6-amino-1-(4-fluorobenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

Base Information

Chemical Name:6-amino-1-(4-fluorobenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid
CAS No.:1616491-20-3
Molecular Formula:C₁₇H₁₃FN₂O₃
Molecular Weight:312.3
Hs Code.:

Synonyms:6-amino-1-(4-fluorobenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

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Chemical Property of 6-amino-1-(4-fluorobenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

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Technology Process of 6-amino-1-(4-fluorobenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

There total 6 articles about 6-amino-1-(4-fluorobenzyl)-4-oxo-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: 80.0%

: 1616491-19-0
1-(4-fluorobenzyl)-6-nitro-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

: 1616491-20-3
6-amino-1-(4-fluorobenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

Guidance literature:: With 5%-palladium/activated carbon; hydrogen; In methanol; at 20 ℃; for 6h;
DOI:10.1016/j.bmc.2014.05.028

Reference yield:

: 709-46-6
2-fluoro-5-nitrobenzoyl chloride

: 1616491-20-3
6-amino-1-(4-fluorobenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

Guidance literature:: Multi-step reaction with 5 steps

1: triethylamine / toluene / Reflux

2: ethanol; diethyl ether / 20 °C

3: potassium carbonate / N,N-dimethyl-formamide / 0.67 h / 100 °C

4: water; hydrogenchloride / methanol / 2 h / Reflux

5: hydrogen; 5%-palladium/activated carbon / methanol / 6 h / 20 °C

With hydrogenchloride; 5%-palladium/activated carbon; water; hydrogen; potassium carbonate; triethylamine; In methanol; diethyl ether; ethanol; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.bmc.2014.05.028

Reference yield:

: 7304-32-7
2-fluoro-5-nitrobenzoic acid

: 1616491-20-3
6-amino-1-(4-fluorobenzyl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1: thionyl chloride / Reflux

2: triethylamine / toluene / Reflux

3: ethanol; diethyl ether / 20 °C

4: potassium carbonate / N,N-dimethyl-formamide / 0.67 h / 100 °C

5: water; hydrogenchloride / methanol / 2 h / Reflux

6: hydrogen; 5%-palladium/activated carbon / methanol / 6 h / 20 °C

With hydrogenchloride; thionyl chloride; 5%-palladium/activated carbon; water; hydrogen; potassium carbonate; triethylamine; In methanol; diethyl ether; ethanol; N,N-dimethyl-formamide; toluene;
DOI:10.1016/j.bmc.2014.05.028