FIELD: substances having antimicrobial activity. SUBSTANCE: azetidine derivatives of the general formula 1 wherein A is a nitrogen atom, or CH or C-Ha; in which Hal is a chlorine or fluorine atom; R1 is lower alkyl or cycloalkyl, lower halogenoalkyl or phenyl substituted by mono- or difluorine; R2,R3 and R5 are the same or different and are hydrogen or lower alkyl; R4 is hydroxyl, amino, aminoalkyl, alkylamino, dialkylamino, pyrrolyl-1 or pyrro lidinyl-1, alkylaminoalkyl, trifluoroacetamido; R6 is hydrogen or amino, or A and R1 together form and in that case have a chiral centre with the R or S consignation; R7 is hydrogen or lower alkyl. EFFECT: improved properties of the title compounds. 1 tbl
Title | Year | Author | Number |
---|---|---|---|
SUBSTITUTED DERIVATIVES OF ISOTHIAZOLE-PYRIDONE-AZETIDYL AND PHARMACEUTICAL COMPOSITION ON THEIR BASIS | 1991 |
|
RU2041226C1 |
AZETHIDINE DERIVATIVES OR THEIR PHARMACEUTICALLY ACCEPTABLE SALTS, METHOD OF THEIR SYNTHESIS AND COMPOSITION BASED ON THEREOF SHOWING ANTIMICROBIAL EFFECT | 1993 |
|
RU2088581C1 |
DERIVATIVES OF BENZATHIAZINES | 1991 |
|
RU2032679C1 |
PROCESS FOR PREPARING AZETIDINE DERIVATIVES OF 1,4-DIHYDRO-4-OXOQUINOLINE-3-CARBOXYLIC ACIDS | 0 |
|
SU1731055A3 |
DERIVATIVE OF THIENYLAZOLYLALKOXYETHANEAMINE, METHOD FOR ITS PREPARING (VARIANTS), PHARMACEUTICAL COMPOSITION, INTERMEDIATE COMPOUND AND METHOD FOR ITS PREPARING (VARIANTS) | 1999 |
|
RU2213743C2 |
AGENT FOR TREATMENT OF NEUROGENIC INFLAMMATION | 1999 |
|
RU2212237C2 |
METHOD OF SEPARATING CARBINOLS | 1996 |
|
RU2162464C2 |
METHOD FOR PREPARING RACEMIC AND PURE ENANTIOMERS OF DERIVATIVES OF 1,5-DIARYL-3-TRIFLUOROMETHYL-2-PYRAZOLINES | 2002 |
|
RU2288915C2 |
BENZIMIDAZOLE DERIVATIVES SHOWING ANTIHISTAMINE ACTIVITY | 1991 |
|
RU2024519C1 |
ANTIBACTERIAL COMPOUND NITRATE SALTS | 2001 |
|
RU2288231C2 |
Authors
Dates
1995-09-27—Published
1991-09-18—Filed