تفاعل #9297

ord-5add00d2fc5045eab00f8af0fde67517

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONwas added in five portions
  2. 2
    workup.STIRRINGstirring
  3. 3
    غسيلthe extract was washed with saturated aqueous sodium hydrogencarbonate and brine
  4. 4
    تجفيفAfter drying over anhydrous magnesium sulfate and filtration
  5. 5
    تركيزthe solvent was concentrated under reduced pressure
  6. 6
    أخرىthe residue was purified by preparative TLC [n-hexane:ethyl acetate (5:1), Rf=0.5]

الإجراء التجريبي

N-[7-(2,4-Dichlorophenyl)-2-ethylpyrazolo[1,5-a]pyridin-3-yl]-N-(2-methoxyethyl)amine (14 mg) was dissolved in tetrahydrofuran (1 mL), and after adding propionaldehyde (0.016 mL) and 3 M aqueous sulfuric acid (0.77 mL), sodium borohydride (5.8 mg) was added in five portions while vigorously stirring on ice, and stirring was continued for 30 minutes. Water was added to the reaction mixture, extraction was performed with diethyl ether and the extract was washed with saturated aqueous sodium hydrogencarbonate and brine. After drying over anhydrous magnesium sulfate and filtration, the solvent was concentrated under reduced pressure and the residue was purified by preparative TLC [n-hexane:ethyl acetate (5:1), Rf=0.5] to obtain the title compound (9.5 mg) as a light yellow oil.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07091215B2uspto-grants-2006_08