TW200740807A - Process for preparing triazole substituted azaindoleoxoacetic piperazine derivatives and novel salt forms produced therein - Google Patents

Process for preparing triazole substituted azaindoleoxoacetic piperazine derivatives and novel salt forms produced therein

Info

Publication number
TW200740807A
TW200740807A TW095122521A TW95122521A TW200740807A TW 200740807 A TW200740807 A TW 200740807A TW 095122521 A TW095122521 A TW 095122521A TW 95122521 A TW95122521 A TW 95122521A TW 200740807 A TW200740807 A TW 200740807A
Authority
TW
Taiwan
Prior art keywords
piperazine derivatives
triazole substituted
salt forms
novel salt
forms produced
Prior art date
Application number
TW095122521A
Other languages
English (en)
Inventor
Nachimuthu Soundararajan
yu-ping Qiu
Wen-Hao Hu
David R Kronenthal
Pierre Sirard
Jean Lajeunesse
Roberto Droghini
Ramakrishnan Chidambaram
Xinhua Qian
Kenneth J Natalie Jr
Shawn K Pack
Nathan Reising
Erqing Tang
Michael G Fakes
Qi Gao
Feng Qian
Blisse J Vakkalagadda
Shan-Ming Kuang
Chiajen Lai
Original Assignee
Bristol Myers Squibb Co
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 Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of TW200740807A publication Critical patent/TW200740807A/zh

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C311/00—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C311/48—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom
    • C07C311/49—Amides of sulfonic acids, i.e. compounds having singly-bound oxygen atoms of sulfo groups replaced by nitrogen atoms, not being part of nitro or nitroso groups having nitrogen atoms of sulfonamide groups further bound to another hetero atom to nitrogen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47—Quinolines; Isoquinolines
    • A61K31/4738—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4745—Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having nitrogen as a ring hetero atom, e.g. phenantrolines
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A61P31/18—Antivirals for RNA viruses for HIV
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D213/00—Heterocyclic 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
    • C07D213/02—Heterocyclic 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
    • C07D213/04—Heterocyclic 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
    • C07D213/24—Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/26—Radicals substituted by halogen atoms or nitro radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Virology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Communicable Diseases (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • AIDS & HIV (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Molecular Biology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pyridine Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
TW095122521A 2005-06-22 2006-06-22 Process for preparing triazole substituted azaindoleoxoacetic piperazine derivatives and novel salt forms produced therein TW200740807A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US69300405P 2005-06-22 2005-06-22

Publications (1)

Publication Number Publication Date
TW200740807A true TW200740807A (en) 2007-11-01

Family

ID=37460063

Family Applications (1)

Application Number Title Priority Date Filing Date
TW095122521A TW200740807A (en) 2005-06-22 2006-06-22 Process for preparing triazole substituted azaindoleoxoacetic piperazine derivatives and novel salt forms produced therein

Country Status (11)

Country Link
US (2) US7601715B2 (zh)
EP (1) EP1907389B1 (zh)
JP (1) JP5010593B2 (zh)
CN (1) CN101243085A (zh)
AR (1) AR055801A1 (zh)
AT (1) ATE517898T1 (zh)
ES (1) ES2368788T3 (zh)
NO (1) NO341136B1 (zh)
PE (1) PE20070122A1 (zh)
TW (1) TW200740807A (zh)
WO (1) WO2007002308A2 (zh)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7601715B2 (en) * 2005-06-22 2009-10-13 Bristol-Myers Squibb Company Process for preparing triazole substituted azaindoleoxoacetic piperazine derivatives and novel salt forms produced therein
US7598380B2 (en) * 2005-08-03 2009-10-06 Bristol-Myers Squibb Company Method of preparation of azaindole derivatives
JP2011527689A (ja) * 2008-07-08 2011-11-04 リヒター ゲデオン エヌワイアールティー. 2−[4−(4−フルオロ−ベンジル)−ピペリジン−1−イル]−2−オキソ−n−(2−オキソ−2,3−ジヒドロ−ベンゾオキサゾール−6−イル)−アセトアミドの結晶形態
EP2323633B1 (en) * 2008-09-04 2012-03-21 Bristol-Myers Squibb Company Stable pharmaceutical composition for optimized delivery of an hiv attachment inhibitor
EP2552893B1 (en) 2010-03-31 2014-10-29 Actelion Pharmaceuticals Ltd. Antibacterial isoquinolin-3-ylurea derivatives
WO2011130500A1 (en) * 2010-04-16 2011-10-20 Novartis Ag Formulations of a pyridazine bipyrazinyl
US20110263701A1 (en) * 2010-04-21 2011-10-27 Sigal Blau Gabapentin enacarbil compositions
CN102372707B (zh) * 2010-08-16 2015-08-19 上海药明康德新药开发有限公司 6-甲基-4-溴-1,6-二氢吡咯[2,3-c]吡啶-7-酮的合成方法
CN103339130B (zh) 2011-01-31 2015-05-06 百时美施贵宝公司 制备hiv附着抑制剂前药化合物的方法及中间体
CN102993109A (zh) * 2012-12-03 2013-03-27 浙江工业大学 一种脒化合物的制备方法
CN105793263B (zh) 2013-12-05 2019-08-23 豪夫迈·罗氏有限公司 一种苯并[e]薁化合物及其晶型的合成
AR099677A1 (es) 2014-03-07 2016-08-10 Sumitomo Chemical Co Compuesto heterocíclico fusionado y su uso para el control de plagas
CN108863917A (zh) * 2017-05-16 2018-11-23 穆云 一种2,5-二甲氧基吡啶的制备方法
EP3911651B1 (en) 2019-01-17 2024-01-10 ViiV Healthcare UK (No.4) Limited Process for preparing fostemsavir

