PT1675846E - Novas formas cristalinas de {2-[1-(3,5-bis-trifluorometilbenzil)-5- iridin-4-il-1h-[1,2,3]triazol-4-il]-piridin-3-il}-(2-clorofenil)-metanona - Google Patents

Novas formas cristalinas de {2-[1-(3,5-bis-trifluorometilbenzil)-5- iridin-4-il-1h-[1,2,3]triazol-4-il]-piridin-3-il}-(2-clorofenil)-metanona Download PDF

Info

Publication number
PT1675846E
PT1675846E PT04793893T PT04793893T PT1675846E PT 1675846 E PT1675846 E PT 1675846E PT 04793893 T PT04793893 T PT 04793893T PT 04793893 T PT04793893 T PT 04793893T PT 1675846 E PT1675846 E PT 1675846E
Authority
PT
Portugal
Prior art keywords
pyridin
trifluoromethylbenzyl
methanone
triazol
chlorophenyl
Prior art date
Application number
PT04793893T
Other languages
English (en)
Inventor
Susan Marie Reutzel-Edens
Alfio Borghese
David Scott Coffey
Pamela Kaye Footman
Steven Wayne Pedersen
Shella Lenyonga Tameze
Carsten Weber
Carsten Timpe
Original Assignee
Lilly Co Eli
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 Lilly Co Eli filed Critical Lilly Co Eli
Publication of PT1675846E publication Critical patent/PT1675846E/pt

Links

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
    • C07D401/14Heterocyclic 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurosurgery (AREA)
  • Neurology (AREA)
  • Biomedical Technology (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Medicinal Preparation (AREA)
PT04793893T 2003-10-24 2004-10-12 Novas formas cristalinas de {2-[1-(3,5-bis-trifluorometilbenzil)-5- iridin-4-il-1h-[1,2,3]triazol-4-il]-piridin-3-il}-(2-clorofenil)-metanona PT1675846E (pt)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US51430003P 2003-10-24 2003-10-24

Publications (1)

Publication Number Publication Date
PT1675846E true PT1675846E (pt) 2010-04-20

Family

ID=34549327

Family Applications (1)

Application Number Title Priority Date Filing Date
PT04793893T PT1675846E (pt) 2003-10-24 2004-10-12 Novas formas cristalinas de {2-[1-(3,5-bis-trifluorometilbenzil)-5- iridin-4-il-1h-[1,2,3]triazol-4-il]-piridin-3-il}-(2-clorofenil)-metanona

Country Status (28)

