AR062125A1 - Compuestos que modulan el receptor cb2 y su utilizacion como medicamentos - Google Patents
Compuestos que modulan el receptor cb2 y su utilizacion como medicamentosInfo
- Publication number
- AR062125A1 AR062125A1 ARP070103333A ARP070103333A AR062125A1 AR 062125 A1 AR062125 A1 AR 062125A1 AR P070103333 A ARP070103333 A AR P070103333A AR P070103333 A ARP070103333 A AR P070103333A AR 062125 A1 AR062125 A1 AR 062125A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- alkyl
- halogen
- halogen atoms
- pyridinyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 3
- 229940079593 drug Drugs 0.000 title 1
- 239000003814 drug Substances 0.000 title 1
- 125000005843 halogen group Chemical group 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 5
- 150000002367 halogens Chemical class 0.000 abstract 5
- 125000000623 heterocyclic group Chemical group 0.000 abstract 4
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 3
- 125000003118 aryl group Chemical group 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- -1 dimethylaminoalkyl Chemical group 0.000 abstract 3
- 125000001072 heteroaryl group Chemical group 0.000 abstract 3
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 2
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 2
- 229910052799 carbon Inorganic materials 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 1
- FTNJQNQLEGKTGD-UHFFFAOYSA-N 1,3-benzodioxole Chemical compound C1=CC=C2OCOC2=C1 FTNJQNQLEGKTGD-UHFFFAOYSA-N 0.000 abstract 1
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 206010061218 Inflammation Diseases 0.000 abstract 1
- KPCZJLGGXRGYIE-UHFFFAOYSA-N [C]1=CC=CN=C1 Chemical group [C]1=CC=CN=C1 KPCZJLGGXRGYIE-UHFFFAOYSA-N 0.000 abstract 1
- 125000004442 acylamino group Chemical group 0.000 abstract 1
- 239000000556 agonist Substances 0.000 abstract 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 1
- 125000000217 alkyl group Chemical group 0.000 abstract 1
- BNBQRQQYDMDJAH-UHFFFAOYSA-N benzodioxan Chemical compound C1=CC=C2OCCOC2=C1 BNBQRQQYDMDJAH-UHFFFAOYSA-N 0.000 abstract 1
- 150000001721 carbon Chemical group 0.000 abstract 1
- 125000006310 cycloalkyl amino group Chemical group 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 1
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 1
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 1
- 230000004054 inflammatory process Effects 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000004043 oxo group Chemical group O=* 0.000 abstract 1
- 125000003854 p-chlorophenyl group Chemical group [H]C1=C([H])C(*)=C([H])C([H])=C1Cl 0.000 abstract 1
- 125000001037 p-tolyl group Chemical group [H]C1=C([H])C(=C([H])C([H])=C1*)C([H])([H])[H] 0.000 abstract 1
- 125000000951 phenoxy group Chemical group [H]C1=C([H])C([H])=C(O*)C([H])=C1[H] 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
Classifications
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- C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
- C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
- C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
- C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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Abstract
Son utiles para tratar la inflamacion. Los compuestos que son agonistas, son adicionalmente utiles para tratar el dolor. Reivindicacion 1: Un compuesto de formula (1) en la que: R1 es arilo o heteroarilo, cada uno de ellos opcionalmente sustituido independientemente con 1 a 3 sustituyentes elegidos entre alquilo C1-6 (que está opcionalmente sustituido con 1 a 3 átomos de halogeno), cicloalquilo C1-6, alcoxi C1-6 (que está opcionalmente sustituido con 1 a 3 átomos de halogeno), alquiltio C1-6, alquilsulfonilo C1-6, alcoxicarbonilo C1-6, alquilamino C1-6, cicloalquilamino C3-6, dialquilamino C1-6, alquilaminocarbonilo C1-6, acilamino, dialquilaminocarbonilo C1-6, hidroxilo, halogeno, ciano, nitro, oxo, heterociclilo, arilo y heteroarilo; R2 y R3 son independientemente hidrogeno o alquilo C1-6 o R2 y R3 junto con el de carbono al que están unidos forman un anillo cicloalquilo o heterocíclico de 3 a 6 miembros; R4 es hidrogeno o metilo; R5 es arilo o heteroarilo, cada uno de ellos opcionalmente sustituido independientemente con 1 a 3 sustituyentes elegidos entre alquilo C1-6 (que está opcionalmente sustituido con 1 a 3 átomos de halogeno o con un grupo heterociclilo), alcoxi C1-6 (que está opcionalmente sustituido con 1 a 3 átomos de halogeno), cicloalquilo C1-6, heterociclilo, fenoxi, halogeno, ciano, dimetilaminoalquilo, fenilo (que está opcionalmente sustituido con 1 a 2 átomos de halogeno o alquilo C1-4 opcionalmente sustituido con halogeno), tienilo (que está opcionalmente sustituido con 1 a 2 átomos de halogeno o alquilo C1-4 opcionalmente sustituido con halogeno) y piridinilo (que está opcionalmente sustituido con 1 a 2 grupos alquilo C1-4 opcionalmente sustituidos con halogeno); donde R2 y R3, junto con el átomo de carbono al que están unidos no forman un anillo ciclopropilo cuando R5 es 5-alcoxi-benzotiazolilo, 3-alquil-2-piridinilo, 3-piridinilo sin sustituir, 1-fenil-5-pirazolilo, 2-tiazolilo, 2,3-dihidro-benzo[1,4]dioxina y benzo[1,3]dioxol, y R1 es un fenilo, 4-clorofenilo o 4-metilfenilo; o un tautomero o una sal farmacéuticamente aceptable del mismo.
