DE60301569T2 - Bestimmte 1-(d-cyclopropylglycinyl)-4-(piperidin-4-yl)piperazin verbindungen als inhibitoren der serin protease factor xa - Google Patents

Bestimmte 1-(d-cyclopropylglycinyl)-4-(piperidin-4-yl)piperazin verbindungen als inhibitoren der serin protease factor xa Download PDF

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Publication number
DE60301569T2
DE60301569T2 DE60301569T DE60301569T DE60301569T2 DE 60301569 T2 DE60301569 T2 DE 60301569T2 DE 60301569 T DE60301569 T DE 60301569T DE 60301569 T DE60301569 T DE 60301569T DE 60301569 T2 DE60301569 T2 DE 60301569T2
Authority
DE
Germany
Prior art keywords
inhibitors
cyclopropylglycinyl
piperidin
certain
piperazine compounds
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 - Fee Related
Application number
DE60301569T
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German (de)
English (en)
Other versions
DE60301569D1 (de
Inventor
Robert Wiley
Lowell Engel
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.)
Eli Lilly and Co
Original Assignee
Eli Lilly and 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 Eli Lilly and Co filed Critical Eli Lilly and Co
Publication of DE60301569D1 publication Critical patent/DE60301569D1/de
Application granted granted Critical
Publication of DE60301569T2 publication Critical patent/DE60301569T2/de
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members 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
    • C07D211/56Nitrogen atoms
    • C07D211/58Nitrogen atoms attached in position 4
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P7/00Drugs for disorders of the blood or the extracellular fluid
    • A61P7/02Antithrombotic agents; Anticoagulants; Platelet aggregation inhibitors
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/42Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/44Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C235/52Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to carbon atoms of six-membered aromatic rings and singly-bound oxygen atoms bound to the same carbon skeleton with carbon atoms of carboxamide groups and singly-bound oxygen atoms bound to carbon atoms of the same non-condensed six-membered aromatic ring having the nitrogen atom of at least one of the carboxamide groups bound to an acyclic carbon atom of a hydrocarbon radical substituted by carboxyl groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C2601/00Systems containing only non-condensed rings
    • C07C2601/02Systems containing only non-condensed rings with a three-membered ring

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Diabetes (AREA)
  • Hematology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
DE60301569T 2002-04-01 2003-03-24 Bestimmte 1-(d-cyclopropylglycinyl)-4-(piperidin-4-yl)piperazin verbindungen als inhibitoren der serin protease factor xa Expired - Fee Related DE60301569T2 (de)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US36852302P 2002-04-01 2002-04-01
PCT/US2003/007794 WO2003084929A1 (en) 2002-04-01 2003-03-24 Certain 1-(d-cyclopropylglycinyl)-4-(piperidin-4-yl)piperazine compounds as inhibitors of the serine protease factor xa

Publications (2)

Publication Number Publication Date
DE60301569D1 DE60301569D1 (de) 2005-10-13
DE60301569T2 true DE60301569T2 (de) 2006-06-14

Family

ID=28791889

Family Applications (1)

Application Number Title Priority Date Filing Date
DE60301569T Expired - Fee Related DE60301569T2 (de) 2002-04-01 2003-03-24 Bestimmte 1-(d-cyclopropylglycinyl)-4-(piperidin-4-yl)piperazin verbindungen als inhibitoren der serin protease factor xa

Country Status (24)

