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Application_Number cess Pate Secondary Title Classific Abstract Inventor 00275/KOLNP/2005 1 0 #N/A #N/A #N/A #N/A 00523/DELNP/2004 1 0 A method A61K-31/0 A topical 0081/DEL/2001 1 0 A process A61K-31/0 The prese 0088/DEL/2001 1 0 a process A61-K 31/ A process 0090/DEL/2001 1 0 A process A61-K 31/ The prese 00951/DELNP/2003 1 0 "A METHOD A61K-9/10 The prese 01005/DELNP/2003 1 0 "A Proces A61K-38/4 A process 01042/KOLNP/2004 1 0 "PROCESS A61K-31/5 A process 01448/DELNP/2003 1 0 PROCESS F A61K-31/0 The prese 01479/KOLNP/2003 1 0 METHOD OF A61K-9/28 An ingest 01584/KOLNP/2004 1 0 A PROCESS A61K-31/4 The enol 01622/KOL-NP/2003 1 0 #N/A #N/A #N/A #N/A 01622/KOLNP/2003 1 0 #N/A #N/A #N/A #N/A 0173/DEL/2001 1 0 "PROCESS A61K-31/5 The inven 01863/KOLNP/2004 1 0 A METHOD A61-K 35/ The inven 02135/DELNP/2003 1 0 "PROCESS A61K-31/4 Process f 0846/DELNP/2003 1 0 PROCESS F A61-K 7/4 Phenylene 0851/DEL/1999 1 0 "PROCESS A61K-31/0 1. Proces 1011/MUM/2008 1 0 COMPOUNDS A61K-1/00 Steroidal 1014/CHE/2005 1 0 AN IMPROV A61K-31/3 The prese 1015/KOL/2006 1 0 METHODS F A61K-31/4 This inve 1018/MUM/2000 1 0 A PROCESS A61-K 9/2 1. A meth 1022/DEL/1996 1 0 "AN IMPRO A61K-31/1 An improv 1023/DEL/2002 1 0 "A METHOD A61K-9/00 The prese 1024/DEL/2006 1 0 "A PROCES A61K-35/7 The prese 1025/MUMNP/2005 1 0 A PARTICU A61K-47/36 1025/MUM/2003 1 0 A PROCESS A61K-9/00 The inven 1031/DEL/2000 1 0 AN IMPROV A61K-31/0 A process 1031/MUM/2003 1 0 IMPROVED A61K-31/0 ABSTRACT TYAGI, OM 1034/CHE/2009 1 0 IMPROVED A61K-31/4 ABSTRACT 103/DELNP/2005 1 0 "A METHOD A61K-9/28 A method 103/DEL/2002 1 0 "PROCESS A61K-35/6 A process 1040/DEL/2003 1 0 "PROCESS A61K-31/0 The prese 10441/DELNP/2008 1 0 "COMPOSIT A61K-9/00 A process 1044/MUMNP/2007 1 0 PROCESS F A61K-47/4 A process 1045/DEL/1998 1 0 "A METHOD A61K-31/4 The prese 1048/CHENP/2003 1 0 A NOVEL P A61K-31/5 Cilazapri 104/CHE/2007 1 0 NOVEL PRO A61K-31/0 Abstract 1050/DEL/2001 1 0 "AN IMPRO A61K-031/ The prese 1051/DEL/1998 1 0 " PROCESS A61K-31/0 The prese 1051/KOLNP/2008 1 0 A METHOD A01N- 63/ (57) Th 1053/DEL/1996 1 0 "A PROCES A61K-31/0 A process 1054/DELNP/2004 1 0 "METHOD F A61K-9/16 A method JEPSEN SV 1054/DEL/2003 1 0 A process A61-K 31/ The inven David Pau Thottappi Thottappi Thottappi RAJARAM S Pilar Pic COOTE STE PREMCHEND NOWAK EDW BARTOLINI PERDRIEUX EVANS CHR PETER SIE ROLAND LA HERBERT M AMIRANASH MEENAKSHI Azaam All CHANDAVAR LALGUDI V RAJIV MAL AMIT NAYY ERACLIS S PATEL, PA SANJAY NA KARAKAL S ALFONS GR SINGH JAS DINOS PAU KIECKBUSC GREENWALD HUBERTUS MURALIDHA DR. CHAVA YATENDRA HERMAN PI MOGNA GIO RAJENDRA Praveen K

