AU2004285855B8 - Novel crystalline forms of {2-[1-(3,5-bis-trifluoromethylbenzyl) -5 -pyridin-4-yl-1H-[1,2,3]triazol-4-yl]-pyridin-3-yl}-(2-chlorophenyl)-methanone - Google Patents

Novel crystalline forms of {2-[1-(3,5-bis-trifluoromethylbenzyl) -5 -pyridin-4-yl-1H-[1,2,3]triazol-4-yl]-pyridin-3-yl}-(2-chlorophenyl)-methanone Download PDF

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Publication number
AU2004285855B8
AU2004285855B8 AU2004285855A AU2004285855A AU2004285855B8 AU 2004285855 B8 AU2004285855 B8 AU 2004285855B8 AU 2004285855 A AU2004285855 A AU 2004285855A AU 2004285855 A AU2004285855 A AU 2004285855A AU 2004285855 B8 AU2004285855 B8 AU 2004285855B8
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AU
Australia
Prior art keywords
pyridin
chlorophenyl
methanone
triazol
bistrifluoromethylbenzyl
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Expired
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AU2004285855A
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English (en)
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AU2004285855A1 (en
AU2004285855B2 (en
Inventor
Alfio Borghese
David Scott Coffey
Pamela Kaye Footman
Steven Wayne Pedersen
Susan Marie Reutzel-Edens
Shella Lenyonga Tameze
Carsten Timpe
Carsten Weber
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Eli Lilly and Co
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Eli Lilly and Co
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Publication of AU2004285855A1 publication Critical patent/AU2004285855A1/en
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Publication of AU2004285855B2 publication Critical patent/AU2004285855B2/en
Publication of AU2004285855B8 publication Critical patent/AU2004285855B8/en
Anticipated expiration legal-status Critical
Expired legal-status Critical Current

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    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/22Anxiolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/24Heterocyclic 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
    • C07D213/44Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
    • C07D213/46Oxygen atoms
    • C07D213/50Ketonic radicals
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Psychiatry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Medicinal Preparation (AREA)
AU2004285855A 2003-10-24 2004-10-12 Novel crystalline forms of {2-[1-(3,5-bis-trifluoromethylbenzyl) -5 -pyridin-4-yl-1H-[1,2,3]triazol-4-yl]-pyridin-3-yl}-(2-chlorophenyl)-methanone Expired AU2004285855B8 (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US51430003P 2003-10-24 2003-10-24
US60/514,300 2003-10-24
PCT/US2004/030914 WO2005042515A1 (en) 2003-10-24 2004-10-12 Novel crystalline forms of {2-[1-(3,5-bis-trifluoromethylbenzyl)-5-pyridin-4-yl-1h-[1,2,3]triazol-4-yl]-pyridin-3-yl}-(2-chlorophenyl)-methanone

Publications (3)

Publication Number Publication Date
AU2004285855A1 AU2004285855A1 (en) 2005-05-12
AU2004285855B2 AU2004285855B2 (en) 2010-12-23
AU2004285855B8 true AU2004285855B8 (en) 2011-04-28

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AU2004285855A Expired AU2004285855B8 (en) 2003-10-24 2004-10-12 Novel crystalline forms of {2-[1-(3,5-bis-trifluoromethylbenzyl) -5 -pyridin-4-yl-1H-[1,2,3]triazol-4-yl]-pyridin-3-yl}-(2-chlorophenyl)-methanone

Country Status (28)

