IP Library Granted Patent US 9,550,741
Granted Patent B2
US 9,550,741 · App. 14/889,831 · Granted Jan 24, 2017

Benzoisothiazole compounds and methods of treating schizophrenia

Inventors: Jianqi Li (Shanghai, CN); Xiaowen Chen (Shanghai, CN); Zhilong Ma (Shanghai, CN); Li Zhang (Shanghai, CN); Ning Cui (Shanghai, CN)
Assignee: Shanghai Institute of Pharmaceutical Industry
C07D275/04C07D417/12
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Quick Facts
Patent No.
US 9,550,741
App. No.
14/889,831
Granted
Jan 24, 2017
Kind
B2
Abstract

Disclosed are benzoisothiazole compounds and a use in the preparation of anti-schizophrenia drugs. The benzoisothiazole compounds of the present invention not only have strong affinity for dopamine D 3 receptor, 5-HT 1A receptor and 5-HT 2A receptor, but also can observably improve the symptoms of schizophrenia relevant to apomorphine model and MK-801 model mice, with oral absorption being good, safety being high and side-effect being less, and having developmental value as new anti-neurotic disease drugs. The present invention is the compounds having a structure of general formula (I), or geometric isomers, free alkalies, salts, hydrates or solvates thereof.

Claims (106)

1. The benzoisothiazole compound, characterized in that it is the compound having the structure of general formula (I) or the geometric isomers, free alkalies, salts, hydrates or solvates thereof:

wherein:

W is:

R 1 and R 2 independently represent heteroaryl or substituted heteroaryl;

n is 0, 1, 2 or 3; m is 0, 1 or 2;

R 3 represents C 1 -C 4 alkyl, substituted C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, substituted C 3 -C 6 cycloalkyl, phenyl, substituted phenyl, benzyl, substituted benzyl, heteroaryl, substituted heteroaryl, heteroarylmethyl, or substituted heteroarylmethyl;

R 4 is hydrogen atom or C 1 -C 4 alkyl;

R 5 is phenyl, substituted phenyl, heteroaryl or substituted heteroaryl;

the heteroaryl represented by R 1 and R 2 is selected from furyl, pyrrolyl, thienyl, benzofuryl, indolyl or benzothienyl;

the substituent of the substituted heteroaryl represented by R 1 and R 2 is selected from halogen, cyano, C 1 -C 2 alkyl carbonyl, nitro, methoxyl or C 1 -C 4 alkyl;

the C 1 -C 4 alkyl represented by R 3 can be substituted by 1-3 fluorine atom(s);

the substituent of the substituted cycloalkyl represented by R 3 is selected from C 1 -C 2 alkyl;

the substituent of the substituted phenyl, substituted benzyl, substituted heteroaryl or substituted heteroarylmethyl represented by R 3 is selected from halogen, C 1 -C 2 alkoxy, nitro or C 1 -C 2 alkyl;

the heteroaryl represented by R 3 is selected from furyl, thienyl, pyridyl or benzofuryl;

the heteroarylmethyl represented by R 3 is selected from furylmethyl, thenyl, picolyl, benzofurylmethyl or benzothenyl;

the substituent of the substituted heteroaryl represented by R3 is selected from halogen, C1-C2 alkoxy, nitro or C1-C2 alkyl-substituted furyl, thienyl, pyridyl or benzofuryl;

the substituent of the substituted heteroarylmethyl represented by R3 is selected from halogen, C1-C2 alkoxy, nitro or C1-C2 alkyl-substituted furylmethyl, thenyl, picolyl, benzofurylmethyl or benzothenyl;

the heteroaryl represented by R 5 is selected from furyl, pyrrolyl, thienyl, pyridyl, benzofuryl, benzothienyl or indolyl; and

the substituent of the substituted phenyl or substituted heteroaryl represented by R 5 is selected from halogen, C 1 -C 2 alkoxy, nitro or C 1 -C 2 alkyl.

