HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 446680Generated: October 30, 2026
Benzenesulfonamide, 3-amino- → HCID 4852487, compound
https://huagongshe.com/reaction/446680
Participants
| Role | Name | HCID | Charge |
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| Reactant | Benzenesulfonamide, 3-amino- | HCID 7377 | — |
| Reactant | 2-Aminobenzenesulfonamide | HCID 72894 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-(Dimethylamino)acetyl chloride hydrochloride | HCID 13994991 | — |
| Solvent | Acetone | HCID 180 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 4852487 | HCID 4852487 | — |
Reaction Steps
A flask was charged with 3-aminobenzene sulfonamide (3.3 g, 19 mmol), and 20 mL of 1:1 acetone:H2O. The solution was stirred at room temperature until the aminobenzene sulfonamide had dissolved. The flask was then cooled in an ice bath and dimethylamino-acetyl chloride HCl (4.6 g, 29 mmol) was added. To the resulting slurry sodium bicarbonate (4.8 g, 57 mmol) was added over a 15 m period. After 30 min the reaction was removed from the ice bath and allowed to stir at room temperature for 15 h. The reaction mixture was then filtered and washed with methanol and acetonitrile. The filtrate was dried on a rotary evaporator to yield 2-(dimethylamino)-N-(3-sulfamoyl-phenyl)acetamide, which was submitted to the next step without further purification. MS (EI) m/z C10H15N3O3S: 258.0 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08481001B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-b8df26f5b4e344f196690545a0f2efdd |
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| Source note | uspto-grants-2013_07 |
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