ATE462700T1 - Neue kristalline formen von ä2-ä1-(3,5- bistrifluormethylbenzyl)-5-pyridin-4-yl-1h-ä1,2 3üütriazol-4-ylü-pyridin-3-ylü-(2- chlorphenyl)methanon - Google Patents
Neue kristalline formen von ä2-ä1-(3,5- bistrifluormethylbenzyl)-5-pyridin-4-yl-1h-ä1,2 3üütriazol-4-ylü-pyridin-3-ylü-(2- chlorphenyl)methanonInfo
- Publication number
- ATE462700T1 ATE462700T1 AT04793893T AT04793893T ATE462700T1 AT E462700 T1 ATE462700 T1 AT E462700T1 AT 04793893 T AT04793893 T AT 04793893T AT 04793893 T AT04793893 T AT 04793893T AT E462700 T1 ATE462700 T1 AT E462700T1
- Authority
- AT
- Austria
- Prior art keywords
- ylü
- pyridine
- bistrifluormethylbenzyl
- chlorphenyl
- methanone
- Prior art date
Links
Classifications
-
- 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
- C07D401/14—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 three or more hetero rings
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/22—Anxiolytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
- A61P25/24—Antidepressants
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic 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
- C07D213/02—Heterocyclic 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
- C07D213/04—Heterocyclic 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
- C07D213/24—Heterocyclic 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
- C07D213/44—Radicals substituted by doubly-bound oxygen, sulfur, or nitrogen atoms, or by two such atoms singly-bound to the same carbon atom
- C07D213/46—Oxygen atoms
- C07D213/50—Ketonic radicals
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
Landscapes
- 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)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US51430003P | 2003-10-24 | 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 (1)
Publication Number | Publication Date |
---|---|
ATE462700T1 true ATE462700T1 (de) | 2010-04-15 |
Family
ID=34549327
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AT04793893T ATE462700T1 (de) | 2003-10-24 | 2004-10-12 | Neue kristalline formen von ä2-ä1-(3,5- bistrifluormethylbenzyl)-5-pyridin-4-yl-1h-ä1,2 3üütriazol-4-ylü-pyridin-3-ylü-(2- chlorphenyl)methanon |
Country Status (28)
Country | Link |
---|---|
US (1) | US7381826B2 (de) |
JP (1) | JP4959336B2 (de) |
KR (1) | KR100848407B1 (de) |
CN (1) | CN1863791B (de) |
AR (1) | AR046131A1 (de) |
AT (1) | ATE462700T1 (de) |
AU (1) | AU2004285855B8 (de) |
BR (1) | BRPI0415010B8 (de) |
CA (1) | CA2542140C (de) |
CL (2) | CL2009001310A1 (de) |
CR (1) | CR8353A (de) |
DE (1) | DE602004026333D1 (de) |
DK (1) | DK1675846T3 (de) |
EA (1) | EA008881B1 (de) |
EC (1) | ECSP066517A (de) |
ES (1) | ES2340772T3 (de) |
HR (1) | HRP20100207T1 (de) |
IL (1) | IL174926A0 (de) |
MA (1) | MA28329A1 (de) |
MY (1) | MY157375A (de) |
NO (1) | NO335090B1 (de) |
NZ (2) | NZ545917A (de) |
PE (1) | PE20050481A1 (de) |
PT (1) | PT1675846E (de) |
TW (1) | TW200524906A (de) |
UA (1) | UA82901C2 (de) |
WO (1) | WO2005042515A1 (de) |
ZA (1) | ZA200603234B (de) |
Families Citing this family (16)
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 |
