HRID1119610

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID6386

tert-Butyl alcohol

C4H10O

HCID108810

(3-tert-Butyl-2-phenyl-1,3-oxazolidin-5-yl)methanol

C14H21NO2

HCID5462222

Potassium

HCID21388031

未命名化合物

HCID21388033

1,7-Dichloro-3-methylisoquinoline

C10H7Cl2N

PRODUCTS

生成物

结构：Cc1cnc(OCC2CN(C(C)(C)C)C(c3ccccc3)O2)c2cc(Cl)ccc12

HCID21388034

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-79fa26f644114cdcb69a00047912f87c
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (7/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (7/10)

反应 SMILES

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