JO2715B1 - مشتقات أمين-ن[(4.5ثنائي فينيل بيريميدين-2-ي ل)ميثيل] وتحضيرها واستخداماتها في العلاج - Google Patents

مشتقات أمين-ن[(4.5ثنائي فينيل بيريميدين-2-ي ل)ميثيل] وتحضيرها واستخداماتها في العلاج

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Publication number
JO2715B1
JO2715B1 JOP/2006/0207A JOP20060207A JO2715B1 JO 2715 B1 JO2715 B1 JO 2715B1 JO P20060207 A JOP20060207 A JO P20060207A JO 2715 B1 JO2715 B1 JO 2715B1
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JO
Jordan
Prior art keywords
unsubstituted
substituted
phenyl
alkyl
therapeutics
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JOP/2006/0207A
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English (en)
Inventor
Francis Barth
Patrick Gueule
Murielle Rinaldi-Carmona
Christian Congy
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Sanofi Aventis
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    • 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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Abstract

يتعلق الاختراع الحالي بمركبات متمثلة بالصيغة :التي فيها X يمثل مجموعة R1 تمثل - ألكيل (C1-12) غير مستبدلة او مستبدلة - شق كربوحلقي (C3-12)غير أروماتي غير مستبدلة او مستبدلة-مثيل ألكيل حلقي (C3-7) غير مستبدلة او مستبدلة - فنيل ، غير مستبدلة او مستبدلة -بنزيل,غير مستبدل او مستبدل- فنثيل، غير مستبدلة او مستبدلة - بنزهيدريل : بنزهيدريل مثيل - 1،2،3،4- رابع هيدرونفثالينيل غير مستبدلة او مستبدلة - شق اروماتي حلقي مخلط - R2 تمثل ذرة هيدروجين او الكيل(C1-3) .ءR3-تمثل ذرة هيدروجين او الكيل (C1-5)ء - R4 تمثل فنيل غير مستبدل او مستبدل - R5 تمثل فنيل غير مستبدل او مستبدل - R6 تمثل ذرة هيدروجين او الكيل (C1-3) n تمثل صفر ، 1 او 2؛ الك تمثل الكيل ((C1-4غير مستبدل او مستبدل بشرط ان R4 و R5 غير متشابهين في وقت واحد وتمثل فنيل مستبدلة مع الكوكسي (C1-4) طريقة التحضير والاستخدام في العلاج.
JOP/2006/0207A 2005-07-08 2006-07-02 مشتقات أمين-ن[(4.5ثنائي فينيل بيريميدين-2-ي ل)ميثيل] وتحضيرها واستخداماتها في العلاج JO2715B1 (ar)

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Application Number Priority Date Filing Date Title
FR0507359A FR2888237B1 (fr) 2005-07-08 2005-07-08 Derives de n-[(4,5-diphenylpyrimidin-2-yl)methyl] amine, leur preparation et leur application en therapeutique

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JO2715B1 true JO2715B1 (ar) 2014-03-15

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US (1) US7541361B2 (ar)
EP (1) EP1937672B1 (ar)
JP (1) JP2009500381A (ar)
AR (1) AR054824A1 (ar)
AT (1) ATE441643T1 (ar)
DE (1) DE602006008971D1 (ar)
DO (1) DOP2006000160A (ar)
FR (1) FR2888237B1 (ar)
GT (1) GT200600298A (ar)
JO (1) JO2715B1 (ar)
PA (1) PA8685401A1 (ar)
PE (1) PE20070346A1 (ar)
TW (1) TW200738691A (ar)
UY (1) UY29658A1 (ar)
WO (1) WO2007006928A1 (ar)

Families Citing this family (4)

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WO2009137404A1 (en) * 2008-05-05 2009-11-12 Amgen Inc. Urea compounds as gamma secretase modulators
GB201103419D0 (ar) 2011-02-28 2011-04-13 Univ Aberdeen
AR094929A1 (es) 2013-02-28 2015-09-09 Bristol Myers Squibb Co Derivados de fenilpirazol como inhibidores potentes de rock1 y rock2
CN105102448B (zh) 2013-02-28 2018-03-06 百时美施贵宝公司 作为rock1和rock2抑制剂的苯基吡唑衍生物

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WO1992002513A1 (en) * 1990-08-06 1992-02-20 Fujisawa Pharmaceutical Co., Ltd. Heterocyclic compounds
CA2499497A1 (en) * 2002-09-27 2004-04-08 Merck & Co., Inc. Substituted pyrimidines
US20040259887A1 (en) * 2003-06-18 2004-12-23 Pfizer Inc Cannabinoid receptor ligands and uses thereof

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GT200600298A (es) 2007-07-10
FR2888237A1 (fr) 2007-01-12
PE20070346A1 (es) 2007-05-04
EP1937672A1 (fr) 2008-07-02
UY29658A1 (es) 2007-01-31
DOP2006000160A (es) 2007-01-31
TW200738691A (en) 2007-10-16
JP2009500381A (ja) 2009-01-08
FR2888237B1 (fr) 2007-08-31
AR054824A1 (es) 2007-07-18
EP1937672B1 (fr) 2009-09-02
ATE441643T1 (de) 2009-09-15
US20080176867A1 (en) 2008-07-24
WO2007006928A1 (fr) 2007-01-18
PA8685401A1 (es) 2007-01-17
US7541361B2 (en) 2009-06-02
DE602006008971D1 (de) 2009-10-15

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