IP Library › Granted Patent US 8,022,076

Granted Patent B2

US 8,022,076 · App. 10/864,771 · Granted Sep 20, 2011

Substituted thieno[2,3-d]pyrimidines as potassium channel inhibitors

Assignee: Xention Limited

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Patent No.: US 8,022,076
App. No.: 10/864,771
Granted: Sep 20, 2011
Kind: B2

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Abstract

This invention relates to novel compound of formula (I) or pharmaceutically acceptable salts thereof. The invention is also directed to the uses of compounds having formula (I) in the treatment or prevention of diseases or disorders which requires potassium channel inhibition to an animal, mammal or human in need thereof. The invention is also directed to the use of compounds having formula (I) in the treatment or prevention of arrhythmia to an animal, mammal or human in need thereof.

Claims (132)

1. A compound of formula (I)

wherein

R2 is H; alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10; nitro; CO 2 R7; CONR4R5 or halo;

R3 is H; NR4R5; NHC(O)R8; halo; trifluoromethyl; alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10; cyano or alkoxy;

R4 and R5 may be the same or different, and may be H; alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10; aryl, which is unsubstituted or substituted at any position with one, two, three, or four substituents selected from the group consisting of cyano, halogen, nitro, trifluoromethyl, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; heteroaryl, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; or cycloalkyl; or R4 and R5 may together form a saturated, unsaturated or partially saturated 4 to 7 member ring, wherein said ring may optionally comprise one or more further heteroatoms selected from N, O or S;

X is O, S or NR6;

R6 is H or alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10;

R7 is hydrogen, methyl or ethyl;

R8 is methyl or ethyl;

R9 and R10 are independently selected from the group consisting of hydrogen, unsubstituted alkyl, unsubstituted aryl, unsubstituted heteroaryl, unsubstituted cycloalkyl, aminoethyl, methylaminoethyl, hydroxyethyl, and alkoxyethyl; or

R9 and R10 taken together form a saturated, unsaturated, or partially saturated 4 to 7 membered ring;

L is (CH 2 ) n , where n is 1, 2 or 3; and

Y is heterocyclic group, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; alkenyl or cycloalkyl;

or a pharmaceutically acceptable salt thereof;

with the proviso that when Y is furanyl; tetrahydrofuranyl; pyrimidinyl; pyrrolidinyl or 1,3-benzodioxolyl, then R1 is not phenyl, phenyl monosubstituted by halogen or phenyl substituted by methyl; and wherein the compound is not:

5-Phenyl-N-(pyridin-2-ylmethyl)thieno[2,3-d]pyrimidin-4-amine;

5-(4-Chlorophenyl)-N-[3-(1H-imidazol-1-yl)propyl]thieno[2,3-d]pyrimidin-4-amine;

5-(4-Chlorophenyl)-N-(pyridin-2-ylmethyl)thieno[2,3-d]pyrimidin-4-amine;

5-(4-Chlorophenyl)-N-(pyridin-3-ylmethyl)thieno[2,3-d]pyrimidin-4-amine;

5-(4-Fluorophenyl)-N-(pyridin-3-ylmethyl)thieno[2,3-d]pyrimidin-4-amine;

N-Allyl-5-phenylthieno[2,3-d]pyrimidin-4-amine;

5-(4-Methylphenyl)-N-(2-thien-2-ylethyl)thieno[2,3-d]pyrimidin-4-amine;

5-(4-Chlorophenyl)-N-(2-thien-2-ylethyl)thieno[2,3-d]pyrimidin-4-amine;

5-(4-Fluorophenyl)-N-(2-thien-2-ylethyl)thieno[2,3-d]pyrimidin-4-amine;

N-Allyl-5-(4-chlorophenyl)thieno[2,3-d]pyrimidin-4-amine;

5-(4-Bromophenyl)-N-(pyridin-3-ylmethyl)thieno[2,3-d]pyrimidin-4-amine;

N-[3-(1H-Imidazol-1-yl)propyl]-5-phenylthieno[2,3-d]pyrimidin-4-amine; or

1-(2-{[5-(4-Methylphenyl)thieno[2,3-d]pyrimidin-4-yl]amino}ethyl)imidazolidin-2-one.

2. A compound as claimed in claim 1 wherein R1 is aryl, which is unsubstituted or substituted at any position with one, two, three, or four substituents selected from the group consisting of cyano, halogen, nitro, trifluoromethyl, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; or heteroaryl, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; R2 is H or alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10; R3 is H; NR4R5; alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10; or alkoxy X is O or NR6, R6 is H, n is 1 or 2 and Y is cycloalkyl, or heteroaryl, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl.

