O-[(5-chlorothiophen-2-yl)methyl]hydroxylamine → HCID 11406179,化合物
反应方程式
FC1C(O[C:9](=[O:24])[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[NH:16][CH2:17][C:18]2[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=2)=C(F)C(F)=C(F)C=1F.[Cl:29][C:30]1[S:34][C:33]([CH2:35][O:36][NH2:37])=[CH:32][CH:31]=1>>[Cl:29][C:30]1[S:34][C:33]([CH2:35][O:36][NH:37][C:9](=[O:24])[C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=2[NH:16][CH2:17][C:18]2[CH:19]=[CH:20][N:21]=[CH:22][CH:23]=2)=[CH:32][CH:31]=1参与物
3
实验过程
Prepared by the same method as described for example 415. Starting materials: 2-[(Pyridin-4-ylmethyl)-amino]-benzoic acid pentafluorophenyl ester (preparation 7C) and O-(5-chloro-thiophen-2-ylmethyl)-hydroxylamine (see preparation 64).
后处理
- customPrepared by the same method
来源与证据
- ORD记录
- ord-271c68b0bd4446229fa4011e0fceeea4
- 来源数据集
- uspto-grants-2011_10
- 专利号
- US08034811B2
反应笔记
加载中…