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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088856Generated: November 2, 2026

Pyridine → 6-Chloro-2-(ethylamino)pyridine-3-carbonyl fluoride

https://huagongshe.com/reaction/2088856

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantCyanuric fluorideHCID 12664—
Reactant6-Chloro-2-(ethylamino)nicotinic acidHCID 63376479—
SolventDichloromethaneHCID 6344—
Product6-Chloro-2-(ethylamino)pyridine-3-carbonyl fluorideHCID 8671457499%

Reaction Steps

To a suspension of 10.5 g (52.3 mmol) of the compound obtained in step 1.1 in dichloromethane (250 ml) are successively added 4.2 ml (52.3 mmol) of pyridine and 8.4 ml (99.6 mmol) of cyanuric fluoride. The mixture is stirred for 3 hours at room temperature and then filtered. The solid is rinsed with dichloromethane (100 ml) and the filtrate is washed twice with ice-cold water (60 ml). The organic phase is dried over Na2SO4 and then concentrated under reduced pressure. 10.44 g of product are obtained, the form of an orange-coloured oil. Yield=99%. The product is used without purification in the following step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08436011B2
Source datasetuspto-grants-2013_05
ORD IDord-3e6fcac51b144091a84abeee34028be9
Source noteuspto-grants-2013_05