WO2002092606A8 - Derives d'imidazolidine fusionnes, leur procede de preparation et d'utilisation - Google Patents

Derives d'imidazolidine fusionnes, leur procede de preparation et d'utilisation

Info

Publication number
WO2002092606A8
WO2002092606A8 PCT/JP2002/004640 JP0204640W WO02092606A8 WO 2002092606 A8 WO2002092606 A8 WO 2002092606A8 JP 0204640 W JP0204640 W JP 0204640W WO 02092606 A8 WO02092606 A8 WO 02092606A8
Authority
WO
WIPO (PCT)
Prior art keywords
same
optionally substituted
fused
preparation
substituted hydrocarbyl
Prior art date
Application number
PCT/JP2002/004640
Other languages
English (en)
Japanese (ja)
Other versions
WO2002092606A1 (fr
Inventor
Yasunori Funabashi
Masayuki Takizawa
Shinji Morimoto
Kohei Notoya
Original Assignee
Takeda Chemical Industries Ltd
Yasunori Funabashi
Masayuki Takizawa
Shinji Morimoto
Kohei Notoya
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
Application filed by Takeda Chemical Industries Ltd, Yasunori Funabashi, Masayuki Takizawa, Shinji Morimoto, Kohei Notoya filed Critical Takeda Chemical Industries Ltd
Publication of WO2002092606A1 publication Critical patent/WO2002092606A1/fr
Publication of WO2002092606A8 publication Critical patent/WO2002092606A8/fr

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D513/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00
    • C07D513/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/542Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/554Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having at least one nitrogen and one sulfur as ring hetero atoms, e.g. clothiapine, diltiazem
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F9/00Compounds containing elements of Groups 5 or 15 of the Periodic Table
    • C07F9/02Phosphorus compounds
    • C07F9/547Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
    • C07F9/6561Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom containing systems of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring or ring system, with or without other non-condensed hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Epidemiology (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Rheumatology (AREA)
  • Biochemistry (AREA)
  • Molecular Biology (AREA)
  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

L'invention concerne des composés représentés par la formule générale (I) et présentant une excellente activité d'inhibition contre la dégradation de la matrice du cartilage; ou leurs sels ou sulfoxydes, formule dans laquelle R1 représente -(S)¿n?-R?2(où R2¿ représente hydrocarbyle facultativement substitué ou analogue; et n représente un nombre entier de 0 à 2) ou analogue; R5 représente hydrogène, hydrocarbyle facultativement substitué ou analogue; le symbole (II) est un groupe représenté par la formule générale (III) ou analogue; et le symbole (IV) est un groupe représenté par la formule générale (V) ou analogue [où R6 représente hydrogène, hydrocarbyle facultativement substitué, ou analogue; R10 représente -ZR15 (où Z représente -SO¿2?- ou analogue; et R?15¿ représente hydrocarbyle facultativement substitué ou analogue) ou analogue; et R11 représente hydrogène ou analogue].
PCT/JP2002/004640 2001-05-15 2002-05-14 Derives d'imidazolidine fusionnes, leur procede de preparation et d'utilisation WO2002092606A1 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2001144608 2001-05-15
JP2001-144608 2001-05-15

Publications (2)

Publication Number Publication Date
WO2002092606A1 WO2002092606A1 (fr) 2002-11-21
WO2002092606A8 true WO2002092606A8 (fr) 2002-12-19

Family

ID=18990527

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/JP2002/004640 WO2002092606A1 (fr) 2001-05-15 2002-05-14 Derives d'imidazolidine fusionnes, leur procede de preparation et d'utilisation

Country Status (1)

Country Link
WO (1) WO2002092606A1 (fr)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004069999A2 (fr) * 2003-02-04 2004-08-19 Takeda Pharmaceutical Company Limited Procede de criblage
ES2265276B1 (es) 2005-05-20 2008-02-01 Laboratorios Almirall S.A. Derivados de 4-(2-amino-1-hidroxietil)fenol como agonistas del receptor beta2 adrenergico.
ES2320961B1 (es) 2007-11-28 2010-03-17 Laboratorios Almirall, S.A. Derivados de 4-(2-amino-1-hidroxietil)fenol como agonistas del receptor adrenergico beta2.
US8450070B2 (en) 2007-12-28 2013-05-28 Takeda Pharmaceutical Company Limited Method for screening of cell-protecting agent
EP2228368A1 (fr) 2009-03-12 2010-09-15 Almirall, S.A. Procédé de fabrication de 5-(2-{[6-(2,2-difluoro-2-ph2nyl2thoxy)hexyl]amino}-1-hydroxy2thyl)-8-hydroxyquinolin-2(1h)-one
EP2578570A1 (fr) 2011-10-07 2013-04-10 Almirall, S.A. Nouveau procédé de fabrication de 5-(2-{[6-(2,2-difluoro-2-phényléthoxy)hexyl]amino}-1-hydroxyéthyl)-8-hydroxyquinolin-2(1h)-one via de nouveaux intermédiaires de synthèse
EP2641900A1 (fr) 2012-03-20 2013-09-25 Almirall, S.A. Nouvelles formes polymorphes de héminapadisylate de 5-(2-{[6-(2,2-difluoro-2-phényléthoxy) hexyl]amino}-1-(R)-hydroxyéthyl)-8-hydroxyquinolin-2(1h)-one en tant qu'agoniste du récepteur adrénergique ß2
TW201512171A (zh) 2013-04-19 2015-04-01 Pfizer Ltd 化學化合物
US10085999B1 (en) 2017-05-10 2018-10-02 Arixa Pharmaceuticals, Inc. Beta-lactamase inhibitors and uses thereof
CN111448182A (zh) 2017-10-02 2020-07-24 阿里萨制药有限公司 氨曲南衍生物及其用途
WO2020072442A1 (fr) 2018-10-01 2020-04-09 Arixa Pharmaceuticals, Inc. Dérivés de relebactam et utilisations associées
CN110156620B (zh) * 2019-07-02 2022-04-15 中节能万润股份有限公司 一种氨甲环酸的制备方法

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4179276A (en) * 1977-02-01 1979-12-18 E. I. Du Pont De Nemours And Company Novel imidazothiazine-1,3 (2H)-diones
GB9212486D0 (en) * 1992-06-12 1992-07-22 Erba Carlo Spa Derivatives of substituted imidazo benzoxazin-1-one and process for their preparation
GB9410469D0 (en) * 1994-05-25 1994-07-13 Erba Farmitalia Imidazolylalkyl derivatives of imidazo (5,1-c) (1,4) benzoxazin-1-one and process for their preparation
AU3106997A (en) * 1996-06-14 1998-01-07 Kaken Pharmaceutical Co., Ltd. Bicyclic hydantoin derivatives, intermediates for the preparation thereof, process for the preparation of them, and herbicides containing the same as active ingredient
EP0931074B1 (fr) * 1996-09-06 2003-05-07 Takeda Chemical Industries, Ltd. 4,5,6,7-tetrahydrobenzo c]thiopenes condenses utilises comme renfor ateurs de l'action des facteurs induisant la differenciation cellulaire
PT977745E (pt) * 1998-03-04 2005-04-29 Pharmacia Corp Compostos de acido tioarilo sulfonamida hidroxamico
EP1307455B1 (fr) * 1999-10-20 2005-04-06 Tanabe Seiyaku Co., Ltd. Inhibiteurs d'adhesion cellulaire induite par alpha-l beta-2

Also Published As

Publication number Publication date
WO2002092606A1 (fr) 2002-11-21

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