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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2373234Generated: November 1, 2026

Diethyl (cyanomethyl)phosphonate → HCID 69184035, compound

https://huagongshe.com/reaction/2373234

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl (cyanomethyl)phosphonateHCID 75676—
ReactantPotassium tert-butoxideHCID 23665647—
ReactantHCID 86602412HCID 86602412—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 69184035HCID 6918403580%

Reaction Steps

To a suspension of diethyl (cyanomethyl)phosphonate (17.4 mg) in THF (0.5 ml) was added potassium tert-butoxide (11.3 mg) at 0° C. and the mixture was stirred at room temperature for 30 minutes. A solution of ethyl 3-[1-ethyl-6-formyl-4-(5-methyl-3-pyridyl)-1H-pyrazolo[3,4-b]pyridin-5-yl]propanoate (20 mg) in THF (0.5 ml) was added at 0° C. and the mixture was stirred at room temperature for 1.5 hours. The reaction mixture was diluted with water and extracted with EtOAc. The organic layer was washed with water, brine, dried over anhydrous MgSO4 and concentrated in vacuo. The residue was purified by preparative thin layer chromatography eluting with a mixture of EtOAc and n-hexane (1:1) to give ethyl 3-[6-[(E)-2-cyanovinyl]-1-ethyl-4-(5-methyl-3-pyridyl)-1H-pyrazolo[3,4-b]pyridin-5-yl]propanoate (17 mg) as a colorless crystal.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07459451B2
Source datasetuspto-grants-2008_12
ORD IDord-6d5b223178f24fd19aafc5807f9af4e2
Source noteuspto-grants-2008_12