AR042658A1 - Derivados de 1,5-diaril-pirrol-3-carboxamida y su uso como moduladores de receptores canabinoides - Google Patents
Derivados de 1,5-diaril-pirrol-3-carboxamida y su uso como moduladores de receptores canabinoidesInfo
- Publication number
- AR042658A1 AR042658A1 ARP030104797A ARP030104797A AR042658A1 AR 042658 A1 AR042658 A1 AR 042658A1 AR P030104797 A ARP030104797 A AR P030104797A AR P030104797 A ARP030104797 A AR P030104797A AR 042658 A1 AR042658 A1 AR 042658A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- alkyl
- optionally substituted
- alkyl group
- groups
- Prior art date
Links
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 8
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 8
- -1 trifluoromethylthio, difluoromethoxy Chemical group 0.000 abstract 7
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 229910052757 nitrogen Inorganic materials 0.000 abstract 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 4
- 125000002777 acetyl group Chemical group [H]C([H])([H])C(*)=O 0.000 abstract 3
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 125000005330 8 membered heterocyclic group Chemical group 0.000 abstract 2
- 208000008589 Obesity Diseases 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 125000004849 alkoxymethyl group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 0.000 abstract 2
- 125000004356 hydroxy functional group Chemical group O* 0.000 abstract 2
- 238000000034 method Methods 0.000 abstract 2
- 235000020824 obesity Nutrition 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 229920006395 saturated elastomer Polymers 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- 125000006594 (C1-C3) alkylsulfony group Chemical group 0.000 abstract 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 1
- 208000012902 Nervous system disease Diseases 0.000 abstract 1
- 208000025966 Neurological disease Diseases 0.000 abstract 1
- 125000005115 alkyl carbamoyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000002178 anthracenyl group Chemical group C1(=CC=CC2=CC3=CC=CC=C3C=C12)* 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 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
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 1
- 239000008194 pharmaceutical composition Substances 0.000 abstract 1
- 239000000651 prodrug Substances 0.000 abstract 1
- 229940002612 prodrug Drugs 0.000 abstract 1
- 208000020016 psychiatric disease Diseases 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 230000001225 therapeutic effect Effects 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 abstract 1
Classifications
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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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
-
- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/402—1-aryl substituted, e.g. piretanide
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- 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
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/4025—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil not condensed and containing further heterocyclic rings, e.g. cromakalim
-
- 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
- A61K31/4523—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
- A61K31/454—Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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- 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
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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- A61P3/08—Drugs for disorders of the metabolism for glucose homeostasis
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- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/30—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
- C07D207/34—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two 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
-
- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Biomedical Technology (AREA)
- Diabetes (AREA)
- Epidemiology (AREA)
- Obesity (AREA)
- Hematology (AREA)
- Psychiatry (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Endocrinology (AREA)
