AR054277A1 - Derivados de piperidin - 4 - il - amida, un proceso para su obtencion, composiciones farmaceuticas que los contienen y su empleo en la fabricacion de medicamentos para el tratamiento de enfermedades asociadas con la modulacion de receptores del subtipo 5 de la sst. - Google Patents
Derivados de piperidin - 4 - il - amida, un proceso para su obtencion, composiciones farmaceuticas que los contienen y su empleo en la fabricacion de medicamentos para el tratamiento de enfermedades asociadas con la modulacion de receptores del subtipo 5 de la sst.Info
- Publication number
- AR054277A1 AR054277A1 AR20060102259A ARP060102259A AR054277A1 AR 054277 A1 AR054277 A1 AR 054277A1 AR 20060102259 A AR20060102259 A AR 20060102259A AR P060102259 A ARP060102259 A AR P060102259A AR 054277 A1 AR054277 A1 AR 054277A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkoxy
- alkyl
- formula
- halogen
- compound
- Prior art date
Links
- 238000000034 method Methods 0.000 title abstract 4
- 201000010099 disease Diseases 0.000 title abstract 2
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 title abstract 2
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- NQRYJNQNLNOLGT-UHFFFAOYSA-N Piperidine Chemical class C1CCNCC1 NQRYJNQNLNOLGT-UHFFFAOYSA-N 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 238000004519 manufacturing process Methods 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 15
- 125000003545 alkoxy group Chemical group 0.000 abstract 13
- 150000001875 compounds Chemical class 0.000 abstract 13
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical class 0.000 abstract 6
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000004076 pyridyl group Chemical group 0.000 abstract 5
- 150000003839 salts Chemical class 0.000 abstract 5
- 150000002431 hydrogen Chemical group 0.000 abstract 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 4
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 3
- -1 2-fluorethyl Chemical group 0.000 abstract 3
- 125000002947 alkylene group Chemical group 0.000 abstract 3
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 3
- 125000001424 substituent group Chemical group 0.000 abstract 3
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 2
- 150000001412 amines Chemical class 0.000 abstract 2
- 230000008878 coupling Effects 0.000 abstract 2
- 238000010168 coupling process Methods 0.000 abstract 2
- 238000005859 coupling reaction Methods 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 125000002883 imidazolyl group Chemical group 0.000 abstract 2
- 125000000714 pyrimidinyl group Chemical group 0.000 abstract 2
- 125000005871 1,3-benzodioxolyl group Chemical group 0.000 abstract 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001350 alkyl halides Chemical class 0.000 abstract 1
- 125000002431 aminoalkoxy group Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 150000001732 carboxylic acid derivatives Chemical class 0.000 abstract 1
- 239000003638 chemical reducing agent Substances 0.000 abstract 1
- 239000007822 coupling agent Substances 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000001207 fluorophenyl group Chemical group 0.000 abstract 1
- 125000002485 formyl group Chemical class [H]C(*)=O 0.000 abstract 1
- 125000005113 hydroxyalkoxy group Chemical group 0.000 abstract 1
- 125000001041 indolyl group Chemical group 0.000 abstract 1
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 125000000168 pyrrolyl group Chemical group 0.000 abstract 1
- 125000003831 tetrazolyl group Chemical group 0.000 abstract 1
- 125000001425 triazolyl group Chemical group 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D211/56—Nitrogen atoms
- C07D211/58—Nitrogen atoms attached in position 4
