【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