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【结 构 式】

【分子编号】24247

【品名】4-chloro-2-methyl-N-[(E)-benzylidene]-2-butanamine

【CA登记号】

【 分 子 式 】C12H16ClN

【 分 子 量 】209.71848

【元素组成】C 68.73% H 7.69% Cl 16.9% N 6.68%

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:(II)

The reaction of 1-(1-propen-2-yl)-2 benzimidazolinone (I) in hexamethylphosphorus triamide with sodium hydride and 3-benzalamino-3,3-dimethylpropyl chloride (II) and treating the reaction product with hydrochloric acid gives 1-(3 amino-3,3-dimethylpropyl)-2 benzimidazolone (III). The amine (III) is refluxed with 1-(1-naphthyloxy)propylene-(2,3)-oxide (IV) yielding the title compound.

1 Hoefke, W.; et al. (Boehringer Ingelheim GmbH); 1-Aryloxy-2-hydroxy-3-[(benzimidazolin-one-substituted alkyl)-amino]-propanes and salts thereof. DE 2644833 .
2 Mentrup, A.; Palluk, R.; Gaida, W.; Hoefke, W.; Adimolol hydrochloride hydrate. Drugs Fut 1986, 11, 1, 9.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(I) 24246 1-isopropenyl-1,3-dihydro-2H-benzimidazol-2-one C10H10N2O 详情 详情
(II) 24247 4-chloro-2-methyl-N-[(E)-benzylidene]-2-butanamine C12H16ClN 详情 详情
(III) 24248 1-(3-amino-3-methylbutyl)-1,3-dihydro-2H-benzimidazol-2-one C12H17N3O 详情 详情
(IV) 22937 2-[(1-naphthyloxy)methyl]oxirane; 1-naphthyl 2-oxiranylmethyl ether C13H12O2 详情 详情
Extended Information