تفاعل #472830
ord-666d45f2885948a2a7f5944b39191f6f
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1workup.STIRRINGthe mixture was stirred at room temperature for 1 hour 30 minutes
- 2أخرىthe organic layer was separated
- 3غسيلwashed sequentially with water
- 4تجفيفa saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate
- 5workup.DISTILLATIONthe solvent was distilled off under reduced pressure
- 6أخرىThe resultant residue was purified by silica gel column chromatography
الإجراء التجريبي
To a solution of 48 mg of tert-butyl (2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)(piperidin-4-yl)carbamate in 2 mL of methanol, 50 mg of (3-oxo-6-(1H-1,2,4-triazol-1-yl)pyrido(2,3-b)pyrazin-4(3H)-yl)acetaldehyde, 2.5 mL of dichloromethane and 20 μL of acetic acid were added, and the mixture was stirred at room temperature for 40 minutes. To the reaction mixture, 9.0 mg of sodium cyanoborohydride was added, and the mixture was stirred at room temperature for 1 hour 30 minutes. Thereto were added a saturated aqueous sodium hydrogen carbonate solution and chloroform, the organic layer was separated, washed sequentially with water and a saturated aqueous sodium chloride solution and dried over anhydrous magnesium sulfate, and the solvent was distilled off under reduced pressure. The resultant residue was purified by silica gel column chromatography using an eluent of chloroform:methanol=50:1 to obtain 35 mg of tert-butyl (2,3-dihydro(1,4)dioxino(2,3-c)pyridin-7-ylmethyl)(1-(2-(3-oxo-6-(1H-1,2,4-triazol-1-yl)pyrido(2,3-b)pyrazin-4(3H)-yl)ethyl)piperidin-4-yl)carbamate as a light yellow oily substance.