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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1948106Generated: November 2, 2026

Ethyl bromoacetate → (3-Methyl-5-nitro-4-oxo-4H-quinolin-1-yl)-acetic acid ethyl ester

https://huagongshe.com/reaction/1948106

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl bromoacetateHCID 7748—
ReactantCesium carbonateHCID 10796—
Reactant3-methyl-5-nitroquinolin-4(1H)-oneHCID 10512369—
Reactant3-methyl-7-nitroquinolin-4(1H)-oneHCID 10560102—
SolventTolueneHCID 1140—
Product(3-Methyl-5-nitro-4-oxo-4H-quinolin-1-yl)-acetic acid ethyl esterHCID 67256021—

Reaction Steps

A suspension of 3-methyl-5-nitroquinolin-4(1H)-one and 3-methyl-7-nitroquinolin-4(1H)-one (Eur. J. Med. Chem. 1997, 32, 547, 500 mg, 2.45 mmol,) and cesium carbonate (800 mg (2.45 mmol) in toluene (50 mL) was treated with ethyl bromoacetate (0.3 mL, 2.45 mmol) and stirred at RT for 3 days. The solid (Cesium salt of starting materials) was filtered and washed with dichloromethane. The filtrate was concentrated to give 400 mg of the crude material which was purified using flash column chromatography (DCM:MeOH, 99:1) to isolate the desired region-isomer: 100 mg 1H NMR (CDCl3, 300 MHz): δ 1.3 (m, 3H, J=7.2 Hz), 2.08 (s, 3H), 4.25 (q, 2H, J=7.2 Hz), 4.8 (s, 2H), 7.3 (m, 2H), 7.4 (s, 1H), 7.65 (t, J=8 Hz, 1H). The other isomer was also recovered: 70 mg.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08399433B2
Source datasetuspto-grants-2013_03
ORD IDord-edd0b8cef1ac46878e5c9e2053ab8732
Source noteuspto-grants-2013_03