Bhise
Amod V. Bhise, Round Rock, TX US
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20140208305 | Automatically Identifying Criticality of Software Fixes Specific to a Client Deployment and Usage of Software Product - A mechanism is provided in a data processing system for identifying criticality of a software fix. The mechanism obtains a criticality description associated with a software fix of a software product deployed on the data processing system. The mechanism determines a criticality value of the software fix based on computing environment of the data processing system and customer usage of the software product on the data processing system. | 07-24-2014 |
20140324511 | BUSINESS PROCESS DISCOVERY USING DOCUMENT TRACKING TECHNOLOGIES - A document tracking module is associated with a physical document utilized within a business organization. Physical movement of the document is monitored through different departments of the business organization using information derived from the document tracking module. A business process flow within the business organization is discovered from the monitored physical movement of the document through the different departments of the business organization. A business process model, including details of the discovered business process flow within the business organization, is generated. | 10-30-2014 |
20140324515 | BUSINESS PROCESS DISCOVERY USING DOCUMENT TRACKING TECHNOLOGIES - A document tracking module is associated with a physical document utilized within a business organization. Physical movement of the document is monitored through different departments of the business organization using information derived from the document tracking module. A business process flow within the business organization is discovered from the monitored physical movement of the document through the different departments of the business organization. A business process model, including details of the discovered business process flow within the business organization, is generated. | 10-30-2014 |
Anil D. Bhise, Pune IN
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20100305314 | GEOMETRIC SYNTHESIS OF PORPHYRIN RODS - A method of making a compound of Formula I′ | 12-02-2010 |
20110184166 | GEOMETRIC SYNTHESIS OF PORPHYRIN RODS - A method of making a compound of Formula I′ | 07-28-2011 |
20130079528 | GEOMETRIC SYNTHESIS OF PORPHYRIN RODS - A method of making a compound of Formula I′ | 03-28-2013 |
Jaimin Rohitkumar Bhise, San Diego, CA US
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20120236002 | 3D TO STEREOSCOPIC 3D CONVERSION - This disclosure describes techniques for modifying application program interface (API) calls in a manner that can cause a device to render native three dimensional (3D) graphics content in stereoscopic 3D. The techniques of this disclosure can be implemented in a manner where API calls themselves are modified, but the API itself and the GPU hardware are not modified. The techniques of the present disclosure include using the same viewing frustum defined by the original content to generate a left-eye image and a right-eye image and shifting the viewport offset of the left-eye image and the right-eye image. | 09-20-2012 |
Mohar H. Bhise, Bellevue, WA US
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20110276863 | Providing Text Content Embedded with Multimedia Content - Text content embedded with multimedia content is provided from a content provider to a client device. The multimedia content may be provided to the client device separate from the text content. In particular, multimedia content metadata indicating a storage location of the multimedia content may be provided to the client device after the text content. The client device may request the multimedia content from the content provider based on the multimedia content metadata. The content provider may send the requested multimedia content to the client device after receiving an authenticated version of the multimedia content metadata. | 11-10-2011 |
Nandu Bhise, Pune IN
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20120237770 | NOVEL PROCESS FOR PREPARATION OF DARUNAVIR AND DARUNAVIR ETHANOLATE OF FINE PARTICLE SIZE - The present invention provides a novel process for preparation of darunavir that involves reduction of [(1S,2R)-3-[[(4-nitrophenyl)sulfonyl](2-methylpropyl)amino]-2-hydroxy -1-(phenylmethyl)propyl]carbamic acid (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl ester, of formula (5). The present invention also provides darunavir ethanolate of particle size wherein d | 09-20-2012 |