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4453—Non condensed piperidines, e.g. piperocaine only substituted in position 1, e.g. propipocaine, diperodon
-
- 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
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4468—Non condensed piperidines, e.g. piperocaine having a nitrogen directly attached in position 4, e.g. clebopride, fentanyl
-
- 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
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/06—Anti-spasmodics, e.g. drugs for colics, esophagic dyskinesia
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P1/12—Antidiarrhoeals
-
- 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
- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
-
- 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
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
- A61P3/10—Drugs for disorders of the metabolism for glucose homeostasis for hyperglycaemia, e.g. antidiabetics
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- 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
- A61P37/02—Immunomodulators
- A61P37/04—Immunostimulants
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- 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
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- A—HUMAN NECESSITIES
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/08—Vasodilators for multiple indications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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- 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
- C07D401/10—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 linked by a carbon chain containing aromatic rings
-
- 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
- C07D401/12—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 linked by a chain containing hetero atoms as chain links
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- 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
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
- C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
- C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
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- C07—ORGANIC CHEMISTRY
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- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
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- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Engineering & Computer Science (AREA)
- Immunology (AREA)
- Diabetes (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Obesity (AREA)
- Rheumatology (AREA)
- Epidemiology (AREA)
- Hematology (AREA)
- Dermatology (AREA)
- Emergency Medicine (AREA)
- Endocrinology (AREA)
- Pain & Pain Management (AREA)
- Vascular Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Nutrition Science (AREA)
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- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Hydrogenated Pyridines (AREA)
Abstract
Composiciones farmacéuticas que contienen tales compuestos, a un proceso para su obtencion y a la utilizacion de los mismos para tratar y/o prevenir enfermedades asociadas con la modulacion de los receptores del subtipo 5 de la SST. Reivindicacion 1: Compuestos de la formula (1) en la que R1 se elige entre el grupo formado por etilo, 2-fluoretilo, isopropilo e isobutio; R2 se elige entre el grupo formado por hidrogeno, alquilo C1-7, hidroxi, alcoxi C1-7 , cicloalquilo C3-7, -O-cicloalquilo C3- 7, halogeno, halogeno-alquilo C1-7; -C(O)OR6, en el que R6 es alquilo C1-7; -NH-C(O)-R7, en el que R7 es alquilo C1-7; amino, fenilo, fenilo sustituido de una a tres veces por sustituyentes elegidos entre el grupo formado por halogeno, halogeno- alquilo C1-7 y halogeno-alcoxi