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【结 构 式】

【分子编号】49089

【品名】2-[1-(6-methyl-3-pyridazinyl)-4-piperidinyl]-1-ethanol

【CA登记号】

【 分 子 式 】C12H19N3O

【 分 子 量 】221.30248

【元素组成】C 65.13% H 8.65% N 18.99% O 7.23%

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)

Treatment of 4-hydroxybenzaldehyde (I) with O-ethylhydroxylamine produced the corresponding O-ethyloxime (II). Coupling of (II) with alcohol (III) under Mitsunobu conditions then gave the title ether.

1 Wu, W.-Y.; Watson, K.; Jin, B.; Krippner, G.; McConnell, D. (Biota Scientific Management Pty Ltd.); Antiviral agents. WO 0078746 .
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) 13433 4-Hydroxybenzaldehyde; p-Hydroxybenzaldehyde 123-08-0 C7H6O2 详情 详情
(II) 49088 4-hydroxybenzaldehyde O-ethyloxime C9H11NO2 详情 详情
(III) 49089 2-[1-(6-methyl-3-pyridazinyl)-4-piperidinyl]-1-ethanol C12H19N3O 详情 详情
Extended Information