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HRID 1360434作成日:2026年10月26日

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

https://huagongshe.com/reaction/1360434

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物Phthalimide potassium saltHCID 24194345—
反応物4-bromo-5-(4-chlorobutyl)-1-ethyl-1H-pyrazole-3-carbonitrileHCID 66958265—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
溶媒DimethylformamideHCID 6228—
生成物4-bromo-1-ethyl-5-(4-phthalimidobutyl)-1H-pyrazole-3-carbonitrileHCID 6695841871.1%

反応条件

温度100 °C

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07879849B2
出典データセットuspto-grants-2011_02
ORD IDord-9bfbb018d7e8437199b1c3c09ca184d7
出典メモuspto-grants-2011_02