AR057627A1 - Compuestos de carbamato como agonistas del receptor 5-ht4 - Google Patents
Compuestos de carbamato como agonistas del receptor 5-ht4Info
- Publication number
- AR057627A1 AR057627A1 ARP060105125A ARP060105125A AR057627A1 AR 057627 A1 AR057627 A1 AR 057627A1 AR P060105125 A ARP060105125 A AR P060105125A AR P060105125 A ARP060105125 A AR P060105125A AR 057627 A1 AR057627 A1 AR 057627A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- nrarb
- compounds
- formula
- 3alkyl
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D451/00—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof
- C07D451/02—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof
- C07D451/04—Heterocyclic compounds containing 8-azabicyclo [3.2.1] octane, 9-azabicyclo [3.3.1] nonane, or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane or granatane alkaloids, scopolamine; Cyclic acetals thereof containing not further condensed 8-azabicyclo [3.2.1] octane or 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring systems, e.g. tropane; Cyclic acetals thereof with hetero atoms directly attached in position 3 of the 8-azabicyclo [3.2.1] octane or in position 7 of the 3-oxa-9-azatricyclo [3.3.1.0<2,4>] nonane ring system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/46—8-Azabicyclo [3.2.1] octane; Derivatives thereof, e.g. atropine, ***e
-
- 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
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/04—Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
-
- 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
- A61P1/10—Laxatives
-
- 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
- A61P1/14—Prodigestives, e.g. acids, enzymes, appetite stimulants, antidyspeptics, tonics, antiflatulents
-
- 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)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Engineering & Computer Science (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Nutrition Science (AREA)
- Emergency Medicine (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
También se proveen composiciones farmacéuticas como compuestos, métodos para utilizar dichos compuestos para tratar enfermedades asociadas con la actividad del receptor 5-HT4, y procesos e intermediarios utiles para preparar dichos compuestos. Reivindicacion 1: Un compuesto caracterizado porque es de formula (1) donde R1 es halo o C1-3 alquilo, donde C1-3 alquilo está opcionalmente sustituido con hidroxi o halo; R2 es H o C1-3 alquilo, donde C1-3 está opcionalmente sustituido con hidroxi; R3 es C1-3 alquilo o H; R4 es -(CH2)1-3C(O)NRaRb, o como se muestra en los compuestos de formulas (2), o R3 y R4 junto con el átomo de N al cual están unidos forman una porcion seleccionada entre: (i) una porcion de formula (3), (ii)una porcion de formula (4); y (iii) una porcion de formula (5), donde R5 es -OC(O)NRaRb, -C(O)NRaRb, -NRdS(O)2C1-3alquilo, -NRdC(O)Rc, -NRdS(O)2NRaRb, o -NRdC(O)ORe; R6 es -C(O)Rf, -(CH2)2ORg, -S(O)2NRaRb, -S(O)2C1-3alquilo, o -S(O)2(CH2)1-3S(O)2C1- 3alquilo; Ra, Rb, y Rc son en forma independiente H o C1-3 alquilo; Rd es H o C1-3 alquilo, donde C1-3 alquilo está opcionalmente sustituido con hidroxi; Re es C1-3 alquilo; Rf es H, C1-3 alquilo, tetrahidrofuranilo, o -NRaRb; Rg es H o C1-3 alquilo; a es 0, 1 o 2; b es 0, 1, 2 o 3, c es 0, 1 o 2; d es 1 o 2; y e es 1 o 2; con la condicion de que cuando c es 0, entonces d es 2, y R5 es -C(O)NRaRb; y cuando c es 2, entonces d es 1; o una sal o solvato o estereoisomero aceptable para uso farmacéutico del mismo.