IP Library › Granted Patent US 7,511,038
Granted Patent B2
US 7,511,038 · App. 10/578,594 · Granted Mar 31, 2009

Pyridazin-3(2H)-one derivatives and their use as PDE4 inhibitors

Assignee: Laboratorios Almirall S.A.
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Quick Facts
Patent No.
US 7,511,038
App. No.
10/578,594
Granted
Mar 31, 2009
Kind
B2
Abstract

New pyridazin-e-(2H)-one derivatives having the chemical structure of general formula (I) are disclosed; as well as processes for their preparation, pharmaceutical compositions comprising them and their use in therapy as inhibitors of phosphodiesterase 4.

Claims (230)

1. A pyridazinone derivative of formula (I)

wherein

R 1 represents:

a hydrogen atom;

a group chosen from acyl, alkoxycarbonyl, carbamoyl, monoalkylcarbamoyl and dialkylcarbamoyl;

an alkyl, alkenyl or alkynyl group, wherein the alkyl, alkenyl or alkynyl group is optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, alkoxy, aryloxy, alkylthio, arylthio, oxo, amino, mono- and di-alkylamino, acylamino, hydroxycarbonyl, alkoxycarbonyl, carbamoyl and mono- and di-alkylcarbamoyl groups;

an aryl or heteroaryl group, wherein the aryl or heteroaryl group is optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, hydroxyalkyl, hydroxycarbonyl, alkoxy, alkylenedioxy, alkoxycarbonyl, aryloxy, acyl, acyloxy, alkylthio, arylthio, amino, nitro, cyano, mono- and di-alkylamino, acylamino, carbamoyl, mono- and di-alkylcarbamoyl, difluoromethyl, trifluoromethyl, difluoromethoxy, and trifluoromethoxy groups;

a saturated or unsaturated heterocyclic group, wherein the saturated or unsaturated heterocyclic group is optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, hydroxyalkyl, hydroxycarbonyl, alkoxy, alkylenedioxy, alkoxycarbonyl, aryloxy, acyl, acyloxy, alkylthio, arylthio, oxo, amino, nitro, cyano, mono- and di-alkylamino, acylamino, carbamoyl, mono- and di-alkylcarbamoyl, difluoromethyl, trifluoromethyl, difluoromethoxy, and trifluoromethoxy groups; or

a group of formula

—(CH 2 ) n —R 6

wherein n is an integer from 0 to 4 and R 6 represents:

a cycloalkyl or cycloalkenyl group;

an aryl group, which is optionally substituted by one or more substituents chosen from halogen atoms, alkyl, hydroxy, alkoxy, alkylenedioxy, alkylthio, amino, mono- and di-alkylamino, nitro, acyl, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, mono- and di-alkylcarbamoyl, cyano, trifluoromethyl, difluoromethoxy, and trifluoromethoxy groups;

or a 3- to 7-membered ring comprising from 1 to 4 heteroatoms chosen from nitrogen, oxygen and sulphur, which ring is optionally substituted by one or more substituents chosen from halogen atoms, alkyl, hydroxy, alkoxy, alkylenedioxy, amino, mono- and di-alkylamino, nitro, cyano and trifluoromethyl groups;

R 2 represents:

a hydrogen atom;

a group chosen from acyl, alkoxycarbonyl, carbamoyl, monoalkylcarbamoyl and dialkylcarbamoyl;

an alkyl, alkenyl or alkynyl group, wherein the alkyl, alkenyl or alkynyl group is optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, alkoxy, hydroxycarbonyl, alkoxycarbonyl, aryloxy, alkylthio, arylthio, oxo, amino, mono- and di-alkylamino, acylamino, carbamoyl, and mono- and di-alkylcarbamoyl groups;

an aryl or heteroaryl group, wherein the aryl or heteroaryl group is optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, hydroxyalkyl, hydroxycarbonyl, alkoxy, alkylenedioxy, alkoxycarbonyl, aryloxy, acyl, acyloxy, alkylthio, arylthio, amino, nitro, cyano, mono- and di-alkylamino, acylamino, carbamoyl, mono- and di-alkylcarbamoyl, difluoromethyl, trifluoromethyl, difluoromethoxy, and trifluoromethoxy groups;

a saturated or unsaturated heterocyclic group, wherein the saturated or unsaturated heterocyclic group is optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, hydroxyalkyl, hydroxycarbonyl, alkoxy, alkylenedioxy, alkoxycarbonyl, aryloxy, acyl, acyloxy, alkylthio, arylthio, oxo, amino, nitro, cyano, mono- and di-alkylamino, acylamino, carbamoyl, mono- and di-alkylcarbamoyl, difluoromethyl, trifluoromethyl, difluoromethoxy and trifluoromethoxy groups; or

a group of formula

—(CH 2 ) n —R 6

wherein n is an integer from 0 to 4 and R 6 represents:

a cycloalkyl or cycloalkenyl group;

an aryl group, which is optionally substituted by one or more substituents chosen from halogen atoms and alkyl, hydroxy, alkoxy, alkylenedioxy, alkylthio, amino, mono- and di-alkylamino, nitro, acyl, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, mono- and di-alkylcarbamoyl, cyano, trifluoromethyl, difluoromethoxy, and trifluoromethoxy groups;

or a 3- to 7-membered ring comprising from 1 to 4 heteroatoms chosen from nitrogen, oxygen and sulphur, which ring is optionally substituted by one or more substituents chosen from halogen atoms, alkyl, hydroxy, alkoxy, alkylenedioxy, amino, mono- and di-alkylamino, nitro, cyano, and trifluoromethyl groups;

