AR071577A1 - Pirazolo-pirimidinona para el tratamiento de trastornos del sistema nervioso central - Google Patents
Pirazolo-pirimidinona para el tratamiento de trastornos del sistema nervioso centralInfo
- Publication number
- AR071577A1 AR071577A1 ARP090101179A AR071577A1 AR 071577 A1 AR071577 A1 AR 071577A1 AR P090101179 A ARP090101179 A AR P090101179A AR 071577 A1 AR071577 A1 AR 071577A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- heterocycloalkyl
- cycloalkyl
- heteroaryl
- alkynyl
- Prior art date
Links
- 210000003169 central nervous system Anatomy 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 17
- 125000000592 heterocycloalkyl group Chemical group 0.000 abstract 13
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 10
- 125000000217 alkyl group Chemical group 0.000 abstract 10
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 7
- 229910052731 fluorine Inorganic materials 0.000 abstract 7
- 239000011737 fluorine Substances 0.000 abstract 7
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 6
- 125000003118 aryl group Chemical group 0.000 abstract 6
- -1 aryl-C1-6- alkyl Chemical group 0.000 abstract 6
- 125000004432 carbon atom Chemical group C* 0.000 abstract 6
- 125000001072 heteroaryl group Chemical group 0.000 abstract 6
- 125000001424 substituent group Chemical group 0.000 abstract 6
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical group [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 4
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 4
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 4
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 4
- 125000000304 alkynyl group Chemical group 0.000 abstract 4
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Chemical group BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 4
- 229910052794 bromium Inorganic materials 0.000 abstract 4
- 229910052801 chlorine Inorganic materials 0.000 abstract 4
- 239000000460 chlorine Chemical group 0.000 abstract 4
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 150000001875 compounds Chemical class 0.000 abstract 3
- 239000003814 drug Substances 0.000 abstract 3
- 125000001153 fluoro group Chemical group F* 0.000 abstract 3
- 229910052757 nitrogen Inorganic materials 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 238000004519 manufacturing process Methods 0.000 abstract 2
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 2
- 125000003566 oxetanyl group Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 230000008447 perception Effects 0.000 abstract 2
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 1
- 208000024827 Alzheimer disease Diseases 0.000 abstract 1
- 125000002619 bicyclic group Chemical group 0.000 abstract 1
- 125000002837 carbocyclic group Chemical group 0.000 abstract 1
- 230000006735 deficit Effects 0.000 abstract 1
- 229940079593 drug Drugs 0.000 abstract 1
- 125000005842 heteroatom Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical group II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 1
- 230000028252 learning or memory Effects 0.000 abstract 1
- 125000002950 monocyclic group Chemical group 0.000 abstract 1
- 125000002757 morpholinyl group Chemical group 0.000 abstract 1
- 125000006574 non-aromatic ring group Chemical group 0.000 abstract 1
- 125000004193 piperazinyl group Chemical group 0.000 abstract 1
- 125000003386 piperidinyl group Chemical group 0.000 abstract 1
- 125000000719 pyrrolidinyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 239000012453 solvate Substances 0.000 abstract 1
- 208000024891 symptom Diseases 0.000 abstract 1
