AR055420A1 - SUBSTITUTED PIRIMIDINE DERIVATIVES - Google Patents
SUBSTITUTED PIRIMIDINE DERIVATIVESInfo
- Publication number
- AR055420A1 AR055420A1 ARP060103924A ARP060103924A AR055420A1 AR 055420 A1 AR055420 A1 AR 055420A1 AR P060103924 A ARP060103924 A AR P060103924A AR P060103924 A ARP060103924 A AR P060103924A AR 055420 A1 AR055420 A1 AR 055420A1
- Authority
- AR
- Argentina
- Prior art keywords
- alq
- ilo
- cycloalq
- yloxy
- halo
- Prior art date
Links
Classifications
-
- 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
- C07D239/50—Three nitrogen atoms
-
- 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
-
- 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
- A61P25/06—Antimigraine agents
-
- 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
-
- 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
- A61P25/20—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
- A61P25/22—Anxiolytics
-
- 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
- A61P25/34—Tobacco-abuse
-
- 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
- A61P25/36—Opioid-abuse
-
- 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
-
- 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
- C07D239/48—Two nitrogen atoms
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Neurology (AREA)
- Biomedical Technology (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Neurosurgery (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Addiction (AREA)
- Psychiatry (AREA)
- Pain & Pain Management (AREA)
- Psychology (AREA)
- Hospice & Palliative Care (AREA)
- Anesthesiology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
Abstract
Reivindicacion 1: Un compuesto que tiene la formula general (1) donde: q es 0 o 1; R1 y R2 se seleccionan independientemente del grupo integrado por H y opcionalmente sustituido aril-alq(en/in)ilo C1-6, siempre que R1 y R2 no sean ambos H, o R1 y R2 junto con el N al cual ellos están unidos forman un anillo de 5 a 7 miembros que contiene opcionalmente otro heteroátomo; R3 y R4 se seleccionan independientemente de H, halogeno, ciano, amino, alq(en/in)ilo C1-6, cicloalq(en)ilo C3-8, halo- alq(en/in)ilo C1-6, halo-cicloalq(en)ilo C3-8 alq(en/in)iloxi C1-6, cicloalq(en)iloxi C3-8, cicloalq(en)il C3-8-alq(en/in)iloxi C1-6, halo-alq(en/in)iloxi C1-6, halo-cicloalq(en)iloxi C3-8 y halo-cicloalq(en)il C3-8-alq(en/in)iloxi C1-6, siempre que R3 y R4 no sean ambos H; R5 se selecciona del grupo integrado por alq(en/in)ilo C1-10, cicloalq(en)il C3-8-alq(en/in)ilo C1-6, opcionalmente sustituido aril-alq(en/in)ilo C1-6- y arilo opcionalmente sustituido; como base libre a sus sales.Claim 1: A compound having the general formula (1) wherein: q is 0 or 1; R1 and R2 are independently selected from the group consisting of H and optionally substituted aryl-alq (en / in) ilo C1-6, provided that R1 and R2 are not both H, or R1 and R2 together with the N to which they are attached they form a 5 to 7 member ring that optionally contains another heteroatom; R3 and R4 are independently selected from H, halogen, cyano, amino, alq (en / in) C1-6 yl, cycloalk (en) C3-8 yl, haloalq (en / in) C1-6 ilo, halo- cycloalq (en) C3-8 yl alq (en / in) C1-6 yloxy, cycloalq (en) C3-8 yloxy, C3-8-cycloalk (en) and C1-6 yloxy, halo- alq (en / in) C1-6 iloxy, halo-cycloalq (en) C3-8 yloxy and halo-C3-8-alq (en / in) C1-6 iloxy, provided that R3 and R4 do not be both H; R5 is selected from the group consisting of alq (en / in) ilo C1-10, cycloalq (en) and C3-8-alq (en / in) ilo C1-6, optionally substituted aryl-alq (en / in) ilo C1 -6- and optionally substituted aryl; as a free base for its salts.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DKPA200501262 | 2005-09-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR055420A1 true AR055420A1 (en) | 2007-08-22 |
