HRID812476

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID72894

2-Aminobenzenesulfonamide

C6H8N2O2S

HCID820700

2-amino-5-bromobenzenesulfonamide

C6H7BrN2O2S

结构：CCOC(=O)c1c(O)c2cc(Cl)cnc2n(Cc2ccccc2)c1=O

HCID54692180

Ethyl 1-benzyl-6-chloro-4-hydroxy-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate

C18H15ClN2O4

结构：CCOC(=O)c1c(O)c2cccnc2n(Cc2ccccc2)c1=O

HCID54729304

Ethyl 1-benzyl-4-hydroxy-2-oxo-1,2-dihydro-1,8-naphthyridine-3-carboxylate

C18H16N2O4

PRODUCTS

生成物

结构：NS(=O)(=O)c1ccccc1NC(=O)c1c(O)c2cc(Cl)cnc2n(Cc2ccccc2)c1=O

HCID67064084

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-dad4b8ce9e79448b8a04f103f8a7e71b
来源数据集: Test data from https://doi.org/10.1039/C8SC04228D
DOI: 10.1039/C8SC04228D
来源说明: Test data from https://doi.org/10.1039/C8SC04228D

反应 SMILES

[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[n:8]1[c:9](=[O:25])[c:10]([C:20](=[O:21])[O:22][CH2:23][CH3:24])[c:11]([OH:19])[c:12]2[cH:13][c:14]([Cl:18])[cH:15][n:16][c:17]12.[CH2:26]([n:27]1[c:28]2[c:29]([cH:30][cH:31][cH:32][n:33]2)[c:34]([OH:35])[c:36]([C:37]([O:38][CH2:39][CH3:40])=[O:41])[c:42]1=[O:43])[c:44]1[cH:45][cH:46][cH:47][cH:48][cH:49]1.[NH2:50][c:51]1[c:52]([S:57](=[O:58])(=[O:59])[NH2:60])[cH:53][cH:54][cH:55][cH:56]1.[NH2:61][c:62]1[cH:63][cH:64][c:65]([Br:66])[cH:67][c:68]1[S:69]([NH2:70])(=[O:71])=[O:72]>>[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[n:8]1[c:9](=[O:25])[c:10]([C:20](=[O:21])[NH:50][c:51]2[c:52]([S:57](=[O:58])(=[O:59])[NH2:60])[cH:53][cH:54][cH:55][cH:56]2)[c:11]([OH:19])[c:12]2[cH:13][c:14]([Cl:18])[cH:15][n:16][c:17]12