IP Library Granted Patent US 6,956,035
Granted Patent B2
US 6,956,035 · App. 10/376,746 · Granted Oct 18, 2005

Isoquinoline derivatives and methods of use thereof

Assignee: Inotek Pharmaceuticals Corporation
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 6,956,035
App. No.
10/376,746
Granted
Oct 18, 2005
Kind
B2
Abstract

The invention provides novel classes of Isoquinoline Derivatives. Pharmaceutical compositions and methods of making and using the compounds, are also described.

Claims (47)

1. A method for making a compound of formula 13

wherein

R 1 , R 2 , R 3 , R 4 , R 7 , R 8 , R 9 and R 10 are independently -hydrogen, -halo, -hydroxy, —O—(C 1 -C 5 alkyl), C 1 -C 10 alkyl, -alkylhalo, —C 2 -C 10 alkenyl, —C 3 -C 8 carbocycle, -aryl, —NH 2 , -alkylamino, —C(O)OH, —C(O)O(C 1 -C 5 alkyl), —OC(O)(C 1 -C 5 alkyl), NO 2 or -A-B;

A is —SO 2 —, —SO 2 NH—, —NHCO—, —NHCONH—, —O—, —CO—, —OC(O)—, —C(O)O—, —CONH—, —CON(C 1 -C 4 alkyl)-, —NH—, —CH 2 —, —S— or —C(S)—;

B is —C 1 -C 10 alkyl, —C 2 -C 10 alkenyl, -heterocycle, —C 3 -C 5 carbocycle, -aryl, —NZ 1 Z 2 —(C 1 -C 5 alkylene)—NZ 1 Z 2 , -alkylamino, -aminodialkyl, -alkylheterocycle, -arylamido, —C(O)OH, —C(O)O—(C 1 -C 5 alkyl), —C(O)O-phenyl or —C(NH)NH 2 , any of which are unsubstituted or substituted with one or more of —O—(C 1 -C 5 alkyl), -halo, -alkylhalo, -alkanol, -alkylamino, -hydroxy, —NO 2 , —NH 2 , —CN, -aminoalkyl, -aminodialkyl, -heterocyclic amine, —C 1 -C 10 alkyl, —C 2 -C 10 alkenyl, —C 2 -C 10 alkynyl, -aryl, -benzyl, -alkylamido, -alkylcarboxy, —C(O)OH, —C 1 -C 5 alkylene-C(O)O—(C 1 -C 5 alkyl) or —C 1 -C 5 alkylene-OC(O)—(C 1 -C 5 alkyl); and

Z 1 and Z 2 are independently —H or —C 1 -C 10 alkyl, which is unsubstituted or substituted with one or more of -halo, —OH or —N(Z 3 )(Z 4 ), where Z 3 and Z 4 are independently, —H or —C 1 -C 5 alkyl, which is unsubstituted or substituted with one or more of -halo, -hydroxy or —NH 2 ; or N, Z 3 and Z 4 are taken together to form an unsubstituted or substituted heterocyclic amine; or N, Z 1 and Z 2 are taken together to form a heterocyclic amine,

comprising contacting a compound of formula 11a

with a compound of formula 12

wherein R b is —Cl, —Br, —I, —OMs, —OTs or —OTf,

in the presence of a base, for a time and at a temperature sufficient to make the compound of formula 13.

2. A compound of the formula

or a pharmaceutically acceptable hydrate or salt thereof,

wherein

R 1 , R 2 , R 3 , R 4 , R 7 , R 8 and R 10 are independently -hydrogen, -halo, -hydroxy, —O—(C 1 -C 5 alkyl), —C 1 -C 10 alkyl, -alkylhalo, —C 2 -C 10 alkenyl, —C 3 -C 8 carbocycle, -aryl, —NH 2 , -alkylamino, —C(O)OH, —C(O)O(C 1 -C 5 alkyl), —OC(O)(C 1 -C 5 alkyl), —NO 2 or -A-B;

R 9 is —SO 2 —B or —SO 2 NH—B;

