1-(2,6-dimethylphenyl)-5-oxo-3-(tetrahydro-pyran-4-yl)-pyrrolidine-3-carboxylic acid (3,5-bis-trifluoromethylphenyl)amide

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Chemical Name:1-(2,6-dimethylphenyl)-5-oxo-3-(tetrahydro-pyran-4-yl)-pyrrolidine-3-carboxylic acid (3,5-bis-trifluoromethylphenyl)amide
CAS No.:1280200-37-4
Molecular Formula:C₂₆H₂₆F₆N₂O₃
Molecular Weight:528.494
Hs Code.:

Synonyms:1-(2,6-dimethylphenyl)-5-oxo-3-(tetrahydro-pyran-4-yl)-pyrrolidine-3-carboxylic acid (3,5-bis-trifluoromethylphenyl)amide

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Chemical Property of 1-(2,6-dimethylphenyl)-5-oxo-3-(tetrahydro-pyran-4-yl)-pyrrolidine-3-carboxylic acid (3,5-bis-trifluoromethylphenyl)amide

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Technology Process of 1-(2,6-dimethylphenyl)-5-oxo-3-(tetrahydro-pyran-4-yl)-pyrrolidine-3-carboxylic acid (3,5-bis-trifluoromethylphenyl)amide

There total 8 articles about 1-(2,6-dimethylphenyl)-5-oxo-3-(tetrahydro-pyran-4-yl)-pyrrolidine-3-carboxylic acid (3,5-bis-trifluoromethylphenyl)amide 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: 100.0%

: 1280200-36-3
3-(3,6-dihydro-2H-pyran-4-yl)-1-(2, 6-dimethylphenyl)-5-oxo-pyrrolidine-3-carboxylic acid (3,5-bis-trifluoromethylphenyl)amide

: 1280200-37-4
1-(2,6-dimethylphenyl)-5-oxo-3-(tetrahydro-pyran-4-yl)-pyrrolidine-3-carboxylic acid (3,5-bis-trifluoromethylphenyl)amide

Guidance literature:: With hydrogen; palladium 10% on activated carbon; In methanol; at 20 ℃; for 5h;

Reference yield:

: 87-62-7
2,6-dimethylaniline

: 1280200-37-4
1-(2,6-dimethylphenyl)-5-oxo-3-(tetrahydro-pyran-4-yl)-pyrrolidine-3-carboxylic acid (3,5-bis-trifluoromethylphenyl)amide

Guidance literature:: Multi-step reaction with 7 steps

1.1: 0.75 h / 130 °C

2.1: acetyl chloride / 1 h / 64 °C

3.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.08 h / -78 °C

3.2: 1 h / -78 - 20 °C

4.1: Burgess Reagent / tetrahydrofuran / 1 h / 75 °C

5.1: water; lithium hydroxide / methanol / 1 h / 75 °C

5.2: pH 4

6.1: N-ethyl-N,N-diisopropylamine; methanesulfonyl chloride / tetrahydrofuran / 0.08 h / 20 °C

6.2: 18 h / 75 °C

7.1: hydrogen / palladium 10% on activated carbon / methanol / 5 h / 20 °C

With Burgess Reagent; water; hydrogen; methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine; acetyl chloride; lithium hydroxide; lithium hexamethyldisilazane; palladium 10% on activated carbon; In tetrahydrofuran; methanol;

Reference yield:

: 97-65-4,25119-64-6
2-methylenesuccinic acid

: 1280200-37-4
1-(2,6-dimethylphenyl)-5-oxo-3-(tetrahydro-pyran-4-yl)-pyrrolidine-3-carboxylic acid (3,5-bis-trifluoromethylphenyl)amide

Guidance literature:: Multi-step reaction with 7 steps

1.1: 0.75 h / 130 °C

2.1: acetyl chloride / 1 h / 64 °C

3.1: lithium hexamethyldisilazane / tetrahydrofuran / 0.08 h / -78 °C

3.2: 1 h / -78 - 20 °C

4.1: Burgess Reagent / tetrahydrofuran / 1 h / 75 °C

5.1: water; lithium hydroxide / methanol / 1 h / 75 °C

5.2: pH 4

6.1: N-ethyl-N,N-diisopropylamine; methanesulfonyl chloride / tetrahydrofuran / 0.08 h / 20 °C

6.2: 18 h / 75 °C

7.1: hydrogen / palladium 10% on activated carbon / methanol / 5 h / 20 °C

With Burgess Reagent; water; hydrogen; methanesulfonyl chloride; N-ethyl-N,N-diisopropylamine; acetyl chloride; lithium hydroxide; lithium hexamethyldisilazane; palladium 10% on activated carbon; In tetrahydrofuran; methanol;