Reacción #4599
ord-ce801baf663247ddbe6aa39a88d06aae
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1Filtraciónthe precipitate filtered off
- 2Otrosolvent removed from the filtrate under reduced pressure
- 3workup.DISSOLUTIONThe residue is dissolved in 5 ml of tetrahydrofuran and to this solution
- 4workup.ADDITIONis added dropwise a solution of ammonia in tetrahydrofuran until the reaction
- 5workup.ADDITIONThe mixture is poured into water
- 6Extracciónextracted with ethyl acetate
- 7SecadoThe organic solution is dried over magnesium sulfate
- 8Otroevaporated to an oil which
- 9Otrois chromatographed on silica gel
- 10Lavadoeluting with a 50:1 mixture of dichloromethane and methanol
- 11workup.STIRRINGThe purified product is stirred with a mixture of ether and hexane
- 12Filtraciónfiltered
Procedimiento
To a solution of 500 mgs of morpholinoethyl (E)-6-(1,3-dihydro-4-hydroxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoate in 10 ml of benzene cooled in an ice bath is added 0.1 ml of pyridine and 6 ml of a 12.5% solution of phosgene in benzene. The solution is stirred at 25° C. overnight, the precipitate filtered off and solvent removed from the filtrate under reduced pressure. The residue is dissolved in 5 ml of tetrahydrofuran and to this solution is added dropwise a solution of ammonia in tetrahydrofuran until the reaction is complete. The mixture is poured into water and extracted with ethyl acetate. The organic solution is dried over magnesium sulfate and evaporated to an oil which is chromatographed on silica gel, eluting with a 50:1 mixture of dichloromethane and methanol. The purified product is stirred with a mixture of ether and hexane and filtered giving morpholinoethyl (E)-6-(1,3-dihydro-4-carbamoyloxy-6-methoxy-7-methyl-3-oxo-5-isobenzofuranyl)-4-methyl-4-hexenoate.