SK8012002A3 - Process for the preparation of imidazolidinone alfagammabeta3/alfagammabeta5 integrin antagonists and intermediates obtained by this method - Google Patents

Process for the preparation of imidazolidinone alfagammabeta3/alfagammabeta5 integrin antagonists and intermediates obtained by this method Download PDF

Info

Publication number
SK8012002A3
SK8012002A3 SK801-2002A SK8012002A SK8012002A3 SK 8012002 A3 SK8012002 A3 SK 8012002A3 SK 8012002 A SK8012002 A SK 8012002A SK 8012002 A3 SK8012002 A3 SK 8012002A3
Authority
SK
Slovakia
Prior art keywords
compound
formula
alkyl
aqueous
solution
Prior art date
Application number
SK801-2002A
Other languages
English (en)
Slovak (sk)
Inventor
Mark S Jensen
Michael Palucki
Nelo R Rivera
Kenneth M Wells
Yi Xiao
Yaling Wang
Chunhua Yang
Nobuyoshi Yasuda
Original Assignee
Merck & Co Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Merck & Co Inc filed Critical Merck & Co Inc
Publication of SK8012002A3 publication Critical patent/SK8012002A3/sk

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/62Oxygen or sulfur atoms
    • C07D213/63One oxygen atom
    • C07D213/64One oxygen atom attached in position 2 or 6
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D233/30Oxygen or sulfur atoms
    • C07D233/32One oxygen atom
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pyridine Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
SK801-2002A 1999-11-08 2000-11-03 Process for the preparation of imidazolidinone alfagammabeta3/alfagammabeta5 integrin antagonists and intermediates obtained by this method SK8012002A3 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US16397999P 1999-11-08 1999-11-08
PCT/US2000/030361 WO2001034602A2 (en) 1999-11-08 2000-11-03 Process and intermediates for the preparation of imidazolidinone alpha v integrin antagonists

Publications (1)

Publication Number Publication Date
SK8012002A3 true SK8012002A3 (en) 2002-10-08

Family

ID=22592461

Family Applications (1)

Application Number Title Priority Date Filing Date
SK801-2002A SK8012002A3 (en) 1999-11-08 2000-11-03 Process for the preparation of imidazolidinone alfagammabeta3/alfagammabeta5 integrin antagonists and intermediates obtained by this method

Country Status (20)

Country Link
EP (1) EP1230240B1 (de)
JP (1) JP2003513974A (de)
KR (1) KR20020048427A (de)
CN (1) CN1414966A (de)
AR (1) AR029407A1 (de)
AT (1) ATE245645T1 (de)
AU (1) AU777919B2 (de)
BR (1) BR0015384A (de)
CA (1) CA2389999A1 (de)
CZ (1) CZ20021508A3 (de)
DE (1) DE60004087T2 (de)
EA (1) EA200200548A1 (de)
ES (1) ES2202191T3 (de)
HU (1) HUP0203246A3 (de)
IL (1) IL149313A0 (de)
MX (1) MXPA02004547A (de)
PL (1) PL355011A1 (de)
SK (1) SK8012002A3 (de)
WO (1) WO2001034602A2 (de)
YU (1) YU32502A (de)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2421792A1 (en) * 2000-09-13 2002-03-21 Merck & Co., Inc. Alpha v integrin receptor antagonists
US20040254211A1 (en) 2000-09-14 2004-12-16 Arison Byron H Alpha v integrin receptor antagonists
US6706885B2 (en) 2001-06-06 2004-03-16 Merck & Co., Inc. Process for preparing integrin antagonist intermediates
US6509347B2 (en) 2001-06-11 2003-01-21 Merck & Co., Inc. Crystalline forms of an integrin receptor antagonist
US6646130B2 (en) 2001-07-19 2003-11-11 Merck & Co., Inc. Process to chiral integrin antagonist beta-amino acid intermediate
AR038189A1 (es) * 2002-01-29 2005-01-05 Merck & Co Inc Proceso para la preparacion de intermediarios de antagonistas de integrina
US20060030581A1 (en) * 2002-09-20 2006-02-09 Debusi Laura A Mannitol formulation for integrin receptor antagonist
RS55856B1 (sr) 2010-07-14 2017-08-31 Novartis Ag Heterociklična jedinjenja agonisti ip receptora
ES2565826T3 (es) 2012-01-13 2016-04-07 Novartis Ag Pirroles fusionados como agonistas del receptor IP para el tratamiento de hipertensión arterial pulmonar (PAH) y trastornos relacionados
JP2016507582A (ja) 2013-02-13 2016-03-10 ノバルティス アーゲー Ip受容体アゴニスト複素環式化合物
GB201305668D0 (en) 2013-03-28 2013-05-15 Glaxosmithkline Ip Dev Ltd Avs6 Integrin Antagonists
DK3929196T3 (da) 2013-09-24 2023-09-25 Fujifilm Corp Farmaceutisk sammensætning af en nitrogenholdig forbindelse eller salt deraf, eller metalkompleks deraf
AP2016009156A0 (en) * 2013-10-25 2016-04-30 Novartis Ag Ring-fused bicyclic pyridyl derivatives as fgfr4 inhibitors
GB201417094D0 (en) 2014-09-26 2014-11-12 Glaxosmithkline Ip Dev Ltd Novel compounds
GB201417011D0 (en) 2014-09-26 2014-11-12 Glaxosmithkline Ip Dev Ltd Novel compounds
GB201417002D0 (en) 2014-09-26 2014-11-12 Glaxosmithkline Ip Dev Ltd Novel compound
GB201417018D0 (en) 2014-09-26 2014-11-12 Glaxosmithkline Ip Dev Ltd Novel compounds
WO2016054483A1 (en) * 2014-10-03 2016-04-07 Novartis Ag Use of ring-fused bicyclic pyridyl derivatives as fgfr4 inhibitors
GB201604681D0 (en) * 2016-03-21 2016-05-04 Glaxosmithkline Ip Dev Ltd Chemical Compounds
GB201604680D0 (en) 2016-03-21 2016-05-04 Glaxosmithkline Ip Dev Ltd Chemical Compounds
WO2017189828A1 (en) * 2016-04-27 2017-11-02 Scifluor Life Sciences, Inc. Nonanoic and decanoic acid derivatives and uses thereof
CA3042693A1 (en) * 2016-11-08 2018-05-17 Bristol-Myers Squibb Company Pyrrole amides as .alpha.v integrin inhibitors

