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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46363Generated: October 25, 2026

Dabco → 5-chloro-2,4-difluoro-N-pyrimidin-4-ylbenzenesulfonamide

https://huagongshe.com/reaction/46363

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDabcoHCID 9237—
Reactant4-AminopyrimidineHCID 68958—
Reactant5-Chloro-2,4-difluorobenzenesulphonyl chlorideHCID 2773527—
SolventAcetonitrileHCID 6342—
Product5-chloro-2,4-difluoro-N-pyrimidin-4-ylbenzenesulfonamideHCID 594365455%

Reaction Steps

A mixture of 4-aminopyrimidine (1.30 g, 13.7 mmol) and 1,4-diazabicyclo[2.2.2]octane (1.54 g, 13.7 mmol) were added concurrently to a solution of 5-chloro-2,4-difluorobenzenesulfonyl chloride (3.4 g, 14 mmol) in anhydrous acetonitrile (63 mL). The reaction mixture immediately turned yellow and a precipitate formed. The reaction mixture was stirred under argon. After 72 hours, the reaction mixture was filtered and the filtrate was concentrated in vacuo to give a residue. The residue was partitioned between 1M hydrochloric acid and ethyl acetate. The organic phase was separated, dried over anhydrous magnesium sulfate and concentrated in vacuo. The residue was partially purified by automated flash column chromatography using an 80 g silica gel ISCO™ column using hexanes to 1% v/v acetic acid in ethyl acetate gradient elution. The product was purified a second time by reverse phase HPLC to give the title compound (193 mg, 5%) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541588B2
Source datasetuspto-grants-2013_09
ORD IDord-e411c3715dc34aff853b7427251500dc
Source noteuspto-grants-2013_09