20140066638 | NOVEL PROCESS FOR PREPARATION OF DARUNAVIR AND DARUNAVIR ETHANOLATE OF FINE PARTICLE SIZE - The present invention provides a novel process for preparation of darunavir that involves reduction of [(1S,2R)-3-[[(4-nitrophenyl)sulfonyl](2-methylpropyl)amino]-2-hydroxy-1-(phenylmethyl)propyl]carbamic acid (3R,3aS,6aR)-hexahydrofuro[2,3-b]furan-3-yl ester, of formula (5). The present invention also provides darunavir ethanolate of particle size wherein d | 03-06-2014 |
Nandu Baban Bhise, Mumbai IN
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20080319226 | Process For the Preparation of Highly Pure (E) N,N-Diethyl-2-Cyano-3-(3,4-Dihydroxy-5-Nitro Phenyl) Acrylamide (Entacapone) - A process for the preparation of highly pure (E)-N,N-diethyl-2-cyano-3-(3,4-dihydroxy-5-nitrophenyl)acrylamide (Entacapone). It comprises condensing 3,4-dihydroxy-5-nitro benzaldehyde with N,N-diethyl cyano acetamide in an organic solvent in the presence of an organic base and an acid under reflux conditions followed by distilling off the solvent under vacuum and treating the residue with a lower aliphatic carboxylic acid at 40-8O0 C. The resulting residue is extracted with a chlorinated solvent and the solvent is distilled off under vacuum. The resulting residue is extracted with an organic solvent to obtain crude N,N-diethyl-2-cyano-3-3,4-dihydroxy-5-nitrophenyl)acrylamide. The crude product N,N-diethyl-2-cyano-3-(3,4-dihydroxy-5-nitrophenyl) acrylamide formed is treated with a mixture of organic alcohol and organic acid in the molar ratio of the crude product to organic alcohol 1:5 to 15 and crude product to organic acid 1:1 to 3 under reflux conditions. | 12-25-2008 |
20090198058 | Process for Preparation of Dextrorotatory Isomer of 6-(5- chloro-pyrid-2-yl)-5-[(4-methyl -1-piperazinyl) carbonyloxy] -7-oxo-6,7-dihydro-5H-pyrrolo [3,4-b] pyrazine (Eszopiclone) - Disclosed herein is the process for preparation of 6-(5-chloro-pyrid-2-yl)-5-[(4-methyl-1-piperazinyl)carbonyloxy]-7-oxo-6,7-dihydro-5H-pyrrolo[3,4-b]pyrazine (Zopiclone), its resolution to get the dextrorotatory isomer of formula (I) substantially free of R(−) enantiomer and recovery of key raw material i.e. 6-(5-chloro pyrid-2-yl)-5-hydroxy-7-oxo-5,6-dihydropyrrolo[3,4-b]pyrazine from the R-isomer of Zopiclone followed by conversion of the recovered compound to get pure Eszopiclone (I) in high yield and high purity. | 08-06-2009 |
Nandu Baban Bhise, Pune IN
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20130225845 | PROCESS FOR PREPARATION OF ESTRADIOL VALERATE AND A NOVEL CRYSTALLINE FORM A OF ESTRADIOL DIVALERATE - The present invention relates to the process for the preparation of estradiol valerate (I) which involves isolation of crystalline estradiol divalerate (III) by crystallization from an alcoholic solvent. | 08-29-2013 |
20140357871 | PROCESS FOR PREPARATION OF RUFINAMIDE - The present invention relates to a novel process for preparation of rufinamide (I) comprising: reacting 2,6-difluorobenzyl azide (II) and propiolic acid (III) in a mixture of alcohol and water to produce 1-(2,6-difluorobenzyl)-1H-1,2,3-triazole-4-carboxylic acid (IV), esterifying the acid (IV) to ester (V) and treating ester (V) with ammonia. The invention further relates to process for purification of 1-(2,6-difluorobenzyl)-1H-1,2,3-triazole-4-carboxylic acid (IV), by crystallization from a mixture of alcohol and water. The present invention also provides process for purification of rufinamide (I) by crystallization from mixture of polar aprotic solvent with water or alcohol. | 12-04-2014 |
Nandu Baban Bhise, Maharashtra IN
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20080275241 | Polymorphic Forms of Dolasetron Base and Processes of Preparing Dolasetron Base, Its Polymorphic Forms and Salt Thereof - The present disclosure relates to a process for the preparation of endo-hexahydro-8-(3-indolylcarbonyloxy)-2,6-methano-2H-quinolizin-3(4H)-one or Dolasetron base. It also discloses a process for the preparation of endo-hexahydro-8-(3-indolylcarbonyloxy)-2,6-methano-2H-quinolizin-3(4H)-one mesylate or Dolasetron mesylate. Further, the present disclosure relates to a process for producing Form I of Dolasetron base, and to the novel crystalline polymorphs, Form II, III, IV and V of Dolasetron base and industrial processes for producing them. | 11-06-2008 |
