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
4.39 g (11 mmoles) of thioisoguanine and 7.10 g (121 mmoles) of neutral Raney-nickel are refluxed in 50 ml of 1-propanol for 4.5 hours. The nickel was filtered off and the filtrate evaporated to dryress. The residue (3.79 g/93.8%) was dissolved in 20 ml of chloroform and 0.4 ml methanol and filtered through 24 g of silicagel in a column also with 2% methanol. The combined fractions were washed with 1N NaOH and the organic phase evaporated to dryness. The residue (2.69 g/66.6%) was dissolved in 30 ml of dichloromethane and 0.6 ml methanol and again filtered through 30 g of silicagel. A total of 1.86 g (46.0%) of 3H-purine was isolated, which was dissolved in 20 ml of methanol, treated with 5.4 ml of 1N methanolic HCl, and evaporated in vacuo to dryness. Crystallization and recrystallization from dichloromethane and ethyl acetate gave 1.75 g (39.4%) of 3H-purine hydrochloride with mp 170-85° C.
WORKUP
后处理
- filtrationThe nickel was filtered off
- customthe filtrate evaporated
- dissolutionThe residue (3.79 g/93.8%) was dissolved in 20 ml of chloroform
- filtration0.4 ml methanol and filtered through 24 g of silicagel in a column also with 2% methanol
- washThe combined fractions were washed with 1N NaOH
- customthe organic phase evaporated to dryness
- dissolutionThe residue (2.69 g/66.6%) was dissolved in 30 ml of dichloromethane
- filtration0.6 ml methanol and again filtered through 30 g of silicagel