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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1984358생성일: 2026년 10월 27일

Sodium Iodide → 4-bromo-1-ethyl-5-(4-phthalimidobutyl)-1H-pyrazole-3-carbonitrile

https://huagongshe.com/reaction/1984358

반응식

참여 물질

역할이름HCID투입량
반응물Sodium IodideHCID 5238—
반응물Phthalimide potassium saltHCID 24194345—
반응물4-bromo-5-(4-chlorobutyl)-1-ethyl-1H-pyrazole-3-carbonitrileHCID 66958265—
용매WaterHCID 962—
용매ChloroformHCID 6212—
용매DimethylformamideHCID 6228—
생성물4-bromo-1-ethyl-5-(4-phthalimidobutyl)-1H-pyrazole-3-carbonitrileHCID 6695841871.1%

반응 조건

온도100 °C

반응 단계

Potassium phthalimide (954 mg, 5.15 mmol), sodium iodide (130 mg, 0.86 mmol), and DMF (5 mL) were added to 4-bromo-5-(4-chlorobutyl)-1-ethyl-1H-pyrazole-3-carbonitrile (1.0 g, 3.4 mmol, prepared as described in Parts A-E of Example 19), and the reaction was heated at 100° C. for 45 minutes under a nitrogen atmosphere and allowed to cool to ambient temperature. Water (50 mL) was added, and the resulting mixture was stirred at 0° C. A precipitate formed, was isolated by filtration, and was dissolved in chloroform. The resulting solution was dried over sodium sulfate, filtered, and concentrated under reduced pressure. An analysis by nuclear resonance spectroscopy (NMR) indicated that starting material was present. The solid was treated with potassium phthalimide (1.27 g, 6.88 mmol), sodium iodide (130 mg, 0.86 mmol), and DMF (5 mL) and heated at 90° C. for three hours. Water (50 mL) was added, and the resulting solid was isolated by filtration to provide 0.97 g of 4-bromo-1-ethyl-5-(4-phthalimidobutyl)-1H-pyrazole-3-carbonitrile as a gray, crystalline solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07544697B2
출처 데이터셋uspto-grants-2009_06
ORD IDord-cefe8cda0a8443deb6cdaf70932fc632
출처 메모uspto-grants-2009_06