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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 527263Generated: October 26, 2026

Hydrazine hydrate (1:1) → 5-amino-3-((4-isopropylphenyl)amino)-1H-pyrazole-4-carboxamide

https://huagongshe.com/reaction/527263

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant2-Cyano-3-((4-isopropylphenyl)amino)-3-(methylthio)acrylamideHCID 86701870—
SolventEthanolHCID 702—
Product5-amino-3-((4-isopropylphenyl)amino)-1H-pyrazole-4-carboxamideHCID 8670187266%

Reaction Conditions

Temperature75 °C

Reaction Steps

2-cyano-3-((4-isopropylphenyl)amino)-3-(methylthio)acrylamide (1.360 g) was suspended in 15 mL of ethanol and hydrazine hydrate (360 μL, 1.5 eq.) was added drop wise to the reaction. Reaction was then heated at 75° C. until the starting material was no longer present and confirmed via HPLC. Once starting material was absent (18 hrs), reaction was brought to room temperature and filtered to obtain 5-amino-3-((4-isopropylphenyl)amino)-1H-pyrazole-4-carboxamide as an off white to yellow powder. The product was allowed to dry under vacuum for 1 hr (850 mg, 66% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09346792B2
Source datasetuspto-grants-2016_05
ORD IDord-7f09d68a8a2346db8cbdc5b070dd9b44
Source noteuspto-grants-2016_05