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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 47067Generated: October 25, 2026

5,6-Dimethoxyindolin-2-one → HCID 178486553, compound

https://huagongshe.com/reaction/47067

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,6-Dimethoxyindolin-2-oneHCID 222993—
ReactantEthylorthoformateHCID 53630039—
ProductHCID 178486553HCID 178486553—

Reaction Steps

As illustrated above in Scheme (A), the intermediate, 5,6-dimethoxy oxindole (I) is reacted with ethyl ortho formate (II) to provide 5,6-dimethoxy-3-hydroxymethylene oxindole (III). This oxindole (III) is then reacted with primary or secondary amines in refluxing benzene in the presence of acetic acid or toluene sulfonic acid to yield 5,6-dimethoxy-3-(substituted amino methylene) oxindoles (IV) or (V), respectively.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04176191
Source datasetuspto-grants-1979_11
ORD IDord-0f88a97320c64033b9dbd7dfa764f397
Source noteuspto-grants-1979_11