- 125000004568 thiomorpholinyl group Chemical group 0.000 abstract 1
Classifications
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- 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
-
- 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
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
-
- 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
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- 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
- A61P15/08—Drugs for genital or sexual disorders; Contraceptives for gonadal disorders or for enhancing fertility, e.g. inducers of ovulation or of spermatogenesis
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P21/00—Drugs for disorders of the muscular or neuromuscular 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
-
- 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
- A61P25/20—Hypnotics; Sedatives
-
- 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
- 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
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- 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
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Neurosurgery (AREA)
- Diabetes (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Epidemiology (AREA)
- Endocrinology (AREA)
- Psychiatry (AREA)
- Reproductive Health (AREA)
- Emergency Medicine (AREA)
- Hospice & Palliative Care (AREA)
- Anesthesiology (AREA)
- Psychology (AREA)
- Child & Adolescent Psychology (AREA)
- Orthopedic Medicine & Surgery (AREA)
- Physical Education & Sports Medicine (AREA)
- Pulmonology (AREA)
- Gynecology & Obstetrics (AREA)
- Pregnancy & Childbirth (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Los compuestos se utilizarán para la fabricacion de medicamentos, en particular medicamentos para el tratamiento de la enfermedad de Alzheimer o los síntomas o consecuencias de la misma tales como el déficit de percepcion, de concentracion, de aprendizaje o de memoria. También el uso se refiere a la utilizacion de estos compuestos para la fabricacion de medicamentos para mejorar la percepcion, la concentracion, el aprendizaje y/o la memoria en pacientes que lo necesiten. Reivindicacion 1: Un compuesto caracterizado porque la formula general (1), en la que Hc es un grupo heterociclilo, definido como un sistema de anillos no aromático monocíclico, bicíclico, o tricíclico, en el cual al menos uno, preferiblemente uno a tres, de los átomos de carbono han sido reemplazados con un heteroátomo seleccionado del grupo de nitrogeno, oxígeno y/o -S(O)r- siendo r 0, 1 o 2; R1 es un grupo seleccionado de alquil C1-8-, alquenil C2-8-, alquinil C2-8-, alquil C1-6-S-, alquil C1-6-S-alquil C1-3-, cicloalquil C3-7-, cicloalquil C3-7-alquil C1-6-, cicloalquil C3-7-alquenil C2-6-, cicloalquil C3-7-alquinil C2-6-, heterocicloalquil C3-7-, heterocicloalquil C3-7-alquil C1-6-, heterocicloalquil C3-7-alquenil C2-6-, heterocicloalquil C3-7-alquinil C2-6-, arilo, aril-alquil C1-6-, aril-alquenil C2-6-, aril-alquinil C2-6-, heteroarilo, heteroaril-alquil C1-6-, heteroaril-alquenil C2-6- y heteroaril-alquinil C2-6-, donde los miembros mencionados antes pueden estar opcionalmente sustituidos independientemente uno de otro con uno o más sustituyentes seleccionados del grupo que consiste en fluor, cloro, bromo, yodo, O=, HO-, NC-, O2N-, F3C-, HF2C-, FH2C-, F3C-CH2-, F3C-O-, HF2C-O-, HO-alquil C1-6-, R10-O-alquil C1-6-, R10-S-alquil C1-6-, alquil C1-6-, alquenil C2-6-, alquinil C2-6-, cicloalquil C3-7-, cicloalquil C3-7-alquil C1-6-, cicloalquil C3-7-O, cicloalquil