CN115504940A - A kind of amide compound, its preparation method and pharmaceutical use - Google Patents

Abstract

The present disclosure relates to an amide compound represented by general formula I, its prodrug, pharmaceutically acceptable salt, complex or solvate. The disclosed compound has a novel structure and significant antiviral activity and antiinflammatory activity.

Description

A kind of amide compound, its preparation method and pharmaceutical use

technical field

The invention belongs to the field of medicinal chemistry, and in particular relates to an amide compound, its preparation method and pharmaceutical application.

Background technique

Niclosamide was approved by the US Food and Drug Administration in 1960 for the treatment of intestinal tapeworm infection. Dead parasites. So far, niclosamide has been used safely for more than 50 years and has been included in the World Health Organization's list of essential medicines. In addition, niclosamide can also be used in the treatment of tapeworm infection in animals, and can also be used to kill snails and prevent schistosomiasis.

Recent studies have shown that niclosamide has a wide range of biological activities and can regulate various signaling pathways and biological processes, such as Wnt/β-catenin, mTORC1, STAT3, NF-κB, Notch, NS2B-NS protein interaction, etc. (Cancer Lett, 2014, 349, 8-14; Cell Res, 27, 1046-1064). Moreover, niclosamide exhibits antiviral pharmacological effects (Tuberculosis, 2019, 116, S28-S33; Nat.Med, 2016, 22, 1101-1107.)

Coronaviruses are a class of widely distributed single-stranded positive-sense RNA viruses that can infect a variety of higher animals and are also common human pathogens. Such as HCoV-229E, HCoV-OC43, HCoV-NL63, HCoV-HKU1 usually cause mild cold symptoms in humans (Academic Press, 2018, 100, 163-188). However, coronaviruses such as SARS-CoV, MERS-CoV, and SARS-CoV-2 can cause severe respiratory diseases and even death in humans. Currently, effective treatments for people infected with coronavirus have yet to be further developed. Wu et al. found that niclosamide can inhibit the replication of SARS-CoV through the new application screening of old drugs on the market, and can completely inhibit the synthesis of viral antigens at 1.5 μM (Antimicrob.Agents Chemother, 2004, 48, 2693- 2696.). Yang et al. found that niclosamide can inhibit the cytopathic effect (CPE) of SARS-CoV at 1 μM, and inhibit the replication of SARS-CoV in Vero E6 cells, and its EC50 value is less than 0.1 μM (J.Med.Chem, 2007, 50, 4087-4095).

Flaviviruses are also single-stranded positive-sense RNA viruses, mainly including Zika virus, dengue virus, Japanese encephalitis virus, West Nile virus, Yellow fever virus, many of these viruses are human pathogens. It is known that niclosamide is a potential inhibitor of Zika virus infection by enzyme screening method, the IC50 of intracellular level is 0.37μM, and niclosamide directly inhibits flavivirus NS2B-NS3 interaction, and niclosamide was also found Salamide is a broad-spectrum inhibitor of flaviviruses (Cell Res, 2017, 27, 1046-1064; Nat. Med, 2016, 22, 1101-1107).

Hepatitis C virus (HCV) is also an envelope-positive single-stranded RNA virus of the Flaviviridae family. About 71 million people in the world suffer from chronic HCV infection. The EC50 of niclosamide to inhibit HCV virus replication is 0.16μM. The mechanism of this inhibition of virus replication is similar to that of nitazoxanide and tizoxanide in regulating host cell processes (Antimicrob. Agents Chemother, 2008, 52, 4069-4071; Antiviral Res, 2011, 91, 233-240; ACS Med. Chem. Lett, 2011, 2, 849-854).

Ebola virus is a severe infectious disease virus that can cause Ebola hemorrhagic fever in humans and primates. Niclosamide has strong Ebola virus inhibitory activity, with EC50 of 1.5 μM (ACS Infect. Dis, 2015, 1, 317-326).

Human rhinovirus is a member of the Picornaviridae family, a genus of the Rhinovirus genus, and is a major cause of the common cold and poses serious health risks to patients with asthma, chronic lung disease, and severe bronchiolitis in infants and young children. Niclosamide is a pH-dependent inhibitor of HRV infection, with IC50 reaching micromolar levels; as a proton carrier, it inhibits the entry of HRV virus by blocking the acidification of endolysosomal compartments (Clin.Microbiol.Rev, 2013 , 26, 135-162; PLoS Pathog, 2012 8, e1002976).

Human adenoviruses are non-enveloped, double-stranded DNA viruses with seven subspecies. Adenoviruses are prevalent in the population, especially in infants and adolescents, mainly associated with respiratory, ocular- and gastrointestinal infections. At present, there is no truly feasible drug for the treatment of such viral infections (FEMS Microbiol.Rev.2019, 43, 380-388; Antimicrob.Agents Chemother.2010, 54, 3871-3877; 55, 3170-3181). Studies have found that niclosamide can significantly inhibit the infection of human adenovirus, with an IC50 of 0.6 μM.

However, niclosamide has some obvious disadvantages, such as low oral bioavailability and insufficient antiviral activity. These factors limit the further development and application of niclosamide as an antiviral active compound. On the basis of the structure of niclosamide, it is of great significance to optimize the structure and find compounds with stronger antiviral activity and higher oral bioavailability, as well as broad-spectrum antiviral active compounds with anti-inflammatory effects.

Contents of the invention

purpose of invention

In order to solve the deficiencies in the prior art, an object of the present invention is to provide a class of amide compounds which have antiviral activity, especially anticoronavirus, bunyavirus and dengue virus activity.

One object of the present invention is to provide a process for the preparation of the above compounds.

Another object of the present invention is to provide the use of the above compounds in the preparation of medicines for treating or preventing viral infections.

Technical solutions

According to one aspect of the present invention, it provides an amide compound represented by the following general formula I, its prodrug, pharmaceutically acceptable salt, complex or solvate:

in,

Y is a benzene ring, a 5-6 membered heteroaromatic ring, a benzene ring with a 5-6 membered heteroaryl ring or a 5-6 membered heteroaryl ring with a 5-6 membered heteroaryl ring; preferably a benzene ring, a pyridine ring or a thiazole ring ;

Z is O or S;

A ₁ is C-OR ₁₁ , C-SR ₁₁ , C-NHR ₁₁ , N or CR ₁₂ ;

C1～C20烷基磷酰基、C1～C20烷基磺酰基、C1～C20烷基取代的6-20元含有1-3个选自O、N或S的杂原子的杂环基羰基或

上述C1～C20烷基任选地被选自羟基、氨基(-NH₂)、C1～C20烷基氨基、氰基、羧基、卤素、

C1-C10烷基磺酰基、C1-C10烷基磷酰基、C1-C10酰基中的一种或多种取代；R ₁₁ is hydrogen atom, C1～C20 alkyl, C1～C20 alkylcarbonyl, C1～C20 alkylaminocarbonyl, C1～C20 alkylcarbonyloxy C1～C20 alkyl,

C1～C20 alkylphosphoryl, C1～C20 alkylsulfonyl, C1～C20 alkyl substituted 6-20 heterocyclic carbonyl containing 1-3 heteroatoms selected from O, N or S or

The above-mentioned C1-C20 alkyl group is optionally selected from hydroxyl, amino (-NH ₂ ), C1-C20 alkylamino, cyano, carboxyl, halogen,

One or more substitutions in C1-C10 alkylsulfonyl, C1-C10 alkyl phosphoryl, C1-C10 acyl;

上述C1～C10烷基任选地被选自羟基、氨基、氰基、羧基、卤素、

C1-C10烷基磺酰基、C1-C10烷基磷酰基、C1-C10烷基羰基中的一种或多种取代；Preferably, R ₁₁ is hydrogen atom, C1～C10 alkyl, C1～C10 alkylcarbonyl, C1～C10 alkylaminocarbonyl, C1～C10 alkylcarbonyloxy C1～C10 alkyl, C1～C10 alkyl substituted The 6-10 membered heterocyclylcarbonyl containing 1-3 heteroatoms selected from O, N or S or

The above-mentioned C1～C10 alkyl groups are optionally selected from hydroxyl, amino, cyano, carboxyl, halogen,

One or more substitutions in C1-C10 alkylsulfonyl, C1-C10 alkylphosphoryl, C1-C10 alkylcarbonyl;

取代的C1～C6烷基羰基、C1～C6烷基取代的6-8元含有1-3个选自O、N或S的杂原子的杂环基羰基或

More preferably, R ₁₁ is a hydrogen atom, C1～C6 alkyl, halogenated C1～C6 alkyl, amino C1～C6 alkyl, hydroxyl, C1～C6 alkyl, C1～C6 alkylcarbonyl, C1～C6 alkane Aminocarbonyl, C1～C6 alkylcarbonyloxy C1～C6 alkyl, C1～C6 alkylamino C1～C6 alkylcarbonyl, amino C1～C6 alkylcarbonyl,

Substituted C1～C6 alkylcarbonyl, C1～C6 alkyl substituted 6-8 membered heterocyclic carbonyl containing 1-3 heteroatoms selected from O, N or S or

取代的C1～C4烷基、取代的C1～C4烷基羰基、

或者

Most preferably, R ₁₁ is hydrogen atom, C1～C4 alkyl, C1～C6 alkylcarbonyl, C1～C5 alkylaminocarbonyl, C1～C5 alkylcarbonyloxy C1～C5 alkyl,

Substituted C1～C4 alkyl, substituted C1～C4 alkylcarbonyl,

or

R ₇ is C1～C10 alkyl, C1～C10 alkylamino C1～C10 alkyl or C3～C10 cycloalkyl, preferably C1～C6 alkyl, C1～C6 alkylamino C1～C6 alkyl or C3～ C7 cycloalkyl, more preferably C1～C4 alkyl, C1～C3 alkylamino C1～C4 alkyl or C3～C6 cycloalkyl;

_R8 is hydrogen atom, halogen or C1～C10 alkyl; preferably hydrogen atom, halogen or C1～C2 alkyl, more preferably hydrogen atom or methyl;

R ₁₂ is hydrogen atom, halogen, cyano, nitro or C1～C20 alkyl, preferably hydrogen atom, halogen, cyano, nitro or C1～C6 alkyl; more preferably hydrogen atom, halogen, cyano or C1～C4 alkyl;

A ₂ , A ₃ , A ₄ , A ₅ are each independently N or CR ₂ ; preferably, at most two of A ₂ , A ₃ , A ₄ , A ₅ are N;

R ₂ are the same or different from each other, and are independently selected from hydrogen, hydroxyl, halogen, C1-C6 alkyloxy, C1-C6 alkyl, amino (-NH ₂ ), nitro, cyano, carboxyl, aldehyde , C1～C6 alkylcarbonyl, C1～C6 alkylsulfonyl, C1～C6 alkylsulfonylamino and C1～C6 alkyloxycarbonyl, the above hydroxyl, amino, carboxyl, C1～C6 alkyl are optionally One or more substitutions in hydroxyl, amino, cyano, carboxyl, halogen, C1-C10 alkylsulfonyl, C1-C10 alkylphosphoryl, C1-C10 alkylcarbonyl;

Preferably, R are the same or different from each other, and are each independently selected from _hydrogen , hydroxyl, halogen, C1-C4 alkyloxy, C1-C4 alkyl, amino, nitro, cyano and C1-C4 alkylcarbonyl , the above-mentioned C1-C4 alkyl group is optionally replaced by one or more of hydroxyl, amino, cyano, carboxyl, halogen, C1-C4 alkylsulfonyl, C1-C4 alkylphosphoryl, C1-C4 alkylcarbonyl kind of substitution;

More preferably, R2 are the same or different from each other, and are independently selected from _hydrogen , hydroxyl, halogen, C1-C2 alkoxy, C1-C2 alkyl, C1-C2 alkylcarbonyl, halogenated C1-C2 alkoxy Group, halogenated C1-C2 alkyl, halogenated C1-C2 alkylcarbonyl, amino and nitro;

R ₃ is a hydrogen atom or a C1-C6 alkyl group, preferably, R ₃ is a hydrogen atom or a C1-C4 alkyl group, more preferably, R ₃ is a hydrogen atom;

R ₄ to R ₆ are each independently selected from hydrogen atom, hydroxyl, amino, halogen, nitro, cyano, C1～C6 alkyl, C1～C6 alkyloxy and C1～C6 alkylthio, the above C1～C6 C6 alkyl is optionally substituted by one or more of hydroxyl, amino, cyano, carboxyl, halogen, C1-C6 alkylsulfonyl, C1-C6 alkylphosphoryl, C1-C6 alkylacyl;

Preferably, R ₄ to R ₆ are each independently selected from a hydrogen atom, hydroxyl, amino, halogen, nitro, cyano, C1-C4 alkyl and C1-C4 alkyloxy, and the above-mentioned C1-C4 alkyl is optionally substituted by one or more of hydroxyl, amino, cyano, carboxyl, halogen;

More preferably, R ₄ to R ₆ are each independently selected from a hydrogen atom, halogen, C1-C4 alkyl, halogenated C1-C4 alkyl, C1-C4 alkoxy, and halogenated C1-C4 alkoxy.

