HRID1523092

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：O=C(OC1C(=O)N(CCc2ccccc2)c2ccc(Cl)cc21)c1ccccc1

HCID90416238

未命名化合物

PRODUCTS

生成物

结构：COc1cc(CC2(OC(=O)c3ccccc3)C(=O)N(CCc3ccccc3)c3ccc(Cl)cc32)cc(OC)c1OC

HCID90418382

未命名化合物

PROCEDURE

实验过程

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

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-54d8021978864bf792b4b81420f72111
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][CH2:56][C:57]2[CH:62]=[CH:61][CH:60]=[CH:59][CH:58]=2)[C:46]1=[O:63])(=[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][CH2:56][C:57]2[CH:58]=[CH:59][CH:60]=[CH:61][CH:62]=2)[C:46]1=[O:63])(=[O:43])[C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1