R 3 represents a monocyclic or polycyclic aryl or a monocyclic or polycyclic heteroaryl group, wherein the monocyclic or polycyclic aryl or the monocyclic or polycyclic heteroaryl group are optionally substituted by one or more substituents chosen from:

halogen atoms;

alkyl and alkylene groups, wherein the alkyl and alkylene groups are optionally substituted by one or more substituents chosen from halogen atoms, phenyl, hydroxy, alkoxy, aryloxy, alkylthio, arylthio, oxo, amino, mono- and di-alkylamino, acylamino, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, and mono- and di-alkylcarbamoyl groups; and

phenyl, hydroxy, hydroxyalkyl, alkoxy, cycloalkoxy, nitro, cyano, aryloxy, alkylthio, arylthio, alkylsulfinyl, alkylsulfonyl, alkylsulfamoyl, acyl, amino, mono- and di-alkylamino, acylamino, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, mono- and di-alkylcarbamoyl, ureido, N′-alkylureido, N′, N′-dialkylureido, alkylsulfamido, aminosulfonyl, mono- and di-alkylaminosulfonyl, difluoromethoxy, and trifluoromethoxy groups;

R 4 represents:

a hydrogen atom;

a hydroxy, alkoxy, amino, monoalkylamino, dialkylamino or cyano group;

an alkyl, alkenyl or alkynyl group, wherein the alkyl, alkenyl or alkynyl group is optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, acyloxy, alkoxy, aryloxy, alkylthio, arylthio, amino, mono- and di-alkylamino, acylamino, hydroxycarbonyl, alkoxycarbonyl, alkoxyimino, carbamoyl, and mono- and di-alkylcarbamoyl groups;

or a group of formula

—(CH 2 ) n —R 6

wherein n is an integer from 0 to 4 and R 6 represents:

a cycloalkyl or cycloalkenyl group;

an aryl group, which is optionally substituted by one or more substituents chosen from halogen atoms, alkyl, hydroxy, alkoxy, alkylenedioxy, alkylthio, amino, mono- and di-alkylamino, nitro, acyl, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, mono- and di-alkylcarbamoyl, cyano, trifluoromethyl, difluoromethoxy, and trifluoromethoxy groups;

or a 3- to 7-membered ring comprising from 1 to 4 heteroatoms chosen from nitrogen, oxygen and sulphur, which ring is optionally substituted by one or more substituents chosen from halogen atoms, alkyl, phenyl, alkoxyphenyl, halophenyl, pyridyl, alkoxycarbonyl, hydroxy, alkoxy, alkylenedioxy, amino, mono- and di-alkylamino, nitro, cyano, and trifluoromethyl groups;

R 5 represents a group —COOR 7 or a monocyclic or polycyclic aryl or a monocyclic or polycyclic heteroaryl group, wherein the monocyclic or polycyclic aryl or the monocyclic or polycyclic heteroaryl group are optionally substituted by one or more substituents chosen from:

halogen atoms;

alkyl and alkenyl groups, wherein the alkyl and alkenyl groups are optionally substituted by one or more substituents chosen from halogen atoms, phenyl, hydroxy, hydroxyalkyl, alkoxy, aryloxy, alkylthio, arylthio, oxo, amino, mono- and di-alkylamino, acylamino, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, mono- and di-alkylcarbamoyl groups; and

phenyl, hydroxy, alkylenedioxy, alkoxy, cycloalkyloxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylsulfamoyl, amino, mono- and di-alkylamino, acylamino, nitro, acyl, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, mono- and di-alkylcarbamoyl, ureido, N′-alkylureido, N′,N′-dialkylureido, alkylsulfamido, aminosulfonyl, mono- and di-alkylaminosulfonyl, cyano, difluoromethoxy, and trifluoromethoxy groups;

wherein R 7 represents

an alkyl, which is optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, alkoxy, aryloxy, alkylthio, arylthio, oxo, amino, mono- and di-alkylamino, acylamino, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, and mono- and di-alkylcarbamoyl groups,

or a group of formula

—(CH 2 ) n —R 6

wherein n is an integer from 0 to 4 and R 6 represents:

a cycloalkyl or cycloalkenyl group;

