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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 642043Generated: October 26, 2026

m-Anisohydrazide → HCID 178490564, compound

https://huagongshe.com/reaction/642043

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-AnisohydrazideHCID 79848—
Reactant5-IodoisatinHCID 88695—
SolventAcetic AcidHCID 176—
ProductHCID 178490564HCID 17849056482%

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 3-methoxybenzohydrazide. 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 345 mg of the title compound (82%) as a yellow solid in 99.7% purity by HPLC (Rt: 5.5, 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-63022755d650403d8a47ae01af29a786
Source noteuspto-grants-2010_04