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【结 构 式】

【分子编号】33967

【品名】1-chloro-3-(3-methylphenoxy)-2-propanol

【CA登记号】

【 分 子 式 】C10H13ClO2

【 分 子 量 】200.66472

【元素组成】C 59.86% H 6.53% Cl 17.67% O 15.95%

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:(IV)

The condensation of 3-methylphenol (I) with epichlorohydrin (II) by means of a catalytic amount of piperidine gives 1-(3-methylphenoxy)-3-chloro-2-propanol (IV), which is then condensed with 3,4-dimethoxyphenylethylamine (V) by heating their mixture at 95-100 C.

1 Holmes, A.; Meyer, R.F.; New aminoalkanol compounds and methods for their production. FR 2163486; GB 1344976; JP 48067232 .
2 Milton, L.H.; et al.; Cardioselective beta-adrenergic blocking agents. 1. 1-[3,4-(dimethoxyphenethyl)amino]-3-aryloxy-2-propanols. J Med Chem 1975, 18, 2, 148-152.
3 Castaner, J.; Weetman, D.F.; Bevantol. Drugs Fut 1977, 2, 8, 500.
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) 17793 m-cresol; m-Methylphenol 108-39-4 C7H8O 详情 详情
(II) 10146 Epichlorohydrin; 2-(Chloromethyl)oxirane 106-89-8 C3H5ClO 详情 详情
(IV) 33967 1-chloro-3-(3-methylphenoxy)-2-propanol C10H13ClO2 详情 详情
(V) 10098 2-(3,4-Dimethoxyphenyl)-1-ethanamine; 3,4-Dimethoxyphenethylamine; 2-(3,4-Dimethoxyphenyl)ethylamine 120-20-7 C10H15NO2 详情 详情
Extended Information