Hydroxyamine hydrochloride → 3-(4-Bromo-phenyl)-1-(2-fluoro-6-methyl-pyridin-4-yl)-3-o-tolyl-propan-1-one oxime
反応式
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[CH3:26])[CH2:9][C:10]([C:12]2[CH:17]=[C:16]([CH3:18])[N:15]=[C:14]([F:19])[CH:13]=2)=O)=[CH:4][CH:3]=1.Cl.[NH2:28][OH:29].C([O-])(O)=O.[Na+]>>[Br:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[CH3:26])[CH2:9][C:10]([C:12]2[CH:17]=[C:16]([CH3:18])[N:15]=[C:14]([F:19])[CH:13]=2)=[N:28][OH:29])=[CH:4][CH:3]=1参加物
4
実験手順
In analogy to example 74, step 7, from 3-(4-bromo-phenyl)-1-(2-fluoro-6-methyl-pyridin-4-yl)-3-o-tolyl-propan-1-one and hydroxylamine hydrochloride in the presence of NaHCO3 was prepared the title compound as a mixture of E and Z isomers (2.4:1) as a colorless oil, MS (ESI+): m/z=427.0804 ([M+H]+, 1Br).
出典と根拠
- ORDレコード
- ord-5ebb52e79fe448f294cf1a4fb0b32b9e
- 出典データセット
- uspto-grants-2014_07
- 特許番号
- US08765730B2
反応ノート
読み込み中…