an aryl group, which is optionally substituted by one or mote substituents chosen from halogen atoms, alkyl, hydroxy, alkoxy, alkylenedioxy, alkylthio, amino, mono- and di-alkylamino, nitro, acyl, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, mono- and di-alkylcarbamoyl, cyano, trifluoromethyl, difluoromethoxy, and trifluoromethoxy groups;

or a 3- to 7-membered ring comprising from 1 to 4 heteroatoms chosen from nitrogen, oxygen and sulphur, which ring is optionally substituted by one or more substituents chosen from halogen atoms, alkyl, phenyl, alkoxyphenyl, halophenyl, pyridyl, alkoxycarbonyl, hydroxy, alkoxy, alkylenedioxy, amino, mono- and di-alkylamino, nitro, cyano, and trifluoromethyl groups;

or a salt thereof, or a N-oxide thereof

with the proviso that when R 1 is methyl, R 2 is H, and both R 3 and R 5 are phenyl then R 4 is not a 1-hydroxyethyl group.

2. A compound according to claim 1 , wherein R 1 is chosen from hydrogen atoms and alkyl groups, wherein the alkyl groups are optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, alkoxy, alkylthio, hydroxycarbonyl and alkoxycarbonyl groups.

3. A compound according to claim 2 wherein R 1 is chosen from unsubstituted C 1-4 alkyl groups.

4. A compound according to claim 1 , wherein R 2 is chosen from:

hydrogen atoms,

an acyl group,

an alkyl group, which is optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, alkoxy, and alkylthio groups; and

aryl and heteroaryl groups, wherein the aryl and heteroaryl groups are optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, hydroxyalkyl, hydroxycarbonyl, alkoxy, alkylenedioxy, alkoxycarbonyl, aryloxy, acyl, acyloxy, alkylthio, arylthio, amino, nitro, cyano, mono- and di-alkylamino, acyiamino, carbamoyl, mono- and di-alkylcarbamoyl, difluoromethyl, trifluoromethyl, difluoromethoxy, and trifluoromethoxy groups.

5. A compound according to claim 4 wherein R 2 is a hydrogen atom.

6. A compound according to claim 1 , wherein R 3 represents a monocyclic or polycyclic aryl or a monocyctic or polycyclic heteroaryl group, wherein the monocyclic or polycyclic, aryl or the monocyclic or polycyclic heteroaryl group are optionally substituted by one or more substituents chosen from:

halogen atoms;

alkyl and alkylene groups, wherein the alkyl and alkylene groups are optionally substituted by one or more substituents chosen from halogen atoms, phenyl, hydroxy, alkoxy, aryloxy, alkylthio, arylthio, oxo, amino, mono- or di-alkylamino, acylamino, hydroxycarbonyl, alkoxycarbonyl, carbamoyl and mono- and di-alkylcarbamoyl groups; and

phenyl, hydroxy, hydroxyalkyl, alkoxycarbonyl, alkoxy, cycloalkoxy, nitro, cyano, aryloxy, alkylthio, arylthio, alkylsuifinyl, alkylsulfonyl, alkylsulfamoyl, acyl, amino, mono- and di-alkylamino, acylamino, hydroxycarbonyl, carbamoyl, mono- and di-alkylcarbamoyl, ureido, N′-alkylureido, N′,N′-dialkylureido, alkylsulfamido, aminosulfonyl, mono- and di-alkylaminosulfonyl, difluoromethoxy, and trifluoromethoxy groups.

7. A compound according to claim 6 , wherein R 3 represents a monocyclic or polycyclic aryl or a monocyclic or polycyclic heteroaryl group, wherein the monocyclic or polycyclic, aryl or the monocyclic or polycyclic heteroaryl group are optionally substituted by one substituent chosen from halogen atoms, alkyl groups and hydroxycarbonyl groups.

8. A compound according to claim 7 , wherein R 3 represents a phenyl group or a monocyclic or polycyclic N-containing heteroaryl group, wherein the phenyl group or the monocyclic or polycyclic N-containing heteroaryl group may be substituted by one substituent chosen from halogen atoms, alkyl groups and hydroxycarbonyl groups.

9. A compound according to claim 1 , wherein R 4 represents:

a hydrogen atom;

a cyano group;

an alkyl, alkenyl or alkynyl group, wherein the alkyl, alkenyl or alkynyl group is optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, acyloxy, alkoxy, aryloxy, alkylthio, arylthio, amino, mono- and di-alkylamino, acylamino, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, and mono- and di-alkylcarbamoyl groups;

or a group of formula

—(CH 2 ) n —R 6

wherein n is an integer from 0 to 4 and R 6 represents a 3- to 7-membered ring comprising from 1 to 4 heteroatoms chosen from nitrogen, oxygen and sulphur, which ring is optionally substituted by one or more substituents chosen from halogen atoms, alkyl, phenyl, alkoxyphenyl, halophenyl, pyridyl, alkoxycarbonyl, hydroxy, alkoxy, alkylenedioxy, amino, mono- and di-alkylamino, nitro, cyano, and trifluoromethyl groups.

