Patents by Inventor Jorge Martin
Jorge Martin 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).
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Patent number: 9466965Abstract: An electrical enclosure wherein an electrical component can be moved between various positions (e.g., connected, disconnected, test, etc.) without opening an enclosure door. The electrical enclosure supports a component for movement between a withdrawn position, a test position, and an inserted position. A handle is accessible by an operator from an exterior of the enclosure and is configured to move the component between the respective positions without having to open the enclosure. The handle is integral with the enclosure and thus an operator needs no special tool or other device to effect movement of the electrical component between its respective positions.Type: GrantFiled: January 9, 2014Date of Patent: October 11, 2016Assignee: Rockwell Automation Technologies, Inc.Inventors: Gregory David Lehtola, Dean Meyer, Arnaldo Hiroyuki Omoto, Paul Krause, Fabio Kazuo Ito, Steven J. Bauer, Jr., Joao Jorge Martins Freitas
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Patent number: 9194287Abstract: An axial engine includes a cam assembly housing moveable away from a cylinder head to reduce a compression ratio during conditions giving rise to detonation and movable towards the cylinder head to raise the compression ratio when operation allows the higher compression ratio. Piston rod ends ride in counter rotating slots balancing lateral forces on the piston rods. Piston dwell at Top Dead Center (TDC) provides for constant volume combustion and extended piston travel during the power stroke allows for over-expansion. Rotary valves improve volumetric efficiency and water injection supports increased compression ratio leading to improved thermodynamic efficiency.Type: GrantFiled: February 27, 2015Date of Patent: November 24, 2015Inventors: Bernard Bon, Jorge Martins, Francisco Brito, Tiago Costa
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Patent number: 8952173Abstract: The invention relates to a novel method for the resolution of the racemic mixture of compound (R,S)-2-amino-6-propylamino-4,5,6,7-tetrahydrobenzothiazole, or the enrichment of same with in one of its enantiomers, and to intermediate compounds which can be used to perform said method.Type: GrantFiled: May 9, 2006Date of Patent: February 10, 2015Assignee: Crystal Pharma, S.A.U.Inventors: Luis Octavio Silva Guisasola, Jorge Martin Juarez
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Publication number: 20140126120Abstract: An electrical enclosure wherein an electrical component can be moved between various positions (e.g., connected, disconnected, test, etc.) without opening an enclosure door. The electrical enclosure supports a component for movement between a withdrawn position, a test position, and an inserted position. A handle is accessible by an operator from an exterior of the enclosure and is configured to move the component between the respective positions without having to open the enclosure. The handle is integral with the enclosure and thus an operator needs no special tool or other device to effect movement of the electrical component between its respective positions.Type: ApplicationFiled: January 9, 2014Publication date: May 8, 2014Applicant: ROCKWELL AUTOMATION TECHNOLOGIES, INC.Inventors: Gregory David Lehtola, Dean Meyer, Arnaldo Hiroyuki Omoto, Paul Krause, Fabio Kazuo Ito, Steven J. Bauer, JR., Joao Jorge Martins Freitas
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Patent number: 8638561Abstract: An electrical enclosure wherein an electrical component can be moved between various positions (e.g., connected, disconnected, test, etc.) without opening an enclosure door. The electrical enclosure supports a component for movement between a withdrawn position, a test position, and an inserted position. A handle is accessible by an operator from an exterior of the enclosure and is configured to move the component between the respective positions without having to open the enclosure. The handle is integral with the enclosure and thus an operator needs no special tool or other device to effect movement of the electrical component between its respective positions.Type: GrantFiled: October 28, 2010Date of Patent: January 28, 2014Assignee: Rockwell Automation Technologies, Inc.Inventors: Gregory David Lehtola, Dean Meyer, Arnaldo Hiroyuki Omoto, Paul Krause, Fabio Kazuo Ito, Steven J. Bauer, Jr., Joao Jorge Martins Freitas
