【摘要】 以（2R,3R,4R,5S）-3,4,5-三（苄氧基）-2-（（苄氧基）甲基）哌啶盐酸盐为起始原料，与取代苯乙酮及多聚甲醛在无水乙醇中经曼尼希反应缩合得到中间体1-（4-取代苯基）-3-（（2R,3R,4R,5S）-3,4,5-三（苄氧基）-2-（（苄氧基）甲基）哌啶-1-基）丙烷-1-酮，该中间体经Pd（OH）₂/C加氢、脱苄、脱氧得到1-脱氧野尻霉素（DNJ）的N-取代苯丙烷衍生物，总收率36.8%～46.8%,并通过¹HNMR、¹³CNMR、LC-MS对产物结构进行了确证。更多还原

【Abstract】 Firstly, we synthesized the intermediate of 1-（4-substituted phenyl）-3-（（2R,3R,4R,5S）-3,4,5-tri（benzyloxy）-2-（（benzyloxy）methyl）piperidine-1-yl）propane-1-one from（2R,3R,4R,5S）-3,4,5-tri（benzyloxy）-2-（（benzyloxy）methyl）piperidine hydrochloride, substituted acetophenone, and paraformaldehyde by Mannich reaction in ethanol.Then, we synthesized the N-substituted phenylpropane derivatives of 1-deoxynojirimycin（DNJ） by Pd（OH）₂/C hydrogenation, debenzylation, and deoxygenation from the intermediate.The total yield can reach 36.8%-46.8%.Moreover, the structures of the products are confirmed by ¹HNMR,¹³CNMR,and LC-MS.更多还原