AR062210A1 - Pirazolopirimidinas sustituidas, un proceso para su preparacion y su uso como medicamento - Google Patents
Pirazolopirimidinas sustituidas, un proceso para su preparacion y su uso como medicamentoInfo
- Publication number
- AR062210A1 AR062210A1 ARP070103439A ARP070103439A AR062210A1 AR 062210 A1 AR062210 A1 AR 062210A1 AR P070103439 A ARP070103439 A AR P070103439A AR P070103439 A ARP070103439 A AR P070103439A AR 062210 A1 AR062210 A1 AR 062210A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkylaminocarbonyl
- alkylamino
- alkyl
- heterocyclyl
- heteroaryl
- Prior art date
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- C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
- C07D487/04—Ortho-condensed systems
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- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/495—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
- A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
- A61K31/519—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
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Abstract
Moduladores de mGluR5 para la prevencion de trastornos neurologicos agudos y cronicos. Proceso de obtencion y composiciones farmacéuticas que los comprende. Reivindicacion 1: Un compuesto pirazolopirimidínico de formula (1) donde, Y1 representa N o C-, Y2 representa N o C-, Y3 representa N o C-, Y4 representa N o C-, mediante la cual al menos dos de los grupos Y1 a Y4 denotan un átomo de carbono, R1 representa cloro o bromo; R2 y R3 cada uno independientemente representa hidrogeno, alquilo C1- 6, cicloalquilo C3-7 o trifluorometilo; o R2 y R3 ambos junto con el átomo de carbono del anillo representan un grupo carbonilo; R4 y R5 cada uno independientemente representa hidrogeno, alquilo C1-6, cicloalquilo C3-7 o trifluorometilo; o R4 y R5 ambos junto con el átomo de carbono del anillo representan un grupo carbonilo; R6 y R7 representan independientemente hidrogeno, alquilo C1-6, cicloalquilo C3-7 o trifluorometilo; o R6 y R7 ambos junto con el átomo de carbono del anillo representan un grupo carbonilo; R2 o R3 junto con R6 y R7 también pueden formar un radical bivalente a partir del grupo CH2-CH2 o CH2-O; R10 y R11 representan independientemente hidrogeno, halogeno, amino, hidroxi, nitro, ciano, trifluorometilo, trifluorometoxi, arilo, alquilo C1-6, cicloalquilo C3-7, alquenilo C2-6, alquinilo C2-6, alcoxi C1-6, cicloalquiloxi C3-7, alqueniloxi C2-6, alquiniloxi C2-6, heteroarilo, heterociclilo, ariloxi, heteroariloxi, heterocicliloxi, alquilamino C1-6, di- alquilamino C1-6, cicloalquilamino C3-7, di-cicloalquilamino C3-7, alquil C1-6-cicloalquilamino C3-7, alquenilamino C2-6, alquinilamino C2-6, di-alquenilamino C2-6, di-alquinilamino C2-6, alquil C1-6-alquenilamino C2-6, alquil C1-6-alquinilamino C2- 6, alquenil C2-6-cicloalquilamino C3-7, alquinil C2-6-cicloalquilamino C3-7, alquenil C2-6-alquinilamino C2-6, arilamino, diarilamino, aril-alquilamino C1-6, aril-alquenilamino C2-6, aril-alquinilamino C2-6, aril-cicloalquilamino C3-7, heteroarilamino, diheteroarilamino, heteroaril-alquilamino C1-6, heteroaril-alquenilamino C2-6, heteroaril-alquinilamino C2-6, heteroaril-cicloalquilamino C3-7, heteroarilarilamino, heterociclilamino, diheterociclilamino, heterociclil-alquilamino C1- 6, heterociclil-alquenilamino C2-6, heterociclil-alquinilamino C2-6, heterociclil-cicloalquilamino C3-7, heterociclilarilamino, heterociclilhetero-arilamino, acilo, aciloxi, acilamino, alcoxicarbonilo