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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 401825Erstellt: 23. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSulfur DioxideHCID 1119—
EduktSodium NitriteHCID 23668193—
Edukt4-Amino-N-{[1-(4-chlorophenyl)cyclopropyl]methyl}-3-fluorobenzamideHCID 57732017—
KatalysatorCupric chloride dihydrateHCID 61482—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
Produkt4-[({[1-(4-Chlorophenyl)cyclopropyl]methyl}amino)carbonyl]-2-fluorobenzenesulfonyl chlorideHCID 57732253—

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08741934B2
Quelldatensatzuspto-grants-2014_06
ORD IDord-677d7dafa3a442ba9b9b94835751e588
Quellennotizuspto-grants-2014_06