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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1644636Generated: November 1, 2026

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

https://huagongshe.com/reaction/1644636

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 methanol 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 numberUS08124610B2
Source datasetuspto-grants-2012_02
ORD IDord-27ac1ea4cfac4afc8bca94b3a51c6756
Source noteuspto-grants-2012_02