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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18185생성일: 2026년 10월 24일

Ethanol → 4-(3-Benzyl-2-carbamoyl-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/ko/reaction/18185

반응식

참여 물질

역할이름HCID투입량
반응물EthanolHCID 702—
반응물Sodium;3-oxidodioxaborirane;tetrahydrateHCID 23693097—
반응물4-(3-Benzyl-2-cyano-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 59344912—
용매WaterHCID 962—
용매Sodium chloride; waterHCID 57417360—
생성물4-(3-Benzyl-2-carbamoyl-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 5934490480%

반응 조건

온도130 °C

반응 단계

4-(3-Benzyl-2-cyano-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl ester (0.302 gm, 0.7 mmol), sodium perborate tetrahydrate (0.43 gm, 2.8 mmol), ethanol (8 ml) and water (8 ml) were combined in a vial and heated in a microwave reactor to 130° C. for 10 minutes. The reaction mixture was cooled to room temperature, diluted with brine and water and extracted three times with ethyl acetate. The solution was dried over magnesium sulfate and purified by column chromatography (methanol/dichloromethane gradient) to give 4-(3-benzyl-2-carbamoyl-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl ester (0.25 gm, 80% yield).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741326B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-6e1cd638c39c4f80be55e1ba89a7d870
출처 메모uspto-grants-2010_06