AR060525A1 - Piridin [3,4-b] pirazinonas. composiciones farmaceuticas - Google Patents
Piridin [3,4-b] pirazinonas. composiciones farmaceuticasInfo
- Publication number
- AR060525A1 AR060525A1 ARP070101657A ARP070101657A AR060525A1 AR 060525 A1 AR060525 A1 AR 060525A1 AR P070101657 A ARP070101657 A AR P070101657A AR P070101657 A ARP070101657 A AR P070101657A AR 060525 A1 AR060525 A1 AR 060525A1
- Authority
- AR
- Argentina
- Prior art keywords
- group
- independently selected
- alkyl
- alkynyl
- alkenyl
- Prior art date
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Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- 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
- A61K31/4985—Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/12—Drugs for disorders of the urinary system of the kidneys
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P25/00—Drugs for disorders of the nervous system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Urology & Nephrology (AREA)
- Vascular Medicine (AREA)
- Epidemiology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Pain & Pain Management (AREA)
- Rheumatology (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Pulmonology (AREA)
- Biomedical Technology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
- Plural Heterocyclic Compounds (AREA)
- Epoxy Compounds (AREA)
- Separation Of Suspended Particles By Flocculating Agents (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Se dan a conocer también las correspondientes composiciones farmacéuticas. Reivindicacion 1: Un compuesto, o una sal farmacéuticamente aceptable del compuesto, en el que el compuesto tiene la estructura de formula 1, y en la que: R2 se selecciona del grupo constituido por arilo y anillo heterociclilo de 3 a 10 miembros, en la que dichos sustituyentes arilo y heterociclilo R2 pueden estar opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados del grupo constituido por halogeno, ciano, nitro, oxo, alquilo, alquenilo, alquinilo, cicloalquilo, -OR201, -C(O)R201, -OC(O)R201, -C(O)OR201, -NR201R202, -N(R202)C(O)R202, -C(O)NR201R202, -C(O)NR201C(O)R202, -SR201, -S(O)R201, y -S(O)2R201, en los que dichos sustituyentes alquilo, alquenilo, alquinilo y cicloalquilo pueden estar opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados del grupo constituido por halogeno, oxo, -OR203 y -C(O)OR203; R201, R202 y R203 se seleccionan independientemente del grupo constituido por hidrogeno y alquilo, en el que dicho alquilo puede estar opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados del grupo constituido por halogeno, hidroxi, alcoxi, carboxi y - C(O)NH2; R6A y R6B, junto con el nitrogeno al que están unidos, forman un anillo heterociclilo parcial o totalmente saturado de 3 a 14 miembros, en el que el heterociclilo puede estar opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados del grupo constituido por hidrogeno, halogeno, oxo, alquilo, alquenilo, alquinilo, ciano, cicloalquilo, arilo y heterociclilo, -OR601, -C(O)R601, -OC(O)R601, -C(O)OR601, -NR6011R602, -N(R601)C(O)R602, - C(O)NR601R602, -C(O)NR601C(O)R602, en los que (a) dichos sustituyentes alquilo, alquenilo, alquinilo y cicloalquilo pueden estar opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados del grupo constituido por halogeno, ciano, oxo, -OR603, -C(O)R603, -C(O)OR603, -OC(O)R603, -NR603R604, -N(R603)C(O)R604, -C(O)NR603R604, -C(O)NR603C(O)R604, -SR603, -S(O)R603, -S(O)2R603, -N(R603)S(O)2R604, y -S(O)2NR603R604, C(O)NR603C(O)R604, -SR603, -S(O)R603, -S(O)2R603, -N(R603)S(O)2R604, y -S(O)2NR603R604, y (b) dichos sustituyentes arilo y heterociclilo pueden estar opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados del grupo constituido por halogeno, alquilo, alquenilo, alquinilo, ciano, oxo, -OR601, -C(O)R601, -C(O)OR601, -OC(O)R601, -NR601R602, -N(R601)C(O)R602, -C(O)NR601R602, -C(O)NR601C(O)R602, -SR601, -S(O)R602, -S(O)2R601, -N(R601)S(O)2R602, y -S(O)2NR601R602; R601, R602, R603 y R604 se seleccionan independientemente del grupo constituido por hidrogeno, alquilo, alquenilo y alquinilo, en el que (a) dicho alquilo R601 y R602 puede estar opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados del grupo constituido por halogeno, ciano, hidroxi, carboxi, oxo, alquenilo, alquinilo, haloalquenilo, hidroxialquenilo, carboxialquilo, haloalquinilo, hidroxialquinilo, carboxialquinilo, alcoxi, haloalcoxi, hidroxialcoxi y carboxialcoxi, y (b) dichos sustituyentes alquenilo y alquinilo R601 y R602 pueden estar opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados del grupo constituido por halogeno, ciano, hidroxi, carboxi, oxo, alcoxi, haloalcoxi, hidroxialcoxi y carboxialcoxi; R8 es alquilo; en el que dicho sustituyente R8 puede estar opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados del grupo constituido por halogeno, ciano, hidroxi, carboxi, alquenilo, alquinilo, - OR801, -C(O)R801, -C(O)OR801, -OC(O)R801, -NR801R802, -N(R801)C(O)R802, -C(O)NR801R802, y -C(O)NR801C(O)R802, en el que dichos sustituyentes alquenilo y alquinilo pueden estar opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados del grupo constituido por halogeno, ciano, hidroxi, carboxi, oxo y alcoxi; y R801 y R802 se seleccionan independientemente del grupo constituido por hidrogeno, alquilo, alquenilo y alquinilo, en el que (a) cuando dicho alquilo es metilo, dicho metilo puede estar opcionalmente sustituido con 1, 2 o 3 sustituyentes fluoro, (b) cuando dicho alquilo comprende al menos dos átomos de carbono, dicho alquilo puede estar opcionalmente sustituido con uno o más sustituyentes independientemente seleccionados del grupo constituido por halogeno, ciano, hidroxi, carboxi, oxo, alquinilo, haloalquinilo, hidroxialquinilo, carboxialquinilo, alcoxi, haloalcoxi, hidroxialcoxi y carboxialcoxi, y (c) dichos sustituyentes alquenilo y alquinilo R801 y R802 pueden estar opcionalmente sustituidos con uno o más sustituyentes independientemente seleccionados del grupo constituido por halogeno, ciano, hidroxi, carboxi, oxo, alcoxi, haloalcoxi, hidroxialcoxi y carboxialcoxi.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US79397106P | 2006-04-21 | 2006-04-21 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR060525A1 true AR060525A1 (es) | 2008-06-25 |
Family
ID=38431249
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP070101657A AR060525A1 (es) | 2006-04-21 | 2007-04-18 | Piridin [3,4-b] pirazinonas. composiciones farmaceuticas |
Country Status (42)
Families Citing this family (33)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2013208B1 (en) | 2006-04-21 | 2011-06-22 | Pfizer Products Inc. | Pyridin[3,4-b]pyrazinones |
| WO2008073928A1 (en) | 2006-12-12 | 2008-06-19 | Gilead Colorado, Inc. | Composition for treating a pulmonary hypertension |
| CA2718402C (en) * | 2008-03-05 | 2017-08-22 | Merck Patent Gmbh | Pyridopyrazinones derivatives insulin secretion stimulators, methods for obtaining them and use thereof for the treatment of diabetes |
