Claims
- 1. A compound selected from those of formula (I): ##STR60## in which m is equal to 0 or 1,
- the symbol ##STR61## representing the pyridine ring when m is equal to 0 and pyridine N-oxide when m is equal to 1,
- the pyridine system ##STR62## being connected to the group ##STR63## which bears it either in the 2-position or in the 3-position of the pyridine ring;
- R.sub.1 and R.sub.2, which may be identical or different, are chosen, independently of each other, from hydrogen, amino, alkylamino, dialkylamino, alkyl, hydroxy, alkoxy, nitro, and halogen,
- R.sub.3 and R.sub.4, which may be identical or different, are chosen, independently of each other, from amino, alkylamino, dialkylamino, alkyl, hydroxy, alkoxy, nitro, and halogen,
- R represents hydrogen or alkyl,
- A represents a single bond; and in this case Het represents a group chosen from pyrazine and substituted pyrazine, or alternatively A represents alkylene which is unsubstituted or substituted with one or more alkyl, or alkenylene which is unsubstituted or substituted with one or more alkyl; and in this case Het also represents a group chosen from pyrazine and substituted pyrazine,
- X represents oxygen, imino, or imino substituted with a group chosen from alkyl, alkoxy, hydroxy, amino, arylalkyloxy, and aryloxy,
- an enantiomer and a diastereoisomer thereof and an addition salt thereof with a pharmaceutically-acceptable acid or base, it being understood that, except where otherwise mentioned:
- the term "substituted" relating to the pyrazine system means that it is substituted with one or more groups chosen from alkyl, alkoxy, trifluoromethyl, hydroxy, halogen, thio, and alkylthio,
- the terms "alkyl", "alkoxy", and "alkylene" denote linear or branched groups containing 1 to 6 carbon atoms, inclusive,
- the term "aryl" denotes phenyl or naphthyl,
- the term "alkenylene" denotes a linear or branched unsaturated chain containing 2 to 6 carbon atoms, inclusive.
- 2. A compound of claim 1, which is selected from those compounds having the formula (IA): ##STR64## in which m represents 0 or 1, and Het represents pyrazine or pyrazine substituted with alkyl and A is a single bond,
- and X represents oxygen, imino or imino substitued with a hydroxyl, a methoxy, a methyl, amino or benzyloxy,
- an enantiomer and a diastereoisomer thereof and an addition salt thereof with a pharmaceutically-acceptable acid.
- 3. A compound of claim 1, which is selected from N-(4,6-dimethyl-2-pyridyl)-2-pyrazinecarbamidoxime, of formula: ##STR65## the N-oxide thereof and an addition salt thereof, with a pharmaceutically-acceptable acid.
- 4. A compound of claim 1, which is selected from N-(4,6-dimethyl-2-pyridyl)-O-methyl-2-pyrazinecarbamidoxime, of formula: ##STR66## the N-oxide thereof, an enantiomer thereof, and an addition salt thereof with a pharmaceutically-acceptable acid.
- 5. A compound of claim 1, which is selected from N-(4,6-dimethyl-2-pyridyl)-5-methyl-2-pyrazinethiocarboxamide, the N-oxide thereof, and an addition salt thereof with a pharmaceutically-acceptable acid.
- 6. A compound of claim 1, which is selected from N-(4,6-dimethyl-2-pyridyl)-2-pyrazinecarboxamidine, the N-oxide thereof, and an addition salt thereof with a pharmaceutically-acceptable acid.
- 7. A compound of claim 1, which is selected from N-(4,6-dimethyl-2-pyridyl)-N'-methyl-2-pyrazinecarboxamidine, the N-oxide thereof, and an addition salt thereof with a pharmaceutically-acceptable acid.
- 8. A pharmaceutical composition useful for treating inflammatory disorders containing as active principle at least one compound selected from those of formula (I): ##STR67## in which m is equal to 0 or 1,
- the symbol ##STR68## representing the pyridine ring when m is equal to 0 and pyridine N-oxide when m is equal to 1,
- the pyridine system ##STR69## being connected to the group ##STR70## which bears it either in the 2-position or in the 3-position of the pyridine ring;
- R.sub.1 and R.sub.2, which may be identical or different, are chosen, independently of each other, from hydrogen, amino, alkylamino, dialkylamino, alkyl, hydroxy, alkoxy, nitro, and halogen,
- R.sub.3 and R.sub.4, which may be identical or different, are chosen, independently of each other, from amino, alkylamino, dialkylamino, alkyl, hydroxy, alkoxy, nitro, and halogen,
- R represents hydrogen or alkyl,
- A represents a single bond; and in this case Het represents a group chosen from pyrazine and substituted pyrazine, or alternatively A represents alkylene which is unsubstituted or substituted with one or more alkyl, or alkenylene which is unsubstituted or substituted with one or more alkyl; and in this case Het also represents a group chosen from pyrazine and substituted pyrazine,
- X represents oxygen, imino, or imino substituted with a group chosen from alkyl, alkoxy, hydroxy, amino, arylalkyloxy, and aryloxy,
- an enantiomer and a diastereoisomer thereof and an addition salt thereof with a pharmaceutically-acceptable acid or base, it being understood that the term "substituted" relating to the pyrazine system means that it is substituted with one or more groups chosen from alkyl, alkoxy, trifluoromethyl, hydroxy, halogen, thio, and alkylthio,
- the terms "alkyl", "alkoxy", and "alkylene" denote linear or branched groups containing 1 to 6 carbon atoms, inclusive,
- the term "aryl" denotes phenyl or naphthyl,
- the term "alkenylene" denotes a linear or branched unsaturated chain containing 2 to 6 carbon atoms, inclusive, in combination with one or more pharmaceutically-acceptable excipients or vehicles.
