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

Base Information

Chemical Name:methyl 6-bromo-3-methyl-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate
CAS No.:1336905-22-6
Molecular Formula:C₂₂H₁₉BrF₃NO₃
Molecular Weight:482.297
Hs Code.:

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

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

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

There total 5 articles about methyl 6-bromo-3-methyl-7-[(1-methylethyl)oxy]-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: 30.0%

: 67-56-1
methanol

: 1336905-20-4
6-bromo-3-methyl-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid

: 1336905-22-6
methyl 6-bromo-3-methyl-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Guidance literature:: 6-bromo-3-methyl-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylic acid; With oxalyl dichloride; N,N-dimethyl-formamide; In dichloromethane; for 1h;

methanol; In dichloromethane; at 20 ℃; for 1h; Product distribution / selectivity;

Reference yield:

: 77337-82-7
1-bromo-2-methoxy-4-nitrobenzene

: 1336905-22-6
methyl 6-bromo-3-methyl-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Guidance literature:: Multi-step reaction with 5 steps

1.1: hydrogen bromide / water / 20 h / Reflux

2.1: potassium carbonate / acetonitrile / 2 h / Reflux

3.1: nickel(II) chloride tetrahydrate / acetonitrile / 0.08 h / 0 °C

3.2: 0.08 h / 0 °C

4.1: ethanol / 1 h / Reflux

4.2: 19 h / 20 °C / Reflux

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

5.2: 1 h / 20 °C

With oxalyl dichloride; hydrogen bromide; potassium carbonate; nickel(II) chloride tetrahydrate; N,N-dimethyl-formamide; In ethanol; dichloromethane; water; acetonitrile;

Reference yield:

: 52427-05-1
2-bromo-5-nitrophenol

: 1336905-22-6
methyl 6-bromo-3-methyl-7-[(1-methylethyl)oxy]-2-[3-(trifluoromethyl)phenyl]-4-quinolinecarboxylate

Guidance literature:: Multi-step reaction with 4 steps

1.1: potassium carbonate / acetonitrile / 2 h / Reflux

2.1: nickel(II) chloride tetrahydrate / acetonitrile / 0.08 h / 0 °C

2.2: 0.08 h / 0 °C

3.1: ethanol / 1 h / Reflux

3.2: 19 h / 20 °C / Reflux

4.1: oxalyl dichloride / N,N-dimethyl-formamide / dichloromethane / 1 h

4.2: 1 h / 20 °C

With oxalyl dichloride; potassium carbonate; nickel(II) chloride tetrahydrate; N,N-dimethyl-formamide; In ethanol; dichloromethane; acetonitrile;