WHERIN X AND X'' MAY BE DIFFERENT AND ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, HALOGEN, ALKYL, ALKOXY, TRIHALOMETHYL AND NITRO, R IS SELECTED FROM THE GROUP CONSISTING OF -COOH, -COOR'', AND
-CO-N(-A)-B
R'' IS SELECTED FROM THE GROUP CONSISTING OF ALIPHATIC AND HHDROXYLATED RESIDUE OF A GLYCOL, A AND B ARE SELECTED FROM THE GROUP CONSISTING OF HYDROGEN AND OPTIONALLY SUBSTITUTED ALIPHATIC AND R1 IS SELECTED FROM THE GROUP CONSISTING OF HYDROGEN, LOWER ALIPHATIC HDROCARBON, UNSUBSTITUTED AND POLYSUBSTITUTED ARYL, ARYLALIPHATIC, A THIENYL, A B-PYRIDYL AND A FURYL WITH THE PROVISO THAT WHEN R1 IS PHENYL, X'' AND X ARE OTHER THAN HALOGEN, ALKOXY AND TRIFLUROMETHYL WHICH COMPOUNDS POSSESS ANTI-INFLAMMATORY AND ANTIVIRAL ACTIVITY AND A NOVEL PROCESS FOR THEIR PREPARATION.
Abstract:
5-THIAZOL CARBOXYLATES OF THE FORMULA WHEREIN R is an alkali-metal atom, the residue of an organic base or the alkyl radical of an aliphatic, arylaliphatic or alkylheterocyclic alcohol having hypolipemiant activity and their preparation.
Abstract:
WHEREIN R is selected from the group consisting of hydrogen, alkyl of one to seven carbon atoms and acyl of an organic carboxylic acid of one to 18 carbon atoms, R1 and R2 are selected from the group consisting of hydrogen, substituted and unsubstituted alkyl of one to seven carbon atoms, aryl and cycloalkyl and when taken together with the nitrogen atom form a heterocyclic which may contain another heteroatom, which products possess outstanding choleretic properties far superior to dehydrocholic acid. The invention also relates to a novel process and novel intermediate for the preparation of the said benzamides of Formula I.
An amide of 2-hydroxy-3-methoxy-5-allyl-benzoic acid of the formula