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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2095142Generated: October 26, 2026

Aniline → 5-Imino-1-phenyl-4-(phenylhydrazinylidene)-3-pyrazolamine

https://huagongshe.com/reaction/2095142

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantPhenylhydrazineHCID 7516—
ReactantMalononitrileHCID 8010—
ReactantCarbonyl cyanide phenylhydrazoneHCID 67541—
Product5-Imino-1-phenyl-4-(phenylhydrazinylidene)-3-pyrazolamineHCID 318030—

Reaction Steps

1-phenyl-4-phenylazo-1H-pyrazole-3,5-diamine was prepared using 200 mg (1.2 mmol) of 2-(phenylhydrazono)malononitrile, which was derived from aniline (10 mL, 107 mmol) and malononitrile (161 mmol), and phenylhydrazine (767 mg, 7.1 mmol). Solids had not formed after heating the reaction at 75° C. for 3 hrs, however, analysis of the reaction solution by TLC indicated that no starting material remained. The solution was allowed to cool to ambient temperature and the solvent was evaporated. The residue was dissolved in ethyl acetate and then precipitated by the addition of hexanes. The resulting solid was isolated by filtration and dried to yield 77 mg (23%) of the compound as an orange coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445694B2
Source datasetuspto-grants-2013_05
ORD IDord-051865f2259045fd856c0bd9d870001d
Source noteuspto-grants-2013_05