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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401829Generated: October 30, 2026

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

https://huagongshe.com/reaction/401829

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 numberUS08741934B2
Source datasetuspto-grants-2014_06
ORD IDord-7d56d7f57c954631b70c8dff89b7cfc0
Source noteuspto-grants-2014_06