HRID942889

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7237

o-Xylene

C8H10

HCID14284

N,N-Dimethylpyridin-4-amine

C7H10N2

HCID459610

4-Chloro-6,7-dimethoxyquinoline

C11H10ClNO2

HCID22132619

(4-Hydroxyphenyl)[2-(trifluoromethyl)phenyl]methanone

C14H9F3O2

PRODUCTS

生成物

结构：COc1cc2nccc(Oc3ccc(C(=O)c4ccccc4C(F)(F)F)cc3)c2cc1OC

HCID22132725

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-d429c86b3c5742f2a60c87d0f841f9d5
来源数据集: Validation data from https://doi.org/10.1039/C8SC04228D
DOI: 10.1039/C8SC04228D
来源说明: Validation data from https://doi.org/10.1039/C8SC04228D

反应 SMILES

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