Реакция #81903
ord-2d0800827d9f443baf068d2045d203c6
Уравнение реакции
Реагенты
Растворители
Условия реакции
Обработка
- 1ФильтрацияThe solids were filtered
- 2Промывкаwashed with 40 mL of 50% aqueous formic acid
- 3ТемператураWith ice bath cooling
- 4workup.ADDITIONa cold saturated solution of potassium carbonate was added slowly to the green filtrate until complete precipitation of a solid
- 5ЭкстракцияThe solid was extracted into 200 mL of ethyl acetate
- 6Сушкаthe solution was dried (potassium carbonate)
- 7Фильтрацияfiltered
- 8Концентрированиеconcentrated
Методика
A solution of 4.00 g (0.022 mol) of 5-cyano-4-methylamino-2-methylsulfanyl-pyrimidine (from Example 3) in 150 mL of 50% aqueous formic acid was reacted with 6.0 g of water-wet Raney Nickel. The mixture was stirred at 25° C. for 12 hours. The solids were filtered and washed with 40 mL of 50% aqueous formic acid. With ice bath cooling, a cold saturated solution of potassium carbonate was added slowly to the green filtrate until complete precipitation of a solid was achieved (pH is still acidic; pH about 5). The solid was extracted into 200 mL of ethyl acetate, and the solution was dried (potassium carbonate), filtered, and concentrated; wt 2.30 g (57%), mp 98°-100° C.; tlc (1:1 hexane:ethyl acetate) one spot Rf 0.5;