HRID892895

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CC(=O)OCC(C)(C)C(OC(C)=O)C(=O)NCCC(=O)O

HCID19893582

未命名化合物

$结构：CCCCCCCC/C=C\CCCCCCCC(=O)Nc1ccc(O)cc1$

HCID67633947

未命名化合物

PRODUCTS

生成物

$结构：CCCCCCCC/C=C\CCCCCCCC(=O)Nc1ccc(OC(=O)CCNC(=O)C(OC(C)=O)C(C)(C)COC(C)=O)cc1$

HCID67795591

未命名化合物

收率 45.3%

PROCEDURE

实验过程

4-Oleoylaminophenol (372 mg) and 259 mg of 3-[N-(2,4-diacetoxy-3,3-dimethyl-1-oxobutyl)amino]propionic acid were reacted in the same manner as in Example 1 to obtain 255 mg of the title compound (yield: 39%).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-a058bd1956724a7ab3ceb97f5e11439b
来源数据集: uspto-grants-1992_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05120738
来源说明: uspto-grants-1992_06

反应 SMILES

[C:1]([NH:20][C:21]1[CH:26]=[CH:25][C:24]([OH:27])=[CH:23][CH:22]=1)(=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18].[C:28]([O:31][CH:32]([C:41]([CH3:48])([CH3:47])[CH2:42][O:43][C:44](=[O:46])[CH3:45])[C:33]([NH:35][CH2:36][CH2:37][C:38](O)=[O:39])=[O:34])(=[O:30])[CH3:29]>>[C:28]([O:31][CH:32]([C:41]([CH3:48])([CH3:47])[CH2:42][O:43][C:44](=[O:46])[CH3:45])[C:33]([NH:35][CH2:36][CH2:37][C:38]([O:27][C:24]1[CH:25]=[CH:26][C:21]([NH:20][C:1](=[O:19])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8]/[CH:9]=[CH:10]\[CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH2:16][CH2:17][CH3:18])=[CH:22][CH:23]=1)=[O:39])=[O:34])(=[O:30])[CH3:29]