تفاعل #438461
ord-34b4645bd74949f7813239f16899fdd3
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1درجة الحرارةThe reaction mixture was cooled to ambient temperature
- 2أخرىwas quenched
- 3workup.ADDITIONby adding saturated aqueous ammonium chloride solution
- 4استخلاصThe mixture was extracted with AcOEt
- 5غسيلThe organic layer was washed with 1M HCl, saturated aqueous sodium bicarbonate solution, saturated aqueous sodium chloride solution
- 6تجفيفdried over magnesium sulfate
- 7تركيزconcentrated in vacuo
- 8أخرىThe residue was purified by preparative thin layer silica gel chromatography
- 9استخلاصThe separated silica gel was extracted with 10% MeOH/CHCl3
- 10أخرىthe solvent was evaporated in vacuo
الإجراء التجريبي
To a solution of cyclopropylmagnesium bromide, which was prepared from cyclopropyl bromide (257 ml) and magnesium (57 mg) in THF (1 ml) as usual method, was added a solution of 5-(4-{2-[(aminocarbonyl)-amino]ethyl}phenyl)-N-methoxy-1-(4-methoxyphenyl)-N-methyl-1H-pyrazole-3-carboxamide (90 mg) in THF (3 ml) dropwise at ambient temperature. The mixture was stirred at 50° C. for 5 hours. The reaction mixture was cooled to ambient temperature and was quenched by adding saturated aqueous ammonium chloride solution. The mixture was extracted with AcOEt. The organic layer was washed with 1M HCl, saturated aqueous sodium bicarbonate solution, saturated aqueous sodium chloride solution, dried over magnesium sulfate, and concentrated in vacuo. The residue was purified by preparative thin layer silica gel chromatography developed by MeOH/CHC3 10%. The separated silica gel was extracted with 10% MeOH/CHCl3 and the solvent was evaporated in vacuo to give N-(2-{4-[3-(cyclopropylcarbonyl)-1-(4-methoxyphenyl)-1H-pyrazol-5-yl]phenyl}ethyl)urea (23 mg) as a powder.