HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2363976Generated: October 31, 2026
p-Toluenesulfonic acid → HCID 66743595, compound
https://huagongshe.com/reaction/2363976
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Toluenesulfonic acid | HCID 6101 | — |
| Reactant | 1,1-Dioxo-tetrahydro-thiopyran-4-one | HCID 262230 | — |
| Reactant | 3-Amino-5-(pyridin-4-yl)thiophene-2-carboxamide | HCID 9920852 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 66743595 | HCID 66743595 | 24.3% |
Reaction Steps
To a stirred solution of 3-amino-5-(pyridin-4-yl)thiophene-2-carboxamide (0.050 g, 0.23 mmol) in acetic acid (3 mL) were added tetrahydro-4H-thiopyran-4-one 1,1-dioxide (0.068 g, 0.46 mmol) and p-toluenesulfonic acid (0.0040 g, 0.023 mmol). The mixture was heated at 80° C. overnight. Then, the solvent was removed and the obtained residue was taken up in methanol (20 mL). Solid NaHCO3 (1.5 g) was added, and the mixture was stirred for 10 min. The cloudy suspension was filtered and the collected solids were washed with methanol (20 mL) followed by water (30 mL) to give the title compound (0.0195 g, 24%) as a yellow solid:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08691828B2 |
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| Source dataset | uspto-grants-2014_04 |
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| ORD ID | ord-591ea1204f9b42659e89d595606b6681 |
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| Source note | uspto-grants-2014_04 |
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