تفاعل #1605840

ord-514b1cdb2fc8441a9eedfe821d093bc7

معادلة التفاعل

O=c1ccc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc2[nH]1
dehydro-aripiprazole
CCN(CC)CC
triethylamine
CCN(CC)C(=O)Cl
diethyl carbamoyl chloride
CCN(CC)C(=O)Oc1ccc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc2n1
7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)quinolin-2-yl diethylcarbamate

الكواشف

لا شيء

المذيبات

ظروف التفاعل

درجة الحرارة
100°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe reaction was quenched with water (50 mL)
  2. 2
    استخلاصextracted with dichloromethane (2×100 mL)
  3. 3
    تجفيفThe combined organics were dried (MgSO4)
  4. 4
    تركيزconcentrated
  5. 5
    أخرىThe crude product was purified by column chromatrography on silica eluting with ethyl acetate to 20% tetrahydrofuran/ethyl acetate
  6. 6
    أخرىto give the product
  7. 7
    أخرىThe product was then triturated with heptane
  8. 8
    أخرىto remove aliphatic impurities
  9. 9
    أخرىdried
  10. 10
    أخرىto give Compound-334 (1.54 g) as a light brown oil

الإجراء التجريبي

A mixture of dehydro-aripiprazole (1.50 g, 3.36 mmol), triethylamine (1.03 mL, 7.39 mmol), diethyl carbamoyl chloride (1.02 mL) were combined in tetrahydrofuran (30 mL). This was then heated to 100° C. for 6 hours by microwave. The reaction was quenched with water (50 mL) and extracted with dichloromethane (2×100 mL). The combined organics were dried (MgSO4) and concentrated. The crude product was purified by column chromatrography on silica eluting with ethyl acetate to 20% tetrahydrofuran/ethyl acetate to give the product. The product was then triturated with heptane to remove aliphatic impurities and then dried to give Compound-334 (1.54 g) as a light brown oil.

المصدر

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