| WO2010041711A1 (ja) * | 2008-10-09 | 2010-04-15 | 杏林製薬株式会社 | イソキノリン誘導体及びそれらを有効成分とするｐｄｅ阻害剤 |
| ES2613664T3 (es) * | 2009-10-26 | 2017-05-25 | Signal Pharmaceuticals, Llc | Procedimientos de síntesis y purificación de compuestos de heteroarilo |
| EP3106163A1 (en) | 2010-10-15 | 2016-12-21 | Gilead Sciences, Inc. | Compositions and methods of treating pulmonary hypertension |
| EP2691393B1 (en) | 2011-03-31 | 2016-09-14 | Pfizer Inc | Novel bicyclic pyridinones |
| WO2012172449A1 (en) | 2011-06-13 | 2012-12-20 | Pfizer Inc. | Lactams as beta secretase inhibitors |
| JP6043355B2 (ja) | 2011-08-31 | 2016-12-14 | ファイザー・インク | ヘキサヒドロピラノ［３，４−ｄ］［１，３］チアジン−２−アミン化合物 |
| ES2585262T3 (es) | 2012-05-04 | 2016-10-04 | Pfizer Inc | Compuestos heterocíclicos de hexahidropiran[3,4-d][1,3]tiazin-2-amina sustituidos como inhibidores de PPA, BACE1 y BACE2 |
| JP2015529239A (ja) | 2012-09-20 | 2015-10-05 | ファイザー・インク | アルキル置換ヘキサヒドロピラノ［３，４−ｄ］［１，３］チアジン−２−アミン化合物 |
| UA110688C2 (uk) | 2012-09-21 | 2016-01-25 | Пфайзер Інк. | Біциклічні піридинони |
| EP2931731A1 (en) | 2012-12-11 | 2015-10-21 | Pfizer Inc. | Hexahydropyrano [3,4-d][1,3]thiazin-2-amine compounds as inhibitors of bace1 |
| EP2935282A1 (en) | 2012-12-19 | 2015-10-28 | Pfizer Inc. | CARBOCYCLIC- AND HETEROCYCLIC-SUBSTITUTED HEXAHYDROPYRANO[3,4-d][1,3]THIAZIN-2-AMINE COMPOUNDS |
| CA2897678A1 (en) | 2013-02-13 | 2014-08-21 | Pfizer Inc. | Heteroaryl-substituted hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds |
| US9233981B1 (en) | 2013-02-15 | 2016-01-12 | Pfizer Inc. | Substituted phenyl hexahydropyrano[3,4-d][1,3]thiazin-2-amine compounds |
| CN105121439A (zh) | 2013-02-19 | 2015-12-02 | 辉瑞公司 | 作为pde4亚型抑制剂用于治疗cns和其他病症的氮杂苯并咪唑化合物 |
| CA2925743C (en) | 2013-10-04 | 2018-03-06 | Pfizer Inc. | Novel bicyclic pyridinones as gamma-secretase modulators |
| JO3466B1 (ar) | 2013-12-20 | 2020-07-05 | Takeda Pharmaceuticals Co | مواد ضابطة لتترا هيدرو بيريدوبيرازينات من gpr6 |
| SG11201607465UA (en) | 2014-04-01 | 2016-10-28 | Pfizer | Chromene and 1,1 a,2,7b-tetrahydrocyclopropa[c]chromene pyridopyrazinediones as gamma-secretase modulators |
| KR20180078347A (ko) | 2014-04-10 | 2018-07-09 | 화이자 인코포레이티드 | 2-아미노-6-메틸-4,4a,5,6-테트라히드로피라노[3,4-d][1,3]티아진-8a(8H)-일-1,3-티아졸-4-일 아미드 |
| EP3172210B1 (en) | 2014-07-24 | 2020-01-15 | Pfizer Inc | Pyrazolopyrimidine compounds |
| KR102061952B1 (ko) | 2014-08-06 | 2020-01-02 | 화이자 인코포레이티드 | 이미다조피리다진 화합물 |
| EP3253755B1 (en) | 2015-02-03 | 2020-08-26 | Pfizer Inc | Novel cyclopropabenzofuranyl pyridopyrazinediones |
| JP6827959B2 (ja) | 2015-06-17 | 2021-02-10 | ファイザー・インク | 三環式化合物およびホスホジエステラーゼ阻害剤としてのそれらの使用 |
| WO2017051303A1 (en) | 2015-09-24 | 2017-03-30 | Pfizer Inc. | Tetrahydropyrano[3,4-d][1,3]oxazin derivatives and their use as bace inhibitors |
| BR112018003489A2 (pt) | 2015-09-24 | 2018-09-25 | Pfizer | n-[2-(2-amino-6,6-dissubstituído-4,4a,5,6-tetra-hidropirano[3,4-d][1,3]tiazin-8a(8h)-il)-1,3-tiazol-4-il]amidas |
| WO2017051294A1 (en) | 2015-09-24 | 2017-03-30 | Pfizer Inc. | N-[2-(3-amino-2,5-dimethyl-1,1-dioxido-5,6-dihydro-2h-1,2,4-thiadiazin-5-yl)-1,3-thiazol-4-yl] amides useful as bace inhibitors |
| PT3419979T (pt) | 2016-02-23 | 2020-03-26 | Pfizer | Compostos de 6,7-dihidro-5h-pirazolo[5,1-b][1,3]oxazina-2-carboxamida |
| KR102470497B1 (ko) | 2016-07-01 | 2022-11-23 | 화이자 인코포레이티드 | 신경계 및 신경변성 질환을 치료하기 위한 5,7-디히드로-피롤로-피리딘 유도체 |
| WO2018234953A1 (en) | 2017-06-22 | 2018-12-27 | Pfizer Inc. | DIHYDRO-PYRROLO-PYRIDINE DERIVATIVES |
