PL1701946T3 - Pochodne 1-piperazyno- i 1-homopiperazyno-karboksylanów, ich wytwarzanie oraz ich zastosowanie jako inhibitorów enzymu FAAH - Google Patents

Pochodne 1-piperazyno- i 1-homopiperazyno-karboksylanów, ich wytwarzanie oraz ich zastosowanie jako inhibitorów enzymu FAAH

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Publication number
PL1701946T3
PL1701946T3 PL04816424T PL04816424T PL1701946T3 PL 1701946 T3 PL1701946 T3 PL 1701946T3 PL 04816424 T PL04816424 T PL 04816424T PL 04816424 T PL04816424 T PL 04816424T PL 1701946 T3 PL1701946 T3 PL 1701946T3
Authority
PL
Poland
Prior art keywords
homopiperazine
carboxylates
piperazine
inhibitors
derivatives
Prior art date
Application number
PL04816424T
Other languages
English (en)
Inventor
Ahmed Abouabdellah
Garcia Antonio Almario
Christian Hoornaert
Adrien Tak Li
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
Publication of PL1701946T3 publication Critical patent/PL1701946T3/pl

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    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D295/00—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/18—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carboxylic acids, or sulfur or nitrogen analogues thereof
    • C07D295/182—Radicals derived from carboxylic acids
    • C07D295/185—Radicals derived from carboxylic acids from aliphatic carboxylic acids
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    • A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/08—Drugs for disorders of the alimentary tract or the digestive system for nausea, cinetosis or vertigo; Antiemetics
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
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    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
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    • C07D213/02—Heterocyclic 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
    • C07D213/04—Heterocyclic 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
    • C07D213/60—Heterocyclic 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
    • C07D213/72—Nitrogen atoms
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    • C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
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    • C07D215/38—Nitrogen atoms
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    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three 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
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    • C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
    • C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more 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, directly attached to ring carbon atoms
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    • C07D295/16—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms
    • C07D295/20—Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms acylated on ring nitrogen atoms by radicals derived from carbonic acid, or sulfur or nitrogen analogues thereof
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    • C07D311/02—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only hetero atom, condensed with other rings ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D311/04—Benzo[b]pyrans, not hydrogenated in the carbocyclic ring
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D317/00—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms
    • C07D317/08—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3
    • C07D317/44—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D317/46—Heterocyclic compounds containing five-membered rings having two oxygen atoms as the only ring hetero atoms having the hetero atoms in positions 1 and 3 ortho- or peri-condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D317/48—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring
    • C07D317/50—Methylenedioxybenzenes or hydrogenated methylenedioxybenzenes, unsubstituted on the hetero ring with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to atoms of the carbocyclic ring
    • C07D317/58—Radicals substituted by nitrogen atoms
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    • 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
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    • 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
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    • C07D405/04—Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
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    • C07D495/04—Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
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  • Neurology (AREA)
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  • Pain & Pain Management (AREA)
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  • Physical Education & Sports Medicine (AREA)
  • Communicable Diseases (AREA)
  • Cardiology (AREA)
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  • Orthopedic Medicine & Surgery (AREA)
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  • Ophthalmology & Optometry (AREA)
  • Anesthesiology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Vascular Medicine (AREA)
  • Otolaryngology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
PL04816424T 2003-12-23 2004-12-17 Pochodne 1-piperazyno- i 1-homopiperazyno-karboksylanów, ich wytwarzanie oraz ich zastosowanie jako inhibitorów enzymu FAAH PL1701946T3 (pl)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
FR0315248A FR2864080B1 (fr) 2003-12-23 2003-12-23 Derives de 1-piperazine-et-1-homopiperazine-carboxylates, leur preparation et leur application en therapeutique
EP04816424A EP1701946B1 (fr) 2003-12-23 2004-12-17 Derives de 1-piperazine- et 1-homopiperazine-carboxylates, leur preparation et leur application en tant qu'inhibiteurs de l'enzyme faah
PCT/FR2004/003289 WO2005070910A2 (fr) 2003-12-23 2004-12-17 Derives de 1 -piperazine- et 1-homopiperazine-carboxylates, leur preparation et leur application en tant qu’ inhibiteurs de l’enzyme faah

Publications (1)

