CL2009001311A1 - Procedimiento para preparar {2-[1-(3,5-bistrifluorometilbencil)-5-piridin-4-il-1h-[1,2,3]triazol-4-il]-piridin-3-il}-(2-clorofenil)metanona a partir de (2-clorofenil)-[2-(2-hidroxi-2-piridin-4-ilvinil)piridin-3-il]metanona y 1-azidometil-3,5-bistrifluorometilbenceno en presencia de una base y un disolvente (div.sol.2680-04). - Google Patents
Procedimiento para preparar {2-[1-(3,5-bistrifluorometilbencil)-5-piridin-4-il-1h-[1,2,3]triazol-4-il]-piridin-3-il}-(2-clorofenil)metanona a partir de (2-clorofenil)-[2-(2-hidroxi-2-piridin-4-ilvinil)piridin-3-il]metanona y 1-azidometil-3,5-bistrifluorometilbenceno en presencia de una base y un disolvente (div.sol.2680-04).Info
- Publication number
- CL2009001311A1 CL2009001311A1 CL2009001311A CL2009001311A CL2009001311A1 CL 2009001311 A1 CL2009001311 A1 CL 2009001311A1 CL 2009001311 A CL2009001311 A CL 2009001311A CL 2009001311 A CL2009001311 A CL 2009001311A CL 2009001311 A1 CL2009001311 A1 CL 2009001311A1
- Authority
- CL
- Chile
- Prior art keywords
- pyridin
- methanone
- chlorophenyl
- bistrifluoromethylbenzyl
- bistrifluoromethylbenzene
- 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)
- 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)
Abstract
Procedimiento para preparar {2-[1-(3,5-bistrifluorometilbencil)-5-piridin-4-il-1h-[1,2,3]triazol-4-il]-piridin-3-il}-(2-clorofenil)metanona a partir de (2-clorofenil)-[2-(2-hidroxi-2-piridin-4-ilvinil)piridin-3-il]metanona y 1-azidometil-3,5-bistrifluorometilbenceno en presencia de una base y un disolvente (Div. Sol. 2680-04).
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US51430003P | 2003-10-24 | 2003-10-24 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CL2009001311A1 true CL2009001311A1 (es) | 2009-10-02 |
Family
ID=34549327
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2009001310A CL2009001310A1 (es) | 2003-10-24 | 2009-05-29 | Compuesto intermediario (2-clorofenil)-[2-(2-hidroxi-2-piridin-4-ilvinil)piridin-3-il]metanona o una sal del mismo en lapreparacion del compuesto {2-[1-(3,5-bistrifluorometilbencil)-5-piridin-4-il-1h-[1,2,3]triazol-4-il]piridin-3-il}-(2-cloofenil)metanona (div. sol. 2680-04). |
| CL2009001311A CL2009001311A1 (es) | 2003-10-24 | 2009-05-29 | Procedimiento para preparar {2-[1-(3,5-bistrifluorometilbencil)-5-piridin-4-il-1h-[1,2,3]triazol-4-il]-piridin-3-il}-(2-clorofenil)metanona a partir de (2-clorofenil)-[2-(2-hidroxi-2-piridin-4-ilvinil)piridin-3-il]metanona y 1-azidometil-3,5-bistrifluorometilbenceno en presencia de una base y un disolvente (div.sol.2680-04). |
Family Applications Before (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CL2009001310A CL2009001310A1 (es) | 2003-10-24 | 2009-05-29 | Compuesto intermediario (2-clorofenil)-[2-(2-hidroxi-2-piridin-4-ilvinil)piridin-3-il]metanona o una sal del mismo en lapreparacion del compuesto {2-[1-(3,5-bistrifluorometilbencil)-5-piridin-4-il-1h-[1,2,3]triazol-4-il]piridin-3-il}-(2-cloofenil)metanona (div. sol. 2680-04). |
Country Status (28)
| Country | Link |
|---|---|
| US (1) | US7381826B2 (es) |
| JP (1) | JP4959336B2 (es) |
| KR (1) | KR100848407B1 (es) |
| CN (1) | CN1863791B (es) |
| AR (1) | AR046131A1 (es) |
| AT (1) | ATE462700T1 (es) |
| AU (1) | AU2004285855B8 (es) |
| BR (1) | BRPI0415010B8 (es) |
| CA (1) | CA2542140C (es) |
| CL (2) | CL2009001310A1 (es) |
| CR (1) | CR8353A (es) |
| DE (1) | DE602004026333D1 (es) |
