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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1260573Generated: November 1, 2026

Pyridine → 2-(Aminoethyl)-6-chloronicotinic acid fluoride

https://huagongshe.com/reaction/1260573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2,4,6-Trifluoro-1,2,3-triazineHCID 21694433—
Reactant2-(Aminoethyl)-6-chloronicotinic acidHCID 86642333—
SolventDichloromethaneHCID 6344—
Product2-(Aminoethyl)-6-chloronicotinic acid fluorideHCID 8740037399.7%

Reaction Steps

2 ml (24.8 mmol) of pyridine and 4.2 ml (49.8 mmol) of 2,4,6-trifluorotriazine are added to a suspension of 5.0 g (24.8 mmol) of 2-(aminoethyl)-6-chloronicotinic acid in 125 ml of dichloromethane. The mixture is stirred for 3 hours at ambient temperature and then filtered. The solid is rinsed with 50 ml of dichloromethane and the filtrate is washed twice with 60 ml of ice-cold water. The organic phase is dried over Na2SO4 and the solvent is evaporated off under reduced pressure. 5.01 g of product are obtained in the form of an orange oil. Yield=99%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08470847B2
Source datasetuspto-grants-2013_06
ORD IDord-e0b571ab32624b038919e26a9dcf91a4
Source noteuspto-grants-2013_06