AR054208A1 - Derivados de oxopiperidina, su preparacion, una composicion farmaceutica y compuestos intermediarios - Google Patents
Derivados de oxopiperidina, su preparacion, una composicion farmaceutica y compuestos intermediariosInfo
- Publication number
- AR054208A1 AR054208A1 AR20050103084A ARP050103084A AR054208A1 AR 054208 A1 AR054208 A1 AR 054208A1 AR 20050103084 A AR20050103084 A AR 20050103084A AR P050103084 A ARP050103084 A AR P050103084A AR 054208 A1 AR054208 A1 AR 054208A1
- Authority
- AR
- Argentina
- Prior art keywords
- cycloalkyl
- heterocycloalkyl
- heteroaryl
- aryl
- alkyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 239000008194 pharmaceutical composition Substances 0.000 title abstract 2
- XUWHAWMETYGRKB-UHFFFAOYSA-N piperidin-2-one Chemical class O=C1CCCCN1 XUWHAWMETYGRKB-UHFFFAOYSA-N 0.000 title abstract 2
- 239000012450 pharmaceutical intermediate Substances 0.000 title 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 24
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 19
- 125000001072 heteroaryl group Chemical group 0.000 abstract 17
- 125000003118 aryl group Chemical group 0.000 abstract 16
- 125000000217 alkyl group Chemical group 0.000 abstract 14
- 125000002877 alkyl aryl group Chemical group 0.000 abstract 7
- 125000005213 alkyl heteroaryl group Chemical group 0.000 abstract 7
- 125000005843 halogen group Chemical group 0.000 abstract 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 7
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 208000024172 Cardiovascular disease Diseases 0.000 abstract 1
- 101100134927 Gallus gallus COR8 gene Proteins 0.000 abstract 1
- 208000008589 Obesity Diseases 0.000 abstract 1
- 201000001880 Sexual dysfunction Diseases 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000004122 cyclic group Chemical group 0.000 abstract 1
- 206010012601 diabetes mellitus Diseases 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 239000000543 intermediate Substances 0.000 abstract 1
- 238000000034 method Methods 0.000 abstract 1
- 235000020824 obesity Nutrition 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 231100000872 sexual dysfunction Toxicity 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 125000003003 spiro group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/10—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms
- C07D295/104—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/10—Drugs for genital or sexual disorders; Contraceptives for impotence
-
- 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
- A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
- A61P25/32—Alcohol-abuse
-
- 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
- A61P3/00—Drugs for disorders of the metabolism
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/04—Anorexiants; Antiobesity agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
- A61P3/06—Antihyperlipidemics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- 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
-
- 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
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
- C07D295/04—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
- C07D295/10—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms
- C07D295/104—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
- C07D295/108—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by doubly bound oxygen or sulphur atoms with the ring nitrogen atoms and the doubly bound oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
-
- 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
- C07D401/06—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 only aliphatic carbon atoms
-
- 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
-
- 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
