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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501074Generated: October 30, 2026

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

https://huagongshe.com/reaction/501074

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 numberUS07772224B2
Source datasetuspto-grants-2010_08
ORD IDord-eb8265386bfb44a286bac4ef26463a27
Source noteuspto-grants-2010_08