C1-7; piridilo, imidazolilo, triazolilo y pirrolilo; R3 se elige entre el grupo formado por hidrogeno, alcoxi C1-7, amino, -NH-C(O)-R8 en el que R8 es alquilo C1-7, -O-bencilo y -O-tetrahidropiranilo; o R2 y R3 junto con los átomos de carbono a los que están unidos forman un anillo y R2 y R3 juntos son -CH=CH-NH-; R4 se elige entre el grupo formado por hidrogeno, halogeno, piridilo y pirimidilo; R5 y R5' con independencia entre si se eligen entre hidrogeno o metilo; A se elige entre el grupo formado por fenilo; fenilo sustituido de una a tres veces por sustituyentes elegidos entre el grupo formado por alquilo C1-7, cicloalquilo C3-7, alquilsulfonilo C1-7, -O-alquilsulfonilo C1-7, alquilsulfonil C1-7- alcoxi C2-7, hidroxi, alcoxi C1-7, -O-cicloalquilo C3-7, cicloalquil C3-7-alcoxi C1-7, hidroxi-alquilo C1-7, hidroxi-alcoxi C2-7, dihidroxi-alcoxi C3-7, alcoxi C1-7-alcoxi C2-7, alcoxi C1-7-hidroxi-alcoxi C3-7, alquilamino C1-7, di(alquil C1- 7)amino, amino-alcoxi C2-7, amino-alquilo C1-7, -C(O)NR10R11, -alquileno C1-7-C(O)NR10R11, -O-alquileno C1-7-C(O)NR10R11, -C(O)OR10, -alquileno C1-7-C(O)OR10, -O-alquileno C1-7-C(O)OR10, halogeno, ciano, halogeno-alquilo C1-7, halogeno-alcoxi C1-7, ciano-alcoxi C1-7; fluorofenilo, piridilo, tetrazolilo y tetrazolil-alcoxi C1-7; 1,3-benzodioxolilo; naftilo; pirimidinilo; piridilo; piridilo sustituido por uno o dos sustituyentes elegidos entre el grupo formado por alquilo C1-7, alcoxi C1-7, amino, alquilamino C1-7, di(alquil C1-7)amino, cicloalquilamino C3-7, halogeno, ciano, morfolinilo, imidazolilo, y -NH-C(O)-R9, en el que R9 es alquilo C1-7 o cicloalquilo C3-7, e indolilo; R10 y R11 con independencia entre si son hidrogeno o alquilo C1-7; y las sales farmacéuticamente aceptables de los mismos. Reivindicacion 23: Un proceso para la obtencion de los compuestos segun una cualquiera de las reivindicaciones de 1 a 22, dicho proceso consiste en: a) hacer reaccionar un compuesto de la formula general (2) en la que A tiene el significado definido en la reivindicacion 1, con un aldehído de la formula (3) en la que R1, R2, R3 y R4 tienen los significados definidos en la reivindicacion 1, empleando un agente reductor para obtener un compuesto de la formula (1) en la que R5 y R5' son hidrogeno, y, si se desea, convertir el compuesto de la formula (1) en una sal farmacéuticamente aceptable, o, como alternativa, b) hacer reaccionar un compuesto de la formula (2) en la que A tiene el significado definido en la reivindicacion 1, con un haluro de alquilo de la formula (4) en la que de R1 a R5 y R5' tienen los significados definidos en la reivindicacion 1 y Hal es halogeno, mediante la adicion de una base idonea para obtener un compuesto de la formula (1) y, si se desea, convertir el compuesto de la formula (1) en una sal farmacéuticamente aceptable, o, como alternativa, c) acoplar una amina de la formula general (5) en la que de R1 a R5 y R5' tienen los significados definidos en la reivindicacion 1, con un ácido carboxílico de la formula HOOC-A, en la que A tiene el significado definido en la reivindicacion 1, empleando un agente de acoplamiento apropiado para obtener un compuesto de la formula (1) y, si se desea, convertir el compuesto de la formula (1) en una sal farmacéuticamente aceptable, o, como alternativa, d) acoplar una amina de la formula general (6) en la que de R1 a R5 y R5' tienen los significados definidos en la reivindicacion 1, con un cloruro de ácido de la formula A-C(:O)Cl, en la que A tiene el significado definido en la reivindicacion 1, mediante la adicion de una base idonea para obtener un compuesto de la formula (1) y, si se desea, convertir el compuesto de la formula (1) en una sal farmacéuticamente aceptable.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP05104774 | 2005-06-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR054277A1 true AR054277A1 (es) | 2007-06-13 |
