HRID1545531

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID11345546

4-Phenyl-1-(piperidin-4-yl)-1,3-dihydro-2H-imidazol-2-one

C14H17N3O

结构：CC(C)(C)CN1Cc2c(cc(Cl)c3[nH]ncc23)CC(CC(=O)N2CCC(N3Cc4ccccc4NC3=O)CC2)C1=O

HCID68826478

未命名化合物

PRODUCTS

生成物

结构：CC(C)(C)CN1Cc2c(cc(Cl)c3[nH]ncc23)CC(CC(=O)N2CCC(n3cc(-c4ccccc4)[nH]c3=O)CC2)C1=O

HCID68826314

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-0eb9250b70314d998fed636a0d61b805
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

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