methyl 7-(ethyloxy)-3-methyl-6-[(1-methylethyl)sulfonyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Base Information

Chemical Name:methyl 7-(ethyloxy)-3-methyl-6-[(1-methylethyl)sulfonyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate
CAS No.:1335116-81-8
Molecular Formula:C₂₄H₂₄F₃NO₅S
Molecular Weight:495.519
Hs Code.:

Synonyms:methyl 7-(ethyloxy)-3-methyl-6-[(1-methylethyl)sulfonyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

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Chemical Property of methyl 7-(ethyloxy)-3-methyl-6-[(1-methylethyl)sulfonyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

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Technology Process of methyl 7-(ethyloxy)-3-methyl-6-[(1-methylethyl)sulfonyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

There total 12 articles about methyl 7-(ethyloxy)-3-methyl-6-[(1-methylethyl)sulfonyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate 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: 83.0%

: 1335116-80-7
methyl 7-hydroxy-3-methyl-6-[(1-methylethyl)sulfonyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

: 75-03-6
ethyl iodide

: 1335116-81-8
methyl 7-(ethyloxy)-3-methyl-6-[(1-methylethyl)sulfonyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Guidance literature:: With caesium carbonate; In N,N-dimethyl-formamide; at 20 ℃;

Reference yield:

: 19056-40-7
4-bromo-3-methoxyaniline

: 1335116-81-8
methyl 7-(ethyloxy)-3-methyl-6-[(1-methylethyl)sulfonyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Guidance literature:: Multi-step reaction with 8 steps

1.1: hydrogenchloride / 1,4-dioxane; water / 50 °C

1.2: 1 h / 80 °C

2.1: sulfuric acid / 1 h / 50 - 80 °C

3.1: potassium hydroxide / ethanol; water / 16 h / Reflux

3.2: pH 3

4.1: caesium carbonate / dimethyl sulfoxide / 2 h / 20 °C

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

5.2: 1 h / 20 °C

6.1: hydrogen bromide; acetic acid / 120 h / Reflux

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

7.2: 0 - 20 °C

8.1: caesium carbonate / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; copper(l) iodide; oxalyl dichloride; sulfuric acid; hydrogen bromide; caesium carbonate; acetic acid; potassium hydroxide; N,N-dimethyl-formamide; In 1,4-dioxane; ethanol; dichloromethane; water; dimethyl sulfoxide; N,N-dimethyl-formamide;

Reference yield:

: 454-89-7
3-Trifluoromethylbenzaldehyde

: 1335116-81-8
methyl 7-(ethyloxy)-3-methyl-6-[(1-methylethyl)sulfonyl]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Guidance literature:: Multi-step reaction with 6 steps

1.1: ethanol / Reflux

1.2: 20 °C / Reflux

2.1: sodium hydride / dimethyl sulfoxide; mineral oil / 0.33 h

2.2: 100 °C

2.3: 2 h / 20 °C

3.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane

4.1: hydrogen bromide; acetic acid / 120 h / Reflux

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

5.2: 0 - 20 °C

6.1: caesium carbonate / N,N-dimethyl-formamide / 20 °C

With oxalyl dichloride; hydrogen bromide; sodium hydride; caesium carbonate; acetic acid; 3-chloro-benzenecarboperoxoic acid; N,N-dimethyl-formamide; In ethanol; dichloromethane; dimethyl sulfoxide; N,N-dimethyl-formamide; mineral oil;