156834-57-0

Basic information

• Product Name: 6-fluoro-1-methyl-4-oxo-7-<4-<(2-oxo-1-methylenepropyl)oxycarbonyl>-1-piperazinyl>-4H-<1,3>thiazeto<3,2-a>quinoline-3-carboxylic acid
• Synonyms: 6-fluoro-1-methyl-4-oxo-7-<4-<(2-oxo-1-methylenepropyl)oxycarbonyl>-1-piperazinyl>-4H-<1,3>thiazeto<3,2-a>quinoline-3-carboxylic acid
• CAS NO: 156834-57-0
• Molecular Weight: 461.471
• Mol File: 156834-57-0.mol
• Article Data: 1

Chemical Properties

• CAS DataBase Reference: 6-fluoro-1-methyl-4-oxo-7-<4-<(2-oxo-1-methylenepropyl)oxycarbonyl>-1-piperazinyl>-4H-<1,3>thiazeto<3,2-a>quinoline-3-carboxylic acid(CAS DataBase Reference)
• NIST Chemistry Reference: 6-fluoro-1-methyl-4-oxo-7-<4-<(2-oxo-1-methylenepropyl)oxycarbonyl>-1-piperazinyl>-4H-<1,3>thiazeto<3,2-a>quinoline-3-carboxylic acid(156834-57-0)
• EPA Substance Registry System: 6-fluoro-1-methyl-4-oxo-7-<4-<(2-oxo-1-methylenepropyl)oxycarbonyl>-1-piperazinyl>-4H-<1,3>thiazeto<3,2-a>quinoline-3-carboxylic acid(156834-57-0)

Safety Data

• Hazardous Substances Data: 156834-57-0(Hazardous Substances Data)

Upstream product

• 80715-22-6 4-bromomethyl-1,3-dioxa-5-methylcyclopentene-2-one 
• 112984-60-8 ulifloxacin 

Relevant articles and documents

Studies on synthesis of antibacterial agent (NM441). I. Kinetics and mechanism of the reaction of 4-(bromomethyl)-5-methyl-1,3-dioxol-2-one with 1-substituted piperazine (NM394)

When a tertiary amine (4,NM441) is synthesized from 4-bromomethyl-5-methyl-1,3-dioxol-2-one (DMDO-Br) and a secondary amine (3,NM394) in N,N-dimethylformamide (DMF), the quaternary ammonium salt 5, the ring-opened compound 6, and the 1,2-adduct 7 are formed as by-products. The tertiary amine 4 is formed by nucleophilic attack of 3 on the α-carbon to the bromine atom of DMDO-Br. The ring-opened compound 6 is formed by nucleophilic attack of 3 on carbonyl carbon of DMDO-Br. The quaternary ammonium salt 5 is formed by the reaction of DMDO-Br with 4 (the Menshutkin reaction). Main pathway for the formation of 7 is the Michael addition of 3 to 6. Kinetics of the reactions have been studied and the methods to obtain 4 suppressing the formations of 5, 6, and 7 have been proposed based on the kinetic results.