6-(methylsulfonyl)-3-[(4-oxo-1-piperidinyl)methyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

Base Information

Chemical Name:6-(methylsulfonyl)-3-[(4-oxo-1-piperidinyl)methyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid
CAS No.:1335117-20-8
Molecular Formula:C₂₄H₂₁F₃N₂O₅S
Molecular Weight:506.502
Hs Code.:

Synonyms:6-(methylsulfonyl)-3-[(4-oxo-1-piperidinyl)methyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

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Chemical Property of 6-(methylsulfonyl)-3-[(4-oxo-1-piperidinyl)methyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

Chemical Property:

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Technology Process of 6-(methylsulfonyl)-3-[(4-oxo-1-piperidinyl)methyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

There total 15 articles about 6-(methylsulfonyl)-3-[(4-oxo-1-piperidinyl)methyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic 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:

: 1533-03-5
3-(trifluoromethyl)propiophenone

: 1335117-20-8
6-(methylsulfonyl)-3-[(4-oxo-1-piperidinyl)methyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium hydroxide / ethanol; water / 3 h / 85 °C

1.2: 0 °C / pH ~ 3

2.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h / 0 °C

2.2: 0 - 20 °C

3.1: copper(l) iodide / dimethyl sulfoxide / 50 - 120 °C / Inert atmosphere

4.1: dibenzoyl peroxide; N-Bromosuccinimide / tetrachloromethane / 100 °C

5.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 50 °C

6.1: sodium hydroxide; methanol / tetrahydrofuran / 20 h / 50 °C

With methanol; N-Bromosuccinimide; copper(l) iodide; oxalyl dichloride; N-ethyl-N,N-diisopropylamine; potassium hydroxide; sodium hydroxide; dibenzoyl peroxide; N,N-dimethyl-formamide; In tetrahydrofuran; tetrachloromethane; ethanol; dichloromethane; water; dimethyl sulfoxide; acetonitrile;

Reference yield:

: 1335117-19-5
methyl 6-(methylsulfonyl)-3-[(4-oxo-1-piperidinyl)methyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

: 1335117-20-8
6-(methylsulfonyl)-3-[(4-oxo-1-piperidinyl)methyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

Guidance literature:: With methanol; sodium hydroxide; In tetrahydrofuran; at 50 ℃; for 20h;

Reference yield:

: 87-48-9
5-Bromo-1H-indole-2,3-dione

: 1335117-20-8
6-(methylsulfonyl)-3-[(4-oxo-1-piperidinyl)methyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

Guidance literature:: Multi-step reaction with 6 steps

1.1: potassium hydroxide / ethanol; water / 3 h / 85 °C

1.2: 0 °C / pH ~ 3

2.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h / 0 °C

2.2: 0 - 20 °C

3.1: copper(l) iodide / dimethyl sulfoxide / 50 - 120 °C / Inert atmosphere

4.1: dibenzoyl peroxide; N-Bromosuccinimide / tetrachloromethane / 100 °C

5.1: N-ethyl-N,N-diisopropylamine / acetonitrile / 50 °C

6.1: sodium hydroxide; methanol / tetrahydrofuran / 20 h / 50 °C

With methanol; N-Bromosuccinimide; copper(l) iodide; oxalyl dichloride; N-ethyl-N,N-diisopropylamine; potassium hydroxide; sodium hydroxide; dibenzoyl peroxide; N,N-dimethyl-formamide; In tetrahydrofuran; tetrachloromethane; ethanol; dichloromethane; water; dimethyl sulfoxide; acetonitrile;