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Application_NumberProcess PatentsSecondary Title Classificat Abstract Inventor Applicant00275/KOLNP/2005 1 0 #N/A #N/A #N/A #N/A #N/A00523/DELNP/2004 1 0 A method oA61K-31/0A topical o Healthpoint, Ltd.,::US::US0081/DEL/2001 1 0 A process fA61K-31/0The present Council of Scientific and Industrial Research::IN::IN0088/DEL/2001 1 0 a process fA61-K 31/0A process f Council of Scientific and Industrial Research::IN::IN0090/DEL/2001 1 0 A process fA61-K 31/1The present Council of Scientific and Industrial Research::IN::IN00951/DELNP/2003 1 0 "A METHODA61K-9/10The present BAXTER INTERNATIONAL INC.::US::US01005/DELNP/2003 1 0 "A ProcessA61K-38/4A process f Healthpoint, Ltd.::US::US01042/KOLNP/2004 1 0 "PROCESS A61K-31/5A process f GLAXO GROUP LIMITED::GB::GB01448/DELNP/2003 1 0 PROCESS FA61K-31/0The present COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH::IN::IN01479/KOLNP/2003 1 0 METHOD OFA61K-9/28An ingestib BIOPROGRESS TECHNOLOGY INTERNATIONAL INC::US::US01584/KOLNP/2004 1 0 A PROCESSA61K-31/4The enol ta POLIFARMA S.P.A.::IT::IT01622/KOL-NP/2003 1 0 #N/A #N/A #N/A #N/A #N/A01622/KOLNP/2003 1 0 #N/A #N/A #N/A #N/A #N/A0173/DEL/2001 1 0 "PROCESS A61K-31/5The inventi ATOFINA::FR::FR01863/KOLNP/2004 1 0 A METHOD A61-K 35/0The inventi THE BRIGHAM AND WOMEN'S HOSPITAL INC.::US::US02135/DELNP/2003 1 0 "PROCESS A61K-31/4Process for BOEHRINGER INGELHEIM PHARMA GMBH & CO. KG.::DE::DE0846/DELNP/2003 1 0 PROCESS FA61-K 7/42Phenylene-b SYMRISE GMBH & CO. KG.::DE::DE0851/DEL/1999 1 0 "PROCESS A61K-31/01. Process LANXESS DEUTSCHLAND GMBH,::DE::DE1011/MUM/2008 1 0 COMPOUNDSA61K-1/00Steroidal d SHELAR ASHOK RANGANATH::IN::IN1014/CHE/2005 1 0 AN IMPROVA61K-31/3The present AUROBINDO PHARMA LIMITED::IN::IN1015/KOL/2006 1 0 METHODS FA61K-31/43This invent JOHNSON & JOHNSON VISION CARE, INC.,::US::US1018/MUM/2000 1 0 A PROCESSA61-K 9/201. A method FDC LIMITED::IN::IN1022/DEL/1996 1 0 "AN IMPROA61K-31/1An improved COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH::IN::IN1023/DEL/2002 1 0 "A METHODA61K-9/00The present RANBAXY LABORATORIES LIMITED::IN::IN1024/DEL/2006 1 0 "A PROCESA61K-35/7The present NATIONAL INSTITUTE OF PHARMACEUTICAL EDUCATION AND RESEARCH::IN::IN1025/MUMNP/2005 1 0 A PARTICUA61K-47/36 ADISSEO FRANCE SAS::FR::FR1025/MUM/2003 1 0 A PROCESSA61K-9/00The inventi CADILA HEALTHCARE LTD::IN::IN1031/DEL/2000 1 0 AN IMPROVA61K-31/0A process f COUNCIL OF SCIENTIFIC AND INDUSTRIAL RESEARCH::IN::IN1031/MUM/2003 1 0 IMPROVED A61K-31/0ABSTRACT ImTYAGI, OM LUPIN LTD.::IN::IN1034/CHE/2009 1 0 IMPROVED A61K-31/4ABSTRACT Th GLAND PHARMA LTD::IN::IN103/DELNP/2005 1 0 "A METHODA61K-9/28A method of BAYER HEALTHCARE AG,::DE::DE103/DEL/2002 1 0 "PROCESS A61K-35/6A process f PANACEA BIOTECH LIMITED::IN::IN1040/DEL/2003 1 0 "PROCESS A61K-31/0The present10441/DELNP/2008 1 0 "COMPOSITA61K-9/00A process f NOVARTIS AG::CH::CH1044/MUMNP/2007 1 0 PROCESS FA61K-47/4A process f ENZON PHARMACEUTICALS, INC.::US::US1045/DEL/1998 1 0 "A METHODA61K-31/4The present DSM N.V..,::NL::NL1048/CHENP/2003 1 0 A NOVEL PA61K-31/5Cilazapril M/S. HETERO DRUGS LIMITED::IN::IN104/CHE/2007 1 0 NOVEL PROA61K-31/0Abstract Th MYLAN LABORATORIES LTD::IN::IN1050/DEL/2001 1 0 "AN IMPROA61K-031/The present RANBAXY LABORATORIES LIMITED::IN::IN1051/DEL/1998 1 0 " PROCESSA61K-31/0The present DSM N.V.::NL::NL1051/KOLNP/2008 1 0 A METHOD A01N- 63/0(57) The Anidral S.R.L.::IT::IT1053/DEL/1996 1 0 "A PROCESA61K-31/0A process f THE CHIEF CONTROLLER RESEARCH & DEVELOPMENT::IN::IN1054/DELNP/2004 1 0 "METHOD FA61K-9/16A method foJEPSEN SVEFERRING BV::NL::NL1054/DEL/2003 1 0 A process fA61-K 31/0The inventi Council of Scientific and Industrial Research::IN::IN1056/CHE/2004 1 0 "AN IMPROA61K-31/0The present ORCHID CHEMICALS & PHARMACEUTICALS LTD::IN::IN1058/DEL/2001 1 0 ''A PROCESA61K-9/19The long ch#N/A1060/MUM/2003 1 0 A PROCESSA61K-31/4the inventi

