Macrolides with antiinflammatory activity
Macrolide compounds of formula (I) wherein X, R, R 1 , R 2 , R 3 and R 4 , have the meanings as defined in the specification, pharmaceutically acceptable salts thereof, pharmaceutical compositions containing them as active ingredient and the use thereof in the treatment and prophylaxis of inflammatory diseases, are described.
1. A compound of formula
wherein
X is a —C(═O)—, —C(═O)—O—, —C(═O)—N—, —SO 2 — or —SO 2 —N group;
R is a hydrogen atom or methyl;
R 1 is a hydrogen atom or a (C 1 -C 3 )-alkyl group;
R 2 is a hydrogen atom, a (C 1 -C 4 )-alkoxy-(C 1 -C 4 )-alkyl group, a (C 5 -C 7 )-cycloalkyl group, a phenyl or a five- or six-membered heteroaryl having from one to three heteroatoms selected among nitrogen, oxygen and sulphur, a phenyl-(C 1 -C 4 )-alkyl or heteroaryl-(C 1 -C 4 )-alkyl group optionally substituted by 1 to 3 substituents selected among a (C 1 -C 4 )-alkyl group, a (C 1 -C 4 )-alkoxy group and halogen, or a chain of formula
—(CH 2 ) r —Y—(CH 2 ) m -A
wherein
A is a phenyl or a five- or six-membered heteroaryl having from one to three heteroatoms selected among nitrogen, oxygen and sulphur, both ones optionally substituted by 1 to 3 substituents selected among a (C 1 -C 4 )-alkyl group, a (C 1 -C 4 )-alkoxy group or halogen;
Y represents O, S or NR 6 wherein R 6 is a hydrogen atom, a linear or branched (C 1 -C 3 ) alkyl, a (C 1 -C 3 )-alkoxycarbonyl group or a benzyloxycarbonyl group;
r is an integer from 1 and 3;
m is an integer from 0 and 3;
R 3 is a hydroxy group or R 3 taken together with R 4 forms a (═O) group or a ═N—O—R 5 group wherein R 5 is a hydrogen atom, a (C 1 -C 4 )-alkyl group, a benzyl or a —X—R 2 group wherein X and R 2 have the corresponding meanings defined above;
R 4 is a hydrogen atom or R 4 taken together with R 3 forms a (═O) group or a ═N—O—R 5 group wherein R 5 has the meanings defined above;
and furthermore R 2 is a (C 1 -C 10 )-alkyl group or a (C 4 -C 10 )-alkyl group when, at the same time, X is a —C(═O)— group, R 1 is a (C 1 -C 3 )-alkyl group and R 3 is a hydroxy group or R 3 taken together with R 4 forms a ═N—O—R 5 group wherein R 5 is different from —X—R 2 ;
and pharmaceutically acceptable salts thereof.
2. A compound according to claim 1 wherein R, R 1 , R 2 have the meanings as defined in formula I, X is a —C(═O)—, —C(═O)—N— or —SO 2 — group and R 3 is a hydroxy group or R 3 taken together with R 4 forms a (═O) group or a ═N—O—R 5 group wherein R 5 is a hydrogen atom, methyl, benzyl or a —X—R 2 group wherein X and R 2 have the meanings as defined in formula I.
3. A compound according to claim 2 wherein R 1 is a hydrogen atom or methyl and R 5 is a hydrogen atom or a —X—R 2 group wherein X and R 2 have the meanings as defined in formula I.