Publication Number Publication Date
PL1701946T3 true PL1701946T3 (pl) 2008-04-30

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PL04816424T PL1701946T3 (pl) 2003-12-23 2004-12-17 Pochodne 1-piperazyno- i 1-homopiperazyno-karboksylanów, ich wytwarzanie oraz ich zastosowanie jako inhibitorów enzymu FAAH

Country Status (28)

Country Link
US (2) US7687503B2 (pl)
EP (1) EP1701946B1 (pl)
JP (1) JP4833080B2 (pl)
KR (1) KR101276427B1 (pl)
CN (2) CN101538254B (pl)
AR (1) AR046982A1 (pl)
AT (1) ATE381552T1 (pl)
AU (1) AU2004314287B2 (pl)
BR (1) BRPI0418134A (pl)
CA (1) CA2550598C (pl)
CY (1) CY1107902T1 (pl)
DE (1) DE602004010848T2 (pl)
DK (1) DK1701946T3 (pl)
ES (1) ES2297533T3 (pl)
FR (1) FR2864080B1 (pl)
HR (1) HRP20080078T3 (pl)
IL (1) IL176478A (pl)
MA (1) MA28234A1 (pl)
NO (1) NO20063229L (pl)
NZ (1) NZ548194A (pl)
PL (1) PL1701946T3 (pl)
PT (1) PT1701946E (pl)
RS (1) RS50544B (pl)
RU (1) RU2356890C2 (pl)
SI (1) SI1701946T1 (pl)
TW (1) TWI339121B (pl)
WO (1) WO2005070910A2 (pl)
ZA (2) ZA200505522B (pl)

