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AR043505A1 - Preparacion de beta-cetoamidas e intermediarios de reaccion - Google Patents

Preparacion de beta-cetoamidas e intermediarios de reaccion

Info

Publication number
AR043505A1
AR043505A1 ARP040100731A AR043505A1 AR 043505 A1 AR043505 A1 AR 043505A1 AR P040100731 A ARP040100731 A AR P040100731A AR 043505 A1 AR043505 A1 AR 043505A1
Authority
AR
Argentina
Prior art keywords
preparation
unsubstituted
structural formula
substituted
cetoamids
Prior art date
Application number
Other languages
English (en)
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 AR043505A1 publication Critical patent/AR043505A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

Reivindicación 1: Procedimiento para la preparación de un compuesto de fórmula estructural (1) en la que R1 es un H o un alquilo C1-4 no sustituido o sustituido conde 1 a 5 F; que comprende el paso de tratar un compuesto de fórmula estructural (2) en la que Ar es un fenilo que no está sustituido o que está sustituido con de 1 a 5 sustituyentes seleccionados independientemente del grupo constituido por halógeno, trifluorometilo y trifluorometoxi, con una 5,6,7,8-tetrahidro[1,2,4]-triazol[4,3-a]pirazina de fórmula estructural (5) o una sal ácida de la misma en presencia de un ácido o base en un disolvente orgánico apropiado. Reivindicación 9: Compuesto de fórmula estructural (1) en el que Ar es un fenilo que no está sustituido o que está sustituido con e 1 a 5 sustituyentes seleccionados independientemente del grupo constituido por halógeno, trifluorometilo y trifluorometoxi; y R1 es un H o un alquilo C1-4 no sustituido o sustituido con de 1 a 5 F.
ARP040100731 2003-03-18 2004-03-08 Preparacion de beta-cetoamidas e intermediarios de reaccion AR043505A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US45545803P 2003-03-18 2003-03-18

Publications (1)

Publication Number Publication Date
AR043505A1 true AR043505A1 (es) 2005-08-03

Family

ID=33030004

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP040100731 AR043505A1 (es) 2003-03-18 2004-03-08 Preparacion de beta-cetoamidas e intermediarios de reaccion

Country Status (3)

Country Link
AR (1) AR043505A1 (es)
TW (1) TW200505923A (es)
WO (1) WO2004083212A1 (es)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ATE374181T1 (de) 2001-06-27 2007-10-15 Smithkline Beecham Corp Fluorpyrrolidine als dipeptidylpeptidaseinhibitoren
US20040242566A1 (en) 2003-03-25 2004-12-02 Syrrx, Inc. Dipeptidyl peptidase inhibitors
EP1625122A1 (en) 2003-05-14 2006-02-15 Takeda San Diego, Inc. Dipeptidyl peptidase inhibitors
CA2535619A1 (en) 2003-08-13 2005-02-24 Takeda Pharmaceutical Company Limited 4-pyrimidone derivatives and their use as peptidyl peptidase inhibitors
CN101087756B (zh) 2004-07-23 2011-04-06 纽阿达有限责任公司 肽酶抑制剂
ME02005B (me) 2005-09-14 2012-08-31 Takeda Pharmaceuticals Co Inhibitori dipeptidil peptidaze za lečenje dijabetesa
CN101360723A (zh) 2005-09-16 2009-02-04 武田药品工业株式会社 制备嘧啶二酮衍生物的方法
US20090156465A1 (en) 2005-12-30 2009-06-18 Sattigeri Jitendra A Derivatives of beta-amino acid as dipeptidyl peptidase-iv inhibitors
WO2007112347A1 (en) 2006-03-28 2007-10-04 Takeda Pharmaceutical Company Limited Dipeptidyl peptidase inhibitors
TW200838536A (en) 2006-11-29 2008-10-01 Takeda Pharmaceutical Polymorphs of succinate salt of 2-[6-(3-amino-piperidin-1-yl)-3-methyl-2,4-dioxo-3,4-dihydro-2H-pyrimidin-1-ylmethy]-4-fluor-benzonitrile and methods of use therefor
US20150025080A1 (en) 2011-06-29 2015-01-22 Ranbaxy Laboratories Limited Solid dispersions of sitagliptin and processes for their preparation
AU2012277403A1 (en) 2011-06-30 2014-01-30 Ranbaxy Laboratories Limited Novel salts of sitagliptin
EP2788352A1 (en) 2011-12-08 2014-10-15 Ranbaxy Laboratories Limited Amorphous form of sitagliptin salts
CN116199691A (zh) * 2022-09-01 2023-06-02 淄博矿业集团有限责任公司 一种西格列汀重要中间体的合成方法
WO2024121301A1 (en) 2022-12-09 2024-06-13 Krka, D.D., Novo Mesto Process for the preparation of sitagliptin
CN116284004A (zh) * 2023-03-29 2023-06-23 宙晟智维生命科学(上海)有限公司 一种合成磷酸西格列汀中间体的连续化方法

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA74912C2 (en) * 2001-07-06 2006-02-15 Merck & Co Inc Beta-aminotetrahydroimidazo-(1,2-a)-pyrazines and tetratriazolo-(4,3-a)-pyrazines as inhibitors of dipeptylpeptidase for the treatment or prevention of diabetes

Also Published As

Publication number Publication date
WO2004083212A1 (en) 2004-09-30
TW200505923A (en) 2005-02-16

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