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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241283Generated: October 27, 2026

4-Fluorobenzenesulfonyl chloride → 4-fluoro-N-[4-(thiazol-2-yl)benzyl]benzenesulfonamide

https://huagongshe.com/reaction/241283

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Fluorobenzenesulfonyl chlorideHCID 9588—
Reactant(4-(Thiazol-2-yl)phenyl)methanamine hydrochlorideHCID 51138530—
Reactant(6-Phenylpyridazin-3-ylmethyl)amine hydrochlorideHCID 66717660—
Product4-fluoro-N-[4-(thiazol-2-yl)benzyl]benzenesulfonamideHCID 5477395885.5%

Reaction Steps

Reaction and post-treatment were carried out in the same manner as in Reference Example 2-(d) except for using 4-fluorobenzenesulfonyl chloride (278 mg, 1.42 mmol) in place of 3-pyridylsulfonyl chloride, and using 4-(thiazol-2-yl)benzylamine hydrochloride (364 mg, 1.38 mmol) obtained in Reference Example 4-(d) in place of (6-phenylpyridazin-3-ylmethyl)amine hydrochloride to afford the title compound (411 mg) as a slightly yellow solid. (Yield: 85%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08648097B2
Source datasetuspto-grants-2014_02
ORD IDord-9d86110553274f6c9b03b23ba218009d
Source noteuspto-grants-2014_02