Ammonia → 4-[2-(2,2,2-Trifluoroethyl)guanidino]-2-methylthiopyrimidine
Reaktionsgleichung
[F:1][C:2]([F:17])([F:16])[CH2:3][NH:4][C:5](=S)[NH:6][C:7]1[CH:12]=[CH:11][N:10]=[C:9]([S:13][CH3:14])[N:8]=1.[NH3:18]>CO>[F:1][C:2]([F:17])([F:16])[CH2:3][N:4]=[C:5]([NH2:18])[NH:6][C:7]1[CH:12]=[CH:11][N:10]=[C:9]([S:13][CH3:14])[N:8]=1Komponenten
4
Edukt 2
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Versuchsvorschrift
A mixture of 4-[3-(2,2,2-trifluoroethyl)thioureido]-2-methylthiopyrimidine (2.15 g.), methanol (100 ml.), saturated ethanolic ammonia (10 ml.) and yellow mercuric oxide (4.3 g.) was stirred at room temperature for 2 hours and then filtered. The filtrate was evaporated to dryness and the residue recrystallised from ethanol to give 4-[2-(2,2,2-trifluoroethyl)guanidino]-2-methylthiopyrimidine (1.5 g.), m.p. 201°-202°.
Aufarbeitung
- filtrationfiltered
- customThe filtrate was evaporated to dryness
- customthe residue recrystallised from ethanol
Quellen und Nachweise
- ORD-Eintrag
- ord-08df52c1668844eb8a0d748ea6ac0aa9
- Quelldatensatz
- uspto-grants-1988_08
- Patentnummer
- US04762932
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