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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 10505생성일: 2026년 10월 26일

N-BOC-ethylenediamine → N-(tert-butoxycarbonyl)-N'-(5-isoquinolyl)ethylenediamine

https://huagongshe.com/reaction/10505

반응식

참여 물질

역할이름HCID투입량
반응물N-BOC-ethylenediamineHCID 187201—
반응물5-BromoisoquinolineHCID 736487—
반응물2-(Di-tert-butylphosphino)biphenylHCID 2734215—
반응물Sodium t-butoxideHCID 23676156—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매TolueneHCID 1140—
용매Ethyl AcetateHCID 8857—
생성물N-(tert-butoxycarbonyl)-N'-(5-isoquinolyl)ethylenediamineHCID 2197991770%

반응 조건

온도80 °C

반응 단계

Under nitrogen atmosphere, a suspension of 5-bromoisoquinoline (416 mg, Spex), tris(dibenzylideneacetone)dipalladium(0) (92 mg), 2-(di-tert-butylphosphino)biphenyl (119 mg), N-(2-aminoethyl)carbamic acid tert-butyl ester (385 mg) and sodium tert-butoxide (269 mg) in toluene (5 ml) was stirred with heating at 80° C. for 2 hours. The reaction mixture was cooled to room temperature and added with ethyl acetate (5 ml). The insoluble matters were removed by filtration through Celite. The solvent was evaporated under reduced pressure, and the residue was purified by silica gel column chromatography (n-hexane:ethyl acetate=2:1) to obtain the title compound (402 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07094789B2
출처 데이터셋uspto-grants-2006_08
ORD IDord-236c7339795b45e393f5e303add9f945
출처 메모uspto-grants-2006_08