2. The benzoisothiazole compound according to claim 1 , characterized in that the hydrate is a hydrate containing 0.5-3 molecules of crystal water wherein the salt comprises a pharmaceutically acceptable anion.

3. The benzoisothiazole compound according to claim 2 , characterized in that the salt further contains 0.5-6 molecules of crystal water.

4. A benzoisothiazole compound, characterized in that the compound is:

I-1 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)furyl-2-carboxamide,

I-2 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)thienyl-2-carboxamide,

I-3 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-1H-pyrrolyl-2-carboxamide,

I-4 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-1H-indolyl-2-carboxamide,

I-5 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)benzofuryl-2-carboxamide,

I-6 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)benzo[b]thienyl-2-carboxamide,

I-7 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-cyano-furyl-2-carboxamide,

I-8 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-tert-butylfuryl-2-carboxamide,

I-9 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-methyl-1 H-pyrrolyl-2-carboxamide,

I-10 trans 5-acetyl-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl) ethyl)cyclohexyl)furyl-2-carboxamide,

I-11 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-methylthienyl-2-carboxamide,

I-12 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-bromothienyl-2-carboxamide,

I-13 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-methylbenzo[b]thienyl-2-carboxamide,

I-14 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-chlorobenzo[b]thienyl-2-carboxamide,

I-15 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-nitro-1H-indolyl-2-carboxamide,

I-16 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-methoxylbenzofuryl-2-carboxamide,

I-17 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-2-(thien-2-yl)acetamide,

I-18 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-2-(benzofuran-3-yl)acetamide,

I-19 cis-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)furyl-2-carboxamide,

I-20 cis-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)thienyl-2-carboxamide,

I-21 cis-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-1H-pyrrolyl-2-carboxamide,

I-22 cis-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-1H-indolyl-2-carboxamide,

I-23 cis-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)benzofuryl-2-carboxamide,

I-24 cis-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)benzo[b]thienyl-2-carboxamide,

II-1 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)thienyl-2-sulfamide,

II-2 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-1H-pyrrolyl-3-sulfamide,

II-3 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)furyl-2-sulfamide,

II-4 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)benzo[b]thienyl-2-sulfamide,

II-5 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)benzofuryl-2-sulfamide,

II-6 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-1H-indolyl-3-sulfamide,

II-7 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-cyanofuryl-2-sulfamide,

II-8 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-chlorofuryl-2-sulfamide,

II-9 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-methylfuryl-2-sulfamide,

II-10 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-tert-butylthienyl-2-sulfamide,

II-11 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-chlorobenzo[b]thienyl-2-sulfamide,

II-12 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-cyanobenzo[b]thienyl-2-sulfamide,

II-13 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-methylbenzo[b]thienyl-2-sulfamide,

II-14 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-nitrobenzo[b]thienyl-2-sulfamide,

II-15 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-methoxylbenzofuryl-2-sulfamide,

II-16 cis-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)thienyl-2-sulfamide,

II-17 cis-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-1H-pyrrolyl-3-sulfamide,

II-18 cis-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)furyl-2-sulfamide,

II-19 cis-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)benzo[b]thienyl-2-sulfamide,

II-20 cis-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)benzofuryl-2-sulfamide,

II-21 cis-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-1H-indolyl-3-sulfamide,

II-22 cis-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-5-methylfuryl-2-sulfamide,

III-1 trans-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)methylcarbamate,

III-2 trans-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)ethylcarbamate,

III-3 trans-N-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)isobutylcarbamate,

III-4 trans-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)cyclopropylcarbamate,

III-5 trans-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)cyclohexylcarbamate,

III-6 trans-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)phenylcarbamate,

III-7 trans-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-methoxylphenylcarbamate,

III-8 trans-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-2-methylphenylcarbamate,

III-9 trans-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-4-chlorophenylcarbamate,

III-10 trans-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-4-nitrophenylcarbamate,

