Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 901258Generated: October 30, 2026

4,6-Dichloro-1-(4-methoxy-benzyl)-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carboxylic Acid Ethyl Ester → 4,6-Dichloro-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/901258

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4,6-Dichloro-1-(4-methoxy-benzyl)-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carboxylic Acid Ethyl EsterHCID 69215698—
SolventTrifluoroacetic acidHCID 6422—
Product4,6-Dichloro-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carboxylic Acid Ethyl EsterHCID 6921726599.3%

Reaction Steps

A solution of 4,6-dichloro-1-(4-methoxy-benzyl)-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carboxylic acid ethyl ester (77) (6.0 g, 14.73 mmol) in neat TFA was refluxed for 3 h. The solution was cooled and the excess TFA was distilled under vacuum. The residue was suspended in saturated NaHCO3 solution, sonicated briefly and filtered. The solids were washed by water, and dried at room temperature to yield 4.2 g (99%) of 4,6-dichloro-2-oxo-1,2-dihydro-[1,8]-naphthyridine-3-carboxylic acid ethyl ester (79) as white solids. MP: 228° C.; 1H-NM (DMSO-d6): δ 1.29 (t, J=7.2 Hz, 3H), 4.37 (q, J=7.2 Hz, 2H), 8.38 (d, J=2.4 Hz, 1H), 8.75 (d, J=2.4 Hz, 1H), 13.10 (s, 1H); EIMS: 287 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07361760B2
Source datasetuspto-grants-2008_04
ORD IDord-01087b1a715846d4928c103158c993db
Source noteuspto-grants-2008_04