C1-6, cicloalcoxi C3-7-carbonilo, alqueniloxicarbonilo C2-6, alquiniloxicarbonilo C2-6, ariloxicarbonilo, heteroariloxicarbonilo, heterocicliloxicarbonilo, aminocarbonilo, alquilamino C1-6-carbonilo, di-alquilaminocarbonilo C1-6, cicloalquilaminocarbonilo C3-7, di- cicloalquilaminocarbonilo C3-7, alquil C1-6-cicloalquilaminocarbonilo C3-7, alquenil C2-6-aminocarbonjlo, alquinilaminocarbonilo C2-6, di-alquenilaminocarbonilo C2-6, di-alquinilaminocarbonilo C2-6, alquil C1-6-alquenilaminocarbonilo C2-6, alquil C1- 6-alquinil C2-6-aminocarbonilo, alquenil C2-6-cicloalquilaminocarbonilo C3-7, alquinil C2-6-cicloalquilaminocarbonilo C3-7, alquenil C2-6-alquinilaminocarbonilo C2-6, arilaminocarbonilo, diarilaminocarbonilo, aril-alquilaminocarbonilo C1-6, aril- alquenilaminocarbonilo C2-6, aril-alquinilaminocarbonilo C2-6, aril-cicloalquilaminocarbonil C3-7 heteroarilaminocarbonilo, diheteroarilaminocarbonilo, heteroaril-alquilaminocarbonilo C1-6, heteroaril-alquenilaminocarbonilo C2-6, heteroaril- alquinilaminocarbonilo C2-6, heteroaril-cicloalquilaminocarbonilo C3-7, heteroarilarilaminocarbonilo, heterociclilaminocarbonilo, diheterociclilaminocarbonilo, heterociclil-alquilaminocarbonilo C1-6, heterociclil-alquenilamino C2-6-carbonilo, heterociclil-alquinilaminocarbonilo C2-6, heterociclil-cicloalquil C3-7-aminocarbonilo, heterociclilarilaminocarbonilo, heterociclilheteroarilaminocarbonilo, alquilsulfinilo C1-6, cicloalquilsulfinilo C3-7, alquenilsulfinilo C2-6, alquinilsulfinilo C2-6, arilsulfinilo, heteroarilsulfinilo, heterociclilsulfinilo, alquilsulfonilo C1-6, cicloalquilsulfonilo C3-7, alquenilsulfonilo C2-6, alquinilsulfonilo C2-6, arilsulfonilo, heteroarilsulfonilo, heterociclilsulfonilo, alquilsulfonilamino C1-6, o arilsulfonilamino; o R10 y R11 junto con los dos átomos de carbono que los portan representan un heteroarilo que posee 5 o 6 miembros de anillo o un grupo heterociclilo que posee 5 o 6 miembros de anillo, que pueden ser sustituidos con uno de los siguientes grupos: halogeno, hidroxi, nitro, ciano, trifluorometilo, trifluorometoxi, alquilo C1-6 y alcoxi C1-6; e isomeros opticos, sales, hidratos, solvatos y polimorfos aceptables para uso farmacéutico de los mismos, con la condicion que el compuesto de formula (1) no representa al compuesto (6-Bromo-pirazolo[1,5-a]pirimidin-2-il)-(3,4-dihidro-1H-isoquinolin-2-il)-metanona.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US83582006P | 2006-08-04 | 2006-08-04 | |
| US87754406P | 2006-12-28 | 2006-12-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR062210A1 true AR062210A1 (es) | 2008-10-22 |
Family
ID=38710494
Family Applications (3)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP070103439A AR062210A1 (es) | 2006-08-04 | 2007-08-03 | Pirazolopirimidinas sustituidas, un proceso para su preparacion y su uso como medicamento |
| ARP070103437A AR063680A1 (es) | 2006-08-04 | 2007-08-03 | Derivados de pirazolo[1, 5-a]pirimidina, metodos e intermediario para su preparacion, composiciones farmaceuticas que los comprenden y su uso en la fabricacion de medicamentos para el tratamiento de enfermedades mediadas por la modulacion de mglur5. |
| ARP070103438A AR062209A1 (es) | 2006-08-04 | 2007-08-03 | Pirazolopirimidinas moduladoras de receptores de glutamato metabotropicos mglur5, proceso para su preparacion, medicamentos que las contienen y usos en la prevencion y/o tratamiento de trastornos neurologicos agudos y cronicos. |
