Reaktion #367558

Reaktionsgleichung

sodium borohydride

tellurium

(3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acid methyl ester

acetic acid

→

2,3-dihydro-3-oxo-5H-thiazolo[2,3-b]quinazoline-2-acetic acid methyl ester

Ausbeute 32.3%

Lösungsmittel

ethanol

ethanol

ethanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   Temperaturwas heated under nitrogen atmosphere for 15 min
2. 2
   Temperaturto warm up to ambient temperature
3. 3
   workup.STIRRINGstirred overnight
4. 4
   FiltrationThen, the mixture was filtered through celite
5. 5
   Sonstigeevaporated under reduced pressure
6. 6
   Extraktionextracted with chloroform
7. 7
   ExtraktionThe organic extract
8. 8
   Trocknenwas dried over anhydrous magnesium sulfate
9. 9
   Sonstigeevaporated under reduced pressure

Vorschrift

A suspension of sodium borohydride (3.03 g, 0.08 mol) and 4.38 g (0.034 mol) tellurium powder in 135 ml anhydrous ethanol was heated under nitrogen atmosphere for 15 min. After cooling to -20° C., 8.08 ml glacial acetic acid in 33.65 ml anhydrous ethanol was added dropwise, and the mixture was stirred at that temperature for 5 min, followed by the addition of 3.50 g (0.013 mol) of (3-oxo-5H-thiazolo[2,3-b]quinazolin-2(3H)-ylidene)acetic acid methyl ester in 13.5 ml anhydrous ethanol. The reaction mixture was allowed to warm up to ambient temperature and stirred overnight. Then, the mixture was filtered through celite, and evaporated under reduced pressure. The residue was taken up in water and extracted with chloroform. The organic extract was dried over anhydrous magnesium sulfate and evaporated under reduced pressure, yielding 1.16 g of 2,3-dihydro-3-oxo-5H-thiazolo[2,3-b]quinazoline-2-acetic acid methyl ester. Mp 143°-144° C. after recrystallization from ethyl acetate.

Quelle