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US73870205P | 2005-11-22 | 2005-11-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR057627A1 true AR057627A1 (es) | 2007-12-05 |
Family
ID=38067868
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060105125A AR057627A1 (es) | 2005-11-22 | 2006-11-22 | Compuestos de carbamato como agonistas del receptor 5-ht4 |
Country Status (20)
Country | Link |
---|---|
US (2) | US7329752B2 (es) |
EP (1) | EP1960396B1 (es) |
JP (1) | JP2009516745A (es) |
KR (1) | KR20080072727A (es) |
CN (1) | CN101312967B (es) |
AR (1) | AR057627A1 (es) |
AT (1) | ATE448224T1 (es) |
AU (1) | AU2006318507A1 (es) |
BR (1) | BRPI0618835A2 (es) |
CA (1) | CA2630222A1 (es) |
DE (1) | DE602006010432D1 (es) |
EA (1) | EA014819B1 (es) |
ES (1) | ES2336952T3 (es) |
MY (1) | MY143574A (es) |
NO (1) | NO20082597L (es) |
NZ (1) | NZ567653A (es) |
PE (1) | PE20070954A1 (es) |
TW (1) | TW200804366A (es) |
WO (1) | WO2007062058A2 (es) |
ZA (1) | ZA200804010B (es) |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2006094063A1 (en) * | 2005-03-02 | 2006-09-08 | Theravance, Inc. | Quinolinone compounds as 5-ht4 receptor agonists |
WO2007097976A1 (en) * | 2006-02-16 | 2007-08-30 | Theravance, Inc. | Process for preparing intermediates to 5-ht4 receptor agonist compounds |
Family Cites Families (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US5223511A (en) * | 1987-09-23 | 1993-06-29 | Boehringer Ingelheim Italia S.P.A. | Benzimidazoline-2-oxo-1-carboxylic acid compounds useful as 5-HT receptor antagonists |
IT1231413B (it) | 1987-09-23 | 1991-12-04 | Angeli Inst Spa | Derivati dell'acido benzimidazolin-2-osso-1-carbossilico utili come antagonisti dei recettori 5-ht |
JP3829879B2 (ja) * | 1994-05-18 | 2006-10-04 | 大正製薬株式会社 | キノリンカルボン酸誘導体 |
IT1275903B1 (it) * | 1995-03-14 | 1997-10-24 | Boehringer Ingelheim Italia | Esteri e ammidi della 1,4-piperidina disostituita |
US6069152A (en) * | 1997-10-07 | 2000-05-30 | Eli Lilly And Company | 5-HT4 agonists and antagonists |
IT1298271B1 (it) | 1998-02-18 | 1999-12-20 | Boehringer Ingelheim Italia | Esteri ed ammidi dell'acido 2-oxo-2,3-diidro-benzimidazol-1- carbossilico |
CN1461216A (zh) * | 1999-04-28 | 2003-12-10 | 呼吸器有限公司 | 用作治疗有关支气管收缩的机能障碍的药物的化合物 |
IT1313625B1 (it) * | 1999-09-22 | 2002-09-09 | Boehringer Ingelheim Italia | Derivati benzimidazolonici aventi affinita' mista per i recettori diserotonina e dopamina. |
JP4181847B2 (ja) * | 2002-10-25 | 2008-11-19 | エルピーダメモリ株式会社 | タイミング調整回路、半導体装置及びタイミング調整方法 |
ES2377484T3 (es) * | 2003-09-03 | 2012-03-28 | Pfizer, Inc. | Compuestos de bencimidazolona que tiene actividad agonista del receptor 5-HT |