Families Citing this family (34)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20030236259A1 (en) * 2002-02-05 2003-12-25 Rolf Hohlweg Novel aryl- and heteroarylpiperazines
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
TW200633990A (en) 2004-11-18 2006-10-01 Takeda Pharmaceuticals Co Amide compound
CN101160287B (zh) 2005-02-17 2011-08-03 安斯泰来制药株式会社 吡啶基非芳香族含氮杂环-1-羧酸酯衍生物
PE20070099A1 (es) 2005-06-30 2007-02-06 Janssen Pharmaceutica Nv N-heteroarilpiperazinil ureas como moduladores de la amida hidrolasa del acido graso
JP5121707B2 (ja) 2005-07-04 2013-01-16 ハイ ポイント ファーマシューティカルズ，エルエルシー 新規医薬
JPWO2007020888A1 (ja) * 2005-08-12 2009-02-26 武田薬品工業株式会社 脳・神経細胞保護剤および睡眠障害治療薬
GB0517184D0 (en) * 2005-08-22 2005-09-28 Glaxo Group Ltd Compounds
FR2892646B1 (fr) * 2005-10-28 2008-06-06 Novalyst Discovery Soc Par Act Systeme catalytique heterogene et son utilisation.
SI2079732T1 (sl) * 2006-05-29 2012-03-30 High Point Pharmaceuticals Llc benzodioksol il ciklopropilpiperazin il piridazin njegove soli in solvati in njegova uporaba kot antagonist histaminskega receptorja H
EP2065369A4 (en) * 2006-08-23 2011-12-28 Astellas Pharma Inc UREA CONNECTION OR SALT THEREOF
EP2014656A3 (en) * 2007-06-11 2011-08-24 High Point Pharmaceuticals, LLC New heteocyclic h3 antagonists
FR2945534B1 (fr) * 2009-05-12 2012-11-16 Sanofi Aventis DERIVES DE CYCLOPENTAL[c]PYRROLE-2-CARBOXYLATES, LEUR PREPARATION ET LEUR APPLICATION EN THERAPEUTIQUE
FR2945533B1 (fr) * 2009-05-12 2011-05-27 Sanofi Aventis Derives de cyclopenta°c!pyrrolyl-alkylcarbamates d'heterocycles a 5 chainons, leur preparation et leur application en therapeutique
TW201044234A (en) * 2009-06-08 2010-12-16 Chunghwa Picture Tubes Ltd Method of scanning touch panel
KR20120125302A (ko) * 2010-01-20 2012-11-14 사노피 알킬-헤테로사이클 카르바메이트 유도체, 그의 제조법 및 그의 치료 용도
FR2955325B1 (fr) * 2010-01-20 2012-01-20 Sanofi Aventis Derives de carbamates d'alkyl-heterocycles, leur preparation et leur application en therapeutique
UA108233C2 (uk) * 2010-05-03 2015-04-10 Модулятори активності гідролази амідів жирних кислот
SI2800565T1 (sl) 2012-01-06 2020-10-30 Lundbeck La Jolla Research Center, Inc. Karbamatne spojine in metode izdelave in uporabe le-teh
EP2945483A4 (en) * 2013-01-18 2016-11-30 Univ City New York Res Found METHOD FOR IMPROVING AMIDOHYDROLASE ACTIVITY OF FATTY ACID AMIDY-DYROLASE
WO2016149401A2 (en) 2015-03-18 2016-09-22 Abide Therapeutics, Inc. Piperazine carbamates and methods of making and using same
MX2017014344A (es) 2015-05-11 2018-04-11 Abide Therapeutics Inc Metodos para el tratamiento de la inflacion o el dolor neuropatico.
WO2017143283A1 (en) 2016-02-19 2017-08-24 Abide Therapeutics, Inc. Radiolabeled monoacylglycerol lipase occupancy probe
ES2892952T3 (es) 2016-09-19 2022-02-07 H Lundbeck As Carbamatos de piperazina como moduladores del MAGL y/o ABHD6 y su uso
JOP20190105A1 (ar) 2016-11-16 2019-05-09 Lundbeck La Jolla Research Center Inc مثبطات أحادي أسيل جليسرول ليباز (magl)
JOP20190106A1 (ar) 2016-11-16 2019-05-09 Lundbeck La Jolla Research Center Inc مثبطات أحادي أسيل جليسرول ليباز (magl)
TW201946906A (zh) 2018-05-15 2019-12-16 美商阿拜德生物製藥公司 Magl抑制劑
CN108912107A (zh) * 2018-08-14 2018-11-30 李敬敬 对人脂肪酰胺水解酶具有选择性抑制活性的化合物及其治疗疼痛的用途
CN110437157B (zh) * 2019-07-05 2022-05-17 西华大学 一种芳基嘧啶类截短侧耳素衍生物及其制备方法和用途
CN110615774B (zh) * 2019-09-19 2022-11-11 安徽中医药大学 具有抗炎活性的苄基哌嗪类化合物、制法及医药用途
CN113195597B (zh) * 2019-11-27 2023-01-03 丸善石油化学株式会社 配位化合物及其制造方法
JP7282017B2 (ja) * 2019-11-27 2023-05-26 丸善石油化学株式会社 アルケニルリン化合物の製造方法
CA3175210A1 (en) 2020-04-21 2021-10-28 Cheryl A. Grice Synthesis of a monoacylglycerol lipase inhibitor

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AT342057B (de) * 1974-04-25 1978-03-10 Thomae Gmbh Dr K Verfahren zur herstellung von neuen 3-piperazino-isochinolinen und deren salzen
JPH05255089A (ja) * 1991-12-18 1993-10-05 Sanwa Kagaku Kenkyusho Co Ltd 抗ウイルス剤
FR2740134B1 (fr) * 1995-10-18 1998-01-09 Pf Medicament Derives d'amines cycliques d'aryl-piperazines, leur preparation et les compositions pharmaceutiques les contenant
PL358618A1 (pl) * 2000-03-31 2004-08-09 Pfizer Products Inc. Nowe pochodne piperazyny
ATE516263T1 (de) * 2002-05-16 2011-07-15 Sunovion Pharmaceuticals Inc Amine, die einen säugetier-anandamidtransporter hemmen; und verfahren zu deren verwendung
FR2850377B1 (fr) * 2003-01-23 2009-02-20 Sanofi Synthelabo Derives d'arylalkylcarbamates, leur preparation et leur application en therapeutique
FR2854633B1 (fr) * 2003-05-07 2005-06-24 Sanofi Synthelabo Derives de piperidinyl-et piperazinyl-alkylcarbamates, leur preparation et leur application en therapeutique
FR2860514A1 (fr) * 2003-10-03 2005-04-08 Sanofi Synthelabo Derives d'arylalkylcarbamates, leur preparation et leur application en therapeutique

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FR2864080A1 (fr) 2005-06-24
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