- 9. A method of treating a mammal afflicted with an inflammatory disorder comprising the step of administering to the said mammal an amount of a compound selected from those of formula (I): ##STR71## in which m is equal to 0 or 1,
- the symbol ##STR72## representing the pyridine ring when m is equal to 0 and pyridine N-oxide when m is equal to 1,
- the pyridine system ##STR73## being connected to the group ##STR74## which bears it either in the 2-position or in the 3-position of the pyridine ring;
- R.sub.1 and R.sub.2, which may be identical or different, are chosen, independently of each other, from hydrogen, amino, alkylamino, dialkylamino, alkyl, hydroxy, alkoxy, nitro, and halogen,
- R.sub.3 and R.sub.4, which may be identical or different, are chosen, independently of each other, from amino, alkylamino, dialkylamino, alkyl, hydroxy, alkoxy, nitro, and halogen,
- R represents hydrogen or alkyl,
- A represents a single bond; and in this case Het represents a group chosen from pyrazine and substituted pyrazine,
- or alternatively A represents alkylene which is unsubstituted or substituted with one or more alkyl, or alkenylene which is unsubstituted or substituted with one or more alkyl; and in this case Het also represents a group chosen from pyrazine and substituted pyrazine,
- X represents oxygen, sulfur, imino, or imino substituted with a group chosen from alkyl, alkoxy, hydroxy, amino, arylalkyloxy, and aryloxy,
- an enantiomer and a diastereoisomer thereof and an addition salt thereof with a pharmaceutically-acceptable acid or base, it being understood that the term "substituted" relating to the pyrazine system means that it is substituted with one or more groups chosen from alkyl, alkoxy, trifluoromethyl, hydroxy, halogen, thio, and alkylthio,
- the terms "alkyl", "alkoxy", and "alkylene" denote linear or branched groups containing 1 to 6 carbon atoms, inclusive,
- the term "aryl" denotes phenyl or naphthyl,
- the term "alkenylene" denotes a linear or branched unsaturated chain containing 2 to 6 carbon atoms, inclusive, which is effective for alleviating the said disorder.
- 10. A pharmaceutical composition according to claim 8 wherein the compound has the formula (IA): ##STR75## in which m represents 0 or 1, and Het represents pyrazine or alkylpyrazine and A represents a single bond,
- and X represents oxygen, imino, or imino substituted with a hydroxyl, a methoxy, a methyl, amino, or benzyloxy,
- an enantiomer and a diastereoisomer thereof and an addition salt thereof with a pharmaceutically-acceptable acid.
- 11. A pharmaceutical composition according to claim 8 wherein the compound is selected from the group consisting of N-(4,6-dimethyl-2-pyridyl)-2-pyrazinecarboxamidoxime or the O-methyl derivative thereof, or an N-oxide of any of the foregoing, and the addition salts thereof with a pharmaceutically-acceptable acid.
- 12. A pharmaceutical composition according to claim 8 wherein the compound is selected from the group consisting of N-(4,6-dimethyl-2-pyridyl)-5-methyl-2-pyrazinethiocarboxamide, N-(4,6-dimethyl-2-pyridyl)-2-pyrazinecarboxamidine or the N'-methyl derivative thereof, or an N-oxide of any of the foregoing, and the addition salts thereof with a pharmaceutically-acceptable acid.
- 13. A method of claim 9, wherein the compound has the formula (IA): ##STR76## in which m represents 0 or 1, and Het represents pyrazine or alkylpyrazine and A represents a single bond,
- and X represents oxygen, sulfur, imino, or imino substituted with a hydroxyl, a methoxy, a methyl, amino, or benzyloxy,
- an enantiomer and a diastereoisomer thereof and an addition salt thereof with a pharmaceutically-acceptable acid.
- 14. A method of claim 9, wherein the compound is selected from the group consisting of N-(4,6-dimethyl-2-pyridyl)-2-pyrazine carboxamidoxime or the O-methyl derivative thereof, or an N-oxide of any of the foregoing, and the addition salts thereof with a pharmaceutically-acceptable acid.
- 15. A method of claim 9, wherein the compound is selected from the group consisting of N-(4,6-dimethyl-2-pyridyl)-5-methyl-2-pyrazinethiocarboxamide, N-(4,6-dimethyl-2-pyridyl)-2-pyrazine-carboxamidine or the N'-methyl derivative thereof, or an N-oxide of any of the foregoing, and the addition salts thereof with a pharmaceutically-acceptable acid.
Priority Claims (1)
Number |
Date |
Country |
Kind |
94 06412 |
May 1994 |
FRX |
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Parent Case Info
The present application is a division of our prior-filed application Ser. No. 08/450,346, filed May 25, 1995, now U.S. Pat. No. 5,712,294.
US Referenced Citations (1)
Number |
Name |
Date |
Kind |
5260320 |
Haga et al. |
Nov 1993 |
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Non-Patent Literature Citations (4)
Entry |
Kinney, W.A. et al. J. Medicinal Chemistry, vol. 33, pp. 327-336 (1990). |
Rodier, N. et al. Chemical Abstracts, Abstract No. 122:68755, obtained via STN (1995). |
Rodier, N. et al. SCISEARCH, Abstract No. 95:31601, obtained via STN (1995). |
Katritzky et al., Heterocyclic Chemistry, pp. 27-51, 1960. |
Divisions (1)
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Number |
Date |
Country |
Parent |
450346 |
May 1995 |
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