MX2017011279A (es) * | 2015-03-04 | 2018-01-25 | Vanda Pharmaceuticals Inc | Metodo de tratamiento con tradipitant. |
WO2017031215A1 (en) * | 2015-08-17 | 2017-02-23 | Eli Lilly And Company | Process development of a pyridine-containing nk-1 receptor antagonist |
JP7347743B2 (ja) | 2017-09-13 | 2023-09-20 | 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アトピー性皮膚炎の改善された治療 |
EP3710000A1 (de) * | 2017-11-17 | 2020-09-23 | Vanda Pharmaceuticals Inc. | Verfahren zur behandlung von magen-darm-erkrankungen mit tradipitant |
BR112020024906A2 (pt) | 2018-06-08 | 2021-03-09 | Vanda Pharmaceuticals Inc. | Métodos para tratar um indivíduo que está sofrendo ou está em risco de sofrer uma consequência indesejada de uso de opioides e uma ânsia por um opioide, e, tradipitant para uso no tratamento de um indivíduo que está sofrendo ou está em risco de sofrer uma consequência indesejada de uso de opioides. |
WO2020069092A1 (en) | 2018-09-28 | 2020-04-02 | Vanda Pharmaceuticals Inc. | Use of tradipitant in motion sickness |
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 |
KR20220145844A (ko) | 2020-02-25 | 2022-10-31 | 반다 파마슈티칼즈, 인코퍼레이티드. | 트라디피탄트를 이용한 아토피 피부염의 개선된 치료 |
US20230145932A1 (en) | 2020-03-26 | 2023-05-11 | 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 |
EP4395778A1 (de) | 2021-08-31 | 2024-07-10 | Vanda Pharmaceuticals Inc. | Behandlung von infektionen der unteren atemwege mit tradipitant |
WO2024138040A1 (en) | 2022-12-21 | 2024-06-27 | Vanda Pharmaceuticals Inc. | Methods of treatment with tradipitant |
Family Cites Families (8)
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 |
KR20020030791A (ko) * | 1999-08-12 | 2002-04-25 | 버텍스 파마슈티칼스 인코포레이티드 | c-JUN N-말단 키나제(JNK) 및 기타의 단백질키나제 억제제 |
AU1343901A (en) * | 1999-10-29 | 2001-05-14 | 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 |
DE60318697T2 (de) * | 2002-04-26 | 2009-01-08 | Eli Lilly And Co., Indianapolis | Triazolderivate als tachykininrezeptor-antagonisten |
-
2004
- 2004-10-12 AT AT04793893T patent/ATE462700T1/de active
- 2004-10-12 PT PT04793893T patent/PT1675846E/pt unknown
- 2004-10-12 EA EA200600829A patent/EA008881B1/ru not_active IP Right Cessation
- 2004-10-12 AU AU2004285855A patent/AU2004285855B8/en active Active
- 2004-10-12 US US10/574,712 patent/US7381826B2/en active Active
- 2004-10-12 DK DK04793893.1T patent/DK1675846T3/da active
- 2004-10-12 KR KR1020067007751A patent/KR100848407B1/ko active IP Right Grant
- 2004-10-12 BR BRPI0415010A patent/BRPI0415010B8/pt active IP Right Grant
- 2004-10-12 CN CN2004800291393A patent/CN1863791B/zh active Active
- 2004-10-12 CA CA2542140A patent/CA2542140C/en active Active
- 2004-10-12 ES ES04793893T patent/ES2340772T3/es active Active
- 2004-10-12 JP JP2006536635A patent/JP4959336B2/ja active Active
- 2004-10-12 NZ NZ545917A patent/NZ545917A/en unknown
- 2004-10-12 NZ NZ580480A patent/NZ580480A/en unknown
- 2004-10-12 WO PCT/US2004/030914 patent/WO2005042515A1/en active Application Filing
- 2004-10-12 DE DE602004026333T patent/DE602004026333D1/de active Active
- 2004-10-20 PE PE2004001008A patent/PE20050481A1/es not_active Application Discontinuation
