Bromine → Methyl 5-amino-1,2,4-thiadiazole-3-carboxylate
Reaktionsgleichung
Br.[CH2:2]([O:4][C:5]([C:7]([NH2:9])=[NH:8])=[O:6])C.[Na].BrBr.[S-:13][C:14]#[N:15].[K+]>CO>[NH2:15][C:14]1[S:13][N:9]=[C:7]([C:5]([O:4][CH3:2])=[O:6])[N:8]=1Komponenten
Edukt 4
Produkt 1
Reagenzien, Katalysatoren, Lösungsmittel 1
Reaktionsbedingungen
- Temperatur
- 0 °C
Versuchsvorschrift
To a solution of 1-ethoxycarbonylformamidine. hydrobromide (16.6 g.) in absolute methanol (84 ml) was added a solution of sodium (1.93 g) in absolute methanol (42 ml) at 0° C. To the mixture were added alternately bromine (12.8 g) and a solution of sodium (1.93 g) in absolute methanol (42 ml) at 0° C. and then to the suspension was added potassium thiocyanate (8.1 g) in absolute methanol (100 ml). The reaction mixture was stirred for an hour at 0° C. and for an additional 6 hours at ambient temperature. The mixture was filtered through cellulose powder and the filtrate was evaporated to dryness. The residue was dissolved in a mixture of ethyl acetate and water, and then the ethyl acetate layer was separated and dried over anhydrous magnesium sulfate. The solvent was evaporated and the residue was triturated with diethyl ether to give the title compound (9.0 g), mp. 202° to 205° C.
Aufarbeitung
- filtrationThe mixture was filtered through cellulose powder
- customthe filtrate was evaporated to dryness
- dissolutionThe residue was dissolved in a mixture of ethyl acetate and water
- customthe ethyl acetate layer was separated
- dry with materialdried over anhydrous magnesium sulfate
- customThe solvent was evaporated
- customthe residue was triturated with diethyl ether
Quellen und Nachweise
- ORD-Eintrag
- ord-18412570489a481fa99941b017428ac0
- Quelldatensatz
- uspto-grants-1981_05
- Patentnummer
- US04268509
Notizen zur Reaktion
Wird geladen…