HRID1523080

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CCN1C(=O)C(Cc2cc(OC)c(OC)c(OC)c2)(OC(=O)c2ccccc2)c2cc(C)ccc21

HCID86300681

未命名化合物

结构：CC(C)CN1C(=O)C(OC(=O)c2ccccc2)c2cc(Cl)ccc21

HCID90418318

未命名化合物

PRODUCTS

生成物

结构：COc1cc(CC2(OC(=O)c3ccccc3)C(=O)N(CC(C)C)c3ccc(Cl)cc32)cc(OC)c1OC

HCID86300541

未命名化合物

PROCEDURE

实验过程

This compound was prepared in an analogous fashion to 1-ethyl-5-methyl-2-oxo-3-(3,4,5-trimethoxybenzyl)indolin-3-yl benzoate using 5-chloro-1-isobutyl-2-oxoindolin-3-yl benzoate.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-2dfbd889b97a42d5b44b1a7d4b3dedc4
来源数据集: uspto-grants-2015_07
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09079853B2
来源说明: uspto-grants-2015_07

反应 SMILES

C(OC1([CH2:23][C:24]2[CH:29]=[C:28]([O:30][CH3:31])[C:27]([O:32][CH3:33])=[C:26]([O:34][CH3:35])[CH:25]=2)C2C(=CC=C(C)C=2)N(CC)C1=O)(=O)C1C=CC=CC=1.[C:36]([O:44][CH:45]1[C:53]2[C:48](=[CH:49][CH:50]=[C:51]([Cl:54])[CH:52]=2)[N:47]([CH2:55][CH:56]([CH3:58])[CH3:57])[C:46]1=[O:59])(=[O:43])[C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1>>[C:36]([O:44][C:45]1([CH2:23][C:24]2[CH:25]=[C:26]([O:34][CH3:35])[C:27]([O:32][CH3:33])=[C:28]([O:30][CH3:31])[CH:29]=2)[C:53]2[C:48](=[CH:49][CH:50]=[C:51]([Cl:54])[CH:52]=2)[N:47]([CH2:55][CH:56]([CH3:57])[CH3:58])[C:46]1=[O:59])(=[O:43])[C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1