트리아졸환 함유 6-엑소메칠렌 펜남 유도체의 합성

The synthesis of new 6-exomethylene penams with triazole ring for $\beta$-lactamase inhibitor was described. The 6,6-dibromopenam 6 was treated with $CH_3$MgBr and carbaldehyde 5 to afford the 6-bromo-6-(1-hydroxy-1-methyl)penicillanate 7, which was reacted with acetic anhydride to give acetoxy comp...

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Veröffentlicht in:Yaghag-hoi-ji 2001-04, Vol.45 (2), p.140-146
Hauptverfasser: 임채욱(Chaeuk Im), 오정석(Jung Suk Oh ), 임철부(Chul Bu Yim)
Format: Artikel
Sprache:kor
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Zusammenfassung:The synthesis of new 6-exomethylene penams with triazole ring for $\beta$-lactamase inhibitor was described. The 6,6-dibromopenam 6 was treated with $CH_3$MgBr and carbaldehyde 5 to afford the 6-bromo-6-(1-hydroxy-1-methyl)penicillanate 7, which was reacted with acetic anhydride to give acetoxy compound 8. The deacetoxybromination of 8 with zinc and acetic acid gave 6-exomethylenepenams, Z-isomer 9 and E-isomer 10, which were oxidized to sulfones 11 and 12 by m-CPBA. The p-methoxybenzyl compounds 9~12 were deprotected by AIC1$_3$and neutralized to give the sodium salts 13~16.
ISSN:0377-9556
2383-9457