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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 622497Generated: October 26, 2026

Ethyl 7-bromoacetyl-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3quinolinecarboxylate → Ethyl 6-fluoro-4-hydroxyquinoline-3-carboxylate

https://huagongshe.com/reaction/622497

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 7-bromoacetyl-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3quinolinecarboxylateHCID 13853634—
Reactant2-(N-acetyl-N-ethylamino)thioacetamideHCID 14023632—
SolventEthanolHCID 702—
ProductEthyl 6-fluoro-4-hydroxyquinoline-3-carboxylateHCID 710779—

Reaction Steps

According to example 30, reacting 7-bromoacetyl-1-ethyl-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid ethyl ester with 2-(N-acetyl-N-ethylamino)thioacetamide in ethanol gave 1-ethyl-7-2-[(N-acetyl-N-ethylamino)methyl]-4-thiazolyl]-6-fluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid ethyl ester, mp 160°-161° C. which was then hydrolyzed in refluxing 6N hydrochloric acid to afford the title compound, mp 289°-300° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04771054
Source datasetuspto-grants-1988_09
ORD IDord-791852a944394ac897f0dde5ce947f3b
Source noteuspto-grants-1988_09