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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074316Generated: November 1, 2026

Oxalic Acid → HCID 69378687, compound

https://huagongshe.com/reaction/2074316

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalic AcidHCID 971—
Reactant3-HydroxypyridineHCID 7971—
ReactantTetrahydrofuranHCID 8028—
Reactant1-Piperidinecarbonyl chlorideHCID 242085—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthanolHCID 702—
SolventWaterHCID 962—
ProductHCID 69378687HCID 6937868761.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

3-Hydroxypyridine (400 mg), TEA (1.17 ml) and DMAP (catalytic amount) were added in that order to a THF (10 ml) solution containing piperidine-1-carbonyl chloride (745 mg), and then heated at 60° C. for 5 hours. The reaction solution was cooled, then water (3 ml) was added thereto, and extracted with EtOAc. The extract was washed with water, and then dried over anhydrous magnesium sulfate. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (eluent: hexane:EtOAc=1:1 (v/v)) to obtain a colorless oil. The resulting oil was dissolved in ethanol, and an ethanol solution of oxalic acid (378 mg) added thereto to obtain a colorless powder. This was recrystallized from hexane/ethanol to obtain (pyridin-3-yl)piperidine-1-carboxylate oxalate (761 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919495B2
Source datasetuspto-grants-2011_04
ORD IDord-da07a447a13b44e5a349118da5f26bb7
Source noteuspto-grants-2011_04