In the present invention, halogen refers to fluorine, chlorine, bromine, iodine; halogenated C1～C4 alkyl refers to C1～C4 alkyl substituted with one or more halogen atoms, preferably trifluoromethyl; halogen Substituted C1-C4 alkoxy refers to C1-C4 alkyloxy substituted with one or more halogen atoms, preferably trifluoromethoxy.

In some embodiments, the amide compound represented by the general formula I is a compound represented by the following general formula II, IIIA or IIIB:

in,

A ₁ is C-OR ₁₁ , C-SR ₁₁ , C-NHR ₁₁ or CR ₁₂ ;

The definitions of R ₁₁ , R ₁₂ , R ₂ , R ₄ to R ₆ and Y are the same as in the general formula I.

In some embodiments, the amide compound represented by the general formula I is a compound represented by the following general formula IV:

in,

The definitions of R ₁₁ , R ₂ , R ₄ and R ₅ are the same as in the general formula I.

In some embodiments, each of the above-mentioned R ₂ is independently selected from a hydrogen atom, a halogen (especially fluorine and chlorine), a hydroxyl group, a formyl group, an acetyl group, and a nitro group.

In some embodiments, the above-mentioned R ₄ and R ₅ are each independently selected from a hydrogen atom, halogen, cyano, methyl, trifluoromethyl, methoxy, trifluoromethoxy, methylthio, trifluoromethyl Sulfur base.

In some embodiments, above-mentioned R ₁₁ is hydrogen.

In some embodiments, the compound or salt is selected from the following structures:

The invention also provides a preparation method of the compound of the general formula.

Wherein, the general formula II, IIIA or IIIB can be prepared by the following method one or method two:

method one:

Preparation of general formula compounds II and IIIA by condensation reaction, the condensation products II and IIIA are obtained in the presence of a condensing agent or phosphorus trichloride;

Method Two:

Using the condensation product as a raw material, compound I and/or IIIA can be reacted to obtain compound IIIB through hydrocarbylation, acylation, phosphorylation or sulfonylation.

Wherein, the definitions of each group are the same as those defined above.

On the other hand, the present invention also provides a pharmaceutical composition, which comprises a therapeutically effective amount of one selected from the above compounds of the present invention, their prodrugs, pharmaceutically acceptable salts, complexes and solvates. or several, and optionally a pharmaceutically acceptable carrier.

In another aspect, the present invention provides the use of the compound, its prodrug, pharmaceutically acceptable salt, complex or solvate or the pharmaceutical composition in the preparation of antiviral drugs.

In some embodiments, the virus is at least one selected from DNA viruses and RNA viruses.

In some embodiments, the DNA virus is selected from hepatitis B virus, human papillomavirus, herpes virus, phage virus; the RNA virus is selected from influenza virus, avian influenza virus, Zika virus, dengue virus, respiratory syndrome Cellular virus, SARS virus, MERS virus, novel coronavirus (SARS-CoV-2), bunya virus, HIV, Ebola virus, hepatitis C virus, Japanese encephalitis virus, rhinovirus, polio Viruses, Coxsackieviruses, Rotaviruses, Tobacco Mosaic Viruses, Phage Viruses, Marburg Viruses, Enteroviruses.

In some embodiments, the RNA virus is at least one of coronavirus, bunya virus, and dengue virus.

In some embodiments, the coronavirus is SARS-CoV-2.

In some embodiments, the bunyavirus is Rift Valley fever virus.

In some embodiments, the virus is dengue virus.

In another aspect, the present invention provides the use of the compound, its prodrug, pharmaceutically acceptable salt, complex or solvate or the pharmaceutical composition in the preparation of anti-inflammatory disease medicine.

In some embodiments, the inflammatory disease is inflammatory skin disease, inflammatory bowel disease, inflammatory joint disease, and other autoimmune diseases.

Beneficial effect

The compound of the invention has the following beneficial effects: novel structure and significant antiviral activity.

detailed description

In order to further understand the present invention, the present invention is further described below in conjunction with embodiment, and these embodiment descriptions are only for further specifying the feature of the present invention, rather than limiting the scope of the present invention or the scope of claims of the present invention. Simple replacements or improvements made by those skilled in the art to the invention shall be included in the technical solutions protected by the present invention.

Wherein the compound of the general formula can be prepared by following various synthetic methods and a series of synthetic steps well known to those skilled in the art.

Example 1: Synthesis of N-(4-trifluoromethylthiazole)-5-chlorosalicylamide (IIIA-1)

Add the weighed 2-hydroxyl-5-chloro-benzoic acid in the eggplant-shaped bottle successively, add the toluene (10 times volume) after molecular sieve drying, add the 2-amino-4-trifluoromethylthiazole of equivalent, Then phosphorus trichloride (about 1.1 equivalents) was added, replaced with nitrogen immediately, the temperature was raised from room temperature to 115°C, and stirred at this temperature for 8 hours, the reaction solution gradually became clear. TLC detects that the aniline reaction is complete before post-processing, adding a small amount of methanol to the reaction solution to quench phosphorus trichloride, then concentrating to remove most of the solvent, then extracting the liquid with ethyl acetate and water, and washing the organic solution with saturated sodium chloride solution. layer, dried over anhydrous sodium sulfate, filtered, mixed, and eluted with petroleum ether and ethyl acetate (50:1) to obtain the corresponding target compound IIIA-1 with a yield of 51.8%. ¹ H NMR (500MHz,DMSO-d ₆ )δ12.34(s,1H),11.73(s,1H),8.05(d,J=1.1Hz,1H),7.90(d,J=2.7Hz,1H) ,7.52(dd,J=8.8,2.8Hz,1H),7.08(d,J=8.8Hz,1H).ESI-MS m/z 307.9(MH) ^- .

Example 2: Synthesis of N-(2-chloro-4-trifluoromethoxyphenyl)-5-chlorosalicylamide (IIIA-2)

Except that 2-amino-4-trifluoromethylthiazole was replaced with 2-chloro-4-trifluoromethoxyaniline, and the reaction time was 5 hours, the same method as in Example 1 was used to prepare IIIA-2, and the yield For: 65.9%. ¹ H NMR (600MHz, DMSO-d6) δ12.31(s, 1H), 10.96(s, 1H), 8.51(d, J=9.1Hz, 1H), 7.98(d, J=2.8Hz, 1H), 7.73(d, J=2.8Hz, 1H), 7.52(dd, J=8.7, 2.8Hz, 1H), 7.47(dt, J=9.1, 1.8Hz, 1H), 7.08(d, J=8.8Hz, 1H ).ESI-MS m/z 363.9(MH) ^- .

Example 3: Synthesis of N-(4-trifluoromethylthiazole)-5-chlorosalicylamide (IIIA-3)

IIIA-3 was prepared according to the same method as in Example 1 except that 2-amino-5-trifluoromethylthiazole was used instead of 2-amino-4-trifluoromethylthiazole, and the yield was 55.5%. ¹ H NMR (500MHz, DMSO-d ₆ )δ12.33(s, 2H), 8.22(s, 1H), 7.87(d, J=2.7Hz, 1H), 7.52(dd, J=8.8, 2.8Hz, 1H),7.06(d,J＝8.8Hz,1H).ESI-MSm/z 320.9(MH) ^- .

Example 4: Synthesis of N-(4-trifluoromethylphenyl)-5-chlorosalicylamide (IIIA-4)

Except that 4-trifluoromethylaniline was used instead of 2-amino-4-trifluoromethylthiazole, and the reaction time was 7 hours, IIIA-4 was prepared according to the same method as in Example 1, and the yield was 67.36%. ¹ H NMR (500MHz,DMSO-d ₆ )δ11.57(s,1H),10.64(s,1H),7.94(d,J=8.5Hz,2H),7.88(d,J=2.7Hz,1H) ,7.77–7.71(m,2H),7.48(dd,J＝8.8,2.7Hz,1H),7.03(d,J＝8.8Hz,1H).ESI-MS m/z 314.0(MH) ^- .

Example 5: Synthesis of N-(4-trifluoromethylphenyl) salicyl (IIIA-5)

IIIA was prepared in the same manner as in Example 1 except that 2-hydroxybenzoic acid was used instead of 2-hydroxy-5-chloro-benzoic acid and 4-trifluoromethylaniline was used instead of 2-amino-4-trifluoromethylthiazole -5, yield: 7.11%. ¹ H NMR (500MHz,DMSO-d ₆ )δ10.41(s,1H),9.48(s,1H),7.82(d,J=8.4Hz,2H),7.66(d,J=8.5Hz,2H) ,7.14(dd,J=7.5,1.7Hz,1H),7.07(td,J=7.7,1.8Hz,1H),6.80(dd,J=8.1,1.2Hz,1H),6.75(td,J=7.4 ,1.2Hz,1H),3.63(s,2H).ESI-MS m/z 280.0(MH) ^- .

Example 6: Synthesis of N-(4-trifluoromethoxyphenyl)-5-chlorosalicylamide (IIIA-6)

Except that 2-amino-4-trifluoromethylthiazole was replaced by 4-trifluoromethoxyaniline, and the reaction time was 5 hours, IIIA-6 was prepared according to the same method as in Example 1, and the yield was: 54.38% . ¹ H NMR (500MHz, DMSO-d ₆ ) δ11.69(s, 1H), 10.53(s, 1H), 7.91(d, J=2.7Hz, 1H), 7.85–7.77(m, 2H), 7.47( dd, J＝8.8, 2.7Hz, 1H), 7.41–7.36(m, 2H), 7.02(d, J＝8.8Hz, 1H). ESI-MS m/z 330.0(MH) ^- .

Example 7: Synthesis of N-(4-trifluoromethoxyphenyl)pyrazinamide (IIIA-7)

Except that pyrazine-2-carboxylic acid was used instead of 2-hydroxy-5-chloro-benzoic acid, 4-trifluoromethoxyaniline was used instead of 2-amino-4-trifluoromethylthiazole, and the reaction time was 6 hours , Compound IIIA-7 was prepared according to the same method as in Example 1, and the yield was: 58.30%. ¹ H NMR (500MHz, DMSO-d ₆ )δ10.97(s, 1H), 9.31(d, J=1.5Hz, 1H), 8.95(d, J=2.5Hz, 1H), 8.83(dd, J= 2.5,1.5Hz,1H),8.06–7.99(m,2H),7.42–7.37(m,2H).ESI-MS m/z 284.0(M+H) ⁺ .

Example 8: Synthesis of N-(4-trifluoromethylphenyl)pyrazinamide (IIIA-8)

Except that pyrazine-2-carboxylic acid was used instead of 2-hydroxy-5-chloro-benzoic acid, 4-trifluoromethylaniline was used instead of 2-amino-4-trifluoromethylthiazole, and the reaction time was 6 hours, Compound IIIA-8 was prepared according to the same method as in Example 1, and the yield was: 56.17%. ¹ H NMR (500MHz, DMSO-d ₆ ) δ11.10(s, 1H), 9.32(d, J=1.5Hz, 1H), 8.96(d, J=2.5Hz, 1H), 8.84(dd, J= 2.5, 1.5Hz, 1H), 8.15(d, J=8.5Hz, 2H), 7.75(d, J=8.6Hz, 2H). ESI-MS m/z 269.0(M+H) ⁺ .

