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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120177Generated: October 31, 2026

Acetic Acid → HCID 23438736, compound

https://huagongshe.com/reaction/2120177

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 23438713HCID 23438713—
SolventAcetoneHCID 180—
SolventMethanolHCID 887—
ProductHCID 23438736HCID 2343873680.4%

Reaction Steps

To a stirring suspension of N-(5-chloropyridin-2-yl)-6-methyl-3-[ (4-piperidinylcarbonyl)amino]pyridine-2-carboxamide trifluoroacetate (0.75 g, 1.54 mmol) in methanol (11 mL) was added acetone (11 mL), followed by acetic acid (0.45 mL, 7.86 mmol), and then sodium cyanoborohydride (0.51 g, 7.7 mmol). After stirring overnight, the solution was treated with saturated aqueous ammonium chloride solution, concentrated, and partitioned between dichloromethane and saturated aqueous sodium bicarbonate. The organic phase was washed with brine, dried over magnesium sulfate, filtered, and concentrated. The crude product was purified by chromatography over silica gel, eluting with a step gradient of 0-10% 2 M solution of ammonia/methanol in dichloromethane. To a stirring solution of the purified product in dichloromethane was added 1.0 N hydrochloric acid in diethyl ether until precipitate formed. The mixture was filtered to give 0.28 g (40%) of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689780B1
Source datasetuspto-grants-2004_02
ORD IDord-d5e3c27435634b36ad1e2dc936022943
Source noteuspto-grants-2004_02