Abstract:
7- OR 8-TRIFLUOROMETHYL-QUINOLINES OF THE FORMULA
WHEREIN N IS 1 OR 2 AND R is selected from the group consisting of saturated and unsaturated heterocyclic having an oxygen atom, a nitrogen atom or both a nitrogen and oxygen atom and their non-toxic, pharmaceutically acceptable acid addition salts having analgesic and anti-inflammatory activity and their preparation.
Abstract:
3-AMINO-4,4-DIHALO-5-PYRAZOLONES OF THE FORMULA
1-Y,3-(R-N(-R1)-),4-X,4-X'',5-(O=)-2-PYRAZOLINE
WHEREIN X AND X'' ARE SELECTED FRO THE GROUP CONSISTING OF CHLORINE AND BROMINE, Y IS SELECTED FROM THE GROUP CONSISTING OF ALKYL, CYCLOALKYL, AND ARYL WHICH MAY BE SUBSTITUTED AND R AND R1 ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, ALKYL, ARYL, CYCLOALKYL AND ARALKYL WHICH POSSES; FUNGICIDAL ACTIVITY AND THEIR PREPARATION.
Abstract:
7- OR 8-TRIFLUOROMETHYL-QUINOLINES OF THE FORMULA
WHEREIN N IS 1 OR 2 AND R is morpholino and their non-toxic, pharmaceutically acceptable acid addition salts having analgesic and anti-inflammatory activity and their preparation.
WHEREIN N IS AN INTEGER FROM 0 TO 10 AND R IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN AND HYDROXYL HAVING ANTI-INFLAMMATORY ACTIVITY AND THEIR PREPARATION.
WHEREIN THE CF3 RADICAL IS IN THE 7 OR 8-POSITION, R AND R'' ARE HYDROGEN AND TAKEN TOGETHER FORM A KETONIDE OF THE FORMULA
-C(-P)(-Q)-
P AND O BEING SELECTED FROM THE GROUP COSISTING OF ALKYL ARALKYL AND ARYL AND THE NON-TOXIC, PHARMACEUTICALLY ACCEPTABLE ADDITION SALTS WHEN R AND R'' ARE HYDROGEN'', WHICH POSSESS NOTABLE ANTI-INFLAMMATORY ACTIVITY AND INTENSE ANALGESIC ACTIVITY.