1-methanesulfonylpiperidine-4-carboxylic acid {4-[isobutyl-(2-trifluoromethylphenyl)sulfamoyl]phenyl}amide

Base Information

Chemical Name:1-methanesulfonylpiperidine-4-carboxylic acid {4-[isobutyl-(2-trifluoromethylphenyl)sulfamoyl]phenyl}amide
CAS No.:1613303-88-0
Molecular Formula:C₂₄H₃₀F₃N₃O₅S₂
Molecular Weight:561.647
Hs Code.:

Synonyms:1-methanesulfonylpiperidine-4-carboxylic acid {4-[isobutyl-(2-trifluoromethylphenyl)sulfamoyl]phenyl}amide

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Chemical Property of 1-methanesulfonylpiperidine-4-carboxylic acid {4-[isobutyl-(2-trifluoromethylphenyl)sulfamoyl]phenyl}amide

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Technology Process of 1-methanesulfonylpiperidine-4-carboxylic acid {4-[isobutyl-(2-trifluoromethylphenyl)sulfamoyl]phenyl}amide

There total 5 articles about 1-methanesulfonylpiperidine-4-carboxylic acid {4-[isobutyl-(2-trifluoromethylphenyl)sulfamoyl]phenyl}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: 65.0%

: 241138-40-9
1-(methylsulfonyl)piperidine-4-carbonyl chloride

: 1613304-91-8
4-amino-N-isobutyl-N-(2-trifluoromethylphenyl)benzenesulfonamide

: 1613303-88-0
1-methanesulfonylpiperidine-4-carboxylic acid {4-[isobutyl-(2-trifluoromethylphenyl)sulfamoyl]phenyl}amide

Guidance literature:: With N-ethyl-N,N-diisopropylamine; In dichloromethane; at 20 ℃; for 3h;

Reference yield:

: 98-74-8
4-Nitrobenzenesulfonyl chloride

: 1613303-88-0
1-methanesulfonylpiperidine-4-carboxylic acid {4-[isobutyl-(2-trifluoromethylphenyl)sulfamoyl]phenyl}amide

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / dichloromethane / 18 h / 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 18 h / 100 °C

3: iron; hydroxylamine hydrochloride / water; ethanol / 1 h / Reflux

4: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 20 °C

With pyridine; hydroxylamine hydrochloride; iron; potassium carbonate; N-ethyl-N,N-diisopropylamine; In ethanol; dichloromethane; water; N,N-dimethyl-formamide;

Reference yield:

: 88-17-5
2-(trifluoromethyl)benzenamine

: 1613303-88-0
1-methanesulfonylpiperidine-4-carboxylic acid {4-[isobutyl-(2-trifluoromethylphenyl)sulfamoyl]phenyl}amide

Guidance literature:: Multi-step reaction with 4 steps

1: pyridine / dichloromethane / 18 h / 20 °C

2: potassium carbonate / N,N-dimethyl-formamide / 18 h / 100 °C

3: iron; hydroxylamine hydrochloride / water; ethanol / 1 h / Reflux

4: N-ethyl-N,N-diisopropylamine / dichloromethane / 3 h / 20 °C

With pyridine; hydroxylamine hydrochloride; iron; potassium carbonate; N-ethyl-N,N-diisopropylamine; In ethanol; dichloromethane; water; N,N-dimethyl-formamide;