Country Link
US (1) US7166606B2 (enExample)
EP (1) EP1492767B1 (enExample)
JP (1) JP2005531529A (enExample)
KR (1) KR20040094892A (enExample)
CN (1) CN1288135C (enExample)
AT (1) ATE303990T1 (enExample)
AU (1) AU2003218147A1 (enExample)
BR (1) BR0308870A (enExample)
CA (1) CA2478340A1 (enExample)
CR (1) CR7497A (enExample)
DE (1) DE60301569T2 (enExample)
DK (1) DK1492767T3 (enExample)
EA (1) EA007300B1 (enExample)
EC (1) ECSP045329A (enExample)
ES (1) ES2248737T3 (enExample)
HR (1) HRP20040900B1 (enExample)
IL (1) IL164018A0 (enExample)
MX (1) MXPA04009640A (enExample)
NO (1) NO20044688L (enExample)
NZ (1) NZ535402A (enExample)
PL (1) PL373066A1 (enExample)
UA (1) UA76849C2 (enExample)
WO (1) WO2003084929A1 (enExample)
ZA (1) ZA200407418B (enExample)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6834308B1 (en) 2000-02-17 2004-12-21 Audible Magic Corporation Method and apparatus for identifying media content presented on a media playing device
US7363278B2 (en) 2001-04-05 2008-04-22 Audible Magic Corporation Copyright detection and protection system and method
US8972481B2 (en) 2001-07-20 2015-03-03 Audible Magic, Inc. Playlist generation method and apparatus
DE102014108210A1 (de) 2014-06-11 2015-12-17 Dietrich Gulba Rodentizid
WO2018093716A1 (en) * 2016-11-18 2018-05-24 Merck Sharp & Dohme Corp. FACTOR XIIa INHIBITORS
EP4070658A1 (de) 2021-04-06 2022-10-12 BIORoxx GmbH Verwendung von blutgerinnungshemmenden verbindungen als rodentizide

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000077027A2 (en) 1999-06-14 2000-12-21 Tularik Limited Serine protease inhibitors
WO1999011657A1 (en) 1997-08-29 1999-03-11 Proteus Molecular Design Ltd. 1-amino-7-isoquinoline derivatives as serine protease inhibitors
JP2003502314A (ja) 1999-06-14 2003-01-21 イーライ・リリー・アンド・カンパニー 化合物
GB0030305D0 (en) 2000-12-13 2001-01-24 Lilly Co Eli Compounds
GB0030303D0 (en) 2000-12-13 2001-01-24 Lilly Co Eli Compounds
GB0030304D0 (en) * 2000-12-13 2001-01-24 Lilly Co Eli Compounds
GB0030306D0 (en) 2000-12-13 2001-01-24 Lilly Co Eli Compounds
TWI257389B (en) 2001-06-12 2006-07-01 Lilly Co Eli Pharmaceutical compound
DE60224805T2 (de) * 2001-07-26 2009-01-22 Eli Lilly And Co., Indianapolis 1-glycinyl-4-(1-methylpiperidin-4-yl)piperazine und -piperidine als faktor-xa-antagonisten

Also Published As

Publication number Publication date
US20050096328A1 (en) 2005-05-05
NO20044688L (no) 2004-10-29
BR0308870A (pt) 2005-01-04
WO2003084929A1 (en) 2003-10-16
ZA200407418B (en) 2005-09-15
US7166606B2 (en) 2007-01-23
MXPA04009640A (es) 2005-01-11
EA200401290A1 (ru) 2005-02-24
PL373066A1 (en) 2005-08-08
CR7497A (es) 2005-01-17
ES2248737T3 (es) 2006-03-16
HK1070363A1 (en) 2005-06-17
WO2003084929A8 (en) 2004-05-21
CN1642914A (zh) 2005-07-20
DK1492767T3 (da) 2005-11-28
EP1492767A1 (en) 2005-01-05
IL164018A0 (en) 2005-12-18
HRP20040900B1 (en) 2006-02-28
HRP20040900A2 (en) 2004-12-31
KR20040094892A (ko) 2004-11-10
DE60301569D1 (de) 2005-10-13
UA76849C2 (uk) 2006-09-15
EA007300B1 (ru) 2006-08-25
ATE303990T1 (de) 2005-09-15
ECSP045329A (es) 2004-11-26
NZ535402A (en) 2006-02-24
EP1492767B1 (en) 2005-09-07
AU2003218147A1 (en) 2003-10-20
CN1288135C (zh) 2006-12-06
JP2005531529A (ja) 2005-10-20
CA2478340A1 (en) 2003-10-16

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8364 No opposition during term of opposition
8339 Ceased/non-payment of the annual fee