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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 46314Generated: October 29, 2026

Hydrochloric Acid → N-(5-chloro-1,3-thiazol-2-yl)-3-cyano-4-(4-fluoro-2-iodophenoxy)benzenesulfonamide

https://huagongshe.com/reaction/46314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantPotassium CarbonateHCID 11430—
Reactant4-Fluoro-2-iodophenolHCID 10171417—
ReactantN-(5-chloro-thiazol-2-yl)-3-cyano-4-fluorobenzenesulfonamideHCID 59436522—
SolventDimethylformamideHCID 6228—
ProductN-(5-chloro-1,3-thiazol-2-yl)-3-cyano-4-(4-fluoro-2-iodophenoxy)benzenesulfonamideHCID 5943663359%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of N-(5-Chloro-1,3-thiazol-2-yl)-3-cyano-4-fluorobenzenesulfonamide (Preparation 52, 100 mg, 0.32 mmol) and potassium carbonate (109 mg, 0.8 mmol) in dimethylformamide (3 ml) was added 4-fluoro-2-iodophenol (Preparation 218, 0.32 mmol) and the reaction heated at 80° C. for 24 hours. The solution was added dropwise into rapidly stirring hydrochloric acid (2M aqueous solution). The fine dark precipitate was filtered and dried in vacuo to afford the title product as a brown solid, 100 mg, 59% yield.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08541588B2
Source datasetuspto-grants-2013_09
ORD IDord-69f75e533d9a46c688a2f550dc3510e0
Source noteuspto-grants-2013_09