Hydrochloric Acid → 5-(Trifluoromethyl)isoxazol-3-ylamine
反応式
[F:1][C:2]([F:16])([F:15])[C:3]1[O:7][N:6]=[C:5]([NH:8]C(=O)C(C)(C)C)[CH:4]=1.Cl>C(O)CO>[F:1][C:2]([F:16])([F:15])[C:3]1[O:7][N:6]=[C:5]([NH2:8])[CH:4]=1参加物
4
実験手順
The reaction was carried out according to the same procedure as described in Example 50 except that 5-trifluoromethyl-3-pivaloylaminoisoxazole (0.7553 g, 3.20 mmole), 36% hydrochloric acid (0.81 g, 8.00 mmole) and ehtylene glycol (3.2 ml) were used. The product was then purified by column chromatography on silica gel to give the title compound. Yield: 0.3686 g (75.7%). The structure of this product was confirmed by NMR.
後処理
- customThe product was then purified by column chromatography on silica gel
出典と根拠
- ORDレコード
- ord-9d540287f89c4dd2b760df357577682f
- 出典データセット
- uspto-grants-1989_01
- 特許番号
- US04797492
反応ノート
読み込み中…