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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 271874Generated: October 30, 2026

Methanol → Methyl 3-[(1-benzylpiperidin-4-yl)amino]pyrazine-2-carboxylate

https://huagongshe.com/reaction/271874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant1-Benzyl-4-piperidylamineHCID 415852—
ReactantMethyl 3-bromopyrazine-2-carboxylateHCID 13318551—
SolventIsopropanolHCID 3776—
SolventEthyl AcetateHCID 8857—
ProductMethyl 3-[(1-benzylpiperidin-4-yl)amino]pyrazine-2-carboxylateHCID 22293191—

Reaction Steps

A mixture of methyl 2-bromopyrazine-3-carboxylate (J. Med. Chem., 1969, 12, 285) (2.2 g, 10.1 mmol) and 4-amino-1-benzylpiperidine (2.0 g, 10.5 mmol) was refluxed in 2-propanol overnight. Thin layer chromatography (10% methanol in ethyl acetate) showed the reaction was complete. The solvent was evaporated, and the crude product dissolved in chloroform (100 mL), which was washed with saturated sodium carbonate solution (20 mL), and dried over magnesium sulfate. The title compound was obtained as a gum (3.8 g). MS 327 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07452903B2
Source datasetuspto-grants-2008_11
ORD IDord-64f69ac92a034f1b92774ff1b91b4a89
Source noteuspto-grants-2008_11