Family
ID=37199174
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060103924A AR055420A1 (en) | 2005-09-09 | 2006-09-08 | SUBSTITUTED PIRIMIDINE DERIVATIVES |
Country Status (15)
Country | Link |
---|---|
EP (1) | EP1937653A1 (en) |
JP (1) | JP2009507052A (en) |
KR (1) | KR20080043314A (en) |
CN (1) | CN101258133A (en) |
AR (1) | AR055420A1 (en) |
AU (1) | AU2006322461A1 (en) |
BR (1) | BRPI0615631A2 (en) |
CA (1) | CA2621854A1 (en) |
EA (1) | EA200800780A1 (en) |
IL (1) | IL189545A0 (en) |
MX (1) | MX2008002294A (en) |
NO (1) | NO20081713L (en) |
UA (1) | UA93387C2 (en) |
WO (1) | WO2007065449A1 (en) |
ZA (1) | ZA200802174B (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20100256145A1 (en) * | 2007-08-01 | 2010-10-07 | H. Lundbeck A/S | Use of kcnq potassium channel openers for reducing symptoms of or treating disorders or conditions wherein the dopaminergic system is disrupted |
US7786146B2 (en) * | 2007-08-13 | 2010-08-31 | Valeant Pharmaceuticals International | Derivatives of 5-amino-4,6-disubstituted indole and 5-amino-4,6-disubstituted indoline as potassium channel modulators |
WO2010097379A1 (en) * | 2009-02-24 | 2010-09-02 | Neurosearch A/S | Substituted pyrimidin derivatives and their medical use |
AU2011275393B2 (en) * | 2010-07-08 | 2014-04-10 | Pfizer Inc. | Piperidinyl pyrimidine amides as Kv7 potassium channel openers |
CA2815131C (en) * | 2010-10-20 | 2020-06-09 | Gruenenthal Gmbh | Substituted 6-amino-nicotinamides as kcnq2/3 modulators |
CN103508960B (en) * | 2012-06-29 | 2017-12-12 | 江苏先声药业有限公司 | Benzheterocyclic derivatives |
CN103508943B (en) * | 2012-06-29 | 2017-06-09 | 江苏先声药业有限公司 | As the compound of potassium channel modulating agents |
MX2017005044A (en) | 2014-10-24 | 2017-07-04 | Ono Pharmaceutical Co | Kcnq2-5 channel activator. |
JP2022543230A (en) * | 2019-08-02 | 2022-10-11 | ハー・ルンドベック・アクチエゼルスカベット | Alcohol derivatives as Kv7 potassium channel openers for use in epilepsy or epileptic seizures |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2005508833A (en) * | 2001-02-20 | 2005-04-07 | ブリストル−マイヤーズ スクイブ カンパニー | 2,4-disubstituted pyrimidine-5-carboxamide derivatives as KCNQ potassium channel modulators |
AU2003202115A1 (en) * | 2002-02-12 | 2003-09-04 | Pfizer Inc. | Non-peptide compounds affecting the action of gonadotropin-releasing hormone (gnrh) |
US20080261918A1 (en) * | 2004-12-17 | 2008-10-23 | Graham Andrew Showell | Silicon Compounds and Their Use |
-
2006
- 2006-09-07 KR KR1020087004306A patent/KR20080043314A/en not_active Application Discontinuation
- 2006-09-07 CA CA002621854A patent/CA2621854A1/en not_active Abandoned
- 2006-09-07 ZA ZA200802174A patent/ZA200802174B/en unknown
- 2006-09-07 WO PCT/DK2006/050039 patent/WO2007065449A1/en active Application Filing
- 2006-09-07 EA EA200800780A patent/EA200800780A1/en unknown
- 2006-09-07 BR BRPI0615631-2A patent/BRPI0615631A2/en not_active IP Right Cessation
- 2006-09-07 CN CNA2006800327125A patent/CN101258133A/en active Pending
