HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 615358Generated: October 30, 2026
Acetic Acid → 6-(1-Methylethyl)amino-2-benzothiazolesulfonamide
https://huagongshe.com/reaction/615358
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetone | HCID 180 | — |
| Reactant | Aminozolamide | HCID 93505 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(1-Methylethyl)amino-2-benzothiazolesulfonamide | HCID 20428105 | — |
Reaction Steps
Sodium borohydride (378 mg, 0.01 mole) and 6-amino-2-benzothiazolesulfonamide (459 mg, 0.002 mole) are ground together, then added very slowly to a mixture of glacial acetic acid (5 ml) and acetone (5 ml) with stirring under nitrogen at 20° C. After vigorous evolution of hydrogen, the reaction mixture is stirred at 20° C. for 2 hrs, treated with H2O, filtered, made basic with 10N NaOH solution, then neutralized with aqueous HCl to give 6-(1-methylethyl)amino-2-benzothiazolesulfonamide.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04499103 |
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| Source dataset | uspto-grants-1985_02 |
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| ORD ID | ord-c8e9362002e14e7c993cd60ddd4fbaf9 |
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| Source note | uspto-grants-1985_02 |
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