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【结 构 式】

【分子编号】39009

【品名】4-[2-(1H-imidazol-1-yl)ethoxy]benzamide

【CA登记号】

【 分 子 式 】C12H13N3O2

【 分 子 量 】231.25424

【元素组成】C 62.33% H 5.67% N 18.17% O 13.84%

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:(III)

This compound can be obtained in several different ways: 1) The condensation of imidazole (I) with 4-(2-chloroethoxy)benzamide (II) by means of NaH in DMF gives 1-[2-(4-carbamoylphenoxy)ethyl]imidazole (III), which is hydrolyzed by refluxing with 5N aqueous HCl. 2) Esters of 4-(2-chloroethoxy)benzoic acid (IV) can also be used instead of (II) in the first step of the synthesis. 3) This compound can also be obtained by direct condensation of imidazole (I) with 4-(2-chloroethoxy)benzoic acid (IV) by means of NaH in THF.

1 DE 2950019 .
2 Sneddon, J.; Castaner, J.; UK-37,248-01. Drugs Fut 1981, 6, 11, 693.
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) 10255 Imidazole; 1H-Imidazole 288-32-4 C3H4N2 详情 详情
(II) 39008 4-(2-chloroethoxy)benzamide C9H10ClNO2 详情 详情
(III) 39009 4-[2-(1H-imidazol-1-yl)ethoxy]benzamide C12H13N3O2 详情 详情
(IV) 39010 4-(2-chloroethoxy)benzoic acid C9H9ClO3 详情 详情
Extended Information