تفاعل #1605831
ord-885bdeb1cb204d6a8d1df64ae87b5019
معادلة التفاعل
الكواشف
المذيبات
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 overnight
- 4أخرىThe 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 0 to 3% tetrahydrofuran in ethyl acetate
- 10أخرىThe product was triturated in heptane
- 11أخرىto remove aliphatic impurities
- 12ترشيحfiltered
- 13أخرىdried
- 14أخرىto afford Compound-59 (0.487 g) as a colorless solid
الإجراء التجريبي
To a solution of diisopropylamine (1.11 mL, 7.87 mmol) in 2-methyltetrahydrofuran (37 mL) at −5° C. was added n-BuLi (3.0 mL, 2.5 M in hexanes, 7.49 mmol) slowly. After 20 minutes, the reaction was cooled to −78° C. and Aripiprazole (1.68 g, 3.74 mmol) was added. After a further 10 minutes, hexylchloroformate (1.53 mL, 9.37 mmol) was added. The reaction was held at −78° C. for 2 hours before allowing to warm to room temperature overnight. 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 0 to 3% tetrahydrofuran in ethyl acetate. The product was triturated in heptane to remove aliphatic impurities and then filtered and dried to afford Compound-59 (0.487 g) as a colorless solid.