Patents by Inventor Michael Kraft

Michael Kraft 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).

  • Patent number: 7096230
    Abstract: A computer-implemented method or computer system develops a process specification for a collaborative process involving distributed computer-based participant systems exchanging messages through an asynchronous messaging network. In operation, a computer retrieves, from a first computer system, information on process states and process state transitions in relation to each participant system. Information on collaboration states and collaboration state transitions of the process are stored in a second computer system and used to generate information on dead-end collaboration states.
    Type: Grant
    Filed: August 1, 2003
    Date of Patent: August 22, 2006
    Assignee: SAP Aktiengesellschaft
    Inventor: Frank Michael Kraft
  • Publication number: 20060160859
    Abstract: A method for treating HIV infection through co-administration of tipranavir and GW873140.
    Type: Application
    Filed: November 17, 2005
    Publication date: July 20, 2006
    Applicant: Boehringer Ingelheim International GmbH
    Inventors: Michael Kraft, Douglas Mayers
  • Publication number: 20060157958
    Abstract: A side airbag device for a vehicle includes an airbag which is deployed in the event of an accident and, in the deployed state, covers a side wall section of the vehicle. In order for the airbag to reliably deploy, provision is made according to embodiments of the invention for the side airbag device to have a deployment control mechanism which deflect the airbag during its deployment around an obstacle situated in a region of a side wall section.
    Type: Application
    Filed: January 12, 2006
    Publication date: July 20, 2006
    Inventors: Benedikt Heudorfer, Stefan Schafer, Holger Rist, Michael Kraft, Christian Weyrich
  • Publication number: 20060142344
    Abstract: A method for treating HIV infection through co-administration of tipranavir and GW695634.
    Type: Application
    Filed: November 16, 2005
    Publication date: June 29, 2006
    Applicant: Boehringer Ingelheim International GmbH
    Inventors: Michael Kraft, Douglas Mayers
  • Publication number: 20060135563
    Abstract: A method for treating HIV infection through co-administration of tipranavir and SCH-417690.
    Type: Application
    Filed: November 17, 2005
    Publication date: June 22, 2006
    Applicant: Boehringer Ingelheim International GmbH
    Inventors: Michael Kraft, Douglas Mayers
  • Publication number: 20060128733
    Abstract: A method for treating HIV infection through co-administration of tipranavir and reverset.
    Type: Application
    Filed: November 15, 2005
    Publication date: June 15, 2006
    Applicant: Boehringer Ingelheim International GmbH
    Inventors: Michael Kraft, Douglas Mayers
  • Publication number: 20060122220
    Abstract: A method for treating HIV infection through co-administration of tipranavir and UK-427,857.
    Type: Application
    Filed: November 15, 2005
    Publication date: June 8, 2006
    Applicant: Boehringer Ingelheim International GmbH
    Inventors: Michael Kraft, Douglas Mayers
  • Publication number: 20060106043
    Abstract: A method for treating HIV infection through co-administration of tipranavir and etravirine.
    Type: Application
    Filed: October 12, 2005
    Publication date: May 18, 2006
    Applicant: Boehringer Ingelheim International GmbH
    Inventors: Michael Kraft, Douglas Mayers
  • Publication number: 20050171359
    Abstract: The present invention is concerned with the resolution of a mixture of enantiomers of N-protected amino acids by crystallization with enantiomerically pure N-unprotected ?-amino acid derivatives.
    Type: Application
    Filed: December 9, 2004
    Publication date: August 4, 2005
    Inventors: Rolf Hoffmann, Michael Kraft
  • Patent number: 6455705
    Abstract: A method of isolating 1-[N2-((S)-ethoxycarbonyl)-3-phenylpropyl)-N6-trifluoroacetyl]-L-lysyl-L-proline (lisinopril (TFA) ethyl ester, LPE). The solvent or solvent mixture used for the extraction is also a main constituent of the solvent or solvent mixture from which the crystallization takes place. High yield as well as good purity of the end product are obtained, without distillation. 1-[N2-((S)-ethoxycarbonyl)-3-phenylpropyl)-N6-trifluoroacetyl]-L-lysyl-L-proline (lisinopril (TFA) ethyl ester, LPE) is described as a precursor for producing an ACE inhibitor.