Country Link
US (1) US7381826B2 (enExample)
JP (1) JP4959336B2 (enExample)
KR (1) KR100848407B1 (enExample)
CN (1) CN1863791B (enExample)
AR (1) AR046131A1 (enExample)
AT (1) ATE462700T1 (enExample)
AU (1) AU2004285855B8 (enExample)
BR (1) BRPI0415010B8 (enExample)
CA (1) CA2542140C (enExample)
CL (2) CL2009001311A1 (enExample)
CR (1) CR8353A (enExample)
DE (1) DE602004026333D1 (enExample)
DK (1) DK1675846T3 (enExample)
EA (1) EA008881B1 (enExample)
EC (1) ECSP066517A (enExample)
ES (1) ES2340772T3 (enExample)
HR (1) HRP20100207T1 (enExample)
IL (1) IL174926A0 (enExample)
MA (1) MA28329A1 (enExample)
MY (1) MY157375A (enExample)
NO (1) NO335090B1 (enExample)
NZ (2) NZ545917A (enExample)
PE (1) PE20050481A1 (enExample)
PT (1) PT1675846E (enExample)
TW (1) TW200524906A (enExample)
UA (1) UA82901C2 (enExample)
WO (1) WO2005042515A1 (enExample)
ZA (1) ZA200603234B (enExample)

Families Citing this family (17)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI2121610T1 (sl) 2006-12-20 2014-08-29 Eli Lilly & Company Nove vmesne spojine in postopek, ki je uporaben pri pripravi (2-(1-(3,5-bistrifluorometil-benzil)-5-piridin-4-il-1h-(1,2,3)triazol- 4-il)-piridin-3-il)-(2-klorofenil)-metanona
WO2009075778A2 (en) * 2007-12-06 2009-06-18 The Regents Of The University Of California Nonpeptidic inhibitors of cruzain
US8080568B1 (en) * 2010-06-29 2011-12-20 Ewha University - Industry Collaboration Foundation 2-pyridyl substituted imidazoles as therapeutic ALK5 and/or ALK4 inhibitors
PT3265087T (pt) 2015-03-04 2020-10-15 Vanda Pharmaceuticals Inc Método de tratamento com tradipitant
US10287287B2 (en) 2015-08-17 2019-05-14 Eli Lilly And Company Process development of a pyridine-containing NK-1 receptor antagonist
US11549147B2 (en) 2017-09-13 2023-01-10 Vanda Pharmaceuticals Inc. Treatment of atopic dermatitis with tradipitant
SI3710000T1 (sl) * 2017-11-17 2025-07-31 Vanda Pharmaceuticals Inc. Tradipitant za uporabo pri zdravljenju gastropareze
CA3101210A1 (en) 2018-06-08 2019-12-12 Vanda Pharmaceuticals Inc. Method of treatment with tradipitant
MX2020008456A (es) * 2018-09-28 2020-09-25 Vanda Pharmaceuticals Inc Uso de tradipitant para tratar la cinetosis.
US10821099B2 (en) 2018-09-28 2020-11-03 Vanda Pharmaceuticals Inc. Use of tradipitant in motion sickness
US20220096449A1 (en) 2018-12-03 2022-03-31 Vanda Pharmaceuticals Inc. Method of treatment with tradipitant
EP4110335B1 (en) 2020-02-25 2025-10-15 Vanda Pharmaceuticals Inc. Improved treatment of atopic dermatitis with tradipitant
WO2021195205A1 (en) 2020-03-26 2021-09-30 Vanda Pharmaceuticals Inc. Treatment of lower respiratory tract infection with tradipitant
WO2023019084A1 (en) 2021-08-12 2023-02-16 Vanda Pharmaceuticals Inc. Treatment of gastric accommodation with tradipitant
US20240350469A1 (en) 2021-08-31 2024-10-24 Vanda Pharmaceuticals Inc. Treatment of lower respiratory tract infection with tradipitant
AU2023413130A1 (en) 2022-12-21 2025-06-05 Vanda Pharmaceuticals Inc. Methods of treatment with tradipitant
US20250255855A1 (en) 2024-02-09 2025-08-14 Vanda Pharmaceuticals Inc. Method of treatment with tradipitant

