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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2304443Generated: November 1, 2026

Aniline → (3,5-Diamino-4-phenylazopyrazol-1-yl)phenylmethanone

https://huagongshe.com/reaction/2304443

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantMalononitrileHCID 8010—
ReactantBenzoylhydrazineHCID 11955—
ReactantCarbonyl cyanide phenylhydrazoneHCID 67541—
Product(3,5-Diamino-4-phenylazopyrazol-1-yl)phenylmethanoneHCID 13541821713.1%

Reaction Steps

This compound was prepared using 85 mg (0.5 mmol) of 2-(phenyl-hydrazono)-malononitrile, which was derived from aniline (10 mL, 107 mmol) and malononitrile (161 mmol) as described in Example 8, and benzoic hydrazide (68 mg, 0.5 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 room temperature and the solvent was evaporated. The residue was dissolved in methanol and then precipitated by the addition of water. The resulting solid was isolated by filtration and dried to yield 20 mg (13%) of the title compound as an orange coloured solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06436915B1
Source datasetuspto-grants-2002_08
ORD IDord-91602f59652444d39dadeedc77bfa00f
Source noteuspto-grants-2002_08