| DK (1) | DK1675846T3 (es) |
| EA (1) | EA008881B1 (es) |
| EC (1) | ECSP066517A (es) |
| ES (1) | ES2340772T3 (es) |
| HR (1) | HRP20100207T1 (es) |
| IL (1) | IL174926A0 (es) |
| MA (1) | MA28329A1 (es) |
| MY (1) | MY157375A (es) |
| NO (1) | NO335090B1 (es) |
| NZ (2) | NZ580480A (es) |
| PE (1) | PE20050481A1 (es) |
| PT (1) | PT1675846E (es) |
| TW (1) | TW200524906A (es) |
| UA (1) | UA82901C2 (es) |
| WO (1) | WO2005042515A1 (es) |
| ZA (1) | ZA200603234B (es) |
Families Citing this family (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP5443168B2 (ja) * | 2006-12-20 | 2014-03-19 | イーライ リリー アンド カンパニー | ｛２−［１−（３，５−ビス−トリフルオロメチル−ベンジル）−５−ピリジン−４−イル−１ｈ−［１，２，３］トリアゾール−４−イル］−ピリジン−３−イル｝−（２−クロロフェニル）−メタノンの調製において有用な新規の中間体及び方法 |
| 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 |
| CA3213864A1 (en) * | 2015-03-04 | 2016-09-09 | Vanda Pharmaceuticals Inc. | Dosing regimen of tradipitant |
| US10287287B2 (en) | 2015-08-17 | 2019-05-14 | Eli Lilly And Company | Process development of a pyridine-containing NK-1 receptor antagonist |
| CN111093671A (zh) | 2017-09-13 | 2020-05-01 | 万达制药公司 | 以托吡坦对特应性皮炎的改进治疗 |
| AU2018367623B2 (en) * | 2017-11-17 | 2024-03-28 | Vanda Pharmaceuticals Inc. | Method of treatment of gastrointestinal diseases with tradipitant |
| US20210228555A1 (en) | 2018-06-08 | 2021-07-29 | Vanda Pharmaceuticals Inc. | Method of treatment with tradipitant |
| BR112020015484A2 (pt) * | 2018-09-28 | 2021-04-27 | Vanda Pharmaceuticals Inc. | métodos para tratamento de um sujeito prestes a se envolver em uma atividade que implica em movimento indutor de enjoo e de um sujeito com enjoo de movimento ou pelo menos um sintoma de enjoo de movimento, composto, e, composição farmacêutica |
| 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 |
| WO2021173641A1 (en) | 2020-02-25 | 2021-09-02 | 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 |
| WO2023034718A1 (en) | 2021-08-31 | 2023-03-09 | 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)
| 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 |
| WO1998015277A2 (en) * | 1996-10-07 | 1998-04-16 | Merck Sharp & Dohme Limited | Cns-penetrant nk-1 receptor antagonists as antidepressant and/or an anti-anxiety agents |
| EP1218369B1 (en) * | 1999-08-13 | 2008-07-23 | Vertex Pharmaceuticals Incorporated | INHIBITORS OF c-JUN N-TERMINAL KINASES (JNK) AND OTHER PROTEIN KINASES |
| EP1228068A1 (en) * | 1999-10-29 | 2002-08-07 | 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 |
| NZ535886A (en) * | 2002-04-26 | 2007-07-27 | Lilly Co Eli | Triazole derivatives as tachykinin receptor antagonists |
-
2004
- 2004-10-12 JP JP2006536635A patent/JP4959336B2/ja active Active
- 2004-10-12 ES ES04793893T patent/ES2340772T3/es active Active
- 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 AU AU2004285855A patent/AU2004285855B8/en active Active
- 2004-10-12 DK DK04793893.1T patent/DK1675846T3/da active
- 2004-10-12 WO PCT/US2004/030914 patent/WO2005042515A1/en active Application Filing
- 2004-10-12 KR KR1020067007751A patent/KR100848407B1/ko active IP Right Grant
- 2004-10-12 NZ NZ580480A patent/NZ580480A/en unknown
- 2004-10-12 EA EA200600829A patent/EA008881B1/ru not_active IP Right Cessation
- 2004-10-12 NZ NZ545917A patent/NZ545917A/en unknown
- 2004-10-12 AT AT04793893T patent/ATE462700T1/de active
- 2004-10-12 PT PT04793893T patent/PT1675846E/pt unknown
- 2004-10-12 DE DE602004026333T patent/DE602004026333D1/de active Active
