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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538310Generated: October 28, 2026

Lawesson's reagent → 5-Chloro-pyridine-2-carboxylic acid [6-(3-fluoromethyl-5-thioxo-morpholin-3-yl)-pyridin-2-yl]-amide

https://huagongshe.com/reaction/538310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLawesson's reagentHCID 87949—
Reactant5-Chloro-pyridine-2-carboxylic acid [6-(3-fluoromethyl-5-oxo-morpholin-3-yl)-pyridin-2-yl]-amideHCID 86668024—
SolventTetrahydrofuranHCID 8028—
Product5-Chloro-pyridine-2-carboxylic acid [6-(3-fluoromethyl-5-thioxo-morpholin-3-yl)-pyridin-2-yl]-amideHCID 86668025—

Reaction Steps

To a solution of 5-chloro-pyridine-2-carboxylic acid [6-(3-fluoromethyl-5-oxo-morpholin-3-yl)-pyridin-2-yl]-amide (0.24 g, 0.658 mmol) in THF (10.0 ml), Lawesson's reagent (0.798 g, 1.974 mmol) was added at rt and heated at reflux temperature for 24 h. Reaction mass was concentrated under reduced pressure. The crude compound was directly purified by column chromatography using 23% ethyl acetate in hexane to furnish title compound as off-white solid. Yield=0.19 g (72% [2 steps]). TLC (50% ethyl acetate in hexane) Rf=0.71; LCMS: RtH8=1.578, [M+1]+=381.1 and 382.9.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865712B2
Source datasetuspto-grants-2014_10
ORD IDord-ee3ce59f5eac4d529d93fb2c75438022
Source noteuspto-grants-2014_10