Abstract:
Production of carbonyl compounds substituted in the Alpha position and having the formula
WHEREIN R1 is alkyl, aralkyl, phenyl, toluyl, naphthyl, alkoxy or amino; R2 is hydrogen,
A is hydrogen, alkyl, halo or
R6 is hydrogen or methyl; and R11 is alkyl, wherein said compounds are formed by reacting a sulfur ylide having the formula
WHEREIN Y is the radical
AND R9 and R10 are alkyl or phenyl, with a solution containing both an electrophilic agent A1 that is converted into the radical A and a nucleophilic agent B1 that is converted into the radical B; and said carbonyl compounds having the formula
WHEREIN Z is nitrile, carboxyl, or carboxyl esterified with an alkanol.
Abstract:
NEW 6-ACYLAMINOPHENYL-4,5-DIHYDROPYRIDAZONES BEARING A SUBSTITUENT IN THE ACYL RADICAL, METHODS FOR THEIR PRODUCTION AND THEIR USE AS MEDICAMENTS, WHICH HAVE THE EFFECT OFLOWERING BLOOD PRESSURE, DILATING THE CARONARY ARTERIES AND COMBATTING INFLAMMATION.
Abstract:
1. A PROCESS FOR THE PRODUCTION OF STERICALLY UNIFORM 4-ENDOTRICYCLO(5,2,10**2,6-ENDO)-DECYLAMINE WHICH COMPRISES: ELECTROCHEMICALLY REDUCING A COMPOUND OF THE FORMULA
2-(X-NH-)-PERHYDRO-4,7-METHANOINDENE
WHEREIN X IS HYDROGEN, HYDROXY OR -OCOR IN WHICH R IS LOWER ALKYL OF 1 TO 4 CARBON ATOMS, SAID REDUCTION BEING CARRIED OUT IN A LIQUID SOLVENT SELECTED FROM THE GROUP CONSISTING OF AN ORGANIC SOLVENT AND AN AQUEOUS ORGANIC SOLVENT REACTION MEDIUM AT A MERCURY, LEAD OR AMALGAM ELECTRODE AT A CURRENT DENSITY OF ABOUT 1 TO 20 AMPS/DM.2 AT A TEMPERATURE OF FROM -20*C. TO 40*C. AND A PH OF ABOUT 5 OR LESS; AND SEPARATING THE SUBSTANTIALLY STERICALLY UNIFORM AMINE PRODUCT FROM THE REACTION MEDIUM.
IN WHICH R IS ALKYL OF 1 TO 8 CARBON ATOMS OR SAID ALKYL MONO SUBSTITUTED BY PHENYL, METHOXY, ETHOXY OR HYDROXY; CYCLOALKYL OF 5 TO 8 CARBON ATOMS; ALLYL; OR BUTYNYL; AND THE PHARMACEUTICALLY COMPATIBLE ACID ADDITION SALTS OF SAID COMPOUND.