- 2004-10-12 US US10/574,712 patent/US7381826B2/en active Active
- 2004-10-20 AR ARP040103801A patent/AR046131A1/es not_active Application Discontinuation
- 2004-10-20 PE PE2004001008A patent/PE20050481A1/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 |
|---|---|---|
| CL2009001311A1 (es) | Procedimiento para preparar {2-[1-(3,5-bistrifluorometilbencil)-5-piridin-4-il-1h-[1,2,3]triazol-4-il]-piridin-3-il}-(2-clorofenil)metanona a partir de (2-clorofenil)-[2-(2-hidroxi-2-piridin-4-ilvinil)piridin-3-il]metanona y 1-azidometil-3,5-bistrifluorometilbenceno en presencia de una base y un disolvente (div.sol.2680-04). | |
| CY1108218T1 (el) | Δισκιο που περιεχει 3-[(2-{[4-(εξυλοξυκαρβονυλαμινο-ιμινο-μεθυλο)-φαινυλαμινο]-μεθυλο}-1 -μεθυλο-1 η-βενζιμιδαζολο5-καρβονυλο)-πυριδιν-2-υλ-αμινο] προπιονικο αιθυλεστερα | |
| CY1112796T1 (el) | Μεθανοσουλφονικος 3-[(2{[4-(εξυλοξυκαρβοονυλαμινο-ιμινο-μεθυλο)-φαινυλαμινο]μεθυλ}-1-μεθυλ-1h-βενζιμιδαζολο-5-καρβονυλο)-πυριδιν-2-υλ-αμινο]-προπιονικος αιθυλεστερας | |
| IL198775A0 (en) | Novel intermediate and process useful in the preparation of {2-[1-(3,5-bis-trifluoromethyl-benzyl)-5-pyridin-4-yl-1h-[1,2,3]triazol-4-yl]-pyridin-3-yl}-(2-chlorophenyl)-methanone | |
| DK1332137T3 (da) | Behandling af gastrointestinale stromale tumorer | |
| CY2013015I2 (el) | Πολυμορφο του 4-[2-[4-[1-(2-αιθοξυαιθυλ)-1η-βενζιμιδαζολ-2-υλ]-1-πιπepιδινυλ]αιθυλ]αιθυλ-αλφα, αλφα-διμεθυλ-βενζενοξικου οξεος | |
| BRPI0606768A2 (pt) | forma de dosagem oral compreendendo rosiglitazona | |
| FR2844975B1 (fr) | Contenant pour cosmetiques | |
| IT1320970B1 (it) | Macchina per realizzare pacchetti di sigarette e metodo di controllodella macchina. | |
| DE60102590D1 (de) | Darreichungsformen zur behandlung von oralen mykosen | |
| ITMI20030454A1 (it) | Macchina per l'immagazzinamento ordinato e il rilascio di banconote. | |
| CY1105354T1 (el) | Ένα παραγωγο θειαζολιδινοδιονης και η χρηση του σαν αντι-διαβητικο | |
| CY1105903T1 (el) | Ενα παραγωγο της θειαζολιδενεδιονης και η χρηση του σαν αντιδιαβητικο | |
| ID26146A (id) | Proses untuk cis-1-{2-[4-(6-metoksi-2-fenil-1,2,3,4-tetrahidronaftalen-1-il]fenoksi]etil} pirolidin | |
| NO20040350L (no) | Anvendelse av LHRH-antagonister i doser som ikke medfører kastrering, for forbedring av T-cellemediert immunitet. | |
| CY1107252T1 (el) | Τρυγικο αλας παραγωγου της θειζολιδινοδιονης | |
| EA200300345A1 (ru) | Гидрохлоридная соль 5-[4-[2-(n-метил-n-(2-пиридил)амино)этокси]бензил]тиазолидин-2,4-диона | |
| ATE289194T1 (de) | Eindämmung der wiederaufnahme von drogenmissbrauch | |
| PT1446404E (pt) | Edisilatos de rosiglitazona e sua utilizacao como antidiabeticos | |
| ITMI20030216A1 (it) | Dispositivo di supporto di contenitori in macchine per il trattamento extracorporeo di sangue o in macchine per il trattamento di insufficienza renale. | |
| NO20071096L (no) | Diarylmetylpiperazinderivater, fremstillinger derav og anvendelser derav | |
| NO20055836L (no) | Intermediater anvendelige ved syntesen av HIV-proteaseinhibitorer og fremgangsmater for fremstilling av samme | |
| ITTO20020114U1 (it) | Dispositivo per l'erogazione o il rilascio di una sostanza in una macchina lavatrice. | |
| ITFI20040078A1 (it) | Metodo e dispositivo utilizzabili per una macchina per la produzione di filato fantasia | |
| ITTO20030762A1 (it) | Metodo per controllare l'istante di funzionamento di una |