AR070074A1 - Derivados 6- heterociclico- imidazo ( 1,2-alfa) piridina -2- carboxamidas, su preparacion y su aplicacion en terapeutica - Google Patents
Derivados 6- heterociclico- imidazo ( 1,2-alfa) piridina -2- carboxamidas, su preparacion y su aplicacion en terapeuticaInfo
- Publication number
- AR070074A1 AR070074A1 ARP080105779A ARP080105779A AR070074A1 AR 070074 A1 AR070074 A1 AR 070074A1 AR P080105779 A ARP080105779 A AR P080105779A AR P080105779 A ARP080105779 A AR P080105779A AR 070074 A1 AR070074 A1 AR 070074A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkoxy
- alkyl
- group
- halogen
- hydrogen atom
- Prior art date
Links
- JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical compound C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 11
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 7
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 6
- 229910003827 NRaRb Inorganic materials 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 150000002367 halogens Chemical class 0.000 abstract 3
- 125000004429 atom Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000005842 heteroatom Chemical group 0.000 abstract 2
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 2
- 229910052757 nitrogen Inorganic materials 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004800 4-bromophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Br 0.000 abstract 1
- 102000002559 Member 2 Group A Nuclear Receptor Subfamily 4 Human genes 0.000 abstract 1
- 108010093175 Member 2 Group A Nuclear Receptor Subfamily 4 Proteins 0.000 abstract 1
- 239000002253 acid Substances 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 201000010099 disease Diseases 0.000 abstract 1
- 208000037265 diseases, disorders, signs and symptoms Diseases 0.000 abstract 1
- 229910052731 fluorine Inorganic materials 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 229910052739 hydrogen Inorganic materials 0.000 abstract 1
- 239000001257 hydrogen Substances 0.000 abstract 1
- -1 hydroxy, amino Chemical group 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
-
- 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
- A61P19/08—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
- A61P19/10—Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease for osteoporosis
-
- 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
- A61P25/08—Antiepileptics; Anticonvulsants
-
- 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
- A61P25/14—Drugs for disorders of the nervous system for treating abnormal movements, e.g. chorea, dyskinesia
- A61P25/16—Anti-Parkinson drugs
-
- 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
- A61P25/18—Antipsychotics, i.e. neuroleptics; Drugs for mania or schizophrenia
-
- 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
-
- 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
- A61P25/26—Psychostimulants, e.g. nicotine, cocaine
-
- 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
- A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
-
- 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
-
- 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
- A61P35/00—Antineoplastic 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
-
- 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
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/02—Silicon compounds
- C07F7/08—Compounds having one or more C—Si linkages
- C07F7/0803—Compounds with Si-C or Si-Si linkages
- C07F7/081—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te
- C07F7/0812—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring
- C07F7/0814—Compounds with Si-C or Si-Si linkages comprising at least one atom selected from the elements N, O, halogen, S, Se or Te comprising a heterocyclic ring said ring is substituted at a C ring atom by Si
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic Table
- C07F7/22—Tin compounds
- C07F7/2208—Compounds having tin linked only to carbon, hydrogen and/or halogen
