CO5261605A1 - PHARMACEUTICAL COMPOUNDS - Google Patents
PHARMACEUTICAL COMPOUNDSInfo
- Publication number
- CO5261605A1 CO5261605A1 CO00082018A CO00082018A CO5261605A1 CO 5261605 A1 CO5261605 A1 CO 5261605A1 CO 00082018 A CO00082018 A CO 00082018A CO 00082018 A CO00082018 A CO 00082018A CO 5261605 A1 CO5261605 A1 CO 5261605A1
- Authority
- CO
- Colombia
- Prior art keywords
- alkyl
- alkanoyl
- group
- substituted
- alkoxy
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 20
- 125000002861 (C1-C4) alkanoyl group Chemical group 0.000 abstract 4
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 3
- 229910052760 oxygen Inorganic materials 0.000 abstract 3
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 3
- 125000002837 carbocyclic group Chemical group 0.000 abstract 2
- 125000005843 halogen group Chemical group 0.000 abstract 2
- 125000000623 heterocyclic group Chemical group 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
- 125000004209 (C1-C8) alkyl group Chemical group 0.000 abstract 1
- -1 C1- haloalkyl C6 Chemical group 0.000 abstract 1
- 125000006577 C1-C6 hydroxyalkyl group Chemical group 0.000 abstract 1
- 102100036834 Metabotropic glutamate receptor 1 Human genes 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000004397 aminosulfonyl group Chemical group NS(=O)(=O)* 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 125000004181 carboxyalkyl group Chemical group 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 1
- 125000004990 dihydroxyalkyl group Chemical group 0.000 abstract 1
- 239000003814 drug Substances 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 238000004519 manufacturing process Methods 0.000 abstract 1
- 108010014719 metabotropic glutamate receptor type 1 Proteins 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 1
- 239000002464 receptor antagonist Substances 0.000 abstract 1
- 229940044551 receptor antagonist Drugs 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001424 substituent group Chemical group 0.000 abstract 1
- 125000006296 sulfonyl amino group Chemical group [H]N(*)S(*)(=O)=O 0.000 abstract 1
- 125000000472 sulfonyl group Chemical group *S(*)(=O)=O 0.000 abstract 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/47—One nitrogen atom and one oxygen or sulfur atom, e.g. cytosine
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/86—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
- C07D239/94—Nitrogen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
- C07D239/72—Quinazolines; Hydrogenated quinazolines
- C07D239/95—Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in positions 2 and 4
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/04—Ortho-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
- C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D495/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Medicinal Chemistry (AREA)
- Psychiatry (AREA)
- Neurology (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Biomedical Technology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Neurosurgery (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Un compuesto de fórmula general <EMI FILE="00082018_1" ID="1" IMF=JPEG >En la queX1 representa O o NH,L representa un enlace o una cadena de alquileno C1-C6 interrumpida opcionalmente por O, S, SO, SO2, o NH y sustituida opcionalmente en un átomo de carbono del alquileno con fluoro, hidroxi, alcoxi C1-C4 u oxo,R1 representa un grupo carbocíclico o heterocíclico sustituido o no sustituidoR2 representa un atomo de hidrógeno, un átomo de halógeno, un grupo carboxilo, un grupo ciano, un SCH2CN, o un grupo de fórmula X2-R5 en la que X2 representa un enlace, O, S, SO, SO2 o NH y R5 representa alquilo C1-C8, cicloalquilo C3-C10, haloalquilo C1-C6, hidroxialquilo C1-C6, dihidroxialquilo C1-C4, (alcoxi C1-C4)(alquilo C1-C4), (alcanoíl C1-C4)(alquilo C1-C4), (alcanoíl C1-C4) oxi (alquilo C1-C4), carboxialquilo C1-C4, (alquil C1-C4) aminocarbonil (alquilo C1-C4), alcanoíl(C1-C4), amino, (alcanoíl C1-C4) amino (alquilo C1-C4), (alcanoíl C1-C4) amino (alquilo C1-C4)2, (alquil C1-C4) tio (alquilo C1-C4), (alquil C1-C4) sufinil (alquilo C1-C4), (alquil C1-C4) sulfonil (alquilo C1-C4), (alquil C1-C4) sulfonilamino (alquilo C1-C4), (alquil C1-C4) aminosulfonil(alquilo C1-C4), (dialquil C1-C4) aminofosfonil (alquilo C1-C4) fenilo o fenialquilo C1-C4, en los que cualquier grupo fenilo no esta sustituido o está sustituido con uno o dos sustituyentes seleccionados independientemente de un átomo de halógeno, alquilo C1-C4 y alcoxi C1-C4, ycada uno de R3 y R4 representa independientemente alquilo C1-C4 o junto con los átomos de carbono a los que están unidos forman un anillo carbocíclico o heterocíclico sustituido