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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401825Generated: October 23, 2026

Hydrochloric Acid → 4-[({[1-(4-Chlorophenyl)cyclopropyl]methyl}amino)carbonyl]-2-fluorobenzenesulfonyl chloride

https://huagongshe.com/en/reaction/401825

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSulfur DioxideHCID 1119—
ReactantSodium NitriteHCID 23668193—
Reactant4-Amino-N-{[1-(4-chlorophenyl)cyclopropyl]methyl}-3-fluorobenzamideHCID 57732017—
CatalystCupric chloride dihydrateHCID 61482—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
Product4-[({[1-(4-Chlorophenyl)cyclopropyl]methyl}amino)carbonyl]-2-fluorobenzenesulfonyl chlorideHCID 57732253—

Reaction Steps

4-Amino-N-{[1-(4-chlorophenyl)cyclopropyl]methyl}-3-fluorobenzamide (Preparation 92, 338 mg, 1.06 mmol) in 6 M of HCl in water (2 mL) was cooled at −5° C. Sodium nitrite (80.5 mg, 1.17 mmol) in water (0.4 mL, 20 mmol) was added slowly. After 20 minutes, sulfur dioxide in AcOH (8:25, sulfur dioxide:AcOH, 3 mL) and copper(II)chloride dihydrate (0.18 g, 1.1 mmol) were added to the reaction mixture. Vigorous gas evolution occurred. After 2 hours, the reaction was poured onto ice and water. The resulting solid was collected by filtration, washed with water, and dried to afford a tan powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741934B2
Source datasetuspto-grants-2014_06
ORD IDord-677d7dafa3a442ba9b9b94835751e588
Source noteuspto-grants-2014_06