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EA003095B1 (ru) * 1997-12-17 2002-12-26 Мерк Энд Ко., Инк. Антагонисты рецепторов интегринов

Also Published As

Publication number Publication date
HUP0203246A3 (en) 2003-12-29
BR0015384A (pt) 2002-10-08
IL149313A0 (en) 2002-11-10
MXPA02004547A (es) 2002-09-02
CZ20021508A3 (cs) 2002-10-16
ATE245645T1 (de) 2003-08-15
DE60004087D1 (de) 2003-08-28
DE60004087T2 (de) 2004-04-15
EP1230240B1 (de) 2003-07-23
YU32502A (sh) 2004-12-31
AU1461401A (en) 2001-06-06
JP2003513974A (ja) 2003-04-15
AU777919B2 (en) 2004-11-04
ES2202191T3 (es) 2004-04-01
WO2001034602A3 (en) 2002-01-17
AR029407A1 (es) 2003-06-25
KR20020048427A (ko) 2002-06-22
HUP0203246A2 (hu) 2003-01-28
CA2389999A1 (en) 2001-05-17
CN1414966A (zh) 2003-04-30
EP1230240A2 (de) 2002-08-14
PL355011A1 (en) 2004-03-22
WO2001034602A2 (en) 2001-05-17
EA200200548A1 (ru) 2002-10-31

Similar Documents

Publication Publication Date Title
SK8012002A3 (en) Process for the preparation of imidazolidinone alfagammabeta3/alfagammabeta5 integrin antagonists and intermediates obtained by this method
AU2017254916B2 (en) Method for producing substituted 5-fluoro-1H-pyrazolopyridines
DE69432611T2 (de) Herstellung einer substituierten 2,5-Diamino-3-hydroxyhexan
US20040248892A1 (en) Process for the preparation of rebeccamycin and analogs thereof
US6407241B1 (en) Process and intermediates for the preparation of imidazolidinone αv integrin antagonists
KR20210127961A (ko) 방법 및 화합물
CA1037047A (en) 2-hydroxymethyl-3-hydroxy-6-(1-hydroxy-2-t-butylaminoethyl)pyridine preparation and intermediate compounds
US6979736B2 (en) Process for the preparation of benazepril hydrochloride
CA3097628A1 (en) Intermediates and processes for the preparation of linagliptin and its salts
KR101299720B1 (ko) 3-아미노-5-플루오로-4-디알콕시펜탄산 에스테르의 새로운제조방법
SK282272B6 (sk) Deriváty kyseliny glutárovej, spôsob ich prípravy a medziprodukt tohto postupu
EP0970029A1 (de) Verfahren zur herstellung von 9-deazaguaninderivaten
JP3144921B2 (ja) ベンジルエステル誘導体及びその製造方法
JP3144920B2 (ja) α−アシルアミノケトン誘導体、その製造方法及びその利用
EP1829870A1 (de) 2-(pyrazol-1-yl)pyridinderivat
DD209630A5 (de) Verfahren zur herstellung von flutrolin