تفاعل #9322
ord-86b007e3ac12424397c9f7c9e7aff08f
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1workup.ADDITIONwere added
- 2درجة الحرارةthe mixture was heated
- 3غسيلthe extract was washed with brine
- 4تجفيفAfter drying the obtained organic layer over anhydrous magnesium sulfate
- 5ترشيحfiltering it
- 6تركيزthe solvent was concentrated under reduced pressure
- 7أخرىthe residue was purified by silica gel column chromatography
الإجراء التجريبي
After dissolving tert-butyl N-(7-bromo-2-methoxypyrazolo[1,5-a]pyridin-3-yl)carbamate (300 mg) in 1,2-dimethoxyethane (10 mL) and water (5 mL), 6-methyl-2,4-dimethoxyphenylboric acid (258 mg), tetrakis (triphenylphosphine)palladium (0) complex (203 mg) and barium hydroxide octahydrate (415 mg) were added and the mixture was heated and stirred at 80° C. for 3 hours. Water was added to the reaction mixture, extraction was performed with ethyl acetate and the extract was washed with brine. After drying the obtained organic layer over anhydrous magnesium sulfate and filtering it, the solvent was concentrated under reduced pressure, the residue was purified by silica gel column chromatography, and the title compound (230 mg) was obtained from the n-hexane:ethyl acetate (5:1) fraction as a brown oil.