HRID260851

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(OCCC(=O)c1cn(CCCC(=O)OCC)c2ccccc12)c1ccc(CC(C)C)cc1

HCID22400508

未命名化合物

PRODUCTS

生成物

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

HCID22400541

未命名化合物

PROCEDURE

实验过程

The procedure of Ex. 16 was repeated except that ethyl 4-[3-[3-[1-(4-isobutylphenyl)pentyloxy]propionyl]-1-indolyl]butyrate obtained in Ex. 34 was used in place of ethyl 4-[3-[8(4-isobutylphenyl)undecanoyl]-1-indolyl]butyrate to give 4-[3-[3-[1-(4-isobutylphenyl)pentyloxy]propionyl]-1-indolyl]butyric acid as an oil.

WORKUP

后处理

customobtained in Ex

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-960bcc4290054cab960b7eeba1546b3e
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]([O:16][CH2:17][CH2:18][C:19]([C:21]2[C:29]3[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=3)[N:23]([CH2:30][CH2:31][CH2:32][C:33]([O:35]CC)=[O:34])[CH:22]=2)=[O:20])[CH2:12][CH2:13][CH2:14][CH3:15])=[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:6]=[CH:7][C:8]([CH:11]([O:16][CH2:17][CH2:18][C:19]([C:21]2[C:29]3[C:24](=[CH:25][CH:26]=[CH:27][CH:28]=3)[N:23]([CH2:30][CH2:31][CH2:32][C:33]([OH:35])=[O:34])[CH:22]=2)=[O:20])[CH2:12][CH2:13][CH2:14][CH3:15])=[CH:9][CH:10]=1)[CH:2]([CH3:4])[CH3:3]