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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049205Generated: October 31, 2026

p-Aminoacetophenone → HCID 86701904, compound

https://huagongshe.com/reaction/1049205

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-AminoacetophenoneHCID 7468—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant2-Cyano-3,3-bis(methylthio)acrylamideHCID 2747746—
SolventEthanolHCID 702—
ProductHCID 86701904HCID 86701904—

Reaction Conditions

Temperature75 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382237B2
Source datasetuspto-grants-2016_07
ORD IDord-00ae0a4c2ce84ddab5e363f5f24d4e20
Source noteuspto-grants-2016_07