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WO2010106269A3 - Derives de n-[(2-aza-bicyclo[2.1.1]hex-1-yl)-aryl-methyl]-heterobenzamide, leur preparation et leur application en therapeutique - Google Patents

Derives de n-[(2-aza-bicyclo[2.1.1]hex-1-yl)-aryl-methyl]-heterobenzamide, leur preparation et leur application en therapeutique Download PDF

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Publication number
WO2010106269A3
WO2010106269A3 PCT/FR2010/050447 FR2010050447W WO2010106269A3 WO 2010106269 A3 WO2010106269 A3 WO 2010106269A3 FR 2010050447 W FR2010050447 W FR 2010050447W WO 2010106269 A3 WO2010106269 A3 WO 2010106269A3
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WIPO (PCT)
Prior art keywords
alkyl
cycloalkyl
groups
therapeutics
halo
Prior art date
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Ceased
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PCT/FR2010/050447
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English (en)
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WO2010106269A2 (fr
Inventor
Geneviève ESTENNE-BOUHTOU
Abdel-Kader Mafroud
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sanofi Aventis France
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Sanofi Aventis France
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
Priority claimed from FR0901219A external-priority patent/FR2943056A1/fr
Priority claimed from FR0901810A external-priority patent/FR2944283B1/fr
Priority to AU2010224720A priority Critical patent/AU2010224720A1/en
Priority to EP10715932A priority patent/EP2408763A2/fr
Priority to SG2011066867A priority patent/SG174434A1/en
Priority to CA2755526A priority patent/CA2755526A1/fr
Priority to RU2011141778/04A priority patent/RU2011141778A/ru
Priority to CN2010800121453A priority patent/CN102356074A/zh
Application filed by Sanofi Aventis France filed Critical Sanofi Aventis France
Priority to BRPI1009496A priority patent/BRPI1009496A2/pt
Priority to JP2012500292A priority patent/JP2012520345A/ja
Priority to MX2011009677A priority patent/MX2011009677A/es
Publication of WO2010106269A2 publication Critical patent/WO2010106269A2/fr
Publication of WO2010106269A3 publication Critical patent/WO2010106269A3/fr
Priority to IL215104A priority patent/IL215104A0/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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    • C07ORGANIC CHEMISTRY
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    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • 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
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • AHUMAN NECESSITIES
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    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
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    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/04Indoles; Hydrogenated indoles
    • C07D209/10Indoles; Hydrogenated indoles with substituted hydrocarbon radicals attached to carbon atoms of the hetero ring
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    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
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    • C07D333/26Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom 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
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Abstract

Les composés de l'invention répondent à la formule générale (I) dans laquelle R représente un atome d'hydrogène ou un groupe choisi parmi les groupes (C1-C6)aIkVIe, (C3-C7)-cycloalkyle, benzyle ou allyle éventuellement substitué par un ou plusieurs groupes choisis indépendamment l'un de l'autre parmi les atomes d'halogène, les groupes (C3-C7)-cycloalkyle, (C1-C6)alkyle, (C1-C6)BlCOXy, hydroxy; R1 représente un groupe phényle ou naphtyle, éventuellement substitué par un ou plusieurs substituants choisis indépendamment l'un de l'autre parmi les atomes d'halogène, les groupes (CrC6)alkyle, (C1-C6)BlCOXy, halo-(C1-C6)alkyle, hydroxy, halo-(C1C6)alcoxy, (C1-C6)alkyle-thio, (C1-C6)alkyle-SO, (C1C6)alkyle-SO2; Het représente un groupe hétéroaryle; R2 représente un ou plusieurs substituants choisis parmi l'atome d'hydrogène, les atomes d'halogène, les groupes halo-(d- C6)alkyle, (C1C6)alkyle, (C3-C7)cycloalkyle, (C3-C7)-cycloalkyl-(C1-C3)alkyle, (C1- C6)alcoxy, benzyl, (C1C6)alkyle-thio, (C1C6)alkyle-SO, (C1C6)alkyle-SO2; à l'état de base ou de sel d'addition à un acide. Utilisation en thérapeutique et procédé de synthèse.
PCT/FR2010/050447 2009-03-16 2010-03-15 Derives de n-[(2-aza-bicyclo[2.1.1]hex-1-yl)-aryl-methyl]-heterobenzamide, leur preparation et leur application en therapeutique Ceased WO2010106269A2 (fr)

Priority Applications (10)