10. A compound according to claim 9 wherein R 4 represents a hydrogen atom or a cyano group.

11. A compound according to claim 1 , wherein R 5 represents a group —COOR 7 , a monocyclic or polycyclic aryl or a monocyclic or polycyclic heteroaryl group, wherein the monocyclic or polycyclic aryl or the monocyclic or polycyclic heteroaryl group are optionally substituted by one or more substituents chosen from:

halogen atoms;

alkyl groups, which are optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, hydroxyalkyl, alkoxy, alkylthio, mono- or di-alkylamino, acylamino, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, and mono- and di-alkylcarbamoyl groups; and

hydroxy, alkylenedioxy, alkoxy, cycloalkyloxy, alkylthio, alkylsulfinyl, alkylsulfonyl, alkylsulfamoyl, amino, mono- and di-alkylamino, acylamino, nitro, acyl, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, mono- and di-alkylcarbamoyl, ureido, N′-alkylureido, N′,N′-dialkylureido, alkylsulfamido, aminosuphonyl, mono- and di-alkylaminosulfonyl, cyano, difluoromethoxy, and trifluoromethoxy groups;

wherein R 7 represents

an alkyl group, which is optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, alkoxy, aryloxy, alkylthio, arylthio, oxo, amino, mono- and di-alkylamino, acylamino, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, and mono- and di-alkylcarbamoyl groups

or a group of formula

—(CH 2 ) n —R 6

wherein n Is an integer from 0 to 4 and R 6 represents:

a cycloalkyl or cycloalkenyl group;

an aryl group, which is optionally substituted by one or more substituents chosen from halogen atoms, alkyl, hydroxy, alkoxy, alkylenedioxy, alkylthio, amino, mono- and di-alkylamino, nitro, acyl, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, mono- and di-alkylcarbamoyl, cyano, trifluorornethyl, difluoromethoxy, and trifluoromethoxy groups;

or a 3- to 7-membered ring comprising from 1 to 4 heteroatoms chosen from nitrogen, oxygen and sulphur, which ring is optionally substituted by one or more substituents chosen from halogen atoms, alkyl, phenyl, hydroxy, alkoxy, alkylenedioxy, amino, mono- and di-alkylamino, nitro, cyano, and trifluoromethyl groups.

12. A compound according to claim 11 , wherein R 5 represents a monocyclic aryl or heteroaryl group, wherein the monocyclic aryl or heteroaryl group is optionally substituted by one or more substituents chosen from halogen atoms and alkyl groups.

13. A compound according to claim 1 , wherein R 1 is chosen from hydrogen atoms and alkyl groups, which are optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, alkoxy, alkylthio, arylthio, hydroxycarbonyl and alkoxycarbonyl groups; and

R 2 is chosen from:

hydrogen atoms,

an acyl group

an alkyl group, which is optionally substituted by one or more substituents chosen from halogen atoms, hydroxy, alkoxy and alkylthio groups; and

aryl and heteroaryl groups, wherein the aryl and heteroaryl groups are optionally substituted by one or more halogen atoms.

14. A compound according to claim 13 , wherein R 1 is chosen from unsubstituted C 1-4 alkyl groups and R 2 is a hydrogen atom.

15. A compound according to claim 14 , wherein R 3 represents a monocyclic or polycyclic aryl or a monocyclic or polycyclic heteroaryl group, wherein the monocyclic or polycyclic aryl or the monocyclic or polycyclic heteroaryl group are optionally substituted by one or more substituents chosen from:

halogen atoms;

alkyl groups, which are optionally substituted by one or more substituents chosen from halogen atoms and hydroxy groups; and

cyano, and hydroxycarbonyl groups.

16. A compound according to claim 15 , wherein R 3 represents a phenyl group or a monocyclic or polycyclic N-containing heteroaryl group, wherein the phenyl group or the monocyclic or polycyclic N-containing heteroaryl group may be substituted by one substituent chosen from halogen atoms, alkyl groups and hydroxycarbonyl groups.

17. A compound according to claim 13 , wherein R 4 represents:

a hydrogen atom;

a cyano group;

an alkyl, alkenyl or alkynyl group, wherein the alkyl, alkenyl or alkynyl group is optionally substituted by one or more substituents chosen from halogen atoms, hydroxyl and alkoxy groups;

or a group of formula

—(CH 2 ) n —R 6

wherein n is 0 and R 6 represents a 3- to 7-membered ring comprising from 1 to 4 heteroatoms chosen from nitrogen, oxygen and sulphur, which ring is optionally substituted by one or more substituents chosen from halogen atoms, alkyl and phenyl groups.