- C07D405/14—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 three or more hetero rings
-
- 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
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Diabetes (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Addiction (AREA)
- Psychiatry (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Gynecology & Obstetrics (AREA)
- Child & Adolescent Psychology (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Emergency Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Abstract
La presente se refiere a derivados de oxopiperidina de formula general (1), a un procedimiento para su preparacion, a medicamentos y composiciones farmacéuticas en base a ellos y a compuestos intermediarios de síntesis. Estos compuestos son de aplicacion en el tratamiento y prevencion de la obesidad, diabetes y disfunciones sexuales y el tratamiento de enfermedades cardiovasculares. Reivindicacion 1: Compuesto que responde a la formula (1): en la cual: n es igual a 1; Ra, Ra', Rb y Rb' son idénticos o diferentes entre sí, y representan un átomo de hidrogeno o un grupo alquilo o cicloalquilo, Rb y Rb' pueden formar juntos, con los átomos de carbono del ciclo al que están unidos, un puente carbonado que comprende de 4 a 5 eslabones; R1 representa un grupo alquilo o cicloalquilo; R2 representa un grupo heteroarilo; R3 representa 1 a 3 grupos, idénticos o diferentes entre sí, situados en posiciones cualesquiera del nucleo al cual están unidos, y elegidos, entre los átomos de halogeno y los grupos alquilos, cicloalquilos, -OR, -NRR', -CO-NRR', -NR-CO-R', -NR-CONRR', -NR-COOR', -NO2, -CN y -COOR; R5 representa un átomo de hidrogeno, un grupo alquilo, o cicloalquilo; R4 se elige entre los grupos de formulas (a), (b) y (c) que se presentan más adelante, eventualmente, substituidos por un grupo oxo, o mono- o polisubstituido por un grupo arilo o heteroarilo; en las cuales p = 0, 1, 2 o 3, m = 0, 1 o 2, y, o bien a) X representa un eslabon -N(R10) -, donde R10, se elige entre: ò un grupo (CH2)x-OR8, (CH2)x-COOR8, -(CH2)x-NR8R9, (CH2)x-CO-NR8R9 o -(CH2)x-NR8-COR9, -(CH2)x-COR8 en los cuales x = 1, 2, 3 o 4; ò un grupo cicloalquilo o heterocicloalquilo fusionado con un grupo arilo o heteroarilo; ò un grupo cicloalquilo, heterocicloalquilo, arilo, heteroarilo, alquilarilo, alquilheteroarilo, -CO-alquilo, -CO-cicloalquilo, -CO-heterocicloalquilo, -CO-arilo, -CO-heteroarilo, -CO-alquilarilo, -CO-alquilheteroarilo, -CS-alquilo, -CS-cicloalquilo, -CS- heterocicloalquilo, -CS-arilo, -CS-heteroarilo, -CS-alquilarilo, -CS-alquilheteroarilo, -CS-NR8R9, C(=NH)-NR8R9, -SO2-alquilo-, -SO2-cicloalquilo, -SO2-heterocicloalquilo, -SO2-arilo, -SO2-heteroarilo, -SO2-alquilarilo, -SO2-alquilheteroarilo o -SO2- NR8R9, los grupos alquilos, cicloalquilos, heterocicloalquilos, arilos, heteroarilos están eventualmente substituidos por 1 o varios grupos elegidos entre los átomos de halogeno y los grupos R, R', OR, NRR', -CO-NRR', -NRCOR', NRCONRR', -NO2, CN, - COOR, OCOR, COR,, OCONRR', NRCOOR'; los grupos cicloalquilos, heterocicloalquilos, están eventualmente fusionados con un grupo arilo o heteroarilo; o bien R10 forma con el átomo de nitrogeno al cual está unido y un átomo de carbono situado en una posicion cualquiera de la estructura cíclica de la formula (a), pero no adyacente a dicho átomo de nitrogeno, un puente que comprende de 3 a 5 eslabones, R8 y R9 se eligen, independientemente entre si, entre un átomo de hidrogeno y los grupos alquilos, cicloalquilos, heterocicloalquilos, arilos, heteroarilos, alquilarilos, alquilheteroarilos, -CO-alquilos, -CO-cicloalquilos, -CO-heterocicloalquilos, -CO-arilos, -CO-heteroarilos, -CO-alquilarilos, -CO-alquilheteroarilos, -SO2-alquilos, - SO2-cicloalquilos, -SO2-heterocicloalquilos, -SO2-arilos, -SO2-heteroarilos, -SO2-alquilarilos, -SO2-alquilheteroarilos, -C(=NH)-NRR', -COOR, -CO-NRR', -CS-NRR' y -(CH2)x-OR, donde x = 0, 1, 2, 3 o 4, los grupos alquilos, cicloalquilos, heterocicloalquilos, arilos y heteroarilos están substituidos, eventualmente, por uno o varios grupos elegidos entre los átomos de halogeno y los grupos R, R', OR, NRR', -CO-NRR', -NRCOR', NRCONRR', -NO2, CN, -COOR, OCOR, COR, OCONRR', NRCOOR'; o bien R8 y R9 forman juntos un cicloalquilo o un heterocicloalquilo; R y R' representan, independientemente entre si, un átomo de hidrogeno o un grupo alquilo, cicloalquilo, heterocicloalquilo, arilo, heteroarilo, alquilarilo o alquilheteroarilo, o pueden formar juntos un cicloalquilo o un heterocicloalquilo; o bien, b) X representa un eslabon -C(R6)(R7)-, donde R6 se elige entre: ò un átomo de hidrogeno, un átomo de halogeno; ò un grupo (CH2)x-OR8, (CH2)x-COOR8, -(CH2)x-NR8R9, (CH2)x-CO-NR8R9 o -(CH2)x-NR8-COR9, -(CH2)x-COR8 en los cuales x = 1, 2, 3 o 4; ò un grupo alquilo, cicloalquilo, heterocicloalquilo, arilo, heteroarilo, alquilarilo, alquilheteroarilo, -CO-alquilo, -CO-cicloalquilo, -CO-heterocicloalquilo, -CO-arilo, -CO- heteroarilo, -CO-alquilarilo, -CO-alquilheteroarilo, -CS-alquilo, -CS-cicloalquilo, -CS-heterocicloalquilo, -CS-arilo, -CS-heteroarilo, -CS-alquilarilo, -CS-alquilheteroarilo, -CS-NR8R9, C(=NH)-NR8R9; ò un grupo cicloalquilo o heterocicloalquilo, fusionado o no, situado en posicion espiro sobre el ciclo de formula (a) al cual está unido; un grupo cicloalquilo o heterocicloalquilo fusionado con un grupo arilo o heteroarilo; los grupos alquilos, cicloalquilos, heterocicloalquilos, arilos o heteroarilos están substituidos, eventualmente, por uno o varios grupos elegidos entre los átomos de halogeno y los grupos R, R', OR, NRR', -CO-NRR', -NRCOR', NRCONRR', -NO2, CN, -COOR, OCOR, COR, OCONRR', NRCOOR'; los grupos cicloalquilos o heterocicloalquilos están eventualmente fusionados con un grupo arilo o heteroarilo; R7 se elige entre los átomos de halogeno y los grupos alquilos, cicloalquilos, arilos, heteroarilos, alquilarilos, alquilheteroarilos, -OR, -O-arilos, -O- heteroarilos, -O-alquilarilos, -O-alquilheteroarilos, -NRR', -CO-NRR', -NR-CO-R', -NR-CO-NRR', -NR-COOR', -NO2, -CN y -COOR; R8 y R9, se eligen, independientemente entre si, entre un átomo de hidrogeno y los grupos alquilos, cicloalquilos, heterocicloalquilos, arilos, heteroarilos, alquilarilos, alquilheteroarilos, -CO-alquilos, -CO-cicloalquilos, -CO-heterocicloalquilos, -CO-arilos, -CO-heteroarilos, -CO-alquilarilos, -CO-alquilheteroarilos, -SO2-alquilos, -SO2-cicloalquilos, -SO2- heterocicloalquilos, -SO2-arilos, -SO2-heteroarilos, -SO2-alquilarilos, -SO2-alquilheteroarilos, -C(=NH)-NRR', -COOR, -CO-NRR', -CS NRR' y -(CH2)x-OR, donde x = 0, 1, 2, 3 o 4, los grupos alquilos, cicloalquilos, heterocicloalquilos, arilos y heteroarilos están substituidos, eventualmente, por uno o varios grupos elegidos entre los átomos de halogeno y los grupos R, R', OR, NRR', -CO-NRR', -NRCOR', NRCONRR', -NO2, CN, -COOR, OCOR, COR, OCONRR', NRCOOR'; o bien R8 y R9 forman juntos un cicloalquilo o un heterocicloalquilo; R y R' representan, independientemente entre si, un átomo de hidrogeno o un grupo alquilo, cicloalquilo, heterocicloalquilo, arilo, heteroarilo, alquilarilo o alquilheteroarilo, o pueden formar juntos un cicloalquilo o un heterocicloalquilo, en estado de base o de sal de adicion con un ácido, así como en estado de hidrato o de solvato.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0408369A FR2873690B1 (fr) | 2004-07-29 | 2004-07-29 | Derives d'oxopiperidine, leur preparation et leur application en therapeutique |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR054208A1 true AR054208A1 (es) | 2007-06-13 |