- 2006-09-07 JP JP2008529473A patent/JP2009507052A/en not_active Withdrawn
- 2006-09-07 EP EP06846967A patent/EP1937653A1/en not_active Withdrawn
- 2006-09-07 UA UAA200803570A patent/UA93387C2/en unknown
- 2006-09-07 MX MX2008002294A patent/MX2008002294A/en active IP Right Grant
- 2006-09-07 AU AU2006322461A patent/AU2006322461A1/en not_active Abandoned
- 2006-09-08 AR ARP060103924A patent/AR055420A1/en not_active Application Discontinuation
-
2008
- 2008-02-14 IL IL189545A patent/IL189545A0/en unknown
- 2008-04-09 NO NO20081713A patent/NO20081713L/en not_active Application Discontinuation
Also Published As
Publication number | Publication date |
---|---|
WO2007065449A1 (en) | 2007-06-14 |
KR20080043314A (en) | 2008-05-16 |
AU2006322461A1 (en) | 2007-06-14 |
NO20081713L (en) | 2008-06-04 |
CN101258133A (en) | 2008-09-03 |
UA93387C2 (en) | 2011-02-10 |
ZA200802174B (en) | 2009-10-28 |
IL189545A0 (en) | 2008-06-05 |
EP1937653A1 (en) | 2008-07-02 |
MX2008002294A (en) | 2008-03-14 |
EA200800780A1 (en) | 2008-06-30 |
BRPI0615631A2 (en) | 2011-05-24 |
JP2009507052A (en) | 2009-02-19 |
CA2621854A1 (en) | 2007-06-14 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AR055420A1 (en) | SUBSTITUTED PIRIMIDINE DERIVATIVES | |
AR055144A1 (en) | ACID SECRETION INHIBITOR | |
PE20061297A1 (en) | CHROME AND CHROME DERIVED COMPOUNDS MODULATING THE SEROTONIN 5-HT2C RECEPTOR | |
AR058776A1 (en) | CONDENSED PYRIDINE COMPOUND | |
AR049784A1 (en) | SUBSTITUTED DERIVATIVES OF MORFOLINA AND TIOMORFOLINA | |
ECSP11010912A (en) | PIRROL COMPOUNDS | |
ECSP055974A (en) | SYNTHESIS OF CHLORIDES OF 4 AMINO-2-BUTENOIL AND ITS USE IN THE PREPARATION OF 3-CYANO QUINOLINAS | |
AR077695A1 (en) | PIRIMIDINE DERIVATIVES AS INHIBITORS OF FACTOR IXA | |
AR062677A1 (en) | DERIVATIVES OF BIARIL-SULFONAMIDE, PRODUCTION PROCESSES AND PHARMACEUTICAL COMPOSITIONS THAT UNDERSTAND THEM | |
AR048778A1 (en) | PIRROLIDINYL DERIVATIVES AS INHIBITORS OF 11-BETA HYDROXIESTEROID DEHYDROGENASE | |
AR052568A1 (en) | DERIVATIVES OF PIRAZOLO-PYRIMIDINE AS ANGLOSTS OF MGLUR2 | |
CR10784A (en) | NEW DERIVATIVES OF AMINOPIRIMIDINE AS PLKI INHIBITORS | |
AR053739A1 (en) | ESPIRO COMPOUNDS CONDENSED AS INHIBITORS OF ALDOSTERONA SINTASA | |
ECSP055987A (en) | HETEROARILCARBAMOILBENCENO DERIVATIVES | |
PE20071322A1 (en) | DERIVATIVES OF 2-MORPHOLINOPYRIMIDINE AS INHIBITORS OF PHOSPHATIDINOINOSITOL (PI) 3-KINASE | |
AR054369A1 (en) | CONDENSED IMIDAZOL COMPOUNDS AND ITS USE AS ALDOSTERONE SINTASA INHIBITORS | |
AR048055A1 (en) | PIRIMIDINE DERIVATIVES AS INHIBITORS OF DIPEPTIDIL PEPTIDASA | |
CR9459A (en) | BENZODIOXAN AND BENZODIOXOLAN DERIVATIVES AND USES OF THE SAME | |
ES2422204T3 (en) | Novel derivatives of imidazolidin-2-one as selective androgen receptor modulators (SARMS) | |
CO6270314A2 (en) | A Y-DERIVATIVE - AMINO BICYCLE ACID THAT HAS AN ACTIVITY AS A BINDING (ALPHA) 2 (OMEGA) | |
UY30897A1 (en) | PENTAFLUOROTIOBENZAMIDOACETONITRILE DERIVATIVES, COMPOSITIONS CONTAINING THEM AND APPLICATIONS | |
PE20080068A1 (en) | COMPOUNDS DERIVED FROM PYRIMIDINE AS INHIBITORS OF KINASE AURORA | |
AR069480A1 (en) | DERIVATIVES OF 2-AMINO-PYRIMIDINE | |
AR051392A1 (en) | NON-PEPTIDIC ANTAGONISTS OF BRADIQUININE AND PHARMACEUTICAL COMPOSITIONS OF THE SAME | |
AR078606A1 (en) | PIPERIDINE DERIVATIVES TO PREVENT AND / OR TREAT DEGENERATIVE DISORDERS OF THE CENTRAL NERVOUS SYSTEM |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
FA | Abandonment or withdrawal |