DE69921358D1 - Stickstoffhaltige heterobicyclen als faktor-xa-hemmer - Google Patents

Stickstoffhaltige heterobicyclen als faktor-xa-hemmer

Info

Publication number
DE69921358D1
DE69921358D1 DE69921358T DE69921358T DE69921358D1 DE 69921358 D1 DE69921358 D1 DE 69921358D1 DE 69921358 T DE69921358 T DE 69921358T DE 69921358 T DE69921358 T DE 69921358T DE 69921358 D1 DE69921358 D1 DE 69921358D1
Authority
DE
Germany
Prior art keywords
heterobicycles
inhibitor
nitrogen
factor
nitrogen heterobicycles
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
DE69921358T
Other languages
English (en)
Other versions
DE69921358T2 (de
Inventor
M Fevig
Joseph Cacciola
G Clark
Yuk Lam
J Pinto
R Pruitt
A Rossi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Bristol Myers Squibb Pharma Co
Original Assignee
Bristol Myers Squibb Pharma 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=26811284&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=DE69921358(D1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Bristol Myers Squibb Pharma Co filed Critical Bristol Myers Squibb Pharma Co
Publication of DE69921358D1 publication Critical patent/DE69921358D1/de
Application granted granted Critical
Publication of DE69921358T2 publication Critical patent/DE69921358T2/de
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00—Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02—Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Vascular Medicine (AREA)
  • Urology & Nephrology (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
DE69921358T 1998-12-23 1999-12-17 Stickstoffhaltige heterobicyclen als faktor-xa-hemmer Expired - Lifetime DE69921358T2 (de)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US11362898P 1998-12-23 1998-12-23
US113628P 1998-12-23
US12763399P 1999-04-02 1999-04-02
US127633P 1999-04-02
PCT/US1999/030316 WO2000039131A1 (en) 1998-12-23 1999-12-17 Nitrogen containing heterobicycles as factor xa inhibitors

Publications (2)

Publication Number Publication Date
DE69921358D1 true DE69921358D1 (de) 2004-11-25
DE69921358T2 DE69921358T2 (de) 2006-03-09

Family

ID=26811284

Family Applications (1)

Application Number Title Priority Date Filing Date
DE69921358T Expired - Lifetime DE69921358T2 (de) 1998-12-23 1999-12-17 Stickstoffhaltige heterobicyclen als faktor-xa-hemmer

Country Status (26)

Country Link
US (2) US6413980B1 (de)
EP (1) EP1140941B1 (de)
JP (1) JP2002533465A (de)
KR (1) KR100628407B1 (de)
CN (1) CN100340559C (de)
AR (1) AR024242A1 (de)
AT (1) ATE280171T1 (de)
AU (1) AU759711B2 (de)
BR (1) BR9917080A (de)
CA (1) CA2349330C (de)
DE (1) DE69921358T2 (de)
DK (1) DK1140941T3 (de)
EA (1) EA004515B1 (de)
ES (1) ES2232202T3 (de)
HK (1) HK1052508B (de)
HR (1) HRP990396A2 (de)
IL (2) IL142959A0 (de)
MX (1) MXPA01006502A (de)
MY (1) MY138239A (de)
NO (1) NO319816B1 (de)
NZ (1) NZ511674A (de)
PT (1) PT1140941E (de)
SI (1) SI1140941T1 (de)
TW (1) TWI225862B (de)
WO (1) WO2000039131A1 (de)
ZA (1) ZA200103795B (de)

