1174020-16-6Relevant articles and documents
A concise synthesis of a β-lactamase inhibitor
Mangion, Ian K.,Ruck, Rebecca T.,Rivera, Nelo,Huffman, Mark A.,Shevlin, Michael
, p. 5480 - 5483 (2011/12/05)
MK-7655 (1) is a β-lactamase inhibitor in clinical trials as a combination therapy for the treatment of bacterial infection resistant to β-lactam antibiotics. Its unusual structural challenges have inspired a rapid synthesis featuring an iridium-catalyzed N-H insertion and a series of late stage transformations designed around the reactivity of the labile bicyclo[3.2.1]urea at the core of the target.
BETA-LACTAMASE INHIBITORS
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Page/Page column 65, (2009/08/16)
Substituted bicyclic beta-lactams of Formula I: (I), are ?-lactamase inhibitors, wherein a, X, R1 and R2 are defined herein. The compounds and pharmaceutically acceptable salts thereof are useful in the treatment of bacterial infections in combination with ?-lactam antibiotics. In particular, the compounds can be employed with a ?-lactam antibiotics (e.g., imipenem, piperacillin, or ceftazidime) against microorganisms resistant to ?-lactam antibiotics due to the presence of the ?-lactamases.