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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910717Generated: November 3, 2026

Acetic Anhydride → HCID 66700168, compound

https://huagongshe.com/reaction/1910717

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AnhydrideHCID 7918—
ReactantTriethylamineHCID 8471—
ReactantHCID 66700199HCID 66700199—
SolventDichloromethaneHCID 6344—
ProductHCID 66700168HCID 66700168—

Reaction Conditions

Temperature40 °C

Reaction Steps

[Step 4] 30 mg of the 4-oxo-2-methyl-2,3-dihydro-1H-[1,6]naphthyridine were dissolved in 2 mL of dichloromethane followed by adding 0.1 mL of triethylamine and 35 μL of acetic anhydride and stirring overnight at 40° C. Following completion of the reaction, the solution was concentrated under reduced pressure and the resulting residue was purified using silica gel chromatography (ethyl acetate) to obtain 7 mg of 1-acetyl-4-oxo-2-methyl-2,3-dihydro-1H-[1,6]naphthyridine in the form of a pale yellow oil (18%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604030B2
Source datasetuspto-grants-2013_12
ORD IDord-662b4ca3ffd549a9ba15a9390a748ae8
Source noteuspto-grants-2013_12