Hydrochloric Acid → 5-(Trifluoromethyl)isoxazol-3-ylamine
Reaktionsgleichung
[F:1][C:2]([F:18])([F:17])[C:3]1[O:7][N:6]=[C:5]([NH:8]C(=O)C2C=CC=CC=2)[CH:4]=1.Cl>C(O)CO>[F:1][C:2]([F:18])([F:17])[C:3]1[O:7][N:6]=[C:5]([NH2:8])[CH:4]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
The reaction was carried out according to the same procedure as described in Example 50 except that 5-trifluoromethyl-3-benzoylaminoisoxazole (0.8738 g, 3.41 mmole), 36% hydrochloric acid (0.87 g, 8.53 mmole) and ethylene glycol (3.4 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.
Aufarbeitung
- customThe product was then purified by column chromatography on silica gel
Quellen und Nachweise
- ORD-Eintrag
- ord-3ef23fb820734c8d92ba7e00da80f798
- Quelldatensatz
- uspto-grants-1989_01
- Patentnummer
- US04797492
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