III-11 trans-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)benzylcarbamate,

III-12 trans-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)benzofuryl-2-methylcarbamate,

III-13 trans-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)thienyl-2-methylcarbamate,

III-14 cis-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)methylcarbamate,

III-15 cis-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)ethylcarbamate,

III-16 cis-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)benzylcarbamate,

IV-1 trans-1-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-phenylurea,

IV-2 trans-1-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-phenylethylurea,

IV-3 trans-1-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-(pyridin-3-yl)urea,

IV-4 trans-1-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-(furan-2-yl)urea,

IV-5 trans-1-(benzo[b]thien-2-yl)-3-(4-(2-(4-(benzo[d]isothiazol-3-yl) piperazin-1-yl)ethyl)cyclohexyl)urea,

IV-6 trans-3-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-1-methyl-1-phenylurea,

IV-7 trans-3-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-1-butyl-1-phenylurea,

IV-8 trans-3-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-1-methyl-1-(thien-2-yl)urea,

IV-9 trans-1-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-(3-methoxylphenyl)urea,

IV-10 trans-1-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-(3-nitrophenyl)urea,

IV-11 trans-1-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-benzylurea,

IV-12 cis-1-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-phenylurea,

IV-13 cis-1-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-benzylurea, or

IV-14 cis-1-(4-(2-(4-(benzo[d]isothiazol-3-yl)piperazin-1-yl)ethyl) cyclohexyl)-3-(furan-2-yl)urea, or a geometric isomer, free alkali, salt, hydrate or solvate thereof.

5. A composition for treating schizophrenia, characterized in that the composition comprises a therapeutically effective amount of an benzoisothiazole compound according to claim 1 or one or more of the geometric isomers, free alkalies, salts, hydrates or solvates thereof and a pharmaceutically acceptable carrier.

6. A method for treating schizophrenia, which comprises administering a therapeutically effective amount of a benzoisothiazole of claim 1 to a patient in need thereof.

7. A method for treating schizophrenia, which comprises administering a therapeutically effective amount of the composition of claim 5 to a patient in need thereof.

8. An anti-schizophrenia composition comprising a benzoisothiazole compound of claim j and a pharmaceutically acceptable carrier.

9. A composition for treating schizophrenia, wherein the composition comprises a therapeutically effective amount of one of the benzoisothiazole compounds according to claim 4 , or a geometric isomer, free alkali, salt, hydrate or solvate thereof, and a pharmaceutically acceptable carrier.

10. A method for treating schizophrenia, which comprises administering a therapeutically effective amount of a benzoisothiazole compound of claim 4 to a patient in need thereof.

11. A method for treating schizophrenia, which comprises administering a therapeutically effective amount of the composition of claim 9 to a patient in need thereof.

12. An anti-schizophrenia composition comprising a benzoisothiazole compound of claim 4 and a pharmaceutically acceptable carrier.

Assignments (3)
CHANGE OF NAME Recorded Sep 11, 2024
From: SHANGHAI INSTITUTE OF PHARMACEUTICAL INDUSTRY
To: SHANGHAI INSTITUTE OF PHARMACEUTICAL INDUSTRY CO., LTD.
Reel/Frame 068933/0725 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 11, 2024
From: SHANGHAI INSTITUTE OF PHARMACEUTICAL INDUSTRY CO., LTD.
To: SHANGHAI ZHONGZE THERAPEUTICS CO., LTD.
Reel/Frame 068933/0766 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 9, 2015
From: LI, JIANQI; CHEN, XIAOWEN; MA, ZHILONG; ZHANG, LI; CUI, NING
To: SHANGHAI INSTITUTE OF PHARMACEUTICAL INDUSTRY
Reel/Frame 037245/0367 →
Priority Claims (1)
CN 2013 1 0166896 · May 8, 2013 · national
Continuity (1)
Related Publication 20160096811A1 · Apr 7, 2016