HRID186016

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID6228

N,N-Dimethylformamide

C3H7NO

HCID19660

Carbonate

CO3-2

HCID104967

Cesium(1+)

Cs+

2 次

HCID314941

2-(chloromethyl)-5-phenyl-1,3,4-oxadiazole

C9H7ClN2O

结构：Cc1nc(-n2ccc(O)cc2=O)sc1C(=O)NCc1ccccc1

HCID54742338

N-Benzyl-2-(4-hydroxy-2-oxo-1(2H)-pyridinyl)-4-methyl-1,3-thiazole-5-carboxamide

C17H15N3O3S

PRODUCTS

生成物

结构：Cc1nc(-n2ccc(OCc3nnc(-c4ccccc4)o3)cc2=O)sc1C(=O)NCc1ccccc1

HCID57744445

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-d19cf942e21a49308217c686be67c72f
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (6/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (6/10)

反应 SMILES

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