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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 862123Generated: October 30, 2026

Hydrochloric Acid → Methyl-2-dimethylcarbamoyl-1-(methoxycarbonylmethyl)piperidine-4-carboxylate

https://huagongshe.com/reaction/862123

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl bromoacetateHCID 60984—
ReactantMethyl 2-(dimethylcarbamoyl)pyridine-4-carboxylateHCID 22097574—
CatalystPlatinum oxide (PtO)HCID 82844—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
ProductMethyl-2-dimethylcarbamoyl-1-(methoxycarbonylmethyl)piperidine-4-carboxylateHCID 2209756696,296.297%

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of compound 28 (55.4 g, 0.27 mmole), conc. HCl (16 ml) in MeOH (62 ml) was hydrogenated over platinum oxide (1 g) at 8 kg/cm2 for 24 hours. The catalyst was removed by filtration. The filtrate was concentrated under reduced pressure and the resulting oil was used without further purification. A mixture of crude intermediate compound hydrochloride, methyl bromoacetate (61 g, 0.4 mole) and K2CO3 (73.5 g, 0.53 mole) in toluene (200 ml) was heated at 70° C. for 3 hours. After cooling the reaction mixture, H2O (200 ml) was added and extracted with EtOAc (200 ml×2). The combined organic extracts were dried over MgSO4 and concentrated down. The crude oil was purified by silica gel chromatography EtOAc as eluent to give 29 (69.8 g, 0.26 mole, 97%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05716965
Source datasetuspto-grants-1998_02
ORD IDord-42f77fa11c424f6bb447d8ac93fe2d2c
Source noteuspto-grants-1998_02