Abstract: There is provided a novel method for producing a bifunctional epoxy monomer which comprises reacting diolefin with a hydrogen peroxide aqueous solution, in the presence of molybdenum or tungsten oxide as a catalyst to selectively epoxidize a double bound at a specific position. The bifunctional epoxy monomers provided by the present invention are substances widely used in various industrial fields such as chemical industry, as materials for resist materials (particularly solder resist materials), and intermediates of agrochemicals and medicines, and various polymers such as plasticizers, adhesives and coating resins.
Abstract: The invention relates to a process for the preparation of pyridylcarboxylic amides and esters I, Formula (I) wherein Hal, X and R1 have the meanings given in claim 1, which comprises the following steps: (a) heating a mixture consisting essentially of trichloromethylpyridine II, Formula (II), wherein Hal has the meaning given, and 1.0 to 1.5 equivalents of concentrated sulfuric acid, characterized in that the trichloromethylpyridine II in a liquid form is added to the concentrated sulfuric acid at a temperature from 110° C. to 160° C.; and (b) reacting the intermediate product obtained in step (a) with an amine or alcohol III, HXR1, wherein X and R1 have the meaning given, optionally in the presence of a solvent and/or a base.
Type:
Grant
Filed:
October 26, 2006
Date of Patent:
April 6, 2010
Assignee:
BASF SE
Inventors:
Monika Brink, Marcus Knell, Jan Hendrik Wevers
Abstract: A method of separating propylene oxide from a mixture (M) comprising propylene oxide and methanol, said method comprising: (i) introducing said mixture (M) into an extractive distillation column; (ii) additionally introducing an extracting solvent into said extractive distillation column; (iii) distilling propylene oxide overhead from said extractive distillation column as top stream; (iv) withdrawing a bottoms stream from said extractive distillation column; (v) compressing the top stream obtained overhead in (iii) by means of at least one compressor to give a compressed vapor.
Type:
Grant
Filed:
July 6, 2005
Date of Patent:
April 6, 2010
Assignees:
BASF Aktiengesellschaft, The Dow Chemical Company
Abstract: A process for making propylene oxide from propylene is disclosed. The process comprises reacting propylene, oxygen, and hydrogen in the presence of a catalyst, a solvent, and a buffer to produce a reaction mixture comprising propylene oxide. Separation of light components from the reaction mixture gives a heavy residue comprising the buffer. The buffer is precipitated from the heavy residue by a precipitating agent.
Abstract: The invention relates to a method for producing chiral organic compounds by asymmetric catalysis, using ionic catalysts comprising a chiral catalyst anion. The claimed method is suitable for reactions which are carried out over cationic intermediate stages, such as iminium ions or acyl pyridinium ions. The invention enables the production of chiral compounds with high ee values, that until now could only be obtained by means of costly purification methods.
Type:
Grant
Filed:
February 27, 2007
Date of Patent:
March 23, 2010
Assignee:
Studiangesellschaft Kohle mbH
Inventors:
Benjamin List, Sonja Mayer, Martin Nolwenn, Wang Xingwang
Abstract: The present invention relates to compounds of the formula (I) wherein R1 and R2 are as defined in the description and claims, and pharmaceutically acceptable salts thereof. The compounds are useful for the treatment and/or prophylaxis of diseases which are associated with DPP-IV, such as diabetes, non-insulin dependent diabetes mellitus and/or impaired glucose tolerance, obesity, and/or metabolic syndrome or ?-cell protection.
Type:
Grant
Filed:
December 14, 2005
Date of Patent:
March 23, 2010
Assignee:
Hoffmann-La Roche Inc.
Inventors:
Markus Boehringer, Daniel Hunziker, Bernd Kuhn, Bernd Michael Loeffler, Thomas Luebbers, Fabienne Ricklin
Abstract: 7-azaindoles inhibit phosphodiesterase 4 (PDE4). Methods for preparing these compounds and methods of treating arthritis and other conditions with the compounds are also provided.
Type:
Grant
Filed:
March 10, 2008
Date of Patent:
March 23, 2010
Assignee:
Biotie Therapies GmbH
Inventors:
Norbert Höfgen, Ute Egerland, Thomas Kronbach, Degenhard Marx, Stefan Szelenyi, Hildegard Kuss, Emmanuel Polymeropoulos
Abstract: A catalyst comprising a spray-dried transition metal zeolite and a noble metal is disclosed. The spray-dried transition metal zeolite comprises a transition metal zeolite and a binder. At least 50 wt. % of the binder is titania. The catalyst is used in a process to produce an epoxide by reacting an olefin, hydrogen, and oxygen. The catalyst is easy to filter from a slurry and produces a reduced level of hydrogenation products.
Type:
Grant
Filed:
January 29, 2008
Date of Patent:
January 19, 2010
Assignee:
Lyondell Chemical Technology, L.P.
Inventors:
Edrick Morales, Guoyi Fu, Roger A. Grey, Kun Qin
Abstract: A process for making propylene oxide from propylene is disclosed. Propylene, hydrogen, and oxygen are reacted in a slurry comprising a catalyst and a solvent to produce a gaseous product stream and a liquid product stream. The gaseous product stream is contacted with an absorbent to produce a gas effluent and a liquid effluent. The gas effluent is recycled to the reaction step.
