5-(4-Methyl-3-nitrophenyl)-pyrimidine → 2-Methyl-5-(pyrimidin-5-YL)aniline
反応式
[CH3:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[CH:9]=[N:10][CH:11]=[N:12][CH:13]=2)=[CH:4][C:3]=1[N+:14]([O-])=O>O1CCCC1.CO.[Pd]>[NH2:14][C:3]1[CH:4]=[C:5]([C:8]2[CH:13]=[N:12][CH:11]=[N:10][CH:9]=2)[CH:6]=[CH:7][C:2]=1[CH3:1]参加物
5
実験手順
A suspension of 5-(4-methyl-3-nitrophenyl)-pyrimidine (258 mg) in tetrahydrofuran (5ml) and methanol (5 ml) was hydrogenated over palladium on carbon (10% w/w, 50% wet, 130 mg) under hydrogen atmosphere for 4 hours. The catalyst was filtered off and the filtrate was evaporated to give 5-(3-amino4-methylphenyl)pyrimidine(410 mg, 96.5%).
後処理
- filtrationThe catalyst was filtered off
- customthe filtrate was evaporated
出典と根拠
- ORDレコード
- ord-2aaf6e3cc2b34a47b1400f7669979dda
- 出典データセット
- uspto-grants-2004_08
- 特許番号
- US06770667B1
反応ノート
読み込み中…