反応 #83849

反応方程式

6-fluoro-3-(4-piperidinyl)-1,2 benzisoxazole hydrochloride

K2CO3

1-[4-(3-chloropropoxy)-3-methoxyphenyl]-ethanone

dimethylformamide

→

1-[4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-propoxy]-3-methoxyphenyl]-ethanone

収率 58.6%

溶媒

water

反応条件

後処理

1. 1
   抽出the aqueous mixture was extracted with ethyl acetate
2. 2
   洗浄The ethyl acetate was washed (water)
3. 3
   乾燥dried (MgSO4)
4. 4
   濃縮concentrated
5. 5
   その他to afford a moist solid
6. 6
   その他Recrystallization (twice) from ethyl alcohol

実験手順

A stirred mixture of 6-fluoro-3-(4-piperidinyl)-1,2 benzisoxazole hydrochloride (5.1 g, 20 mmol), K2CO3 (5.2 g, 40 mmol), 1-[4-(3-chloropropoxy)-3-methoxyphenyl]-ethanone (5.3 g, 22 mmol), and dimethylformamide (60 ml) was heated at 90° C. for 16 hours. The reaction was poured into water, and the aqueous mixture was extracted with ethyl acetate. The ethyl acetate was washed (water), dried (MgSO4) and concentrated to afford a moist solid. Recrystallization (twice) from ethyl alcohol afforded 5.0 g (58%) of 1-[4-[3-[4-(6-fluoro-1,2-benzisoxazol-3-yl)-1-piperidinyl]-propoxy]-3-methoxyphenyl]-ethanone as a beige solid, m.p.=118°-120° C.

出典