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Publication number: 20110319666Abstract: The invention relates to a method of obtaining 3,3-diphenylpropylamines (I), wherein R1 is H, alkyl, haloalkyl or alkoxyalkyl, R2 is alkyl, alkoxy, halogen, NO2, CN, CHO, which may be free or protected, CH2OH or COOR6, and R2 and R1 are selected independently from H and alkyl or together with the nitrogen to which they are bound form a ring having 3 to 7 members. The inventive method consists in reacting a propylenephenylamine and a disubstituted aromatic hydrocarbon and, if necessary, separating the desired enantiomer or the mixture of enantiomers, and/or converting the compound (I) into a salt. Compounds (I) are muscarinic receptor antagonists which can be used in the treatment of urinary incontinence and other symptoms of urinary bladder hyperactivity. Said compounds include tolterodine.Type: ApplicationFiled: September 7, 2011Publication date: December 29, 2011Inventors: Antonio Lorente Bonde-Larsen, Pablo Martin Pascual, Jorge Martin Juarez, Miquel Armengol Montserrat
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Publication number: 20110262761Abstract: This utility model relates to a new device for decorating containers and utensils used for selected juices and cocktails generally characterized in that it comprises a clip or grip dividing the device into two in its position of use, a) on the upper edge of the clip having a closed U shape and following its curvature, it has in one and the same plane a set of elongated triangular surfaces ending in points, of a different size and spaced equidistantly, resembling a crest of a cockerel, b) at one end of the U-shaped curvature it has a shaft (support) arranged perpendicular to both sides of the plane containing the elongated triangular surfaces, which serves to afford greater rigidity to the clip during the use thereof, c) in the lower part of the clip and at one of its ends it has a triangular surface with curved downward-facing sides, which serves for placing any desired advertisement. An overall impression of the device resembles the physiognomy of the neck and head of a crested bird.Type: ApplicationFiled: September 15, 2009Publication date: October 27, 2011Inventor: Jorge Martin Rivero Kennedy
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Patent number: 8039672Abstract: The invention relates to a method of obtaining 3,3-diphenylpropylamines (I), wherein R1 is H, alkyl, haloalkyl or alkoxyalkyl, R2 is alkyl, alkoxy, halogen, NO2, CN, CHO, which may be free or protected, CH2OH or COOR6, and R3 and R4 are selected independently from H and alkyl or together with the nitrogen to which they are bound form a ring having 3 to 7 members. The inventive method consists in reacting a propylenephenylamine and a disubstituted aromatic hydrocarbon and, if necessary, separating the desired enantiomer or the mixture of enantiomers, and/or converting the compound (I) into a salt. Compounds (I) are muscarinic receptor antagonists which can be used in the treatment of urinary incontinence and other symptoms of urinary bladder hyperactivity. Said compounds include tolterodine.Type: GrantFiled: August 3, 2006Date of Patent: October 18, 2011Assignee: Interquim, S.A.Inventors: Antonio Lorente Bonde-Larsen, Pablo Martin Pascual, Jorge Martin Juarez, Miquel Armengol Montserrat
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Publication number: 20110161181Abstract: A system and method for the management of advertisements in an graphic object such as an application or web page The system includes an ad-server manager that is configured: to receive (from a user-side process that generates graphic objects such as application windows or web pages) a request for an ad-server to be used; to select the ad-server to be used; and to send information related to the selected ad-server to the user-side process. The user-side process then requests the selected ad-server to provide at least one advertisement; and receives said at least one advertisement from the selected ad-server. As a result, the ad-server manager is able to choose the most suitable ad-server for each request, taking account of issues such as temporary unavailability or backwards compatibility. In addition, the applications/web pages may be made lighter, easier to construct and cheaper because they do not need to include the code to recover advertisements.Type: ApplicationFiled: July 30, 2010Publication date: June 30, 2011Applicant: VODAFONE GROUP PLCInventors: Guillermo Esteve Asensio, Juan Jose Valverde Fuster, Lucia Garate Mutiloa, Diego Martinez Rellan, Enrique Jorge Martin Hormigos
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Publication number: 20110110049Abstract: An electrical enclosure wherein an electrical component can be moved between various positions (e.g., connected, disconnected, test, etc.) without opening an enclosure door. The electrical enclosure supports a component for movement between a withdrawn position, a test position, and an inserted position. A handle is accessible by an operator from an exterior of the enclosure and is configured to move the component between the respective positions without having to open the enclosure. The handle is integral with the enclosure and thus an operator needs no special tool or other device to effect movement of the electrical component between its respective positions.Type: ApplicationFiled: October 28, 2010Publication date: May 12, 2011Applicant: ROCKWELL AUTOMATION TECHNOLOGIES, INC.Inventors: Gregory David Lehtola, Dean Meyer, Arnaldo Hiroyuki Omoto, Paul Krause, Fabio Kazuo Ito, Steven J. Bauer, JR., Joao Jorge Martins Freitas
