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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1365944Generated: November 1, 2026

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

https://huagongshe.com/reaction/1365944

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 numberUS07893052B2
Source datasetuspto-grants-2011_02
ORD IDord-2804ef6b0b684cc888da2710a1ca890a
Source noteuspto-grants-2011_02