HRID684651

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID8028

Tetrahydrofuran

C4H8O

HCID13489605

Phenyl (5-tert-butyl-1,2-oxazol-3-yl)carbamate

C14H16N2O3

结构：Nc1ccc(-c2cn3c(n2)sc2cc(OCCCl)ccc23)cc1

HCID66794019

7-(2-Chloro-ethoxy)-2-(4-amino-phenyl)-benzo[d]imidazo[2,1-b]thiazole

C17H14ClN3OS

PRODUCTS

生成物

结构：CC(C)(C)c1cc(NC(=O)Nc2ccc(-c3cn4c(n3)sc3cc(OCCCl)ccc34)cc2)no1

HCID66794183

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-2edd4389f960447db9be3949dff7630e
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (3/10)

反应 SMILES

[C:24]([CH3:25])([CH3:26])([CH3:27])[c:28]1[cH:29][c:30]([NH:33][C:34]([O:35][c:37]2[cH:38][cH:39][cH:40][cH:41][cH:42]2)=[O:36])[n:31][o:32]1.[CH2:43]1[O:44][CH2:45][CH2:46][CH2:47]1.[Cl:1][CH2:2][CH2:3][O:4][c:5]1[cH:6][c:7]2[c:8]([n:9]3[c:10]([s:11]2)[n:12][c:13](-[c:15]2[cH:16][cH:17][c:18]([NH2:21])[cH:19][cH:20]2)[cH:14]3)[cH:22][cH:23]1>>[Cl:1][CH2:2][CH2:3][O:4][c:5]1[cH:6][c:7]2[c:8]([n:9]3[c:10]([s:11]2)[n:12][c:13](-[c:15]2[cH:16][cH:17][c:18]([NH:21][C:34]([NH:33][c:30]4[cH:29][c:28]([C:24]([CH3:25])([CH3:26])[CH3:27])[o:32][n:31]4)=[O:35])[cH:19][cH:20]2)[cH:14]3)[cH:22][cH:23]1