HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049205Generated: October 31, 2026
p-Aminoacetophenone → HCID 86701904, compound
https://huagongshe.com/reaction/1049205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | p-Aminoacetophenone | HCID 7468 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 2-Cyano-3,3-bis(methylthio)acrylamide | HCID 2747746 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86701904 | HCID 86701904 | — |
Reaction Steps
Dissolved 0.500 g 2-cyano-3,3-bis(methylthio)acrylamide in 15 mL EtOH and added 4′-aminoacetophenone (1.0 eq.). Stirred reaction at 75 degrees C. until starting amide was absent by HPLC. Once complete (18 hrs), reaction was brought to room temperature and filtered to obtain a light yellow powder as product. Product was allowed to dry under vacuum for 1 hr. Product was then suspended in 10 mL EtOH and hydrazine hydrate (1 eq.) was added dropwise. Reaction was heated at 75° C. until intermediate was absent (HPLC). Once intermediate was absent (18 hrs), reaction was brought to room temperature and filtered to obtain 3-((4-acetylphenyl)amino)-5-amino-1H-pyrazole-4-carboxamide as a yellow powder. Product was allowed to dry under vacuum for 1 hr.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09382237B2 |
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| Source dataset | uspto-grants-2016_07 |
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| ORD ID | ord-00ae0a4c2ce84ddab5e363f5f24d4e20 |
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| Source note | uspto-grants-2016_07 |
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