HRID1544468

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID31275

1,4-Dioxane

C4H8O2

HCID108029

5-Methoxy-3-(1,2,3,6-tetrahydro-4-pyridinyl)-1H-indole

C14H16N2O

结构：CN(C)C1(c2ccccc2)CCC(CNC(=O)Oc2ccccc2)CC1

HCID67531743

未命名化合物

PRODUCTS

生成物

结构：COc1ccc2[nH]cc(C3=CCN(C(=O)NCC4CCC(c5ccccc5)(N(C)C)CC4)CC3)c2c1

HCID10009749

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-1e0e7bd839644d468f08e7eb2d087887
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

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