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STUTI SRIVASTAVA::IN::INPRASHANT SHARMA::IN::INAJIT KUMAR HAZARIKA::IN::INJIBON C SARMA KATAKY::IN::IN

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A process for the synthesis of 5-(N-ethyl-N-2-hydroxyethylamino)-2-pentylamine (Hydroxy Novoldamine), 5-(N,N-diethylamino)-2-pentylamine(Novoldamine) wherein the said process comprises a) ketalization of 1-chloro-4-pentanone carried out by treating it with glycol selected from ethylene glycol or neopentyl glycol in a molar ratio of 1:2 in presence of non polar organic solvent selected from toluene, cyclohexane, xylene, heptane and hexane and catalyst selected from para-toluene sulphonic acid, methane sulphonic acid, perchloric acid at temperature range of 80-140°C for 20-25 hours to obtain compound of formula (I) 2(3'-chloropropyl)2-methyl-1,3-dioxalane, 2-(3 '-chloropropyl) -2,5,5-Trimethyl 1,3-dioxane; 0) b) condensation of said compound of formula (I) 2(3'-chloropropyl)2-methyl- 1,3-dioxalane, 2-(3'-chIoropropyl) -2,5,5-Trimethyl 1,3-dioxane with substituted amine derivatives of formula (V) N-ethyl-N-2-hydroxy ethyl amine, N,N-diethylamine in a molar ratio of 2:5 in presence of non-polar solvents selected from toluene, xylene and cyclohexane at temperature ranging from 90°C-140°C for 18 hours to obtain compound of formula (II) 2-(3' -N-ethy 1- N-2-hydroxyethylaminopropyl)-2-methyl-1,3 -dioxalane (HNK Ketal); 3 H< 1 NR2 R1=R2=Ethyl or R1R2=Ethyl Rl=Ethyl; R1 =Ethyl R2=Hydroxy ethyl (11) (V) c) deprotection of the ketal group of compound of formula (II), 2-(3,-N-ethyI-N-2-hydroxyethylaminopropyl)-2-methyl-l,3-dioxalane (HNK Ketal) under acidic conditions at temperature range of 10- 50°C for 6-7 hours to obtain compound of formula (III) 5-(N-ethyl-N-2-hyd^xyethylamino)-4-pentanone or 5-(N.N-diethylamino)-4-pentanone; and 0 NT Ri = R2 = Ethyl (or) R1=Ethyl; R2=Hydroxy ethyl d) reductive amination of compound of formula (III), 5-(N-ethyl-N-2-hydroxyethylamino)-4-pentanone or 5-(N,N-diethylamino)-4-pentanone is carried out by treating it with alcoholic ammonia in presence of catalyst such as Raney Nickel under mild hydrogenation conditions such as 10-30 kg/cm2 and temperature ranging from 40-130°C for 2-5 hours to yield compound of formula (IV) namely 5-(N-ethyl-N-2-hydroxyethylamino)-2-pentylamine and 5-(N,N'diethyIamino)-2-pentylamine. 10 (IV) i)Ri ,R2= Ethylâ€â€Â>- 5-[N,N-diethylamino]-2-pentylamine] ii) R, = Ethyl, R2 = hydroxy ethyl â€â€Â*â– 5-[N-ethyl-N-2-hydroxyethylamino]-2-pent� �KALAWADIA RAMESH M::IN::INBOSE MILINA::IN::INBASAVARAJ K. NANJWADE::IN::INF. V. MANVI::IN::IN

