HRID838349

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2468184

N-(tert-butyl)-2-piperazin-1-ylacetamide

C10H21N3O

结构：CCOc1cc(C(C)(C)C#N)ccc1C1=NC(c2ccc(Cl)cc2)C(c2ccc(Cl)cc2)N1C(=O)Cl

HCID178466492

未命名化合物

PRODUCTS

生成物

结构：CCOc1cc(C(C)(C)C#N)ccc1C1=NC(c2ccc(Cl)cc2)C(c2ccc(Cl)cc2)N1C(=O)N1CCN(CC(=O)NC(C)(C)C)CC1

HCID178466498

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-9c0eb0ff144942d5af82cf88905f7854
来源数据集: Test data from https://doi.org/10.1039/C8SC04228D
DOI: 10.1039/C8SC04228D
来源说明: Test data from https://doi.org/10.1039/C8SC04228D

反应 SMILES

[C:37]([CH3:38])([CH3:39])([CH3:40])[NH:41][C:42]([CH2:43][N:44]1[CH2:45][CH2:46][NH:47][CH2:48][CH2:49]1)=[O:50].[Cl:1][c:2]1[cH:3][cH:4][c:5]([CH:8]2[N:9]=[C:10]([c:23]3[c:24]([O:34][CH2:35][CH3:36])[cH:25][c:26]([C:29]([CH3:30])([CH3:31])[C:32]#[N:33])[cH:27][cH:28]3)[N:11]([C:20](=[O:21])[Cl:22])[CH:12]2[c:13]2[cH:14][cH:15][c:16]([Cl:19])[cH:17][cH:18]2)[cH:6][cH:7]1>>[Cl:1][c:2]1[cH:3][cH:4][c:5]([CH:8]2[N:9]=[C:10]([c:23]3[c:24]([O:34][CH2:35][CH3:36])[cH:25][c:26]([C:29]([CH3:30])([CH3:31])[C:32]#[N:33])[cH:27][cH:28]3)[N:11]([C:20](=[O:21])[N:47]3[CH2:46][CH2:45][N:44]([CH2:43][C:42]([NH:41][C:37]([CH3:38])([CH3:39])[CH3:40])=[O:50])[CH2:49][CH2:48]3)[CH:12]2[c:13]2[cH:14][cH:15][c:16]([Cl:19])[cH:17][cH:18]2)[cH:6][cH:7]1