- 2004-10-20 AR ARP040103801A patent/AR046131A1/es not_active Application Discontinuation
- 2004-10-21 MY MYPI20044338A patent/MY157375A/en unknown
- 2004-10-22 TW TW093132097A patent/TW200524906A/zh unknown
- 2004-12-10 UA UAA200604473A patent/UA82901C2/uk unknown
-
2006
- 2006-04-11 IL IL174926A patent/IL174926A0/en unknown
- 2006-04-21 ZA ZA200603234A patent/ZA200603234B/en unknown
- 2006-04-21 CR CR8353A patent/CR8353A/es not_active Application Discontinuation
- 2006-04-21 EC EC2006006517A patent/ECSP066517A/es unknown
- 2006-05-22 MA MA29043A patent/MA28329A1/fr unknown
- 2006-05-24 NO NO20062371A patent/NO335090B1/no unknown
-
2009
- 2009-05-29 CL CL2009001310A patent/CL2009001310A1/es unknown
- 2009-05-29 CL CL2009001311A patent/CL2009001311A1/es unknown
-
2010
- 2010-04-13 HR HR20100207T patent/HRP20100207T1/hr unknown
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
ATE462700T1 (de) | Neue kristalline formen von ä2-ä1-(3,5- bistrifluormethylbenzyl)-5-pyridin-4-yl-1h-ä1,2 3üütriazol-4-ylü-pyridin-3-ylü-(2- chlorphenyl)methanon | |
PT1381363E (pt) | Derivados de imidazo-(1,2-a)-piridina como antagonistas mglur5 | |
DE602004019298D1 (de) | Polymorphe Formen von Rifaximin als Antibiotica | |
DK1515969T3 (da) | Spiroindolinpiperidinderivater | |
ATE525377T1 (de) | Imidazoä1,5-aüpyrazine als inhibitoren von tyrosinkinase | |
IS6561A (is) | Bensóamíð píperidín efnasambönd sem P-efnis mótlyf | |
ATE460407T1 (de) | Kristalline formen von duloxetin als freie base | |
DE50111292D1 (de) | Neue sulfonamid-substituierte pyrazolopyridinderivate | |
DE50202178D1 (de) | Neue sulfonat-substituierte pyrazolopyridinderivate | |
ATE305002T1 (de) | Substituierte 2-phenylaminoimidazolin-phenyl- ketonderivate als ip-antagonisten | |
NO20011436L (no) | 2,2,6,6-dietyl-dimetyl-1-alkoksy-piperidin-forbindelser og deres korresponderende 1-oksider | |
ATE292128T1 (de) | Piperidinderivate als neurokinin 1 antagonisten | |
DE60302137D1 (de) | Piperidinderivate | |
IS6704A (is) | Fenoxýbensýlamínafleiður sem valvísir serótónín endurupptöku hindrar | |
ATE500256T1 (de) | Neue kondensierte pyrrolocarbazole | |
ATE339405T1 (de) | Neue kristalline modifikation des anhydrates von boscalid | |
IS8007A (is) | 4-(2-fenýlsúlfanýl-fenýl)-1,2,3,6-tetrahýdrópýridín afleiður sem serótónín endurupptöku hindrar | |
ATE374183T1 (de) | Nk1-antagonisten | |
DE60222217D1 (de) | Tintenzusammensetzung zum Phasenaustausch | |
DE50100358D1 (de) | Neue N-Triazolylmethyl-Piperazinderivate als Neurokininrezeptor-Antagonisten | |
ATE320418T1 (de) | Substituierte benzo(b)azepin-2-on-verbindungen als schmerzmittel | |
DE60210058D1 (de) | Alkoxycarbonylamino-heteroaryl-carbonsäurederivate als ip-antagonisten | |
NO20042980L (no) | 3,4-dihydro-1H-isokinolin-2-yl-derivater | |
ATE299138T1 (de) | Mandelatsalze von substituierten tetrazyklischen tetrahydrofuranderivaten | |
ATE327226T1 (de) | Substituierte y-lactonverbindungen als nmda- antagonisten |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
UEP | Publication of translation of european patent specification |
Ref document number: 1675846 Country of ref document: EP |