BASAVARAJ K. NANJWADE::IN::INF. V. MANVI::IN::INKUMAR, RAJIV::IN::IN

AGARWAL VIRENDRA KUMAR::IN::INBRENDAN JOHN MURPHY::US::USBARBARA ALICE JOHNSON::US::USVILAS GAJANAN GAIKAR::IN::INGIRIJA RAMAN::IN::IN

FRANK MOLOCK::US::USAZAAM ALLI::US::KUMAR ASHOK::IN::INDalavi Dadaso Shankar::IN::IN

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process for preparing an acylated cellobiose satisfying the general formula in which X epresents_ani acyl group -R-CO- or II. Z represents an acyl group R" -CO- m*i Kand not more than a minority of R + 11' residues represent H and in the remaining R + R' residues. R represents a saturated or unsaturated, linear or branched chain hydrocarbon residue containing from 5 to 31 carbon atoms and R" represents a residue which is different fromJ3_aLd_which is > (0 a saturated or unsaturated, linear or branched chain hydrocarbon residue containing from 1 to 31 carbon atoms optionally substituted or \ii) an aiorr.ai hydrocarbon residue, optionally substituted or (iii) a cycloaiiphatic hydrocarbon, optionally substituted <""" \ -â– '" said process comprising the step ot reacting an acylated dfellobiose having general r lormula 2 V Ol in which X represents an acyl group (R-CO-) or H. being not more than a minority X residues and R represents a saturated or unsatuniicd. linear or branched chain hydrocarbon residue containing from 5 to 31 carbon atoms with an acylating agent 1 icontainiim a residue R' preferentially at the anomenc carbon of the cellobiosc.WEBB, NICHOLAS::GB::WHITE, MICHAEL STEPHEN::GB::LOHRAY VIDYA BHUSHAN::IN::IN

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ADD ADVANCED DRUG DELIVERY TECHNOLOGIES LTD::CH::CHADD TECHNOLOGIES LTD.::CH::CH

CIBA HOLDING INC::CH::CHVESIFACT AG::CH::CH

PATEL DINESH SHANTILAL::IN::INKURANI SHASHIKANT PRABHUDAS::IN::IN

M/S. MATRIX LABORATORIES LTD::IN::INCADILA HEALTHCARE LIMITED::IN::INWYETH.::US::USGALDERMA S.A.::CH::CH

WHITE FLOWER ASSOCIATES LLP::US::USTIANJIN TASLY PHARMACEUTICAL CO. LTD::CN::CNM/S. ARCH PHARMALABS LIMITED::IN::INAMERICAN HOME PRODUCTS CORPORATION::US::USNANO CUTTING EDGE TECHNOLOGY PVT. LTD.::IN::INL M. COLLEGE OF PHARMACY::IN::INVASCULAR BIOGENICS LTD::IL::ILJOHN CLAUDE SAVOIR::MX::MXKUREHA CORPORATION::JP::JP

IND-SWIFT LABORATORIES LIMITED::IN::INDIVI'S LABORATORIES LIMITED::IN::INOTSUKA PHARMACEUTICAL CO., LTD.::JP::JPM/S.F HOFFMANN-LA ROCHE AG::SZ::SZELI LILLY AND COMPANY::US::USORCHID CHEMICALS & PHARMACEUTICALS LTD::IN::INSEOUL NATIONAL UNIVERSITY INDUSTRY FOUNDATION::KR::KRNATCO PHARMA LIMITED::IN::INLES LABORATOIRES SERVIER::FR::FRACTAVIS PHARMA MANUFACTURING PRIVATE LIMITED::IN::INNYCOMED PHARMA AS::NO::NO

