AR047818A1 - Derivados de piperidinilalquilcarbamatos, su preparacion y su aplicacion en terapeutica - Google Patents
Derivados de piperidinilalquilcarbamatos, su preparacion y su aplicacion en terapeuticaInfo
- Publication number
- AR047818A1 AR047818A1 ARP050100668A ARP050100668A AR047818A1 AR 047818 A1 AR047818 A1 AR 047818A1 AR P050100668 A ARP050100668 A AR P050100668A AR P050100668 A ARP050100668 A AR P050100668A AR 047818 A1 AR047818 A1 AR 047818A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- naphthinyl
- cycloalkyl
- alkyl
- pyrimidyl
- Prior art date
Links
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- C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D207/04—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D207/08—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon radicals, substituted by hetero atoms, attached to ring carbon atoms
- C07D207/09—Radicals substituted by nitrogen atoms, not forming part of a nitro radical
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- C07D211/04—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D211/06—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
- C07D211/08—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
- C07D211/18—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms
- C07D211/34—Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with substituted hydrocarbon radicals attached to ring carbon atoms with hydrocarbon radicals, substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
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- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
- A61K31/445—Non condensed piperidines, e.g. piperocaine
- A61K31/4468—Non condensed piperidines, e.g. piperocaine having a nitrogen directly attached in position 4, e.g. clebopride, fentanyl
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- Emergency Medicine (AREA)
Abstract
Composicion farmacéutica que los comprende y usos. Reivindicacion 1: Compuestos que responden a la formula (1), en donde: m representa un numero entero de 1 a 4; n representa un numero entero igual a 1, 2 o 3; o un numero entero igual a 1 o 2; A es seleccionado entre uno o más grupos X, Y y/o Z; X representa un grupo metileno eventualmente sustituido por uno o dos grupos alquilo-C1-6, cicloalquilo-C3-7 o cicloalquilo-C3-7-alquileno-C1-3; Y representa o bien un grupo alquinileno-C2 eventualmente sustituido por uno o dos grupos alquilo-C1-6, cicloalquilo-C3-7 o cicloalquilo-C3-7-alquileno-C1-3; o bien un grupo; Z representa un grupo de formulas (2), p representa un numero entero de 1 a 5, q y r representan numeros enteros y son definidos de tal modo que r + q sea un numero de 1 a 5; B representa un enlace covalente o un grupo alquileno-C1-6; G representa un enlace covalente, un átomo de oxígeno o de azufre o un grupo -CH(OH)-, CO, SO o SO2; R1 representa un grupo R4 eventualmente sustituido por uno o más grupos R5 y/o R6; R4 representa un grupo seleccionado entre un