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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 733367Erstellt: 25. Oktober 2026

Hydrochloric Acid → 3-[[2-(2-Tert-butylsulfamoyl-4-isopropylphenyl)ethyl]sulfamoyl]-4-methoxybenzamide

https://huagongshe.com/reaction/733367

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktTriethylamineHCID 8471—
Edukt5-Carbamoyl-2-methoxybenzenesulfonyl chlorideHCID 15922008—
Edukt2-(2-aminoethyl)-N-tert-butyl-5-isopropylbenzenesulfonamideHCID 17856312—
LösungsmittelWaterHCID 962—
LösungsmittelDimethylformamideHCID 6228—
Produkt3-[[2-(2-Tert-butylsulfamoyl-4-isopropylphenyl)ethyl]sulfamoyl]-4-methoxybenzamideHCID 1845694586,3%

Reaktionsschritte

To a suspension of 241 mg of 5-carbamoyl-2-methoxybenzene-sulfonyl chloride and 288 mg of 2-(2-aminoethyl)-N-tert-butyl-5-isopropylbenzenesulfonamide in 10 mL of N,N-dimethyl-formamide was added 0.32 mL of triethylamine, and the mixture was stirred at room temperature for 3 days. To the reaction mixture was added 30 mL of water, and the mixture was stirred at the same temperature for 1 hour. To the mixture was added 10 mL of 1 mol/L hydrochloric acid, and the mixture was extracted three times with 20 mL of ethyl acetate. The organic layers were combined and washed with 30 mL of water, and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure to give 426 mg of 3-[[2-(2-tert-butylsulfamoyl-4-isopropylpheyl)ethyl]sulfamoyl]-4-methoxybenzamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07589126B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-206c150509ee4b36b96d262dda5148fd
Quellennotizuspto-grants-2009_09