Expedient protocols based on the versalility of oxo ketenedithio acetals in synthesis ,has been develop ed to the preparation of the library of many amino acids and sulpha drugs embellished analogues of the privilege d 1,4 benzodiazepines for their possible use as CCK A antagonists .The process to its preparation proce eded with the reaction of 3-oxoketene dithio acetal analogues of 1,4 benzodiazepin-2- one with amino acids and sulp ha drugs followed by treatment of the resulting species with alkali to deliver 3(a-d) ,4(a-b), 5(e-f) and (6 c- d) respectively ,in acceptable yields
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