Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1768171Generated: November 1, 2026

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

https://huagongshe.com/reaction/1768171

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 numberUS07235545B2
Source datasetuspto-grants-2007_06
ORD IDord-2c59a441ba984f31ad33340ca41a0f1c
Source noteuspto-grants-2007_06