Sodium Hydroxide → 2-Amino-6-(trifluoromethoxy)-5-benzothiazolol

HRID 482272ノート

反応式

HRID 482272 の反応式
[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

4

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

  1. temperatureto reflux for 20 hours
  2. extractionThe organic phase is then extracted with ethyl acetate
  3. dry with materialdried over magnesium sulphate
  4. filtrationfiltered
  5. concentrationconcentrated to dryness under reduced pressure (15 mm Hg, 2 kPa)
  6. customThe crude product thus obtained
  7. 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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