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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1360434생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1360434

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 번호US07879849B2
출처 데이터셋uspto-grants-2011_02
ORD IDord-9bfbb018d7e8437199b1c3c09ca184d7
출처 메모uspto-grants-2011_02