Family
ID=36763959
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AR20060102259A AR054277A1 (es) | 2005-06-02 | 2006-05-31 | Derivados de piperidin - 4 - il - amida, un proceso para su obtencion, composiciones farmaceuticas que los contienen y su empleo en la fabricacion de medicamentos para el tratamiento de enfermedades asociadas con la modulacion de receptores del subtipo 5 de la sst. |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US7772253B2 (es) |
| EP (1) | EP1893603B1 (es) |
| JP (1) | JP4949387B2 (es) |
| KR (1) | KR100962732B1 (es) |
| CN (1) | CN101189226A (es) |
| AR (1) | AR054277A1 (es) |
| AT (1) | ATE445612T1 (es) |
| AU (1) | AU2006254256B2 (es) |
| BR (1) | BRPI0611138A2 (es) |
| CA (1) | CA2608819A1 (es) |
| DE (1) | DE602006009804D1 (es) |
| DK (1) | DK1893603T3 (es) |
| ES (1) | ES2330788T3 (es) |
| IL (1) | IL187426A (es) |
| MX (1) | MX2007014928A (es) |
| NO (1) | NO20076060L (es) |
| PL (1) | PL1893603T3 (es) |
| PT (1) | PT1893603E (es) |
| RU (1) | RU2403250C2 (es) |
| TW (1) | TWI315305B (es) |
| WO (1) | WO2006128803A1 (es) |
| ZA (1) | ZA200710169B (es) |
Families Citing this family (17)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7799806B2 (en) * | 2007-04-04 | 2010-09-21 | Hoffmann-La Roche Inc. | Substituted n-benzyl piperidines as somatostatin receptor modulators |
| US8026365B2 (en) * | 2007-05-25 | 2011-09-27 | Hoffman-La Roche Inc. | 4,4-disubstituted piperidine derivatives |
| JP2013508350A (ja) * | 2009-10-20 | 2013-03-07 | ファイザー・インク | ガンマ−セクレターゼモジュレーターとしての新規なヘテロアリールイミダゾールおよびヘテロアリールトリアゾール |
| KR20120125332A (ko) | 2010-02-01 | 2012-11-14 | 바스프 에스이 | 동물 해충을 퇴치하기 위한 치환된 케톤계 이속사졸린 화합물 및 유도체 |
| EP2605658B1 (en) | 2010-08-18 | 2016-03-23 | Merck Sharp & Dohme Corp. | Spiroxazolidinone compounds |
| BR112013007056A2 (pt) | 2010-10-01 | 2019-09-24 | Basf Se | compostos de imina |
| AR083646A1 (es) | 2010-10-01 | 2013-03-13 | Basf Se | Compuestos de imina, composiciones veterinarias y agricolas que los contienen y su uso en el control de plagas de invertebrados |
| TWI834637B (zh) | 2018-03-01 | 2024-03-11 | 日商武田藥品工業有限公司 | 六氫吡啶基-3-(芳氧基)丙醯胺及丙酸酯 |
| CN114945560B (zh) | 2019-10-07 | 2024-08-13 | 卡尔优普公司 | Gpr119激动剂 |
| CN115667277A (zh) | 2020-02-28 | 2023-01-31 | 卡尔优普公司 | Gpr40激动剂 |
| AR121682A1 (es) | 2020-03-31 | 2022-06-29 | Takeda Pharmaceuticals Co | Derivados de n-(heterociclil y heterociclilalquil)-3-bencilpiridin-2-amina como agonistas de sstr4 |
| WO2021199310A1 (ja) * | 2020-03-31 | 2021-10-07 | エヌ・イーケムキャット株式会社 | 芳香族化合物の製造方法 |
| UY39222A (es) | 2020-05-19 | 2021-11-30 | Kallyope Inc | Activadores de la ampk |
| CA3183575A1 (en) | 2020-06-26 | 2021-12-30 | Iyassu Sebhat | Ampk activators |
| CN115215787A (zh) * | 2021-04-19 | 2022-10-21 | 中国科学院上海药物研究所 | 生长抑素受体5拮抗剂及其用途 |
| KR20250157553A (ko) | 2023-03-27 | 2025-11-04 | 가부시키가이샤 스코히아 파마 | 성장 호르몬 분비 촉진제 |
| WO2025176114A1 (en) * | 2024-02-20 | 2025-08-28 | Rezubio Pharmaceuticals Co., Ltd | Compounds and compositions |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH598231A5 (es) | 1973-07-27 | 1978-04-28 | Hoffmann La Roche | |
| AR216043A1 (es) * | 1974-03-21 | 1979-11-30 | Anphar Sa | Procedimiento para la preparacion de 1-derivados de benzoilamino-4-piperidina y sus sales fisiologicamente aceptables |
| GB1574418A (en) * | 1976-11-16 | 1980-09-03 | Anphar Sa | Piperidine derivatives |
| CH628885A5 (en) * | 1978-01-01 | 1982-03-31 | Anphar Sa | Piperidine derivative |
| JPS5592384A (en) * | 1978-12-30 | 1980-07-12 | Beecham Group Ltd | Compound having pharmacological activity |
| US5098915A (en) * | 1989-09-05 | 1992-03-24 | G. D. Searle & Co. | Substituted N-benzylpiperidine amides |
