HRID139104

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2155

2-Aminothiazole

C3H4N2S

HCID6228

N,N-Dimethylformamide

C3H7NO

HCID8471

Triethylamine

C6H15N

HCID9886

Hexafluorophosphate ion

F6P-

HCID102808

2-(1,3-Dioxo-1,3-dihydro-2H-isoindol-2-yl)-4-methylpentanoato

C14H15NO4

HCID130500

未命名化合物

PRODUCTS

生成物

结构：CC(C)CC(C(=O)Nc1nccs1)N1C(=O)c2ccccc2C1=O

HCID2831706

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-cfeea201c28c4ad0b2a137947aa2f05f
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

[CH3:50][CH2:51][N:52]([CH2:53][CH3:54])[CH2:55][CH3:56].[NH2:20][c:21]1[s:22][cH:23][cH:24][n:25]1.[O:1]=[C:2]1[N:3]([CH:12]([C:13](=[O:14])[OH:15])[CH2:16][CH:17]([CH3:18])[CH3:19])[C:4](=[O:11])[c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]21.[O:57]=[CH:58][N:59]([CH3:60])[CH3:61].[P-:26]([F:27])([F:28])([F:29])([F:30])([F:31])[F:32].[n:33]1([O:34][C:35]([N:36]([CH3:37])[CH3:38])=[N+:39]([CH3:40])[CH3:41])[c:42]2[cH:43][cH:44][cH:45][cH:46][c:47]2[n:48][n:49]1>>[O:1]=[C:2]1[N:3]([CH:12]([C:13](=[O:15])[NH:20][c:21]2[s:22][cH:23][cH:24][n:25]2)[CH2:16][CH:17]([CH3:18])[CH3:19])[C:4](=[O:11])[c:5]2[cH:6][cH:7][cH:8][cH:9][c:10]21