4. A compound according to claim 3 wherein R 2 is a hydrogen atom, a (C 1 -C 4 )-alkoxy-(C 1 -C 4 )-alkyl group, a (C 5 -C 7 )-cycloalkyl group, a phenyl or a five- or six-membered heteroaryl having from one to three heteroatoms selected among nitrogen, oxygen and sulphur, a phenyl-(C 1 -C 4 )-alkyl or heteroaryl-(C 1 -C 4 )-alkyl group optionally substituted by 1 to 3 substituents selected among a (C 1 -C 4 )-alkyl group, a (C 1 -C 4 )-alkoxy group and halogen, or a chain to formula
—(CH 2 ) r —Y—(CH 2 ) m -A
wherein
A is a phenyl or a heteroaryl selected among furan, thiophene, oxazole, imidazole, pyridine, pyrimidine and triazole both ones optionally substituted by 1 to 3 substituents selected among a (C 1 -C 4 )-alkyl group, a (C 1 -C 4 )-alkoxy group or halogen;
Y represents O, S or NR 6 wherein R 6 is a hydrogen atom or methyl;
r is an integer from 1 and 3;
m is an integer from 0 and 3;
and furthermore R 2 is a (C 1 -C 10 )-alkyl group or a (C 4 -C 10 )-alkyl group when, at the same time, X is a —C(═O)— group, R 1 is a (C 1 -C 3 )-alkyl group and R 3 is a hydroxy group or R 3 taken together with R 4 forms a ═N—O—R 5 group wherein R 5 is different from —X—R 2 .
5. A compound according to claim 1 wherein R 1 is methyl and R 2 is a metoxy-(C 1 -C 3 )-alkyl group, a (C 5 -C 7 )-cycloalkyl group, a phenyl or a heteroaryl selected among furan, thiophene, oxazole and pyridine, a benzyl or heteroaryl-(C 1 -C 4 )-alkyl group optionally substituted by a substituent selected among a (C 1 -C 4 )-alkyl group, a metoxy group and halogen, or a chain of formula
—(CH 2 ) r —Y—(CH 2 ) m -A
wherein
A is a phenyl or a heteroaryl selected among furan, thiophene, oxazole and pyridine, both ones optionally substituted by a substituent selected among a (C 1 -C 4 )-alkyl group, a metoxy group or halogen;
Y represents O, S or NR 6 wherein R 6 is a hydrogen atom;
r is an integer from 1 and 3;
m is an integer selected among 0 and 1;
and furthermore R 2 is a (C 1 -C-7)-alkyl group or a (C 4 -C 10 )-alkyl group when, at the same time, X is a —C(═O)— group, R 1 is a (C 1 -C 3 )-alkyl group and R 3 is a hydroxy group or R 3 taken together with R 4 forms a ═N—O—R 5 group wherein R 5 is different from —X—R 2 .
6. A compound according to claim 1 wherein R, R 1 , R 2 and X have the meanings as defined in formula I, R 3 is a hydroxy group and R 4 is a hydrogen atom.
7. A compound according to claim 6 wherein R 1 is a hydrogen atom or methyl and X is a —C(═O)—, —C(═O)—N— or —SO 2 — group.
8. A compound according to claim 7 wherein R 2 is a hydrogen atom, a (C 1 -C 4 )-alkoxy-(C 1 -C 3 )-alkyl group, a (C 5 -C 7 )-cycloalkyl group, a phenyl or a five- or six-membered heteroaryl having from one to three heteroatoms selected among nitrogen, oxygen and sulphur, a phenyl-(C 1 -C 4 )alkyl or heteroaryl-(C 1 -C 4 )-alkyl group optionally substituted by a substituent selected among a (C 1 -C 4 )-alkyl group, a (C 1 -C 4 )-alkoxy group and halogen, or a chain of formula
—(CH 2 ) r —Y—(CH 2 ) m -A
wherein
A is a phenyl or a heteroaryl selected among furan, thiophene, oxazole, imidazole, pyridine, pyrimidine and triazole both ones optionally substituted by a substituent selected among a (C 1 -C 4 )-alkyl group, a (C 1 -C 4 )-alkoxy group or halogen;
Y represents O, S or NR 6 wherein R 6 is a hydrogen atom or methyl;
r is an integer comprised between 1 and 3;
m is an integer selected among 0 and 3;
and furthermore R 2 is a (C 1 -C 7 )-alkyl group or a (C 4 -C 10 )-alkyl group when, at the same time, X is a —C(═O)— group, R 1 is a (C 1 -C 3 )-alkyl group and R 3 is a hydroxy group or R 3 taken together with R 4 forms a ═N—O—R 5 group wherein R 5 is different from —X—R 2 .