Family Applications After (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP070103437A AR063680A1 (es) | 2006-08-04 | 2007-08-03 | Derivados de pirazolo[1, 5-a]pirimidina, metodos e intermediario para su preparacion, composiciones farmaceuticas que los comprenden y su uso en la fabricacion de medicamentos para el tratamiento de enfermedades mediadas por la modulacion de mglur5. |
| ARP070103438A AR062209A1 (es) | 2006-08-04 | 2007-08-03 | Pirazolopirimidinas moduladoras de receptores de glutamato metabotropicos mglur5, proceso para su preparacion, medicamentos que las contienen y usos en la prevencion y/o tratamiento de trastornos neurologicos agudos y cronicos. |
Country Status (21)
| Country | Link |
|---|---|
| US (4) | US7947689B2 (es) |
| EP (3) | EP2295439A1 (es) |
| JP (2) | JP2009545569A (es) |
| KR (1) | KR20090047450A (es) |
| AR (3) | AR062210A1 (es) |
| AT (2) | ATE488520T1 (es) |
| AU (2) | AU2007280429A1 (es) |
| BR (2) | BRPI0714622A2 (es) |
| CA (2) | CA2659876A1 (es) |
| CY (1) | CY1112003T1 (es) |
| DE (2) | DE602007010640D1 (es) |
| DK (1) | DK2054416T3 (es) |
| HR (1) | HRP20110128T1 (es) |
| IL (2) | IL196008A0 (es) |
| MX (2) | MX2009000919A (es) |
| PL (1) | PL2054416T3 (es) |
| PT (1) | PT2054416E (es) |
| RU (2) | RU2009107688A (es) |
| TW (3) | TW200815432A (es) |
| WO (3) | WO2008015270A1 (es) |
| ZA (1) | ZA200810605B (es) |
Families Citing this family (28)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2008056176A1 (en) * | 2006-11-10 | 2008-05-15 | Scottish Biomedical Limited | Pyrazolopyrimidines as phosphodiesterase inhibitors |
| HK1136565A1 (en) * | 2007-03-31 | 2010-07-02 | Intervet Int Bv | Processes for making zilpaterol and salts thereof |
| EP2090576A1 (en) * | 2008-02-01 | 2009-08-19 | Merz Pharma GmbH & Co.KGaA | 6-halo-pyrazolo[1,5-a]pyridines, a process for their preparation and their use as metabotropic glutamate receptor (mGluR) modulators |
| RU2496494C2 (ru) | 2008-06-30 | 2013-10-27 | Новартис Аг | КОМБИНАЦИИ, СОДЕРЖАЩИЕ МОДУЛЯТОРЫ mGluR, ДЛЯ ЛЕЧЕНИЯ БОЛЕЗНИ ПАРКИНСОНА |
| JP2013512216A (ja) | 2009-11-25 | 2013-04-11 | メルツ・ファルマ・ゲゼルシヤフト・ミト・ベシュレンクテル・ハフツング・ウント・コンパニー・コマンデイトゲゼルシヤフト・アウフ・アクティーン | 置換ピラゾロピリミジン類の結晶形 |
| CA2820262A1 (en) | 2010-12-08 | 2012-06-14 | Vanderbilt University | Bicyclic pyrazole compounds as allosteric modulators of mglur5 receptors |
| US8865725B2 (en) | 2011-03-15 | 2014-10-21 | Vanderbilt University | Substituted imidazopyrimidin-5(6H)-ones as allosteric modulators of MGLUR5 receptors |
| CA2830220A1 (en) * | 2011-03-15 | 2012-09-20 | Vanderbilt University | Substituted imidazopyrimidin-5(6h)-ones as allosteric modulators of mglur5 receptors |
| WO2012139876A1 (en) | 2011-04-14 | 2012-10-18 | Merz Pharma Gmbh & Co. Kgaa | Enteric formulations of metabotropic glutamate receptor modulators |
| US8791108B2 (en) | 2011-08-18 | 2014-07-29 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
| WO2013087808A1 (en) | 2011-12-15 | 2013-06-20 | Merz Pharma Gmbh & Co. Kgaa | Pharmaceutical composition comprising a pyrazolopyrimidme and cyclodextrin |
| WO2013087815A1 (en) | 2011-12-15 | 2013-06-20 | Merz Pharma Gmbh & Co. Kgaa | Liquid pharmaceutical composition containing a pyrazolopyrimidine derivative and pharmaceutical uses thereof |
| US9006235B2 (en) | 2012-03-06 | 2015-04-14 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
| EP2831074B1 (en) * | 2012-03-29 | 2016-09-14 | Boehringer Ingelheim International GmbH | Novel pyrazolopyrimidines as metabotropic glutamate 5 receptor antagonists for the treatment of psychiatric diseases |
