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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Trimethylsilyl cyanide | HCID 82115 | — |
| Reactant | (2-Phenylfuro[3,2-c]pyrazolo[1,5-a]pyridin-1-yl)methanol | HCID 59179389 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Sodium Bicarbonate | HCID 516892 | — |
| Product | (2-Phenylfuro[3,2-c]pyrazolo[1,5-a]pyridin-1-yl)acetonitrile | HCID 59179406 | 73% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08273761B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-d2489c6f33e342068a777baa59328844 |
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| Source note | uspto-grants-2012_09 |
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