HRID161792

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)c2cccnc2n(Cc2ccccc2)c1=O

HCID54729304

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

C18H16N2O4

结构：CCOC(=O)c1c(O)c2cc(-c3ccccc3)cnc2n(Cc2ccccc2)c1=O

HCID67064088

未命名化合物

PRODUCTS

生成物

结构：NS(=O)(=O)c1ccccc1NC(=O)c1c(O)c2cc(-c3ccccc3)cnc2n(Cc2ccccc2)c1=O

HCID67063821

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-f7787e119bc741eebafd68dc65bf1320
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (9/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (9/10)

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:30])[c:10]([C:25](=[O:26])[O:27][CH2:28][CH3:29])[c:11]([OH:24])[c:12]2[cH:13][c:14](-[c:18]3[cH:19][cH:20][cH:21][cH:22][cH:23]3)[cH:15][n:16][c:17]12.[CH2:31]([n:32]1[c:33]2[c:34]([cH:35][cH:36][cH:37][n:38]2)[c:39]([OH:40])[c:41]([C:42]([O:43][CH2:44][CH3:45])=[O:46])[c:47]1=[O:48])[c:49]1[cH:50][cH:51][cH:52][cH:53][cH:54]1.[NH2:55][c:56]1[c:57]([S:62](=[O:63])(=[O:64])[NH2:65])[cH:58][cH:59][cH:60][cH:61]1.[NH2:66][c:67]1[cH:68][cH:69][c:70]([Br:71])[cH:72][c:73]1[S:74]([NH2:75])(=[O:76])=[O:77]>>[CH2:1]([c:2]1[cH:3][cH:4][cH:5][cH:6][cH:7]1)[n:8]1[c:9](=[O:30])[c:10]([C:25](=[O:26])[NH:55][c:56]2[c:57]([S:62](=[O:63])(=[O:64])[NH2:65])[cH:58][cH:59][cH:60][cH:61]2)[c:11]([OH:24])[c:12]2[cH:13][c:14](-[c:18]3[cH:19][cH:20][cH:21][cH:22][cH:23]3)[cH:15][n:16][c:17]12