C3-7-alquil C1-6-O-, arilo, aril-alquil C1-6-, heteroarilo, heteroaril-alquil C1-6-, heteroaril-O-, heteroaril-alquil C1-6-O-, N-enlazada-piridina-2-ona, N-enlazada-piridina-2-ona-alquil C1-6-, N-enlazada-piridina-2-ona-alquil C1-6-O, heterocicloalquil C3-7-, heterocicloalquil C3-7-alquil C1-6-, heterocicloalquil C3-7-O- estando el heterocicloalquil C3-7- unido al O mediante uno de sus átomos C del anillo, heterocicloalquil C3-7-alquil C1-6-O- estando el heterocicloalquil C3-7- unido al alquil C1-6- mediante uno de sus átomos C del anillo, (R10)2N-, (R10)2N-alquil C1-6, R10-O-, R10-S-, R10-CO-, R10O-CO-, (R10)2N-CO-, (R10)2N-CO-alquil C1-6, R10-CO-(R10)N-, R10-CO-(R10)N-alquil C1-6-, R10-CO-O-, R10-O-CO-O-, R10O-CO-O-alquil C1-6-, R10O-CO-(R10)N-, R10O-CO-(R10)N-alquil C1-6-, (R10)2N-CO-O-alquil C1-6-, (R10)2N-CO-(R10)N-alquil C1-6-, R10-SO2-(R10)N-, R10-SO2-(R10)N-alquil C1-6-, (R10)2N-SO2-(R10)N-alquil C1-6-, (R10)2N-SO2-, (R10)2N-SO2- alquil C1-6-, y alquil C1-6-SO2-; donde cualquiera de los grupos cicloalquil C3-7-, heterocicloalquil C3-7-, aril-, heteroaril-, N-enlazada-piridina-2-ona, (R10)2N-CO-alquil C1-6-, mencionados antes puede estar opcionalmente sustituido independientemente con uno o más del grupo de fluor, cloro, bromo, HO-, NC-, O2N-, F3C-, HF2C-, FH2C-, F3C-CH2-, F3C-O-, HF2C-O-, heterocicloalquil C3-7-, R10-O-alquil C1-6-, R10-S-alquil C1-6-, alquil C1-6-, (R10)2N-, (R10)2N-alquil C1-6-, R10-O-, R10-S-, R10-CO-, R10O-CO-, (R10)2N-CO-, (R10)2N-CO-alquil C1-6, R10-CO-(R10)N-, R10-CO-(R10)N-alquil C1-6-, R10-CO-O-, R10-O-CO-O-, R10O-CO-O-alquil C1-6-, R10O-CO-(R10)N-, R10O-CO-(R10)N-alquil C1-6-, (R10)2N-CO-O-, (R10)2N-CO-(R10)N-; (R10)2N-SO2-(R10)N-, (R10)2N-CO-O-alquil C1-6-, (R10)2N-CO-(R10)N-alquil C1-6-, R10-SO2-(R10)N-, R10-SO2-(R10)N-alquil C1-6-, (R10)2N-SO2-(R10)N-alquil C1-6-, (R10)2N-SO2-, (R10)2N-SO2-alquil C1-6, y/o alquil C1-6-SO2-; R2 independientemente de cualquier otro R2 es un grupo seleccionado de: H-, fluor, NC-, F3C-, HF2C-, FH2C-, F3C-CH2-, carboxi-, alquil C1-6-, alquenil C2-6-, alquinil C2-6-, alquil C1-6-S-, alquil C1-6-S-alquil C1-3-, preferiblemente alquil C1-6-S-alquil C2-3-, cicloalquil C3-7-, cicloalquil C3-7-alquil C1-6-, cicloalquil C3-7-alquenil C2-6-, cicloalquil C3-7-alquinil C2-6-, heterocicloalquil C3-7-, heterocicloalquil C3-7-alquil C1-6-, heterocicloalquil C3-7-alquenil C2-6-, heterocicloalquil C3-7-alquinil C2-6, arilo, aril-alquil C1-6-, aril-alquenil C2-6-, aril-alquinil C2-6, heteroarilo, heteroaril-alquil C1-6-, heteroaril-alquenil C2-6-, heteroaril-alquinil C2-6-, R10-O-alquil C2-3-, (R10)2N-, R10O-CO-, (R10)2N-CO-, R10-CO-(R10)N-, R10-CO-, (R10)2N-CO-(R10)N-, R10-CO-(R10)N-, R10-SO2-(R10)N-, alquil C1-6-SO2-, =O, donde los miembros mencionados antes pueden estar opcionalmente sustituidos independientemente uno de otro con uno o más sustituyentes seleccionados del grupo que consiste en fluor, cloro, bromo, NC-, O2N-, F3C-, HF2C-, FH2C-, F3C-CH2-, HO-alquil C1-6-, alquil C1-6-O-, alquil C1-6-O-alquil C1-6-, alquil C1-6-, (R10)2N-, (R10)2N-alquil C1-3-, y (R10)2N-CO-, y en los casos en que Hc comprende NR2 como un miembro del anillo, R2 será independientemente de cualquier otro R2: H-, F3C-CH2-, HF2C-CH2-, alquil C1-6, alquenil C2-6-, alquinil C2-6-, alquil C1-6-S-alquil C1-3-, cicloalquil C3-7-, cicloalquil C3-7-alquil C1-6-, cicloalquil C3-7-alquenil C2-6-, cicloalquil C3-7-alquinil C2-6-, heterocicloalquil C3-7-, heterocicloalquil C3-7-alquil C1-6-, heterocicloalquil C3-7-alquenil C2-6-, heterocicloalquil C3-7-alquinil C2-6-, arilo, aril-alquil