3. A compound as claimed in claim 2 wherein X is NR6, n is 1 and Y is heteroaryl, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl.

4. A compound as claimed in any one of claims 1 to 3 wherein Y is furanyl, thienyl or pyridyl.

5. A compound as claimed in any one of claims 1 to 3 wherein Y is optionally substituted furan-2-yl or optionally substituted pyridin-2-yl.

6. A compound which is:

2-{5-Phenyl-4-[(pyridin-2-ylmethyl)-amino]-thieno[2,3-d]pyrimidin-2-yl}-propane-1,3-diol;

2-{5-(4-Fluorophenyl)-4-[(pyridin-2-ylmethyl)-amino]thieno[2,3-d]pyrimidin-2-ylamino}-ethanol;

Pyridin-2-ylmethyl-(5-p-tolyl-thieno[2,3-d]pyrimidin-4-yl)-amine;

2-{5-Phenyl-4-[(pyridin-2-ylmethyl)-amino]-thieno[2,3-d]pyrimidin-2-ylamino}-ethanol;

2-{5-Phenyl-4-[(pyridin-2-ylmethyl)amino]thieno[2,3-d]pyrimidin-2-yl}ethanol;

2-((2-Hydroxy-ethyl)-{5-phenyl-4-[(pyridin-2-ylmethyl)-amino]-thieno[2,3-d]pyrimidin-2-yl}-amino)-ethanol;

2-Methyl-N-(2-pyridyl)methyl-5-phenylthieno[2,3-d]pyrimidin-4-ylamine;

2-{4-[(Furan-2-ylmethyl)-amino]-5-phenyl-thieno[2,3-d]pyrimidin-2-yl}-ethanol;

[2-(2-Methoxy-ethoxy)-5-phenyl-thieno[2,3-d]pyrimidin-4-yl]-pyridin-2-ylmethylamine;

(2-Methoxy-5-phenyl-thieno[2,3-d]pyrimidin-4-yl)-pyridin-2-ylmethyl-amine;

5-(4-Fluorophenyl)-N 2 -(2-methoxy-ethyl)-N 4 -pyridin-2-ylmethyl-thieno[2,3-d]pyrimidine-2,4-diamine;

[5-(4-Dimethylamino-phenyl)-thieno[2,3-d]pyrimidin-4-yl]-pyridin-2-ylmethyl-amine;

5-(4-Fluorophenyl)-N 2 ,N 2 -dimethyl-N 4 -pyridin-2-ylmethyl-thieno[2,3-d]pyrimidine-2,4-diamine;

Pyridin-2-ylmethyl-[5-(4-trifluoromethyl-phenyl)-thieno[2,3-d]pyrimidin-4-yl]-amine;

[5-(1H-Indol-6-yl)-thieno[2,3-d]pyrimidin-4-yl]-pyridin-2-ylmethyl-amine;

(5-Benzo[1,3]dioxol-5-yl-thieno[2,3-d]pyrimidin-4-yl)-pyridin-2-ylmethyl-amine;

2-{5-Phenyl-4-[(pyridin-2-ylmethyl)-amino]-thieno[2,3-d]pyrimidin-2-ylamino}-propane-1,3-diol;

3-{5-Phenyl-4-[(pyridin-2-ylmethyl)-amino]-thieno[2,3-d]pyrimidin-2-ylamino}-propane-1,2-diol;

N-Methyl-2-{5-phenyl-4-[(pyridin-2-ylmethyl)amino]thieno[2,3-d]pyrimidin-2-yl}acetamide; or

6-Methyl-N-[(6-methylpyridin-2-yl)methyl]-5-phenylthieno[2,3-d]pyrimidin-4-amine;

or a pharmaceutically acceptable salt thereof.

7. A process for preparing a compound as claimed in claim 1 comprising:

(i) reacting a compound of formula II with a suitable nucleophile X-L-Y, optionally in the presence of a solvent and a base, and optionally at elevated temperature or with microwave irradiation; or

(ii) reacting a compound of formula X by displacement of the 2-chloro substituent with a suitable nucleophilic species; or

(iii) reacting a compound of formula XVII with an aryl or heteroaryl boronic acid, optionally in the presence of a palladium catalyst, and optionally at elevated temperature or with microwave irradiation

wherein R1, R2, R3, X, L and Y are as defined in claim 1 .

8. A pharmaceutical composition comprising at least one compound and one or more excipients, diluents or carriers, wherein said compound has the formula

wherein

X is O, S or NR6;

R7 is hydrogen, methyl or ethyl;

R8 is methyl or ethyl;

R9 and R10 taken together form a saturated, unsaturated, or partially saturated 4 to 7 membered ring;

L is (CH2) n , where n is 1, 2 or 3; and

or a pharmaceutically acceptable salt thereof;

with the proviso that when Y is furanyl; tetrahydrofuranyl; pyrimidinyl;

pyrrolidinyl or 1,3-benzodioxolyl, then R1 is not phenyl, phenyl monosubstituted by halogen or phenyl substituted by methyl.

