HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 606498Generated: October 30, 2026
Cyanoacetamide → 2-Aminothiophene-3-carboxamide
https://huagongshe.com/reaction/606498
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cyanoacetamide | HCID 7898 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1,4-Dithiane-2,5-diol | HCID 98330 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 2-Aminothiophene-3-carboxamide | HCID 699495 | 69.4% |
Reaction Steps
A solution of 2,5-dihydroxy-1,4-dithiane (11.8 g, 155 mmol), cyanoacetamide (17.0 g, 202 mmol) and triethylamine (20 ml) in ethanol (100 mL) was stirred under heating at 70° C. for 4 hr. The reaction mixture was cooled to room temperature, and concentrated under reduced pressure to an about half volume. Water was added to the residue, the precipitated insoluble material was collected by filtration, and the solid was washed with water to give 2-amino-3-thiophenecarboxamide as a brown powder (15.3 g, 69%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07915267B2 |
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| Source dataset | uspto-grants-2011_03 |
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| ORD ID | ord-92d1389d9369420db15f4d1a383f6c05 |
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| Source note | uspto-grants-2011_03 |
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