Example 9: Synthesis of N-(3,5-bis(trifluoromethyl)phenyl)-5-chlorosalicylamide (IIIA-9)

Except that 2-amino-4-trifluoromethylthiazole was replaced with 3,5-bis(trifluoromethyl)aniline, and the reaction time was 7 hours, compound IIIA-9 was prepared according to the same method as in Example 1, and the obtained Rate: 44.38%. ¹ H NMR (500MHz,DMSO-d ₆ )δ11.38(s,1H),10.84(s,1H),8.84(m,2H),7.83-7.86(m,2H),7.47-7.51(m,1H ),7.03-7.05(m,1H).ESI-MS m/z 382.0(MH) ^- .

Example 10: Synthesis of N-(4-trifluoromethylphenyl)-3,5-dichlorosalicylamide (IIIA-10)

Except for 2-hydroxy-3,5-dichlorobenzoic acid instead of 2-hydroxy-5-chloro-benzoic acid, 4-trifluoromethylaniline instead of 2-amino-4-trifluoromethylthiazole, and reaction times Compound IIIA-10 was prepared according to the same method as in Example 1 except for 6 hours, and the yield was 67.33%. ¹ H NMR (500MHz, DMSO-d ₆ )δ12.22(s, 1H), 10.88(d, J=4.2Hz, 1H), 8.05(d, J=2.5Hz, 1H), 7.93(d, J= 8.4Hz, 2H), 7.83(d, J=2.5Hz, 1H), 7.77(d, J=8.5Hz, 2H). ESI-MS m/z 348.2.

Example 11: Synthesis of N-(4-trifluoromethylphenyl)-2-cyano-5-chlorobenzamide (IIIA-11)

Except for 2-cyano-5-chlorobenzoic acid instead of 2-hydroxy-5-chloro-benzoic acid, 4-trifluoromethylaniline instead of 2-amino-4-trifluoromethylthiazole, and a reaction time of 6 After 1 hour, compound IIIA-11 was prepared according to the same method as in Example 1, and the yield was 37.57%. ¹ H NMR (500MHz,DMSO-d ₆ )δ10.53(s,1H),8.34–8.28(m,1H),8.00–7.96(m,2H),7.90(d,J＝8.4Hz,2H), 7.74(d,J＝8.2Hz,2H).ESI-MS m/z 323.1(MH) ^- .

Example 12: Synthesis of N-(4-trifluoromethoxyphenyl)-4-fluoro-5-chlorosalicylamide (IIIA-12)

In addition to substituting 2-hydroxy-4-fluoro-5-chlorobenzoic acid for 2-hydroxy-5-chloro-benzoic acid, substituting 4-trifluoromethoxyaniline for 2-amino-4-trifluoromethylthiazole, and Except that the reaction time was 10 hours, compound IIIA-12 was prepared according to the same method as in Example 1, and the yield was: 51.72%. ¹ H NMR (500MHz, DMSO-d ₆ ) δ12.20(s, 1H), 10.51( s,1H), 8.12(d,J=8.5Hz,1H),7.86–7.79(m,2H),7.43–7.38(m,2H),7.04(d,J=10.8Hz,1H).ESI-MS m/z 348.2(MH) ^- .

Example 13: Synthesis of N-(5-trifluoromethylthiazole)-4-fluoro-5-chlorosalicylamide (IIIA-13)

In addition to replacing 2-hydroxy-5-chloro-benzoic acid with 2-hydroxy-4-fluoro-5-chlorobenzoic acid and replacing 2-amino-4-trifluoromethyl with 2-amino-5-trifluoromethylthiazole Thiazole, and the reaction time was 3 hours, according to the same method as Example 1 to prepare compound IIIA-13, the yield: 51.47%. ¹ H NMR (500MHz,DMSO-d ₆ )δ12.65(s,2H),8.25(s,1H),8.05(d,J=8.7Hz,1H),7.03(d,J=8.7Hz,1H) .ESI-MS m/z 339.1(MH) ^- .

Example 14: Synthesis of N-(4-trifluoromethylphenyl)-5-fluorosalicylamide (IIIA-14)

Except for 2-hydroxy-5-fluorobenzoic acid instead of 2-hydroxy-5-chloro-benzoic acid, 4-trifluoromethylaniline instead of 2-amino-4-trifluoromethylthiazole, and a reaction time of 9 hours Otherwise, compound IIIA-14 was prepared according to the same method as in Example 1, and the yield was: 53.29%. ¹ H NMR (500MHz,DMSO-d ₆ )δ11.55(s,1H),10.56(s,1H),7.86(d,J=8.3Hz,2H),7.80(d,J=2.7Hz,1H) ,7.77–7.73(m,2H),7.48(dd,J＝8.3,2.7Hz,1H),7.03(d,J＝8.8Hz,1H).ESI-MS m/z 298.0(MH) ^- .

Example 15: Synthesis of N-(4-trifluoromethylphenyl)-3,5-difluorosalicylamide (IIIA-15)

Except for 2-hydroxy-3,5-difluorobenzoic acid instead of 2-hydroxy-5-chloro-benzoic acid, 4-trifluoromethylaniline instead of 2-amino-4-trifluoromethylthiazole, and reaction times Except for 6 hours, compound IIIA-15 was prepared according to the same method as in Example 1, and the yield was: 75.23%. ¹ H NMR (500MHz,DMSO-d ₆ )δ11.32(s,1H),10.72(s,1H),7.93(d,J=8.5Hz,2H),7.76(d,J=8.5Hz,2H) ,7.55(s,1H),7.53(d,J=3.5Hz,1H).ESI-MS m/z316.2(MH) ^- .

Example 16: Synthesis of N-(4-trifluoromethoxyphenyl)-3,5-difluorosalicylamide (IIIA-16)

In addition to substituting 2-hydroxy-3,5-difluorobenzoic acid for 2-hydroxy-5-chloro-benzoic acid, substituting 4-trifluoromethoxyaniline for 2-amino-4-trifluoromethylthiazole, and the reaction Except for 11 hours (whether there are other different reaction conditions), compound IIIA-16 was prepared according to the same method as in Example 1, and the yield was 50.05%. ¹ H NMR (500MHz,DMSO-d ₆ )δ11.48(s,1H),10.60(s,1H),7.84–7.79(m,2H),7.60–7.52(m,2H),7.40(m,2H ).ESI-MS m/z 332.2(MH) ^- .

Example 17: Synthesis of N-(3,5-bis(trifluoromethyl)phenyl)-4-fluoro-5-chlorosalicylamide (IIIA-17)

Except for 2-hydroxy-4-fluoro-5-chlorobenzoic acid instead of 2-hydroxy-5-chloro-benzoic acid and 3,5-bis(trifluoromethyl)aniline instead of 2-amino-4-trifluoromethane Based on thiazole, and the reaction time is 9 hours, compound IIIA-17 was prepared according to the same method as in Example 1, and the yield was 65%. ¹ H NMR (500MHz, DMSO-d6) δ11.90(s, 1H), 10.85(s, 1H), 8.44(d, J=1.6Hz, 2H), 8.07(d, J=8.6Hz, 1H), 7.87(s,1H),7.05(d,J=10.8Hz,1H).ESI-MS m/z 400.2(MH) ^- .

Example 18: Synthesis of N-(4-trifluoromethylphenyl)-4-fluoro-5-chlorosalicylamide (IIIA-18)

In addition to substituting 2-hydroxy-4-fluoro-5-chlorobenzoic acid for 2-hydroxy-5-chloro-benzoic acid, substituting 4-trifluoromethylaniline for 2-amino-4-trifluoromethylthiazole, and the reaction Except for 7 hours, compound IIIA-18 was prepared according to the same method as in Example 1, and the yield was 45.04%. ¹ H NMR (500MHz,DMSO-d ₆ )δ12.07(s,1H),10.63(s,1H),8.07(d,J=8.6Hz,1H),7.93(d,J=8.5Hz,2H) ,7.74(d,J=8.5Hz,2H),7.02(d,J=10.8Hz,1H).ESI-MS m/z 332.1(MH) ^- .

Example 19: Synthesis of N-(4-trifluoromethylphenyl)-2-hydroxy-5-chloronicotinamide (IIIA-19)

Except that 2-hydroxy-5-chloronicotinic acid was used instead of 2-hydroxy-5-chloro-benzoic acid, 4-trifluoromethylaniline was used instead of 2-amino-4-trifluoromethylthiazole, and the reaction time was 12 hours Otherwise, compound IIIA-19 was prepared according to the same method as in Example 1, and the yield was: 69.72%. ¹ H NMR (500MHz,DMSO-d ₆ )δ13.25(s,1H),12.32(s,1H),8.36(d,J=3.0Hz,1H),8.13(d,J=3.1Hz,1H) ,7.90(d,J=8.4Hz,2H),7.73(d,J=8.5Hz,2H).ESI-MS m/z 315.0(MH) ^- .

Example 20: Synthesis of N-(2-chloro-4-trifluoromethylphenyl)-3,4,5-trihydroxybenzamide (IIIA-20)

Add 3,4,5-trihydroxybenzoic acid (500mg), methanol (10mL) and sulfuric acid (100uL) into the eggplant-shaped flask, stir and reflux for 12 hours, and the raw materials basically react completely. The reaction solution was spin-dried, extracted, and dried to obtain methyl 3,4,5-trihydroxybenzoate (510 mg), which was directly used for the next step.

Add acetone and potassium nitrite (2.8 g) to the above product, dropwise add benzyl bromide (1.4 mL), and reflux at 66° C. for 6 hours. TLC detects that the reaction of the raw materials is complete. The reaction solution was directly filtered, and the filtrate was spin-dried to obtain methyl 3,4,5-tribenzyloxybenzoate, which was directly used for the next step.

Add methanol/water (3:2) to the above product, add sodium hydroxide (480mg, 5eq), and reflux at 66°C overnight. Post-processing: remove methanol by rotary evaporation, extract with ethyl acetate, adjust pH to 5-6, separate liquid, wash with water, wash with saturated saline, separate liquid and dry, spin dry the filtrate, obtain light yellow 3,4, 5-Tribenzyloxybenzoic acid (800 mg).

Add light yellow solid (330mg), dry toluene (8mL), and 2-chloro-4-trifluoromethylaniline (78uL) to the eggplant-shaped flask in turn, add phosphorus trichloride (56uL) at room temperature, and immediately protect with nitrogen. At this time, the reaction solution was a milky white suspension, which was heated to 115° C. and refluxed overnight. Add water to the reaction solution, a small amount of sodium bicarbonate solution, extract with ethyl acetate, wash with saturated brine, dry, and elute with petroleum ether and ethyl acetate (100:1) to obtain white N-(2-chloro- 220 mg of 4-trifluoromethylphenyl)-3,4,5-tribenzyloxybenzamide as a solid.

Dissolve the white solid in methanol:tetrahydrofuran (1:1), add palladium carbon (20 mg), replace with hydrogen, react overnight, and detect by TLC the next day. The reaction of the raw materials is complete, and the reaction is thorough. Post-treatment: Diatomaceous earth filter aid, spin the filtrate to dry, mix the sample, and elute with dichloromethane and methanol (50:1) to obtain 60 mg of the target compound IIIA-20 with a yield of 45.80%. ¹ H NMR (500MHz, DMSO-d ₆ ) δ9.71(s,1H), 9.24(s,2H), 8.91(s,1H), 8.00–7.93(m,2H), 7.74(dd, J=8.6 ,2.1Hz,1H),6.99(s,2H).ESI-MS m/z 453.1(MH) ^- .

Example 21: Synthesis of N-(4-trifluoromethoxyphenyl)-2,3,4-trihydroxybenzamide (IIIA-21)

Add 2,3,4-tribenzyloxybenzoic acid (330mg), dry toluene (8mL), 4-trifluoromethoxyaniline (100uL) to the eggplant-shaped flask in turn, add phosphorus trichloride (75uL ), immediately under nitrogen protection. At this time, the reaction solution was a milky white suspension, which was heated to 115° C. and refluxed overnight. The next day, it was cleared and detected by TLC, and the reaction of the raw materials was complete. Add water to the reaction solution, a small amount of sodium bicarbonate solution, extract with ethyl acetate, wash with saturated brine, dry, and elute with petroleum ether and ethyl acetate (100:1) to obtain white N-(4-trifluoromethane Oxyphenyl)-2,3,4-tribenzyloxybenzamide solid 370mg.

