Реакция #604545

ord-59318fa5b4e04808ac4a6061b813a5f9

Уравнение реакции

c1cn[nH]c1
1H-pyrazole
CN(C)S(=O)(=O)Cl
dimethylsulfamoyl chloride
[H-].[Na+]
sodium hydride
Clc1ccn(-c2cccnc2)n1
3-(3-chloro-1H-pyrazol-1-yl)pyridine
Brc1cccnc1
3-bromopyridine
Clc1cc[nH]n1
3-chloropyrazole
Clc1cc[nH]n1
3-chloropyrazole
CN(C)S(=O)(=O)n1cccn1
N,N-dimethyl-1H-pyrazole-1-sulfonamide

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    ДругоеThe route to prepare such compounds

Методика

US 20130288893(A1) describes, inter alia, certain (3-halo-1-(pyridin-3-yl)-1H-pyrazol-4-yl)amides and carbamates and their use as pesticides. The route to prepare such compounds involved the preparation of 3-(3-chloro-1H-pyrazol-1-yl)pyridine by the direct coupling of 3-bromopyridine with 3-chloropyrazole. The 3-chloropyrazole was prepared by a) treating 1H-pyrazole with 2 dimethylsulfamoyl chloride and sodium hydride to provide N,N-dimethyl-1H-pyrazole-1-sulfonamide, b) treating the N,N-dimethyl-1H-pyrazole-1-sulfonamide with perchloroethane and n-butyl lithium to provide 3-chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamide, and c) removing the N,N-dimethylsulfonamide from 3-chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamide with trifluoroacetic acid to give the 3-chloropyrazole.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US09115115B1uspto-grants-2015_08