HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 613561Generated: October 29, 2026
Acetic Anhydride → HCID 19592733, compound
https://huagongshe.com/reaction/613561
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | HCID 19592706 | HCID 19592706 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | HCID 19592733 | HCID 19592733 | — |
| Product | HCID 178474000 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06008230 |
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| Source dataset | uspto-grants-1999_12 |
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| ORD ID | ord-fc2558baac1e4a9fb35b0f1bdd1d8b0f |
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| Source note | uspto-grants-1999_12 |
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