Dissolve the white solid in methanol:tetrahydrofuran (1:1), add palladium carbon (100mg), replace with hydrogen, react overnight, TLC detection the next day, the raw materials are completely reacted, and the reaction is thorough. Post-treatment: Diatomaceous earth filter aid, the filtrate was spin-dried, mixed the sample, and eluted with dichloromethane and methanol (50:1) to obtain 140 mg of the target compound IIIA-21 with a yield of 70%. ¹ H NMR (500MHz,DMSO-d ₆ )δ12.11(s,1H),10.27(s,1H),9.73(s,1H),8.57(s,1H),7.82–7.75(m,2H), 7.43(d, J=8.9Hz, 1H), 7.39–7.34(m, 2H), 6.42(d, J=8.8Hz, 1H).ESI-MS m/z 328.2(MH) ^- .

Example 22: Synthesis of N-(4-trifluoromethylphenyl)-2,3,4-trihydroxybenzamide (IIIA-22)

Add 2,3,4-tribenzyloxybenzoic acid (330mg), dry toluene (8mL), 4-trifluoromethylaniline (94uL) to the eggplant-shaped flask in sequence, and add phosphorus trichloride (78uL) at room temperature , Immediately under nitrogen protection. At this time, the reaction solution was a milky white suspension, which was heated to 115° C. and refluxed overnight. The next day, it was cleared and detected by TLC, and the reaction of the raw materials was complete. Add water to the reaction solution, a small amount of sodium bicarbonate solution, extract with ethyl acetate, wash with saturated brine, dry, and elute with petroleum ether and ethyl acetate (100:1) to obtain white N-(4-trifluoromethane phenyl)-2,3,4-tribenzyloxybenzamide solid 390mg.

Dissolve the white solid in methanol:tetrahydrofuran (1:1), add palladium carbon (100mg), replace with hydrogen, react overnight, TLC detection the next day, the raw materials are completely reacted, and the reaction is thorough. Post-processing: Diatomaceous earth filter aid, the filtrate was spin-dried, mixed the sample, and eluted with dichloromethane and methanol (50:1) to obtain 130 mg of the target compound IIIA-22 with a yield of 53%. ¹ H NMR (500MHz, DMSO-d ₆ )δ11.91(s,1H),10.40(s,1H),9.79(s,1H),8.62(s,1H),7.92(d,J＝8.5Hz, 2H), 7.72(d, J=8.5Hz, 2H), 7.45(d, J=8.8Hz, 1H), 6.43(d, J=8.8Hz, 1H).ESI-MS m/z 312.2(MH) ^- .

Example 23: Synthesis of N-(4-trifluoromethylphenyl)-2-methoxy-5-chlorobenzamide (IIIA-23)

Add 5-chloro-2-methoxybenzoic acid (186mg), dry toluene (5ml), p-trifluoromethylaniline (125uL) to the eggplant-shaped bottle in turn, add phosphorus trichloride (105uL) at room temperature, nitrogen Protect. At this time, the reaction solution was a white suspension, which was heated to 115° C. and refluxed overnight. TLC detected that the reaction of the raw materials was complete. Add water to the reaction solution, a small amount of sodium bicarbonate solution, extract with ethyl acetate, wash with saturated brine, dry, and elute with petroleum ether and ethyl acetate (100:1) to obtain white solid compound IIIA-23, weighing 150mg . ¹ H NMR (500MHz, DMSO-d6) δ10.54(s, 1H), 7.93(d, J=8.4Hz, 2H), 7.71(d, J=8.5Hz, 2H), 7.61(d, J=2.7 Hz,1H),7.56(dd,J=8.9,2.8Hz,1H),7.22(d,J=8.9Hz,1H),3.88(s,3H).ESI-MS m/z 328.0(MH) ^- .

Example 24: Synthesis of N-(4-trifluoromethylphenyl)-5-chloro-2-acetamidobenzamide (IIIA-24)

2-Amino-5-chlorobenzoic acid (1.368g) was dissolved in acetic acid (15mL), and acetic anhydride (1.34mL) was added, and the temperature was increased to 75°C. After 30 minutes, TLC detected that the reaction was complete. Post-treatment: Pour the reaction solution into ice water, stir, filter with suction, wash the filter cake with water, and dry to obtain 2-acetylamino-5-chlorobenzoic acid, which will be used in the next step.

Add dry toluene, p-trifluoromethylaniline (878uL), and phosphorus trichloride (800uL) to the above solid, and reflux overnight at 115°C. The next day, the solution is not clear, and the reaction is about 90%. Post-processing: add water and a small amount of sodium bicarbonate solution to the reaction solution, remove toluene by rotary evaporation, extract with ethyl acetate, wash with saturated brine, dry, and elute with petroleum ether and ethyl acetate (100:1) to obtain the compound IIIA-24, weighing 1.9 g. ¹ H NMR (500MHz, DMSO-d ₆ ) δ8.06 (d, J = 2.5Hz, 1H), 7.99 (d, J = 8.2Hz, 2H), 7.91 (d, J = 8.7, 1H), 7.77 ( d,J=8.2Hz,2H),7.73(d,J=8.7Hz,1H),2.14(s,3H).ESI-MS m/z 355.1(MH) ^- .

Example 25: Synthesis of N-(4-trifluoromethoxyphenyl)-5-chloro-2-acetamidobenzamide (IIIA-25)

Add white solid (277mg) obtained in the first step in Example 24, dry toluene (5mL), p-trifluoromethoxyaniline (171.6uL), phosphorus trichloride (146uL) to the round-bottomed flask successively, replace with nitrogen, From room temperature to 115°C, stirring for 12 hours, the reaction phase was always in a turbid state. After cooling, TLC detection showed that about 90% of the raw material was reacted. Post-processing: add a small amount of methanol to quench the reaction, remove part of the toluene by rotary evaporation, add ethyl acetate and water to the system, separate layers, separate liquids, wash the organic phase with saturated brine, dry, filter, mix the sample, and add petroleum ether Eluted with ethyl acetate (100:1), and the eluent of the target product point was ethyl acetate:methanol=30:1, to obtain the target compound IIIA-25, 304 mg, and the NMR was correct. ¹ H NMR (500MHz, DMSO-d ₆ )δ8.04(s, 1H), 7.90(d, J=8.7Hz, 1H), 7.73(d, J=8.6Hz, 1H), 7.65(d, J= 8.3Hz, 2H), 7.60(d, J=8.3Hz, 2H), 2.15(s, 3H). ESI-MS m/z 395.0(M+Na) ⁺ .

Example 26: Synthesis of N-(4-trifluoromethylphenyl)-5-chloro-3-acetyl salicylamide (IIIA-26)

Add 5-chlorosalicylic acid (5g), dichloromethane (15mL), and DMF (10 drops) to the reaction flask in sequence, add oxalyl chloride (3.5mL) dropwise in an ice bath, and turn to room temperature for about 3 hours The response is complete. Add this solution dropwise to methanol (25mL), after the addition is complete, stir for 10 minutes, concentrate, extract with ethyl acetate and water, wash the organic phase with saturated brine, dry, filter, and concentrate the filtrate to give 5-chloro-2 -Methyl hydroxybenzoate (5.10g), waiting to be thrown.

Acetic anhydride (5 mL) and sulfuric acid (100 uL) were added to methyl 5-chloro-2-hydroxybenzoate (5.10 g) obtained in the previous step, and stirred at room temperature for 30 minutes. Ethyl acetate (15 mL) and saturated sodium bicarbonate solution (added slowly in batches) were added to the reaction system until no bubbles were generated after the addition. The liquid was separated, and the organic phase was washed with saturated brine, dried, filtered, and concentrated to obtain methyl 5-chloro-2-acetoxybenzoate, which was to be used in the next step.

Transfer methyl 5-chloro-2-acetoxybenzoate to a two-necked flask, add aluminum trichloride (30g), sodium chloride (16g), nitrogen protection, mechanical stirring at 120°C for 3 hours, TLC detection The basic reaction of raw materials is complete. Add 1M hydrogen chloride solution (slowly) to the reaction system under an ice bath, and add ethyl acetate (30 mL) after stirring evenly, extract and separate the layers, and extract the water layer several times. The organic phases were combined, washed with saturated brine, dried, filtered, concentrated and mixed, and eluted with petroleum ether and ethyl acetate (10:1) to obtain white 5-chloro-3-acetyl-2-hydroxybenzoic acid solid 1.1 g.

Add 5-chloro-3-acetyl 2-hydroxybenzoic acid (990mg), dry toluene (25mL), p-trifluoromethylaniline (554uL), phosphorus trichloride (446uL) to the reaction flask in sequence, nitrogen protection, The temperature was raised from room temperature to 115° C., and the reaction was carried out for 10 hours. TLC showed that the reaction was not complete. Post-treatment: add a small amount of methanol to the reaction system, concentrate, mix the sample, and elute with petroleum ether and ethyl acetate (100:1) to obtain the target compound IIIA-26, 150 mg. ¹ H NMR (500MHz,DMSO-d ₆ )δ13.01(s,1H),10.80(s,1H),8.13(d,J=2.7Hz,1H),8.06(d,J=2.8Hz,1H) ,7.95(d,J=8.3Hz,2H),7.76(d,J=8.4Hz,2H),2.74(s,3H).ESI-MS m/z 356.1(MH) ^- .

Example 27: Synthesis of N-(4-trifluoromethoxyphenyl)-5-chloro-3-acetyl salicylamide (IIIA-27)

Add the solid obtained in the third step in Example 26 (85mg), dry toluene (2mL), p-trifluoromethoxyaniline (54uL), phosphorus trichloride (45uL) to the reaction flask in sequence, nitrogen protection, and increase the temperature from room temperature to 115°C and react for 13 hours. TLC showed that the reaction was not complete. Post-treatment: add a small amount of methanol to the reaction system, concentrate, extract with ethyl acetate and water, wash with saturated brine, dry, and elute with petroleum ether and ethyl acetate (100:1) to obtain the target compound IIIA-27, 18 mg. ¹ H NMR (500MHz,DMSO-d ₆ )δ13.07(s,1H),10.72(s,1H),8.09–8.04(m,2H),7.85–7.79(m,2H),7.39(d,J =8.6Hz,2H),2.71(s,3H).ESI-MS m/z 372.0(MH) ^- .

Example 28: Synthesis of N-(4-trifluoromethylphenyl)-5-chloro-3-nitrosalicylicamide (IIIA-28)

5-Chlorosalicylic acid (342 mg) was dissolved in concentrated sulfuric acid, ice-bathed, concentrated nitric acid (232 mg) was added, and reacted in ice-bath for 4 hours, TLC detection showed that the raw materials were completely reacted. The reaction solution was dropped into ice water, stirred for 30 minutes, filtered, and the filter cake was washed with water, dried, concentrated to obtain 3-nitro-5-chloro-2-hydroxybenzoic acid, which was to be used in the next step.

3-nitro-5-chloro-2-hydroxybenzoic acid (310mg), p-trifluoromethylaniline (230mg), dry toluene (20mL), phosphorus trichloride (149uL), reflux at 115°C. Add water and a small amount of sodium bicarbonate solution to the reaction solution, remove toluene by rotary evaporation, extract with ethyl acetate, wash with saturated brine, dry, and elute with petroleum ether and ethyl acetate (100:1) to obtain the target compound IIIA- 28, 150 mg. ¹ H NMR (500MHz,DMSO-d ₆ )δ11.83(s,1H),8.17–8.15(m,1H),8.14–8.10(m,1H),7.91(d,J＝8.5Hz,2H), 7.75(d,J＝8.4Hz,2H).ESI-MS m/z 359.0(MH) ^- .

Example 29: Synthesis of N-(4-trifluoromethylmercaptophenyl)-4-fluoro-5-chlorosalicylamide (IIIA-29)

Reaction 5, except that 2-hydroxy-4-fluoro-5-chlorobenzoic acid was substituted for 2-hydroxy-5-chloro-benzoic acid and 4-trifluoromethylmercaptoaniline was substituted for 2-amino-4-trifluoromethylthiazole After 1 hour, compound IIIA-29 was prepared according to the same method as in Example 1, and the yield was 69.23%. ¹ H NMR (400MHz, DMSO-d6) δ12.08(s,1H),10.58(s,1H),8.06(d,J=8.6Hz,1H),7.90–7.83(m,2H),7.76–7.69 (m,2H),7.02(d,J＝10.8Hz,1H).ESI-MS m/z363.0(MH) ^- .

