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A process for the preparation of 5-substituted 5,10-dihydro-11H-dibenzo (b, e) (1,4) diazepin-11-ones or 11-substituted 5, 11-dihydro-6H-pyrido (2,3-b ) (1,4) benzodiazepin-6-ones or acid addition salts thereof.
A process for the preparation of 5-substituted 5,10-dihydro-11H-dibenzo (b, e) (1,4) diazepin-11-ones or 11-substituted 5, 11-dihydro-6H-pyrido (2,3-b ) (1,4) benzodiazepin-6-ones or acid addition salts thereof.
Compounds of the formula WHEREIN R1 is hydrogen or alkyl of one to four carbon atoms, R2 and R3 are each hydrogen or halogen, Y is nitrogen or -CH-, and A is alkylene of one to two carbon atoms, AND THEIR NON-TOXIC, PHARMACOLOGICALLY ACCEPTABLE ACID ADDITION SALTS; THE COMPOUNDS AS WELL AS THEIR SALTS ARE USEFUL AS ULCER INHIBITORS AND STOMACH JUICE SECRETION INHIBITORS IN WARM-BLOODED ANIMALS.
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