Reaktion #430550
ord-e5e6a276d85a4793814838fd4c543719
Reaktionsgleichung
Reagenzien
Lösungsmittel
Reaktionsbedingungen
Aufarbeitung
- 1SonstigeVolatile material was removed by evaporation and dichloromethane (250 ml)
- 2workup.ADDITIONwas added to the residue
- 3SonstigeInsoluble material was removed by filtration
- 4Waschenthe filtrate was washed with water (100 ml) and saturated sodium chloride solution (100 ml)
- 5workup.ADDITIONThe solution was treated with charcoal
- 6Trocknendried (MgSO4)
- 7SonstigeThe solvent was removed by evaporation
- 8Sonstigethe residue was purified by flash chromatography
- 9Wascheneluting with ethyl acetate/hexane (1:4 v/v)
- 10SonstigeThe resulting solid was triturated with ether
- 11Sonstigerecrystallised from ethanol
Vorschrift
5-Dimethylamino-1-naphthalenesulphonyl chloride (15.2 g) and 2-amino-5-bromo-3-methoxypyrazine (obtained as described in Gazz. Chim. Ital. 1960, 90, 1807) (9.5 g) were mixed intimately in a mortar and pestle and added to pyridine (150 ml) at 0° C. The solution was kept at 0° C. for 1 hour and then heated at 80° C. for 18 hours. Volatile material was removed by evaporation and dichloromethane (250 ml) was added to the residue. Insoluble material was removed by filtration and the filtrate was washed with water (100 ml) and saturated sodium chloride solution (100 ml). The solution was treated with charcoal and dried (MgSO4). The solvent was removed by evaporation and the residue was purified by flash chromatography, eluting with ethyl acetate/hexane (1:4 v/v). The resulting solid was triturated with ether and recrystallised from ethanol to give 5-dimethylamino-N-(5-bromo-3-methoxy-2-pyrazinyl)-1-naphthalenesulphonamide (4.7 g), m.p. 166°-167° C.; 1H NMR (d6 -DMSO): 2.8 (s,6H), 3.9 (s,3H), 7.2 (d,1H), 7.55-7.7 (d,2H), 7.8 (s,1H), 8.3 (d,1H), 8.4-8.5 (m,2H), 11.5 (s,1H); mass spectrum (+ve CI): 437 (M+H)+.