HRID260860

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID22400458

未命名化合物

HCID22400462

未命名化合物

结构：CCCCCCCC(=CC(=O)c1c[nH]c2ccccc12)CCCCCCC

HCID22400518

未命名化合物

PRODUCTS

生成物

结构：CCCCCCCC(=CC(=O)c1cn(CCCC(=O)OCc2ccc(OC)cc2)c2ccccc12)CCCCCCC

HCID22400467

未命名化合物

PROCEDURE

实验过程

The procedure of Ex. 1 was repeated except that 3-(3-heptyl-2-decenoyl)indole obtained in Pre. Ex. 26 was used in place of 3-heptanoylindole, and 4-methoxybenzyl 4-bromobutyrate was used in place of 4-bromobutyrate to give 4-methoxybenzyl 4-[3-(3-heptyl-2-decenoyl)-1-indolyl]butyrate as an oil.

WORKUP

后处理

customobtained in Pre

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-5703ae5ba6714d25842f56e99bf9c614
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:8]([CH2:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27])=[CH:9][C:10]([C:12]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[NH:14][CH:13]=1)=[O:11])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7].C(C1C2C(=CC=CC=2)NC=1)(=O)CCCCCC.Br[CH2:46][CH2:47][CH2:48][C:49]([O:51][CH2:52][C:53]1[CH:58]=[CH:57][C:56]([O:59][CH3:60])=[CH:55][CH:54]=1)=[O:50]>>[CH2:21]([C:8]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH3:7])=[CH:9][C:10]([C:12]1[C:20]2[C:15](=[CH:16][CH:17]=[CH:18][CH:19]=2)[N:14]([CH2:46][CH2:47][CH2:48][C:49]([O:51][CH2:52][C:53]2[CH:58]=[CH:57][C:56]([O:59][CH3:60])=[CH:55][CH:54]=2)=[O:50])[CH:13]=1)=[O:11])[CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH3:27]