    Type: Grant
    Filed: December 24, 1998
    Date of Patent: September 24, 2002
    Assignee: Degussa Aktiengesellschaft
    Inventors: Matthias Kottenhahn, Roland Möller, Michael Kraft, Karlheinz Drauz, Klaus Stingl
  • Patent number: 5907044
    Abstract: A method of isolating 1-?N.sup.2 -((S)-ethoxycarbonyl)-3-phenylpropyl)-N.sup.6 -trifluoroacetyl!-L-lysyl-L-proline (lisinopril (TFA) ethyl ester, LPE). The solvent or solvent mixture used for the extraction is also a main constituent of the solvent or solvent mixture from which the crystallization takes place. High yield as well as good purity of the end product are obtained, without distillation. 1-?N.sup.2 -((S)-ethoxycarbonyl)-3-phenylpropyl)-N.sup.6 -trifluoroacetyl!-L-lysyl-L-proline (lisinopril (TFA) ethyl ester, LPE) is described as a precursor for producing an ACE inhibitor.
    Type: Grant
    Filed: October 16, 1997
    Date of Patent: May 25, 1999
    Assignee: Degussa Aktiengellschaft
    Inventors: Matthias Kottenhahn, Roland Moller, Michael Kraft, Karlheinz Drauz, Klaus Stingl
  • Patent number: 5585500
    Abstract: A method of producing optically active pyrrolidines of the general formula ##STR1## in which R.sup.1 is hydrogen or OH,R.sup.2 is a benzyl group which can have one or more alkyl-, alkoxy- and/or halogen substituents on the aromatic, and* is and/or can be an asymmetric center,by reducing the corresponding, enantiomerically pure pyrrolidinediones using activated alkali boron hydride.
    Type: Grant
    Filed: July 17, 1995
    Date of Patent: December 17, 1996
    Assignee: Degussa Aktiengesellschaft
    Inventors: Karlheinz Drauz, Matthias Kottenhahn, Michael Kraft, Michael Schwarm
  • Patent number: 5387734
    Abstract: The invention relates to a process for the decomposition of polyhalogenated aliphatic compounds having 1 to 8 carbon atoms, polyhalogenated cycloalkyl compounds having 5 to 8 carbon atoms and polyhalogenated aromatic compounds having at least 5 carbon atoms. A contaminated substrate or the polychlorinated compounds per se are heated with a suitable catalyst to 150.degree. to 550.degree. C. The process according to the invention is especially suitable for the decomposition of polychlorinated dibenzodioxins and dibenzofurans in soils, scrap loads and waste gases and for decontaminating filter dust from refuse and waste incineration plants.
    Type: Grant
    Filed: October 18, 1993
    Date of Patent: February 7, 1995
    Inventors: Hanspaul Hagenmaier, Karl-Heinz Tichaczek, Michael Kraft, Roland Haag, Hermann Brunner
  • Patent number: 5276250
    Abstract: The invention relates to a process for the decomposition of polyhalogenated aliphatic compounds having 1 to 8 carbon atoms, polyhalogenated cycloalkyl compounds having 5 to 8 carbon atoms and polyhalogenated aromatic compounds having at least 5 carbon atoms. A contaminated substrate or the polychlorinated compounds per se are heated with a suitable catalyst to 150 to 550.degree. C. The process according to the invention is especially suitable for the decomposition of polychlorinated dibenzodioxins and dibenzofurans in soils, scrap loads and waste gases and for decontaminating filter dust from refuse and waste incineration plants.
    Type: Grant
    Filed: January 19, 1993
    Date of Patent: January 4, 1994
    Inventors: Hanspaul Hagenmaier, Karl-Heinz Tichaczek, Michael Kraft, Roland Haag, Hermann Brunner
  • Patent number: 4579979
    Abstract: A method of preparation for acetals utilizing saturated or unsaturated aldehydes, in particular, the preparation of dimethylacetals of acetaldehyde, acrolein and methacrolein. The production of the acetal takes place in a liquid phase in the presence of a solid acid catalyst, such as a strongly acidic ion exchange resin or zeolite. The conversion mixture is extracted by means of water and by means of water insoluble organic solvents. There is obtained not only the desired acetals, but in addition also the unconverted initial quantities of the starting materials by a simple method and with very good yields.
    Type: Grant
    Filed: January 24, 1985
    Date of Patent: April 1, 1986
    Assignee: Degussa Aktiengesellschaft
    Inventors: Juan Andrade, Dietrich Arntz, Michael Kraft, Gunter Prescher