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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1272427Generated: October 26, 2026

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

https://huagongshe.com/reaction/1272427

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
Reactant5-Carbamoyl-2-methoxybenzenesulfonyl chlorideHCID 15922008—
Reactant2-(2-aminoethyl)-N-tert-butyl-5-isopropylbenzenesulfonamideHCID 17856312—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product3-[[2-(2-Tert-butylsulfamoyl-4-isopropylphenyl)ethyl]sulfamoyl]-4-methoxybenzamideHCID 1845694586.3%

Reaction Steps

To a suspension of 241 mg of 5-carbamoyl-2-methoxybenzenesulfonyl chloride and 288 mg of 2-(2-aminoethyl)-N-tert-butyl-5-isopropylbenzenesulfonamide in 10 mL of N,N-dimethylformamide 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07208524B2
Source datasetuspto-grants-2007_04
ORD IDord-1c68fb56289049f99cff2b5e572f73af
Source noteuspto-grants-2007_04