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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 346813생성일: 2026년 10월 24일

Dimethylformamide → HCID 58799476, 화합물

https://huagongshe.com/ko/reaction/346813

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물Oxalyl chlorideHCID 65578—
반응물2-Amino-4'-chlorobiphenylHCID 262261—
반응물1-methyl-3-(trifluoromethyl)-1H-pyrazole-4-carboxylic acidHCID 2775665—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물HCID 58799476HCID 5879947660.4%

반응 단계

A solution of 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid (0.68 g) and oxalyl chloride (0.49 g) in methylene chloride (30 ml) is stirred for 2 hours at room temperature in the presence of a catalytic amount of DMF. The resulting acid chloride solution is then added to a solution of 4′-chlorobiphenyl-2-ylamine (0.71 g) and triethylamine (0.36 g) in 15 ml of methylene chloride at 0° C. The reaction mixture is then stirred for 4 hours at room temperature. After distilling off the solvent in a water-jet-vacuum, the residue is taken up in ethylacetate/water. The ethylacetate phase is extracted twice with water. After drying of the organic phase with Na2SO4, the solvent is distilled off in a water-jet-vacuum and the residue purified by column chromatography (silica gel; eluant: ethylacetate/hexane=1:1). 0.8 g of 1-methyl-3-trifluoromethyl-1H-pyrazole-4-carboxylic acid (4′-chlorobiphenyl-2-yl) amide are obtained in the form of slightly brownish crystals having a melting point of 144–146° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07173055B1
출처 데이터셋uspto-grants-2007_02
ORD IDord-99ae9128fab0475badea545ca848a26e
출처 메모uspto-grants-2007_02