AUROBINDO PHARMA LIMITED::IN::INHEMOTEQ AG::DE::DECYMABAY THERAPEUTICS, INC::US::USSMITHKLINE BEECHAM CORPORATION::US::USWARNER CHILCOTT COMPANY, LLC::US::USUNIVERSITY OF DELHI,::IN::INF HOFFMANN-LA ROCHE AG::CH::CHSMITHKLINE BEECHAM CORPORATION::US::USUNILEVER PLC::PY::PYTHE PROCTER & GAMBLE COMPANY::US::USMYLAN LABORATORIES LTD::IN::INNEKTAR THERAPEUTICS AL, CORPORATION::US::US

GRUNENTHAL GMBH::DE::DEVITAL HEALTH SCIENCES PTY LTD.::AU::AUSENJU PHARMACEUTICAL Co.,Ltd.,::JP::JPM/S. MATRIX LABORATORIES LTD::IN::INIPCA LABORATORIES LTD.::IN::INSANOFI-AVENTIS DEUTSCHLAND GMBH::DE::DEORTHO MCNEIL PHARMACEUTICAL, INC::US::USWACKER METROARK CHEMICALS PVT,LTD.::IN::IN

HOPCKE Reiner::DE::DEAND DESEVAUX Cyril::CA::CA

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JOSHI ADVAIT ARUN::IN::INNARKHEDE SACHIN SURESH::IN::IN

LTS LOHMANN THERAPIE-SYSTEME AG::DE::DEBRISTOL-MYERS SQUIBB COMPANY::US::USIPCA LABORATORIES LIMITED::IN::INORCHID CHEMICALS & PHARMACEUTICALS LTD.::IN::INTHE PROCTER & GAMBLE COMPANY::US::USHANMI HOLDINGS CO., LTD.::KR::KRCADILA HEALTHCARE LIMITED::IN::IN

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PATEL DINESH SHANTILAL::IN::INKURANI SHASHIKANT PRABHUDAS::IN::IN

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CADILA HEALTHCARE LTD.::IN::IN

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M/S. ORCHID CHEMICALS & PHARMACEUTICALS LTD,::IN::INORCHID CHEMICALS & PHARMACEUTICALS LTD,::IN::IN

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ARRAY BIOPHARMA INC.::US::USASTRAZENECA AB,::SE::SE

SOCIETE LABORATORIES DES PRODUITS ETHIQUES-ETHYPHARM::FR::FRBioMedicines Inc.::US::USTHE UNIVERSITY OF KANSAS::US::US

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PENWEST PHARMACEUTICAL CO.::US::USCOLGATE-PALMOLIVE COMPANY::US::USDERMATECH LIMITED::GB::GB

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AVENTIS PHARMACEUTICALS, INC::US::USH. LUNDBECK A/S::DK::DK

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TEVA PHARMACEUTICAL INDUSTRIES LTD::IL::ILTEVA PHARMACEUTICAL INDUSTRIES LTD.::IL::IL

LTS LOHMANN THERAPIE-SYSTEM AG::DE::DELTS LOHMANN THERAPIE-SYSTEME AG::DE::DE

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GADOR S.A::AR::ARLEIDEN UNIVERSITY MEDICAL CENTER::NL::NL

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TEMPLE UNIVERSITY - OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION::US::USTEMPLE UNIVERSITY OF THE COMMONWEALTH SYSTEM OF HIGHER EDUCATION::US::USKOPRAN RESEARCH LABORATORIES LIMITED::IN::INTEVA PHARMACEUTICAL INDUSTRIES LTD.::IL::ILYISSUM RESEARCH DEVELOPMENT COMPANY OF THE HEBREW UNIVERSITY OF JERUSALEM::IL::ILGE HEALTHCARE BIO-SCIENCES AB::SE::SETHE PROCTER & GAMBLE COMPANY::US::USSEPRACOR INC::US::US

VECTURA LIMITED::GB::GBEPICEPT, INC::US::USM/S. ROHM GMBH & CO. KG::DE::BIOLIFE, L.L.C::US::USM/S. RECKITT BENCKISER HEALTHCARE (UK) LIMITED::GB::GBF. HOFFMANN-LA ROCHE AG::CH::CHM/S. VECTURA LIMITED::GB::GBH LUNDBECK A/S::DK::DKSHEARWATER CORPORATION::US::USNOVARTIS AG::CH::CHPHARMATOP SCR::FR::FR

BPSI HOLDINGS, INC.::US::USROHM GMBH & CO. KG CHEMISCHE FABRIK::DE::DE

THE GOVERNMENT OF THE UNITED STATES OF AMERICA AS REPRESENTED BY THE SECRETARY OF THE DEPARTMENT OF HEALTH AND HUMAN SERVICES::US::US