تفاعل #1605842
ord-10e6b9d31115409a9c134e705e92bd90
معادلة التفاعل
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1تركيزAfter 2 hours the reaction mixture was concentrated in vacuo
- 2workup.DISSOLUTIONThe residue was dissolved in 2-methyltetrahydrfuran (5 mL)
- 3أخرىwas quenched with water (25 mL) and 28% aq NH3 (15 mL)
- 4workup.STIRRINGstirred for 10 minutes
- 5استخلاصThe reaction mixture was then extracted with ethyl acetate (2×40 mL)
- 6غسيلThe combined organics were washed with water (50 mL) and brine (50 mL)
- 7تجفيفthen dried (MgSO4)
- 8تركيزconcentrated in vacuo
- 9أخرىThe crude mixture was purified by column chromatography
- 10غسيلeluting with 5% methanol (1:1 ethyl acetate/dichloromethane)
- 11أخرىto give the product
- 12أخرىto remove these impurities
الإجراء التجريبي
To a solution of dibenzyl phosphate (2.48 g, 8.91 mmol) in dichloromethane (25 ml) was added N,N-dimethyl formamide (1 drop) followed by oxalyl chloride (0.75 mL, 8.91 mmol). After 2 hours the reaction mixture was concentrated in vacuo. The residue was dissolved in 2-methyltetrahydrfuran (5 mL) and added to a suspension of dehydro-aripiprazole (1.66 g, 3.71 mmol) and potassium t-butoxide (0.92 g, 8.17 mmol) in 2-methyltetrahydrfuran (35 mL) at 0° C. under argon gas, then allowed to gradually warm to room temperature. After stirring overnight the reaction was quenched with water (25 mL) and 28% aq NH3 (15 mL) and stirred for 10 minutes. The reaction mixture was then extracted with ethyl acetate (2×40 mL). The combined organics were washed with water (50 mL) and brine (50 mL) then dried (MgSO4) and concentrated in vacuo. The crude mixture was purified by column chromatography eluting with 5% methanol (1:1 ethyl acetate/dichloromethane) to give the product. The 1H-NMR showed minor impurities still present (impurities not observed by LCMS). Various further purifications were attempted but failed to remove these impurities.