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20020099067A1 (en) * 1993-07-08 2002-07-25 Ulrich Posanski Pharmaceutical compositions for sparingly soluble therapeutic agents
GB9505492D0 (en) * 1995-03-18 1995-05-03 Merck Sharp & Dohme Therapeutic agents
GB9525296D0 (en) * 1995-12-11 1996-02-07 Merck Sharp & Dohme Therapeutic agents
DE69736390T2 (de) * 1996-10-07 2007-07-26 Merck Sharp & Dohme Ltd., Hoddesdon Zns-penetrierende nk-1 rezeptorantagonisten als antidepressivum und / oder anxiolytikum
HK1045507A1 (zh) * 1999-08-12 2002-11-29 Vertex Pharmaceuticals Incorporated C-jun n-末端激酶(jnk)及其他蛋白质激酶的抑制物
JP2003513095A (ja) * 1999-10-29 2003-04-08 メルク エンド カムパニー インコーポレーテッド タキキニン受容体アンタゴニストの多形
US20020044971A1 (en) * 2000-07-07 2002-04-18 Amidon Gordon L. Dissolution rate of poorly soluble drugs
DK1501809T3 (da) * 2002-04-26 2008-05-13 Lilly Co Eli Trizolderivater som tachykininreceptorantagonister

Also Published As

Publication number Publication date
NO20062371L (no) 2006-05-24
NZ580480A (en) 2010-02-26
NZ545917A (en) 2009-11-27
IL174926A0 (en) 2006-08-20
PT1675846E (pt) 2010-04-20
UA82901C2 (en) 2008-05-26
EA008881B1 (ru) 2007-08-31
MA28329A1 (fr) 2006-12-01
TW200524906A (en) 2005-08-01
DK1675846T3 (da) 2010-05-31
US20070078166A1 (en) 2007-04-05
EA200600829A1 (ru) 2006-08-25
PE20050481A1 (es) 2005-09-20
KR100848407B1 (ko) 2008-07-28
JP2007509143A (ja) 2007-04-12
CA2542140C (en) 2012-05-29
JP4959336B2 (ja) 2012-06-20
ES2340772T3 (es) 2010-06-09
ATE462700T1 (de) 2010-04-15
CN1863791B (zh) 2011-12-07
CL2009001311A1 (es) 2009-10-02
CR8353A (es) 2006-06-06
AR046131A1 (es) 2005-11-23
CA2542140A1 (en) 2005-05-12
AU2004285855A1 (en) 2005-05-12
WO2005042515A1 (en) 2005-05-12
MY157375A (en) 2016-06-15
ECSP066517A (es) 2006-10-10
CN1863791A (zh) 2006-11-15
CL2009001310A1 (es) 2009-12-04
US7381826B2 (en) 2008-06-03
DE602004026333D1 (de) 2010-05-12
ZA200603234B (en) 2007-07-25
AU2004285855B2 (en) 2010-12-23
NO335090B1 (no) 2014-09-08
BRPI0415010A (pt) 2006-11-07
BRPI0415010B1 (pt) 2019-07-09
HRP20100207T1 (hr) 2010-05-31
KR20060061388A (ko) 2006-06-07
BRPI0415010A8 (pt) 2018-05-08
BRPI0415010B8 (pt) 2021-05-25

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FGA Letters patent sealed or granted (standard patent)
TH Corrigenda

Free format text: IN VOL 24, NO 51, PAGE(S) 5988 UNDER THE HEADING APPLICATIONS ACCEPTED - NAME INDEX UNDER THE NAME ELI LILLY AND COMPANY, APPLICATION NO. 2004285855, UNDER INID (54) CORRECT THE TITLE TO READ NOVEL CRYSTALLINE FORMS OF {2-[1-(3,5-BIS-TRIFLUOROMETHYLBENZYL) -5 - PYRIDIN- 4-YL-1H-[1,2,3]TRIAZOL-4-YL]-PYRIDIN-3-YL}-(2-CHLOROPHENYL)-METHANONE

MK14 Patent ceased section 143(a) (annual fees not paid) or expired