AR054090A1 - Derivados de quinuclidina como antagonistas del receptor muscarinico m3. composiciones farmaceuticas y proceso de obtencion - Google Patents
Derivados de quinuclidina como antagonistas del receptor muscarinico m3. composiciones farmaceuticas y proceso de obtencionInfo
- Publication number
- AR054090A1 AR054090A1 ARP050104547A ARP050104547A AR054090A1 AR 054090 A1 AR054090 A1 AR 054090A1 AR P050104547 A ARP050104547 A AR P050104547A AR P050104547 A ARP050104547 A AR P050104547A AR 054090 A1 AR054090 A1 AR 054090A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- hydroxy
- hydrogen
- alkoxy
- positions
- Prior art date
Links
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D453/00—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids
- C07D453/02—Heterocyclic compounds containing quinuclidine or iso-quinuclidine ring systems, e.g. quinine alkaloids containing not further condensed quinuclidine ring systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/08—Bronchodilators
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/16—Central respiratory analeptics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Immunology (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Hydrogenated Pyridines (AREA)
- Cosmetics (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Se describen composiciones farmacéuticas que contienen a los compuestos, y un proceso para la preparacion de los compuestos. Reivindicacion 1: Un compuesto de la formula (1), en forma de sal o zwiterionica, en donde: R1 y R2 son cada uno independientemente fenilo, estando uno o ambos de R1 y R2 sustituido en una, dos, o tres posiciones por halogeno, alquilo C1-8, o alcoxilo C1-8, y R3 es hidrogeno, hidroxilo, alquilo C1-8, alcoxilo C1-8, o tioalquilo C1-8; o R1 y R2 son cada uno fenilo insustituidos, y R3 es hidrogeno, alquilo C1-8, alcoxilo C1-8, o tioalquilo C1-8; o R1 es cicloalquilo C3-8. o un grupo heterocíclico de 4 a 6 miembros que contiene cuando menos un heteroátomo del anillo seleccionado a partir de nitrogeno, oxígeno, y azufre; R2 es fenilo opcionalmente sustituido en una, dos, o tres posiciones por halogeno, alquilo C1-8, o alcoxilo C1-8; o R2 es un grupo heterocíclico de 4 a 6 miembros que contiene cuando menos un heteroátomo del anillo seleccionado a partir de nitrogeno, oxígeno y azufre, y R3 es hidrogeno, hidroxilo, alquilo C1-8, alcoxilo C1-8, o tioalquilo C1-8; -CR1R2R3 denota 9H-fluoren-9-ilo, 9,10,-dihidroantracenil-9-ilo, 9-hidroxi-9,10-dihidroantracenil-9-ilo, 9-hidroxi-9H-fluoren-9-ilo, 9H-xanten-9-ilo, 9-hidroxi-9H-xanten-9-ilo, 5H-dibenzo-[a,d]-ciclohepten-5-ilo o 5-hidroxi-5H-dibenzo[a,d]-ciclohepten-5-ilo; y R4 es alquilo C1-8 sustituido en una, dos o tres posiciones por -CO-N(R5)R6, en donde R5 es hidrogeno o alquilo C1-8, y R6 es un grupo heterocíclico de 4 a 6 miembros que contiene cuando menos un heteroátomo del anillo seleccionado a partir de nitrogeno, oxígeno, y azufre; o R1 y R2 son cada uno fenilo insustituido, R3 es hidroxi, y R4 es alquilo C1-8 sustituido en una, do o tres posiciones por -CO-N(R5)R6, en donde R5 es hidrogeno o alquilo C1-4, y R6 es 5-metil-3-isoxazolilo; o R1 y R2 son cada uno fenilo insustituido, R3 es hidroxilo, y R4 es 1-etilo en una, dos, o tres posiciones por -CO-N(R5)R6, en donde R5 es hidrogeno o alquilo C1-4, y R6 es un grupo heterocíclico de 4 a 6 miembros que contiene cuando menos un heteroátomo del anillo seleccionado a partir de nitrogeno, oxígeno, y azufre; con la condicion de que el compuesto de la formula (1) no es (R)-3-(2-hidroxi-2,2-di-tiofen-2-il-acetoxi)-l-(pirazin-2-ilcarbamoil-metil)-l-azonia-biciclo[2.2.2]-octano, bromuro de (R)-3-(2-hidroxi-2,2-di-tiofen-2-il-acetoxi)-l-(isoxazol-3-ilcarbamoil-metil)-l-azonia-biciclo-[2.2.2]octano, o bromuro de (R)-3- (2-hidroxi-2,2-di-tiofen-2-il-acetoxi)-l-(pirimidin-4-ilcarbamoil-metil)-l-azonia-biciclo-[2.2.2]-octano.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GBGB0424284.8A GB0424284D0 (en) | 2004-11-02 | 2004-11-02 | Organic compounds |
Publications (1)
Publication Number | Publication Date |
---|---|
AR054090A1 true AR054090A1 (es) | 2007-06-06 |
Family
ID=33515948
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP050104547A AR054090A1 (es) | 2004-11-02 | 2005-10-31 | Derivados de quinuclidina como antagonistas del receptor muscarinico m3. composiciones farmaceuticas y proceso de obtencion |
Country Status (33)
Country | Link |
---|---|
US (2) | US7723356B2 (es) |
EP (2) | EP2206499A1 (es) |
