HRID1985119

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：COc1ccc(CN2CC(CCOS(=O)(=O)c3ccc(C)cc3)N(C)C2=O)cc1

HCID57719164

未命名化合物

HCID68742930

未命名化合物

PRODUCTS

生成物

结构：CCCc1cc(OC(C)(C)C(=O)OCC)ccc1OCCC1CN(Cc2ccc(OC)cc2)C(=O)N1C

HCID68866714

未命名化合物

PROCEDURE

实验过程

The titled compound is prepared, according to the procedure of Example 1, Step A, using toluene-4-sulfonic acid 2-[1-(4-methoxy-benzyl)-3-methyl-2-oxo-imidazolidin-4-yl]-ethyl ester (0.200 g, 0.478 mmole) and 2-(4-hydroxy-3-propyl-phenoxy)-2-methyl-propionic acid ethyl ester (0.140 g, 0.526 mmole) to produce a colorless oil (0.122 g, 50%). Mass [EI+] 513 (M+H)+.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-77f50433312a4ab285bbd0af5fc0a025
来源数据集: uspto-grants-2009_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07544812B2
来源说明: uspto-grants-2009_06

反应 SMILES

[CH3:1][O:2][C:3]1[CH:29]=[CH:28][C:6]([CH2:7][N:8]2[CH2:12][CH:11]([CH2:13][CH2:14][O:15]S(C3C=CC(C)=CC=3)(=O)=O)[N:10]([CH3:26])[C:9]2=[O:27])=[CH:5][CH:4]=1.[CH2:30]([O:32][C:33](=[O:48])[C:34]([O:37][C:38]1[CH:43]=[CH:42][C:41](O)=[C:40]([CH2:45][CH2:46][CH3:47])[CH:39]=1)([CH3:36])[CH3:35])[CH3:31]>>[CH2:30]([O:32][C:33](=[O:48])[C:34]([O:37][C:38]1[CH:43]=[CH:42][C:41]([O:15][CH2:14][CH2:13][CH:11]2[CH2:12][N:8]([CH2:7][C:6]3[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:29][CH:28]=3)[C:9](=[O:27])[N:10]2[CH3:26])=[C:40]([CH2:45][CH2:46][CH3:47])[CH:39]=1)([CH3:35])[CH3:36])[CH3:31]