| JO3407B1 (ar) * | 2012-05-31 | 2019-10-20 | Eisai R&D Man Co Ltd | مركبات رباعي هيدرو بيرازولو بيريميدين |
| WO2014035707A1 (en) * | 2012-08-25 | 2014-03-06 | The Johns Hopkins University | Gapdh cascade inhibitor compounds and methods of use and treatment of stress induced disorders including mental illness |
| EP2958915B1 (en) | 2013-02-19 | 2017-07-05 | Pfizer Inc | Azabenzimidazole compounds as inhibitors of pde4 isozymes for the treatment of cns and other disorders |
| WO2014164467A1 (en) | 2013-03-13 | 2014-10-09 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
| WO2014164428A1 (en) | 2013-03-13 | 2014-10-09 | Bristol-Myers Squibb Company | Inhibitors of human immunodeficiency virus replication |
| CN105008369B (zh) | 2013-03-14 | 2017-07-11 | 百时美施贵宝公司 | 人类免疫缺陷病毒复制抑制剂 |
| EP3036219A4 (en) * | 2013-06-04 | 2017-08-23 | Temple University Of The Commonwealth System Of Higher Education | Novel beta lactams as modulators of glutamate uptake and methods for use thereof |
| MX2016005994A (es) | 2013-11-05 | 2017-01-11 | Univ Temple | Anifífilos policatónicos como agentes antimicrobianos. |
| US10398142B2 (en) | 2013-11-05 | 2019-09-03 | Temple University Of The Commonwealth System Of Higher Education | Polycationic amphiphiles as antimicrobial agents |
| GB201320905D0 (en) | 2013-11-27 | 2014-01-08 | Takeda Pharmaceutical | Therapeutic compounds |
| US9273067B2 (en) | 2014-02-19 | 2016-03-01 | Bristol-Myers Squibb Company | Pyrazolopyrimidine macrocycles as inhibitors of human immunodeficiency virus replication |
| WO2016012896A1 (en) | 2014-07-24 | 2016-01-28 | Pfizer Inc. | Pyrazolopyrimidine compounds |
| JP6506833B2 (ja) | 2014-08-06 | 2019-04-24 | ファイザー・インク | イミダゾピリダジン化合物 |
| CA3222584A1 (en) | 2016-01-27 | 2017-08-03 | Universitat Zurich | Use of gabaa receptor modulators for treatment of itch |
Family Cites Families (35)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CH603545A5 (es) | 1972-04-20 | 1978-08-31 | Merz & Co | |
| GB1383409A (en) * | 1972-09-09 | 1974-02-12 | Pfizer Ltd | Derivatives of 2-amino- and 4-amino-quinazoline and pharmaceutical compositions containing them |
| US3988339A (en) * | 1974-02-08 | 1976-10-26 | Smithkline Corporation | Pharmaceutical compositions and methods of inhibiting phenylethanolamine N-methyltransferase |
| US3974283A (en) * | 1974-03-18 | 1976-08-10 | Sandoz, Inc. | N-substituted-4-T-butyl-1-pyridinethiocarboxamides and their use for treatment of inflammation or pain |
| NZ190915A (en) * | 1978-07-31 | 1984-07-31 | Hoffmann La Roche | Oxadiazolotriazine derivatives and pharmaceutical compositions |
| DE2856393C2 (de) | 1978-12-27 | 1983-04-28 | Merz + Co GmbH & Co, 6000 Frankfurt | Arzneimittel zur Behandlung von Morbus Parkinson |
| SU768177A1 (ru) * | 1979-04-23 | 1985-08-07 | МГУ им.М.В.Ломоносова | Способ получени ( @ )-(-) или ( @ )-(+)-1=метил-1,2,3,4-тетрагидроизохинолина |
| ZA803591B (en) * | 1979-07-09 | 1981-06-24 | American Cyanamid Co | Substituted pyrazolo(1,5-a)pyrimidines |
| US4340597A (en) * | 1981-04-13 | 1982-07-20 | Schering Corporation | 1-Substituted-4-aryl-1,2,5,6-tetrahydro and hexahydropyridines |
| DE3308554A1 (de) * | 1983-03-10 | 1984-09-13 | Hoechst Ag, 6230 Frankfurt | 1-/1,3-dioxolan-2-ylmethyl)-azole, ihre salze, verfahren zu ihrer herstellung und ihre verwendung |
| WO1989005643A1 (en) * | 1987-12-18 | 1989-06-29 | Pfizer Inc. | Heterocyclic-substituted quinoline-carboxylic acids |