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP3545461B2 (ja) 1993-09-10 2004-07-21 エーザイ株式会社 二環式ヘテロ環含有スルホンアミド誘導体
ZA949293B (en) 1993-12-08 1995-08-17 Nihon Nohyaku Co Ltd Hydrazine derivatives and uses thereof
US20020061892A1 (en) 2000-02-22 2002-05-23 Tao Wang Antiviral azaindole derivatives
US6476034B2 (en) 2000-02-22 2002-11-05 Bristol-Myers Squibb Company Antiviral azaindole derivatives
RU2303038C2 (ru) 2001-02-02 2007-07-20 Бристол-Маерс Сквибб Компани Азаиндолоксоуксусные производные пиперазины и фармацевтическая композиция на их основе
US20030207910A1 (en) 2001-02-02 2003-11-06 Tao Wang Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives
US20040110785A1 (en) 2001-02-02 2004-06-10 Tao Wang Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives
US20040063744A1 (en) 2002-05-28 2004-04-01 Tao Wang Indole, azaindole and related heterocyclic 4-alkenyl piperidine amides
US7745625B2 (en) * 2004-03-15 2010-06-29 Bristol-Myers Squibb Company Prodrugs of piperazine and substituted piperidine antiviral agents
US20060100432A1 (en) 2004-11-09 2006-05-11 Matiskella John D Crystalline materials of 1-(4-benzoyl-piperazin-1-yl)-2-[4-methoxy-7-(3-methyl-[1,2,4]triazol-1-yl)-1H-pyrrolo[2,3-c]pyridin-3-yl]-ethane-1,2-dione
US7601715B2 (en) 2005-06-22 2009-10-13 Bristol-Myers Squibb Company Process for preparing triazole substituted azaindoleoxoacetic piperazine derivatives and novel salt forms produced therein

Also Published As

Publication number Publication date
ATE517898T1 (de) 2011-08-15
JP2008546795A (ja) 2008-12-25
JP5010593B2 (ja) 2012-08-29
NO341136B1 (no) 2017-08-28
AR055801A1 (es) 2007-09-05
US20060293304A1 (en) 2006-12-28
WO2007002308A2 (en) 2007-01-04
PE20070122A1 (es) 2007-03-11
EP1907389A2 (en) 2008-04-09
US20100076191A1 (en) 2010-03-25
CN101243085A (zh) 2008-08-13
US7601715B2 (en) 2009-10-13
ES2368788T3 (es) 2011-11-22
WO2007002308A3 (en) 2007-07-12
WO2007002308A9 (en) 2007-03-01
NO20076575L (no) 2008-03-18
US7968718B2 (en) 2011-06-28
EP1907389B1 (en) 2011-07-27

Similar Documents

Publication Publication Date Title
NO20076575L (no) Fremgangsmåte for fremstilling av triazol substituerte azaindoloksoeddikpiperazinderivater og nye saltformer derved fremstilt
HUE037560T2 (hu) Glikolipid-származékok, eljárás elõállításukra, szintézis-köztitermékeik, és eljárás a köztitermékek elõállítására
ZA200307450B (en) Process for the production of synthesis gas.
AU2003284371A8 (en) Improved ethanol production process
MXPA05009068A (es) Dihidro-pteridinonas, metodo para la produccion y uso del mismo en la forma de farmacos.
SG158848A1 (en) Method for producing annelated piperazin-2-one derivatives and intermediates of said method
MXPA05012362A (es) Yodopirazolilcarboxanilidas.
IL174469A0 (en) Rearranged pentanols, a method for the production thereof, and their use as antiphlogistics
MY143519A (en) Process for the production of ethers
GB0607249D0 (en) Process for the production of multipurpose energy sources and multipurpose energy sources produced by said process
MXNL04000051A (es) Proceso para la produccion de un inmunosupresor.
AU2002219127A1 (en) Process for the production of ceftifur sodium salt
TW200504066A (en) Crystal of intermediate for carbapenem synthesis
IL166374A0 (en) Novel process for producing imidazoÄ1,2-bÜpyridazine derivative
AU2003264365A1 (en) Process for producing oxycarbonyl-substituted piperazine derivative
AU9223601A (en) 5-phenylbenzylamine compounds, process for their production and intermediates for their synthesis
AU2002358557A1 (en) Improved method for the production of biphosphites
IL166793A0 (en) Process for producing indolopyrrolocarbazole derivative
TW200626555A (en) A process for the preparation of 1, 3, 5-trisubstituted pyrazoles via [3+2] cycloaddition
ATE266099T1 (de) Produktionsverfahren für biomasse
TW200740811A (en) Process for producing benzylamine derivatives
AU2003280976A1 (en) Process for producing 2,3,6-trialkyl-8-fluoro-4-quinoline derivative
HUP0402558A3 (en) Process for production of 3,3-dimethyl-2-formylcyclopropanecarboxylic acid derivatives
AU2003255148A1 (en) Process for producing 2-alkyl-3-aminothiophene derivative
AU2003238198A1 (en) Method for producing 4,6-dichloro-5-fluoropyrimidine