TW200533348A (en) * | 2004-02-18 | 2005-10-16 | Theravance Inc | Indazole-carboxamide compounds as 5-ht4 receptor agonists |
TWI351282B (en) * | 2004-04-07 | 2011-11-01 | Theravance Inc | Quinolinone-carboxamide compounds as 5-ht4 recepto |
ES2332808T3 (es) * | 2004-11-05 | 2010-02-12 | Theravance, Inc. | Compuestos agonistas del receptor 5-ht4. |
EP1807423B1 (en) * | 2004-11-05 | 2009-05-20 | Theravance, Inc. | Quinolinone-carboxamide compounds |
RU2404179C2 (ru) * | 2004-12-22 | 2010-11-20 | Тереванс, Инк. | Индазол-карбоксамидные соединения |
WO2006094063A1 (en) | 2005-03-02 | 2006-09-08 | Theravance, Inc. | Quinolinone compounds as 5-ht4 receptor agonists |
US7351304B2 (en) * | 2005-05-24 | 2008-04-01 | General Electric Company | Method and apparatus for reducing surface defects |
DE602006019595D1 (de) | 2005-06-07 | 2011-02-24 | Theravance Inc | Benzimidazoloncarbonsäureamidverbindungen als agonisten des 5-ht4-rezeptors |
-
2006
- 2006-11-09 MY MYPI20064472A patent/MY143574A/en unknown
- 2006-11-15 TW TW095142293A patent/TW200804366A/zh unknown
- 2006-11-21 CA CA002630222A patent/CA2630222A1/en not_active Abandoned
- 2006-11-21 JP JP2008542415A patent/JP2009516745A/ja active Pending
- 2006-11-21 NZ NZ567653A patent/NZ567653A/en unknown
- 2006-11-21 DE DE602006010432T patent/DE602006010432D1/de active Active
- 2006-11-21 AT AT06838207T patent/ATE448224T1/de not_active IP Right Cessation
- 2006-11-21 EP EP06838207A patent/EP1960396B1/en active Active
- 2006-11-21 CN CN2006800433139A patent/CN101312967B/zh not_active Expired - Fee Related
- 2006-11-21 EA EA200801402A patent/EA014819B1/ru not_active IP Right Cessation
- 2006-11-21 ES ES06838207T patent/ES2336952T3/es active Active
- 2006-11-21 KR KR1020087014898A patent/KR20080072727A/ko not_active Application Discontinuation
- 2006-11-21 PE PE2006001486A patent/PE20070954A1/es not_active Application Discontinuation
- 2006-11-21 WO PCT/US2006/045099 patent/WO2007062058A2/en active Application Filing
- 2006-11-21 US US11/602,888 patent/US7329752B2/en active Active
- 2006-11-21 BR BRPI0618835-4A patent/BRPI0618835A2/pt not_active IP Right Cessation
- 2006-11-21 AU AU2006318507A patent/AU2006318507A1/en not_active Abandoned
- 2006-11-22 AR ARP060105125A patent/AR057627A1/es not_active Application Discontinuation
-
2007
- 2007-12-06 US US11/999,609 patent/US7851467B2/en not_active Expired - Fee Related
-
2008
- 2008-05-09 ZA ZA200804010A patent/ZA200804010B/xx unknown
- 2008-06-10 NO NO20082597A patent/NO20082597L/no not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
AU2006318507A1 (en) | 2007-05-31 |
TW200804366A (en) | 2008-01-16 |
WO2007062058A2 (en) | 2007-05-31 |
CN101312967A (zh) | 2008-11-26 |
ZA200804010B (en) | 2009-02-25 |
US20080090811A1 (en) | 2008-04-17 |
EP1960396A2 (en) | 2008-08-27 |
ATE448224T1 (de) | 2009-11-15 |
PE20070954A1 (es) | 2007-09-10 |
US7851467B2 (en) | 2010-12-14 |
WO2007062058A3 (en) | 2007-09-07 |
US20070117796A1 (en) | 2007-05-24 |
NZ567653A (en) | 2011-06-30 |
CA2630222A1 (en) | 2007-05-31 |
US7329752B2 (en) | 2008-02-12 |
NO20082597L (no) | 2008-06-10 |
DE602006010432D1 (de) | 2009-12-24 |
BRPI0618835A2 (pt) | 2011-09-13 |
