HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 229597Generated: October 25, 2026
Hydrochloric Acid → 3-[[2-(2-Tert-butylsulfamoyl-4-isopropylphenyl)ethyl]sulfamoyl]-4-methoxybenzamide
https://huagongshe.com/reaction/229597
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Carbamoyl-2-methoxybenzenesulfonyl chloride | HCID 15922008 | — |
| Reactant | 2-(2-aminoethyl)-N-tert-butyl-5-isopropylbenzenesulfonamide | HCID 17856312 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-[[2-(2-Tert-butylsulfamoyl-4-isopropylphenyl)ethyl]sulfamoyl]-4-methoxybenzamide | HCID 18456945 | 86.3% |
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-isopropylphenyl)ethyl]sulfamoyl]-4-methoxybenzamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07563822B2 |
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| Source dataset | uspto-grants-2009_07 |
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| ORD ID | ord-6f88be331235461f85541c4536fc3719 |
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| Source note | uspto-grants-2009_07 |
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