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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1268103Erstellt: 26. Oktober 2026

Thionyl Chloride → 3-(4-t-Butylbenzyloxy)-N-(2-sulfamoylphenyl)benzamide

https://huagongshe.com/reaction/1268103

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktThionyl ChlorideHCID 24386—
Edukt2-AminobenzenesulfonamideHCID 72894—
EduktNurr1 agonist 7HCID 18544100—
LösungsmittelBenzeneHCID 241—
Produkt3-(4-t-Butylbenzyloxy)-N-(2-sulfamoylphenyl)benzamideHCID 1204130968,4%

Reaktionsschritte

A benzene (30 ml) solution containing 4.00 g (14.0 mmol) of 3-(4-t-butylbenzyloxy)benzoic acid and 3 ml of thionyl chloride was heated under reflux for 2 hours and then the solvent was evaporated under a reduced pressure. The resulting residue was dissolved in methylene chloride (30 ml), this solution was added dropwise under ice-cooling to a pyridine (50 ml) solution containing 2.42 g (14.0 mmol) of 2-aminobenzenesulfonamide, the mixture was stirred at room temperature for 18 hours and then methylene chloride was evaporated under a reduced pressure. The resulting residue was dissolved in ethyl acetate, washed with a 1 N hydrochloric acid aqueous solution, water and saturated brine in that order and dried over anhydrous sodium sulfate, and then the solvent was evaporated under a reduced pressure. The thus obtained crude crystals were recrystallized from an ether-hexane mixed solvent to obtain 4.2 g (yield: 68.0%) of the title compound.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06555584B1
Quelldatensatzuspto-grants-2003_04
ORD IDord-0ab645b4f253488c8e8c06febf39e4b6
Quellennotizuspto-grants-2003_04