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- General Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Physical Education & Sports Medicine (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Cardiology (AREA)
- Psychology (AREA)
- Addiction (AREA)
- Heart & Thoracic Surgery (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
Abstract
Composicion farmacéutica y usos para tratar enfermedades que implican los receptores nucleares Nurr-1 Reivindicacion 1: Compuestos de formula (1) en la que: X representa un grupo fenilo sustituido opcionalmente con uno o varios grupos elegidos independientemente los unos de los otros entre los átomos o grupos siguientes: halogeno, alcoxi C1-6, alquilo C1-6, NRaRb, ciano, alcoxi C1-6carbonilo, estando los grupos alquilo C1-6 y alcoxi C1-6 sustituidos opcionalmente con uno o varios átomos de halogeno; R1 representa un átomo de hidrogeno, un halogeno, un grupo alcoxi C1-6, alquilo C1-6 o NRaRb, pudiendo estar los grupos alquilo y alcoxi sustituidos opcionalmente con uno o varios halogeno, hidroxi, amino o grupo alcoxi C1-6; R2 representa un grupo heterocíclico aromático, insaturado, parcialmente saturado o totalmente saturado, sustituido opcionalmente con uno o varios grupos elegidos independientemente los unos de los otros entre los átomos o grupos siguientes: hidroxi, alcoxi C1-6, halogeno, ciano, NRaRb, -CO-R5, -CO-NR6R7, -CO-O-R8, -NR9-CO-R10, cicloalquilo C3-7-alquilo C1-6, cicloalquilo C3-7-alcoxi C1-6, un grupo alquilo C1-6, sustituido opcionalmente con uno o varios hidroxi o NRaRb, un grupo oxido; R3 representa un átomo de hidrogeno, un grupo alquilo C1-6, alcoxi C1-6 o un átomo de halogeno; R4 representa un átomo de hidrogeno, un grupo alquilo C1-4, alcoxi C1-4 o un átomo de fluor; R5 representa un átomo de hidrogeno, un grupo fenilo o un grupo alquilo C1-6; R6 y R7, idénticos o diferentes, representan un átomo de hidrogeno, un grupo alquilo C1-6 o forman con el átomo de nitrogeno un ciclo de 4 a 7 eslabones que incluye opcionalmente otro heteroátomo elegido entre N, O o S; R8 representa un grupo alquilo C1-6; R9 y R10, idénticos o diferentes, representan un átomo de hidrogeno o un grupo alquilo C1-6; Ra y Rb son independientemente el uno del otro, hidrogeno, alquilo C1-6 o forman con el átomo de nitrogeno al que están unidos un ciclo de 4 a 7 eslabones; que incluye opcionalmente otro heteroátomo elegido entre N, O o S; con la excepcion de N-(4-bromofenil)-6-(1-metil-2-piperidinil)imidazo[1,2-a]-piridina2-carboxamida; en el estado de base o de sal de adicion a un ácido.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR0800005A FR2925903B1 (fr) | 2008-01-02 | 2008-01-02 | DERIVES 6-HETEROCYCLIQUE-IMIDAZO°1,2-a!PYRIDINE-2- CARBOXAMIDES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR070074A1 true AR070074A1 (es) | 2010-03-10 |
Family
ID=39745373
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080105779A AR070074A1 (es) | 2008-01-02 | 2008-12-30 | Derivados 6- heterociclico- imidazo ( 1,2-alfa) piridina -2- carboxamidas, su preparacion y su aplicacion en terapeutica |
Country Status (25)
| Country | Link |
|---|---|
| US (2) | US8314109B2 (es) |
| EP (1) | EP2225240B1 (es) |
| JP (1) | JP5258899B2 (es) |
| KR (1) | KR101600635B1 (es) |
| CN (1) | CN101959884B (es) |
| AR (1) | AR070074A1 (es) |
| AU (1) | AU2008351928B2 (es) |
| BR (1) | BRPI0821458A2 (es) |
| CA (1) | CA2710947C (es) |
| CL (1) | CL2008003928A1 (es) |
| CO (1) | CO6331309A2 (es) |
| EA (1) | EA019122B1 (es) |
| FR (1) | FR2925903B1 (es) |
| HK (1) | HK1148016A1 (es) |
| IL (1) | IL206669A (es) |
| MA (1) | MA32527B1 (es) |
| ME (1) | ME01157B (es) |
| MX (1) | MX2010007353A (es) |
| MY (1) | MY155468A (es) |
| NZ (1) | NZ586474A (es) |
| SG (1) | SG187408A1 (es) |
| TW (1) | TWI432432B (es) |
| UY (1) | UY31589A1 (es) |
| WO (1) | WO2009106750A2 (es) |
| ZA (1) | ZA201004644B (es) |
