反应 #933775

反应方程式

ammonium chloride

ethyl 7-(4'-fluorophenyl)-2-methyl-5-(1'-methylethyl)pyrazolo [1,5-a]pyrimidin-6-ylcarboxylate

diisobutylaluminium hydride toluene

Diethyl ether

→

desired compound

收率 84.0%

7-(4'-fluorophenyl)-6-hydroxymethyl-2-methyl-5-(1'-methylethyl)pyrazolo [1,5-a]pyrimidin

收率 84.0%

溶剂

toluene

反应条件

后处理

1. 1
   其他at 0° C. to terminate
2. 2
   其他the reaction
3. 3
   其他the organic layer was separated
4. 4
   workup.DISSOLUTIONThe gelled substance was dissolved by an addition of a sodium hydroxide aqueous solution
5. 5
   萃取newly extracted with ethyl ether
6. 6
   干燥dried over anhydrous magnesium sulfate
7. 7
   过滤The extract was subjected to filtration
8. 8
   workup.DISTILLATIONthe solvent was distilled off
9. 9
   其他the residue was recrystallized from ethyl acetate

实验过程

4.40 g (12.9 mmol) of ethyl 7-(4'-fluorophenyl)-2-methyl-5-(1'-methylethyl)pyrazolo [1,5-a]pyrimidin-6-ylcarboxylate was dissolved in 40 ml of dry toluene under a nitrogen atmosphere and cooled to 0° C. in an ice bath. To this solution, 33 ml of a 16 weight % diisobutylaluminium hydride-toluene solution was dropwise added, and then, the mixture was stirred at 0° C. for one hour. After confirming the complete disappearance of ethyl 7-(4'-fluorophenyl)-2-methyl-5-(1'-methylethyl) pyrazolo[1,5-a]pyrimidin-6-ylcarboxylate by thin layer chromatography, a saturated ammonium chloride aqueous solution was added thereto at 0° C. to terminate the reaction. Diethyl ether was added to the reaction mixture, and the organic layer was separated. The gelled substance was dissolved by an addition of a sodium hydroxide aqueous solution and newly extracted with ethyl ether. The ethyl ether extracts were put together and dried over anhydrous magnesium sulfate. The extract was subjected to filtration, and the solvent was distilled off and the residue was recrystallized from ethyl acetate to obtain 3.24 g (yield: 84%) of the slightly yellow desired compound.

来源