18. A compound according to claim 17 wherein R 4 represents a hydrogen atom or a cyano group.

19. A compound according to claim 13 , wherein R 5 represents a group —COOR 7 , a monocyclic or polycyclic aryl or a monocyclic or polycyclic heteroaryl group, wherein the monocyclic or polycyclic aryl or the monocyclic or polycyclic heteroaryl group are optionally substituted by one or more substituents chosen from:

halogen atoms;

alkyl groups, which are optionally substituted by one or more substituents chosen from halogen atoms, hydroxyl and alkoxy groups; and

alkoxy, alkoxycarbonyl and hydroxycarbonyl groups;

wherein R 7 represents

an alkyl group, which is optionally substituted by one or more substituents chosen from halogen atoms, hydroxyl and alkoxy groups

or a group of formula

—(CH 2 ) n —R 6

wherein n is an integer from 0 to 4 and R 6 represents:

a cycloalkyl or cycloalkenyl group;

an aryl group, which is optionally substituted by one or more substituents chosen from halogen atoms, alkyl, hydroxy, alkoxy, alkylenedioxy, alkylthio, amino, mono- and di-alkylamino, nitro, acyl, hydroxycarbonyl, alkoxycarbonyl, carbamoyl, mono- and di-alkylcarbamoyl, cyano, trifluoromethyl, difluoromethoxy and trifluoromethoxy groups;

or a 3- to 7-membered ring comprising from 1 to 4 heteroatoms chosen from nitrogen, oxygen and sulphur, which ring is optionally substituted by one or more substituents chosen from halogen atoms, alkyl, phenyl, hydroxy, alkoxy, alkylenedioxy, amino, mono- and di-alkylamino, nitro, cyano and trifluoromethyl groups.

20. A compound according to claim 19 , wherein R 5 represents a monocyclic or polycyclic aryl or a monocyclic or polycyclic heteroaryl group, wherein the monocyclic or polycyclic aryl or the monocyclic or polycyclic heteroaryl group are optionally substituted by one or more substituents chosen from:

halogen atoms;

alkyl groups, which are optionally substituted by one or more substituents chosen from halogen atoms, hydroxyl and alkoxy groups; and

alkoxy groups.

21. A compound according to claim 20 , wherein R 5 represents a monocyclic aryl or heteroaryl group, which is optionally substituted by one or more substituents chosen from halogen atoms and alkyl groups.

22. A compound according to claim 1 , wherein R 1 represents an alkyl group, R 2 represents a hydrogen atom or a group chosen from acyl, alkyl, aryl and heteroaryl groups, wherein the acyl, alkyl, aryl and heteroaryl groups are optionally substituted by one or more halogen atoms, R 3 represents a monocyclic or polycyclic aryl or a monocyclic or polycyclic heteroaryl group, wherein the monocyclic or polycyclic aryl or the monocyclic or polycyclic heteroaryl group are optionally substituted by one or more substituents chosen from halogen atoms, cyano, hydroxycarbonyl and alkyl groups, which are optionally substituted by one or more hydroxy groups, R 4 represents a hydrogen atom, a cyano group, an alkyl or alkenyl group, wherein the alkyl or alkenyl groups are optionally substituted by one substituent chosen from hydroxyl and alkoxy groups or R 4 represents a group of formula (—R 6 ) wherein R 6 represents a 4- to 6-membered ring comprising from 1 to 3 heteroatoms chosen from nitrogen, oxygen and sulphur, which ring is optionally substituted by one substituent chosen from alkyl and phenyl groups and R 5 represents a monocyclic aryl or monocyclic heteroaryl group, wherein the monocyclic aryl or the monocyclic heteroaryl group are optionally substituted by one substituent chosen from halogen atoms, alkyl and alkoxy groups.

23. A compound according to claim 1 , wherein R 1 is chosen from unsubstituted C 1-4 alkyl groups; R 2 is a hydrogen atom; R 3 represents a phenyl group or a monocyclic or polycyclic N-containing heteroaryl group, wherein the phenyl group or the monocyclic or polycyclic N-containing heteroaryl group may be substituted by one substituent chosen from halogen atoms, alkyl groups and hydroxycarbonyl groups; R 4 represents a hydrogen atom or a cyano group and R 5 represents a monocyclic aryl or monocyclic heteroaryl group, wherein the monocyclic aryl or the monocyclic heteroaryl group are optionally substituted by one or more substituents chosen from halogen atoms and alkyl groups.

24. A compound according to claim 1 , chosen from:

4-[(3-chlorophenyl)amino]-2-ethyl-5-(1-hydroxyethyl)-6-phenylpyridazin-3(2H)-one

4-[(3-chlorophenyl )amino]-2-ethyl-5-(1-methoxyethyl)-6-phenylpyridazin-3(2H)-one

4-[(3-chlorophenyl)amino]-2-ethyl-6-phenyl-5-vinylpyridazin-3(2H)-one

4-anilino-2,5-diethyl-6-phenylpyridazin-3(2H)-one

5-[(3-chlorophenyl)amino]-1-ethyl-6-oxo-3-phenyl-1,6-dihydropyridazine-4-carbaldehyde O-methyloxime

5-[(3-chlorophenyl)amino]-1-ethyl-6-oxo-3-phenyl-1,6-dihydropyridazine-4-carbonitrile

