | 2016-06-02 | 2017-12-07 | Cadent Therapeutics, Inc. | Potassium channel modulators |
WO2018136917A1 (en) | 2017-01-23 | 2018-07-26 | Cadent Therapeutics, Inc. | Potassium channel modulators |
CN113226466A (zh) | 2018-10-22 | 2021-08-06 | 科登特治疗公司 | 钾通道调节剂的结晶形式 |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
NO122123B (ru) | 1966-03-25 | 1971-05-24 | Miles Lab | |
US3592824A (en) | 1970-03-12 | 1971-07-13 | Miles Lab | 3-substituted amino-1,2,3,4-tetrahydrocarbazoles |
DE4239151A1 (de) | 1992-11-20 | 1994-05-26 | Thomae Gmbh Dr K | N,N-Disubstituierte Arylcycloalkylamine, deren Salze, diese Verbindungen enthaltende Arzneimittel und deren Verwendung sowie Verfahren zu ihrer Herstellung |
TW438774B (en) * | 1993-07-14 | 2001-06-07 | Hoffmann La Roche | Pharmaceutical composition for lowering cholesterol containing phenalkylamines and certain novel phenalkylamines |
DK0832069T3 (da) * | 1995-06-07 | 2003-04-22 | Pfizer | Biphenyl-2-carboxylsyre-tetrahydroisoquinolin-6-ylamidderivater, deres fremstilling og deres anvendelse som inhibitorer af sekretion af mikrosomalt triglyceridoverførselsprotein og/eller apolipoprotein B (Apo B) |
CA2190699A1 (en) | 1995-12-08 | 1997-06-09 | Johannes Aebi | Tertiary amines |
US6964974B2 (en) | 2000-09-08 | 2005-11-15 | Hoffmann-La Roche Inc. | 2,3-oxidosqualene-lanosterol cyclase inhibitors |
ES2233703T3 (es) | 2000-11-02 | 2005-06-16 | F. Hoffmann-La Roche Ag | Benzo(b)tiofenos y benzo (d)isotiazoles hipocolesterolemiantes.. |
-
2002
- 2002-12-05 US US10/310,559 patent/US7012077B2/en not_active Expired - Fee Related
- 2002-12-11 CN CNB028256654A patent/CN1296357C/zh not_active Expired - Fee Related
- 2002-12-11 MX MXPA04005907A patent/MXPA04005907A/es unknown
- 2002-12-11 BR BR0215257-6A patent/BR0215257A/pt not_active IP Right Cessation
- 2002-12-11 ES ES02790481T patent/ES2275939T3/es not_active Expired - Lifetime
- 2002-12-11 CA CA2469380A patent/CA2469380C/en not_active Expired - Fee Related
- 2002-12-11 AU AU2002366732A patent/AU2002366732B2/en not_active Ceased
- 2002-12-11 KR KR10-2004-7009921A patent/KR20040075905A/ko not_active Withdrawn
- 2002-12-11 WO PCT/EP2002/014037 patent/WO2003053933A1/en active IP Right Grant
- 2002-12-11 DE DE60216319T patent/DE60216319T2/de not_active Expired - Lifetime
- 2002-12-11 PL PL02370713A patent/PL370713A1/xx not_active Application Discontinuation
- 2002-12-11 AT AT02790481T patent/ATE346045T1/de not_active IP Right Cessation
- 2002-12-11 EP EP02790481A patent/EP1458683B1/en not_active Expired - Lifetime
- 2002-12-11 RU RU2004122480/04A patent/RU2286987C2/ru not_active IP Right Cessation
- 2002-12-11 JP JP2003554649A patent/JP4316384B2/ja not_active Expired - Fee Related
- 2002-12-18 AR ARP020104958A patent/AR038549A1/es not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
RU2286987C2 (ru) | 2006-11-10 |
EP1458683B1 (en) | 2006-11-22 |
DE60216319D1 (en) | 2007-01-04 |
JP2005517667A (ja) | 2005-06-16 |
AU2002366732A1 (en) | 2003-07-09 |
ES2275939T3 (es) | 2007-06-16 |
DE60216319T2 (de) | 2007-05-31 |
