HRID983961

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID16742967

未命名化合物

结构：COC(=O)C(=O)c1c[nH]c2c(CO[Si](C(C)C)(C(C)C)C(C)C)cccc12

HCID69742759

未命名化合物

PRODUCTS

生成物

结构：CC(C)[Si](OCc1cccc2c(C3=C(c4cn5c6c(cccc46)CCC5)C(=O)NC3=O)c[nH]c12)(C(C)C)C(C)C

HCID69742936

未命名化合物

PROCEDURE

实验过程

Beginning with 7-((triisopropylsilyloxy)methyl)indole-3-glyoxylic acid methyl ester and 2-(5,6-dihydro-4H-pyrrolo[3,2,1-ij]quinolin-1-yl)acetamide, the title compound was prepared essentially as described in Example 1.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-441a983b41dc46e69a910d2dc9132a95
来源数据集: uspto-grants-2005_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06867198B2
来源说明: uspto-grants-2005_03

反应 SMILES

CO[C:3](=[O:27])[C:4]([C:6]1[C:14]2[C:9](=[C:10]([CH2:15][O:16][Si:17]([CH:24]([CH3:26])[CH3:25])([CH:21]([CH3:23])[CH3:22])[CH:18]([CH3:20])[CH3:19])[CH:11]=[CH:12][CH:13]=2)[NH:8][CH:7]=1)=O.[C:28]1([CH2:40][C:41]([NH2:43])=[O:42])[C:38]2=[C:39]3[C:34](=[CH:35][CH:36]=[CH:37]2)[CH2:33][CH2:32][CH2:31][N:30]3[CH:29]=1>>[CH:24]([Si:17]([CH:18]([CH3:20])[CH3:19])([CH:21]([CH3:23])[CH3:22])[O:16][CH2:15][C:10]1[CH:11]=[CH:12][CH:13]=[C:14]2[C:9]=1[NH:8][CH:7]=[C:6]2[C:4]1[C:3](=[O:27])[NH:43][C:41](=[O:42])[C:40]=1[C:28]1[C:38]2=[C:39]3[C:34](=[CH:35][CH:36]=[CH:37]2)[CH2:33][CH2:32][CH2:31][N:30]3[CH:29]=1)([CH3:26])[CH3:25]