o no sustituido, o una sal farmacéuticamente aceptable del mismo para ser usado en la fabricación de un medicamento para el tratamiento de una dolencia que requiera la administración de un antagonista de los receptores mGluR1.A compound of the general formula <EMI FILE = "00082018_1" ID = "1" IMF = JPEG> Where X1 represents O or NH, L represents a C1-C6 alkylene bond or chain optionally interrupted by O, S, SO, SO2, or NH and optionally substituted on an alkylene carbon atom with fluoro, hydroxy, C1-C4 alkoxy or oxo, R1 represents a substituted or unsubstituted carbocyclic or heterocyclic group R2 represents a hydrogen atom, a halogen atom, a group carboxyl, a cyano group, a SCH2CN, or a group of formula X2-R5 in which X2 represents a bond, O, S, SO, SO2 or NH and R5 represents C1-C8 alkyl, C3-C10 cycloalkyl, C1- haloalkyl C6, C1-C6 hydroxyalkyl, C1-C4 dihydroxyalkyl, (C1-C4 alkoxy) (C1-C4 alkyl), (C1-C4 alkanoyl) (C1-C4 alkyl), (C1-C4 alkanoyl) oxy (C1-C4 alkyl ), C1-C4 carboxyalkyl, (C1-C4 alkyl) aminocarbonyl (C1-C4 alkyl), alkanoyl (C1-C4), amino, (C1-C4 alkanoyl) amino (C1-C4 alkyl), (C1-C4 alkanoyl) amino (C1-C4 alkyl) 2, (C1-C4 alkyl) ti or (C1-C4 alkyl), (C1-C4 alkyl) sufinyl (C1-C4 alkyl), (C1-C4 alkyl) sulfonyl (C1-C4 alkyl), (C1-C4 alkyl) sulfonylamino (C1-C4 alkyl), (C1-C4 alkyl) aminosulfonyl (C1-C4 alkyl), (C1-C4 dialkyl) aminophosphonyl (C1-C4 alkyl) phenyl or C1-C4 phenyl alkyl, in which any phenyl group is unsubstituted or substituted with one or two substituents independently selected from a halogen atom, C1-C4 alkyl and C1-C4 alkoxy, and each one of R3 and R4 independently represents C1-C4 alkyl or together with the carbon atoms to which they are attached form a substituted carbocyclic or heterocyclic ring or unsubstituted, or a pharmaceutically acceptable salt thereof for use in the manufacture of a medicament for the treatment of a condition that requires the administration of an mGluR1 receptor antagonist.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US16290099P | 1999-11-01 | 1999-11-01 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CO5261605A1 true CO5261605A1 (en) | 2003-03-31 |
Family
ID=22587589
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CO00082018A CO5261605A1 (en) | 1999-11-01 | 2000-10-27 | PHARMACEUTICAL COMPOUNDS |
Country Status (7)
| Country | Link |
|---|---|
| EP (1) | EP1230225A2 (en) |
| AR (1) | AR026275A1 (en) |
| AU (1) | AU1071301A (en) |
| CO (1) | CO5261605A1 (en) |
| PE (1) | PE20010854A1 (en) |
| SV (1) | SV2002000205A (en) |
| WO (1) | WO2001032632A2 (en) |
Families Citing this family (97)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
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|---|---|---|---|---|
| GB1582407A (en) * | 1977-06-07 | 1981-01-07 | Worcester Controls Uk Ltd | Annular seals |
| US5034393A (en) * | 1989-07-27 | 1991-07-23 | Dowelanco | Fungicidal use of pyridopyrimidine, pteridine, pyrimidopyrimidine, pyrimidopyridazine, and pyrimido-1,2,4-triazine derivatives |
| PT100905A (en) * | 1991-09-30 | 1994-02-28 | Eisai Co Ltd | BICYCLE HYGIENEOUS HETEROCYCLIC COMPOUNDS CONTAINING BENZENE, CYCLOHEXAN OR PYRIDINE AND PYRIMIDINE, PYRIDINE OR IMIDAZOLE SUBSTITUTES AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM |
| GB9300059D0 (en) * | 1992-01-20 | 1993-03-03 | Zeneca Ltd | Quinazoline derivatives |
| GB9613021D0 (en) * | 1996-06-21 | 1996-08-28 | Pharmacia Spa | Bicyclic 4-aralkylaminopyrimidine derivatives as tyrosine kinase inhibitors |
| GB9823845D0 (en) * | 1998-11-02 | 1998-12-23 | Lilly Co Eli | Pharmaceutical compounds |
| DE19904710A1 (en) * | 1999-02-05 | 2000-08-10 | Aventis Pharma Gmbh | Substituted 4-amino-2-aryl-tetrahydroquinazolines, their preparation, their use and pharmaceutical compositions containing them |
| SE9903290D0 (en) * | 1999-09-15 | 1999-09-15 | Astra Pharma Prod | Novel compounds |
-
2000
- 2000-10-19 AU AU10713/01A patent/AU1071301A/en not_active Abandoned
- 2000-10-19 WO PCT/US2000/026261 patent/WO2001032632A2/en not_active Ceased
- 2000-10-19 EP EP00971987A patent/EP1230225A2/en not_active Withdrawn
- 2000-10-19 SV SV2000000205A patent/SV2002000205A/en unknown
- 2000-10-20 PE PE2000001131A patent/PE20010854A1/en not_active Application Discontinuation
- 2000-10-27 AR ARP000105680A patent/AR026275A1/en unknown
- 2000-10-27 CO CO00082018A patent/CO5261605A1/en unknown
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| SV2002000205A (en) | 2002-06-07 |
| WO2001032632A2 (en) | 2001-05-10 |
| AR026275A1 (en) | 2003-02-05 |
| EP1230225A2 (en) | 2002-08-14 |
| WO2001032632A3 (en) | 2001-11-08 |
| AU1071301A (en) | 2001-05-14 |
| PE20010854A1 (en) | 2001-08-28 |
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