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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503789Generated: November 2, 2026

Pyridine-2-carbonitrile → HCID 178420108, compound

https://huagongshe.com/reaction/503789

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine-2-carbonitrileHCID 7522—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 4-(hydrazinecarbonyl)piperidine-1-carboxylateHCID 22713165—
ReactantHCID 86630689HCID 86630689—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 178420108HCID 178420108—

Reaction Steps

0.51 ml triethylamine is added to a solution of 581 mg 2-(5-piperidin-4H[1,2,4]triazol-3-yl)-pyridine*2HCl (prepared from tert-butyl 4-(hydrazinocarbonyl)piperidine-1-carboxylate and pyridine-2-carbonitrile according to a procedure described in U.S. Pat. No. 4,011,218 or WO2005100344) in 15 ml methanol. To this solution a solution of 500 mg 4-(2-methyl-6-phenylpyrazolo[1,5-a]pyrimidin-5-yl)benzaldehyde in 15 ml DMF is added, followed by 0.23 ml glacial acetic acid and 676 mg NaBH(OAc)3. The resulting mixture is stirred at room temperature. Fife additional portions of 2 equivalents NaBH(OAc)3 are added over 8 h. The solvent is removed by evaporation after 24 h and the residue is purified by chromatography on silica gel (dichloromethane/[dichloromethane+7M NH3 in methanol]) to yield the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07776864B2
Source datasetuspto-grants-2010_08
ORD IDord-a904f6f94de5476aa98674f8abb17f48
Source noteuspto-grants-2010_08