HRID332704

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID552072

2-(3-Chloropropyl)-1,3-dioxolane

C6H11ClO2

结构：CC(C)(C)OC(=O)NC(c1ccccc1)c1cccc(OCc2ccc(C(=O)O)cc2)c1

HCID71093158

未命名化合物

PRODUCTS

生成物

结构：CC(C)(C)OC(=O)NC(c1ccccc1)c1cccc(OCc2ccc(C(=O)OCCCC3OCCO3)cc2)c1

HCID71093448

未命名化合物

PROCEDURE

实验过程

The title compound was prepared from 4-((3-(((tert-butoxycarbonyl)amino)-(phenyl)methyl)phenoxy)methyl)benzoic acid and 2-(3-chloropropyl)-1,3-dioxolane according to the method of Chiral Example 5 Step 1.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-69658d2672a74654830c239efa1b0306
来源数据集: uspto-grants-2014_11
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08877774B2
来源说明: uspto-grants-2014_11

反应 SMILES

[C:1]([O:5][C:6]([NH:8][CH:9]([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[C:10]1[CH:11]=[C:12]([CH:24]=[CH:25][CH:26]=1)[O:13][CH2:14][C:15]1[CH:23]=[CH:22][C:18]([C:19]([OH:21])=[O:20])=[CH:17][CH:16]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].Cl[CH2:34][CH2:35][CH2:36][CH:37]1[O:41][CH2:40][CH2:39][O:38]1>>[C:1]([O:5][C:6]([NH:8][CH:9]([C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[C:10]1[CH:11]=[C:12]([CH:24]=[CH:25][CH:26]=1)[O:13][CH2:14][C:15]1[CH:23]=[CH:22][C:18]([C:19]([O:21][CH2:34][CH2:35][CH2:36][CH:37]2[O:41][CH2:40][CH2:39][O:38]2)=[O:20])=[CH:17][CH:16]=1)=[O:7])([CH3:4])([CH3:2])[CH3:3]