HRID1220209

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID180

Acetone

C3H6O

HCID8471

Triethylamine

C6H15N

HCID190100

Benzenesulfonyl chloride, 4-(benzoyloxy)-

C13H9ClO4S

HCID22146946

N-(6-Hydroxy-1H-benzimidazol-2-yl)-N′-(2-methoxyethyl)urea

C11H14N4O3

PRODUCTS

生成物

结构：COCCNC(=O)Nc1nc2cc(OS(=O)(=O)c3ccc(OC(=O)c4ccccc4)cc3)ccc2[nH]1

HCID178496034

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-adae7225ac374a3aba8cb2e52b94802c
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (5/10)

反应 SMILES

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