| SE9702794D0 (sv) | 1997-07-24 | 1997-07-24 | Astra Pharma Prod | New compounds |
| CZ20013940A3 (cs) | 1999-05-04 | 2002-04-17 | Schering Corporation | Piperazinové deriváty uľitečné jako CCR5 antagonisté |
| US6344358B1 (en) * | 1999-05-28 | 2002-02-05 | Fujisawa Pharmaceutical Co., Ltd. | Agent for expression of long-term potentiation of synaptic transmission comprising compound having brain somatostatin activation property |
| FR2802206B1 (fr) * | 1999-12-14 | 2005-04-22 | Sod Conseils Rech Applic | Derives de 4-aminopiperidine et leur utilisation en tant que medicament |
| HRP20050993A2 (en) * | 2003-06-17 | 2006-03-31 | Pfizer Inc. | N-pyrrolidin-3-yl-amide derivatives as serotonin and noradrenaline re-uptake inhibitors |
| AU2004291262C1 (en) | 2003-11-05 | 2011-08-11 | F. Hoffmann-La Roche Ag | Phenyl derivatives as PPAR agonists |
-
2006
- 2006-05-23 RU RU2007148224/04A patent/RU2403250C2/ru not_active IP Right Cessation
- 2006-05-23 DE DE602006009804T patent/DE602006009804D1/de active Active
- 2006-05-23 AT AT06755285T patent/ATE445612T1/de active
- 2006-05-23 CN CNA2006800194138A patent/CN101189226A/zh active Pending
- 2006-05-23 KR KR1020077028019A patent/KR100962732B1/ko not_active Expired - Fee Related
- 2006-05-23 DK DK06755285T patent/DK1893603T3/da active
- 2006-05-23 CA CA002608819A patent/CA2608819A1/en not_active Abandoned
- 2006-05-23 BR BRPI0611138-6A patent/BRPI0611138A2/pt not_active IP Right Cessation
- 2006-05-23 AU AU2006254256A patent/AU2006254256B2/en not_active Ceased
- 2006-05-23 PT PT06755285T patent/PT1893603E/pt unknown
- 2006-05-23 EP EP06755285A patent/EP1893603B1/en not_active Not-in-force
- 2006-05-23 MX MX2007014928A patent/MX2007014928A/es active IP Right Grant
- 2006-05-23 ES ES06755285T patent/ES2330788T3/es active Active
- 2006-05-23 WO PCT/EP2006/062515 patent/WO2006128803A1/en not_active Ceased
- 2006-05-23 JP JP2008514062A patent/JP4949387B2/ja not_active Expired - Fee Related
- 2006-05-23 PL PL06755285T patent/PL1893603T3/pl unknown
- 2006-05-26 US US11/442,619 patent/US7772253B2/en not_active Expired - Fee Related
- 2006-05-30 TW TW095119084A patent/TWI315305B/zh not_active IP Right Cessation
- 2006-05-31 AR AR20060102259A patent/AR054277A1/es not_active Application Discontinuation
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2007
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- 2007-11-26 NO NO20076060A patent/NO20076060L/no not_active Application Discontinuation
- 2007-11-26 ZA ZA200710169A patent/ZA200710169B/xx unknown
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| Publication number | Publication date |
|---|---|
| PT1893603E (pt) | 2009-11-24 |
| BRPI0611138A2 (pt) | 2010-08-17 |
| DK1893603T3 (da) | 2009-11-30 |
| NO20076060L (no) | 2007-12-28 |
| ES2330788T3 (es) | 2009-12-15 |
| JP2008545730A (ja) | 2008-12-18 |
| TW200716547A (en) | 2007-05-01 |
| AU2006254256B2 (en) | 2012-04-12 |
| ATE445612T1 (de) | 2009-10-15 |
| ZA200710169B (en) | 2008-12-31 |
| MX2007014928A (es) | 2008-02-15 |
| IL187426A0 (en) | 2008-02-09 |
| IL187426A (en) | 2011-10-31 |
| EP1893603B1 (en) | 2009-10-14 |
| US7772253B2 (en) | 2010-08-10 |
| PL1893603T3 (pl) | 2010-03-31 |
| WO2006128803A1 (en) | 2006-12-07 |
| RU2403250C2 (ru) | 2010-11-10 |
| AU2006254256A1 (en) | 2006-12-07 |
| EP1893603A1 (en) | 2008-03-05 |
| KR100962732B1 (ko) | 2010-06-09 |
| CN101189226A (zh) | 2008-05-28 |
| KR20080008391A (ko) | 2008-01-23 |
| JP4949387B2 (ja) | 2012-06-06 |
| CA2608819A1 (en) | 2006-12-07 |
| DE602006009804D1 (de) | 2009-11-26 |
| US20060276508A1 (en) | 2006-12-07 |
| TWI315305B (en) | 2009-10-01 |
| RU2007148224A (ru) | 2009-07-20 |
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