发明名称 |
Preparation of 4-haloazetidin-2-ones from 4-sulfinoazetidin-2-ones |
摘要 |
Process for 4-halo azetidinones of the formula <IMAGE> wherein R1 is acylamino or diacylamino, X is chloro, bromo or iodo, and R is a carboxy-protecting group which comprises treating a 4-sulfinoazetidinone of the formula <IMAGE> with positive halogen reagent, eg. N-chlorosuccinimide, N-bromosuccinimide, N-iodosuccinimide, hypohalite. The 4-haloazetidinones are useful intermediate for beta -lactam antibiotics.
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申请公布号 |
US4368156(A) |
申请公布日期 |
1983.01.11 |
申请号 |
US19810241872 |
申请日期 |
1981.03.09 |
申请人 |
ELI LILLY AND COMPANY |
发明人 |
SPITZER, WAYNE A.;KUKOLJA, STJEPAN;GOODSON, JR., THEODORE;LAMMERT, STEVEN R. |
分类号 |
C07D205/08;C07D205/085;C07D205/095;C07D403/04;C07D409/12;C07D498/04;C07D503/00;(IPC1-7):C07D205/08;C07B9/00;C07D401/04 |
主分类号 |
C07D205/08 |
代理机构 |
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代理人 |
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主权项 |
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地址 |
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