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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1808252Generated: October 31, 2026

2-Aminothiazole → 4-Iodo-N-(thiazol-2-yl)benzenesulfonamide

https://huagongshe.com/reaction/1808252

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-AminothiazoleHCID 2155—
Reactant4-Iodobenzenesulfonyl chlorideHCID 7399—
SolventPyridineHCID 1049—
Product4-Iodo-N-(thiazol-2-yl)benzenesulfonamideHCID 101931853.7%

Reaction Steps

4-Iodobenzenesulfonyl chloride (1.8 g, 6.0 mmol, 1.0 equiv) was added portion-wise to a 0° C. solution of 2-aminothiazole (654 mg, 6.53 mmol, 1.1 equiv) in 4.91 mL of anhydrous pyridine. After addition was complete, the reaction mixture was warmed to ambient temperature. After 3 d, the reaction mixture was concentrated in vacuo. The residue was treated with MeOH and ether to precipitate the product. The solid was collected by filtration, washing with ether, to afford the product as a light brown solid (1.18 g, 49%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357711B2
Source datasetuspto-grants-2013_01
ORD IDord-62c0879b7c7b4cbcb1792f130acba41e
Source noteuspto-grants-2013_01