HRID124782

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID259

Bromide

Br-

HCID1049

Pyridine

C5H5N

HCID6344

Dichloromethane

CH2Cl2

HCID11776

Triphenylphosphine

C18H15P

HCID202185

1,3,4-Oxadiazole, 2-amino-5-(2-furyl)-

C6H5N3O2

HCID3604519

8-Methyl-2-(thiophen-2-yl)quinoline-4-carboxylic acid

C15H11NO2S

PRODUCTS

生成物

结构：Cc1cccc2c(C(=O)Nc3nnc(-c4ccco4)o3)cc(-c3cccs3)nc12

HCID67204226

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-7c67214879cd4822893e84d7f7ad5170
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (2/10)

反应 SMILES

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