Reacción #56066
ord-6a63ee114ab542759a6f79ccfdf47334
Ecuación de reacción
Reactantes
Reactivos
Condiciones de reacción
Tratamiento posterior
- 1workup.ADDITIONwas added to the suspension
- 2ConcentraciónThe mixture was then concentrated to dryness
- 3workup.DISSOLUTIONthe resulting residue was dissolved in 10 ml of dimethylformamide
- 4workup.DISSOLUTION593 mg of piperonylyl chloride dissolved in 5 ml of dimethylformamide
- 5workup.ADDITIONwas then added dropwise to the mixture
- 6Temperaturawhile cooling with ice-water
- 7workup.ADDITIONwater was added to the mixture
- 8Extracciónfollowed by extraction with chloroform
- 9OtroChloroform was removed by distillation, and diethyl ether
- 10workup.ADDITIONwas added to the residue
- 11Otroto crystallize the product
- 12OtroThe crystals thus obtained
- 13Otrowere separated by filtration
- 14Lavadowashed with diethyl ether
- 15Otrorecrystallized from a mixture of chloroform and diethyl ether
Procedimiento
1 g of 5-(1-hydroxy-2-tert-butylaminopropyl)-8-hydroxycarbostyril hydrochloride was suspended in 15 ml of methanol, and sodium methylate prepared from 155 mg of sodium metal and 3.3 ml of absolute methanol was added to the suspension. The mixture was then concentrated to dryness, and the resulting residue was dissolved in 10 ml of dimethylformamide. 593 mg of piperonylyl chloride dissolved in 5 ml of dimethylformamide was then added dropwise to the mixture while cooling with ice-water. The mixture was then stirred for 1 hour, and water was added to the mixture followed by extraction with chloroform. Chloroform was removed by distillation, and diethyl ether was added to the residue to crystallize the product. The crystals thus obtained were separated by filtration, washed with diethyl ether and recrystallized from a mixture of chloroform and diethyl ether to obtain 520 mg of 8-(3,4-methylenedioxyphenylcarbonyloxy)-5-(1-hydroxy-2-tert-butylaminopropyl)carbostyril having a melting point of 156°-157° C.