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| EA200900403A1 (ru) * | 2006-09-25 | 2009-10-30 | Бёрингер Ингельхайм Интернациональ Гмбх | Соединения, которые модулируют рецептор св2 |
| WO2008048914A1 (en) | 2006-10-17 | 2008-04-24 | Boehringer Ingelheim International Gmbh | Polycyclic compounds which modulate the cb2 receptor |
| US8173638B2 (en) | 2006-11-21 | 2012-05-08 | Boehringer Ingelheim International Gmbh | Compounds which modulate the CB2 receptor |
| CA2679185A1 (en) | 2007-02-28 | 2008-09-04 | Advinus Therapeutics Private Limited | 2,2,2-tri-substituted acetamide derivatives as glucokinase activators, their process and pharmaceutical application |
| EP2215080A1 (en) * | 2007-10-25 | 2010-08-11 | Boehringer Ingelheim International GmbH | Diazepane compounds which modulate the cb2 receptor |
| WO2009061652A1 (en) * | 2007-11-07 | 2009-05-14 | Boehringer Ingelheim International Gmbh | Compounds which modulate the cb2 receptor |
| CA2716515A1 (en) * | 2008-02-21 | 2009-08-27 | Boehringer Ingelheim International Gmbh | Amine and ether compounds which modulate the cb2 receptor |
| JP2011520884A (ja) | 2008-05-13 | 2011-07-21 | 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受容体を変調するスルホン化合物 |
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2007
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- 2007-07-23 WO PCT/US2007/074076 patent/WO2008014199A2/en not_active Ceased
- 2007-07-23 CA CA002657247A patent/CA2657247A1/en not_active Abandoned
- 2007-07-23 EP EP07813203A patent/EP2081905B1/en active Active
- 2007-07-23 JP JP2009522937A patent/JP5448164B2/ja active Active
- 2007-07-26 CL CL200702199A patent/CL2007002199A1/es unknown
- 2007-07-26 PE PE2007000975A patent/PE20080409A1/es not_active Application Discontinuation
- 2007-07-27 TW TW096127596A patent/TW200821306A/zh unknown
- 2007-07-27 AR ARP070103333A patent/AR062125A1/es not_active Application Discontinuation
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2010
- 2010-11-30 US US12/956,322 patent/US8299111B2/en active Active
Also Published As
| Publication number | Publication date |
|---|---|
| EP2081905A2 (en) | 2009-07-29 |
| JP2009544755A (ja) | 2009-12-17 |
| US20110071127A1 (en) | 2011-03-24 |
| CL2007002199A1 (es) | 2008-03-07 |
| US8299111B2 (en) | 2012-10-30 |
| WO2008014199A3 (en) | 2008-04-03 |
| PE20080409A1 (es) | 2008-06-16 |
| TW200821306A (en) | 2008-05-16 |
| US20080039464A1 (en) | 2008-02-14 |
| CA2657247A1 (en) | 2008-01-31 |
| US7935715B2 (en) | 2011-05-03 |
| WO2008014199A2 (en) | 2008-01-31 |
| JP5448164B2 (ja) | 2014-03-19 |
| EP2081905B1 (en) | 2012-09-12 |
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