Bromine → 4,6-Dibromothiazolo[5,4-c]pyridin-2-amine
反応式
[Br:1][C:2]1[CH:7]=[C:6]([NH:8][C:9]([NH2:11])=[S:10])[CH:5]=[C:4]([Br:12])[N:3]=1.BrBr>C1COCC1>[Br:1][C:2]1[C:7]2[S:10][C:9]([NH2:11])=[N:8][C:6]=2[CH:5]=[C:4]([Br:12])[N:3]=1参加物
反応条件
- 温度
- 2.5 °C
実験手順
To a cooled (−60-65° C.) solution of 2,6-dibromo-pyridin-4-yl-thiourea (0.50 g, 1.61 mmol) in THF (100 mL) was added bromine solution (0.20 mL in 45 mL THF, 3.69 mmol) drop wise over a period of 30 min maintaining the temperature to −60-65° C. The reaction mixture was stirred for 15 min at the same temperature and then slowly allowed to come to room temperature. The resulting mixture was heated up to 40° C. for 5 h. After completion of reaction (TLC monitoring), THF was distilled off, basified with aq. NH3 (25% solution, pH 10-12) and then extracted with ethyl acetate (3×50 mL). The combined organics was washed with water, dried (Na2SO4), filtered and concentrated. The crude residue was purified over silica gel (100-200 M, 10% ethyl acetate:hexane) to get the desired product as a white solid (0.10 g, 20%).
後処理
- customto come to room temperature
- temperatureThe resulting mixture was heated up to 40° C. for 5 h
- distillationwas distilled off
- extractionextracted with ethyl acetate (3×50 mL)
- washThe combined organics was washed with water
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated
- customThe crude residue was purified over silica gel (100-200 M, 10% ethyl acetate:hexane)
出典と根拠
- ORDレコード
- ord-7daa89b30327451db42a391c9e987bf7
- 出典データセット
- uspto-grants-2013_07
- 特許番号
- US08481544B2
反応ノート
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