NO20045064L - Indol-, azaindol- og beslektede heterocykliske 4-alkenyl-piperidin-amider - Google Patents

Indol-, azaindol- og beslektede heterocykliske 4-alkenyl-piperidin-amider

Info

Publication number
NO20045064L
NO20045064L NO20045064A NO20045064A NO20045064L NO 20045064 L NO20045064 L NO 20045064L NO 20045064 A NO20045064 A NO 20045064A NO 20045064 A NO20045064 A NO 20045064A NO 20045064 L NO20045064 L NO 20045064L
Authority
NO
Norway
Prior art keywords
azaindole
indole
alkenyl
related heterocyclic
piperidine amides
Prior art date
Application number
NO20045064A
Other languages
English (en)
Other versions
NO329691B1 (no
Inventor
Carol Bachand
Edward H Ruediger
John F Kadow
Nicholas A Meanwell
Tao Wang
Zhongxing Zhang
Kap-Sun Yeung
Zhiwei Yin
Zhilei Qiu
Daniel H Deon
Clint A James
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=32312411&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=NO20045064(L) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bristol Myers Squibb Co filed Critical Bristol Myers Squibb Co
Publication of NO20045064L publication Critical patent/NO20045064L/no
Publication of NO329691B1 publication Critical patent/NO329691B1/no

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • 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
    • A61K31/4353—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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/437—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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Virology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • General Health & Medical Sciences (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)
NO20045064A 2002-05-28 2004-11-22 Indol-, azaindol- og beslektede heterocykliske 4-alkenyl-piperidinamider, farmasøytiske preparater omfattende slike samt anvendelse av slike for fremstilling av farmasøytiske preparater for behandling av sykdom NO329691B1 (no)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US38350902P 2002-05-28 2002-05-28
PCT/US2003/013324 WO2004043337A2 (en) 2002-05-28 2003-04-30 Indole, azaindole and related heterocyclic 4-alkenyl piperidine amides

Publications (2)

Publication Number Publication Date
NO20045064L true NO20045064L (no) 2005-02-23
NO329691B1 NO329691B1 (no) 2010-11-29

Family

ID=32312411

Family Applications (1)

Application Number Title Priority Date Filing Date
NO20045064A NO329691B1 (no) 2002-05-28 2004-11-22 Indol-, azaindol- og beslektede heterocykliske 4-alkenyl-piperidinamider, farmasøytiske preparater omfattende slike samt anvendelse av slike for fremstilling av farmasøytiske preparater for behandling av sykdom

Country Status (31)

Country Link
US (1) US20040063744A1 (no)
EP (1) EP1513832B1 (no)
JP (1) JP4446889B2 (no)
KR (1) KR101001811B1 (no)
CN (1) CN100528866C (no)
AR (1) AR040230A1 (no)
AU (1) AU2003301958B2 (no)
BR (2) BR0311541A (no)
CA (1) CA2487542C (no)
CL (1) CL2003001087A1 (no)
CO (1) CO5631440A2 (no)
DK (1) DK1513832T3 (no)
ES (1) ES2460728T3 (no)
GE (1) GEP20074152B (no)
HR (1) HRP20041137B1 (no)
IL (1) IL165200A (no)
IS (1) IS2945B (no)
MX (1) MXPA04011670A (no)
MY (1) MY139058A (no)
NO (1) NO329691B1 (no)
NZ (1) NZ536661A (no)
PE (1) PE20040526A1 (no)
PL (1) PL216388B1 (no)
PT (1) PT1513832E (no)
RS (1) RS53021B (no)
RU (1) RU2323934C2 (no)
SI (1) SI1513832T1 (no)
TW (1) TWI310381B (no)
UA (1) UA79470C2 (no)
WO (1) WO2004043337A2 (no)
ZA (1) ZA200409504B (no)

Families Citing this family (34)

