Reaktion #169902

Reaktionsgleichung

N,N-diisopropylethylamine

NaHCO3

4-amino-1,2,5-oxadiazole-3-carboxylic acid

6-chloropyridin-2-amine

N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate

→

desired product

4-Amino-N-(6-chloropyridin-2-yl)-1,2,5-oxadiazole-3-carboxamide

Lösungsmittel

N,N-dimethylformamide

Reaktionsbedingungen

Aufarbeitung

1. 1
   Extraktionextracted with ethyl acetate (100 mL)
2. 2
   SonstigeThe organic layer was separated
3. 3
   Waschenwashed with brine (25 mL)
4. 4
   Trocknendried with sodium sulfate
5. 5
   Filtrationfiltered
6. 6
   Einengenconcentrated to a crude solid
7. 7
   WaschenThe crude solid was washed with ethyl acetate
8. 8
   Filtrationfiltered
9. 9
   EinengenThe filtrate was concentrated
10. 10
    Sonstigepurified on silica gel

Vorschrift

A solution of 4-amino-1,2,5-oxadiazole-3-carboxylic acid (0.4 g, 3.1 mmol) and 6-chloropyridin-2-amine (0.56 g, 4.3 mmol) in N,N-dimethylformamide (6.2 mL) was treated with N,N,N′,N′-tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (1.4 g, 3.7 mmol) followed by N,N-diisopropylethylamine (0.76 mL, 4.3 mmol) at 0° C. The reaction mixture was stirred at 25° C. for 2 h, poured into saturated NaHCO3 (50 mL) and extracted with ethyl acetate (100 mL). The organic layer was separated and washed with brine (25 mL), dried with sodium sulfate, filtered, and concentrated to a crude solid. The crude solid was washed with ethyl acetate and filtered. The filtrate was concentrated and purified on silica gel to give the desired product with some impurities. The impurities were removed by washing the solid with chloroform to yield the desired product (65 mg, 9%). LCMS for C8H7ClN5O2 (M+H)+: m/z=240.1.

Quelle