تفاعل #11473
ord-b80539dc2ef344d398c44bf5d354c5d7
معادلة التفاعل
المتفاعلات
الكواشف
المذيبات
ظروف التفاعل
المعالجة
- 1تركيزthe reaction mixture was concentrated under reduced pressure
- 2workup.ADDITIONtreated with 3 mL of triethylamine
- 3درجة الحرارةThe solution was heated
- 4درجة الحرارةto reflux for 4 d
- 5تركيزThe reaction mixture was then concentrated
- 6workup.DISSOLUTIONredissolved in 50 mL of xylenes
- 7workup.ADDITIONtreated with pyridinium hydrochloride (0.5 g)
- 8درجة الحرارةthe mixture was heated
- 9درجة الحرارةto reflux for 4 d
- 10تركيزThe reaction mixture was concentrated
- 11غسيلwashed with saturated NaHCO3 solution, H2O (2×) and brine
- 12تجفيفThe organic portion was dried over Na2SO4
- 13تركيزconcentrated
- 14أخرىThe resulting syrup was purified by column chromatography (SiO2, 80% EtOAc/hexanes)
الإجراء التجريبي
A solution of N-{2-[(3-amino-5,6-dimethyl-2-phenoxypyridin-4-yl)amino]-1,1-dimethylethyl}acetamide (1.80 g, 5.23 mmol) in 50 mL of CH2Cl2 was cooled to 0° C., under N2, and treated with triethylamine (728 μL, 5.23 mmol) and ethoxyacetyl chloride (574 μL, 5.23 mmol). After stirring overnight, the reaction mixture was concentrated under reduced pressure. The resulting syrup was taken up in 50 mL of EtOH and treated with 3 mL of triethylamine. The solution was heated to reflux for 4 d. The reaction mixture was then concentrated and redissolved in 50 mL of xylenes and treated with pyridinium hydrochloride (0.5 g) and the mixture was heated to reflux for 4 d. The reaction mixture was concentrated and taken up in 100 mL of EtOAc and washed with saturated NaHCO3 solution, H2O (2×) and brine. The organic portion was dried over Na2SO4 and concentrated. The resulting syrup was purified by column chromatography (SiO2, 80% EtOAc/hexanes) to give N-{2-[2-(ethoxymethyl)-6,7-dimethyl-4-phenoxy-1H-imidazo[4,5-c]pyridin-1-yl]-1,1-dimethylethyl}acetamide (980 mg) as a mustard colored foam.