Family
ID=34947722
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| AR20050103084A AR054208A1 (es) | 2004-07-29 | 2005-07-26 | Derivados de oxopiperidina, su preparacion, una composicion farmaceutica y compuestos intermediarios |
Country Status (25)
| Country | Link |
|---|---|
| US (1) | US20070149562A1 (es) |
| EP (1) | EP1773796B1 (es) |
| JP (1) | JP4871866B2 (es) |
| KR (1) | KR20070047802A (es) |
| CN (1) | CN101010309A (es) |
| AR (1) | AR054208A1 (es) |
| AT (1) | ATE459608T1 (es) |
| AU (1) | AU2005276353C1 (es) |
| BR (1) | BRPI0512680A (es) |
| CA (1) | CA2577177A1 (es) |
| CY (1) | CY1110124T1 (es) |
| DE (1) | DE602005019743D1 (es) |
| DK (1) | DK1773796T3 (es) |
| ES (1) | ES2341722T3 (es) |
| FR (1) | FR2873690B1 (es) |
| IL (1) | IL180770A (es) |
| MX (1) | MX2007001139A (es) |
| PE (1) | PE20060563A1 (es) |
| PL (1) | PL1773796T3 (es) |
| PT (1) | PT1773796E (es) |
| RU (1) | RU2376298C2 (es) |
| SI (1) | SI1773796T1 (es) |
| TW (1) | TW200609217A (es) |
| UY (1) | UY29036A1 (es) |
| WO (1) | WO2006021655A2 (es) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2873691B1 (fr) * | 2004-07-29 | 2006-10-06 | Sanofi Synthelabo | Derives d'amino-piperidine, leur preparation et leur application en therapeutique |
| KR20090047458A (ko) | 2006-08-08 | 2009-05-12 | 사노피-아벤티스 | 아릴아미노아릴-알킬-치환된 이미다졸리딘-2,4-디온, 이의 제조방법, 이들 화합물을 포함하는 약제 및 이의 용도 |
| EP2020405A1 (en) * | 2007-07-30 | 2009-02-04 | Santhera Pharmaceuticals (Schweiz) AG | Substituted aryl or heteroarylpiperidine derivatives as melanocortin-4 receptor modulators |
| EP2025674A1 (de) | 2007-08-15 | 2009-02-18 | sanofi-aventis | Substituierte Tetrahydronaphthaline, Verfahren zu ihrer Herstellung und ihre Verwendung als Arzneimittel |
| UY31968A (es) | 2008-07-09 | 2010-01-29 | Sanofi Aventis | Nuevos derivados heterocíclicos, sus procesos para su preparación, y sus usos terapéuticos |
| WO2012120052A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit carbozyklen oder heterozyklen substituierte oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| EP2683703B1 (de) | 2011-03-08 | 2015-05-27 | Sanofi | Neue substituierte phenyl-oxathiazinderivate, verfahren zu deren herstellung, diese verbindungen enthaltende arzneimittel und deren verwendung |
| US8710050B2 (en) | 2011-03-08 | 2014-04-29 | Sanofi | Di and tri- substituted oxathiazine derivatives, method for the production, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| WO2012120053A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Verzweigte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| US8809324B2 (en) | 2011-03-08 | 2014-08-19 | Sanofi | Substituted phenyl-oxathiazine derivatives, method for producing them, drugs containing said compounds and the use thereof |
| WO2012120056A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Tetrasubstituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| US8828994B2 (en) | 2011-03-08 | 2014-09-09 | Sanofi | Di- and tri-substituted oxathiazine derivatives, method for the production thereof, use thereof as medicine and drug containing said derivatives and use thereof |
| WO2012120051A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit adamantan- oder noradamantan substituierte benzyl-oxathiazinderivate, diese verbindungen enthaltende arzneimittel und deren verwendung |
| WO2012120058A1 (de) | 2011-03-08 | 2012-09-13 | Sanofi | Mit benzyl- oder heteromethylengruppen substituierte oxathiazinderivate, verfahren zu deren herstellung, ihre verwendung als medikament sowie sie enthaltendes arzneimittel und deren verwendung |
| US9744171B2 (en) | 2012-03-06 | 2017-08-29 | Vanderbilt University | Positive allosteric modulators for melanocortin receptors |
