HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061914Generated: November 2, 2026
Hydrochloric Acid → 3-[(sulfamoylamino)methyl]-1-benzothiophene
https://huagongshe.com/reaction/2061914
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 | Lithium borohydride | HCID 4148881 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[(sulfamoylamino)methyl]-1-benzothiophene | HCID 11687376 | — |
Reaction Steps
Thianaphthene-3-carboxaldehyde (5 g, 30.8 mmol) was dissolved in THF (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 and filtered through a sintered glass funnel. The resulting solution was treated with lithium borohydride (2.0 M in THF, 5 mL, 10 mmol) via addition funnel. After addition (5 minutes) the reaction mixture was stirred for 1 hour. 1N HCl (20 mL, 20 mmol) was added and the reaction mixture concentrated to remove THF. The resulting suspension was treated with water (100 mL) and vigorously stirred. The resulting solid was filtered and dried to yield the title compound as a light pink 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-094c2ccc1d7f4316b81aac5dcb21e71e |
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| Source note | uspto-grants-2012_10 |
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