Dichloromethane → 2-[(1-Amino-4-methyl-1-oxopentan-2-yl)-(4-chlorophenyl)sulfonylamino]acetic acid

反応式

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

参加物

反応物 3

HCID 6344Dichloromethane

HCID 6422Trifluoroacetic acid

HCID 72486021Tert-butyl 2-[(1-amino-4-methyl-1-oxopentan-2-yl)-(4-chlorophenyl)sulfonylamino]acetate

生成物 1

HCID 724860282-[(1-Amino-4-methyl-1-oxopentan-2-yl)-(4-chlorophenyl)sulfonylamino]acetic acid

出典と根拠

ORDレコード: ord-feed301869954652b5f426515855c2b1
出典データセット: Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI: 10.1039/C8SC04228D

反応ノート

読み込み中…