Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049176Generated: October 25, 2026

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

https://huagongshe.com/reaction/1049176

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant3-((3-Chlorophenyl)amino)-2-cyano-3-(methylthio)acrylamideHCID 86698955—
SolventEthanolHCID 702—
Product5-amino-3-((3-chlorophenyl)amino)-1H-pyrazole-4-carboxamideHCID 8669895683%

Reaction Conditions

Temperature75 °C

Reaction Steps

3-((3-chlorophenyl)amino)-2-cyano-3-(methylthio)acrylamide (6.00 g) was suspended in 100 mL of ethanol and hydrazine hydrate (1.478 mL, 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-((3-chlorophenyl)amino)-1H-pyrazole-4-carboxamide as an off white to yellow powder. Product was allowed to dry under vacuum for 1 hr (4.40 g, 83% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382237B2
Source datasetuspto-grants-2016_07
ORD IDord-bebf3c731b344bdea22574b94f4991ec
Source noteuspto-grants-2016_07