Abstract:
LOWER ALKYL ESTERS OF FLAVONE-7-OXYACETIC ACID ARE MADE BY REACTING CHLOROACETONITRILE WITH RESACETOPHENONE TO GIVE 2''-HYDROXY-4''-XYANOMETHOXY ACETOPHENONE, REACTING THE LATTER COMPOUND WITH BENZOYL CHLORIDE TO GIVE 1-(2HYDROXY-4-CYANOMETHOXY PHENYL)-3-PHENYL PROPANE-1,3DIONE AND THEN REACTING THE LATTER COMPOUND WITH AN ANHYDROUS LOWER ALKANOL IN THE PRESENCE OF A MINERAL ACID.
Abstract:
N-ALKYL- AND N-(SUBSTITUTED ALKYL)-DIMETHYLAMINES ARE PREPARED BY REACTING AN UNSUBSTITUTED OR SUBSTITUTED ALKYL HALIDE WITH DIMETHYLAMINE IN AN AQUEOUS MEDIUM FREE FROM ORGANIC SOLVENT AND AT A TEMPERATURE NOT HIGHER THAN ABOUT 30*C.
Abstract:
3-PROPIONYLSALICYLIC ACID IS MADE BY ISOMERISING 2-HYDROXY - 3 - ALLYLPROPIOPHENONE TO 2-HYDROXY-3-PROPENYLPROPIOPHENONE, OXIDIZING THE LATTER TO 3-PROPIONYLSALICYLIC ALDEHYDE AND OXIDIZING THE LATTER TO 3-PROPIONYLSALICYLIC ACID. THIS PRODUCT CAN BE CONVERTED TO LOWER ALKYL ESTERS WHICH CAN BE USED FOR THE PRODUCTION OF 3-METHYLFLAVONE-8-CARBOXYLIC ACID AND ITS ESTERS, PARTICULARLY THE AMINOALKYL ESTERS WHICH ARE THERAPEUTICALLY ACTIVE.
Abstract:
A 3- OR 4-OXO-DIHYDROBENZOLTHIAZINE-S-DIOXIDE OF THE GENERAL FORMULA:
X IN WHICH EITHER X OF Y STAND FOR A SINGLE BOND AND THE OTHER STANDS FOR METHYLENE (CH2) AND R REPRESENTS HYDROGEN OR ALKYL, ALKENYL, PROPARGYL, BENZYL, CARBETHOXY, DIALKYL AMINOALKYL OR CYCLOAMINOALKYL OR A GROUP OF THE FORMULA -CH2-COOR1, IN WHICH R1 REPRESENTS HYDROGEN OR ALKYL, DIALKYLAMINOALKYL OR CYCLOAMINOALKYL, OR R REPRESENTS A GROUP OF THE FORMULA:
-CH2-CO-N(-R2)(-R3)
IN WHICH R2 AND R3 ARE IDENTICAL OR DIFFERENT AND EACH REPRESENT HYDROGEN, ALKYL OR ALKENYL OR DIALKYLAMINOALKYL OR CYCLOAMINO-ALKYL GROUP OR, TOGETHER WITH THE NITROGEN ATOM TO WHICH THEY ARE ATTACHED, FORM A HETEROCYCLIC AMINO GROUP, OR R REPRESENTS AN UNSUBSTITUTED PHENYL AND OR AOR A CHLORO-SUBSTITUTED OR SULFAMYL-SUBSTITUTED PHENYL AND METHODS FOR THE PREPARATION THEREOF. THESE COMPOUNDS ARE THERAPEUTICALLY ACTIVE PARTICULARLY ON THE CENTRAL NERVOUS SYSTEM, E.G., HYPNOTIC ACTIVITY.