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WO2002000655A1 (en) * 2000-06-23 2002-01-03 Bristol-Myers Squibb Pharma Company 1 - (heteroaryl-phenyl) - condensed pyrazol derivatives as factor xa inhibitors
US20040077605A1 (en) * 2001-06-20 2004-04-22 Salvati Mark E. Fused heterocyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function
EP1854798A3 (de) 2000-09-19 2007-11-28 Bristol-Myers Squibb Company Kondensierte heterozyklische Succinimid-Verbindungen und Analoga daraus, Modulatoren der nuklearen Hormonrezeptorfunktion
US20040087548A1 (en) 2001-02-27 2004-05-06 Salvati Mark E. Fused cyclic succinimide compounds and analogs thereof, modulators of nuclear hormone receptor function
US6960595B2 (en) * 2001-03-23 2005-11-01 Bristol-Myers Squibb Pharma Company 5-6 to 5-7 Heterobicycles as factor Xa inhibitors
WO2002085356A1 (en) * 2001-04-18 2002-10-31 Bristol-Myers Squibb Company 1, 4, 5, 6-tetrahydropyrazolo-[3, 4-c]-pyrid in-7-ones as factor xa inhibitors
EP1379244A4 (de) 2001-04-18 2006-03-15 Bristol Myers Squibb Co 1,4,5,6-tetrahydropyrazolo- 3,4-c]-pyridin-7-one als faktor xa hemmer
US6878710B2 (en) * 2001-05-22 2005-04-12 Bristol-Myers Squibb Pharma Company Bicyclic inhibitors of factor Xa
UA78232C2 (uk) 2001-09-21 2007-03-15 Брістол-Майерс Сквібб Компані Лактамвмісні сполуки та їх похідні як інгібітори фактора ха
TWI320039B (en) 2001-09-21 2010-02-01 Lactam-containing compounds and derivatives thereof as factor xa inhibitors
TW200302225A (en) 2001-12-04 2003-08-01 Bristol Myers Squibb Co Substituted amino methyl factor Xa inhibitors
AU2002350217A1 (en) * 2001-12-04 2003-06-17 Bristol-Myers Squibb Company Glycinamides as factor xa inhibitors
TW200738672A (en) * 2001-12-10 2007-10-16 Bristol Myers Squibb Co Intermediated for the preparation of 4,5-dihydro-pyrazolo [3,4-c] pyrid-2-ones
ES2310622T3 (es) * 2001-12-19 2009-01-16 Bristol-Myers Squibb Company Compuestos heterociclicos condensados y analogos de los mismos, moduladores de la funcion de los receptores nucleares de hormonas.
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US7312214B2 (en) 2002-05-10 2007-12-25 Bristol-Myers Squibb Company 1, 1-disubstituted cycloalkyl derivatives as factor Xa inhibitors
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EP1479678A1 (de) * 2003-05-19 2004-11-24 Aventis Pharma Deutschland GmbH Pyrazolderivate als Faktor-Xa-Inhibitoren
US7135469B2 (en) * 2003-03-18 2006-11-14 Bristol Myers Squibb, Co. Linear chain substituted monocyclic and bicyclic derivatives as factor Xa inhibitors
US7122557B2 (en) * 2003-03-18 2006-10-17 Bristol-Myers Squibb Company Sulfonyl-amidino-containing and tetrahydropyrimidino-containing compounds as factor Xa inhibitors
EP1479675A1 (de) 2003-05-19 2004-11-24 Aventis Pharma Deutschland GmbH Indazolderivate als Faktor Xa-Inhibitoren
ZA200508300B (en) * 2003-05-20 2007-03-28 Transtech Pharma Inc RAGE antagonists as agents to reverse amyloidosis and diseases associated therewith
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CN104109165A (zh) * 2013-04-19 2014-10-22 四川海思科制药有限公司 4,5-二氢-吡唑并[3,4-c]吡啶-2-酮衍生物、其制备方法以及应用
CN103992310B (zh) * 2013-05-14 2016-07-06 中国医学科学院医药生物技术研究所 一组取代苯并杂环胺衍生物及其制备方法和作为impdh抑制剂的相关应用
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CN105745212B (zh) * 2013-12-06 2017-09-12 四川海思科制药有限公司 取代的4,5‑二氢吡唑并[3,4‑c]吡啶‑2‑酮的螺环衍生物及应用
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WO2015176625A1 (zh) * 2014-05-22 2015-11-26 南京明德新药研发股份有限公司 作为凝血因子Xa抑制剂的酰肼类化合物
CN105085515B (zh) * 2014-05-22 2019-02-01 华北制药股份有限公司 作为凝血因子Xa抑制剂的酰肼类化合物
CN105384739B (zh) * 2014-09-02 2020-03-20 石药集团中奇制药技术（石家庄）有限公司 吡唑并[3,4-c]吡啶类衍生物
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CN104311557B (zh) * 2014-09-19 2016-01-06 广东东阳光药业有限公司 含有二酮取代基的吡唑并哌啶酮类化合物及其组合物及用途
CN104277039B (zh) * 2014-09-19 2016-06-01 广东东阳光药业有限公司 含有取代丁炔基的吡唑并哌啶酮类化合物及其组合物及用途
CN104277037B (zh) * 2014-09-19 2015-12-09 广东东阳光药业有限公司 含有螺环的吡唑并哌啶酮类化合物及其组合物及用途
CN104311575B (zh) * 2014-09-19 2016-04-20 广东东阳光药业有限公司 含有稠环的吡唑并哌啶酮类化合物及其组合物及用途
CN104311555B (zh) * 2014-09-19 2016-04-20 广东东阳光药业有限公司 吡唑并哌啶酮类化合物及其组合物及用途
CN104311574B (zh) * 2014-09-19 2016-04-20 广东东阳光药业有限公司 含有噻唑的吡唑并哌啶酮类化合物及其组合物及用途
CN104311556B (zh) * 2014-09-19 2016-06-01 广东东阳光药业有限公司 含有环氧烷基取代基的吡唑并哌啶酮类化合物及其组合物及用途
CN104530029B (zh) * 2014-12-09 2017-04-12 广东东阳光药业有限公司 作为Xa因子抑制剂的杂环化合物及其使用方法和用途
CN104513239B (zh) * 2014-12-10 2017-08-22 沈阳药科大学 吡唑并[3,4‑c]吡啶‑7‑酮类化合物及其应用
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CN107235986B (zh) * 2017-05-27 2019-04-12 华南师范大学 一种合成氮氧杂桥联唑啉化合物的方法
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AU2019339777B2 (en) 2018-09-12 2022-09-01 Novartis Ag Antiviral pyridopyrazinedione compounds
KR102128509B1 (ko) * 2018-12-19 2020-07-01 한국과학기술연구원 말단 아민기에 아릴 또는 헤테로아릴기가 치환된 신규한 히드라존 유도체 및 이의 용도
KR20220070005A (ko) 2019-09-26 2022-05-27 노파르티스 아게 항바이러스성 피라졸로피리디논 화합물
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Also Published As