A is —SO 2 —, —SO 2 NH—, —NHCO—, —NHCONH—, —O—, —CO—, —OC(O)—, —C(O)O—, —CONH—, —CON(C 1 -C 4 alkyl)-, —NH—, —CH 2 —, —S— or —C(S)—;

B is —C 1 -C 10 alkyl, —C 2 -C 10 alkenyl, -heterocycle, —C 3 -C 8 carbocycle, -aryl, —NZ 1 Z 2 , —(C 1 -C 5 alkylene)—NZ 1 Z 2 , -alkylamino, -aminodialkyl, -alkylheterocycle, -arylamido, —C(O)OH, —C(O)O—(C 1 -C 5 alkyl), —C(O)O-phenyl or —C(NH)NH 2 , any of which are unsubstituted or substituted with one or more of —O—(C 1 -C 5 alkyl), -halo, -alkylhalo, -alkanol, -alkylamino, -hydroxy, —NO 2 , —NH 2 , —CN, -aminoalkyl, -aminodialkyl, -heterocyclic amine, —C 1 -C 10 alkyl, —C 2 -C 10 alkenyl, —C 2 -C 10 alkynyl, -aryl, -benzyl, -alkylamido, -alkylcarboxy, —C(O)OH, —C 1 -C 5 alkylene-C(O)O—C 1 -C 5 alkyl or —C 1 -C 5 alkylene-OC(O)—C 1 -C 5 alkyl; and

Z 1 and Z 2 are independently —H or —C 1 -C 10 alkyl, which is unsubstituted or substituted with one or more of -halo, —OH or —N(Z 3 )(Z 4 ), where Z 3 and Z 4 are independently, —H or —C 1 -C 5 alkyl, which is unsubstituted or substituted with one or more of-halo, -hydroxy or —NH 2 ; or N, Z 3 and Z 4 are taken together to form an unsubstituted or substituted heterocyclic amine; or N, Z 1 and Z 2 are taken together to form a heterocyclic amine.

3. A method for treating Parkinson's disease, the method comprising administering to a subject in need thereof a compound or a pharmaceutically acceptable hydrate or salt of a compound of claim 2 in amount sufficient to treat Parkinson's disease.

4. A method for treating an inflammatory disease, the method comprising administering to a subject in need thereof a compound or a pharmaceutically acceptable hydrate or salt of the compound of claim 2 in an amount sufficient to treat the inflammatory disease, wherein the inflammatory disease is an inflammatory disease of a joint, a chronic inflammatory disease of the gum, an inflammatory bowel disease, an inflammatory lung disease, an inflammatory disease of the central nervous system, or an inflammatory disease of the eye.

5. A method for treating a reperfusion disease, the method comprising administering to a subject in need thereof a compound or a pharmaceutically acceptable hydrate or salt of the compound of claim 2 in an amount sufficient to treat the reperfusion disease, wherein the reperfusion disease is myocardial infarction or stroke.

6. A method for treating diabetes, the method comprising administering to a subject in need thereof a compound or a pharmaceutically acceptable hydrate or salt of the compound of claim 2 in an amount sufficient to treat the diabetes.

7. A method for treating reoxygenation injury resulting from organ transplantation, the method comprising administering to a subject in need thereof a compound or a pharmaceutically acceptable hydrate or salt of the compound of claim 2 in an amount sufficient to treat the reoxygenation injury resulting from organ transplantation.

8. A composition comprising an effective amount of a compound or pharmaceutically acceptable salt or hydrate of the compound of claim 2 and a pharmaceutically acceptable carrier.