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US6476034B2 (en) * 2000-02-22 2002-11-05 Bristol-Myers Squibb Company Antiviral azaindole derivatives
US20040110785A1 (en) * 2001-02-02 2004-06-10 Tao Wang Composition and antiviral activity of substituted azaindoleoxoacetic piperazine derivatives
US20050075364A1 (en) * 2003-07-01 2005-04-07 Kap-Sun Yeung Indole, azaindole and related heterocyclic N-substituted piperazine derivatives
US20050124623A1 (en) 2003-11-26 2005-06-09 Bender John A. Diazaindole-dicarbonyl-piperazinyl antiviral agents
US7087610B2 (en) * 2004-06-03 2006-08-08 Bristol-Myers Squibb Company Benzothiazole antiviral agents
PE20060430A1 (es) 2004-06-09 2006-05-25 Glaxo Group Ltd Derivados de pirrolopiridina como moduladores de los receptores cannabinoides
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
US20060100209A1 (en) * 2004-11-09 2006-05-11 Chong-Hui Gu Formulations 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
JP2009504587A (ja) * 2005-08-09 2009-02-05 グラクソ グループ リミテッド ナンナビノイド受容体リガンドとしてのイミダゾピリジン誘導体
US7851476B2 (en) * 2005-12-14 2010-12-14 Bristol-Myers Squibb Company Crystalline forms of 1-benzoyl-4-[2-[4-methoxy-7-(3-methyl-1H-1,2,4-triazol-1-YL)-1-[(phosphonooxy)methyl]-1H-pyrrolo[2,3-C]pyridin-3-YL]-1,2-dioxoethyl]-piperazine
US7807671B2 (en) 2006-04-25 2010-10-05 Bristol-Myers Squibb Company Diketo-piperazine and piperidine derivatives as antiviral agents
US7572810B2 (en) * 2006-06-08 2009-08-11 Bristol-Myers Squibb Company Alkene piperidine derivatives as antiviral agents
US7504399B2 (en) * 2006-06-08 2009-03-17 Bristol-Meyers Squibb Company Piperazine enamines as antiviral agents
JP5615700B2 (ja) * 2007-05-25 2014-10-29 アボット ゲーエムベーハー ウント カンパニー カーゲー 代謝型グルタミン酸受容体２（ｍｇｌｕ２受容体）の陽性調節剤としての複素環化合物
WO2009011912A1 (en) * 2007-07-18 2009-01-22 Bristol-Myers Squibb Company A composition for treating hiv comprising virus-like particles
JP5433690B2 (ja) * 2008-06-25 2014-03-05 ブリストル−マイヤーズ スクイブ カンパニー 抗−ｈｉｖ薬としてのジケト縮合アゾロピペリジンおよびアゾロピペラジン
US8242124B2 (en) * 2008-06-25 2012-08-14 Bristol-Myers Squibb Company Diketopiperidine derivatives as HIV attachment inhibitors
DK2323633T3 (da) * 2008-09-04 2012-07-09 Bristol Myers Squibb Co Stabil, farmaceutisk sammensætning til optimeret indgivelse af en hiv-bindingshæmmer
EP2400845B1 (en) 2009-02-27 2017-02-22 Siga Technologies, Inc. Thienopyridine derivatives for the treatment and prevention of dengue virus infections
US8895551B2 (en) 2009-04-02 2014-11-25 Shionogi & Co., Ltd. Acrylamide compounds and the use thereof
EP2308866A1 (de) 2009-10-09 2011-04-13 Bayer CropScience AG Phenylpyri(mi)dinylpyrazole und ihre Verwendung als Fungizide
US8450361B2 (en) * 2010-08-06 2013-05-28 Bristol-Myers Squibb Company Substituted indole and azaindole oxoacetyl piperazinamide derivatives
WO2012075235A1 (en) 2010-12-02 2012-06-07 Bristol-Myers Squibb Company Alkyl amides as hiv attachment inhibitors
EP2696937B1 (en) 2011-04-12 2017-05-17 VIIV Healthcare UK (No.5) Limited Thioamide, amidoxime and amidrazone derivatives as hiv attachment inhibitors
US8835454B2 (en) 2011-08-29 2014-09-16 Bristol-Myers Squibb Company Fused bicyclic diamine derivatives as HIV attachment inhibitors
ES2609579T3 (es) 2011-08-29 2017-04-21 VIIV Healthcare UK (No.5) Limited Derivados espiro de diamina bicíclica como inhibidores de la unión del VIH
CN104080785B (zh) * 2012-02-08 2016-08-31 百时美施贵宝公司 用于制备hiv附着抑制剂哌嗪前药化合物的方法
WO2013138436A1 (en) 2012-03-14 2013-09-19 Bristol-Myers Squibb Company Cyclolic hydrazine derivatives as hiv attachment inhibitors
EP2895471B1 (en) * 2012-08-09 2016-11-23 VIIV Healthcare UK (No.5) Limited Piperidine amide derivatives as hiv attachment inhibitors
WO2014025852A1 (en) * 2012-08-09 2014-02-13 Bristol-Myers Squibb Company Tricyclic alkene derivatives as hiv attachment inhibitors
WO2017112576A1 (en) * 2015-12-21 2017-06-29 Dow Global Technologies Llc Methods for external base-free suzuki couplings
CN108059611A (zh) * 2018-01-22 2018-05-22 济南舜景医药科技有限公司 一种用于治疗心率不齐药物中间体的合成方法
CN109053575A (zh) * 2018-08-24 2018-12-21 遵义医学院 3-环丙基-1-甲基-1h-吡唑-4-甲醛的制备工艺

