作者:Billy B. Wylie、Eugene I. Isaacson、Jaime N. Delgado
DOI:10.1002/jps.2600540932
日期:1965.9
were synthesized as potential medicinal agents. The esterifications were effected by treating the oximes with benzoyl, 3,4,5-trimethoxybenzoyl, and diphenylcarbamyl chlorides. The O -alkylations of benzophenone oxime and dibenzosuberone oxime were accomplished by the nucleophilic substitution of γ -dimethylaminopropyl, β -dimethylaminoethyl, and benzyl chlorides. In the course of this investigation,
合成了二苯甲酮肟和二苯并亚甲基酮肟的酯和醚作为潜在的药物。通过用苯甲酰基,3,4,5-三甲氧基苯甲酰基和二苯基氨基甲酰氯处理肟来进行酯化。二苯甲酮肟和二苯并亚甲基酮肟的O-烷基化是通过γ-二甲基氨基丙基,β-二甲基氨基乙基和苄基氯的亲核取代实现的。在此研究过程中,制备了13种化合物用于药理评估。