- Heart & Thoracic Surgery (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Vascular Medicine (AREA)
- Child & Adolescent Psychology (AREA)
- Communicable Diseases (AREA)
- Urology & Nephrology (AREA)
- Oncology (AREA)
- Hospice & Palliative Care (AREA)
- Emergency Medicine (AREA)
- Pulmonology (AREA)
- Reproductive Health (AREA)
- Nutrition Science (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Un compuesto de fórmula (1), procesos para preparar tales compuestos, su uso en el tratamiento de obesidad, trastornos psiquiátricos y neurológicos, particularmente obesidad, métodos para su uso terapéutico y composiciones farmacéuticas que los contienen. Reivindicación 1: Un compuesto caracterizado porque responde a la fórmula (1), y sales, profármacos y solvatos aceptables para uso farmacéutico del mismo, en donde R1 y R2 representan en forma independiente fenilo, tienilo o piridilo cada uno de los cuales está opcionalmente sustituido por uno, dos o tres grupos representados por Z; Z representa un grupo alquilo C1-3, un grupo alcoxi C1-3, hidroxi, halo, trifluorometilo, trifluorometiltio, difluorometoxi, trifluorometoxi, trifluorometilsulfonilo, amino, mono o di-alquilamino (C1-3), mono o di-alquilamido (C1-3), alquilsulfonilo C1-3, alcoxicarbonilo C1-3, carboxi, ciano, carbamoílo, mono o di-alquilo (C1-3) carbamoílo, sulfamoilo y acetilo; y R3 es H, un grupo alquilo C1-3, un grupo alcoximetilo C1-3, trifluorometilo, un grupo amino-alquilo (C1-3), un grupo hidroxi-alquilo (C1-3), alcoxicarbonilo C1-3, carboxi, ciano, carbamoílo, mono o di-alquilcrbamoilo (C1-3), acetilo, o hidrazinocarbonilo de fórmula -CONHNRaRb donde Ra y Rb son como se define para R4 y R5 respectivamente y; X es CO o SO2; Y está ausente o representa NH opcionalmente sustituido con un grupo alquilo C1-3; R4 y R5 representan en forma independiente un grupo alquilo C1-6; un grupo (amino)alquilo C1-4 en donde el amino está opcionalmente sustituido con uno o más grupos alquilo C1-3; un grupo carbocíclico C3-15 no aromático opcionalmente sustituido; un grupo cicloalquil(C3-12)-alquilo(C1-3); un grupo -(CH2)r(fenil)s en donde r es 0, 1, 2, 3 ó 4, s es 1 cuando r es 0, caso contrario, s es 1 ó 2 y los grupos fenilo están sustituidos opcionalmente en forma independiente por uno, dos o tres grupos representados por Z; naftilo; antracenilo; un grupo heterocíclico saturado de 5 a 8 miembros que contiene un nitrógeno y opcionalmente uno de los siguientes: oxígeno, azufre o un nitrógeno adicional donde el grupo heterocíclico está opcionalmente sustituido con uno o más grupos alquilo C1-3, hidroxi o bencilo; 1-adamantilmetilo; un grupo -(CH2)thet en donde t es 0, 1, 2, 3 ó 4, y la cadena alquileno está opcionalmente sustituida por uno o más grupos alquilo C1-3 y Het representa un heterociclo aromático opcionalmente sustituido por uno, dos o tres grupos seleccionados entre un grupo alquilo C1-6; un grupo alcoxi C1-6 o halo; o R4 representa H y R5 tiene los valores que se han definido; o R4 y R5 junto con el átomo de nitrógeno al cual están unidos representan un grupo heterocíclico saturado de 5 a 8 miembros que contiene un nitrógeno y opcionalmente uno de los siguientes: oxígeno, azufre o un nitrógeno adicional; donde el grupo heterocíclico está opcionalmente sustituido con uno o más grupos alquilo C1-3, hidroxi o bencilo; R6 es H, un grupo alquilo C1-3, un grupo alcoximetilo C1-3, trifluorometilo, un grupo hidroxi-alquilo (C1-3), alcoxicarbonilo C1-3, carboxi, ciano, carbamoílo, mono o di-alquilcarbamoilo (C1-3), acetilo, o hidrazinocarbonilo de fórmula -CONHRaRb donde Ra y Rb son como se define para R4 y R5 respectivamente y; con la salvedad de que cuando R6 es metilo entonces el grupo X-Y-NR4R5 no representa CONHC6H13, CONHC12H25, CONH2, CONHCH3, CON(CH3)2, o un resto de fórmula (2), y con la salvedad adicional de que cuando R1 y R2 representan en forma independiente fenilo entonces Z no es un grupo ortometilo.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0230088.7A GB0230088D0 (en) | 2002-12-24 | 2002-12-24 | Therapeutic agents |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR042658A1 true AR042658A1 (es) | 2005-06-29 |