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US5023265A (en) * 1990-06-01 1991-06-11 Schering Corporation Substituted 1-H-pyrrolopyridine-3-carboxamides
US5124327A (en) * 1991-09-06 1992-06-23 Merck & Co., Inc. HIV reverse transcriptase
US5424329A (en) * 1993-08-18 1995-06-13 Warner-Lambert Company Indole-2-carboxamides as inhibitors of cell adhesion
TW429256B (en) * 1995-12-27 2001-04-11 Janssen Pharmaceutica Nv 1-(1,2-disubstituted piperidinyl)-4-(benzimidazolyl- and imidazopyridinyl)-piperidine derivatives
WO1998028292A1 (en) * 1996-12-23 1998-07-02 Smithkline Beecham Corporation Novel piperidine containing compounds
US6469006B1 (en) * 1999-06-15 2002-10-22 Bristol-Myers Squibb Company Antiviral indoleoxoacetyl piperazine derivatives
US6476034B2 (en) * 2000-02-22 2002-11-05 Bristol-Myers Squibb Company Antiviral azaindole derivatives
US20020061892A1 (en) * 2000-02-22 2002-05-23 Tao Wang Antiviral azaindole derivatives
US6573262B2 (en) * 2000-07-10 2003-06-03 Bristol-Myers Sqibb Company Composition and antiviral activity of substituted indoleoxoacetic piperazine derivatives

Also Published As

Publication number Publication date
IL165200A (en) 2011-01-31
KR20050013558A (ko) 2005-02-04
CO5631440A2 (es) 2006-04-28
US20040063744A1 (en) 2004-04-01
EP1513832A4 (en) 2010-03-10
AU2003301958B2 (en) 2009-10-01
CA2487542C (en) 2011-09-27
AU2003301958A1 (en) 2004-06-03
ES2460728T3 (es) 2014-05-14
IS2945B (is) 2016-05-15
UA79470C2 (en) 2007-06-25
TWI310381B (en) 2009-06-01
ZA200409504B (en) 2006-05-31
CL2003001087A1 (es) 2005-02-11
PL373603A1 (en) 2005-09-05
WO2004043337A2 (en) 2004-05-27
WO2004043337A3 (en) 2004-11-11
MY139058A (en) 2009-08-28
BR0311541A (pt) 2006-06-06
RU2323934C2 (ru) 2008-05-10
PL216388B1 (pl) 2014-03-31
SI1513832T1 (sl) 2014-04-30
RS53021B (en) 2014-04-30
GEP20074152B (en) 2007-07-10
IS7546A (is) 2004-11-22
TW200406397A (en) 2004-05-01
NZ536661A (en) 2007-12-21
PE20040526A1 (es) 2004-08-28
EP1513832B1 (en) 2014-03-05
NO329691B1 (no) 2010-11-29
HRP20041137A2 (en) 2005-06-30
CN100528866C (zh) 2009-08-19
CA2487542A1 (en) 2004-05-27
IL165200A0 (en) 2005-12-18
PT1513832E (pt) 2014-05-22
JP2006507326A (ja) 2006-03-02
MXPA04011670A (es) 2005-03-07
AR040230A1 (es) 2005-03-23
DK1513832T3 (da) 2014-05-26
RS101304A (sr) 2006-10-27
BRPI0311541B1 (pt) 2018-04-24
KR101001811B1 (ko) 2010-12-15
JP4446889B2 (ja) 2010-04-07
CN1671697A (zh) 2005-09-21
RU2004138565A (ru) 2005-07-20
EP1513832A2 (en) 2005-03-16
HRP20041137B1 (hr) 2014-11-21

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Legal Events

Date Code Title Description
CHAD Change of the owner's name or address (par. 44 patent law, par. patentforskriften)

Owner name: VIIV HEALTHCARE UK (NO. 5) LIMITED, GB

MM1K Lapsed by not paying the annual fees