166381-24-4

Upstream product

• 166381-23-3 ethyl 4-benzoyloxy-6,7-difluoro-2-(methoxymethyl)thioquinoline-3-carboxylate 
• 113028-77-6 ethyl 6,7-difluoro-4-hydroxy-2-<(methoxymethyl)thio>-quinoline-3-carboxylate 

Downstream Products

• 166381-26-6 ethyl 4-benzoyloxy-2-(1-chloro-2-fluoroethyl)thio-6,7-difluoroquinoline-3-carboxylate 
• 166381-36-8 ethyl 2-(2-acetoxyethylthio)-4-benzoyloxy-6,7-difluoroquinoline-3-carboxylate 
• 166381-25-5 ethyl 4-benzoyloxy-6,7-difluoro-2-(2-fluoroethyl)thioquinoline-3-carboxylate 
• 166381-37-9 ethyl 2-(2-acetoxy-1-chloroethylthio)-4-benzoyloxy-6,7-difluoroquinoline-3-carboxylate 

Relevant academic research and scientific papers

Synthesis and antibacterial activity of novel 7-substituted 6-fluoro-1- methylene-4-oxo-4H-[1,3]-thiazeto[3,2-a]quinoline-3-carboxylic acid derivatives

A series of 7-substituted 6-fluoro-1-methylene-4-oxo-4H- [1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid derivatives (2) and (3) was prepared and evaluated for antibacterial activity. These compounds were obtained by the treatment of the 1-methanesulfonyloxymethyl or 1-fluoromethyl thiazetoquinolone-3-carboxylates (12, 14 and 20) with potassium hydroxide. Compounds (2) and (3) showed excellent in vitro antibacterial activity against both gram-negative and gram-positive bacteria including quinolone and Methicillin-resistant Staphylococcus aureus.

Synthesis and antibacterial activity of novel 7-substituted-6-fluoro-1- fluoromethyl-4-oxo-4H-[1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid derivatives

A series of 7-substituted-6-fluoro-1-fluoromethyl-4-oxo-4H- [1,3]thiazeto[3,2-a]quinoline-3-carboxylic acid derivatives (2a - I) was prepared and evaluated for antibacterial activity. These compounds were obtained by deacylation of 4-benzoyloxy-2-(1-chloro-2-fluoroethyl)thio-6,7- difluoroquinoline-3-carboxylate (10) and subsequent intramolecular cyclization followed by substitution with cyclic amines and then hydrolysis. The intramolecular cyclization reaction of 18, one of the diastereomers (17, 18) revealed that the cyclization reaction proceeded through an inversion to afford (-)-11a in good chemical and optical yield. The enantiomers of 2a were prepared from the enantiomers of 11a, which were obtained by the optical resolution of the racemate using high-performance liquid chromatography (HPLC). Compounds 2a,b showed excellent in vitro and in vivo antibacterial activity against both gram-negative and gram-positive bacteria including quinolone and Methicillin-resistant Staphylococcus aureus.