Family
ID=9950373
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP030104797A AR042658A1 (es) | 2002-12-24 | 2003-12-22 | Derivados de 1,5-diaril-pirrol-3-carboxamida y su uso como moduladores de receptores canabinoides |
Country Status (20)
| Country | Link |
|---|---|
| US (1) | US20060122230A1 (es) |
| EP (1) | EP1578417A1 (es) |
| JP (1) | JP2006513201A (es) |
| KR (1) | KR20050086931A (es) |
| CN (1) | CN1753668A (es) |
| AR (1) | AR042658A1 (es) |
| AU (1) | AU2003290292A1 (es) |
| BR (1) | BR0317705A (es) |
| CA (1) | CA2511601A1 (es) |
| CL (1) | CL2003002720A1 (es) |
| GB (1) | GB0230088D0 (es) |
| IS (1) | IS7944A (es) |
| MX (1) | MXPA05006919A (es) |
| NO (1) | NO20052995L (es) |
| PL (1) | PL377296A1 (es) |
| RU (1) | RU2005117783A (es) |
| TW (1) | TW200503692A (es) |
| UY (1) | UY28144A1 (es) |
| WO (1) | WO2004058249A1 (es) |
| ZA (1) | ZA200504822B (es) |
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0403780D0 (en) * | 2004-02-20 | 2004-03-24 | Astrazeneca Ab | Therapeutic agents |
| CN101006052B (zh) * | 2004-07-30 | 2013-11-06 | 埃克塞利希斯股份有限公司 | 作为药用制剂的吡咯衍生物 |
| EP1773768B8 (en) * | 2004-07-30 | 2018-12-26 | Exelixis, Inc. | Pyrrole derivatives as pharmaceutical agents |
| FR2874012B1 (fr) * | 2004-08-09 | 2008-08-22 | Sanofi Synthelabo | Derives de pyrrole, leur preparation et leur utlisation en therapeutique |
| FR2882054B1 (fr) * | 2005-02-17 | 2007-04-13 | Sanofi Aventis Sa | Derives de 1,5-diarylpyrrole, leur preparation et leur application en therapeutique |
| FR2887548B1 (fr) * | 2005-06-27 | 2007-09-21 | Sanofi Aventis Sa | Derives de 4,5-diarylpyrrole, leur preparation et leur application en therapeutique |
| PE20070182A1 (es) | 2005-07-29 | 2007-03-06 | Wyeth Corp | Derivados cianopirrol-fenil amida como moduladores del receptor de progesterona |
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-
2002
- 2002-12-24 GB GBGB0230088.7A patent/GB0230088D0/en not_active Ceased
-
2003
- 2003-12-18 RU RU2005117783/04A patent/RU2005117783A/ru not_active Application Discontinuation
- 2003-12-18 PL PL377296A patent/PL377296A1/pl not_active Application Discontinuation
- 2003-12-18 AU AU2003290292A patent/AU2003290292A1/en not_active Abandoned
- 2003-12-18 JP JP2004563346A patent/JP2006513201A/ja not_active Withdrawn
- 2003-12-18 CN CNA2003801099724A patent/CN1753668A/zh active Pending
- 2003-12-18 WO PCT/GB2003/005569 patent/WO2004058249A1/en not_active Ceased
- 2003-12-18 MX MXPA05006919A patent/MXPA05006919A/es not_active Application Discontinuation
- 2003-12-18 KR KR1020057011696A patent/KR20050086931A/ko not_active Withdrawn
- 2003-12-18 BR BR0317705-0A patent/BR0317705A/pt not_active Application Discontinuation
- 2003-12-18 EP EP03782654A patent/EP1578417A1/en not_active Withdrawn
- 2003-12-18 TW TW092135979A patent/TW200503692A/zh unknown
- 2003-12-18 US US10/540,276 patent/US20060122230A1/en not_active Abandoned
- 2003-12-18 CA CA002511601A patent/CA2511601A1/en not_active Abandoned
- 2003-12-22 UY UY28144A patent/UY28144A1/es unknown
- 2003-12-22 AR ARP030104797A patent/AR042658A1/es unknown
- 2003-12-22 CL CL200302720A patent/CL2003002720A1/es unknown
-
2005
- 2005-06-17 NO NO20052995A patent/NO20052995L/no not_active Application Discontinuation
- 2005-07-18 IS IS7944A patent/IS7944A/is unknown
-
2006
- 2006-01-19 ZA ZA200504822A patent/ZA200504822B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| US20060122230A1 (en) | 2006-06-08 |
| NO20052995D0 (no) | 2005-06-17 |
| CA2511601A1 (en) | 2004-07-15 |
| AU2003290292A1 (en) | 2004-07-22 |
| UY28144A1 (es) | 2004-07-30 |
| GB0230088D0 (en) | 2003-01-29 |
| MXPA05006919A (es) | 2005-08-18 |
| BR0317705A (pt) | 2005-11-22 |
| NO20052995L (no) | 2005-07-22 |
| PL377296A1 (pl) | 2006-01-23 |
| TW200503692A (en) | 2005-02-01 |
| CL2003002720A1 (es) | 2005-01-07 |
| CN1753668A (zh) | 2006-03-29 |
| ZA200504822B (en) | 2006-03-29 |
| JP2006513201A (ja) | 2006-04-20 |
| KR20050086931A (ko) | 2005-08-30 |
| EP1578417A1 (en) | 2005-09-28 |
| WO2004058249A1 (en) | 2004-07-15 |
| RU2005117783A (ru) | 2006-02-10 |
| IS7944A (is) | 2005-07-18 |
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