Patents by Inventor Nancy Barta

Nancy Barta has filed for patents to protect the following inventions. This listing includes patent applications that are pending as well as patents that have already been granted by the United States Patent and Trademark Office (USPTO).

  • Publication number: 20060154972
    Abstract: This invention relates to certain ?-amino acids that bind to the alpha-2-delta (?2?) subunit of a calcium channel. These compounds and their pharmaceutically acceptable salts are useful in the treatment of a variety of psychiatric, pain and other disorders.
    Type: Application
    Filed: March 14, 2006
    Publication date: July 13, 2006
    Inventors: Nancy Barta, Jacob Schwarz, Andrew Thorpe, David Wustrow
  • Publication number: 20050245519
    Abstract: This invention relates to compounds of the formulae I wherein R1-R8, A, X, and Z are defined as in the specification, pharmaceutical compositions containing them and their use in the treatment of central nervous system disorders.
    Type: Application
    Filed: April 29, 2005
    Publication date: November 3, 2005
    Inventors: Nancy Barta, Shelly Glase, David Gray, Gregory Reichard, Lloyd Simons, Weijan Xu
  • Publication number: 20050014804
    Abstract: This invention relates to novel tetrazole and oxadiazalone ?-amino acids derivatives of the formula wherein G is wherein R1 through R4 are defined as in the specification, pharmaceutical compositions containing them and their use for the treatment of various central nervous system and other disorders. The cyclopropyl ?-amino acids derivatives of this invention exhibit activity as alpha2delta ligands (?2? ligands). Such compounds have affinity for the ?2? subunit of a calcium channel.
    Type: Application
    Filed: March 8, 2004
    Publication date: January 20, 2005
    Inventors: Nancy Barta, Norman Colbry, Raymond Hudack, Kristin Lin, Jacob Schwarz, Andrew Thorpe, David Wustrow, Zhijian Zhu
  • Patent number: 6372911
    Abstract: A process for preparing a &bgr;-hydroxy carbamate product is disclosed. The process comprises reacting an olefin compound containing at least one carbon-carbon double bond with a carbamate in an aqueous solvent and in the presence of a base, an osmium catalyst, a co-oxidant selected from a halohydantoin, a haloisocyanuric acid, and an alkali metal salt of a haloisocyanuric acid, and optionally an asymmetric ligand, to form a reaction mixture containing the &bgr;-hydroxy carbamate product. The process optionally further comprises treating the &bgr;-hydroxy carbamate product with additional base to form an oxazolidinone. The oxazolidinones are useful as chiral auxiliary agents and as intermediates for the formation of pharmaceutically active substances such as alpha 1 a adrenergic receptor antagonists. A process for preparing nitrogen-functionalized derivatives of the oxazolidinones is also disclosed.
    Type: Grant
    Filed: January 13, 2000
    Date of Patent: April 16, 2002
    Assignee: Merck & Co., Inc.
    Inventors: Nancy Barta, Robert D. Larsen, Daniel R. Sidler, Steven A. Weissman