Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2365456Generated: October 26, 2026

2-Fluoropyridine → 6-chloro-N-2-pyridinyl-3-pyridinemethanamine

https://huagongshe.com/reaction/2365456

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-FluoropyridineHCID 9746—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(Aminomethyl)-2-chloropyridineHCID 7020927—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Product6-chloro-N-2-pyridinyl-3-pyridinemethanamineHCID 82676215154.8%

Reaction Conditions

Temperature230 °C

Reaction Steps

A mixture of 2-fluoropyridine (1.4 g, 15 mmol) and 6-chloro-3-pyridinemethanamine (2.55 g, 18 mmol) in N-methylpyrrolidinone (5 mL) was heated at 230° C. in a microwave reactor for 30 min. This reaction was repeated four times using the same amounts of starting materials for each repetition. All five of the reaction mixtures were then poured into saturated aqueous sodium bicarbonate solution and extracted into ethyl acetate. The organic layer was washed with saturated aqueous sodium bicarbonate solution, dried over Na2SO4, and concentrated under reduced pressure. The crude product was then purified by chromatography on silica gel using 10% ethyl acetate in hexanes as the eluent to provide the title compound as an oil (5.1 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08697707B2
Source datasetuspto-grants-2014_04
ORD IDord-1a6a27dc3add4f539f87f04d5c828c22
Source noteuspto-grants-2014_04