AR065864A1 - COMPOSITE OF OXI-CICLOHEXIL-PIPERIDINIL-DIHIDRO-BENZIMIDAZOL-2-ONA PHARMACEUTICAL COMPOSITION THAT IS INCLUDED IN ITS USE FOR THE PREPARATION OF A MEDICINAL PRODUCT AND INTERMEDIARY COMPOUNDS FOR PREPARATION - Google Patents

COMPOSITE OF OXI-CICLOHEXIL-PIPERIDINIL-DIHIDRO-BENZIMIDAZOL-2-ONA PHARMACEUTICAL COMPOSITION THAT IS INCLUDED IN ITS USE FOR THE PREPARATION OF A MEDICINAL PRODUCT AND INTERMEDIARY COMPOUNDS FOR PREPARATION

Info

Publication number
AR065864A1
AR065864A1 ARP080101269A ARP080101269A AR065864A1 AR 065864 A1 AR065864 A1 AR 065864A1 AR P080101269 A ARP080101269 A AR P080101269A AR P080101269 A ARP080101269 A AR P080101269A AR 065864 A1 AR065864 A1 AR 065864A1
Authority
AR
Argentina
Prior art keywords
preparation
alkyl
optionally substituted
group
fluorine atoms
Prior art date
Application number
ARP080101269A
Other languages
Spanish (es)
Original Assignee
Glaxo Group Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=38050489&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR065864(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Glaxo Group Ltd filed Critical Glaxo Group Ltd
Publication of AR065864A1 publication Critical patent/AR065864A1/en

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
    • C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
    • C07D235/04—Benzimidazoles; Hydrogenated benzimidazoles
    • C07D235/24—Benzimidazoles; Hydrogenated benzimidazoles 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 in position 2
    • C07D235/26—Oxygen atoms
    • 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
    • A61P25/18—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
    • A61P25/28—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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D211/00—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/36—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no 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
    • C07D211/56—Nitrogen atoms
    • C07D211/58—Nitrogen atoms attached in position 4
    • 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

Abstract

Compuesto de oxi-ciclohexil-piperidinil-dihidro-benzimidazol-2-ona caracterizado por la formula (1) o una sal del mismo: en la qué: R4 se selecciona entre el grupo que consiste en hidrogeno y fluor R5 se selecciona entre el grupo que consiste enhidrogeno, ciano, halogeno, alquilo C1-6 (opcionalmente sustituido con uno o más átomos de fluor) y alcoxi C1-6 (opcionalmente sustituido con uno o más átomos de fluor) R6 se selecciona entre el grupo que consiste en hidrogeno, halogeno, ciano,alquilo C1-6 (opcionalmente sustituido con uno o más átomos de fluor), alquilsulfonilo C1-6, cicloalquilo C3-6 (opcionalmente sustituido con uno o más átomos de fluor) y alcoxi C1-6 (opcionalmente sustituido con uno o más átomos de fluor); n seselecciona entre 2, 3 y 4 Q se selecciona entre el grupo que consiste en hidrogeno y alquilo C1-6 y R se selecciona entre el grupo que consiste en alquilo C1-6, cicloalquilo C3-6, cicloalquil C3-6-alquilo C1-6 y alquinilo C2-6, estando cualquiergrupo alquilo o cicloalquilo opcionalmente sustituido con uno o más átomos de fluor. Composicion farmacéutica que lo comprende. Uso de dicho compuesto para la preparacion de un medicamento util para el tratamiento de una afeccion donde serábeneficioso el agonismo de un receptor muscarínico M1, como ser para el tratamiento de un trastorno psicotico o un deterioro cognitivo. Compuestos intermedios para la preparacion de dicho compuesto.Compound of oxy-cyclohexyl-piperidinyl-dihydro-benzimidazol-2-one characterized by the formula (1) or a salt thereof: in which: R4 is selected from the group consisting of hydrogen and fluorine R5 is selected from the group consisting of hydrogen, cyano, halogen, C1-6 alkyl (optionally substituted with one or more fluorine atoms) and C1-6 alkoxy (optionally substituted with one or more fluorine atoms) R6 is selected from the group consisting of hydrogen, halogen, cyano, C1-6 alkyl (optionally substituted with one or more fluorine atoms), C1-6 alkylsulfonyl, C3-6 cycloalkyl (optionally substituted with one or more fluorine atoms) and C1-6 alkoxy (optionally substituted with one or more fluorine atoms); n is selected from 2, 3 and 4 Q is selected from the group consisting of hydrogen and C1-6 alkyl and R is selected from the group consisting of C1-6 alkyl, C3-6 cycloalkyl, C3-6 cycloalkyl-C1 alkyl -6 and C2-6 alkynyl, any alkyl or cycloalkyl group being optionally substituted with one or more fluorine atoms. Pharmaceutical composition that includes it. Use of said compound for the preparation of a medicament useful for the treatment of a condition where agonism of an M1 muscarinic receptor will be beneficial, such as for the treatment of a psychotic disorder or cognitive impairment. Intermediate compounds for the preparation of said compound.