9. A compound according to claim 8 wherein R 1 is methyl and R 2 is a hydrogen atom, a methoxy-(C 1 -C 3 )-alkyl group, a (C 5 -C 7 )-cycloalkyl group, a phenyl or a heteroaryl selected among furan, thiophene, oxazole and pyridine, a benzyl or heteroaryl-methyl group wherein heteroaryl is selected among furan, thiophene, oxazole and pyridine, optionally substituted by a substituent selected among a (C 1 -C 4 )-alkyl group, a metoxy group and halogen, or a chain of formula
—(CH 2 ) r —Y—(CH 2 ) m -A
wherein
A is a phenyl or a heteroaryl selected among furan, thiophene, oxazole and pyridine, both ones optionally substituted by a substituent selected among a methyl group, a metoxy group or halogen;
Y represents O, S or NR 6 wherein R 6 is a hydrogen atom;
r is an integer comprised between 1 and 3;
m is an integer selected among 0 and 1;
and furthermore R 2 is a (C 1 -C 7 )-alkyl group or a (C 4 -C 10 )-alkyl group when, at the same time, X is a —C(═O)— group, R 1 is a (C 1 -C 3 )-alkyl group and R 3 is a hydroxy group or R 3 taken together with R 4 forms a ═N—O—R 5 group wherein R 5 is different from —X—R 2 .
10. A compound according to claim 9 wherein R 2 is a methoxy-methyl group, a cycloesyl, a phenyl or a heteroaryl selected among furan, thiophene, oxazole and pyridine, a benzyl or thiophen-il-methyl group optionally substituted by a substituent selected among a methyl group, a metoxy group and halogen, or a chain of formula
—(CH 2 ) r —Y—(CH 2 ) m -A
wherein
A is a phenyl or pyridine, both ones optionally substituted by a metoxy group;
Y represents O, S or NR 6 wherein R 6 is a hydrogen atom;
r is an integer comprised between 1 and 3;
m is an integer selected between 0 and 1;
and furthermore R 2 is a (C 1 -C 7 )-alkyl group or a (C 4 -C 10 )-alkyl group when, at the same time, X is a —C(═O)— group, R 1 is a (C 1 -C 3 )-alkyl group and R 3 is a hydroxy group or R 3 taken together with R 4 forms a ═N—O—R 5 group wherein R 5 is different from —X—R 2 .
11. A compound according to claim 1 wherein the —X—R 2 substituent in the meanings of R 5 has the same meanings of the X and R 2 substituents at 3′ position.
12. A process for the preparation of a compound according to claim 1 which comprises:
a. the demethylation of the dimethylamino group at 3′ position of a compound of formula
wherein
R, R 3 and R 4 are as defined as in claim 1 ;
b. the removal of L-cladinose by a hydrolysis reaction;
c. the amidation reaction of the primary or secondary aminic group obtained by item a.
13. A process according to claim 12 wherein R 3 in formula II is a hydroxy group and R 4 is a hydrogen atom.
14. A process according to claim 12 wherein the removal of the cladinose is carried out by an acid catalyzed hydrolysis in presence of a mineral acid and of a protic organic solvent.
15. A pharmaceutical composition comprising a therapeutically effective amount of a compound according to claim 1 in admixture with a pharmaceutically acceptable carrier.
16. A pharmaceutical composition according to claim 15 useful in the treatment of inflammatory diseases.
17. A pharmaceutical composition according to claim 15 useful in the treatment of respiratory diseases.
18. A pharmaceutical composition according to claim 16 useful in the treatment of gastrointestinal diseases.