HRID201758

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID41541757

4-[3-(Phenylmethyl)-1,2,4-oxadiazol-5-yl]piperidine

C14H17N3O

结构：CN(CC1(c2ccccc2)CC1C=O)S(=O)(=O)c1ccccc1

HCID178482558

未命名化合物

PRODUCTS

生成物

结构：CN(CC1(c2ccccc2)CC1CN1CCC(c2nc(Cc3ccccc3)no2)CC1)S(=O)(=O)c1ccccc1

HCID9893941

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-2151d0b5ee1c45ed85759da08dea4117
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

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