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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1744561생성일: 2026년 10월 26일

Triethylamine → N-(3-Cyano-4-isobutoxyphenyl)-1-(4-fluorophenyl)-5-methylpyrazole-4-carboxamide

https://huagongshe.com/reaction/1744561

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물Diethyl cyanophosphonateHCID 76257—
반응물1-(4-fluorophenyl)-5-methyl-1H-pyrazole-4-carboxylic acidHCID 4270263—
반응물5-Amino-2-isobutoxybenzonitrileHCID 19366028—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-(3-Cyano-4-isobutoxyphenyl)-1-(4-fluorophenyl)-5-methylpyrazole-4-carboxamideHCID 982187334.2%

반응 단계

1-(4-Fluorophenyl)-5-methylpyrazole-4-carboxylic acid (2 g), 5-amino-2-isobutoxybenzonitrile (1.7 g), triethylamine (2.7 g) and diethyl cyanophosphate (2.2 g) were added to dimethylformamide (20 ml) and the mixture was stirred at room temperature for 1 h. The reaction mixture was added into water and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, after which the solvent was evaporated under reduced pressure. Diisopropyl ether was added to the residue to allow crystallization. The crystals were recrystallized from a mixed solvent of ethyl acetate-n-hexane to give the title compound (1.2 g), melting point: 177–178° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07015218B1
출처 데이터셋uspto-grants-2006_03
ORD IDord-b2fd98bfe31741838dc65fa990f303a6
출처 메모uspto-grants-2006_03