Example 30: Synthesis of N-(3-trifluoromethyl-4-cyanophenyl)-4-fluoro-5-chlorosalicylamide (IIIA-30)

Except for 2-hydroxy-4-fluoro-5-chlorobenzoic acid instead of 2-hydroxy-5-chloro-benzoic acid and 3-trifluoromethyl-4-cyanoaniline instead of 2-amino-4-trifluoromethane Except for base thiazole, compound IIIA-30 was prepared according to the same method as in Example 1, and the yield was 37.23%. ¹ H NMR(500MHz,DMSO-d6)δ11.83(s,1H),10.90(s,1H),8.40(s,1H),8.16(s,2H),7.99(d,J＝8.6Hz,1H ), 7.02(d, J=10.8Hz, 1H).ESI-MS m/z 358.0(MH) ^- .

Example 31: Synthesis of N-(3-trifluoromethyl-4-cyanopyridine)-4-fluoro-5-chlorosalicylamide (IIIA-31)

In addition to replacing 2-hydroxy-5-chloro-benzoic acid with 2-hydroxy-4-fluoro-5-chlorobenzoic acid and replacing 2-amino-4 with 2-cyano-3-trifluoromethyl-5-aminopyridine - Trifluoromethylthiazole, except that the reaction time was 6 hours, compound IIIA-31 was prepared according to the same method as in Example 1, and the yield was 36.13%. ¹ H NMR (500MHz, DMSO-d6) δ11.90(s, 1H), 11.16(s, 1H), 9.24(d, J=2.3Hz, 1H), 8.82(d, J=2.3Hz, 1H), 7.99(d, J=8.6Hz, 1H), 7.03(d, J=10.8Hz, 1H).ESI-MS m/z 359.0(MH) ^- .

Example 32: Synthesis of N-(3-chloro-4-trifluoromethyl)-5-chlorosalicylamide (IIIA-32)

Except for 2-hydroxy-5-chlorobenzoic acid instead of 2-hydroxy-5-chloro-benzoic acid and 3-chloro-4-trifluoromethylaniline instead of 2-amino-4-trifluoromethylthiazole, the reaction times Except for 5 hours, compound IIIA-32 was prepared according to the same method as in Example 1, and the yield was 40.23%. ¹ H NMR (500MHz, DMSO-d6) δ11.92(s, 1H), 10.78(d, J=6.0Hz, 1H), 8.14(d, J=1.9Hz, 1H), 8.02(d, J=8.6 Hz, 1H), 7.89–7.81(m, 2H), 7.01(d, J=10.8Hz, 1H). ESI-MS m/z 348.01(MH) ^- .

Example 33: (4-Chloro-5-fluoro-2-(((4-(trifluoromethyl)phenyl)carbamoyl)phenoxy)methylisopropylcarbonate (IIIB-1) synthesis

Add acetone (1 mL), chloromethyl isopropyl carbonate (46 mg), sodium iodide (45 mg,) to the reaction flask in sequence, and stir at 60° C. for 3 hours. Filter and wash the filter cake with a small amount of acetone.

Potassium carbonate (40mg), compound IIIA-18 (70mg), acetone (2mL), DMF (10 drops) were added successively to the reaction flask to aid dissolution, and the filtrate obtained in the above steps was added under stirring, and the reaction was detected by TLC after stirring for 2 hours. Concentrate the reaction solution, add ethyl acetate and water to the concentrate, adjust the pH of the aqueous phase with saturated ammonium chloride solution, separate the liquids, wash the organic phase with saturated brine, dry, filter, concentrate, and the concentrate with petroleum ether (1.5mL ) and ethyl acetate (10 drops), and filtered to obtain compound IIIB-160mg, and the NMR was correct. ¹ H NMR (500MHz, DMSO-d ₆ )δ10.60(s, 1H), 7.90(d, J=8.4Hz, 2H), 7.88(d, J=8.4Hz, 1H), 7.74(d, J= 8.6Hz, 2H), 7.55(d, J=8.6Hz, 1H), 5.88(s, 2H), 4.76(m, J=6.3Hz, 1H), 1.20(d, J=6.3Hz, 6H).ESI -MS m/z 447.8(MH) ^- .

Example 34: 5-chloro-4-fluoro-2-((5-methyl-2-oxo-1,3-dioxolan-4-yl)methoxy)-N-(4-( Synthesis of Trifluoromethyl)phenyl)benzamide (IIIB-2)

Add acetone (1mL), 4-chloromethyl-5-methyl-1,3-dioxol-2-one (44m), sodium iodide (45mg) to the reaction flask in turn, and stir at 60°C 3 hours. Filter and wash the filter cake with a small amount of acetone.

Add potassium carbonate (50 mg), compound IIIA-18 (70 mg), acetone (2 mL), DMF (10 drops) to the reaction flask in order to aid in dissolution, add the filtrate obtained in step a under stirring, stir for 5 hours, and TLC detects that the remaining raw materials of the reaction are . Post-processing: spin dry the organic solvent, add ethyl acetate and water to the concentrate, adjust the pH of the aqueous phase to be acidic with saturated ammonium chloride, separate the liquid, wash the organic phase with saturated saline, dry, filter, concentrate, and use the concentrate Petroleum ether (1.5 mL) and ethyl acetate (10 drops) were slurried and filtered to obtain 56 mg of compound IIIB-2, and the NMR was correct. ¹ H NMR (500MHz, DMSO-d ₆ )δ10.53(s, 1H), 7.89(d, J=8.4Hz, 2H), 7.84(d, J=8.5Hz, 1H), 7.72(d, J= 8.6Hz, 2H), 7.57(d, J=11.4Hz, 1H), 5.18(s, 2H), 2.18(s, 3H). ESI-MS m/z 444.1(MH) ^- .

Example 35: Synthesis of N-(4-trifluoromethylphenyl)-2-acetoxy-4-fluoro-5-chlorobenzamide (IIIB-3)

Add the weighed salicylamide derivative IIIA-18, acetic anhydride (0.5mL) and concentrated sulfuric acid (1 drop) to the eggplant-shaped bottle in turn, stir at room temperature for 45 minutes, and TLC detects that the raw materials are almost completely converted. Add ethyl acetate (4mL) and ice water (4mL) to the reaction solution, extract and separate the layers, wash the ethyl acetate layer with saturated sodium chloride solution, dry over anhydrous sodium sulfate, filter, mix the sample, and wash with petroleum ether and acetic acid Eluted with ethyl ester (100:1), the corresponding target compound IIIB-3 was obtained with a yield of 30%. ¹ H NMR (500MHz, DMSO-d6) δ10.79(s, 1H), 8.04(d, J=8.1Hz, 1H), 7.89(d, J=8.4Hz, 2H), 7.73(d, J=8.5 Hz,3H),7.57(d,J=9.7Hz,1H),2.21(s,3H).

Example 36: Synthesis of N-(4-trifluoromethylphenyl)-2-acetoxy-3,5-difluorobenzamide (IIIB-4)

IIIB-4 was prepared according to the same method as in Example 35 except that compound IIIA-15 was used instead of IIIA-18, and the yield was 72%. ¹ H NMR (500MHz, DMSO-d6) δ10.89 (s, 1H), 7.91 (d, J = 8.4Hz, 2H), 7.79–7.69 (m, 3H), 7.57 (ddd, J = 8.3, 2.9, 1.6Hz,1H),2.28(s,3H).

Example 37: Synthesis of N-(4-trifluoromethoxyphenyl)-2-acetoxy-4-fluoro-5-chlorobenzamide (IIIB-5)

IIIB-5 was prepared according to the same method as in Example 35 except that compound IIIA-12 was used instead of IIIA-18, and the yield was 34%. ¹ H NMR (500MHz, DMSO-d6) δ10.64(s, 1H), 8.01(d, J=8.2Hz, 1H), 7.81–7.75(m, 2H), 7.56(d, J=9.8Hz, 1H ),7.42–7.31(m,2H),2.21(s,3H).

Example 38: Synthesis of N-(4-trifluoromethylphenyl)-2-isobutyryloxy-4-fluoro-5-chlorobenzamide (IIIB-6)

Except that isobutyric anhydride was used instead of acetic anhydride, and the reaction time was 1 hour, IIIB-6 was prepared according to the same method as in Example 35, and the yield was 74%. ¹ H NMR (500MHz, DMSO-d6) δ10.82(s, 1H), 8.02(d, J=8.1Hz, 1H), 7.90(d, J=8.4Hz, 2H), 7.74(d, J=8.6 Hz, 2H), 7.60(d, J=9.8Hz, 1H), 2.76(m, 1H), 1.15(d, J=7.0Hz, 5H).

Example 39: Synthesis of N-(4-trifluoromethylphenyl)-2-isobutyryloxy-3,5-difluorobenzamide (IIIB-7)

IIIB-7 was prepared according to the same method as in Example 35, except that compound IIIA-15 was used instead of IIIA-18, isobutyric anhydride was used instead of acetic anhydride, and the reaction time was 1 hour. The yield was 76%. ¹ H NMR (500MHz, DMSO-d6) δ10.88(s, 1H), 7.89(d, J=8.4Hz, 2H), 7.74(d, J=8.8Hz, 2H), 7.72–7.69(m, 1H ),7.56–7.51(m,1H),2.82(m,1H),1.15(d,J=7.0Hz,5H).

Example 40: Synthesis of N-(4-trifluoromethoxyphenyl)-2-isobutyryloxy-4-fluoro-5-chlorobenzamide (IIIB-8)

IIIB-8 was prepared according to the same method as in Example 36, except that compound IIIA-12 was used instead of IIIA-18, isobutyric anhydride was used instead of acetic anhydride, and the reaction time was 1 hour. The yield was 65%. ¹ H NMR (500MHz, DMSO-d6) δ10.64(s, 1H), 7.98(d, J=8.2Hz, 1H), 7.80–7.75(m, 2H), 7.58(d, J=9.8Hz, 1H ),7.37(d,J=8.6Hz,2H),2.75(m,1H),1.14(d,J=7.0Hz,5H).

Example 41: Synthesis of N-(4-trifluoromethylphenyl)-2-(L-alanine)oxy-4-fluoro-5-chlorobenzamide hydrochloride (IIIB-9)

Add IIIA-18 (150mg), N-triphenylmethyl-L-alanine (150mg), N,N-dimethylformamide (3mL) to the eggplant-shaped bottle in turn, stir at -10°C, add Cyclohexylcarbodiimide (94 mg) was maintained at this temperature for 1 hour, and then turned to room temperature for 6 hours. A white solid was precipitated during the period, filtered, the filtrate was extracted with ethyl acetate and water, the ethyl acetate layer was washed with saturated sodium chloride solution, dried, and eluted with petroleum ether and ethyl acetate (50:1) for column chromatography to obtain IIIB -9-1200mg, to be administered in the next step.

The IIIB-9-1 obtained in the previous step was dissolved in dichloromethane (1.5 mL), cooled on ice, added trifluoroacetic acid (0.3 mL), and stirred for 1 hour. The solvent was spin-dried, extracted with ethyl acetate and water, washed with saturated sodium chloride solution, dried, concentrated, and eluted with petroleum ether and ethyl acetate (2:1) to obtain the free state of IIIB-9. Methanol was added to the free compound, followed by 1.5 N methanolic hydrogen chloride solution, stirred for 15 minutes, concentrated, and then mixed with toluene and water (3 times) to obtain 70 mg of IIIB-9. ¹ H NMR (500MHz, DMSO-d6) δ12.73(s, 1H), 10.54(s, 1H), 9.09(d, J=6.6Hz, 1H), 8.26(d, J=8.6Hz, 1H), 7.82(d, J=8.5Hz, 2H), 7.69(d, J=8.6Hz, 2H), 7.01(d, J=10.8Hz, 1H), 4.65(p, J=7.0Hz, 1H), 1.47( d,J＝7.1Hz,3H).ESI-MS m/z 403.04(MH) ^- .

