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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049220Generated: October 25, 2026

Hydrazine hydrate (1:1) → 5-amino-3-((4-(4-methyl-1H-imidazol-1-yl)phenyl)amino)-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/1049220

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant2-Cyano-3,3-bis(methylthio)acrylamideHCID 2747746—
Reactant4-(4-Methyl-1h-imidazol-1-yl)benzenamineHCID 16005170—
SolventEthanolHCID 702—
Product5-amino-3-((4-(4-methyl-1H-imidazol-1-yl)phenyl)amino)-1H-pyrazole-4-carboxamideHCID 86701914—

Reaction Conditions

Temperature75 °C

Reaction Steps

Dissolved 0.500 g 2-cyano-3,3-bis(methylthio)acrylamide in 15 mL EtOH and added 4-methyl-1-(4-aminophenyl)-1H-imidazole (1.0 eq.). Stirred reaction at 75° 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 5-amino-3-((4-(4-methyl-1H-imidazol-1-yl)phenyl)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-e9700085dff04113a156072f1b81ef5e
Source noteuspto-grants-2016_07