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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915604Generated: October 30, 2026

Pyridine-2-carbonitrile → HCID 178483024, compound

https://huagongshe.com/reaction/1915604

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridine-2-carbonitrileHCID 7522—
ReactantSodium triacetoxyborohydrideHCID 5049666—
Reactanttert-Butyl 4-(hydrazinecarbonyl)piperidine-1-carboxylateHCID 22713165—
ReactantHCID 86630696HCID 86630696—
SolventAcetic AcidHCID 176—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
SolventTriethylamineHCID 8471—
ProductHCID 178483024HCID 178483024—

Reaction Steps

0.138 ml triethylamine are added to a solution of 207 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 10 ml methanol. To this solution a solution of 196 mg 4-[2-(dimethylamino)-6-phenyl[1,2,4]triazolo[1,5-a]pyrimidin-5-yl]benzaldehyde in 10 ml DMF is added, followed by 0.09 ml glacial acetic acid and 242 mg NaBH(OAc)3. The resulting mixture is stirred at room temperature. Two additional portions of 2 equivalents NaBH(OAc)3 are added after 1 and 2 hours. The solvent is removed by evaporation after 3 h and the residue is dissolved in dichloromethane and water. The phases are separated and the water phase is extracted with dichloromethane. The combined organic layers are dried over Na2SO4 and the solvent is evaporated. The crude product is purified by RP HPLC (water, 10 mM NH4COOH, pH 3.7/ACN) to yield the desired compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08614218B2
Source datasetuspto-grants-2013_12
ORD IDord-f212ea07d5bc454d98e9884a53e3c707
Source noteuspto-grants-2013_12