Example 42: Synthesis of N-(4-trifluoromethylphenyl)-2-(L-alanine)oxy-3,5-difluorobenzamide hydrochloride (IIIB-10)

Add IIIA-15 (143mg), N-triphenylmethyl-L-alanine (150mg), N,N-dimethylformamide (3mL) to the eggplant-shaped bottle in turn, stir at -10°C, add Cyclohexylcarbodiimide (94 mg) was maintained at this temperature for 1 hour, and then turned to room temperature for 6 hours. A white solid was precipitated during the period, filtered, the filtrate was extracted with ethyl acetate and water, the ethyl acetate layer was washed with saturated sodium chloride solution, dried, and eluted with petroleum ether and ethyl acetate (50:1) to obtain IIIB-10-1 195mg, to be administered in the next step.

The IIIB-10-1 obtained in the previous step was dissolved in dichloromethane (1.5 mL), cooled on ice, added trifluoroacetic acid (0.3 mL), and stirred for 1 hour. The solvent was spin-dried, extracted with ethyl acetate and water, washed with saturated sodium chloride solution, dried, concentrated, and eluted with petroleum ether and ethyl acetate (2:1) to obtain the free form of IIIB-10. Add methanol to the free compound, add 1.5 N methanolic hydrogen chloride solution, stir for 15 minutes, concentrate, and add water with toluene (3 times) to obtain 70 mg of IIIB-10. ¹ H NMR (500MHz, DMSO-d6) δ12.26(s, 1H), 10.55(s, 1H), 9.19(d, J=6.6Hz, 1H), 7.83(d, J=8.6Hz, 2H), 7.74(dt, J=10.0, 2.4Hz, 1H), 7.69(d, J=8.6Hz, 2H), 7.55(ddd, J=11.3, 8.4, 3.1Hz, 1H), 4.67(p, J=7.0Hz ,1H),1.48(d,J=7.1Hz,3H).ESI-MS m/z 387.04(MH) ^- .

Example 43: Synthesis of N-(4-trifluoromethoxyphenyl)-2-(L-alanine)oxy-4-fluoro-5-chlorobenzamide hydrochloride (IIIB-11)

Add IIIA-12 (136mg), N-triphenylmethyl-L-alanine (132mg), N,N-dimethylformamide (3mL) to the eggplant-shaped bottle in turn, stir at -10°C, add Cyclohexylcarbodiimide (83 mg) was maintained at this temperature for 1 hour, and then turned to room temperature for 6 hours. A white solid was precipitated during the period, filtered, the filtrate was extracted with ethyl acetate and water, the ethyl acetate layer was washed with saturated sodium chloride solution, dried, and eluted with petroleum ether and ethyl acetate (50:1) to obtain IIIB-11-1 170mg, to be administered in the next step.

The IIIB-11-1 obtained in the previous step was dissolved in dichloromethane (1.5 mL), cooled on ice, added trifluoroacetic acid (0.3 mL), and stirred for 1 hour. The solvent was spin-dried, extracted with ethyl acetate and water, washed with saturated sodium chloride solution, dried, concentrated, and eluted with petroleum ether and ethyl acetate (2:1) to obtain the free form of IIIB-11. Methanol was added to the free compound, followed by 1.5 N methanolic hydrogen chloride solution, stirred for 15 minutes, concentrated, and then mixed with toluene and water (3 times) to obtain 70 mg of IIIB-11. ¹ H NMR (500MHz, DMSO-d6) δ12.73(s, 1H), 10.36(s, 1H), 9.08(d, J=6.7Hz, 1H), 8.25(d, J=8.6Hz, 1H), 7.74–7.70(m,2H),7.33(d,J=8.7Hz,2H),7.00(d,J=10.8Hz,1H),4.63(p,J=7.0Hz,1H),1.45(d,J =7.0Hz,3H).ESI-MS m/z 419.02(MH) ^- .

Example 44: Synthesis of N-(4-trifluoromethylphenyl)-2-(L-alanine)oxy-4-fluoro-5-chlorobenzamide hydrochloride (IIIB-12)

Add IIIA-18 (166mg), N-tert-butoxycarbonyl-L-valine (108mg), N,N-dimethylformamide (3mL) to the eggplant-shaped flask in turn, stir at -10°C, add ring Hexylcarbodiimide (155 mg) was maintained at this temperature for 1 hour, and then turned to room temperature for 6 hours. A white solid was precipitated during the period, filtered, the filtrate was extracted with ethyl acetate and water, the ethyl acetate layer was washed with saturated sodium chloride solution, dried, and eluted with petroleum ether and ethyl acetate (50:1) to obtain IIIB-12-1 150mg, to be administered in the next step.

The IIIB-12-1 obtained in the previous step was dissolved in dichloromethane (1.5 mL), cooled on ice, added trifluoroacetic acid (0.3 mL), and stirred for 1 hour. The solvent was spin-dried, extracted with ethyl acetate and water, washed with saturated sodium chloride solution, dried, concentrated, and eluted with petroleum ether and ethyl acetate (2:1) to obtain the free form of IIIB-12. Add methanol to the free compound, add 1.5 N methanolic hydrogen chloride solution, stir for 15 minutes, concentrate, and add water with toluene (3 times) to obtain 30 mg of IIIB-12. ¹ H NMR (500MHz, DMSO-d6) δ12.60(s, 1H), 10.65(s, 1H), 8.93(d, J=8.1Hz, 1H), 8.23(d, J=8.7Hz, 1H), 7.85(d, J=8.5Hz, 2H), 7.78–7.68(m, 2H), 7.00(d, J=10.7Hz, 1H), 4.57(t, J=7.6Hz, 1H), 2.21(h, J =6.8Hz,1H),0.99(dd,J=6.7,1.5Hz,6H).ESI-MS m/z431.05(MH) ^- .

Example 45: Synthesis of N-(4-trifluoromethoxyphenyl)-2-(L-valine)oxy-4-fluoro-5-chlorobenzamide hydrochloride (IIIB-13)

Add IIIA-12 (170mg), N-tert-butoxycarbonyl-L-valine (105mg), N,N-dimethylformamide (3mL) to the eggplant-shaped flask in turn, stir at -10°C, add ring Hexylcarbodiimide (83 mg) was maintained at this temperature for 1 hour, and then turned to room temperature for 6 hours. A white solid was precipitated during the period, filtered, the filtrate was extracted with ethyl acetate and water, the ethyl acetate layer was washed with saturated sodium chloride solution, dried, and eluted with petroleum ether and ethyl acetate (50:1) to obtain IIIB-13-1 90mg, to be administered in the next step.

The IIIB-13-1 obtained in the previous step was dissolved in dichloromethane (1.5 mL), cooled on ice, added trifluoroacetic acid (0.3 mL), and stirred for 1 hour. The solvent was spin-dried, extracted with ethyl acetate and water, washed with saturated sodium chloride solution, dried, concentrated, and eluted with petroleum ether and ethyl acetate (2:1) to obtain the free state of IIIB-13. Methanol was added to the free compound, followed by 1.5 N methanolic hydrogen chloride solution, stirred for 15 minutes, concentrated, and then mixed with toluene and water (3 times) to obtain 45 mg of IIIB-13. ¹ H NMR (500MHz, DMSO-d6) δ12.63–12.60(m,1H),10.48(s,1H),8.93(d,J=8.2Hz,1H),8.23(d,J=8.7Hz,1H ),7.76–7.71(m,2H),7.35(d,J=8.6Hz,2H),6.99(d,J=10.7Hz,1H),4.54(t,J=7.7Hz,1H),2.20(h , J=6.6Hz, 1H), 0.98 (dd, J=6.8, 1.6Hz, 6H). ESI-MS m/z 447.08 (MH) ⁻ .

Example 46: (4-Chloro-5-fluoro-2-(((4-(trifluoromethoxy)phenyl)carbamoyl)phenoxy)methylisopropylcarbonate (IIIB-14) Synthesis

Add acetone (1 mL), chloromethyl isopropyl carbonate (61 mg) and sodium iodide (62 mg) to the reaction flask in sequence, and stir at 60° C. for 3 hours. Filter and wash the filter cake with a small amount of acetone.

Potassium carbonate (66mg), compound IIIA-12 (70mg), acetone (2mL), DMF (10 drops) were added successively to the reaction flask to aid in dissolution, and the filtrate obtained in the above steps was added under stirring, and the reaction was detected by TLC after stirring for 2 hours. Concentrate the reaction solution, add ethyl acetate and water to the concentrate, adjust the pH of the aqueous phase with saturated ammonium chloride solution, separate the liquids, wash the organic phase with saturated brine, dry, filter, concentrate, and the concentrate with petroleum ether (1.5mL ) and ethyl acetate (10 drops), and filtered to obtain compound IIIB-1470mg, and the NMR was correct. ¹ H NMR (500MHz, DMSO-d6) δ10.41(s, 1H), 7.85(d, J=8.4Hz, 1H), 7.83–7.77(m, 2H), 7.53(d, J=11.0Hz, 1H ), 7.38(d, J=8.7Hz, 2H), 5.88(s, 2H), 4.76(hept, J=6.2Hz, 1H), 1.20(d, J=6.2Hz, 6H).

Example 47: N-(4-Trifluoromethoxyphenyl)-2-(valinecarboxymethyleneoxy)-4-fluoro-5-chlorobenzamide hydrochloride (IIIB-15) Synthesis

Add acetone (3mL), (S)-2-((tert-butoxycarbonyl)amino)-3-methylbutanoic acid chloromethyl ester (397mg), sodium iodide (220mg) to the reaction flask in turn, 60°C Stir for 3 hours. Filter and wash the filter cake with a small amount of acetone.

Potassium carbonate (66 mg), compound IIIA-12 (349 mg), and acetone (10 mL) were sequentially added to the reaction flask, and the filtrate obtained in the above steps was added with stirring, and stirred for 12 hours. Concentrate the reaction solution, add ethyl acetate and water to the concentrate, adjust the pH of the aqueous phase with saturated ammonium chloride solution, wash the organic phase with saturated brine, dry, filter, concentrate, mix the sample, and mix with petroleum ether and ethyl acetate ( 2:1) was eluted to obtain 300 mg of compound IIIB-15-1.

Dissolve IIIB-15-1 in dichloromethane (6 mL), add trifluoroacetic acid (0.75 mL) under ice-cooling, after the addition is complete, stir at room temperature for 3 hours. Concentrate, extract with dichloromethane and water, adjust the pH of the aqueous layer to alkaline, wash with saturated sodium chloride solution, filter, and concentrate. Methanol was added to the concentrate, followed by 1.5 N methanolic hydrogen chloride solution, stirred for 15 minutes, concentrated, and then mixed with toluene and water (3 times) to obtain 180 mg of IIIB-15. NMR is correct. ¹ H NMR (500MHz,) δ10.49 (d, J = 3.6Hz, 1H), 8.49 (s, 2H), 7.88–7.79 (m, 3H), 7.56 (d, J = 11.0Hz, 1H), 7.37 (d,J=8.6Hz,2H),6.06(d,J=6.9Hz,1H),6.01(d,J=6.8Hz,1H),4.01(s,1H),2.13(dq,J=11.4, 6.9 Hz, 1H), 0.89 (t, J = 7.2 Hz, 6H). ESI-MS m/z 479.1 (M+H) ⁻ .

Example 48: N-(4-Trifluoromethoxyphenyl)-2-(4-methylpiperazinoyloxy)-4-fluoro-5-chlorobenzamide hydrochloride (IIIB-16) Synthesis

Add compound IIIA-12 (175 mg), 4-dimethylaminopyridine (18 mg), 4-methylpiperazine-1-formyl chloride hydrochloride (199 mg), and pyridine to the reaction flask in sequence, and reflux for 3 hours. After concentration, extract with ethyl acetate and water, wash the aqueous layer with saturated ammonium chloride, dry over anhydrous sodium sulfate, mix the sample, and elute with petroleum ether and ethyl acetate (1:1) to obtain the target compound IIIB-16 40mg . ¹ H NMR (500MHz, DMSO-d6) δ10.59(s, 1H), 7.91(d, J=8.2Hz, 1H), 7.80–7.74(m, 2H), 7.56(d, J=10.0Hz, 1H ), 7.38(d, J=8.6Hz, 2H), 3.50(s, 2H), 3.31(s, 2H), 2.14(s, 4H), 2.05(s, 3H). ESI-MS m/z 476.1( M+H) ^- .

