4-bromo-2,6-dichloro-N-(difluoromethyl)-N-(1,3,5-trimethyl-1H-pyrazol-4-yl)benzenesulfonamide

Base Information

Chemical Name:4-bromo-2,6-dichloro-N-(difluoromethyl)-N-(1,3,5-trimethyl-1H-pyrazol-4-yl)benzenesulfonamide
CAS No.:1215013-18-5
Molecular Formula:C₁₃H₁₂BrCl₂F₂N₃O₂S
Molecular Weight:463.13
Hs Code.:

Synonyms:4-bromo-2,6-dichloro-N-(difluoromethyl)-N-(1,3,5-trimethyl-1H-pyrazol-4-yl)benzenesulfonamide

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Chemical Property of 4-bromo-2,6-dichloro-N-(difluoromethyl)-N-(1,3,5-trimethyl-1H-pyrazol-4-yl)benzenesulfonamide

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Technology Process of 4-bromo-2,6-dichloro-N-(difluoromethyl)-N-(1,3,5-trimethyl-1H-pyrazol-4-yl)benzenesulfonamide

There total 4 articles about 4-bromo-2,6-dichloro-N-(difluoromethyl)-N-(1,3,5-trimethyl-1H-pyrazol-4-yl)benzenesulfonamide 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: 62.0%

: 1215009-29-2
4-bromo-2,6-dichloro-N-(1,3,5-trimethyl-1H-pyrazol-4-yl)-benzenesulfonamide

: 1895-39-2
sodium chlorodifluoroacetate

: 1215013-18-5
4-bromo-2,6-dichloro-N-(difluoromethyl)-N-(1,3,5-trimethyl-1H-pyrazol-4-yl)benzenesulfonamide

Guidance literature:: With potassium carbonate; In acetonitrile; at 60 ℃; for 48h; Inert atmosphere;
DOI:10.1021/jm500809c

Reference yield:

: 1895-39-2
sodium chlorodifluoroacetate

: 1215013-18-5
4-bromo-2,6-dichloro-N-(difluoromethyl)-N-(1,3,5-trimethyl-1H-pyrazol-4-yl)benzenesulfonamide

Guidance literature:: With potassium carbonate; In acetonitrile;

Reference yield:

: 351003-54-8
4-bromo-2,6-dichlorobenzenesulfonyl chloride

: 1215013-18-5
4-bromo-2,6-dichloro-N-(difluoromethyl)-N-(1,3,5-trimethyl-1H-pyrazol-4-yl)benzenesulfonamide

Guidance literature:: Multi-step reaction with 2 steps

1: pyridine / 24 h / 20 °C / Inert atmosphere

2: potassium carbonate / acetonitrile / 48 h / 60 °C / Inert atmosphere

With pyridine; potassium carbonate; In acetonitrile;
DOI:10.1021/jm500809c