反応式
[C:1]([O:5][C:6]([C:8]1[CH:9]=[C:10]([C:14]2[C:19]([CH3:20])=[CH:18][CH:17]=[CH:16][N+:15]=2[O-])[CH:11]=[CH:12][CH:13]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[N:22]1C=CC=CC=1.CS(OS(C)(=O)=O)(=O)=O.C(CN)O>CC#N.O>[C:1]([O:5][C:6](=[O:7])[C:8]1[CH:13]=[CH:12][CH:11]=[C:10]([C:14]2[C:19]([CH3:20])=[CH:18][CH:17]=[C:16]([NH2:22])[N:15]=2)[CH:9]=1)([CH3:4])([CH3:3])[CH3:2]参加物
反応条件
- 温度
- 10 °C
実験手順
A solution of 2-(3-(tert-butoxycarbonyl)phenyl)-3-methylpyridine-1-oxide (1 eq) and pyridine (4 eq) in MeCN (8 vol) is heated to 70° C. A solution of methanesulfonic anhydride (1.5 eq) in MeCN (2 vol) is added over 50 min via addition funnel maintaining the temperature at less than 75° C. The mixture is stirred for an additional 0.5 hours after complete addition. The mixture is then allowed to cool to ambient. Ethanolamine (10 eq) is added via addition funnel. After stirring for 2 hours, water (6 vol) is added and the mixture is cooled to 10° C. After stirring for NLT 3 hours, the solid is collected by filtration and washed with water (3 vol), 2:1 MeCN/water (3 vol), and MeCN (2×1.5 vol). The solid is dried to constant weight (<1% difference) in a vacuum oven at 50° C. with a slight N2 bleed to afford tert-butyl-3-(6-amino-3-methylpyridin-2-yl)benzoate as a red-yellow solid (53% yield).
後処理
- temperaturemaintaining the temperature at less than 75° C
- additionafter complete addition
- temperatureto cool to ambient
- stirringAfter stirring for 2 hours
- stirringAfter stirring for NLT 3 hours
- filtrationthe solid is collected by filtration
- washwashed with water (3 vol), 2:1 MeCN/water (3 vol), and MeCN (2×1.5 vol)
- dry with materialThe solid is dried to constant weight (<1% difference) in a vacuum oven at 50° C. with a slight N2
出典と根拠
- ORDレコード
- ord-14d765b789694ef7b1146b515aeb83ba
- 出典データセット
- uspto-grants-2014_09
- 特許番号
- US08846718B2
関連ノート
読み込み中…