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HRID 53961作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
反応物(7-Cyano-2-naphthyl)methyltriphenylphosphonium bromideHCID 9936048—
反応物Ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-2-oxoacetateHCID 10316641—
反応物Ethyl acetate hexaneHCID 21226206—
溶媒EthanolHCID 702—
溶媒TetrahydrofuranHCID 8028—
生成物ethyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(7-cyano-2-naphthyl)acrylateHCID 5700554585.9%

反応手順

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.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05620991
出典データセットuspto-grants-1997_04
ORD IDord-fa242b898191430a8c61beb93bbd339f
出典メモuspto-grants-1997_04