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Patent number: 7875750Abstract: The present invention relates to a process for preparing 2-amino-6-alkyl-amino-4,5,6,7-tetrahydrobenzothiazoles (I) wherein the asterisk (*) represents an asymmetric carbon and R1 is C1-C6 alkyl; their enantiomers or mixtures thereof, their solvates, hydrates or pharmaceutically acceptable salts, comprising: (a) reacting a compound (II) with a secondary amine, optionally in the presence of an acid and a solvent 1, to form an enamine; (b) optionally removing said acid and said solvent 1, and then reacting said enamine with sulfur in the presence of a solvent 2; and (c) reacting the previously obtained compound with cyanamide to obtain the compound (I). Pramipexole, a compound with dopamine D-2 agonist activity, is among the compounds (I) and is useful for the treatment of Parkinson's disease and schizophrenia.Type: GrantFiled: November 16, 2009Date of Patent: January 25, 2011Assignee: Ragactives, S.L.Inventors: Gustavo Pascual Coca, Jorge Martin Juarez
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Patent number: 7842821Abstract: The invention is aimed at a compound of formula (I) wherein n is 0, 1 or 2, R1 is a linear or branched alkyl group, R2 is selected from a substituted or non substituted alkyl group, substituted or non substituted aryl group, substituted or non substituted aralkyl group, substituted or non substituted heterocyclyl group, or a substituted or non substituted heterocyclylalkyl group. Another object of the invention is a process for obtaining these compounds from the corresponding compound with a hydroxy group in position 4 by means of reacting with a sulfonamide in the presence of a phosphine and a dialkyl azadicarboxylate. The deprotection of the compound of formula (I) gives rise to the corresponding amine. The intermediate and the processes described are very useful in the synthesis of pharmaceutical products.Type: GrantFiled: November 4, 2005Date of Patent: November 30, 2010Assignee: Ragactives, S.L.Inventors: José María Gorgojo Lobato, Luis Octavio Silva Guisasola, Jorge Martín Juárez
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Publication number: 20100286446Abstract: The invention relates to a method of obtaining 3,3-diphenylpropylamines (I), wherein R1 is H, alkyl, haloalkyl or alkoxyalkyl, R2 is alkyl, alkoxy, halogen, NO2, CN, CHO, which may be free or protected, CH2OH or COOR6, and R3 and R4 are selected independently from H and alkyl or together with the nitrogen to which they are bound form a ring having 3 to 7 members. The inventive method consists in reacting a propylenephenylamine and a disubstituted aromatic hydrocarbon and, if necessary, separating the desired enantiomer or the mixture of enantiomers, and/or converting the compound (I) into a salt. Compounds (I) are muscarinic receptor antagonists which can be used in the treatment of urinary incontinence and other symptoms of urinary bladder hyperactivity. Said compounds include tolterodine.Type: ApplicationFiled: August 3, 2006Publication date: November 11, 2010Applicant: Interquim, S.A.Inventors: Antonio Lorente Bonde-Larsen, Pablo Martin Pascual, Jorge Martin Juarez, Miquel Armengol Montserrat
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Patent number: 7795435Abstract: The process includes the steps of (i) dissolving finasteride in a substantially anhydrous organic solvent selected among n-butyl acetate, iso-butyl acetate, sec-butyl acetate, tert-butyl acetate, C5 alkyl acetate and mixtures thereof, at a temperature equal to or lower than the boiling point of said organic solvent; (ii) slowly cooling said finasteride solution to a cooling temperature determined on the basis of the chosen solvent; (iii) maintaining the resulting suspension at the cooling temperature for a period of time equal to or less than 16 hours; and (iv) recovering the resulting solid phase containing Form I of finasteride, for example by means of filtration, and removing the solvent, for example by means of drying said crystals. The process allows for obtaining the Form I of finasteride only and in a pure form.Type: GrantFiled: April 29, 2005Date of Patent: September 14, 2010Assignee: Ragactives, S.L.Inventors: Luis Octavio Silva Guisasola, Mario Laderas Muñoz, Jorge Martin Juarez
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Publication number: 20100063324Abstract: The present invention relates to a process for preparing 2-amino-6-alkyl-amino-4,5,6,7-tetrahydrobenzothiazoles (I) wherein the asterisk (*) represents an asymmetric carbon and R1 is C1-C6 alkyl; their enantiomers or mixtures thereof, their solvates, hydrates or pharmaceutically acceptable salts, comprising: (a) reacting a compound (II) with a secondary amine, optionally in the presence of an acid and a solvent 1, to form an enamine; (b) optionally removing said acid and said solvent 1, and then reacting said enamine with sulfur in the presence of a solvent 2; and (c) reacting the previously obtained compound with cyanamide to obtain the compound (I). Pramipexole, a compound with dopamine D-2 agonist activity, is among the compounds (I) and is useful for the treatment of Parkinson's disease and schizophrenia.Type: ApplicationFiled: November 16, 2009Publication date: March 11, 2010Applicant: RAGACTIVES, S.L.Inventors: Gustavo Pascual Coca, Jorge Martín Juárez
