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止吐药昂丹司琼的合成[J]. 中国药科大学学报, 1999, (4): 6-8.
引用本文: 止吐药昂丹司琼的合成[J]. 中国药科大学学报, 1999, (4): 6-8.
Synthesis of Ondansetron Hydrochloride[J]. Journal of China Pharmaceutical University, 1999, (4): 6-8.
Citation: Synthesis of Ondansetron Hydrochloride[J]. Journal of China Pharmaceutical University, 1999, (4): 6-8.

止吐药昂丹司琼的合成

Synthesis of Ondansetron Hydrochloride

  • 摘要: 以1 ,3环己二酮为起始原料,形成单苯腙后,经过环合、甲基化得9甲基1 ,2 ,3 ,9四氢4 H咔唑4酮(3) ,与吗啉及多聚甲醛进行 Mannich 反应,再与2甲基咪唑反应、成盐得标题化合物,总收率为491 % 。

     

    Abstract: An improved process for the preparation of ondansetron hydrochloride (1) is described . Compound 1 wassynthesized from 1 ,2 ,3 ,9 tetrahydro 9 methyl 4 H carbazol 4 one(3) by Mannich reaction and condensation with 2 methylimidazole . The compou

     

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