furanilo, pirrolilo, tienilo, isoxazolilo, tiazolilo, isotiazolilo, imidazolilo, pirazolilo, tiadiazolilo, isotiadiazolilo, oxadiazolilo, tiadiazolilo, triazolilo, tetrazolilo, fenilo, piridinilo, piridazinilo, pirimidinilo, pirazinilo, triazinilo, naftalenilo, quinolinilo, tetrahidroquinolinilo, isoquinolinilo, tetrahidroisoquinolinilo, ftalazinilo, quinazolinilo, quinoxalinilo, cinnolinilo, naftiridinilo, imidazopirimidinilo, tienopirimidinilo, benzofuranilo, dihidrobenzofuranilo, benzotienilo, dihidrobenzotienilo, benzimidazolilo, benzoxazolilo, benzisoxazolilo, benzotiazolilo, benzisotiazolilo, indolilo, isoindolilo, indazolilo, pirrolopiridinilo, furopiridinilo, dihidrofuropiridinilo, tienopiridinilo, dihidrotienopiridinilo, imidazopiridinilo, pirazolopiridinilo, oxazolopiridinilo, isoxazolopiridinilo, tiazolopiridinilo; R5 representa un átomo de halogeno, un grupo ciano, nitro, hidroxilo, alquilo-C1-6, alcoxi-C1-6, tioalquilo-C1-6, fluoroalquilo-C1-6, fluoroalcoxi-C1-6, fluorotioalquilo-C1-6, cicloalquilo-C3-7, cicloalquilo-C3-7-alquileno-C1-3, NR7R8, NR7COR8, NR7CO2R8, NR7SO2R8, COR7, CO2R7, CONR7R8, SO2R7, SO2NR7R8, u -O-(alquileno-C1-3)-O; R6 representa un grupo fenilo, feniloxi, benziloxi, piridinilo, pirazinilo, piridazinilo, pirimidinilo o pirimidiniloxi; pudiendo el o los grupos R6 estar sustituidos por uno o más grupos R5 idénticos o diferentes uno del otro; R7 y R8 representan independientemente uno del otro un átomo de hidrogeno o un grupo alquilo-C1-6, o forman con el o los átomos que los llevan un ciclo seleccionado entre un ciclo azetidina, pirrolidina, piperidina, morfolina, tiomorfolina, azepina o piperazina, estando este ciclo eventualmente sustituido por un grupo alquilo-C1-6 o benzilo; R2 representa un átomo de hidrogeno o un grupo alquilo-C1-6; R3 representa un átomo de hidrogeno o un grupo alquilo-C1-6, cicloalquilo-C3-7, cicloalquiklo-C3-7-alquileno-C1-3; en el estado de base, de sal de adicion de un ácido, de hidrato o de solvato.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR0401952A FR2866885B1 (fr) | 2004-02-26 | 2004-02-26 | Derives de piperidinylalkylcarbamates, leur prepation et leur application en therapeutique |
Publications (1)
Publication Number | Publication Date |
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AR047818A1 true AR047818A1 (es) | 2006-02-22 |
Family
ID=34834069
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP050100668A AR047818A1 (es) | 2004-02-26 | 2005-02-24 | Derivados de piperidinilalquilcarbamatos, su preparacion y su aplicacion en terapeutica |
Country Status (26)
Country | Link |
---|---|
US (2) | US7781590B2 (es) |
EP (1) | EP1720550B1 (es) |
JP (1) | JP4796046B2 (es) |
KR (1) | KR20060134081A (es) |
CN (1) | CN1921858A (es) |
AR (1) | AR047818A1 (es) |
AT (1) | ATE428417T1 (es) |
AU (1) | AU2005224140B2 (es) |
BR (1) | BRPI0508072A (es) |
CA (1) | CA2554608A1 (es) |
CY (1) | CY1109231T1 (es) |
DE (1) | DE602005013923D1 (es) |
DK (1) | DK1720550T3 (es) |
ES (1) | ES2325376T3 (es) |
FR (1) | FR2866885B1 (es) |
HR (1) | HRP20090294T1 (es) |
IL (1) | IL177534A (es) |
MA (1) | MA28366A1 (es) |
NZ (1) | NZ550007A (es) |
PL (1) | PL1720550T3 (es) |
PT (1) | PT1720550E (es) |
RU (1) | RU2384569C2 (es) |
SI (1) | SI1720550T1 (es) |
TW (1) | TW200529816A (es) |
WO (1) | WO2005089759A1 (es) |
ZA (1) | ZA200606964B (es) |
Families Citing this family (20)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2866888B1 (fr) * | 2004-02-26 | 2006-05-05 | Sanofi Synthelabo | Derives de alkylpiperazine- et alkylhomopiperazine- carboxylates, 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 |
