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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 483290Generated: October 30, 2026

Diethyl Malonate → 1-Cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid Ethyl Ester

https://huagongshe.com/reaction/483290

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl MalonateHCID 7761—
ReactantAcetic AnhydrideHCID 7918—
ReactantEthyl orthoformateHCID 31214—
ReactantOxalyl chlorideHCID 65578—
ReactantCyclopropylamineHCID 69828—
Reactant2,3,4,5-Tetrafluorobenzoic acidHCID 297549—
ReactantEthyl 3-oxo-(2,3,4,5-tetrafluorophenyl)propanoateHCID 600916—
ReactantSodiumHCID 5360545—
ReactantMagnesiumHCID 5462224—
Product1-Cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic Acid Ethyl EsterHCID 535415—
ProductHCID 178471877HCID 178471877—

Reaction Steps

The starting materials for the present invention are known, or if new, may be prepared from known materials by known means. Thus, ethyl 1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylate is prepared as described in Belgian Pat. No. 899,399 or No. DE3318145. Alternatively, it may be prepared by a series of reactions starting from 2,3,4,5-tetrafluorobenzoic acid. The sodium salt of 2,3,4,5-tetrafluorobenzoic acid is reacted with oxalyl chloride and the product condensed with diethyl malonate in the presence of magnesium turnings to afford after hydrolysis 2,3,4,5-tetrafluorobenzoylacetic acid, ethyl ester. This compound is, in turn, treated with triethylorthoformate and acetic anhydride, followed by cyclopropylamine to afford 2-(2,3,4,5-tetrafluorobenzoyl)-3-cyclopropylamino acrylic acid, ethyl ester, which is then ring closed to give the desired starting material. The corresponding methyl ester is prepared using dimethylmalonate in the sequence described above.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04578473
Source datasetuspto-grants-1986_03
ORD IDord-3292f44d3208476cb08631810f010c12
Source noteuspto-grants-1986_03