9. A compound of claim 2 having the formula:

or pharmaceutically acceptable salt thereof,

wherein:

R is —NHCH 2 CH 2 CN, —NHCH(NH)NH 2 , —NH[4-(1,2,4-triazole)], —NH[4-(N-morpholino)phenyl], —NHCH 2 CH 2 (4-N-benzylpiperidine), —NHCH 2 CH 2 (2-thienyl), —NH[1-(4-azabenzimidazole)], —NH[1-(4-(2′-pyridyl)piperazine)], —NHCH 2 CH 2 N(CH 2 CH 2 OH) 2 , —NH[1-(4-benzylpiperazine)], —NH 2 , —NHCH 2 CH 2 -phenyl, —NHCH 2 CH 2 (4-methoxyphenyl), —NHC(O)(N-morpholine), —NHCH((CH 2 ) 4 NH 2 )COOH, —NHCH(CH 2 COOH)COOH, —NH(CH 2 ) n COOH, —NHCH(CH 2 CH 2 COOH)COOH, or —NHCH(CH 2 OH)COOH; and

n is an integer ranging from 1 to 5.

10. A method for treating Parkinson's disease, the method comprising administering to a subject in need thereof the compound having the formula

or a pharmaceutically acceptable hydrate or salt thereof in an amount sufficient to treat Parkinson's disease.

11. A method for treating an inflammatory disease, the method comprising administering to a subject in need thereof the compound having the formula

or a pharmaceutically acceptable hydrate or salt thereof in an amount sufficient to treat an inflammatory disease, wherein the inflammatory disease is an inflammatory disease of a joint, a chronic inflammatory disease of the gum, an inflammatory bowel disease, an inflammatory lung disease, an inflammatory disease of the central nervous system, or an inflammatory disease of the eye.

12. A method for treating a reperfusion disease, the method comprising administering to a subject in need thereof the compound having the formula

or a pharmaceutically acceptable hydrate or salt thereof in an amount sufficient to treat a reperfusion disease, wherein the reperfusion disease is myocardial infarction or stroke.

13. A method for treating diabetes, the method comprising administering to a subject in need thereof the compound having the formula

or a pharmaceutically acceptable hydrate or salt thereof in an amount sufficient to treat diabetes.

14. A method for treating a reoxygenation injury resulting from organ transplantation, the method comprising administering to a subject in need thereof the compound having the formula

or a pharmaceutically acceptable hydrate or salt thereof in an amount sufficient to treat a reoxygenation injury resulting from organ transplantation.

15. The pharmaceutically acceptable salt of the compound of claim 2 , wherein the salt is a mesylate salt.

16. A mesylate salt of the compound having the formula:

17. A method for treating Parkinson's disease, the method comprising administering to a subject in need thereof the mesylate salt of claim 16 in an amount sufficient to treat Parkinson's disease.

18. A method for treating an inflammatory disease, the method comprising administering to a subject in need thereof the mesylate salt of claim 16 in an amount sufficient to treat the inflammatory disease, wherein the inflammatory disease is an inflammatory disease of a joint, a chronic inflammatory disease of the gum, an inflammatory bowel disease, an inflammatory lung disease, an inflammatory disease of the central nervous system, or an inflammatory disease of the eye.

19. A method for treating a reperfusion disease, the method comprising administering to a subject in need thereof the mesylate salt of claim 16 in an amount sufficient to treat the reperfusion disease, wherein the reperfusion disease is myocardial infarction or stroke.

20. A method for treating diabetes, the method comprising administering to a subject in need thereof the mesylate salt of claim 16 in an amount sufficient to treat the diabetes.

21. A method for treating reoxygenation injury resulting from organ transplantation, the method comprising administering to a subject in need thereof the mesylate salt of claim 16 in an amount sufficient to treat the reoxygenation injury resulting from organ transplantation.

22. A composition comprising an effective amount of the mesylate salt of claim 16 and a pharmaceutically acceptable carrier.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Oct 8, 2003
From: JAGTAP, PRAKASH; BALOGLU, ERKAN; VAN DUZER, JOHN H.; SZABO, CSABA; SALZMAN, ANDREW L.; ROY, ALOKA,; WILLIAMS, WILLIAM; NIVOROKSHKIN, ALEXANDER
To: INOTEK PHARMACEUTICALS CORPORATION
Reel/Frame 014582/0396 →
Continuity (3)
Continuation In Part 1023319800 · Aug 30, 2002
Continuation In Part 0994452400 · Aug 31, 2001
Related Publication 20040039009A1 · Feb 26, 2004