Country Link
US (1) US7381826B2 (pt)
JP (1) JP4959336B2 (pt)
KR (1) KR100848407B1 (pt)
CN (1) CN1863791B (pt)
AR (1) AR046131A1 (pt)
AT (1) ATE462700T1 (pt)
AU (1) AU2004285855B8 (pt)
BR (1) BRPI0415010B8 (pt)
CA (1) CA2542140C (pt)
CL (2) CL2009001310A1 (pt)
CR (1) CR8353A (pt)
DE (1) DE602004026333D1 (pt)
DK (1) DK1675846T3 (pt)
EA (1) EA008881B1 (pt)
EC (1) ECSP066517A (pt)
ES (1) ES2340772T3 (pt)
HR (1) HRP20100207T1 (pt)
IL (1) IL174926A0 (pt)
MA (1) MA28329A1 (pt)
MY (1) MY157375A (pt)
NO (1) NO335090B1 (pt)
NZ (2) NZ545917A (pt)
PE (1) PE20050481A1 (pt)
PT (1) PT1675846E (pt)
TW (1) TW200524906A (pt)
UA (1) UA82901C2 (pt)
WO (1) WO2005042515A1 (pt)
ZA (1) ZA200603234B (pt)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX2009006636A (es) * 2006-12-20 2009-06-30 Lilly Co Eli Nuevos intermediarios y procesos utiles en la rpeparacion de {2-[1-(3,5-bis-trifluorometil-bencil)-5-piridin-4-il-1h-[1,2,3]tr iazol-4-il]-piridin-3-il}-(2-clorofenil)-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
AU2016226006B2 (en) 2015-03-04 2021-03-04 Vanda Pharmaceuticals Inc. Method of treatment with tradipitant
US10287287B2 (en) 2015-08-17 2019-05-14 Eli Lilly And Company Process development of a pyridine-containing NK-1 receptor antagonist
BR112020004964A2 (pt) 2017-09-13 2020-09-15 Vanda Pharmaceuticals Inc. método que consiste em administrar uma quantidade de tradipitant eficaz, aperfeiçoamento, método aperfeiçoado para tratar um paciente que sofre de prurido ou dermatite atópica com tradipitant, e, métodos para tratar um paciente com prurido ou dermatite atópica, para selecionar e para determinar uma dosagem de tradipitant eficaz, para determinar que um paciente tem probabilidade de responder ao tratamento de dermatite atópica com tradipitant e para identificar um paciente.
EP3710000A1 (en) * 2017-11-17 2020-09-23 Vanda Pharmaceuticals Inc. Method of treatment of gastrointestinal diseases with tradipitant
CN112218636A (zh) 2018-06-08 2021-01-12 万达制药公司 使用川地匹坦进行治疗的方法
JP7468964B2 (ja) * 2018-09-28 2024-04-16 バンダ・ファーマシューティカルズ・インコーポレイテッド 動揺病におけるトラジピタントの使用
US10821099B2 (en) 2018-09-28 2020-11-03 Vanda Pharmaceuticals Inc. Use of tradipitant in motion sickness
EP3890735A1 (en) * 2018-12-03 2021-10-13 Vanda Pharmaceuticals Inc. Method of treatment with tradipitant
EP4110335A1 (en) 2020-02-25 2023-01-04 Vanda Pharmaceuticals Inc. Improved treatment of atopic dermatitis with tradipitant
JP2023520369A (ja) 2020-03-26 2023-05-17 バンダ・ファーマシューティカルズ・インコーポレイテッド トラジピタントによる下気道感染症の治療
WO2023019084A1 (en) 2021-08-12 2023-02-16 Vanda Pharmaceuticals Inc. Treatment of gastric accommodation with tradipitant
EP4395778A1 (en) 2021-08-31 2024-07-10 Vanda Pharmaceuticals Inc. Treatment of lower respiratory tract infection with tradipitant
WO2024138040A1 (en) 2022-12-21 2024-06-27 Vanda Pharmaceuticals Inc. Methods 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
ATE333879T1 (de) * 1996-10-07 2006-08-15 Merck Sharp & Dohme Zns-penetrierende nk-1 rezeptorantagonisten als antidepressivum und / oder anxiolytikum
BR0013551A (pt) * 1999-08-13 2003-06-17 Vertex Pharma Inibidores de cinases n-terminal cjun (jnk) e outras cinases de proteìnas
CA2388202A1 (en) * 1999-10-29 2001-05-10 Merck & Co., Inc. Polymorphic form of a tachykinin receptor antagonist
US20020044971A1 (en) 2000-07-07 2002-04-18 Amidon Gordon L. Dissolution rate of poorly soluble drugs
PE20040600A1 (es) 2002-04-26 2004-09-15 Lilly Co Eli Derivados de triazol como antagonistas del receptor de taquicinina

Also Published As

Publication number Publication date
BRPI0415010A (pt) 2006-11-07
ATE462700T1 (de) 2010-04-15
NO335090B1 (no) 2014-09-08
WO2005042515A1 (en) 2005-05-12
ZA200603234B (en) 2007-07-25
BRPI0415010B8 (pt) 2021-05-25
NZ580480A (en) 2010-02-26
CL2009001310A1 (es) 2009-12-04
AR046131A1 (es) 2005-11-23
CA2542140A1 (en) 2005-05-12
CN1863791A (zh) 2006-11-15
AU2004285855B8 (en) 2011-04-28
DK1675846T3 (da) 2010-05-31
KR100848407B1 (ko) 2008-07-28
HRP20100207T1 (hr) 2010-05-31
AU2004285855B2 (en) 2010-12-23
KR20060061388A (ko) 2006-06-07
BRPI0415010B1 (pt) 2019-07-09
BRPI0415010A8 (pt) 2018-05-08
ES2340772T3 (es) 2010-06-09
JP2007509143A (ja) 2007-04-12
EA008881B1 (ru) 2007-08-31
EA200600829A1 (ru) 2006-08-25
US7381826B2 (en) 2008-06-03
NO20062371L (no) 2006-05-24
AU2004285855A1 (en) 2005-05-12
CA2542140C (en) 2012-05-29
IL174926A0 (en) 2006-08-20
CR8353A (es) 2006-06-06
MY157375A (en) 2016-06-15
JP4959336B2 (ja) 2012-06-20
MA28329A1 (fr) 2006-12-01
UA82901C2 (en) 2008-05-26
TW200524906A (en) 2005-08-01
NZ545917A (en) 2009-11-27
PE20050481A1 (es) 2005-09-20
CN1863791B (zh) 2011-12-07
DE602004026333D1 (de) 2010-05-12
US20070078166A1 (en) 2007-04-05
ECSP066517A (es) 2006-10-10
CL2009001311A1 (es) 2009-10-02

