HRID292536

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID62325

2-Methylpropanoyl chloride

C4H7ClO

结构：COC(=O)C(Cc1ccc(-c2ccc(C#N)cc2)cc1)NC(=O)C1Cc2cc3c(cc2CN1S(=O)(=O)c1sc(N)nc1C)OC(c1ccc(OCc2ccc(Cl)c(Cl)c2)cc1)CO3

HCID76761717

未命名化合物

PRODUCTS

生成物

结构：COC(=O)C(Cc1ccc(-c2ccc(C#N)cc2)cc1)NC(=O)C1Cc2cc3c(cc2CN1S(=O)(=O)c1sc(NC(=O)C(C)C)nc1C)OC(c1ccc(OCc2ccc(Cl)c(Cl)c2)cc1)CO3

HCID87325212

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-e5586674761b45c593ec22d9b1b488ed
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (8/10)

反应 SMILES

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