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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 57795생성일: 2026년 10월 24일

Triethylamine → 5-nitro-1H-pyrazole-3-carboxylic acid [2-(4-chloro-phenyl)-ethyl]-amide

https://huagongshe.com/ko/reaction/57795

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물2-(4-Chlorophenyl)ethylamineHCID 67430—
반응물5-Nitro-1H-pyrazole-3-carboxylic acidHCID 86222684—
반응물HCID 178418300HCID 178418300—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물5-nitro-1H-pyrazole-3-carboxylic acid [2-(4-chloro-phenyl)-ethyl]-amideHCID 13634435443%

반응 단계

To a solution of 5-nitro-1H-pyrazole-3-carboxylic acid (200 mg, 1.3 mmol, 1 eq) in tetrahydrofuran (5 mL) were added triethylamine (350 μL, 1.9 mmol, 1.5 eq), hydroxybenzotriazole (HOBT) (257 mg, 1.27 mmol, 1 eq), 2-(4-chloro-phenyl)-ethylamine (180 μL, 1.27 mmol, 1 eq) and EDCI (364 mg, 1.9 mmol, 1.5 eq). The mixture was stirred at room temperature during 20 h. Water (10 mL) was then added and the aqueous phase was extracted with ethyl acetate (2×15 mL). The organic layers were dried over magnesium sulfate, filtered and evaporated in vacuo. The crude residue was purified by flash chromatography using cyclohexane and ethyl acetate (100/0) to (50/50) to afford 5-nitro-1H-pyrazole-3-carboxylic acid [2-(4-chloro-phenyl)-ethyl]-amide as white solid (160 mg, 43% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09434745B2
출처 데이터셋uspto-grants-2016_09
ORD IDord-7a0f096c90634fb5b970bdaed8626bd8
출처 메모uspto-grants-2016_09