Sodium Hydroxide → 2-Amino-6-(trifluoromethoxy)-5-benzothiazolol
反応式
[NH2:1][C:2]1[S:3][C:4]2[CH:10]=[C:9]([O:11][C:12]([F:15])([F:14])[F:13])[C:8]([O:16]C)=[CH:7][C:5]=2[N:6]=1.[OH-].[Na+]>Br>[NH2:1][C:2]1[S:3][C:4]2[CH:10]=[C:9]([O:11][C:12]([F:15])([F:13])[F:14])[C:8]([OH:16])=[CH:7][C:5]=2[N:6]=1参加物
反応条件
- 温度
- 20 °C
実験手順
0.74 g of 2-amino-5-methoxy-6-(trifluoromethoxy)benzothiazole, in solution in 20 ml of 47% hydrobromic acid, are brought to reflux for 20 hours. After cooling to a temperature in the region of 20° C., the reaction mixture is poured in 20 ml of ice-cold water and the solution is basified using concentrated sodium hydroxide. The organic phase is then extracted with ethyl acetate, dried over magnesium sulphate, filtered and concentrated to dryness under reduced pressure (15 mm Hg, 2 kPa). The crude product thus obtained is purified by flash chromatography on a silica column, a dichloromethane/methanol (98/2 by volume) mixture being used as eluent. 0.49 g of 2-amino-5-hydroxy-6-(trifluoromethoxy)benzothiazole are thus isolated in the form of a white powder melting at 216° C. [(Analysis % calculated C: 38.40, H: 2.01, F: 22.78, N: 11.20, S: 12.82; % found C: 38.3, H: 1.9, F: 22.9, N: 11.2, S: 13.0); 1H N.M.R. spectrum (250 MHz, d6-(CD3)2SO, δ in ppm): 6.96 (broad s, 1H, aromatic H ortho to the OH), 7.54 (broad s, 2H, NH2), 7.61 (broad s, 1H, aromatic H meta to the OH), 9.95 (unresolved peak, 1H, OH)].
後処理
- temperatureto reflux for 20 hours
- extractionThe organic phase is then extracted with ethyl acetate
- dry with materialdried over magnesium sulphate
- filtrationfiltered
- concentrationconcentrated to dryness under reduced pressure (15 mm Hg, 2 kPa)
- customThe crude product thus obtained
- customis purified by flash chromatography on a silica column
出典と根拠
- ORDレコード
- ord-5584a96ff730463d9505f0647d2e95ef
- 出典データセット
- uspto-grants-1998_08
- 特許番号
- US05795903
反応ノート
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