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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642039Generated: October 29, 2026

p-Phenylbenzhydrazide → N'-(5-iodo-2-oxoindol-3-yl)-4-phenylbenzohydrazide

https://huagongshe.com/reaction/642039

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-PhenylbenzhydrazideHCID 72718—
Reactant5-IodoisatinHCID 88695—
SolventAcetic AcidHCID 176—
ProductN'-(5-iodo-2-oxoindol-3-yl)-4-phenylbenzohydrazideHCID 17851719186%

Reaction Conditions

Temperature100 °C

Reaction Steps

Following the general method as outlined in Example 1, into a suspension of 5-iodo-1H-indole-2,3-dione in acetic acid was added (1,1′-biphenyl)-4-carbohydrazide. After stirring at 100° C., the reaction mixture was cooled to rt and a yellow solid precipitated out. Filtration on a fritté, washing with AcOH, water and drying under vacuo at 60° C. overnight gave 201 mg of the title compound (86%) as a yellow solid in 99.8% purity by HPLC (Rt: 6.49, gradient of 10 min, MaxPlot detection between 230 and 400 nm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07696231B2
Source datasetuspto-grants-2010_04
ORD IDord-af79eee4a2cf42efbe2279eb192ef061
Source noteuspto-grants-2010_04