20100009977 | Process for the preparation of (R)-(+)-4-(Ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1- ,2-thiazine-6-sulfonamide-1,1-dioxide. - Disclosed herein is an improved process for the preparation of (R)-(+)-4-(Ethylamino)-3,4-dihydro-2-(3-methoxypropyl)-2H-thieno[3,2-e]-1,2-thiazine-6-sulfonamide-1,1-dioxide (Brinzolamide) and novel intermediates thereof. | 01-14-2010 |
Nupura S. Bhise, Baltimore, MD US
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20120128782 | Multicomponent Degradable Cationic Polymers - Degradable polymers were synthesized that self-assemble with DNA to form particles that are effective for gene delivery. Small changes to polymer synthesis conditions, particle formulation conditions, and polymer structure provides significant changes to efficacy in a cell-type dependent manner. Polymers presented here are more effective than commercially available materials, such as LIPOFECTAMINE | 05-24-2012 |
20150250881 | Multicomponent Degradable Cationic Polymers - Degradable polymers were synthesized that self-assemble with DNA to form particles that are effective for gene delivery. Small changes to polymer synthesis conditions, particle formulation conditions, and polymer structure provides significant changes to efficacy in a cell-type dependent manner. Polymers presented here are more effective than commercially available materials, such as LIPOFECTAMINE 2000™, FUGENE®, or polyethylenimine (PEI), for gene delivery to cancerous fibroblasts or human primary fibroblasts. The presently disclosed materials may be useful for cancer therapeutics and regenerative medicine. | 09-10-2015 |
Onkar Bhise, Pune IN
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20150247594 | QUICK CONNECT COUPLING WITH SWAGED VALVE COMPONENTS AND METHOD FOR ASSEMBLING - The present disclosure relate to coupling components including valve structures and methods for forming the valve structures. The method includes attaching together a male valve piece ( | 09-03-2015 |
Rahul Bhise, Ahmednagar IN
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20150051172 | PHARMACEUTICAL COMPOSITIONS COMPRISING BORONIC ACID COMPOUNDS - A pharmaceutical composition and preparing processes thereof. The composition comprises bortezomib or pharmaceutically acceptable salt or solvate thereof, tromethamine and an organic carboxylic acid, and the pH of the composition is from about 3.0 to 6.0. | 02-19-2015 |
Sanjay Shashikant Bhise US
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20160052919 | PROCESS FOR THE PREPARATION OF RIVAROXABAN - Disclosed is a process for the preparation of rivaroxaban and purifying rivaroxaban. | 02-25-2016 |
Tejas N. Bhise, Pune IN
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20120084332 | Orphan Management in File Systems - A method, computer program product, and apparatus for managing a file system is presented. An object in the file system is identified in which one of a first pointer from the object to a first folder in the file system and a second pointer from the first folder to the object is incorrect. A number of folders is generated within a second folder in the file system that represents a path from a root of the file system to the first folder. The first pointer for the object is set to a last folder in the number of folders in which the last folder represents the first folder. | 04-05-2012 |
Umesh Bhise, Ahmednagar IN
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20090156604 | FUSED BICYCLIC IMIDAZOLES - Compounds of formula (I) | 06-18-2009 |
20140088110 | FUSED BICYCLIC IMIDAZOLES - Compounds of formula (I) | 03-27-2014 |
Vijay S. Bhise, North Caldwell, NJ US
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20120041217 | TWO-STAGE CALCINATION FOR CATALYST PRODUCTION - The invention relates to an improved process for producing a catalyst useful for the epoxidation of ethylene to ethylene oxide. In forming the catalyst, a silver-impregnated support is subjected to two calcinations. The support is subjected to a first calcination in a first atmosphere comprising air. Next the support is subjected to a second calcination in a second atmosphere which is substantially entirely comprised of inert gas, and which second atmosphere is substantially absent of hydrogen. This two-stage calcination produces an improved catalyst which contains fewer organics left over under standard conditions of air calcination alone, while costing less than calcination in an inert gas alone. | 02-16-2012 |