HRID662349

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID949

N,N-Dimethylaniline

C8H11N

HCID78282

Benzoyl chloride, 3,4,5-trimethoxy-

C10H11ClO4

结构：O=C1CC(CCOC2CCCCO2)(c2ccc(Cl)c(Cl)c2)CN1

HCID21197671

4-(2-Tetrahydropyranyloxyethyl)-4-(3,4-dichlorophenyl)-2-pyrrolidone

C17H21Cl2NO3

PRODUCTS

生成物

结构：COc1cc(C(=O)N2CC(CCOC3CCCCO3)(c3ccc(Cl)c(Cl)c3)CC2=O)cc(OC)c1OC

HCID53799801

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-8c32084c2cb8462688089813f38bdfcf
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (3/10)

反应 SMILES

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