FR2866886B1 (fr) * | 2004-02-26 | 2007-08-31 | Sanofi Synthelabo | Derives d'aryl-et d'heteroaryl-akylcarbamates, leur preparation et leur application en therapeutique |
PE20070099A1 (es) | 2005-06-30 | 2007-02-06 | Janssen Pharmaceutica Nv | N-heteroarilpiperazinil ureas como moduladores de la amida hidrolasa del acido graso |
WO2007061862A2 (en) * | 2005-11-18 | 2007-05-31 | Janssen Pharmaceutica N.V. | 2-keto-oxazoles as modulators of fatty acid amide hydrolase |
JP2009519349A (ja) | 2005-12-15 | 2009-05-14 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Cb2受容体を変調する化合物 |
WO2008014199A2 (en) | 2006-07-28 | 2008-01-31 | Boehringer Ingelheim International Gmbh | Sulfonyl compounds which modulate the cb2 receptor |
CA2664310A1 (en) | 2006-09-25 | 2008-04-03 | Boehringer Ingelheim International Gmbh | Compounds which modulate the cb2 receptor |
WO2009061652A1 (en) | 2007-11-07 | 2009-05-14 | Boehringer Ingelheim International Gmbh | Compounds which modulate the cb2 receptor |
US8178568B2 (en) | 2008-07-10 | 2012-05-15 | Boehringer Ingelheim International Gmbh | Sulfone compounds which modulate the CB2 receptor |
CA2737639A1 (en) | 2008-09-25 | 2010-04-01 | Boehringer Ingelheim International Gmbh | Compounds which selectively modulate the cb2 receptor |
FR2941696B1 (fr) * | 2009-02-05 | 2011-04-15 | Sanofi Aventis | Derives d'azaspiranyl-alkylcarbamates d'heterocycles a 5 chainons, leur preparation et leur application en therapeutique |
FR2945531A1 (fr) * | 2009-05-12 | 2010-11-19 | Sanofi Aventis | Derives de 7-aza-spiro°3,5!nonane-7-carboxylates, leur preparation et leur application en therapeutique |
US8299103B2 (en) | 2009-06-15 | 2012-10-30 | Boehringer Ingelheim International Gmbh | Compounds which selectively modulate the CB2 receptor |
EP2443107B1 (en) | 2009-06-16 | 2018-08-08 | Boehringer Ingelheim International GmbH | Azetidine 2 -carboxamide derivatives which modulate the cb2 receptor |
JP2013505295A (ja) | 2009-09-22 | 2013-02-14 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Cb2受容体を選択的に調節する化合物 |
JP2013517271A (ja) | 2010-01-15 | 2013-05-16 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Cb2受容体を調節する化合物 |
EP2542539B1 (en) | 2010-03-05 | 2014-02-26 | Boehringer Ingelheim International GmbH | Tetrazole compounds which selectively modulate the cb2 receptor |
JP5746764B2 (ja) | 2010-07-22 | 2015-07-08 | ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング | Cb2受容体を調節する化合物 |
EP2803668A1 (en) | 2013-05-17 | 2014-11-19 | Boehringer Ingelheim International Gmbh | Novel (cyano-dimethyl-methyl)-isoxazoles and -[1,3,4]thiadiazoles |
Family Cites Families (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3235565A1 (de) * | 1982-09-25 | 1984-03-29 | Boehringer Ingelheim KG, 6507 Ingelheim | Piperidinderivate, ihre herstellung und verwendung |
JP2001523695A (ja) * | 1997-11-24 | 2001-11-27 | ザ スクリップス リサーチ インスティテュート | ギャップ結合連絡の阻害剤 |
IL158300A0 (en) * | 2001-04-27 | 2004-05-12 | Bristol Myers Squibb Co | Bisarylimidazol derivatives and pharmaceutical compositions containing the same |
US6949574B2 (en) * | 2002-02-08 | 2005-09-27 | Bristol-Myers Squibb Company | (Oxime)carbamoyl fatty acid amide hydrolase inhibitors |
FR2843964B1 (fr) * | 2002-08-29 | 2004-10-01 | Sanofi Synthelabo | Derives de dioxane-2-alkylcarbamates, leur preparation et leur application en therapeutique |