JP (1) | JP4950896B2 (es) |
KR (1) | KR101252307B1 (es) |
CN (1) | CN101056634B (es) |
AR (1) | AR054090A1 (es) |
AT (1) | ATE481099T1 (es) |
AU (1) | AU2005300710B2 (es) |
BR (1) | BRPI0517945A (es) |
CA (1) | CA2583237C (es) |
CY (1) | CY1110952T1 (es) |
DE (1) | DE602005023639D1 (es) |
DK (1) | DK1811999T3 (es) |
EC (1) | ECSP077424A (es) |
ES (1) | ES2353142T3 (es) |
GB (1) | GB0424284D0 (es) |
HR (1) | HRP20100693T1 (es) |
IL (1) | IL182695A0 (es) |
JO (1) | JO2613B1 (es) |
MA (1) | MA29080B1 (es) |
MX (1) | MX2007005189A (es) |
MY (1) | MY145207A (es) |
NO (1) | NO20072371L (es) |
NZ (1) | NZ554302A (es) |
PE (1) | PE20060609A1 (es) |
PL (1) | PL1811999T3 (es) |
PT (1) | PT1811999E (es) |
RU (1) | RU2399620C2 (es) |
SI (1) | SI1811999T1 (es) |
TN (1) | TNSN07164A1 (es) |
TW (1) | TW200628154A (es) |
WO (1) | WO2006048225A1 (es) |
ZA (1) | ZA200702772B (es) |
Families Citing this family (31)
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AR044134A1 (es) | 2003-05-02 | 2005-08-24 | Novartis Ag | Derivados de quinuclidina, metodo de preparacion y composiciones farmaceuticas. |
US7994211B2 (en) | 2005-08-08 | 2011-08-09 | Argenta Discovery Limited | Bicyclo[2.2.1]hept-7-ylamine derivatives and their uses |
WO2007022030A2 (en) * | 2005-08-11 | 2007-02-22 | University Of Massachusetts | Methods and compositions for the efficient delivery of therapeutic agents to cells and animals |
GB0601951D0 (en) | 2006-01-31 | 2006-03-15 | Novartis Ag | Organic compounds |
EP1894568A1 (en) * | 2006-08-31 | 2008-03-05 | Novartis AG | Pharmaceutical compositions for the treatment of inflammatory or obstructive airway diseases |
TW200825084A (en) * | 2006-11-14 | 2008-06-16 | Astrazeneca Ab | New compounds 521 |
UA97492C2 (ru) * | 2006-11-14 | 2012-02-27 | Астразенека Аб | Хиниклидиновые производные (гетеро) арилциклогептанкарбоксиловой кислоты как антагонисты мускаринового рецептора |
RU2009120229A (ru) * | 2006-12-19 | 2011-01-27 | Астразенека Аб (Se) | Производные хинуклидинола в качестве антагонистов мускариновых рецепторов |
WO2009035542A2 (en) | 2007-09-07 | 2009-03-19 | Theravance, Inc. | Guanidine-containing compounds useful as muscarinic receptor antagonists |
EP2222637A1 (en) | 2007-12-14 | 2010-09-01 | Theravance, Inc. | Amidine-containing compounds useful as muscarinic receptor antagonists |
PL2231642T3 (pl) | 2008-01-11 | 2014-04-30 | Novartis Ag | Pirymidyny jako inhibitory kinazy |
EA017627B1 (ru) * | 2008-05-13 | 2013-01-30 | Астразенека Аб | Хинуклидиновые производные в качестве антагонистов мускаринового м3 рецептора |
GB0808708D0 (en) * | 2008-05-13 | 2008-06-18 | Astrazeneca Ab | New compounds 274 |
BRPI0912657A2 (pt) * | 2008-05-13 | 2016-01-26 | Astrazeneca Ab | produto farmacêutico compreendendo um antagonista de receptor muscarínico e um agonista beta2-adrenorreceptor |
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GB0811100D0 (en) * | 2008-06-17 | 2008-07-23 | Astrazeneca Ab | New combination |
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US8263623B2 (en) | 2008-07-11 | 2012-09-11 | Pfizer Inc. | Triazol derivatives useful for the treatment of diseases |
EP2206712A1 (en) * | 2008-12-23 | 2010-07-14 | CHIESI FARMACEUTICI S.p.A. | "Alkaloid aminoester derivatives and medicinal composition thereof" |
WO2010115937A1 (en) | 2009-04-09 | 2010-10-14 | Novartis Ag | Process for preparing pyrrolidinium salts |
EP2585457B1 (en) * | 2010-06-22 | 2015-07-22 | Chiesi Farmaceutici S.p.A. | Alkaloid aminoester derivatives and medicinal composition thereof |
WO2011160920A1 (en) * | 2010-06-22 | 2011-12-29 | Chiesi Farmaceutici S.P.A. | Dry powder formulation comprising an antimuscarinic drug |
WO2012034095A1 (en) | 2010-09-09 | 2012-03-15 | Irm Llc | Compounds and compositions as trk inhibitors |
UY33597A (es) | 2010-09-09 | 2012-04-30 | Irm Llc | Compuestos y composiciones como inhibidores de la trk |
US9102671B2 (en) | 2011-02-25 | 2015-08-11 | Novartis Ag | Compounds and compositions as TRK inhibitors |
JP2011195593A (ja) * | 2011-06-30 | 2011-10-06 | Astrazeneca Ab | ムスカリンm3受容体アンタゴニストとしてのキヌクリジン誘導体 |
KR20150095888A (ko) | 2012-12-19 | 2015-08-21 | 노파르티스 아게 | 오토탁신 억제제 |
EP3134398A1 (en) | 2014-04-24 | 2017-03-01 | Novartis Ag | Autotaxin inhibitors |
US20170065589A1 (en) * | 2014-05-06 | 2017-03-09 | Anthony G. Visco | Methods of treating or preventing preterm labor |
CN109851615B (zh) * | 2019-04-22 | 2021-06-08 | 上海旭东海普药业有限公司 | 纯化戊乙奎醚的方法 |
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