Example 49: (4,6-Difluoro-2-(((4-(trifluoromethoxy)phenyl)carbamoyl)phenoxy)methylisopropylcarbonate (IIIB-17) synthesis

Add acetone (1 mL), chloromethyl isopropyl carbonate (61 mg) and sodium iodide (62 mg) to the reaction flask in sequence, and stir at 60° C. for 3 hours. Filter and wash the filter cake with a small amount of acetone.

Potassium carbonate (66mg), compound IIIA-15 (85mg), acetone (2mL), DMF (10 drops) were added successively to the reaction flask to aid in dissolution, and the filtrate obtained from the above steps was added under stirring, and the reaction was detected by TLC after stirring for 2 hours. Concentrate the reaction solution, add ethyl acetate and water to the concentrate, adjust the pH of the aqueous phase with saturated ammonium chloride solution, separate the liquids, wash the organic phase with saturated brine, dry, filter, concentrate, and the concentrate with petroleum ether (1.5mL ) and ethyl acetate (10 drops), and filtered to obtain 110 mg of compound IIIB-17. ¹ H NMR (500MHz, DMSO-d6) δ10.74(s, 1H), 7.90(d, J=8.4Hz, 2H), 7.74(d, J=8.5Hz, 2H), 7.64(ddd, J=11.3 ,8.5,3.1Hz,1H),7.40(dt,J=8.2,2.3Hz,1H),5.62(s,2H),4.61(hept,J=6.3Hz,1H),1.12(d,J=6.2Hz ,6H).

Example 50: 3-((((4-Chloro-5-fluoro-2-(4-(trifluoromethoxy)phenylcarbamoyl)phenoxy)methoxy)carbonyloxy)-N -methylpropane-1-ammonium chloride)

Acetone (3mL), 3-(N-methyl-N-tert-butoxycarbonyl) propyl chloromethyl carbonate (422mg, 1.5mmol), sodium iodide (300mg, 2mmol), 60 °C and stirred for 3 hours. Filter and wash the filter cake with a small amount of acetone.

Potassium carbonate (276 mg), compound IIIA-12 (349 mg), acetone (10 mL), DMF (10 drops) were sequentially added to the reaction flask, and the filtrate obtained in the above steps was added under stirring, and stirred for 12 hours. Concentrate the reaction solution, add ethyl acetate and water to the concentrate, adjust the pH of the aqueous phase with saturated ammonium chloride solution, wash the organic phase with saturated brine, dry, filter, concentrate, mix the sample, and mix with petroleum ether and ethyl acetate ( 2:1) was eluted to obtain 300 mg of compound IIIB-18-1.

Add IIIB-18-1 (300 mg) and 2M HCl (diluted from 4M HCl methanol solution with THF) solution to the reaction flask in turn, stir at room temperature for 16 hours, and TLC detects that the reaction of the raw materials is complete. After concentration, 200 mg of oily compound IIIB-18 was obtained by thin layer chromatography. ¹ H NMR (600MHz, DMSO-d6) δ10.56(s, 1H), 8.63(d, J=9.2Hz, 1H), 8.54(s, 2H), 8.46(d, J=2.7Hz, 1H), 8.31(dd, J=9.2,2.7Hz,1H),7.97(d,J=2.7Hz,1H),7.74(dd,J=8.9,2.8Hz,1H),7.47(d,J=8.9Hz,1H ),6.05(s,2H),4.19(t,J＝6.3Hz,2H),2.95(t,J＝6.8Hz,2H),2.57–2.54(m,3H),1.99–1.95(m,2H) .ESI-MS m/z 495.2 (M+H) ^- .

Pharmacological experiment:

Anti-new coronavirus (SRAS-CoV-2) activity test experiment

The experimental cells were seeded into 24-well cell culture plates at a cell density of 80,000 per well, and cultured overnight in a 5% CO ₂ , 37° C. incubator. The next day, compounds (1 μM or 10 μM, double wells) and SRAS-CoV-2 (infected according to MOI=0.01) were added. After cultured in an incubator for 1 day under the condition of 5% CO ₂ and 37° C., the supernatant was collected, and the copy number of virus RNA in the supernatant was detected. If the copy number of viral RNA in the supernatant of the well containing the compound is significantly lower than that of the group without the addition of the compound, it indicates that the compound has an inhibitory effect on the tested SRAS-CoV-2.

The anti-SRAS-CoV-2 activity of the compound is expressed by the inhibition rate (%) of the compound on the RNA copy number of the virus supernatant, see Table 1 and Table 2. The calculation formula is as follows: inhibition rate (%)=1-compound group virus RNA copy number/no compound group virus RNA copy number×100%

Table 1. Inhibition rate of RNA copy number of new coronavirus at 10 μM

test compound 10μM inhibition rate (%) IIIA-1 N/A IIIA-2 * IIIA-3 ＊＊＊＊ IIIA-4 ＊＊＊＊ IIIA-5 N/A IIIA-6 ＊＊＊＊ IIIA-7 ＊＊ IIIA-8 N/A IIIA-20 ＊＊＊＊ IIIA-21 * IIIA-22 ＊＊＊ IIIA-29 ＊＊＊

Table 2. Inhibition rate of SARS-CoV-2 RNA copy number at 1 μM

Description: N/A: No suppression; ＊: 1-25; ＊＊: 26-50; ＊＊＊: 51-75; ＊＊＊＊: 76-100

Anti-Rift Valley fever virus (RVFV) and febrile thrombocytopenia syndrome virus (SFTSV) activity test

Vero cells were seeded into 96-well cell culture plates at 1×10 ⁴ /well, and cultured overnight in a 5% CO ₂ , 37°C incubator. On the second day, different concentrations of compounds (see Table 1) were added, and 2 replicate wells were prepared for each concentration gradient. The same volume of DMSO was used as a negative control, and 10 μM Benidipine was used as a positive control. After compound pretreatment for 1 hour, RVFV-eGFP was added, SFTSV was infected (MOI=0.5), and culture was continued for 24 hours in a 5% CO ₂ , 37° C. incubator. Cells were fixed with 4% paraformaldehyde 24 hours after virus infection. After the RVFV-eGFP infection group was fixed, the cell nuclei were stained with DAPI dye (1:2000, at room temperature in the dark for 10 min), and the Operetta high-content drug screening system was used for detection. After the SFTSV infection group was fixed, incubate specific NP antibody (1:2000, 1h at room temperature or overnight at 4°C) and fluorescent secondary antibody (1:1000, 1h at room temperature in the dark) before using DAPI dye (1:2000, 10min at room temperature in the dark) ) to stain the nuclei, and finally, use the Operetta high-content drug screening system for detection. The nuclei were detected by channel 405. Compared with the DMSO group, the less number of nuclei stained by DAPI indicated that the compound was cytotoxic at this concentration. The virus signal was detected by channel 488. Compared with the DMSO group, the less number of detected cells indicated that the compound had an antiviral effect at this concentration.

The antiviral activity of the compound is represented by the inhibition rate (%) of the compound on virus replication, see Table 3 and Table 4. The calculation formula is as follows: inhibition rate (%)=(average reading value of DMSO group-average reading value of drug wells)/average reading value of DMSO group×100.

Table 3 Different concentrations of compounds on the inhibition rate of RVFV

test compound 1μM inhibition rate (%) 0.1μM inhibition rate (%) 0.01μM inhibition rate (%) IIIA-4 ＊＊＊＊ * * IIIA-9 ＊＊＊＊ * * IIIA-14 ＊＊＊＊ * * IIIA-18 ＊＊＊＊ * * Niclosamide ＊＊＊ * *

Description: N/A: No suppression; ＊: 1-25; ＊＊: 26-50; ＊＊＊: 51-75; ＊＊＊＊: 76-100

Table 4 Different concentrations of compounds have an inhibitory rate on SFTSV

test compound 1μM inhibition rate (%) 0.1μM inhibition rate (%) 0.01μM inhibition rate (%) IIIA-4 ＊＊＊ * * IIIA-9 ＊＊＊＊ * * IIIA-14 ＊＊＊ * * IIIA-18 ＊＊＊＊ * * IIIA-25 N/A N/A N/A IIIA-27 ＊＊ N/A N/A IIIA-12 ＊＊ N/A N/A IIIA-13 * N/A N/A IIIA-16 ＊＊ N/A N/A IIIA-17 ＊＊＊＊ * * IIIA-30 ＊＊＊＊ * * IIIA-31 * N/A N/A IIIA-32 ＊＊ N/A N/A IIIA-33 ＊＊＊ * N/A IIIB-1 * N/A N/A IIIB-3 ＊＊＊＊ * * IIIB-6 ＊＊＊＊ * * IIIB-7 * N/A N/A IIIB-4 * N/A N/A IIIB-8 ＊＊＊ * N/A IIIB-9 * N/A N/A IIIB-5 ＊＊＊ * N/A IIIB-10 * N/A N/A IIIB-11 * N/A N/A IIIB-12 * N/A N/A IIIB-13 * N/A N/A IIIB-14 * N/A N/A Niclosamide ＊＊＊ * *

Description: N/A: No suppression; ＊: 1-25; ＊＊: 26-50; ＊＊＊: 51-75; ＊＊＊＊: 76-100

Anti-dengue virus activity test experiment

The Vero cells were seeded into 6-well cell culture plates at a density of 600,000 cells per well, and cultured overnight in a 5% CO ₂ , 37° C. incubator. Compounds (1-5 concentration points, single point) and virus (40-50 PFU/well) were added the next day. The cells were cultured in an incubator at 5% CO2 and 37° C. for 2 hours, then the supernatant was aspirated, and the low-melting point agarose culture solution containing the corresponding concentration of the compound was added. The cells were cultured in an incubator at 5% CO2 at 33°C or 37°C for 6-7 days until obvious virus plaques could be observed in the virus-infected control wells without compounds under the microscope. Cells were fixed with 4% paraformaldehyde and stained with crystal violet (see Table 5). Count the number of plaques in each well.

Cytotoxicity experiments were performed in parallel with antiviral experiments. The Vero cells were seeded into 96-well cell culture plates at a density of 20,000 cells per well, and cultured overnight in a 5% CO ₂ , 37° C. incubator. Compounds were added the next day (1-5 concentration points, single point). The cells were cultured in an incubator for 6-7 days under the conditions of 5% CO2, 33°C or 37°C. Then CCK-8 was used to detect cell viability in each well.

The antiviral activity and cytotoxicity of the compound are represented by the compound's inhibition rate (%) and cell viability (%) on viral plaques respectively, and the inhibition rate is shown in Table 6. Calculated as follows:

Inhibition rate (%)=100-the number of plaques in test wells/the number of plaques in virus control wells×100

Cell viability (%) = (reading value of test well - average value of medium control) / (average value of cell control - average value of medium control) × 100

EC ₅₀ and CC ₅₀ values were calculated by Prism software (version 5), and the inhibition curve fitting method was "log(inhibitor) vs. response--Variable slope".

Table 5 Anti-dengue virus activity test processing method

Table 6 Anti-dengue virus activity test results

test compound 1μM inhibition rate (%) Niclosamide ＊＊＊ IIIA-4 ＊＊＊＊ IIIA-6 ＊＊＊＊ IIIA-10 ＊＊＊＊ IIIA-21 N/A

Description: N/A: No suppression; ＊: 1-25; ＊＊: 26-50; ＊＊＊: 51-75; ＊＊＊＊: 76-100

Inhibition of interleukin-6 secretion activity test experiment

The cells were seeded into 48-well cell culture plates at a density of 50,000 cells per well, and cultured overnight in a 5% CO ₂ , 37° C. incubator. The next day, first add the compound (1 concentration point, double wells), then add the cytokine interleukin-6 20 minutes later, keep it in a 5% CO ₂ , 37°C incubator for 8 hours, collect the cells and measure the report after 8 hours Gene. See Table 7 for the inhibition rate results.

