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【结 构 式】

【分子编号】48622

【品名】N-[2-hydroxy-2-(3,4,5-trimethoxyphenyl)ethyl]-1-methyl-1H-indole-5-carboxamide

【CA登记号】

【 分 子 式 】C21H24N2O5

【 分 子 量 】384.43204

【元素组成】C 65.61% H 6.29% N 7.29% O 20.81%

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:(VIII)

In a closely related procedure, amino alcohol (III) was coupled with 1-methyl-5-indolecarboxylic acid (VII) to afford amide (VIII). This was then cyclized to the target oxazoline by using the Burgess reagent.

1 Liu, G.; Jae, H.-S.; Szczepankiewicz, B.G.; et al.; New antimitotic agents with activity in multi-drug-resistant cell lines and in vivo efficacy in murine tumor models. J Med Chem 2001, 44, 25, 4416.
2 Sorensen, B.K.; Liu, G.; Tasker, A.S.; et al.; Antimitotic agents with activity in multidrug-resistant tumor cell lines. 221st ACS Natl Meet (April 1 2001, San Diego) 2001, Abst MEDI 139.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(III) 48617 2-amino-1-(3,4,5-trimethoxyphenyl)-1-ethanol C11H17NO4 详情 详情
(VII) 48621 1-methyl-1H-indole-5-carboxylic acid C10H9NO2 详情 详情
(VIII) 48622 N-[2-hydroxy-2-(3,4,5-trimethoxyphenyl)ethyl]-1-methyl-1H-indole-5-carboxamide C21H24N2O5 详情 详情
Extended Information