C1-6-, heteroarilo, heteroaril-alquil C1-6, R10-O-alquil C1-3, R10O-CO-, (R10)2N-CO-, R10-CO-, R10-SO2-, o alquil C1-6-SO2-, donde los miembros mencionados antes pueden estar opcionalmente sustituidos independientemente uno de otro con uno o más sustituyentes seleccionados independientemente del grupo que consiste en fluor, HO-, NC-, O2N-, F3C-, HF2C-, FH2C-, F3C-CH2, HO-alquil C1-6-, R10-O-alquil C1-6-, alquil C1-6-, R10-O-, (R10)2N-, (R10)2N-alquil C1-3-, y (R10)2N-CO-; R3 es independientemente, un grupo seleccionado de H-, hidroxi y R10-O-; R4 y R5 son independientemente uno de otro H-, fluor, F3C-, HF2C-, FH2C-, y alquil C1-3; o R4 y R5 junto con el átomo de carbono al que están unidos forman un grupo cicloalquilo de 3 a 6 miembros, donde los miembros mencionados antes incluyendo el anillo carbocíclico formado, pueden estar opcionalmente sustituidos independientemente uno de otro con uno o más sustituyentes seleccionados del grupo que consiste en fluor, HO-, NC-, O2N-, F3C-, HF2C-, FH2C-, F3C-CH2, HO-alquil C1-6, CH3-O-alquil C1-6-, alquil C1-6-, alquil C1-6-O- y (alquil C1-6-)2N-CO-; R10 independientemente de cualquier otro R10, es un grupo seleccionado de H- (pero no en el caso en que es parte de un grupo que se selecciona de R10O-CO-, R10-SO2 o R10-CO-), F3C-CH2-, alquil C1-6-, alquenil C2-6-, cicloalquil C3-7-, cicloalquil C3-7-alquil C1-3-, heterocicloalquil C3-7, heterocicloalquil C3-7-alquil C1-6-, arilo, aril-alquil C1-3-, heteroarilo, y heteroaril-alquil C1-3-, y en el caso en que dos grupos R10 estén ambos unidos al mismo átomo de nitrogeno pueden formar junto con dicho átomo de nitrogeno un anillo de heterocicloalquilo de 3 a 7 miembros, y donde uno de los grupos -CH2- del anillo heterocicloalquilo formado puede estar reemplazado por -O-, -S-, -NH-, -N(cicloalquil C3-6)-, -N(cicloalquil C3-6-alquil C1-4)- o -N(alquil C1-4)- y, en particular, en el caso de (R10)2N-CO- entonces R10 se selecciona preferiblemente del grupo de piperidinilo, piperazinilo, pirrolidinilo, morfolinilo y tiomorfolinilo, y donde los miembros mencionados antes pueden estar opcionalmente sustituidos independientemente uno de otro con uno o más sustituyentes seleccionados del grupo que consiste en fluor, cloro, bromo, HO-, NC-, O2N-, F3C-, HF2C-, FH2C-, F3C-CH2, HO-alquil C1-6-, CH3-O-alquil C1-6-, alquil C1-6- y alquil C1-6-O-; x es 0, 1, 2, 3 o 4, y preferiblemente es 0, 1 o 2, más preferiblemente 0 o 1 y más preferiblemente 0; y es 0 o 1, preferiblemente 0; y sus sales y solvatos farmacéuticamente aceptables; con la condicion de que si Hc es oxetanilo, que está unido mediante el átomo de carbono proximo al oxígeno del oxetanilo, no hay ningun sustituyente unido a dicho átomo de carbono mediante un separador -CH2-.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP08153987 | 2008-04-02 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR071577A1 true AR071577A1 (es) | 2010-06-30 |
Family
ID=39790395
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP090101179 AR071577A1 (es) | 2008-04-02 | 2009-04-01 | Pirazolo-pirimidinona para el tratamiento de trastornos del sistema nervioso central |
Country Status (33)
| Country | Link |
|---|---|
| US (2) | US8623879B2 (es) |
| EP (1) | EP2300478B1 (es) |
| JP (1) | JP5391264B2 (es) |
| KR (1) | KR101623762B1 (es) |
| CN (1) | CN101983199B (es) |
| AR (1) | AR071577A1 (es) |
| AU (1) | AU2009232017B2 (es) |
| BR (1) | BRPI0910690B8 (es) |
| CA (1) | CA2716410C (es) |
| CL (1) | CL2009000800A1 (es) |
| CO (1) | CO6321264A2 (es) |
| CY (1) | CY1117626T1 (es) |
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