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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13840Generated: October 29, 2026

Acetic Anhydride → N-acetyl-N-(7-(2,4-dichlorophenyl)-6-(4-chlorophenyl)-3-(dimethylamino)-1,2-dihydro-1-methyl-2-oxo-1,8-naphthyridin-4-yl)acetamide

https://huagongshe.com/reaction/13840

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
Reactant1,4-DioxaneHCID 31275—
ReactantHCID 11306006HCID 11306006—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventEthyl AcetateHCID 8857—
ProductN-acetyl-N-(7-(2,4-dichlorophenyl)-6-(4-chlorophenyl)-3-(dimethylamino)-1,2-dihydro-1-methyl-2-oxo-1,8-naphthyridin-4-yl)acetamideHCID 11157205—

Reaction Conditions

Temperature105 °C

Reaction Steps

To the product of EXAMPLE 72 (48.8 mg) in 1,4-dioxane (1 mL) was added acetic anhydride (2 mL) and DMAP (20 mg). The reaction was heated to 105° C. After about 1 hour the reaction was cooled to room temperature and diluted with EtOAc. The solution washed with saturated aqueous NaHCO3/1 M aqueous NaOH solution (1:1). The organic layer was dried (Na2SO4). The concentrated residue was purified by flash chromatography on silica gel gradient eluted with 0-100% EtOAc in hexane affording the title compound. HPLC/MS: 557.1 (M+1), 559.1 (M+3); Rt=4.40 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728141B2
Source datasetuspto-grants-2010_06
ORD IDord-4140ec28afeb4a8e8b1a008adda1825e
Source noteuspto-grants-2010_06