1-ethyl-5-{[4-(hydroxymethyl)phenyl]amino}-6-oxo-3-phenyl-1,6-dihydropyridazine-4-carbonitrile

1-ethyl-6-oxo-3-phenyl-5-[(3,4,5-trifluorophenyl)amino]-1,6-dihydropyridazine-4-carbonitrile

5-[(4-cyanophenyl)amino]-1-ethyl-6-oxo-3-phenyl-1,6-dihydropyridazine-4-carbonitrile

1-ethyl-3-(4-fluorophenyl)-5-{[4-(hydroxymethyl)phenyl]amino}-6-oxo-1,6-dihydropyridazine-4-carbonitrile

5-[(4-cyanophenyl)amino]-1-ethyl-3-(4-fluorophenyl)-6-oxo-1,6-dihydropyridazine-4-carbonitrile

1-ethyl-3-(4-fluorophenyl)-6-oxo-5-[(3,4,5-trifluorophenyl)amino]-1,6-dihydropyridazine-4-carbonitrile

1-ethyl-3-(4-fluorophenyl)-6-oxo-5-(pyridin-3-ylamino)-1,6-dihydropyridazine-4-carbonitrile

1-ethyl-3-(3-fluorophenyl)-5-{[4-(hydroxymethyl)phenyl]amino}-6-oxo-1,6-dihydropyridazine-4-carbonitrile

5-[(4-cyanophenyl)amino]-1-ethyl-3-(3-fluorophenyl)-6-oxo-1,6-dihydropyridazine-4-carbonitrile

1-ethyl-3-(3-fluorophenyl)-6-oxo-5-[(3,4,5-trifluorophenyl)amino]-1,6-dihydropyridazine-4-carbonitrile

4-[(3-chlorophenyl)amino]-2-ethyl-5-(2-methyl-1,3-thiazol-4-yl)-6-phenylpyridazin-3(2H)-one

4-[(3-chlorophenyl)amino]-2-ethyl-6-phenyl-5-(2-phenyl-1,3-thiazol-4-yl)pyridazin-3(2H)-one

4-[(3-chlorophenyl)amino]-2-ethyl-5-(1-methyl-1H-pyrazol-5-yl)-6-phenylpyddazin-3(2H)-one

4-{[2-ethyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)-3-oxo-6-phenyl-2,3-dlhydropyridazin-4-yl]amino}benzonltrile

2-ethyl-5-(5-methyl-1,3,4-oxadiazol-2-yl)-6-phenyl-4-[(3,4,5-trifluorophenyl) amino]pyridazin-3(2H)-one

4-[(3-chlorophenyl)amino]-2-ethyl-6-phenylpyridazin-3(2H)-one

2-ethyl-4-[(3-fluorophenyl)amino]-6-phenylpyridazin-3(2H)-one

2-ethyl-4-(1-naphthylamino)-6-phenylpyridazin-3(2H)-one

2-ethyl-6-phenyl-4-(pyridin-3-ylamino)pyridazin-3(2H)-one

2-ethyl-6-phenyl-4-(quinolin-5-ylamino)pyridazin-3(2H)-one

4-(diquinolin-5-ylamino)-2-ethyl-6-phenylpyridazin-3(2H)-one

4-[bis(3,4,5-trifluorophenyl)amino]-2-ethyl-6-phenylpyridazin-3(2H)-one

4-[bis(3,4-difluorophenyl)amino]-2-ethyl-6-phenylpyridazin-3(2H)-one

4-[(3,4-difluorophenyl)amino]-2-ethyl-6-phenylpyridazin-3(2H)-one

4-[(3-chloro-4-fluorophenyl)amino]-2-ethyl-6-phenylpyridazin-3(2H)-one

4-[(2-ethyl-3-oxo-6-phenyl-2,3-dihydropyridazin-4-yl)amino]benzonitrile

2-ethyl-4-[(1-oxidopyridin-3-yl)amino]-6-phenylpyridazin-3(2H)-one

2-ethyl-6-pyridin-3-yl-4-(pyridin-3-ylamino)pyridazin-3(2H)-one

2-ethyl-4-[(1-oxidoquinolin-5-yl)amino]-6-phenylpyridazin-3(2H)-one

2-ethyl-6-pyridin-4-yl-4-(pyridin-3-ylamino)pyridazin-3(2H)-one

2-ethyl-4-(isoquinolin-4-ylamino)-6-phenylpyridazin-3(2H)-one

2-ethyl-6-phenyl-4-[(3,4,5-trifluorophenyl)amino]pyridazin-3(2H)-one

2-ethyl-4-[(4-fluorophenyl)amina]-6-phenylpyridazin-3(2H)-one

2-ethyl-6-pyridin-3-yl-4-(quinolin-5-ylamino)pyridazin-3(2H)-one

2-methyl-6-pyridin-3-yl-4-(quinolin-5-ylamino)pyridazin-3(2H)-one

2-ethyl-6-pyridin-4-yl-4-(quinolin-5-ylamino)pyridazin-3(2H)-one

2-ethyl-4-{[4-(hydroxymethyl)phenyl]amino}-6-phenylpyridazin-3(2H)-one

4-[(2-methyl-3-oxo-6-pyridin-3-yl-2,3-dihydropyridazin-4-yl)amino]benzonitrile

4-[(2-ethyl-3-oxo-6-pyridin-3-yl-2,3-dihydropyridazin-4-yl)amino]benzonitrile methyl 4-[(2-ethyl-3-oxo-6-phenyl-2,3-dihydropyridazin-4-yl)amino]benzoate

