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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| 반응물 | Binap, (A+-)- | HCID 634876 | — |
| 반응물 | 3-Benzyl-7-bromo-5-methyl-benzofuran-2-carbonitrile | HCID 59344894 | — |
| 촉매 | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-(3-Benzyl-2-cyano-5-methyl-benzofuran-7-yl)-piperazine-1-carboxylic acid tert-butyl ester | HCID 59344912 | 45% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07741326B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-5d5e6fac3ee94d0f999f7f0d1c6c0653 |
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| 출처 메모 | uspto-grants-2010_06 |
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