تفاعل #1605831

ord-885bdeb1cb204d6a8d1df64ae87b5019

معادلة التفاعل

CCCCCCOC(=O)Cl
hexylchloroformate
O=C1CCc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc2N1
Aripiprazole
CC(C)NC(C)C
diisopropylamine
[Li][CH2]CCC
n-BuLi
CCCCCCOC(=O)N1C(=O)CCc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc21
Hexyl 7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)-2-oxo-3,4-dihydroquinoline-1(2H)-carboxylate

الكواشف

لا شيء

المذيبات

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 overnight
  4. 4
    أخرىThe 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 0 to 3% tetrahydrofuran in ethyl acetate
  10. 10
    أخرىThe product was triturated in heptane
  11. 11
    أخرىto remove aliphatic impurities
  12. 12
    ترشيحfiltered
  13. 13
    أخرىdried
  14. 14
    أخرىto 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.

المصدر

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