HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061913Generated: October 29, 2026
Hydrochloric Acid → 3-[(sulfamoylamino)methyl]-1-benzothiophene
https://huagongshe.com/reaction/2061913
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Sulfamic Acid | HCID 5987 | — |
| Reactant | Sulfamide | HCID 82267 | — |
| Reactant | 1-Benzothiophene-3-carbaldehyde | HCID 227328 | — |
| Reactant | Sodium borohydride | HCID 4311764 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-[(sulfamoylamino)methyl]-1-benzothiophene | HCID 11687376 | — |
Reaction Steps
Thianaphthene-3-carboxaldehyde (5 g, 30.8 mmol) was dissolved in anhydrous ethanol (50 mL). Sulfamide (12.22 g, 123.30 mmoles) and sulfamic acid (0.29 g, 3.08 mmoles) were added and the reaction mixture heated to 45° C. for 18 h. The reaction mixture was then cooled to room temperature. Sodium borohydride (1.2 g, 30.8 mmol) was added and the reaction mixture was stirred for 1 hour. 1N HCl (30 mL, 30 mmol) was added and the reaction mixture was filtered through Celite. The filtered solution was then diluted with water (100 mL). The precipitate was filtered to yield the title compound as a off white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08283478B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-66b4b7554a1c4be28ed497df2d21f345 |
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| Source note | uspto-grants-2012_10 |
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