돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 18184생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/18184

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물tert-Butyl piperazine-1-carboxylateHCID 143452—
반응물Binap, (A+-)-HCID 634876—
반응물3-Benzyl-7-bromo-5-methyl-benzofuran-2-carbonitrileHCID 59344894—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매DimethylformamideHCID 6228—
생성물4-(3-Benzyl-2-cyano-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl esterHCID 5934491245%

반응 조건

온도80 °C

반응 단계

In an oven dried flask was added BINAP (racemic, 0.17 g, 0.913 mmol), cesium carbonate (0.35 g, 1.07 mmol), tris(dibenzylideneacetone)dipalladium (0.0207 g, 0.0226 mmol), 1-BOC-piperazine (0.17 g, 0.913 mmol) and 5 ml DMF. The flask was evacuated and refilled with nitrogen. 3-benzyl-7-bromo-5-methyl-benzofuran-2-carbonitrile (0.29 g, 0.90 mmol) in 5 ml DMF was added via syringe and the mixture heated to 80° C. overnight, then to 100° C. for another 24 hours. The mixture was concentrated on a rotary evaporator and purified by column chromatography (1:9 ethyl acetate/hexane) to give 4-(3-benzyl-2-cyano-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl ester (0.174 g, 45% yield) as a yellow solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07741326B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-5d5e6fac3ee94d0f999f7f0d1c6c0653
출처 메모uspto-grants-2010_06