AR038549A1 (es) | 2005-01-19 |
US7012077B2 (en) | 2006-03-14 |
PL370713A1 (en) | 2005-05-30 |
JP4316384B2 (ja) | 2009-08-19 |
BR0215257A (pt) | 2004-12-07 |
EP1458683A1 (en) | 2004-09-22 |
CN1610669A (zh) | 2005-04-27 |
US20030186984A1 (en) | 2003-10-02 |
CA2469380C (en) | 2010-01-26 |
WO2003053933A1 (en) | 2003-07-03 |
CA2469380A1 (en) | 2003-07-03 |
KR20040075905A (ko) | 2004-08-30 |
CN1296357C (zh) | 2007-01-24 |
AU2002366732B2 (en) | 2006-11-02 |
ATE346045T1 (de) | 2006-12-15 |
MXPA04005907A (es) | 2004-09-13 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN106458930B (zh) | 2-氨基嘧啶类化合物及其药物组合物和应用 | |
JP6021880B2 (ja) | 免疫抑制剤としてのチアゾロピリミジン調節因子 | |
US12006328B2 (en) | Thieno[2,3-d]pyrimidin-4-one derivatives as NMDAR modulators and uses related thereto | |
RU2002117422A (ru) | 4-пиримидинил-N-ацил-L-фенилаланины | |
RU2007108861A (ru) | Трифтометилзамещенные бензамиды в качестве ингибиторов киназ | |
RU2005117340A (ru) | Производные пиримидо {4,5-d}пиримидина, обладающие противораковой активностью | |
RU2008123839A (ru) | Соединение оксазола и фармацевтическая композиция | |
RU2006112593A (ru) | Производные 2, 4-ди(гетеро)ариламинопиримидина в качестве ингибиторов zap-70 и/или syk | |
RU2005102004A (ru) | Замещенные хинолины как антагонисты рецептора ccr5 | |
HUP0401735A2 (hu) | CCR1 receptor antagonista hatású piperazinszármazékok és ezeket tartalmazó gyógyászati készítmények | |
NO2014030I1 (no) | (E)-4-[[4-[[4-(2-cyanoetenyl)-2,6-dimetylfenyl]-amino]-2-pyrimidinyl]-amino]-benzonitril("Rilpivirine") samt enhver terapeutisk form derav som er dekket av det aktuelle patentet så som farmasøytisk akseptable salter av Rilpivirie innbefattende hydrokloridsaltet av Rilpivirine, og emtricitabine. | |
RU2004113207A (ru) | Хинолиновые производные в качестве антагонистов нейропептида y | |
JP2007534695A5 (ru) | ||
RU2004111979A (ru) | Производные 1н-имидазола, обладающие св1-агонистической, частичной св1-агонистической или св1-антагонистической активностью | |
RU2002104935A (ru) | ПРОИЗВОДНЫЕ 8-ФЕНИЛ-6,9-ДИГИДРО[1,2,4]ТРИАЗОЛО[3,4-i]ПУРИН-5-ОНА | |
RU2008136187A (ru) | Новое производное кумарина, обладающее противоопухолевой активностью | |
RU96104356A (ru) | Производные амидина, обладающие активностью против синтетазы оксида азота (у) | |
RU2007118653A (ru) | Пиримидиновое производное, сконденсированное с неароматическим кольцом | |
RU2006134020A (ru) | Конденсированные производные пиразола | |
RU2004122480A (ru) | Производные гетероарил-замещенного аминоциклодекана | |
JPS6025974A (ja) | アミノピリミジン誘導体 | |
RU2010143455A (ru) | Имидазохинолины и производные пиримидина в качестве потенциальных модуляторов vegf-стимулируемых ангиогенных процессов | |
RU2002117419A (ru) | 4-пиридинил-N-ацил-L-фенилаланины | |
JP2012526082A5 (ru) | ||
RU2003121307A (ru) | (диазоло-пиридинил)-пиримидины для применения в лечении нарушений центральной нервной системы и диабета |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
MM4A | The patent is invalid due to non-payment of fees |
Effective date: 20071212 |