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HRID 346814생성일: 2026년 10월 25일

Sodium Carbonate → 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid (4'-chlorobiphenyl-2-yl) amide

https://huagongshe.com/reaction/346814

반응식

참여 물질

역할이름HCID투입량
반응물Sodium CarbonateHCID 10340—
반응물4-Chlorophenylboronic acidHCID 74299—
반응물1-Methyl-3-trifluoromethyl-1h-pyrazole-4-carboxylic acid(2-bromo-phenyl)amideHCID 17947996—
촉매Tetrakis(triphenylphosphine)palladiumHCID 11979704—
용매WaterHCID 962—
용매1,2-DimethoxyethaneHCID 8071—
생성물1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid (4'-chlorobiphenyl-2-yl) amideHCID 58799476—

반응 단계

A solution of 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid(2-bromo-phenyl)amide (0.64 g), 4-chlorobenzene boronic acid (0.29 g), powdered sodium carbonate (0.25 g) and tetrakis(triphenylphosphine) palladium (0.04 g) in 25 ml 1,2-dimethoxyethane (DME) and 2 ml water is heated at reflux temperature for 20 hours. After cooling, the solvent is removed in a water jet vacuum and the residue taken up in ethylacetate/water. The ethylacetate phase is washed twice with water and brine and then dried over sodium sulfate. Distilling off the solvent left the raw material which can be further purified by column chromatography (silicagel; eluant: ethylacetate/hexane 1:1) or recrystallization from TBME/hexane. The yield after purification is 0.6 g; m.p.=145–146° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07173055B1
출처 데이터셋uspto-grants-2007_02
ORD IDord-6c221704ba22411d94f61e1a06afe252
출처 메모uspto-grants-2007_02