Table 7 Inhibition of interleukin-6 secretion activity test results

test compound 1μM inhibition rate (%) Niclosamide ＊＊＊ IIIA-4 ＊＊ IIIA-3 ＊＊ IIIA-2 * IIIA-9 ＊＊＊ IIIA-24 * IIIA-15 * IIIA-26 * IIIA-18 ＊＊＊

Description: N/A: No suppression; ＊: 1-25; ＊＊: 26-50; ＊＊＊: 51-75; ＊＊＊＊: 76-100

Inhibition of interleukin-33 secretion activity test experiment

The test method is the same as the test for inhibiting interleukin-6 activity except that the cytokine interleukin-6 is changed to the cytokine interleukin-33. See Table 8 for the inhibition rate results.

Table 8 inhibits interleukin-33 secretion activity test result

test compound 1μM inhibition rate (%) 5μM inhibition rate (%) Niclosamide ＊＊ ＊＊＊ IIIA-4 ＊＊ ＊＊ IIIA-9 N/A N/A IIIA-15 ＊＊ ＊＊＊ IIIA-18 ＊＊＊＊ ＊＊＊＊ IIIA-14 * ＊＊ IIIA-12 ＊＊＊＊ ＊＊＊＊ IIIA-30 ＊＊＊＊ ＊＊＊ IIIA-31 N/A * IIIA-32 ＊＊＊ ＊＊＊＊

Description: N/A: No suppression; ＊: 1-25; ＊＊: 26-50; ＊＊＊: 51-75; ＊＊＊＊: 76-100

Inhibition of interleukin 1b secretion activity test experiment

The test method is the same as the test for inhibiting interleukin 6 activity except that the cytokine interleukin 6 is changed to cytokine interleukin 1b. See Table 9 for the inhibition rate results.

Table 9 inhibits interleukin 1b secretion activity test result

Description: N/A: No suppression; ＊: 1-25; ＊＊: 26-50; ＊＊＊: 51-75; ＊＊＊＊: 76-100

Inhibition of TNF-α activity test experiment

The test method is the same as the test for inhibiting interleukin 6 activity except that the cytokine interleukin 6 is changed to the cytokine interleukin TNF-α. See Table 10 for the inhibition rate results.

Table 10 inhibits TNF-α activity test result

test compound 1μM inhibition rate (%) 5μM inhibition rate (%) Niclosamide * ＊＊ IIIA-4 * ＊＊＊＊ IIIA-9 N/A N/A IIIA-15 ＊＊ ＊＊ IIIA-18 ＊＊＊ ＊＊＊＊ IIIA-14 ＊＊ ＊＊＊ IIIA-12 ＊＊＊＊ ＊＊＊＊ IIIA-30 ＊＊＊ ＊＊＊＊ IIIA-31 N/A N/A IIIA-32 ＊＊ ＊＊

Description: N/A: No suppression; ＊: 1-25; ＊＊: 26-50; ＊＊＊: 51-75; ＊＊＊＊: 76-100

As can be seen from the data in the above Tables 1-10, the compounds of the embodiments of the present application are superior to niclosamide in terms of anti-new coronavirus, Rift Valley fever virus and fever with thrombocytopenia syndrome virus activity, and can inhibit LPS The induced secretion of interleukin-6 shows that some of the compounds in the examples of this application have broad-spectrum antiviral and anti-inflammatory activities, and can be developed into antiviral drugs or anti-inflammatory disease drugs.

Claims (10)

1. A amide compound represented by the following general formula I, its prodrug, pharmaceutically acceptable salt, complex or solvate:

in, Y is a benzene ring, a 5-6-membered heteroaryl ring, a 5-6-membered heteroaryl ring with a benzene ring, or a 5-6-membered heteroaryl ring and a 5-6-membered heteroaryl ring; Z is O or S; A ₁ is C-OR ₁₁ , C-SR ₁₁ , C-NHR ₁₁ , N or CR ₁₂ ; R ₁₁ is hydrogen atom, C1～C20 alkyl, C1～C20 alkylcarbonyl, C1～C20 alkylaminocarbonyl, C1～C20 alkylcarbonyloxy C1～C20 alkyl,

C1～C20 alkylphosphoryl, C1～C20 alkylsulfonyl, C1～C20 alkyl substituted 6-20 heterocyclic carbonyl containing 1-3 heteroatoms selected from O, N or S or

The above-mentioned C1-C20 alkyl group is optionally selected from hydroxyl, -NH ₂ , C1-C20 alkylamino, cyano, carboxyl, halogen,

One or more substitutions in C1-C10 alkylsulfonyl, C1-C10 alkyl phosphoryl, C1-C10 acyl; _R7 is C1～C10 alkyl, C1～C10 alkylamino, C1～C10 alkyl or C3～C10 cycloalkyl; R ₈ is hydrogen atom, halogen or C1～C10 alkyl; R ₁₂ is a hydrogen atom, halogen, cyano, nitro or C1-C20 alkyl; A ₂ , A ₃ , A ₄ , A ₅ are each independently N or CR ₂ ; R ₂ are the same or different from each other, and are independently selected from hydrogen, hydroxyl, halogen, C1-C6 alkyloxy, C1-C6 alkyl, amino (-NH ₂ ), nitro, cyano, carboxyl, aldehyde , C1～C6 alkylcarbonyl, C1～C6 alkylsulfonyl, C1～C6 alkylsulfonylamino and C1～C6 alkyloxycarbonyl, the above hydroxyl, amino, carboxyl, C1～C6 alkyl are optionally One or more substitutions in hydroxyl, amino, cyano, carboxyl, halogen, C1-C10 alkylsulfonyl, C1-C10 alkylphosphoryl, C1-C10 alkylcarbonyl; R ₃ is a hydrogen atom or a C1-C6 alkyl group; R ₄ to R ₆ are each independently selected from hydrogen atom, hydroxyl, amino, halogen, nitro, cyano, C1～C6 alkyl, C1～C6 alkyloxy and C1～C6 alkylthio, the above C1～C6 C6 alkyl is optionally substituted by one or more of hydroxyl, amino, cyano, carboxyl, halogen, C1-C6 alkylsulfonyl, C1-C6 alkylphosphoryl, C1-C6 alkylacyl. 2. amides compound according to claim 1, its prodrug, pharmaceutically acceptable salt, complex or solvate, wherein, Y is a benzene ring, a pyridine ring or a thiazole ring; R ₁₁ is hydrogen atom, C1～C10 alkyl, C1～C10 alkylcarbonyl, C1～C10 alkylcarbonyl, C1～C10 alkylaminocarbonyloxy C1～C10 alkyl, C1～C10 alkyl substituted 6- 10-membered heterocyclylcarbonyl containing 1-3 heteroatoms selected from O, N or S or

The above-mentioned C1～C10 alkyl groups are optionally selected from hydroxyl, amino, cyano, carboxyl, halogen,

One or more substitutions in C1-C10 alkylsulfonyl, C1-C10 alkylphosphoryl, C1-C10 alkylcarbonyl; R ₇ is C1～C6 alkyl, C1～C6 alkylamino C1～C6 alkyl or C3～C7 cycloalkyl; R ₈ is hydrogen atom, halogen or C1～C2 alkyl; R ₁₂ is a hydrogen atom, halogen, cyano, nitro or C1-C6 alkyl; R2 are the same or different from each other, and each independently selected from _hydrogen , hydroxyl, halogen, C1～C4 alkyloxy, C1～C4 alkyl, amino, nitro, cyano and C1～C4 alkylcarbonyl, the above C1 ~C4 alkyl is optionally substituted by one or more of hydroxyl, amino, cyano, carboxyl, halogen, C1-C4 alkylsulfonyl, C1-C4 alkylphosphoryl, C1-C4 alkylcarbonyl; R ₃ is a hydrogen atom or a C1-C4 alkyl group; R ₄ to R ₆ are each independently selected from a hydrogen atom, hydroxyl, amino, halogen, nitro, cyano, C1～C4 alkyl and C1～C4 alkyloxy, and the above C1～C4 alkyl is optionally replaced by hydroxyl , amino, cyano, carboxyl, halogen in one or more substitutions. 3. amides compound according to claim 2, its prodrug, pharmaceutically acceptable salt, complex or solvate, wherein, R ₁₁ is hydrogen atom, C1～C6 alkyl, halogenated C1～C6 alkyl, amino C1～C6 alkyl, hydroxyl, C1～C6 alkyl, C1～C6 alkylcarbonyl, C1～C6 alkylaminocarbonyl, C1～C6 alkylcarbonyloxy C1～C6 alkyl, C1～C6 alkylamino C1～C6 alkylcarbonyl, amino C1～C6 alkylcarbonyl,

Substituted C1～C6 alkylcarbonyl, C1～C6 alkyl substituted 6-8 membered heterocyclic carbonyl containing 1-3 heteroatoms selected from O, N or S or

R ₇ is C1～C4 alkyl, C1～C3 alkylamino C1～C4 alkyl or C3～C6 cycloalkyl; R ₈ is a hydrogen atom or a methyl group; R ₁₂ is a hydrogen atom, halogen, cyano or C1-C4 alkyl; At most two of A ₂ , A ₃ , A ₄ and A ₅ are N; R2 are the same or different from each other, and are independently selected from _hydrogen , hydroxyl, halogen, C1-C2 alkoxy, C1-C2 alkyl, C1-C2 alkylcarbonyl, halogenated C1-C2 alkoxy, halogenated C1～C2 alkyl, halogenated C1～C2 alkylcarbonyl, amino and nitro; R ₃ is a hydrogen atom; R ₄ to R ₆ are each independently selected from a hydrogen atom, halogen, C1-C4 alkyl, halogenated C1-C4 alkyl, C1-C4 alkoxy, and halogenated C1-C4 alkoxy. 4. amides compound according to claim 3, its prodrug, pharmaceutically acceptable salt, complex or solvate, wherein, R ₁₁ is hydrogen atom, C1～C4 alkyl, C1～C6 alkylcarbonyl, C1～C5 alkylaminocarbonyl, C1～C5 alkylcarbonyloxy C1～C5 alkyl,

Substituted C1～C4 alkyl, substituted C1～C4 alkylcarbonyl,

or

5. The amide compound according to claim 1, its prodrug, pharmaceutically acceptable salt, complex or solvate, wherein, the amide compound represented by the general formula I is the following general formula II , IIIA or IIIB compound:

Wherein, A ₁ is C-OR ₁₁ , C-SR ₁₁ , C-NHR ₁₁ or CR ₁₂ ; The definitions of R ₁₁ , R ₁₂ , R ₂ , R ₄ to R ₆ and Y are the same as those in claim 1 . 6. amide compound according to claim 1, its prodrug, pharmaceutically acceptable salt, complex or solvate, wherein, the amide compound represented by the general formula I is the following general formula IV Compounds shown:

Wherein, the definitions of R ₁₁ , R ₂ , R ₄ and R ₅ are the same as those in claim 1. 7. The amide compound, its prodrug, pharmaceutically acceptable salt, complex or solvate according to claim 1, wherein the compound or salt is selected from the following structures:

8. A pharmaceutical composition comprising a therapeutically effective amount of a compound selected from any one of claims 1 to 7, its prodrugs, pharmaceutically acceptable salts, complexes and solvates One or more, and optional pharmaceutically acceptable carrier. 9. The compound according to any one of claims 1 to 7, its prodrug, pharmaceutically acceptable salt, complex and solvate or the pharmaceutical composition described in claim 8 in the preparation of antiviral drugs Or use in medicines for the treatment of anti-inflammatory diseases. 10. The use according to claim 9, wherein the virus is at least one selected from DNA viruses and RNA viruses; In particular, the DNA virus is selected from hepatitis B virus, human papillomavirus, herpes virus, and phage virus; the RNA virus is selected from influenza virus, avian influenza virus, Zika virus, dengue virus, respiratory syncytial virus, SARS virus, MERS virus, novel coronavirus (SARS-CoV-2), bunya virus, HIV, Ebola virus, hepatitis C virus, Japanese encephalitis virus, rhinovirus, poliovirus, Ke Saatchi virus, rotavirus, tobacco mosaic virus, bacteriophage virus, Marburg virus, enterovirus, Particularly, the RNA virus is at least one of coronavirus, bunya virus, dengue virus; In particular, the coronavirus is SARS-CoV-2; the bunya virus is Rift Valley fever virus; More particularly, said virus is dengue virus; The inflammatory diseases are inflammatory skin diseases, inflammatory bowel diseases, inflammatory joint diseases and other autoimmune diseases.