| 摘要 |
<p>The present invention provides a novel intermediate represented by formula (1), (3), or (4) for efficiently producing a 1beta-methylcarbapenem compound for oral administration, and a process for producing the intermediate. That is, the present invention provides a process for producing a novel beta-lactam compound represented by formula (4), the process including allowing a beta-lactam compound represented by formula (5) as a starting material to react with a compound represented by formula (6) in the presence of a base to obtain a novel beta-lactam compound represented by formula (1), protecting the hydroxyl group, subsequently performing cyclization in the presence of a strong base, allowing the cyclized compound to react with diphenylphosphoryl chloride to obtain a novel beta-lactam compound represented by formula (3), and eliminating the protecting group therefrom. The formulae referred to are diagrammed as follows: (In the formulae, R1 represents a trimethylsilyl group or a triethylsilyl group; R2 represents an aryl group or a heteroaryl group; R2 represents an aryl group or a heteroaryl group; R3 represents an alkyl group having 1 to 10 carbon atoms or a cycloalkyl group having 3 to 10 carbon atoms; and X represents a halogen atom.)</p> |
