Hydrochloric Acid → 5-(Trifluoromethyl)isoxazol-3-ylamine
Reaction equation
[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]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
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.
Workup
- customThe product was then purified by column chromatography on silica gel
Sources & evidence
- ORD record
- ord-9d540287f89c4dd2b760df357577682f
- Source dataset
- uspto-grants-1989_01
- Patent number
- US04797492
Reaction notes
Loading…