HRID464771
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
24.8 g (70 mmol) of methyl 2-amino-6-[(p-toluenesulfonyl)oxy]-4-pyrimidinecarbamate-3-oxide and 14.5 g (175 mmol) of 1,2,5,6-tetrahydropyridine are boiled at reflux under argon in 400 ml of chloroform. After 90 minutes, the resulting precipitate is filtered off and the chloroform solution is washed with water. The organic phase is separated, dried over sodium sulfate and evaporated under reduced pressure, whereby there is obtained a crystalline solid. A sample of this material is recrystallized from methylene chloride/ether. The thus-obtained methyl 2-amino-6-[3,6-dihydro-1(2H)-pyridyl]-4-pyrimidinecarbamate-3-oxide melts at 221°-223° with decomposition.
WORKUP
后处理
- filtrationthe resulting precipitate is filtered off
- washthe chloroform solution is washed with water
- customThe organic phase is separated
- dry with materialdried over sodium sulfate
- customevaporated under reduced pressure
- customwhereby there is obtained a crystalline solid
- customA sample of this material is recrystallized from methylene chloride/ether