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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1474062Generated: October 26, 2026

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

https://huagongshe.com/reaction/1474062

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 82676215—

Reaction Conditions

Temperature230 °C

Reaction Steps

A mixture of 2-fluoropyridine (1.4 g, 15 mmol) and 6-chloro-3-pyridinemethanamine (alternatively named 5-aminomethyl-2-chloropyridine) (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 numberUS09018220B2
Source datasetuspto-grants-2015_04
ORD IDord-fb6357a063f44f61b208d1e1ba05ec76
Source noteuspto-grants-2015_04