反応 #48834
ord-2597c2f8d12542899d7e61dc3fdf9d90
反応方程式
3-{4-[(Hydroxyamino)(imino)methyl]phenoxy}-5-[(1S)-2-methoxy-1-methylethoxy]-N-(1-methyl-1H-pyrazol-3-yl)benzamide
trimethyl orthoformate
→
desired compound
3-[(1S)-2-Methoxy-1-methylethoxy]-N-(1-methyl-1H-pyrazol-3-yl)-5-[4-(1,2,4-oxadiazol-3-yl)phenoxy]benzamide
反応物
試薬
なし
反応条件
温度
55°CELSIUS
詳細条件
See reaction.notes.procedure_details.
後処理
- 1workup.ADDITION2 drops of borontrifluoroetherate added
- 2その他The volatiles were removed under reduced pressure
- 3その他the resulting oil chromatographed on silica
- 4洗浄eluting with 0-100% ethyl acetate in iso-hexane
実験手順
3-{4-[(Hydroxyamino)(imino)methyl]phenoxy}-5-[(1S)-2-methoxy-1-methylethoxy]-N-(1-methyl-1H-pyrazol-3-yl)benzamide was taken up in trimethyl orthoformate (3 mL) and 2 drops of borontrifluoroetherate added. The resulting solution was heated to 55° C. in a CEM explorer microwave for 80 mins. The volatiles were removed under reduced pressure and the resulting oil chromatographed on silica, eluting with 0-100% ethyl acetate in iso-hexane, to give the desired compound as a white foam (295 mg)