1344700-14-6Relevant articles and documents
METHOD FOR USING NOVEL HYDROXAMIC ACID DERIVATIVE AND ANTIBACTERIAL SUBSTANCE IN COMBINATION
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, (2017/08/01)
Pharmacological compositions containing a hydroxamic acid derivative selected from (2S)-2-((4-((4-((1S)-1,2-dihydroxyethyl)phenyl)ethynyl)benzoyl)(methyl)amino)-N-hydroxy-N',2-dimethylmalonamide, (2S)-2-((4-((4-((1R)-1,2-dihydroxyethyl)phenyl)ethynyl)benzoyl)(methyl)amino)-N-hydroxy-N',2-dimethylmalonamide, and (2S)-N-hydroxy-2-((4-((4-((1S)-1-hydroxy-2-methoxyethyl)phenyl)ethynyl)benzoyl)(methyl)amino)-N',2-dimethylmalonamide, or a salt of said derivatives, and an antibiotic substance are useful in the treatment of gram-negative bacterial infections.
MANUFACTURING METHOD OF NOVEL HYDROXAMIC ACID DERIVATIVE
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Paragraph 0072, (2017/04/27)
PROBLEM TO BE SOLVED: To provide an industrial manufacturing method of a compound high in optical purity and having excellent uridyldiphospho-3-O-acyl-N acetylglucosamine deacetylase (LpxC) inhibitory activity. SOLUTION: There is provided a manufacturing method of a compound having a LpxC inhibitory activity represented by (2S)-2-((4-((4-((1S-1,2-dihydroxyethyl)phenyl)ethynyl)benzoyl)(methyl)amino)-N-hydroxy-N',2-dimethyl malonamide or a salt, of which an intermediate is represented by the formula [3] or [4], where R1 and R2 are each independently substituted/unsubstituted C1-6 alkyl group, Ra is an amino protective group, Rb is a carboxyl protective group and Rc is a hydroxyl protective group. SELECTED DRAWING: None COPYRIGHT: (C)2017,JPOandINPIT