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HRID 1064811作成日:2026年10月27日

Acetyl nitrate → 2-[4-[2-(benzoxazol-2-ylthio)ethyl]piperazin-1-yl]-N-(2,6-diisopropyl-3-hydroxy-4-nitrophenyl)acetamide

https://huagongshe.com/reaction/1064811

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl nitrateHCID 11557—
反応物Sodium BicarbonateHCID 516892—
反応物2-[4-[2-(benzoxazol-2-ylthio)ethyl]piperazin-1-yl]-N-(2,6-diisopropyl-3-hydroxyphenyl)acetamideHCID 22272616—
溶媒WaterHCID 962—
溶媒AcetonitrileHCID 6342—
生成物2-[4-[2-(benzoxazol-2-ylthio)ethyl]piperazin-1-yl]-N-(2,6-diisopropyl-3-hydroxy-4-nitrophenyl)acetamideHCID 2227286351%

反応手順

Acetyl nitrate (145 mg, 0.75 mmol) was added to a solution of 2-[4-[2-(benzoxazol-2-ylthio)ethyl]piperazin-1-yl]-N-(2,6-diisopropyl-3-hydroxyphenyl)acetamide (107 mg, 0.22 mmol) in acetonitrile (3 ml) with ice cooling followed by stirring for 10 minutes. The reaction solution was diluted with water, made alkaline by adding an aqueous solution of sodium bicarbonate thereto and extracted with chloroform twice. The organic layer was washed with a saturated sodium chloride solution and dried over anhydrous sodium sulfate and the solvent was evaporated therefrom. The residue was purified by a preparative thin layer chromatography (developing solvent, chloroform:methanol=20:1) and the resulting crude crystals were recrystallized from chloroform-ethyl acetate-hexane to provide 60 mg (yield 51%) of the desired compound as yellow powdery crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06969711B2
出典データセットuspto-grants-2005_11
ORD IDord-810afe70c9a247f5b9f52cdb59e3e5ce
出典メモuspto-grants-2005_11