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Patent number: 7638542Abstract: A process for preparing 2-amino-6-alkyl-amino-4,5,6,7-tetrahydrobenzothiazoles of formula (I) wherein the asterisk (*) represents an asymmetric carbon and R1 is C1-C6 alkyl; and enantiomers and mixtures thereof, and their solvates, hydrates and pharmaceutically acceptable salts. The process involves (a) reacting with a secondary amine, optionally in the presence of an acid and a first solvent, to form an enamine; (b) optionally removing the acid and first solvent, and then reacting the enamine with sulfur in the presence of a second solvent; and (c) reacting the previously obtained compound with cyanamide to obtain the formula (I) compound. Pramipexole, a dopamine D-2 agonist, can be made by such process, and is useful for the treatment of Parkinson's disease and schizophrenia.Type: GrantFiled: June 24, 2005Date of Patent: December 29, 2009Assignee: Ragactives, S.L.Inventors: Gustavo Pascual Coca, Jorge Martín Juárez
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Publication number: 20090076287Abstract: The invention is aimed at a compound of formula (I) wherein n is 0, 1 or 2, R1 is a linear or branched alkyl group, R2 is selected from a substituted or non substituted alkyl group, substituted or non substituted aryl group, substituted or non substituted aralkyl group, substituted or non substituted heterocyclyl group, or a substituted or non substituted heterocyclylalkyl group. Another object of the invention is a process for obtaining these compounds from the corresponding compound with a hydroxy group in position 4 by means of reacting with a sulfonamide in the presence of a phosphine and a dialkyl azadicarboxylate. The deprotection of the compound of formula (I) gives rise to the corresponding amine. The intermediate and the processes described are very useful in the synthesis of pharmaceutical products.Type: ApplicationFiled: November 4, 2005Publication date: March 19, 2009Applicant: RAGACTIVES, S.L.Inventors: Jose Maria Gorgojo Lobato, Luis Octavio Silva Guisasola, Jorge Martin Juarez
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Patent number: 7473805Abstract: The process comprises reacting a compound of formula (II), where R is a hydroxyl protecting group, and the asterisk indicates an asymmetric carbon atom, with diisopropylamine in the presence of a reducing agent; optionally converting the resulting intermediate into a salt and, if so desired, isolating it; removing the hydroxyl protecting group; and if so desired, separating the desired (R) or (S) enantiomer, or the mixture of enantiomers and/or converting the obtained compound into a pharmaceutically acceptable salt thereof. Tolterodine is a muscarinic receptor antagonist useful in treating urinary incontinence and other symptoms of urinary bladder hyperactivity.Type: GrantFiled: December 21, 2004Date of Patent: January 6, 2009Assignee: Ragactives, S.L. Parque Tecnologico de BoecilloInventors: Gustavo Pascual Coca, Pablo Martin Pascual, Jorge Martin Juarez
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Publication number: 20080194832Abstract: The invention relates to a novel method for the resolution of the racemic mixture of compound (R,S)-2-amino-6-propylamino-4,5,6,7-tetrahydrobenzothiazole, or the enrichment of same with in one of its enantiomers, and to intermediate compounds which can be used to perform said method.Type: ApplicationFiled: May 9, 2006Publication date: August 14, 2008Applicant: Ragactives, S.L.Inventors: Luis Octavio Silva Guisasola, Jorge Martin Juarez
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Publication number: 20070254959Abstract: The process comprises reacting a compound of formula (II), where R is a hydroxyl protecting group, and the asterisk indicates an asymmetric carbon atom, with diisopropylamine in the presence of a reducing agent; optionally converting the resulting intermediate into a salt and, if so desired, isolating it; removing the hydroxyl protecting group; and if so desired, separating the desired (R) or (S) enantiomer, or the mixture of enantiomers and/or converting the obtained compound into a pharmaceutically acceptable salt thereof. Tolterodine is a muscarinic receptor antagonist useful in treating urinary incontinence and other symptoms of urinary bladder hyperactivity.Type: ApplicationFiled: December 21, 2004Publication date: November 1, 2007Applicant: RAGACTIVES, S.L.Inventors: Gustavo Pascual Coca, Pablo Martin Pascual, Jorge Martin Juarez