ARP080101269A 2007-03-29 2008-03-27 COMPOSITE OF OXI-CICLOHEXIL-PIPERIDINIL-DIHIDRO-BENZIMIDAZOL-2-ONA PHARMACEUTICAL COMPOSITION THAT IS INCLUDED IN ITS USE FOR THE PREPARATION OF A MEDICINAL PRODUCT AND INTERMEDIARY COMPOUNDS FOR PREPARATION AR065864A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0706167.4A GB0706167D0 (en) 2007-03-29 2007-03-29 Compounds

Publications (1)

Publication Number Publication Date
AR065864A1 true AR065864A1 (en) 2009-07-08

Family

ID=38050489

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080101269A AR065864A1 (en) 2007-03-29 2008-03-27 COMPOSITE OF OXI-CICLOHEXIL-PIPERIDINIL-DIHIDRO-BENZIMIDAZOL-2-ONA PHARMACEUTICAL COMPOSITION THAT IS INCLUDED IN ITS USE FOR THE PREPARATION OF A MEDICINAL PRODUCT AND INTERMEDIARY COMPOUNDS FOR PREPARATION

Country Status (6)

Country Link
AR (1) AR065864A1 (en)
CL (1) CL2008000865A1 (en)
GB (1) GB0706167D0 (en)
PE (1) PE20090553A1 (en)
TW (1) TW200901979A (en)
WO (1) WO2008119721A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1960389B1 (en) 2005-09-30 2012-08-15 Glaxo Group Limited Compounds which have activity at m1 receptor and their uses in medicine
ATE492537T1 (en) 2005-09-30 2011-01-15 Glaxo Group Ltd COMPOUNDS WITH M1 RECEPTOR ACTIVITY AND THEIR USE IN MEDICINE
EP1937670A1 (en) 2005-09-30 2008-07-02 Glaxo Group Limited Benzimidazolones which have activity at m1 receptor
GB0718415D0 (en) 2007-09-20 2007-10-31 Glaxo Group Ltd Compounds
JP2010539217A (en) 2007-09-20 2010-12-16 グラクソ グループ リミテッド Compounds having activity at the M1 receptor and their use as medicaments

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2002515008A (en) * 1994-10-27 2002-05-21 メルク エンド カンパニー インコーポレーテッド Muscarinic antagonist
AU7478396A (en) * 1995-10-31 1997-05-22 Merck & Co., Inc. Muscarine agonists
CA2387535A1 (en) * 1999-10-13 2001-04-19 Banyu Pharmaceutical Co., Ltd. Substituted imidazolidinone derivatives
AU2003245565B2 (en) * 2002-06-17 2008-01-03 Banyu Pharmaceutical Co., Ltd. Ophthalmic compositions for treating ocular hypertension
GB0605785D0 (en) * 2006-03-22 2006-05-03 Glaxo Group Ltd Compounds
GB0605784D0 (en) * 2006-03-22 2006-05-03 Glaxo Group Ltd Compounds
GB0605786D0 (en) * 2006-03-22 2006-05-03 Glaxo Group Ltd Compounds

Also Published As

Publication number Publication date
PE20090553A1 (en) 2009-06-06
CL2008000865A1 (en) 2008-10-03
GB0706167D0 (en) 2007-05-09
WO2008119721A1 (en) 2008-10-09
TW200901979A (en) 2009-01-16

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