Pyridine → 4-Acetamido-2-bromo-thiazole
反応式
Br.[NH2:2][C:3]1[N:4]=[C:5]([Br:8])[S:6][CH:7]=1.N1C=CC=CC=1.[C:15]([O-])(=[O:17])[CH3:16].[Na+]>C(OC(=O)C)(=O)C>[C:15]([NH:2][C:3]1[N:4]=[C:5]([Br:8])[S:6][CH:7]=1)(=[O:17])[CH3:16]参加物
5
反応条件
- 温度
- 0 °C
実験手順
4-Amino-2-bromothiazole hydrobromide (52 g, 0.2 m) was suspended in acetic anhydride (200 ml) then treated dropwise with pyridine (100 ml), maintaining the temperature at 0° C. by means of an ice bath. After the addition was complete, the reaction mixture was stirred for 2 h. at room temperature then poured onto 20% aqueous sodium acetate (2 l). The solution was cooled, filtered and the precipitate washed with water (2×200 ml.). The product was air dried and recrystallised from acetone to give the title compound (35 g, 80%). m.p. 165° C. Found: C, 27.5; H, 2.5; N, 12.7. C5H5BrN2OS requires C, 27.2; H, 2.3; N, 12.7%.
後処理
- additionAfter the addition
- temperatureThe solution was cooled
- filtrationfiltered
- washthe precipitate washed with water (2×200 ml.)
- customdried
- customrecrystallised from acetone
出典と根拠
- ORDレコード
- ord-1b27dabd453244c981454e92d07e796b
- 出典データセット
- uspto-grants-1979_04
- 特許番号
- US04148904
反応ノート
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