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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613561Generated: October 29, 2026

Acetic Anhydride → HCID 19592733, compound

https://huagongshe.com/reaction/613561

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 19592706HCID 19592706—
Solvent1,2-DichloroethaneHCID 11—
ProductHCID 19592733HCID 19592733—
ProductHCID 178474000HCID 178474000—

Reaction Steps

To a suspension of 3-amino-6-(2,6-dichlorobenzoylamino)-1H-pyrazolo[4,3-c]quinoline (200 mg) in 1,2-dichloroethane (2 ml) was added acetic anhydride (302 mg), and the reaction mixture was refluxed for 12 hours. The solution was allowed to cool to ambient temperature and the solvent was evaporated in vacuo. The residue was triturated with water-ethanol, and the precipitate was collected. The crude product was purified by column chromatography on silica gel (ethyl acetate-n-hexane) to give 2-acetyl-6-(2,6-dichlorobenzoylamino)-2,3-dihydro-3-imino-1H-pyrazolo[4,3-c]-quinoline as a yellow crystal (60 mg) and 3-acetamido-6-(2,6-dichlorobenzoylamino)-1H-pyrazolo[4,3-c]quinoline as a white crystal (30 mg). 2-Acetyl-6-(2,6-dichlorobenzoylamino)-2,3-dihydro-3-imino-1H-pyrazolo[4,3-cilquinoline

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06008230
Source datasetuspto-grants-1999_12
ORD IDord-fc2558baac1e4a9fb35b0f1bdd1d8b0f
Source noteuspto-grants-1999_12