HRID189302

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID3776

Isopropanol

C3H8O

HCID258688

2,3-Dimethyl-1H-indol-5-ylamine

C10H12N2

HCID11782230

4-Chloro-6-methoxy-7-((1-methylpiperidin-4-yl)methoxy)quinazoline

C16H20ClN3O2

PRODUCTS

生成物

HCID313

Hydrochloric Acid

ClH

结构：COc1cc2c(Nc3ccc4[nH]c(C)c(C)c4c3)ncnc2cc1OCC1CCN(C)CC1

HCID22030664

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-8f41da7eb9fb407cac1c4ebef55620b5
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

[CH:35]([OH:36])([CH3:37])[CH3:38].[Cl:1][c:2]1[n:3][cH:4][n:5][c:6]2[cH:7][c:8]([O:14][CH2:15][CH:16]3[CH2:17][CH2:18][N:19]([CH3:22])[CH2:20][CH2:21]3)[c:9]([O:12][CH3:13])[cH:10][c:11]12.[NH2:23][c:24]1[cH:25][c:26]2[c:27]([CH3:34])[c:28]([CH3:33])[nH:29][c:30]2[cH:31][cH:32]1>>[ClH:1].[c:2]1([NH:23][c:24]2[cH:25][c:26]3[c:27]([CH3:34])[c:28]([CH3:33])[nH:29][c:30]3[cH:31][cH:32]2)[n:3][cH:4][n:5][c:6]2[cH:7][c:8]([O:14][CH2:15][CH:16]3[CH2:17][CH2:18][N:19]([CH3:22])[CH2:20][CH2:21]3)[c:9]([O:12][CH3:13])[cH:10][c:11]12