| US11382918B2 (en) * | 2017-06-28 | 2022-07-12 | Ptc Therapeutics, Inc. | Methods for treating Huntington's Disease |
| US11524954B2 (en) | 2018-03-23 | 2022-12-13 | Pfizer Inc. | Piperazine azaspiro derivatives |
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| TW274550B (es) * | 1992-09-26 | 1996-04-21 | Hoechst Ag | |
| JP2000154139A (ja) | 1998-09-16 | 2000-06-06 | Kyowa Hakko Kogyo Co Ltd | 縮環ピラジン誘導体 |
| US6369056B1 (en) * | 1999-05-04 | 2002-04-09 | American Home Products Corporation | Cyclic urea and cyclic amide derivatives |
| US6465465B1 (en) * | 2000-03-14 | 2002-10-15 | Arzneimittelwerk Dresden Gmbh | Process for the treatment of erectile dysfunction and product therefor |
| KR100540623B1 (ko) * | 2001-02-26 | 2006-01-11 | 다나베 세이야꾸 가부시키가이샤 | 피리도피리미딘 또는 나프틸리딘 유도체 |
| WO2002076954A1 (en) | 2001-03-23 | 2002-10-03 | Smithkline Beecham Corporation | Compounds useful as kinase inhibitors for the treatment of hyperproliferative diseases |
| US20030114469A1 (en) * | 2001-09-27 | 2003-06-19 | Cohen David Saul | Combinations |
| US7067658B2 (en) * | 2002-09-30 | 2006-06-27 | Bristol-Myers Squibb Company | Pyridino and pyrimidino pyrazinones |
| EP1624900A4 (en) * | 2003-05-20 | 2007-05-02 | Univ California | METHOD OF BINDING AGENTS AT BETA AMYLOID PLAQUE |
| CA2529196A1 (en) * | 2003-06-26 | 2005-02-17 | Merck & Co., Inc. | Benzodiazepine cgrp receptor antagonists |
| DE102004033670A1 (de) * | 2004-07-09 | 2006-02-02 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Neue Pyridodihydropyrazinone, Verfahren zu Ihrer Herstellung und Ihre Verwendung als Arzneimittel |
| CA2593005A1 (en) * | 2005-01-03 | 2006-07-13 | Myriad Genetics Inc. | Pharmaceutical compounds as activators of caspases and inducers of apoptosis and the use thereof |
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2007
- 2007-04-10 EP EP07734320A patent/EP2013208B1/en active Active
- 2007-04-10 CA CA2649775A patent/CA2649775C/en not_active Expired - Fee Related
- 2007-04-10 MX MX2008012456A patent/MX2008012456A/es active IP Right Grant
- 2007-04-10 SI SI200730675T patent/SI2013208T1/sl unknown
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- 2007-04-10 BR BRPI0710658-0A patent/BRPI0710658A2/pt not_active IP Right Cessation
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- 2007-04-10 ES ES07734320T patent/ES2366239T3/es active Active
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- 2007-04-10 DK DK07734320.0T patent/DK2013208T3/da active
- 2007-04-10 WO PCT/IB2007/001001 patent/WO2007122466A1/en active Application Filing
- 2007-04-10 EA EA200801998A patent/EA014919B1/ru not_active IP Right Cessation
- 2007-04-10 ME MEP-238/08A patent/MEP23808A/xx unknown
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- 2007-04-10 JP JP2009505983A patent/JP4436892B2/ja not_active Expired - Fee Related
- 2007-04-10 AT AT07734320T patent/ATE513831T1/de active
- 2007-04-10 AP AP2008004640A patent/AP2408A/xx active
- 2007-04-11 NL NL2000583A patent/NL2000583C2/nl not_active IP Right Cessation
- 2007-04-18 AR ARP070101657A patent/AR060525A1/es not_active Application Discontinuation
- 2007-04-18 UY UY30291A patent/UY30291A1/es not_active Application Discontinuation
- 2007-04-19 PE PE2007000483A patent/PE20080192A1/es not_active Application Discontinuation
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- 2007-04-20 PA PA20078724201A patent/PA8724201A1/es unknown
- 2007-04-20 US US11/737,966 patent/US7902195B2/en not_active Expired - Fee Related
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