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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1510108Generated: November 3, 2026

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

https://huagongshe.com/reaction/1510108

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Fluoro-2-methylbenzenesulphonyl chlorideHCID 136286—
Reactant5-(2-Chlorophenyl)pyridin-2-amineHCID 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 numberUS08211913B2
Source datasetuspto-grants-2012_07
ORD IDord-b27e0bee4a6d48d79d9cee63786e4180
Source noteuspto-grants-2012_07