| DE10299048I2 (de) | 1989-04-14 | 2006-07-13 | Merz Pharma Gmbh & Co Kgaa | Verwendung von Adamantan-Derivaten zur Pr{vention und Behandlung der cerebralen Isch{mie |
| US6177443B1 (en) * | 1997-03-07 | 2001-01-23 | Novo Nordisk A/S | 4,5,6,7-tetrahydro-thieno[3, 2-C]pyridine derivatives, their preparation and use |
| US6071966A (en) | 1997-06-30 | 2000-06-06 | Merz + Co. Gmbh & Co. | 1-amino-alkylcyclohexane NMDA receptor antagonists |
| IL133235A (en) | 1997-06-30 | 2004-02-19 | Merz Pharma Gmbh & Co Kgaa | 1-amino-alkylcyclohexane nmda receptor antagonists and pharmaceutical compositions comprising them |
| DE19732589A1 (de) * | 1997-07-29 | 1999-02-04 | Huels Chemische Werke Ag | Verfahren zur Herstellung von 1,2,3,6-tetrahydro-2,2,6,6-tetramethylpyridin |
| FR2769313B1 (fr) * | 1997-10-06 | 2000-04-21 | Sanofi Sa | Derives d'esters hydroxyacetiques, leur procede de preparation et leur utilisation comme intermediaires de synthese |
| NZ505207A (en) | 1997-11-21 | 2003-10-31 | Nps Pharma Inc | Metabotropic glutamate receptor antagonists for treating central nervous system diseases |
| ATE290527T1 (de) * | 1997-12-25 | 2005-03-15 | Meiji Seika Kaisha | Tetrahydrobenzindol-derivate |
| CN1261098C (zh) | 1998-08-28 | 2006-06-28 | 西奥斯股份有限公司 | p38－α激酶的抑制剂 |
| US20020049223A1 (en) | 1999-11-05 | 2002-04-25 | Elmore Steven W. | Quinoline and naphthyridine carboxylic acid antibacterials |
| MXPA02006474A (es) * | 1999-12-28 | 2002-11-29 | Eisai Co Ltd | Compuestos heterociclicos que contienen sulfonamida. |
| GB0110338D0 (en) | 2001-04-27 | 2001-06-20 | Sb Pharmco Inc | Novel processes |
| GB0118752D0 (en) * | 2001-08-01 | 2001-09-26 | Pfizer Ltd | Process for the production of quinazolines |
| EP1506196B1 (en) * | 2001-11-01 | 2012-01-18 | Icagen, Inc. | Pyrazolopyrimidines as sodium channel inhibitors |
| AU2003227437A1 (en) * | 2002-04-23 | 2003-11-10 | Shionogi And Co., Ltd. | PYRAZOLO(1,5-a)PYRIMIDINE DERIVATIVE AND NAD(P)H OXIDASE INHIBITOR CONTAINING THE SAME |
| WO2003101993A1 (en) | 2002-06-04 | 2003-12-11 | Neogenesis Pharmaceuticals, Inc. | Pyrazolo` 1,5a! pyrimidine compounds as antiviral agents |
| WO2004014902A2 (en) * | 2002-08-09 | 2004-02-19 | Astrazeneca Ab | Compounds having an activity at metabotropic glutamate receptors |
| WO2004087153A2 (en) | 2003-03-28 | 2004-10-14 | Chiron Corporation | Use of organic compounds for immunopotentiation |
| JP2006522750A (ja) | 2003-04-11 | 2006-10-05 | ノボ ノルディスク アクティーゼルスカブ | 代謝性症候群ならびに関連の疾患および障害を治療するために、１１β−ヒドロキシステロイドデヒドロゲナーゼ１型阻害剤および抗高血圧剤を使用する併用療法 |
| WO2004089471A2 (en) | 2003-04-11 | 2004-10-21 | Novo Nordisk A/S | NEW PYRAZOLO[1,5-a] PYRIMIDINES DERIVATIVES AND PHARMACEUTICAL USE THEREOF |
| JP2006522744A (ja) | 2003-04-11 | 2006-10-05 | ノボ ノルディスク アクティーゼルスカブ | グルココルチコイド受容体アゴニスト療法に伴う副作用を最小化するための、１１β−ヒドロキシステロイドデヒドロゲナーゼ１型阻害剤およびグルココルチコイド受容体アゴニストを使用する併用療法 |
| EP1773880A4 (en) | 2004-06-08 | 2009-09-09 | Novartis Vaccines & Diagnostic | ENV POLYPEPTIDE COMPLEXES AND METHOD FOR THEIR USE |
| WO2006015737A1 (de) | 2004-08-02 | 2006-02-16 | Schwarz Pharma Ag | Carboxamide des indolizins und seiner aza- und diazaderivate |
| JP2008527031A (ja) | 2005-01-19 | 2008-07-24 | バイオリポックス エービー | 炎症の治療に有用なピロロピリジン誘導体 |
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- 2007-08-03 TW TW096128665A patent/TW200823215A/zh unknown
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- 2007-08-03 AT AT07788196T patent/ATE494289T1/de active
- 2007-08-03 EP EP07788196.9A patent/EP2054416B8/en active Active
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