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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372485Generated: October 26, 2026

Methanol → N-(5-Iodo-pyridin-2-YL)-4-methyl-benzenesulfonamide

https://huagongshe.com/reaction/1372485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
Reactant4-Toluenesulfonyl chlorideHCID 7397—
Reactant2-Pyridinamine, 5-iodo-HCID 88579—
SolventPyridineHCID 1049—
ProductN-(5-Iodo-pyridin-2-YL)-4-methyl-benzenesulfonamideHCID 21772024—

Reaction Steps

p-Toluenesulfonyl chloride (2.00 g, 10.4 mmol) was added to a solution of 5-iodo-2-aminopyridine (2.50 g, 11.4 mmol) in 6 mL of pyridine, and the resultant solution was warmed at 90° C. for 18 h. After cooling to room temperature, the solution was added portionwise to 75 mL of ice-water with stirring. The resultant precipitate was collected, washed with water, and dried in vacuo to afford a pale yellow powder, which was stirred with 20 mL of methanol for several minutes. The solid product was then collected, washed with methanol, and dried in vacuo to provide the title compound as an off-white powder. LC/MS 374.8 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07157490B2
Source datasetuspto-grants-2007_01
ORD IDord-082c0a7fcb6c40b98fc0d69b25098261
Source noteuspto-grants-2007_01