Publication number Publication date
MXPA01006502A (es) 2002-04-08
IL142959A0 (en) 2002-04-21
AU2371700A (en) 2000-07-31
US6413980B1 (en) 2002-07-02
PT1140941E (pt) 2005-02-28
CN1391575A (zh) 2003-01-15
US6673810B2 (en) 2004-01-06
EP1140941B1 (de) 2004-10-20
HK1052508B (zh) 2008-08-01
AU759711B2 (en) 2003-04-17
EA004515B1 (ru) 2004-04-29
US20030004167A1 (en) 2003-01-02
CA2349330A1 (en) 2000-07-06
ZA200103795B (en) 2002-08-12
HRP990396A2 (en) 2000-08-31
CN100340559C (zh) 2007-10-03
SI1140941T1 (en) 2005-04-30
NZ511674A (en) 2003-11-28
EA200100688A1 (ru) 2001-12-24
JP2002533465A (ja) 2002-10-08
WO2000039131A1 (en) 2000-07-06
IL142959A (en) 2010-05-31
NO20013072D0 (no) 2001-06-20
NO20013072L (no) 2001-06-20
EP1140941A1 (de) 2001-10-10
HK1052508A1 (en) 2003-09-19
CA2349330C (en) 2009-09-29
MY138239A (en) 2009-05-29
TWI225862B (en) 2005-01-01
ES2232202T3 (es) 2005-05-16
DK1140941T3 (da) 2005-02-14
KR20010092754A (ko) 2001-10-26
AR024242A1 (es) 2002-09-25
BR9917080A (pt) 2002-03-12
NO319816B1 (no) 2005-09-19
ATE280171T1 (de) 2004-11-15
KR100628407B1 (ko) 2006-09-26
DE69921358T2 (de) 2006-03-09

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