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【结 构 式】

【分子编号】62796

【品名】2-chloro-1-methyl-1H-benzimidazole

【CA登记号】

【 分 子 式 】C8H7ClN2

【 分 子 量 】166.60976

【元素组成】C 57.67% H 4.23% Cl 21.28% N 16.81%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(VII)

Alkylation of 2-chlorobenzimidazole (VI) with iodomethane and NaOH leads to 2-chloro-1-methylbenzimidazole (VII). The 2-chloro group of (VII) is then displaced with hydrazine hydrate to afford hydrazine (VIII). Finally, condensation between ketone (V) and hydrazine (VIII) gives rise to the target hydrazone.

1 Easmon, J.; Fürtinger, S.; Lackner, G. ; Magreiter, E.; Hofmann, J.; Heinisch, G.; Puerstinger, G.; Hydrazones derived from monosubstitued 2-acetylpyridines and 2-hydrazino-1-methylbenzimidazole: Synthesis and biological studies. Eur J Cancer 2002, 38, Suppl. 7.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(V) 62795 1-(5-methyl-2-pyridinyl)-1-ethanone C8H9NO 详情 详情
(VI) 26761 2-chloroimidazo[1,2-a]pyridine; 2-chlorobenzimidazole; 2-Amino-4'-chlorodiphenylether; 2-Aminodiphenylether; 2-chloro-1H-benzimidazole 4857-06-1 C7H5ClN2 详情 详情
(VII) 62796 2-chloro-1-methyl-1H-benzimidazole C8H7ClN2 详情 详情
(VIII) 62797 2-hydrazino-1-methyl-1H-benzimidazole C8H10N4 详情 详情
Extended Information