Similar Documents

Publication Publication Date Title
IL174926A0 (en) 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
MXPA03002297A (es) Compuestos de triazol utiles como inhibidores de proteina cinasa.
GB2415304B (en) Magnetic memory elements using 360 degree walls
IL173735A0 (en) Phenyl or pyridyl amide compounds as prostaglandin e2 antagonists
PL2121610T3 (pl) Nowy półprodukt oraz sposób przydatny w wytwarzaniu {2-[1-(3,5-bistrifluorometylo-benzylo)-5-pirydyn-4-ylo-1H-[1,2,3]triazol-4-ilo]-pirydyn-3-ylo}-(2-chlorofenylo)-metanonu
HK1080843A1 (en) (3z)-3-(3-hydro-isobenzofuran-1-ylidene)-1, 3-dihydro-2h-indol-2-ones as kinase inhibitors
PT1471065E (pt) Novos compostos de 1,2,4-triazole
HK1075839A1 (en) Crystalline 2,5-dione-3-(1-methyl-1h-indol-3yl)-4-1-(pyridin-2-ylmethyl)piperidin-4-yl-1h-pyrrole mono-hydrochloride
ZA200408423B (en) Novel tetrahydropyridine derivatives as renin inhibitors.
SI1311488T1 (sl) Substituirani imidazoli kot inhibitorji TAFIA
HRP20041048A2 (en) Polymorph of 4-[2-[1-(2-ethoxyethyl)-1H-benzimidazol-2-yl]-1-piperidinyl]ethyl]-alpha,alpha-dimethylbenzeneacetic acid
MXPA03004540A (es) Derivados de 4-(bifenilcarbonilamino) piperidina, composiciones que los comprenden y uso de los mismos.
ZA200500515B (en) Crystal modification II of 2-Ä2-(1-chloro-cyclopropyl)-3-(2-chlorophenyl)-2-hydroxy-propylÜ-2,4-dihydro-3h-1,2,4-triazole-3 thions
GB0123437D0 (en) Heterocyclic compounds
AU2003290500A1 (en) Encapsulation of ferroelectric capacitors
IL151566A0 (en) Stepwise alkylation of 5-substituted 1-(4-fluorophenyl)-1,3-dihydroisobenzofurans
PL1675846T3 (pl) Nowe krystaliczne postacie {2-[1-(3,5-bis-trifluoro-metylobenzylo)-5-pirydyn-4-ylo-1H-[1,2,3]triazol-4-ilo]-pirydyn-3-ylo}-(2-chlorofenylo)metanonu
EG22745A (en) 2-(3,5-Disbustituted-4-pyridyl)-4-(thienyl) thiazolyl or arylphenyl)1,30xazoline compounds
PL378329A1 (pl) Związki o aktywności hamującej wobec oligopeptydazy prolilowej
IL164377A0 (en) Methods of preparation of the 2-(7-chloro-1,8-naphthyridine-2yl)-3-(5-methyl-2-oxo-hexyl)-1-isoindolinone
ITTO20030762A1 (it) Metodo per controllare l'istante di funzionamento di una
SI1490363T1 (sl) Postopki za pripravo 2-(7-kloro-1,8-naftiridin-2-il) -3-(5-metil-2-okso-heksil)-1-izoindolinona
IL175791A0 (en) New 5,6-dihydropyrin-2-one compounds useful as inhibitors of thrombin
PL377494A1 (pl) Krystaliczny, niesolwatowany chlorowodorek 1-(4-(2-pipe-rydynyloetoksy) fenoksy)-2-(4-metanosulfonylofenylo)-6- hydroksynaftalenu
ZA200301704B (en) Triazole compounds useful as protein kinase inhibitors.