9. A method of treating or preventing arrhythmia or atrial fibrillation, comprising administering to a subject in need thereof an effective amount of at least one compound or a pharmaceutical composition comprising said at least one compound and one or more excipients, diluents or carriers wherein said compound has the formula:

wherein

R1 is aryl, which is unsubstituted or substituted at any position with one, two, three, or four substituents selected from the group consisting of cyano, halogen, nitro, trifluoromethyl, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; heteroaryl, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; cycloalkyl or alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10;

X is O, S or NR6;

R7 is hydrogen, methyl or ethyl;

R8 is methyl or ethyl;

R9 and R10 taken together form a saturated, unsaturated, or partially saturated 4 to 7 membered ring;

L is (CH 2 ) n , where n is 1, 2 or 3; and

Y is aryl, which is unsubstituted or substituted at any position with one, two, three, or four substituents selected from the group consisting of cyano, halogen, nitro, trifluoromethyl, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; heterocyclic group, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10; alkenyl or cycloalkyl;

or a pharmaceutically acceptable salt thereof.

10. A process as claimed in claim 7 , wherein R1 is aryl, which is unsubstituted or substituted at any position with one, two, three, or four substituents selected from the group consisting of cyano, halogen, nitro, trifluoromethyl, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; or heteroaryl, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; R2 is H or alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10; R3 is H; NR4R5; alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10; or alkoxy X is O or NR6, R6 is H, n is 1 or 2 and Y is cycloalkyl; or heteroaryl, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl.

11. A process as claimed in claim 7 , wherein R1 is aryl, which is unsubstituted or substituted at any position with one, two, three, or four substituents selected from the group consisting of cyano, halogen, nitro, trifluoromethyl, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; or heteroaryl, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; R2 is H or methyl, R3 is H; NR4R5; alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10; or alkoxy X is NR6, R6 is H, n is 1 and Y is heteroaryl, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl.

12. A process as claimed in claim 11 , wherein Y is furanyl, thienyl or pyridyl.

13. A process as claimed in claim 11 , wherein Y is optionally substituted furan-2-yl or optionally substituted pyridin-2-yl.

14. A method as claimed in claim 9 , wherein R1 is aryl, which is unsubstituted or substituted at any position with one, two, three, or four substituents selected from the group consisting of cyano, halogen, nitro, trifluoromethyl, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; or heteroaryl, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; R2 is H or alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10 R3 is H; NR4R5; alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10; or alkoxy X is O or NR6, R6 is H, n is 1 or 2, and Y is cycloalkyl, or heteroaryl, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl.

15. A method as claimed in claim 9 , wherein R1 is aryl, which is unsubstituted or substituted at any position with one, two, three, or four substituents selected from the group consisting of cyano, halogen, nitro, trifluoromethyl, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; or heteroaryl, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl; R2 is H or methyl, R3 is H; NR4R5; alkyl, which is unsubstituted or substituted at any position with one or two substituents selected from the group consisting of halogen, cyano, nitro, NR9R10, alkoxy, hydroxyl, unsubstituted aryl, unsubstituted heteroaryl, CO 2 R7, C(O)NR9R10, NHC(O)R8, and SO 2 NR9R10; or alkoxy X is NR6, R6 is H, n is 1 and Y is heteroaryl, which is unsubstituted or substituted at any position with a substituent selected from the group consisting of cyano, nitro, halogen, alkyl, alkylthio, alkoxy, NR9R10, CO 2 R7, C(O)NR9R10, NHC(O)R8, SO 2 NR9R10, and hydroxyl.

16. A method as claimed in claim 15 , wherein Y is furanyl, thienyl or pyridyl.

17. A method as claimed in claim 15 , wherein Y is optionally substituted furan-2-yl or optionally substituted pyridin-2-yl.

18. A method of treating or preventing arrhythmia or atrial fibrillation, comprising administering to a subject in need thereof an effective amount of at least one compound or a pharmaceutical composition comprising said at least one compound and one or more excipients, diluents or carriers wherein said compound is:

2-{5-Phenyl-4-[(pyridin-2-ylmethyl)-amino]-thieno[2,3-d]pyrimidin-2-yl}-propane-1,3-diol;

2-{5-(4-Fluorophenyl)-4-[(pyridin-2-ylmethyl)-amino]-thieno[2,3-d]pyrimidin-2-ylamino}-ethanol;