HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569049Generated: October 29, 2026
2-Sulfamoyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine → 2-Sulfamoyl-4,5-dihydrothieno[2,3-c]pyridine
https://huagongshe.com/reaction/569049
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Sulfamoyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine | HCID 20148589 | — |
| Catalyst | HCID 178418406 | HCID 178418406 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Sulfamoyl-4,5-dihydrothieno[2,3-c]pyridine | HCID 20148584 | 26.5% |
Reaction Steps
To a partial suspension of 2-sulfamoyl-4,5,6,7-tetrahydrothieno[2,3-c]pyridine (3.05 g, 14 mmol) in ethyl acetate (200 ml) was added activated manganese dioxide (3.0 g). This mixture was warmed to 80° C. Every two hours an additional 3.0 g of activated manganese dioxide was added until 12 g total had been added. This mixture was filtered hot and the collected manganese dioxide was re-extracted with hot ethyl acetate. The combined ethyl acetate extracts were evaporated to give 2.1 g of crude product. This material was purified by chromatography on silica gel eluting with a gradient 0-5% methanol/ethyl acetate. Recrystallization from ethyl acetate gave pure product (0.8 g, 26.5% yield); m.p. 161°-164° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04731368 |
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| Source dataset | uspto-grants-1988_03 |
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| ORD ID | ord-6c2faa2194c74971a021659bf646e7f7 |
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| Source note | uspto-grants-1988_03 |
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