1-ethyl-6-fluoro-4-oxo-7-(4-[4-(trifluoromethyl)benzoylhydrazonomethyl]piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid

Base Information

Chemical Name:1-ethyl-6-fluoro-4-oxo-7-(4-[4-(trifluoromethyl)benzoylhydrazonomethyl]piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid
CAS No.:1340587-08-7
Molecular Formula:C₂₅H₂₃F₄N₅O₄
Molecular Weight:533.482
Hs Code.:

Synonyms:1-ethyl-6-fluoro-4-oxo-7-(4-[4-(trifluoromethyl)benzoylhydrazonomethyl]piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid

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Chemical Property of 1-ethyl-6-fluoro-4-oxo-7-(4-[4-(trifluoromethyl)benzoylhydrazonomethyl]piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid

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Technology Process of 1-ethyl-6-fluoro-4-oxo-7-(4-[4-(trifluoromethyl)benzoylhydrazonomethyl]piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid

There total 2 articles about 1-ethyl-6-fluoro-4-oxo-7-(4-[4-(trifluoromethyl)benzoylhydrazonomethyl]piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 56.0%

: 1340587-12-3
C₁₁H₁₁F₃N₂O₂

: 70458-96-7
1-ethyl-6-fluoro-1,4-dihydro-4-oxo-7-(1-piperazinyl)-3-quinoline carboxylic acid

: 1340587-08-7
1-ethyl-6-fluoro-4-oxo-7-(4-[4-(trifluoromethyl)benzoylhydrazonomethyl]piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid

Guidance literature:: With acetic acid; In acetonitrile; at 20 - 50 ℃; for 5.66667h;
DOI:10.1016/j.ejmech.2011.07.052

Reference yield:

: 339-59-3
4-(trifluoromethyl)benzoic acid hydrazide

: 1340587-08-7
1-ethyl-6-fluoro-4-oxo-7-(4-[4-(trifluoromethyl)benzoylhydrazonomethyl]piperazin-1-yl)-1,4-dihydroquinoline-3-carboxylic acid

Guidance literature:: Multi-step reaction with 2 steps

1: acetonitrile / 0.17 h / 20 °C

2: acetic acid / acetonitrile / 5.67 h / 20 - 50 °C

With acetic acid; In acetonitrile;
DOI:10.1016/j.ejmech.2011.07.052