تفاعل #1605836
ord-181d6d2f5cce4d7088c86beb8f9b13dc
معادلة التفاعل
الكواشف
ظروف التفاعل
المعالجة
- 1workup.WAITAfter a further 10 minutes
- 2workup.WAITThe reaction was held at −78° C. for 2 hours
- 3درجة الحرارةto warm to room temperature
- 4أخرىAfter 2 hours the reaction was quenched with saturated aqueous ammonium chloride solution (30 mL)
- 5استخلاصextracted with ethyl acetate (2×30 mL)
- 6غسيلwashed with saturated aqueous sodium hydrogen carbonate solution (30 mL), brine (30 mL)
- 7تجفيفdried over MgSO4
- 8تركيزconcentrated
- 9أخرىThe crude product was purified by column chromatography on silica eluting with 1:1 ethyl acetate to dichloromethane to 10% methanol in 1:1 ethyl acetate to dichloromethane
- 10أخرىto give the product
- 11أخرىThe product was triturated in heptane
- 12أخرىto remove aliphatic impurities
- 13ترشيحfiltered
- 14أخرىto afford Compound-74 (0.824 g) as a colorless solid
الإجراء التجريبي
To a solution of diisopropylamine (0.99 mL, 7.02 mmol) in 2-methyltetrahydrfuran (33 mL) at −5° C. was added n-BuLi (2.67 mL, 2.5 M in hexanes, 6.69 mmol) slowly. After 20 minutes, the reaction was cooled to −78° C. and aripiprazole (1.50 g, 3.34 mmol) was added. After a further 10 minutes, methylchloroformate (0.65 mL, 8.36 mmol) was added. The reaction was held at −78° C. for 2 hours before allowing to warm to room temperature. After 2 hours the reaction was quenched with saturated aqueous ammonium chloride solution (30 mL) and extracted with ethyl acetate (2×30 mL). The organics were combined, washed with saturated aqueous sodium hydrogen carbonate solution (30 mL), brine (30 mL), dried over MgSO4 and concentrated. The crude product was purified by column chromatography on silica eluting with 1:1 ethyl acetate to dichloromethane to 10% methanol in 1:1 ethyl acetate to dichloromethane to give the product. The product was triturated in heptane to remove aliphatic impurities and then filtered to afford Compound-74 (0.824 g) as a colorless solid.