ATE409184T1 - Dioxan-2-alkylkarbamaten derivaten, deren herstellung und deren therapeutischen verwendung - Google Patents

Dioxan-2-alkylkarbamaten derivaten, deren herstellung und deren therapeutischen verwendung

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Publication number
ATE409184T1
ATE409184T1 AT03758282T AT03758282T ATE409184T1 AT E409184 T1 ATE409184 T1 AT E409184T1 AT 03758282 T AT03758282 T AT 03758282T AT 03758282 T AT03758282 T AT 03758282T AT E409184 T1 ATE409184 T1 AT E409184T1
Authority
AT
Austria
Prior art keywords
dioxane
production
therapeutic use
alkyl carbamates
derivatives
Prior art date
Application number
AT03758282T
Other languages
English (en)
Inventor
Ahmed Abouabdellah
Michele Bas
Gihad Dargazanli
Christian Hoornaert
Adrien Li
Florence Medaisko
Original Assignee
Sanofi Aventis
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 Sanofi Aventis filed Critical Sanofi Aventis
Application granted granted Critical
Publication of ATE409184T1 publication Critical patent/ATE409184T1/de

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D319/00Heterocyclic compounds containing six-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D319/041,3-Dioxanes; Hydrogenated 1,3-dioxanes
    • C07D319/061,3-Dioxanes; Hydrogenated 1,3-dioxanes not condensed with other rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61P1/04Drugs 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
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C235/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms
    • C07C235/02Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton
    • C07C235/04Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated
    • C07C235/06Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by oxygen atoms having carbon atoms of carboxamide groups bound to acyclic carbon atoms and singly-bound oxygen atoms bound to the same carbon skeleton the carbon skeleton being acyclic and saturated having the nitrogen atoms of the carboxamide groups bound to hydrogen atoms or to acyclic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links

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  • Chemical Kinetics & Catalysis (AREA)
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  • Physical Education & Sports Medicine (AREA)
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  • Pulmonology (AREA)
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  • Communicable Diseases (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Psychiatry (AREA)
  • Ophthalmology & Optometry (AREA)
  • Molecular Biology (AREA)
  • Otolaryngology (AREA)
  • Psychology (AREA)
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  • Hospice & Palliative Care (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Anesthesiology (AREA)
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AT03758282T 2002-08-29 2003-08-27 Dioxan-2-alkylkarbamaten derivaten, deren herstellung und deren therapeutischen verwendung ATE409184T1 (de)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0210707A FR2843964B1 (fr) 2002-08-29 2002-08-29 Derives de dioxane-2-alkylcarbamates, leur preparation et leur application en therapeutique

Publications (1)

Publication Number Publication Date
ATE409184T1 true ATE409184T1 (de) 2008-10-15

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ID=31502974

Family Applications (2)

Application Number Title Priority Date Filing Date
AT03758282T ATE409184T1 (de) 2002-08-29 2003-08-27 Dioxan-2-alkylkarbamaten derivaten, deren herstellung und deren therapeutischen verwendung
AT07013954T ATE434598T1 (de) 2002-08-29 2003-08-27 Zwischenprodukte für die herstellung von dioxan-2-alkylcarbamaten

Family Applications After (1)

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AT07013954T ATE434598T1 (de) 2002-08-29 2003-08-27 Zwischenprodukte für die herstellung von dioxan-2-alkylcarbamaten

Country Status (34)

Country Link
US (4) US7119116B2 (de)
EP (2) EP1537096B1 (de)
JP (2) JP4585854B2 (de)
KR (2) KR101051192B1 (de)
CN (3) CN101906071A (de)
AR (1) AR041053A1 (de)
AT (2) ATE409184T1 (de)
AU (1) AU2003274292B2 (de)
BR (1) BR0313846A (de)
CA (2) CA2700319C (de)
CO (1) CO5700820A2 (de)
CY (2) CY1108792T1 (de)
DE (2) DE60328138D1 (de)
DK (2) DK1840125T3 (de)
EA (1) EA008218B1 (de)
ES (2) ES2329181T3 (de)
FR (1) FR2843964B1 (de)
HR (2) HRP20090270B1 (de)
IL (1) IL166882A (de)
IS (1) IS2733B (de)
MA (1) MA27390A1 (de)
ME (2) MEP24208A (de)
MX (1) MXPA05002319A (de)
NO (2) NO331165B1 (de)
NZ (1) NZ538404A (de)
PL (1) PL209339B1 (de)
PT (2) PT1840125E (de)
RS (2) RS51085B (de)
SI (2) SI1840125T1 (de)
TN (1) TNSN05057A1 (de)
TW (2) TWI294878B (de)
UA (1) UA82847C2 (de)
WO (1) WO2004020430A2 (de)
ZA (1) ZA200501537B (de)

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FR2843964B1 (fr) * 2002-08-29 2004-10-01 Sanofi Synthelabo Derives de dioxane-2-alkylcarbamates, leur preparation et leur application en therapeutique
JP4515911B2 (ja) * 2002-10-07 2010-08-04 ザ リージェンツ オブ ザ ユニバーシティ オブ カリフォルニア アナンダミド加水分解の遮断による不安の調節
FR2854633B1 (fr) * 2003-05-07 2005-06-24 Sanofi Synthelabo Derives de piperidinyl-et piperazinyl-alkylcarbamates, leur preparation et leur application en therapeutique
FR2865205B1 (fr) * 2004-01-16 2006-02-24 Sanofi Synthelabo Derives de type aryloxyalkylcarbamates, leur preparation et leur application en therapeutique
FR2866886B1 (fr) * 2004-02-26 2007-08-31 Sanofi Synthelabo Derives d'aryl-et d'heteroaryl-akylcarbamates, leur preparation et leur application en therapeutique
FR2866884B1 (fr) * 2004-02-26 2007-08-31 Sanofi Synthelabo Derives d'aryl-et d'heteroaryl-piperidinecarboxylates, leur preparation et leur application en therapeutique
FR2866885B1 (fr) 2004-02-26 2007-08-31 Sanofi Synthelabo Derives de piperidinylalkylcarbamates, leur prepation et leur application en therapeutique
FR2866888B1 (fr) * 2004-02-26 2006-05-05 Sanofi Synthelabo Derives de alkylpiperazine- et alkylhomopiperazine- carboxylates, leur preparation et leur application en therapeutique
US7269708B2 (en) * 2004-04-20 2007-09-11 Rambus Inc. Memory controller for non-homogenous memory system
US20080103209A1 (en) * 2004-04-23 2008-05-01 The Regents Of The University Of California Compounds And Methods For Treating Non-Inflammatory Pain Using Ppar Alpha Agonists
DE102004039326A1 (de) * 2004-08-12 2006-02-16 Abbott Gmbh & Co. Kg Neue medizinische Verwendungen und Verfahren
EP1849773B1 (de) 2005-02-17 2013-10-16 Astellas Pharma Inc. Piperazinderivate zur Behandlung von Harninkontinenz und Schmerz
FR2885364B1 (fr) * 2005-05-03 2007-06-29 Sanofi Aventis Sa Derives d'alkyl-, alkenyl-et alkynylcarbamates, leur preparation et leur application en therapeutique
CA2661085A1 (en) * 2006-08-18 2008-02-21 N.V. Organon Combination faah inhibitor and analgesic, anti-inflammatory or anti-pyretic agent
US20080089845A1 (en) * 2006-09-07 2008-04-17 N.V. Organon Methods for determining effective doses of fatty acid amide hydrolase inhibitors in vivo
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