반응 #9994
ord-74fde67f2a9f47cb945db7fa6bea0160
반응 방정식
반응 조건
후처리
- 1workup.ADDITIONare added at room temperature
- 2기타the reaction to completion
- 3workup.STIRRINGthe reaction mixture is stirred at 45° C. for a further 24 hours
- 4세척washed with water (2 times) and saturated sodium chloride solution
- 5건조dried over magnesium sulfate
- 6여과After filtration
- 7농축the filtrate is concentrated under reduced pressure at 35° C.
- 8기타the residue is dried under an HV
- 9기타The resulting crude product is purified by crystallization from diethyl ether/hexane
실험 절차
500 mg (1.78 mmol) of 2-chloro-6-(3-chloro-phenyl-amino)-purine are dissolved in a mixture of 29.5 ml of DMF/water (85/15) and 5 ml of dioxane by means of gentle heating. 870 mg (2.67 mmol) of caesium carbonate, followed by 1.78 ml (17.8 mmol) of isopropyl iodide are added at room temperature. The reaction mixture is stirred at room temperature for 18 hours. To bring the reaction to completion, the reaction mixture is stirred at 45° C. for a further 24 hours. When the reaction has ended, the reaction mixture is diluted with ethyl acetate, washed with water (2 times) and saturated sodium chloride solution and dried over magnesium sulfate. After filtration, the filtrate is concentrated under reduced pressure at 35° C. and the residue is dried under an HV. The resulting crude product is purified by crystallization from diethyl ether/hexane. 2-Chloro-6-(3-chloro-phenyl-amino)-9-isopropyl-9H-purine is obtained; Rf=0.46 (ethyl acetate); m.p. 128–129° C.