Application Number Priority Date Filing Date Title
JP2012500292A JP2012520345A (ja) 2009-03-16 2010-03-15 N−[(2−アザ−ビシクロ[2.1.1]ヘキス−1−イル)−アリール−)メチル]−ヘテロベンズアミドの誘導体、その調製および治療におけるその用途
MX2011009677A MX2011009677A (es) 2009-03-16 2010-03-15 Derivados de n-[(2-aza-biciclo[2.1.1]hex-1-il)-aril-metil]-heterob enzamida, su preparacion y su aplicacion en terapeutica.
BRPI1009496A BRPI1009496A2 (pt) 2009-03-16 2010-03-15 derivados de n-[(2-aza-biciclo[2.1.1] hex-1-il)-aril-metil]-heterobenzamida, o respectivo preparo e a respectiva aplicação em terapêutica
SG2011066867A SG174434A1 (en) 2009-03-16 2010-03-15 Derivatives of n-[(2-aza-bicyclo[2.1.1]hex-1-yl)-aryl-methyl]-heterobenzamide, preparation thereof and application of same in therapeutics
CA2755526A CA2755526A1 (fr) 2009-03-16 2010-03-15 Derives de n-[(2-aza-bicyclo[2.1.1]hex-1-yl)-aryl-methyl]-heterobenzamide, leur preparation et leur application en therapeutique
RU2011141778/04A RU2011141778A (ru) 2009-03-16 2010-03-15 Производные n-[(2-азабицикло[2.1.1]гекс-1-ил)арилметил]гетеробензамида, их получение и их применение в терапии
CN2010800121453A CN102356074A (zh) 2009-03-16 2010-03-15 N-[(2-氮杂-二环[2.1.1]己-1-基)-芳基-)甲基]-杂苯甲酰胺的衍生物,它们的制备和它们在治疗中的应用
AU2010224720A AU2010224720A1 (en) 2009-03-16 2010-03-15 Derivatives of N-[(2-aza-bicyclo [2.1.1]hex-1-yl)-aryl-methyl]-heterobenzamide, preparation thereof and application of same in therapeutics
EP10715932A EP2408763A2 (fr) 2009-03-16 2010-03-15 Derives de n-ý(2-aza-bicycloý2.1.1¨hex-1-yl)-aryl-methyl¨-heterobenzamide, leur preparation et leur application en therapeutique
IL215104A IL215104A0 (en) 2009-03-16 2011-09-12 Derivatives of n-[(2-aza-bicyclo[2.1.1]hex-1-yl)-aryl-methyl]-heterobenzamide, preparation thereof and application of same in therapeutics

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
FR0901219A FR2943056A1 (fr) 2009-03-16 2009-03-16 Derives de n-°2-aza-bicyclo°2.1.1!hex-1-yl)-aryl-methyl!- heterobenzamide, leur preparation et leur application en therapeutique
FR09/01219 2009-03-16
FR09/01810 2009-04-14
FR0901810A FR2944283B1 (fr) 2009-04-14 2009-04-14 Derives de n-°(2-aza-bicyclo°2.1.1!hex-1-yl)-aryl-methyl!- heterobenzamide, leur preparation et leur application en therapeutique

Publications (2)

Publication Number Publication Date
WO2010106269A2 WO2010106269A2 (fr) 2010-09-23
WO2010106269A3 true WO2010106269A3 (fr) 2010-12-02

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PCT/FR2010/050447 Ceased WO2010106269A2 (fr) 2009-03-16 2010-03-15 Derives de n-[(2-aza-bicyclo[2.1.1]hex-1-yl)-aryl-methyl]-heterobenzamide, leur preparation et leur application en therapeutique

Country Status (14)

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EP (1) EP2408763A2 (fr)
JP (1) JP2012520345A (fr)
KR (1) KR20110132565A (fr)
CN (1) CN102356074A (fr)
AR (1) AR075837A1 (fr)
AU (1) AU2010224720A1 (fr)
CA (1) CA2755526A1 (fr)
IL (1) IL215104A0 (fr)
MX (1) MX2011009677A (fr)
RU (1) RU2011141778A (fr)
SG (1) SG174434A1 (fr)
TW (1) TW201036980A (fr)
UY (1) UY32495A (fr)
WO (1) WO2010106269A2 (fr)

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1992012128A1 (fr) * 1991-01-14 1992-07-23 The Du Pont Merck Pharmaceutical Company Analgesiques a base de composes heterocycliques d'azote(amidomethyle)
WO2004013100A2 (fr) * 2002-07-29 2004-02-12 Sanofi-Aventis Derives de n-[phenyl(piperidin-2-yl)methyl]benzamide, leur preparation et leur application en therapeutique
WO2004013101A2 (fr) * 2002-07-29 2004-02-12 Sanofi-Aventis Derives de n-[phenyl(piperidin-2-yl)methyl]benzamide, leur preparation et leur application en therapeutique
WO2005037785A2 (fr) * 2003-10-17 2005-04-28 Sanofi-Aventis Derives de n-[phenyl(pyrrolidin-2-yl)methyl]benzamide, et n-[azepan-2-yl) phenylmethyl]benzamide, leur preparation et leur application en therapeutique
WO2005037782A2 (fr) * 2003-10-17 2005-04-28 Sanofi-Aventis Derives de n-[phenyl(alkylpiperidin-2-yl)methyl]benzamide, leur preparation et leur application en therapeutique
WO2005037792A1 (fr) * 2003-10-17 2005-04-28 Sanofi-Aventis Derives de n-``phenyl(piperidin-2-yl)methyl !benzamide, leur preparation et leur application en therapeutique
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AU2010224720A1 (en) 2011-10-06
SG174434A1 (en) 2011-10-28
CA2755526A1 (fr) 2010-09-23
TW201036980A (en) 2010-10-16
EP2408763A2 (fr) 2012-01-25
AR075837A1 (es) 2011-04-27
JP2012520345A (ja) 2012-09-06
KR20110132565A (ko) 2011-12-08
UY32495A (es) 2010-10-29
CN102356074A (zh) 2012-02-15
RU2011141778A (ru) 2013-04-27

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