Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 490669Generated: October 29, 2026

5-Fluoro-2-methylbenzenesulphonyl chloride → HCID 11625024, compound

https://huagongshe.com/reaction/490669

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-2-methylbenzenesulphonyl chlorideHCID 136286—
ReactantHCID 20099815HCID 20099815—
SolventPyridineHCID 1049—
ProductHCID 11625024HCID 1162502457%

Reaction Steps

A solution of 0.2 g (0.98 mmol) of 5-(2-chloro-phenyl)-pyridin-2-ylamine and 0.23 g of 5-fluoro-2-methyl-benzenesulfonyl chloride (1.1 mmol) in pyridine (10 ml) was stirred at RT until completion of reaction according to HPLC analysis (48 h). After concentration in vacuo the residue was taken up in EtOAc, the solution washed with 1 N aqueous HCl, saturated brine then dried over sodium sulphate and concentrated in vacuo. The precipitate was collected by filtration and dried in a high vacuum to give 0.21 g (57%) of N-[5-(2-chloro-phenyl)-pyridin-2-yl]-5-fluoro-2-methyl-benzenesulfonamide as an off-white crystalline solid. ISN mass spectrum, m/e: 375.2 (M−1 calculated for C18H14ClFN2O2S: 375).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07528159B2
Source datasetuspto-grants-2009_05
ORD IDord-4fa92e0d9d934643871fb2e4f4b21349
Source noteuspto-grants-2009_05