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HRID 517364作成日:2026年10月25日

Hexachloroethane → 3-Chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamide

https://huagongshe.com/reaction/517364

反応式

関与物質

役割名称HCID仕込み量
反応物HexachloroethaneHCID 6214—
反応物N,N-dimethyl-1H-pyrazole-1-sulfonamideHCID 10954038—
反応物ButyllithiumHCID 178418339—
生成物3-Chloro-N,N-dimethyl-1H-pyrazole-1-sulfonamideHCID 21113388—

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09115115B1
出典データセットuspto-grants-2015_08
ORD IDord-7bd55377661046e8bc48de53f4f03188
出典メモuspto-grants-2015_08