Families Citing this family (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2925907B1 (fr) * | 2008-01-02 | 2010-10-15 | Sanofi Aventis | DERIVES DE 2-HETEROAROYL-IMIDAZO°1,2-a!PYRIDINE, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE |
| CA2852615A1 (en) * | 2011-10-21 | 2013-04-25 | Torrent Pharmaceuticals Limited | Novel substituted imidazopyrimidines as gpbar1 receptor modulators |
| JP5965499B2 (ja) | 2012-12-25 | 2016-08-03 | 日本曹達株式会社 | ハロゲン化アニリンおよびその製造方法 |
| CN108295074B (zh) * | 2018-02-01 | 2020-08-28 | 华中农业大学 | 一种噻二唑并三嗪类化合物在制备单胺氧化酶抑制剂中的用途 |
Family Cites Families (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| FR2638161B1 (fr) * | 1988-10-24 | 1991-01-11 | Centre Nat Rech Scient | Nouvelles benzoyl-2 imidazo (1,2-a) pyridines et leurs sels, leur procede de preparation, leur application a titre de medicaments et les compositions pharmaceutiques les renfermant |
| IE904346A1 (en) * | 1989-12-04 | 1991-06-05 | Searle & Co | IMIDAZO[1,2-a]PYRIDINYLALKYL COMPOUNDS FOR TREATMENT OF¹NEUROTOXIC INJURY |
| WO2004029229A2 (en) * | 2002-09-24 | 2004-04-08 | Neuro Therapeutics Ab | Methods for promoting dopaminergic neuronal development by using ng4a-subfamily and wnt-ligands |
| EP1567527A1 (en) * | 2002-11-27 | 2005-08-31 | Eli Lilly And Company | Condensed pyrazolo derivatives |
| WO2004103991A1 (fr) * | 2003-05-20 | 2004-12-02 | 'chemical Diversity Research Institute', Ltd. | Piperidines 2-substituees, bibliotheque focalisee et composition pharmaceutique |
| DE102005019181A1 (de) * | 2005-04-25 | 2006-10-26 | Novartis Ag | Peptid-Deformylase (PDF) Inhibitoren 1 |
| FR2903107B1 (fr) * | 2006-07-03 | 2008-08-22 | Sanofi Aventis Sa | Derives d'imidazopyridine-2-carboxamides, leur preparation et leur application en therapeutique |
| FR2903106B1 (fr) * | 2006-07-03 | 2010-07-30 | Sanofi Aventis | Utilisations de 2-benzoyl-imidazopyridines en therapeutique |
| FR2903108B1 (fr) * | 2006-07-03 | 2008-08-29 | Sanofi Aventis Sa | Utilisation de derives d'imidazo[1,2-a] pyridine-2-carboxamides en therapeutique. |
-
2008
- 2008-01-02 FR FR0800005A patent/FR2925903B1/fr not_active Expired - Fee Related
- 2008-12-30 CL CL2008003928A patent/CL2008003928A1/es unknown
- 2008-12-30 UY UY31589A patent/UY31589A1/es not_active Application Discontinuation
- 2008-12-30 AR ARP080105779A patent/AR070074A1/es unknown
- 2008-12-31 EA EA201070814A patent/EA019122B1/ru not_active IP Right Cessation
- 2008-12-31 WO PCT/FR2008/001836 patent/WO2009106750A2/fr active Application Filing
- 2008-12-31 JP JP2010541085A patent/JP5258899B2/ja not_active Expired - Fee Related
- 2008-12-31 NZ NZ586474A patent/NZ586474A/en not_active IP Right Cessation
- 2008-12-31 CA CA2710947A patent/CA2710947C/fr not_active Expired - Fee Related
- 2008-12-31 MX MX2010007353A patent/MX2010007353A/es active IP Right Grant
- 2008-12-31 BR BRPI0821458-1A patent/BRPI0821458A2/pt not_active IP Right Cessation
- 2008-12-31 TW TW097151708A patent/TWI432432B/zh not_active IP Right Cessation
- 2008-12-31 EP EP08872775.5A patent/EP2225240B1/fr active Active
- 2008-12-31 AU AU2008351928A patent/AU2008351928B2/en not_active Ceased
- 2008-12-31 ME MEP-2010-103A patent/ME01157B/me unknown
- 2008-12-31 CN CN2008801277669A patent/CN101959884B/zh not_active Expired - Fee Related
- 2008-12-31 KR KR1020107017143A patent/KR101600635B1/ko not_active IP Right Cessation
- 2008-12-31 MY MYPI2010003073A patent/MY155468A/en unknown
- 2008-12-31 SG SG2012096269A patent/SG187408A1/en unknown
-
2010
- 2010-06-28 IL IL206669A patent/IL206669A/en not_active IP Right Cessation
- 2010-07-01 US US12/828,374 patent/US8314109B2/en not_active Expired - Fee Related
- 2010-07-01 ZA ZA2010/04644A patent/ZA201004644B/en unknown
- 2010-07-02 CO CO10080887A patent/CO6331309A2/es active IP Right Grant
- 2010-07-27 MA MA33051A patent/MA32527B1/fr unknown
-
2011
- 2011-03-07 HK HK11102219.8A patent/HK1148016A1/xx not_active IP Right Cessation
-
2012
- 2012-10-10 US US13/648,731 patent/US8691990B2/en not_active Expired - Fee Related
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