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 |
FR2866886B1 (fr) * | 2004-02-26 | 2007-08-31 | Sanofi Synthelabo | Derives d'aryl-et d'heteroaryl-akylcarbamates, leur preparation et leur application en therapeutique |
-
2004
- 2004-02-26 FR FR0401952A patent/FR2866885B1/fr not_active Expired - Fee Related
-
2005
- 2005-02-24 AR ARP050100668A patent/AR047818A1/es unknown
- 2005-02-25 PT PT05732905T patent/PT1720550E/pt unknown
- 2005-02-25 DE DE602005013923T patent/DE602005013923D1/de active Active
- 2005-02-25 KR KR1020067017251A patent/KR20060134081A/ko active IP Right Grant
- 2005-02-25 EP EP05732905A patent/EP1720550B1/fr active Active
- 2005-02-25 CN CNA2005800058637A patent/CN1921858A/zh active Pending
- 2005-02-25 BR BRPI0508072-0A patent/BRPI0508072A/pt not_active IP Right Cessation
- 2005-02-25 PL PL05732905T patent/PL1720550T3/pl unknown
- 2005-02-25 SI SI200530727T patent/SI1720550T1/sl unknown
- 2005-02-25 NZ NZ550007A patent/NZ550007A/en unknown
- 2005-02-25 WO PCT/FR2005/000452 patent/WO2005089759A1/fr active Application Filing
- 2005-02-25 AT AT05732905T patent/ATE428417T1/de active
- 2005-02-25 DK DK05732905T patent/DK1720550T3/da active
- 2005-02-25 ES ES05732905T patent/ES2325376T3/es active Active
- 2005-02-25 JP JP2007500261A patent/JP4796046B2/ja not_active Expired - Fee Related
- 2005-02-25 CA CA002554608A patent/CA2554608A1/fr not_active Abandoned
- 2005-02-25 RU RU2006134025/04A patent/RU2384569C2/ru not_active IP Right Cessation
- 2005-02-25 TW TW094105855A patent/TW200529816A/zh unknown
- 2005-02-25 AU AU2005224140A patent/AU2005224140B2/en not_active Ceased
- 2005-02-25 ZA ZA200606964A patent/ZA200606964B/xx unknown
-
2006
- 2006-08-16 IL IL177534A patent/IL177534A/en not_active IP Right Cessation
- 2006-08-21 US US11/465,825 patent/US7781590B2/en not_active Expired - Fee Related
- 2006-08-22 MA MA29284A patent/MA28366A1/fr unknown
-
2009
- 2009-05-20 HR HR20090294T patent/HRP20090294T1/xx unknown
- 2009-07-14 CY CY20091100744T patent/CY1109231T1/el unknown
-
2010
- 2010-07-12 US US12/834,267 patent/US20100279998A1/en not_active Abandoned
Also Published As
Publication number | Publication date |
---|---|
EP1720550B1 (fr) | 2009-04-15 |
US20070021403A1 (en) | 2007-01-25 |
RU2006134025A (ru) | 2008-04-10 |
ES2325376T3 (es) | 2009-09-02 |
AU2005224140A1 (en) | 2005-09-29 |
DE602005013923D1 (de) | 2009-05-28 |
PT1720550E (pt) | 2009-06-04 |
HRP20090294T1 (en) | 2009-06-30 |
IL177534A (en) | 2011-01-31 |
BRPI0508072A (pt) | 2007-07-17 |
AU2005224140B2 (en) | 2010-12-02 |
RU2384569C2 (ru) | 2010-03-20 |
ATE428417T1 (de) | 2009-05-15 |
PL1720550T3 (pl) | 2009-09-30 |
ZA200606964B (en) | 2008-01-30 |
MA28366A1 (fr) | 2006-12-01 |
IL177534A0 (en) | 2006-12-10 |
WO2005089759A1 (fr) | 2005-09-29 |
NZ550007A (en) | 2010-06-25 |
KR20060134081A (ko) | 2006-12-27 |
EP1720550A1 (fr) | 2006-11-15 |
JP4796046B2 (ja) | 2011-10-19 |
JP2007524706A (ja) | 2007-08-30 |
US20100279998A1 (en) | 2010-11-04 |
SI1720550T1 (sl) | 2009-10-31 |
CY1109231T1 (el) | 2014-07-02 |
FR2866885B1 (fr) | 2007-08-31 |
CA2554608A1 (fr) | 2005-09-29 |
FR2866885A1 (fr) | 2005-09-02 |
US7781590B2 (en) | 2010-08-24 |
CN1921858A (zh) | 2007-02-28 |
DK1720550T3 (da) | 2009-08-10 |
TW200529816A (en) | 2005-09-16 |
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