HRID1541316

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID679

Dimethyl sulfoxide

C2H6OS

HCID8471

Triethylamine

C6H15N

HCID8857

Ethyl acetate

C4H8O2

HCID5462222

Potassium

HCID11175458

4,6-Dichloro-5-(2-methoxyphenoxy)-2-(pyridin-4-yl)pyrimidine

C16H11Cl2N3O2

HCID18680390

未命名化合物

PRODUCTS

生成物

结构：COc1ccccc1Oc1c(Cl)nc(-c2ccncc2)nc1NS(=O)(=O)CCc1ccccn1

HCID86592474

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-6f242444e82643fbbaf7bcef4a0527bd
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (1/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (1/10)

反应 SMILES

[CH3:37][CH2:38][N:39]([CH2:40][CH3:41])[CH2:42][CH3:43].[CH3:44][S:45]([CH3:46])=[O:47].[CH3:48][CH2:49][O:50][C:51](=[O:52])[CH3:53].[Cl:1][c:2]1[n:3][c:4](-[c:18]2[cH:19][cH:20][n:21][cH:22][cH:23]2)[n:5][c:6]([Cl:17])[c:7]1[O:8][c:9]1[c:10]([O:15][CH3:16])[cH:11][cH:12][cH:13][cH:14]1.[K:24].[n:25]1[c:26]([CH2:31][CH2:32][S:33](=[O:34])(=[O:35])[NH2:36])[cH:27][cH:28][cH:29][cH:30]1>>[c:2]1([NH:36][S:33]([CH2:32][CH2:31][c:26]2[n:25][cH:30][cH:29][cH:28][cH:27]2)(=[O:34])=[O:35])[n:3][c:4](-[c:18]2[cH:19][cH:20][n:21][cH:22][cH:23]2)[n:5][c:6]([Cl:17])[c:7]1[O:8][c:9]1[c:10]([O:15][CH3:16])[cH:11][cH:12][cH:13][cH:14]1