HRID1204324

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID6342

Acetonitrile

C2H3N

HCID8471

Triethylamine

C6H15N

HCID66982

Decanoyl chloride

C10H19ClO

结构：Nc1ccc(S(=O)(=O)Nc2nnc(S(N)(=O)=O)s2)cc1

HCID134560

1,3,4-Thiadiazole-2-sulfonamide, 5-(((4-aminophenyl)sulfonyl)amino)-

C8H9N5O4S3

PRODUCTS

生成物

结构：CCCCCCCCCC(=O)Nc1ccc(S(=O)(=O)Nc2nnc(S(N)(=O)=O)s2)cc1

HCID53318404

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-2b50b67504874c729c6760868a9f5331
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (5/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (5/10)

反应 SMILES

[C:28]([CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH3:37])(=[O:38])[Cl:39].[CH3:21][CH2:22][N:23]([CH2:24][CH3:25])[CH2:26][CH3:27].[CH3:40][C:41]#[N:42].[NH2:1][c:2]1[cH:3][cH:4][c:5]([S:8](=[O:9])(=[O:10])[NH:11][c:12]2[n:13][n:14][c:15]([S:17](=[O:18])(=[O:19])[NH2:20])[s:16]2)[cH:6][cH:7]1>>[NH:1]([c:2]1[cH:3][cH:4][c:5]([S:8](=[O:9])(=[O:10])[NH:11][c:12]2[n:13][n:14][c:15]([S:17](=[O:18])(=[O:19])[NH2:20])[s:16]2)[cH:6][cH:7]1)[C:28]([CH2:29][CH2:30][CH2:31][CH2:32][CH2:33][CH2:34][CH2:35][CH2:36][CH3:37])=[O:38]