HRID260842

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CCCC(CCCCCCC(=O)c1cn(CCCC(=O)OCC)c2ccccc12)c1ccc(CC(C)C)cc1

HCID22400460

未命名化合物

结构：CCCCC(CCCCC(=O)c1cn(CCCC(=O)OCC)c2ccccc12)c1ccc(CC(C)C)cc1

HCID22400512

未命名化合物

PRODUCTS

生成物

结构：CCCCC(CCCCC(=O)c1cn(CCCC(=O)O)c2ccccc12)c1ccc(CC(C)C)cc1

HCID22400557

未命名化合物

PROCEDURE

实验过程

The procedure of Ex. 16 was repeated except that ethyl 4-[3-[6-(4-isobutylphenyl)decanoyl]-1-indolyl]butyrate obtained in Ex. 17 was used in place of ethyl 4-[3-[8-(4-isobutylphenyl)undecanoyl]-1-indolyl]butyrate to give 4-[3-[6-(4-isobutylphenyl)decanoyl]-1-indolyl]butyric acid.

WORKUP

后处理

customobtained in Ex

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-772f585fc77142d389c3d6973277174b
来源数据集: uspto-grants-1996_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05530019
来源说明: uspto-grants-1996_06

反应 SMILES

[CH2:1]([C:5]1[CH:10]=[CH:9][C:8]([CH:11]([CH2:35][CH2:36][CH2:37][CH3:38])[CH2:12][CH2:13][CH2:14][CH2:15][C:16]([C:18]2[C:26]3[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=3)[N:20]([CH2:27][CH2:28][CH2:29][C:30]([O:32]CC)=[O:31])[CH:19]=2)=[O:17])=[CH:7][CH:6]=1)[CH:2]([CH3:4])[CH3:3].C(C1C=CC(C(CCC)CCCCCCC(C2C3C(=CC=CC=3)N(CCCC(OCC)=O)C=2)=O)=CC=1)C(C)C>>[CH2:1]([C:5]1[CH:10]=[CH:9][C:8]([CH:11]([CH2:35][CH2:36][CH2:37][CH3:38])[CH2:12][CH2:13][CH2:14][CH2:15][C:16]([C:18]2[C:26]3[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=3)[N:20]([CH2:27][CH2:28][CH2:29][C:30]([OH:32])=[O:31])[CH:19]=2)=[O:17])=[CH:7][CH:6]=1)[CH:2]([CH3:3])[CH3:4]