4-{[2-ethyl-6-(1-oxidopyridin-3-yl)-3-oxo-2,3-dihydropyridazin-4-yl]amino}benzonitrile

2-ethyl-4-(isoquinolin-4-ylamino)-6-pyridin-3-ylpyridazin-3(2H)-one

2-ethyl-4-[(4-methylpyridin-3-yl)amino]-6-pyridin-3-ylpyridazin-3(2H)-one

2-ethyl-4-(isoquinolin-4-ylamino)-6-pyridin-4-ylpyridazin-3(2H)-one

4-[(2-ethyl-3-oxo-6phenyl-2,3-dihydropyridazin-4-yl)amino]benzoic acid

2-ethyl-4-[(4-methylpyridin-3-yl)amino]-6-pyridin-4-ylpyridazin-3(2H)-one

4-[(2-ethyl-3-oxo-6-pyridin-4-yl-2,3-dihydropyridazin-4-yl)amino]benzonitrile

4-[(2-ethyl-3-oxo-6-phenyl-2,3-dihydropyridazin-4-yl)(methyl)amino]benzonitrile N-(4-cyanophenyl)-N-(2-ethyl-3-oxo-6-phenyl-2,3-dihydropyridazin-4-yl)acetamide

6-(3-chlorophenyl)-2-ethyl-4-(pyridin-3-ylamino)pyridazin-3(2H)-one

2-ethyl-4-[methyl(quinolin-5-yl)amino]-6-phenylpyridazin-3(2H)-one

6-(3-chlorophenyl)-2-ethyl-4-(isoquinolin-4-ylamino)pyridazin-3(2H)-one

N-(2-ethyl-3-oxo-6-phenyl-2,3-dihydropyridazin-4-yl)-N-quinolin-5-yl)acetamide

2-Ethyl-4-(4-hydroxymethyl-phenylamino)-6-pyridin-3-ylpyridazin-3(2H)-one

2-ethyl-4-(isoquinolin-4-ylamino)6-(4-methoxyphenyl)pyridazin-3(2H)-one

2-ethyl-6-(4-methoxyphenyl)-4-(quinolin-5-ylamino)pyridazin-3(2H)-one

4-anilino-2-ethyl-6-phenylpyridazin-3(2H)-one

2-ethyl-6-(4-methylphenyl)-4-(quinolin-5-ylamino)pyridazin-3(2H)-one

2-ethyl-6-(4-methylphenyl)-4-[(1-oxidoquinolin-5-yl)amino]pyridazin-3(2H)-one

2-Ethyl-6-phenyl-4-(thieno[2,3-c]pyridin-3-ylamino)pyridazin-3(2H)-one

1-Ethyl-6-oxo-3-phenyl-5-(pyridin-3-ylamino)-1,6-dihydropyridazine-4-carbonitrile

1-Ethyl-3-(3-methylphenyl)-6-oxo-5-(pyridin-3-ylamino)-1,6-dihydropyridazine-4-carbonitrile

2-Ethyl-5-(1-hydroxyethyl)-6-phenyl-4-(quinolin-5-ylamino)pyridazin-3(2H)-one

2-Ethyl-6-(4-methylphenyl)-4-(pyridin-3-ylamino)pyridazin-3(2H)-one

2-Ethyl-4-(isoquinolin-4-ylamino)-6-(4-methylphenyl)pyridazin-3(2H)-one

2-Ethyl-6-(4-methylphenyl)-4-[(4-methylpyridin-3-yl)amino]pyridazin-3(2H)-one

2-Ethyl-6-(3-methylphenyl)-4-(pyridin-3-ylamino)pyridazin-3(2H )-one

2-Ethyl-4-(isoquinolin-4-ylamino)-6-(3-methylphenyl)pyridazin-3(2H)-one

2-Ethyl-6-(3-methylphenyl)-4-[(4-methylpyridin-3-yl)amino]pyridazin-3(2H)-one

4-{[2-Ethyl-6-(3-methylphenyl)-3-oxo-2,3-dihydropyridazin-4-yl]amino}benzoic acid

2-Ethyl-6-(5-methylpyridin-3-yl)-4-(pyridin-3-ylamino)pyridazin-3(2H)-one

2-Ethyl-4-(isoquinolin-4-ylamino)-6-(5-methylpyridin-3-yl)pyridazin-3(2H)-one

2-Ethyl-6-(5-methylpyridin-3-yl)-4-[(4-methylpyridin-3-yl)amino]pyridazin-3(2H)-one

