HRID1229804

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID313

Hydrochloric Acid

ClH

HCID3283

Diethyl Ether

C4H10O

HCID8028

Tetrahydrofuran

C4H8O

HCID16028

Tetrabutylammonium

C16H36N+

HCID28179

Fluoride

F-

结构：CC(CO[Si](C)(C)C(C)(C)C)Oc1cc(Oc2ccc(S(C)(=O)=O)cc2)cc(C(=O)Nc2nccs2)c1

HCID72260583

未命名化合物

PRODUCTS

生成物

结构：CC(CO)Oc1cc(Oc2ccc(S(C)(=O)=O)cc2)cc(C(=O)Nc2nccs2)c1

HCID10366412

3-[(1-Hydroxypropan-2-yl)oxy]-5-[4-(methanesulfonyl)phenoxy]-N-(1,3-thiazol-2-yl)benzamide

C20H20N2O6S2

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-9c560ca98f2a44ca9e13c86dc553aade
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:19]([Si:20]([CH3:21])([CH3:22])[O:24][CH2:25][CH:26]([O:27][c:28]1[cH:29][c:30]([C:31](=[O:32])[NH:33][c:34]2[s:35][cH:36][cH:37][n:38]2)[cH:39][c:40]([O:42][c:43]2[cH:44][cH:45][c:46]([S:49](=[O:50])(=[O:51])[CH3:52])[cH:47][cH:48]2)[cH:41]1)[CH3:53])([CH3:23])([CH3:54])[CH3:55].[CH2:2]([N+:3]([CH2:4][CH2:5][CH2:6][CH3:7])([CH2:8][CH2:9][CH2:10][CH3:11])[CH2:12][CH2:13][CH2:14][CH3:15])[CH2:16][CH2:17][CH3:18].[CH2:56]1[O:57][CH2:58][CH2:59][CH2:60]1.[CH3:61][CH2:62][O:63][CH2:64][CH3:65].[ClH:66].[F-:1]>>[OH:24][CH2:25][CH:26]([O:27][c:28]1[cH:29][c:30]([C:31](=[O:32])[NH:33][c:34]2[s:35][cH:36][cH:37][n:38]2)[cH:39][c:40]([O:42][c:43]2[cH:44][cH:45][c:46]([S:49](=[O:50])(=[O:51])[CH3:52])[cH:47][cH:48]2)[cH:41]1)[CH3:53]