HRID1782772

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2724641

未命名化合物

结构：CCOC(=O)c1ccc(OCCCc2ccc(OCc3ccc(-c4ccccc4)cc3)cc2)c(C(=O)O)c1

HCID57589042

未命名化合物

PRODUCTS

生成物

结构：CCOC(=O)c1ccc(OCCCc2ccc(OCc3ccc(-c4ccccc4)cc3)cc2)c(C(=O)N[C@@H]2CCCC[C@@H]2C(=O)OCC)c1

HCID57589228

未命名化合物

PROCEDURE

实验过程

The compound is prepared in analogy to the process described in Example 6 from 2-{3-[4-(1,1′-biphenyl-4-ylmethoxy)phenyl]propoxy}-5-(ethoxycarbonyl)benzoic acid and ethyl cis-2-amino-1-cyclohexanecarboxylate hydrochloride.

WORKUP

后处理

customThe compound is prepared in analogy to the process

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-969d106c55664a6ea8e261b2cbb9ca78
来源数据集: uspto-grants-2009_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07498460B2
来源说明: uspto-grants-2009_03

反应 SMILES

[C:1]1([C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)[CH:6]=[CH:5][C:4]([CH2:7][O:8][C:9]2[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][CH2:17][O:18][C:19]3[CH:27]=[CH:26][C:25]([C:28]([O:30][CH2:31][CH3:32])=[O:29])=[CH:24][C:20]=3[C:21](O)=[O:22])=[CH:11][CH:10]=2)=[CH:3][CH:2]=1.Cl.[NH2:40][C@H:41]1[CH2:46][CH2:45][CH2:44][CH2:43][C@H:42]1[C:47]([O:49][CH2:50][CH3:51])=[O:48]>>[C:1]1([C:33]2[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=2)[CH:2]=[CH:3][C:4]([CH2:7][O:8][C:9]2[CH:10]=[CH:11][C:12]([CH2:15][CH2:16][CH2:17][O:18][C:19]3[CH:27]=[CH:26][C:25]([C:28]([O:30][CH2:31][CH3:32])=[O:29])=[CH:24][C:20]=3[C:21]([NH:40][C@@H:41]3[CH2:46][CH2:45][CH2:44][CH2:43][C@@H:42]3[C:47]([O:49][CH2:50][CH3:51])=[O:48])=[O:22])=[CH:13][CH:14]=2)=[CH:5][CH:6]=1