HRID2153977

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID7237

o-Xylene

C8H10

HCID8028

Tetrahydrofuran

C4H8O

HCID65578

Ethanedioyl dichloride

C2Cl2O2

HCID87678

4-(3-Phenylpropyl)piperidine

C14H21N

HCID257501

2-Phenylethenesulfonamide

C8H9NO2S

HCID54089736

未命名化合物

PRODUCTS

生成物

结构：O=C(NS(=O)(=O)C=Cc1ccccc1)N1CCC(CCCc2ccccc2)CC1

HCID54287481

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-cf75259b436f4e26bdc807143641fb66
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (4/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (4/10)

反应 SMILES

[Cl:13][C:14]([C:15]([Cl:16])=[O:17])=[O:18].[O:56]1[CH2:57][CH2:58][CH2:59][CH2:60]1.[c:19]1([CH:25]=[CH:26][S:27](=[O:28])(=[O:29])[N:30]=[C:31]=[O:32])[cH:20][cH:21][cH:22][cH:23][cH:24]1.[c:1]1([CH:2]=[CH:3][S:4]([NH2:5])(=[O:6])=[O:7])[cH:8][cH:9][cH:10][cH:11][cH:12]1.[c:33]1([CH2:39][CH2:40][CH2:41][CH:42]2[CH2:43][CH2:44][NH:45][CH2:46][CH2:47]2)[cH:34][cH:35][cH:36][cH:37][cH:38]1.[c:48]1([CH3:49])[c:50]([CH3:51])[cH:52][cH:53][cH:54][cH:55]1>>[c:19]1([CH:25]=[CH:26][S:27](=[O:28])(=[O:29])[NH:30][C:31](=[O:32])[N:45]2[CH2:44][CH2:43][CH:42]([CH2:41][CH2:40][CH2:39][c:33]3[cH:34][cH:35][cH:36][cH:37][cH:38]3)[CH2:47][CH2:46]2)[cH:20][cH:21][cH:22][cH:23][cH:24]1