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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 53961생성일: 2026년 10월 26일

1,8-Diazabicyclo(5.4.0)undec-7-ene → ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(7-cyano-2-naphthyl)acrylate

https://huagongshe.com/reaction/53961

반응식

참여 물질

역할이름HCID투입량
반응물1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
반응물(7-Cyano-2-naphthyl)methyltriphenylphosphonium bromideHCID 9936048—
반응물Ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-2-oxoacetateHCID 10316641—
반응물Ethyl acetate hexaneHCID 21226206—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
생성물ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(7-cyano-2-naphthyl)acrylateHCID 5700554585.9%

반응 단계

8.40 g of (7-cyano-2-naphthyl)methyltriphenylphosphoniumbromide and 5.0 g of ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-2-oxoacetate were suspended in a mixture of 100 ml of tetrahydrofuran and 100 ml of ethanol. With stirring, to the resulting suspension was added 2.51 g of 1,8-diazabicyclo[5.4.0]-7-undecene, followed by stirring for 3 hours at room temperature. After distilling off the solvent, the residue thus obtained was subjected to silica gel column chromatography using a n-hexane/ethyl acetate mixture as an elution solvent, thereby obtaining 6.06 g of ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(7-cyano-2-naphthyl)acrylate as a mixture of E and Z forms. A portion of the thus obtained compound was separated into E and Z forms.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05620991
출처 데이터셋uspto-grants-1997_04
ORD IDord-fa242b898191430a8c61beb93bbd339f
출처 메모uspto-grants-1997_04