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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915563Generated: November 1, 2026

Pyridine-2-carbonitrile → HCID 178486596, compound

https://huagongshe.com/reaction/1915563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine-2-carbonitrileHCID 7522—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 4-(hydrazinecarbonyl)piperidine-1-carboxylateHCID 22713165—
Reactant4-(7-Methoxy-6-phenylpyrazolo[1,5-a]pyrimidin-5-yl)benzaldehydeHCID 86630673—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 178486596HCID 178486596—

Reaction Steps

0.32 ml triethylamine is added to a solution of 0.42 g 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 10 ml methanol. To this solution a solution of 0.37 g 4-(7-methoxy-6-phenylpyrazolo[1,5-a]pyrimidin-5-yl)benzaldehyde in 10 ml DMF is added, followed by 0.15 ml glacial acetic acid and 0.43 g NaBH(OAc)3. The resulting mixture is stirred at room temperature. Four additional portions of 2 equivalents NaBH(OAc)3 are added after 1, 2, 3 and 7 hours. The solvent is removed by evaporation after 20 h and the residue is purified by chromatography on silica gel (dichloromethane/[dichloromethane+7M NH3 in methanol]) to yield the product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614218B2
Source datasetuspto-grants-2013_12
ORD IDord-f4e45336289047b7a7f153b021a8d2ad
Source noteuspto-grants-2013_12