CN101312967B (zh) | 2011-08-24 |
EA200801402A1 (ru) | 2008-10-30 |
KR20080072727A (ko) | 2008-08-06 |
EA014819B1 (ru) | 2011-02-28 |
EP1960396B1 (en) | 2009-11-11 |
ES2336952T3 (es) | 2010-04-19 |
MY143574A (en) | 2011-05-31 |
JP2009516745A (ja) | 2009-04-23 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR047098A1 (es) | Derivados de arilanilina como agonistas del receptor adrenergico beta2 | |
PE20230249A1 (es) | Compuestos de heteroarilo biciclicos y usos de estos | |
AR072952A1 (es) | Compuestos de 2-imino-3-metilpirrolopirimidinona fenilo-sustituida como inhibidores de bace-1, composiciones y su uso | |
PE20040164A1 (es) | Mimeticos de glucocorticoides, procedimientos para su preparacion y composiciones farmaceuticas | |
AR050407A1 (es) | Compuestos quinolinon-carboxamida como agonistas del receptor 5-ht4. procesos de obtencion y composiciones farmaceuticas | |
PE20212112A1 (es) | Analogos de rapamicina ligados a c40, c28 y c-32 como inhibidores de mtor | |
AR074459A1 (es) | Pirrolopirazinil-ureas utiles para el tratamiento de enfermedades autoinmunes e inflamatorias. | |
HK1167658A1 (en) | Composition for the preparation of 17-vinyl- triflates as intermediates 17-- | |
AR111813A2 (es) | Compuestos y composiciones para el control de nematodos | |
ATE431345T1 (de) | Als modulatoren von dopamin-d3-rezeptoren geeignete azabicyclo-(3,1,0)-hexan-derivate | |
AR046085A1 (es) | Agonistas etilamino amino sustituidos del receptor beta 2 adrenergico | |
AR049446A1 (es) | Preparacion de pregabalina ((s)-(+)-aminometil-5-metilhexanoico) y compuestos relacionados | |
AR078408A1 (es) | Derivados de indol como moduladores de los crac | |
MA28422B1 (fr) | Derives de n- (1,5-diphenyl-1h-pyrazol-3-yl) sulfonamide avec une affinite pour les recepteurs cb1 | |
EA200701745A1 (ru) | Циклопропанкарбоксамидные производные | |
CR7950A (es) | Sintesis de los cloruros de 4amino -2butenoilo y su uso en la preparacion of 3- cianoquinolinas | |
AR038536A1 (es) | N-aril-2-oxazolidinona-5- carboxamidas y sus derivados | |
AR051754A1 (es) | Metodos para preparar compuestos de indazol | |
AR058701A1 (es) | Derivados de piracinil-s-espiro-oxacinoquinolin-pirimidin-triona como agentes antibacterianos | |
AR116474A1 (es) | DERIVADOS DEL ÁCIDO 6,7-DIHIDRO-2H-BENZOFURO[2,3-a]QUINOLIZIN-3-CARBOXÍLICO COMO AGENTES ANTIVIRALES PARA EL TRATAMIENTO O PREVENCIÓN DE UNA INFECCIÓN POR HBV | |
AR083760A1 (es) | Agentes antibacterianos y composiciones farmaceuticas | |
AR065583A1 (es) | Compuestos macrociclicos y composicion farmaceutica | |
AR057327A1 (es) | Compuestos de benzimidazol-carboxamida como agonistas del receptor 5-ht4. procesos de obtencion y composiciones farmaceuticas | |
AR042002A1 (es) | Benzoxazinonas sustituidas, proceso de obtencion y usos para tratamiento de enfermedades del sistema nervioso central. | |
AR076362A1 (es) | Arilsulfonamidas 2,5-disustituidas antagonistas de ccr3, composiciones farmaceuticas que las contienen y uso de las mismas para el tratamiento y/o prevencion de patologias autoinmunes e inflamatorias, entre otras. |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |