تفاعل #1605842

ord-10e6b9d31115409a9c134e705e92bd90

معادلة التفاعل

O=P([O-])(OCc1ccccc1)OCc1ccccc1
dibenzyl phosphate
O=C(Cl)C(=O)Cl
oxalyl chloride
O=c1ccc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc2[nH]1
dehydro-aripiprazole
CC(C)(C)[O-].[K+]
potassium t-butoxide
CCOP(=O)(OCC)Oc1ccc2ccc(OCCCCN3CCN(c4cccc(Cl)c4Cl)CC3)cc2n1
7-(4-(4-(2,3-dichlorophenyl)piperazin-1-yl)butoxy)quinolin-2-yl diethyl phosphate

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    تركيزAfter 2 hours the reaction mixture was concentrated in vacuo
  2. 2
    workup.DISSOLUTIONThe residue was dissolved in 2-methyltetrahydrfuran (5 mL)
  3. 3
    أخرىwas quenched with water (25 mL) and 28% aq NH3 (15 mL)
  4. 4
    workup.STIRRINGstirred for 10 minutes
  5. 5
    استخلاصThe reaction mixture was then extracted with ethyl acetate (2×40 mL)
  6. 6
    غسيلThe combined organics were washed with water (50 mL) and brine (50 mL)
  7. 7
    تجفيفthen dried (MgSO4)
  8. 8
    تركيزconcentrated in vacuo
  9. 9
    أخرىThe crude mixture was purified by column chromatography
  10. 10
    غسيلeluting with 5% methanol (1:1 ethyl acetate/dichloromethane)
  11. 11
    أخرىto give the product
  12. 12
    أخرىto remove these impurities

الإجراء التجريبي

To a solution of dibenzyl phosphate (2.48 g, 8.91 mmol) in dichloromethane (25 ml) was added N,N-dimethyl formamide (1 drop) followed by oxalyl chloride (0.75 mL, 8.91 mmol). After 2 hours the reaction mixture was concentrated in vacuo. The residue was dissolved in 2-methyltetrahydrfuran (5 mL) and added to a suspension of dehydro-aripiprazole (1.66 g, 3.71 mmol) and potassium t-butoxide (0.92 g, 8.17 mmol) in 2-methyltetrahydrfuran (35 mL) at 0° C. under argon gas, then allowed to gradually warm to room temperature. After stirring overnight the reaction was quenched with water (25 mL) and 28% aq NH3 (15 mL) and stirred for 10 minutes. The reaction mixture was then extracted with ethyl acetate (2×40 mL). The combined organics were washed with water (50 mL) and brine (50 mL) then dried (MgSO4) and concentrated in vacuo. The crude mixture was purified by column chromatography eluting with 5% methanol (1:1 ethyl acetate/dichloromethane) to give the product. The 1H-NMR showed minor impurities still present (impurities not observed by LCMS). Various further purifications were attempted but failed to remove these impurities.

المصدر

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