Reaction #927275
ord-1ac3116c907f45cda0261f99cd095297
Reaction equation
Reagents
Solvents
Conditions
Workup
- 1TemperatureThe solution slowly became cloudy as it was chilled for 1 hour on ice
- 2Otherprecipitation by centrifugation at 1000 g for 5 minutes
- 3Otherthe pellet dried for 2 days in a vacuum desiccator
- 4workup.ADDITIONcontaining phosphorus pentoxide
- 5workup.DISSOLUTIONIn 5 cc of a solution of 4:1 acetonitrile and water, 46.5 mg prazosin free base and an equimolar amount of alprostadil, 43 mg, were dissolved
- 6workup.ADDITIONwas added
- 7Temperatureto increase the volume 50%
- 8Otherwas removed azeotropically
- 9OtherThe mother liquor was decanted
- 10OtherThe crystals were dried in a vacuum dessicator
- 11workup.ADDITIONcontaining phosphorus pentoxide
Procedure
Prazosin alprostadilate was synthesized as follows. Of prazosin hydrochloride (Sigma), (202.2 mg) were dissolved in 300 cc sterile water (Baxter). To the solution was added 481.5 μL of 1 M sodium hydroxide (Fisher). The solution slowly became cloudy as it was chilled for 1 hour on ice. The cloudy solution was transferred to conical tubes in order to hasten precipitation by centrifugation at 1000 g for 5 minutes. Pellets were consolidated and recentrifuged. The pellet was resuspended in 10 cc sterile water, and after centrifugation, the supernatant was discarded and the pellet dried for 2 days in a vacuum desiccator containing phosphorus pentoxide. In 5 cc of a solution of 4:1 acetonitrile and water, 46.5 mg prazosin free base and an equimolar amount of alprostadil, 43 mg, were dissolved by heating to 50° C. for 5 minutes. The volume was reduced by one-half under a stream of nitrogen and acetonitrile was added to increase the volume 50%. This was repeated until water was removed azeotropically and only acetonitrile remained. As the volume of acetonitrile decreased, white crystals appeared. The mother liquor was decanted and discarded. The crystals were dried in a vacuum dessicator containing phosphorus pentoxide.