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US 6,649,652 B2Granted
Prodrugs for antimicrobial amidines
AssigneesThe University of North Carolina at Chapel Hill, Georgia State University Research Foundation, Inc.
InventorsDavid W. Boykin, M. Syed Rahmathullah, Richard R. Tidwell, James E. Hall
Life of this patent
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Abstract
A methods of treating an infection comprises administering a therapeutically effective amount of a compound described by the Formula (I)
Claims10
A process for making a pharmaceutically active bis-aryl carbamate, said process comprising:
- reacting an aryl carbonate with bis-amidine in the presence of an organic solvent to form the bis-aryl carbamate, wherein the pharmaceutically active bis-aryl carbamate may-se is represented by the formula:
- wherein:
- X is O or S;
- R1 and R2 may be independently selected from the group consisting of H, loweralkyl, oxyalkyl, alkoxyalkyl, cycloalkyl, aryl, hydroxyalkyl, aminoalkyl, and alkylaminoalkyl;
- R3 and R4 are each independently selected from the group consisting of H, loweralkyl, halogen, oxyalkyl, oxyaryl, and oxyarylalkyl;
- R5 is represented by a formula selected from the group consisting of:
- wherein:
- X1, X2, and X3 are independently selected from O and S;
- and
- R6 and R7 are independently selected from the group consisting of loweralkyl, aryl, alkylaryl, oxyaryl, an ester-containing substituent, and oxyalkyl.
7 more elements
Dependencies are inferred from the claim text.