تفاعل #1605836

ord-181d6d2f5cce4d7088c86beb8f9b13dc

الكواشف

لا شيء

ظروف التفاعل

درجة الحرارة
-78°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.WAITAfter a further 10 minutes
  2. 2
    workup.WAITThe reaction was held at −78° C. for 2 hours
  3. 3
    درجة الحرارةto warm to room temperature
  4. 4
    أخرىAfter 2 hours the reaction was quenched with saturated aqueous ammonium chloride solution (30 mL)
  5. 5
    استخلاصextracted with ethyl acetate (2×30 mL)
  6. 6
    غسيلwashed with saturated aqueous sodium hydrogen carbonate solution (30 mL), brine (30 mL)
  7. 7
    تجفيفdried over MgSO4
  8. 8
    تركيزconcentrated
  9. 9
    أخرىThe 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
  10. 10
    أخرىto give the product
  11. 11
    أخرىThe product was triturated in heptane
  12. 12
    أخرىto remove aliphatic impurities
  13. 13
    ترشيحfiltered
  14. 14
    أخرىto 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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09072788B2uspto-grants-2015_07