Family Cites Families (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2719311B1 (fr) * | 1994-03-18 | 1998-06-26 | Sanofi Sa | Composés antagonistes sélectifs du récepteur NK3 humain et leur utilisation comme médicaments et outils de diagnostic. |
| US5968929A (en) * | 1996-10-30 | 1999-10-19 | Schering Corporation | Piperazino derivatives as neurokinin antagonists |
| WO2000074679A1 (en) * | 1999-06-04 | 2000-12-14 | Merck & Co., Inc. | Substituted piperidines as melanocortin-4 receptor agonists |
| AU2001249296B2 (en) * | 2000-03-23 | 2005-03-24 | Merck Sharp & Dohme Corp. | Substituted piperidines as melanocortin receptor agonists |
| AU2001288285B2 (en) * | 2000-08-23 | 2005-09-29 | Merck & Co., Inc. | Substituted piperidines as melanocortin receptor agonists |
| JP2005511475A (ja) * | 2001-03-02 | 2005-04-28 | ブリストル−マイヤーズ スクイブ カンパニー | メラノコルチン受容体のモジュレーターとして有用な化合物及びそれを含む製薬組成物 |
| JP4336196B2 (ja) * | 2001-07-18 | 2009-09-30 | メルク エンド カムパニー インコーポレーテッド | メラノコルチン受容体作動薬としての架橋ピペリジン誘導体 |
| US6977264B2 (en) * | 2001-07-25 | 2005-12-20 | Amgen Inc. | Substituted piperidines and methods of use |
| US20040010010A1 (en) * | 2002-04-30 | 2004-01-15 | Ebetino Frank Hallock | Melanocortin receptor ligands |
| US7049323B2 (en) * | 2003-04-25 | 2006-05-23 | Bristol-Myers Squibb Company | Amidoheterocycles as modulators of the melanocortin-4 receptor |
| KR20050045927A (ko) * | 2003-11-12 | 2005-05-17 | 주식회사 엘지생명과학 | 멜라노코틴 수용체의 항진제 |
| FR2873691B1 (fr) * | 2004-07-29 | 2006-10-06 | Sanofi Synthelabo | Derives d'amino-piperidine, leur preparation et leur application en therapeutique |
| FR2873693B1 (fr) * | 2004-07-29 | 2006-09-15 | Sanofi Synthelabo | Derives d'amino-tropane, leur preparation et leur application en therapeutique |
-
2004
- 2004-07-29 FR FR0408369A patent/FR2873690B1/fr not_active Expired - Fee Related
-
2005
- 2005-07-20 ES ES05790990T patent/ES2341722T3/es not_active Expired - Lifetime
- 2005-07-20 CA CA002577177A patent/CA2577177A1/fr not_active Abandoned
- 2005-07-20 DE DE602005019743T patent/DE602005019743D1/de not_active Expired - Lifetime
- 2005-07-20 SI SI200531010T patent/SI1773796T1/sl unknown
- 2005-07-20 MX MX2007001139A patent/MX2007001139A/es active IP Right Grant
- 2005-07-20 DK DK05790990.5T patent/DK1773796T3/da active
- 2005-07-20 PT PT05790990T patent/PT1773796E/pt unknown
- 2005-07-20 EP EP05790990A patent/EP1773796B1/fr not_active Expired - Lifetime
- 2005-07-20 CN CNA2005800292206A patent/CN101010309A/zh active Pending
- 2005-07-20 WO PCT/FR2005/001854 patent/WO2006021655A2/fr not_active Ceased
- 2005-07-20 AU AU2005276353A patent/AU2005276353C1/en not_active Ceased
- 2005-07-20 RU RU2007107374/04A patent/RU2376298C2/ru not_active IP Right Cessation
- 2005-07-20 BR BRPI0512680-0A patent/BRPI0512680A/pt not_active IP Right Cessation
- 2005-07-20 PL PL05790990T patent/PL1773796T3/pl unknown
- 2005-07-20 KR KR1020077004655A patent/KR20070047802A/ko not_active Ceased
- 2005-07-20 JP JP2007523108A patent/JP4871866B2/ja not_active Expired - Fee Related
- 2005-07-20 AT AT05790990T patent/ATE459608T1/de active
- 2005-07-26 AR AR20050103084A patent/AR054208A1/es not_active Application Discontinuation
- 2005-07-27 PE PE2005000879A patent/PE20060563A1/es not_active Application Discontinuation
- 2005-07-27 UY UY29036A patent/UY29036A1/es not_active Application Discontinuation
- 2005-07-28 TW TW094125682A patent/TW200609217A/zh unknown
-
2007
- 2007-01-17 IL IL180770A patent/IL180770A/en not_active IP Right Cessation
- 2007-01-25 US US11/626,970 patent/US20070149562A1/en not_active Abandoned
-
2010
- 2010-06-01 CY CY20101100481T patent/CY1110124T1/el unknown
Also Published As
| Publication number | Publication date |
|---|---|
| EP1773796A2 (fr) | 2007-04-18 |
| CY1110124T1 (el) | 2015-01-14 |
| WO2006021655A2 (fr) | 2006-03-02 |
| AU2005276353C1 (en) | 2012-03-29 |