2-Ethyl-4-(1,7-naphthyridin-5-ylamino)-6-phenylpyridazin-3(2H)-one

[1-Ethyl-6-oxo-3-phenyl-5-(pyridin-3-ylamino)-1,6-dihydropyridazin-4-yl]methyl acetate

[1-Ethyl-6-oxo-3-phenyl-5-(pyridin-3-ylamino)-1,6-dihydropyridazin-4-yl]methyl butyrate

2-Ethyl-5-[2-(4-methoxyphenyl)-1,3-thiazol-4-yl]-6-phenyl-4-(pyridin-3-ylamino) pyridazin-3(2H)-one

2-Ethyl-4-(isoquinolin-4-ylamino)-6-(6-methylpyridin-3-yl)pyridazin-3(2H)-one

2-Ethyl-6-(6-methylpyridin-3-yl)-4-(pyridin-3-ylamino)pyridazin-3(2H)-one

2-Ethyl-5-[2-(4-methoxyphenyl)-1,3-thiazol-4-yl]-4-[(4-methylpyridin-3-yl)amino]-6-phenylpyridazin-3(2H)-one

2-Ethyl-6-phenyl-4-(pyridin-3-ylamino)-5-(2-pyridin-4-yl-1,3-thiazol-4-yl)pyridazin-3(2H)-one

Ethyl 4-[1-ethyl-6-oxo-3-phenyl-5-(pyridin-3-ylamino)-1,6-dihydropyridazin-4-yl]-1,3-thiazole-2-carboxylate

2-Ethyl-4-(isoquinolin-4-ylamino)-5-[2-(4-methoxyphenyl)-1,3-thiazol-4-yl]-6-phenylpyridazin-3(2H)-one

2-Ethyl-4-[(4-methylpyridin-3-yl)amino]-6-phenyl-5-(2-pyridin-4-yl-1,3-thiazol-4-yl) pyridazin-3(2H)-one

5-[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]-2-ethyl-4-[(4-methylpyridin-3-yl)amino]-6-phenylpyridazin-3(2H)-one

5-[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]-2-ethyl-6-phenyl-4-(pyridin-3-ylamino)pyridazin-3(2H)-one

5-[2-(4-Chlorophenyl)-1,3-thiazol-4-yl]-2-ethyl-4-(isoquinolin-4-ylamino)-6-phenylpyridazin-3(2H)-one

2-Ethyl-4-[(4-methylpyridin-3-yl)amino]-6-phenylpyridazin-3(2H)-one

2-Ethyl-4-[(4-methyl-1-oxidopyridin-3-yl)amino]-6-phenylpyridazin-3(2H)-one

Ethyl 4-[(2-ethyl-3-oxo-6-phenyl-2,3-dihydropyridazin-4-yl)amino]benzoate.

or a pharmaceutically acceptable salt thereof.

25. A pharmaceutical composition, comprising a compound according to claim 1 and a pharmaceutically acceptable diluent or carrier.

26. A method for treating a subject afflicted with a pathological condition or disease susceptible to amelioration by inhibition of phosphodiesterase 4, comprising administering to said subject an effective amount of a compound according to claim 1 , wherein the pathological condition or disease is chosen from asthma, atopic dermatitis and psoriasis.

27. A combination product comprising:

(i) a compound according to claim 1 ; and

(ii) another compound chosen from (a) steroids, (b) immunosuppressive agents, (c) T-cell receptor blockers and (d) antiinflammatory drugs.

28. A method for treating a subject afflicted with a pathological condition or disease susceptible to amelioration by inhibition of phosphodiesterase 4, comprising administering to said subject an effective amount of a compound according to claim 1 , and further comprising the simultaneous, separate or sequential administration to said subject of another compound chosen from (a) steroids, (b) immunosuppressive agents, (c) T-cell receptor blockers and (d) antiinflammatory drugs, wherein the pathological condition or disease is chosen from asthma, atopic dermatitis and psoriasis.

Assignments (2)
CHANGE OF NAME Recorded Jan 22, 2007
From: ALMIRALL PRODESFARMA S.A.
To: LABORATORIOS ALMIRALL, S.A.
Reel/Frame 018786/0571 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 7, 2006
From: DAL PIAZ, VITTORIO; AGUILAR IZQUIERDO, NURIA; BUIL ALBERO, MARIA ANTONIA; GARRIDO RUBIO, YOLANDA; GIOVANNONI, MARIA PAOLA; GRACIA FERRER, JORDI; LUMERAS AMADOR, WENCESLAO; VERGELLI, CLAUDIA
To: ALMIRALL PRODESFARMA, S.A.
Reel/Frame 018060/0912 →
Priority Claims (1)
ES 200302613 · Nov 10, 2003 · national
Continuity (1)
Related Publication 20070197536A1 · Aug 23, 2007