A PRACTICAL CONVERSION OF AN AZETIDINONE TO PENEM - SYNTHESIS OF SCH 34343

被引:1
作者
GALA, D
CHIU, JS
GANGULY, AK
GIRIJAVALLABHAN, VM
JARET, RS
JENKINS, JK
MCCOMBIE, SW
NYCE, PL
ROSENHOUSE, S
STEINMAN, M
机构
[1] Schering Plough Research, Bloomfield, NJ 07003
关键词
D O I
10.1016/S0040-4020(01)90781-1
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A synthesis of penems from azetidinone 1 is described in detail. This synthesis is used to prepare multikilo batches of (5R,6S)-2-[[-(carbamoyloxy)ethyl]thio]-6-[(R)-1-hydroxyethyl]penem-3-carboxylic acid (10), (Sch 34343). It is practical as all chemical steps progress in high yields, and isolation of all unstable intermediates is avoided. The eight step conversion of (3S,4R)-3-[(R)-1-hydroxyethyl]-4-triphenylmethylthio-2-azetidinone (1) to penem 10 via intermediacy of stable, solid (3S,4R)-1-[[(allyloxy)carbonyl]methyl]-3[(R)-hydroxyethyl]-4-(argenitiothio)-2-azetidinone (4), and (3S,4R)-1-[[(allyloxy)carbonyl]methyl]-3-[(R)-1-hydroxyethyl]-4-beta-naphthoxy (thiocarbonyl)thio-2-azetidinone (5) is achieved in 43% yield.
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收藏
页码:1175 / 1182
页数:8
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