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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1241720Generated: November 1, 2026

Acetic Anhydride → HCID 21936635, compound

https://huagongshe.com/reaction/1241720

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 21936644HCID 21936644—
SolventPyridineHCID 1049—
ProductHCID 21936635HCID 21936635100%

Reaction Conditions

Temperature100 °C

Reaction Steps

A mixture of 1-(3-nitrophenyl)-3-[3-hydroxy-3-(pyridin-4-yl)propyl]-1,8-naphthyridin-2(1H)-one (50 mg, 0.12 mmol; prepared in Example 20) in acetic anhydride (0.2 ml) and pyridine (0.3 ml) was heated at 100° C. for 20 min, concentrated, and extracted with chloroform. The extract was treated according to conventional techniques, concentrated, and then purified by flash column chromatography to afford 1-(3-nitrophenyl)-3-[3-acetyloxy-3-(pyridin-4-yl)propyl]-1,8-naphthyridin-2(1H)-one (55.2 mg, 100%; mp 69–71° C.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07115623B2
Source datasetuspto-grants-2006_10
ORD IDord-6147352068f74fabaf8b055cf2fe14e4
Source noteuspto-grants-2006_10