HRID695114

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID69688174

未命名化合物

结构：CC(C)(C)OC(=O)CC(=O)c1cccc(-c2cc(COC3CCCCO3)no2)c1

HCID69688926

(RS)-3-oxo-3-{3-[3-(tetrahydro-pyran-2-yloxymethyl)-isoxazol-5-yl]-phenyl}-propionic acid tert.-butyl ester

C22H27NO6

PRODUCTS

生成物

结构：CN(C)c1cc(NC(=O)OC(C)(C)C)c(NC(=O)CC(=O)c2cccc(-c3cc(COC4CCCCO4)no3)c2)cc1F

HCID86586834

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-d06661700b07415fa5efa5adc50d6e06
来源数据集: Training data from https://doi.org/10.1039/C8SC04228D (3/10)
DOI: 10.1039/C8SC04228D
来源说明: Training data from https://doi.org/10.1039/C8SC04228D (3/10)

反应 SMILES

[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([NH:7][c:8]1[c:9]([NH2:18])[cH:10][c:11]([F:17])[c:12]([N:14]([CH3:15])[CH3:16])[cH:13]1)=[O:19].[C:20]([CH3:22])([CH3:23])([O:24][C:25](=[O:21])[CH2:26][C:27]([c:28]1[cH:29][c:30](-[c:34]2[cH:35][c:36]([CH2:39][O:40][CH:41]3[O:42][CH2:43][CH2:44][CH2:45][CH2:46]3)[n:37][o:38]2)[cH:31][cH:32][cH:33]1)=[O:47])[CH3:48]>>[C:1]([CH3:2])([CH3:3])([CH3:4])[O:5][C:6]([NH:7][c:8]1[c:9]([NH:18][C:25](=[O:24])[CH2:26][C:27]([c:28]2[cH:29][c:30](-[c:34]3[cH:35][c:36]([CH2:39][O:40][CH:41]4[O:42][CH2:43][CH2:44][CH2:45][CH2:46]4)[n:37][o:38]3)[cH:31][cH:32][cH:33]2)=[O:47])[cH:10][c:11]([F:17])[c:12]([N:14]([CH3:15])[CH3:16])[cH:13]1)=[O:19]