| TW200609217A (en) | 2006-03-16 |
| FR2873690A1 (fr) | 2006-02-03 |
| IL180770A0 (en) | 2007-06-03 |
| ATE459608T1 (de) | 2010-03-15 |
| JP4871866B2 (ja) | 2012-02-08 |
| BRPI0512680A (pt) | 2008-04-01 |
| SI1773796T1 (sl) | 2010-07-30 |
| DK1773796T3 (da) | 2010-06-21 |
| PL1773796T3 (pl) | 2010-08-31 |
| RU2376298C2 (ru) | 2009-12-20 |
| WO2006021655A3 (fr) | 2006-04-20 |
| RU2007107374A (ru) | 2008-09-10 |
| AU2005276353A1 (en) | 2006-03-02 |
| EP1773796B1 (fr) | 2010-03-03 |
| UY29036A1 (es) | 2006-02-24 |
| IL180770A (en) | 2011-10-31 |
| PE20060563A1 (es) | 2006-07-12 |
| CA2577177A1 (fr) | 2006-03-02 |
| CN101010309A (zh) | 2007-08-01 |
| DE602005019743D1 (de) | 2010-04-15 |
| WO2006021655A8 (fr) | 2007-05-24 |
| FR2873690B1 (fr) | 2006-10-13 |
| KR20070047802A (ko) | 2007-05-07 |
| PT1773796E (pt) | 2010-06-01 |
| ES2341722T3 (es) | 2010-06-25 |
| AU2005276353B2 (en) | 2011-12-01 |
| JP2008508240A (ja) | 2008-03-21 |
| MX2007001139A (es) | 2007-04-19 |
| US20070149562A1 (en) | 2007-06-28 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| AR054208A1 (es) | Derivados de oxopiperidina, su preparacion, una composicion farmaceutica y compuestos intermediarios | |
| AR050186A1 (es) | Derivados de amino-piperidina, su preparacion y su aplicacion en terapeutica. | |
| CO6251201A2 (es) | Composiciones y metodos para el tratamiento de3 enfermedades y desordenes oftalmicos | |
| HRP20191469T1 (hr) | Novi kondenzirani spojevi piridina kao inhibitori kazeinske kinase | |
| AR044874A1 (es) | Derivados de 4- cianopirazol-3 - carboxamida, su preparacion y su aplicacion en terapeutica | |
| AR081848A1 (es) | Inhibidores de la proteina ns5a del vhc | |
| AR037489A1 (es) | Quinolinas sustituidas y proceso para su preparacion | |
| AR045010A1 (es) | Pirimidinas utiles como moduladores de canales ionicos cuya activacion es controlada por tension | |
| AR043700A1 (es) | Derivados de 3-substituida-4-pirimidona | |
| AR070437A1 (es) | Moduladores de beta - amiloide | |
| AR038843A1 (es) | Derivados de fenetanolamina para el tratamiento de enfermedades respiratorias | |
| AR054186A1 (es) | Derivados de tetrahidroindazolona y tetrahidroindolona | |
| AR067845A1 (es) | Compuestos para tratar trastornos relacionados con la modulacion de receptores de rianodina y composicion farmaceutica | |
| AR067027A1 (es) | Derivados de 2, 3-dihidro-1h-pirrol[3, 4b]quinolin-1-ona, una composicion farmaceutica que los comprende y su uso en la fabricacion de un medicamento para el tratamiento de enfermedades mediadas por la modulacion de la actividad del receptor gaba a. | |
| AR084430A1 (es) | Di/tri-aza-espiro-alcanos c | |
| ES2603931T3 (es) | Compuestos de triazolo | |
| AR085398A1 (es) | Ureas asimetricas y usos medicos de las mismas | |
| AR076866A1 (es) | Tetrahidroisoquinolinas sustituidas con arilo, heteroarilo y heterociclo y el uso de las mismas | |
| AR057959A1 (es) | 5-pirazolpiperidinas-(sustituidas) | |
| AR069813A1 (es) | Derivados de 2- amino-pirimidina, una composicion farmaceutica, un metodo de preparacion del compuesto y uso del mismo para preparar un medicamento | |
| CO2020001326A2 (es) | Nuevos compuestos heterocíclicos como inhibidores de cdk8/19 | |
| AR064136A1 (es) | Derivados de espiro-piperidina, metodos para su preparacion, una composicion farmaceutica que los comprende y su uso en la fabricacion de medicamentos para el tratamiento de enfermedades relacionadas con la accion antagonista del receptor v1a. | |
| AR044906A1 (es) | Derivados de difenilpiridina, su preparacion y su aplicacion en terapeutica | |
| AR039988A1 (es) | Derivados de benzoxazina como moduladores de 5-ht6 y usos de los mismos | |
| AR040133A1 (es) | Derivados de n-acilamino bencil eter |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FA | Abandonment or withdrawal |