Type:
Grant
Filed:
March 28, 2008
Date of Patent:
January 19, 2010
Assignee:
Lyondell Chemical Technology, L.P.
Inventors:
Te Chang, Arsam Behkish, Jude T. Ruszkay, John H. Speidel, Jr.
Abstract: The invention is directed to compounds and methods of synthesizing hydroxyethylamino amides and their use in treatment of aspartyl protease mediated diseases and conditions.
Type:
Grant
Filed:
July 1, 2008
Date of Patent:
January 19, 2010
Assignee:
Janssen Pharmaceutica N.V.
Inventors:
Steve J. Coats, Dennis J. Hlasta, Mark J. Schulz
Abstract: Reaction gases such as hydrogen, oxygen and propylene are reacted in a slurry of solid catalyst in solvent, the reaction being carried out in a series of separate zones with intermediate removal of the exothermic heat of reaction by indirect heat exchange.
Abstract: The present invention relates to compounds of formula (I) or a pharmaceutically acceptable derivatives thereof, useful in the treatment of prophylazis of CCR5-related diseases and disorders, for example, in the inhibition of HIV replication, the prevention or treatment of HIV infection, and in the treatment of the resulting acquired immune deficiency syndrome (AIDS).
Type:
Grant
Filed:
December 12, 2003
Date of Patent:
January 12, 2010
Assignee:
SmithKline Beecham Corp.
Inventors:
Wieslaw Mieczyslaw Kazmierski, Chrisopher Joseph Aquino, Neil Bifulco, Eric Eugene Boros, Brian Andrew Chauder, Pek Yoke Chong, Maosheng Duan, Felix Deanda, Jr., Cecilia Suarez Koble, Ed Williams McLean, Jennifer Poole Peckham, Angilique C Perkins, James Benjamin Thompson, Dana Vanderwall
Abstract: A method for preparing a prostaglandin derivative represented by the following general formula (I): (wherein Ph represents phenyl group, R1 represents a C1-7 alkyl group, a C1-7 alkenyl group, phenyl group, or benzyl group), which comprises the successive steps (1) to (8) described in the specification, or any one step or two or more successive steps selected from the group consisting of the steps (1) to (8). A method for efficiently, inexpensively and safely preparing prostaglandin derivatives, of which typical example is latanoprost, is provided.
Abstract: Disclosed are intermediates and processes for preparing epoxides of the formula: where R and PROT are defined herein. These epoxides are useful as intermediates in the production of biologically active compounds, i.e., in the production of pharmaceutical agents.
Abstract: A composition comprising compound of formula I, a process for preparing the composition comprising compound of formula I, methods of authentication for an article comprising compound of formula I or compound of formula II, authentication technology for polymer based articles comprising compound of formula I or formula II, methods of facilitating such authentication and method of making articles capable of authentication.
Abstract: This invention relates to a new method for the stereospecific thiocarboxylation of organic compounds for the preparation of compounds according to formula (I): wherein a compound of formula (II): is reacted with a compound of formula (IIIa) or (IIIb): then treating the obtained product with a thiocarboxylic acid or a salt thereof, and subsequently carrying out a nitration reaction.
Type:
Grant
Filed:
February 17, 2009
Date of Patent:
December 22, 2009
Assignee:
Lacer, S.A.
Inventors:
Francisco Pubill Coy, Anna Modolell Saladrigas, Jose Repolles Moliner
Abstract: The invention encompasses compounds of Formula I, including pharmaceutically acceptable salts, their pharmaceutical compositions, and their use in treating CNS disorders.
Type:
Grant
Filed:
November 7, 2008
Date of Patent:
December 15, 2009
Assignee:
Bristol-Myers Squibb Company
Inventors:
Joanne J. Bronson, Andrew P. Degnan, William D. Schmitz
Abstract: A new compound of formula (IV) R represents a protecting group which is removable by hydrogenation, and use thereof as an intermediate for preparing paliperidone.
Abstract: The present invention relates to an improved process for preparing himbacine analogs. The compounds are useful as thrombin receptor antagonists. The improved process may allow for at least one of easier purification by crystallization, easier scalability, and improved process yield on the desired enantiomer.
Type:
Grant
Filed:
April 23, 2009
Date of Patent:
December 1, 2009
Assignee:
Schering Corporation
Inventors:
Tiruvettipuram K. Thiruvengadam, Tao Wang, Jing Liao, John S. Chiu, David J. S. Tsai, Hong-Chang Lee, Wenxue Wu, Xiaoyong Fu
Abstract: This invention is directed to selective antagonists of H1 histamine receptors having the general formula (I); to processes for their preparation; to pharmaceutical compositions comprising them; and to their use in therapy.
Type:
Grant
Filed:
April 1, 2003
Date of Patent:
November 24, 2009
Assignee:
Laboratorios Almirall S.A.
Inventors:
Silvia Fonquerna Pou, Luis Miguel Pages Santacana, Carlos Puig Duran, Jose Manuel Prieto Soto, Aranzazu Cardus Figueras