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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2389881Generated: November 4, 2026

Trimethylsilyl cyanide → (2-Phenylfuro[3,2-c]pyrazolo[1,5-a]pyridin-1-yl)acetonitrile

https://huagongshe.com/reaction/2389881

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylsilyl cyanideHCID 82115—
Reactant(2-Phenylfuro[3,2-c]pyrazolo[1,5-a]pyridin-1-yl)methanolHCID 59179389—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product(2-Phenylfuro[3,2-c]pyrazolo[1,5-a]pyridin-1-yl)acetonitrileHCID 5917940673%

Reaction Steps

To a solution of boron trifluoride diethyl ether complex (460 μL, 3.63 mmol) and trimethylsilyl cyanide (645 μL, 4.84 mmol) in dichloromethane (12 mL) was added a solution of (2-phenylfuro[3,2-c]pyrazolo[1,5-a]pyridin-1-yl)methanol (320 mg, 1.21 mmol) in dichloromethane (12 mL) under ice-cooling and an argon atmosphere, and the mixture was stirred for 2 hr. The reaction solution was diluted with saturated aqueous sodium hydrogen carbonate solution, and the mixture was extracted with ethyl acetate. The extract was dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure and the residue was purified by silica gel column chromatography (ethyl acetate/hexane=10/90→50/50) to give the title compound (240 mg, yield 73%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08273761B2
Source datasetuspto-grants-2012_09
ORD IDord-d2489c6f33e342068a777baa59328844
Source noteuspto-grants-2012_09