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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2182141생성일: 2026년 10월 27일

Piperazine → 2-[(3-Cyanobenzyl)Oxy]-6-(1-Piperazinyl)Pyrazine

https://huagongshe.com/reaction/2182141

반응식

참여 물질

역할이름HCID투입량
반응물PiperazineHCID 4837—
반응물Binap, (A+-)-HCID 634876—
반응물3-(6-Chloro-pyrazin-2-yloxymethyl)-benzonitrileHCID 22481973—
반응물Sodium t-butoxideHCID 23676156—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
생성물2-[(3-Cyanobenzyl)Oxy]-6-(1-Piperazinyl)PyrazineHCID 985733522.4%

반응 조건

온도90 °C

반응 단계

A mixture of 3-(6-chloro-pyrazin-2-yloxymethyl)-benzonitrile I-3f (667.2 mg, 2.716 mmol), piperazine (297 mg, 3.531 mmol), sodium t-butoxide (287 mg, 2.987 mmol), BINAP (67.7 mg, 0.109 mmol), and Pd2(dba)3 (49.7 mg, 0.054 mmol) in toluene (10 mL) was heated at 90° C. overnight. The solution was cooled to room temperature and filtered through a celite pad. The celite pad was washed with ethyl acetate several times. The combined filtrate was concentrated in vacuo to give the crude title compound. The product was purified by chromatography (silica, 10% MeOH/dichlormethane with 1% NH4OH) to give 180 mg 3-(3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl-6′-yloxymethyl)-benzonitrile (3-E).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06894050B2
출처 데이터셋uspto-grants-2005_05
ORD IDord-e6a659b29715454186b3e8c2350cf27b
출처 메모uspto-grants-2005_05