AR061581A1 - Compuestos de pirro[1,2-b]piridazinona,composiciones farmaceuticas que los contienen y usos para tratar hepatitis c. - Google Patents
Compuestos de pirro[1,2-b]piridazinona,composiciones farmaceuticas que los contienen y usos para tratar hepatitis c.Info
- Publication number
- AR061581A1 AR061581A1 ARP070102753A ARP070102753A AR061581A1 AR 061581 A1 AR061581 A1 AR 061581A1 AR P070102753 A ARP070102753 A AR P070102753A AR P070102753 A ARP070102753 A AR P070102753A AR 061581 A1 AR061581 A1 AR 061581A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- alkylene
- heterocyclyl
- aryl
- cycloalkyl
- Prior art date
Links
Classifications
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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
- A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
- A61K31/541—Non-condensed thiazines containing further heterocyclic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P1/00—Drugs for disorders of the alimentary tract or the digestive system
- A61P1/16—Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
- A61P31/12—Antivirals
- A61P31/14—Antivirals for RNA viruses
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Oncology (AREA)
- Communicable Diseases (AREA)
- Virology (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Engineering & Computer Science (AREA)
- Gastroenterology & Hepatology (AREA)
- Molecular Biology (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
Composiciones farmacéuticas que contienen dichos compuestos que son de utilidad para el tratamiento de infecciones por el virus de hepatitis C. Reivindicacion 1: Un compuesto caracterizado por la formula 1: en donde R1 es, de modo independiente, 1- 3 restos seleccionados de hidrogeno, halo, ciano, nitro, hidroxi, -NR8R9, cicloalquilo C3-8, alquilo C1-6, alquenilo, alquinilo, haloalquilo C1-6, hidroxialquilo C1-6, alcoxi C1-6, -alquilen C1-6-NR8R9, -C(O)OH, -C(O)Oalquilo C1-6, - C(O)NH-alquilo C1-6 , -C(O)alquilo C1-6 , arilo o heterociclilo con 1, 2 o 3 átomos de N, O o S, en donde R8 y R9 son, de modo independiente, H, alquilo C1-6, cicloalquilo C3C8, arilo o heterociclilo o R8 y R9 se combinan con el átomo de N al que están unidos para formar un anillo heterociclilo de 5 o 6 miembros , R2 es hidrogeno, cicloalquilo C3-8, alquilo C1-7, alquenilo, alquinilo, haloalquilo C1-6, hidroxialquilo C1-6, alcoxi C1-6, arilo o heterociclilo con 1, 2 o 3 átomos de N, O o S, R3 es hidrogeno o alquilo C1-6, R4 está seleccionado de grupo de formulas (2), en donde n es 0, 1 o 2, R5 es hidrogeno o alquilo C1-6, R6 es hidrogeno, halo o alquilo C1-6, y anillo A es arilo o heterociclilo de 5 a 6 miembros, opcionalmente sustituido con 1-3 restos R7, en donde R7 es H, alquilo, alquenilo, alquinilo, arilo, heterociclilo, halo, ciano, nitro, OH, -O-alquilo, -O-hidroxialquilo C1-6, -O-alcoxi C1-6, -O-alquilen C1-6 -ciano, -O-alquilen C1-6-C(O)R10, - OCHR10C(O)O-R11, - OCHR10C(O)NHOH, -O-alquil C1-6-C(O)NR11R12, -O-alquilen C1-6-NR10C(O)R11, -O-alquilen C1-6-NR10C(O)OR11, -O-alquilen C1-6-NR10C(O)NR11R12, -OCHR10C(O)NR11R12, -Oalquilen C1-6-S(O)-R10, -O-alquil C1-6-S(O)2R10, -O-alquilen C1-6-S(O)2NR11R12, -O- alquilen C1-6- NR10S(O)2NR11R12, -O-alquilen C1-6-NR10S(O)2R11, -O-alquilen C1-6-S(O)2R10, -O-alquilen C1-6-NR11R12, -alquilen C1-6-S(O)2R10, -alquilen C1-6-S(O)2NR11R12, -alquilen C1-6-S(O)R10, -alquilen C1-6-C(O)R10, -alquilen C1-6-C(O)NR11R12, - alquilen C1-6- NR10C(O)R11, -alquilen C1-6-NR10S(O)2R11, -alquilen C1-6-NR10C(O)OR11, -alquilen C1-6-NR10C(O)NR11R12, -alquilen C1-6-NR10S(O)NR11R12, -alquilen C1-6-C(O)OR10, -alquilen C1-6-NR11R12, -NR11R12, -NR11C(O)R12, NR10S(O)2R11, - NR10S(O)2NR11R12, - C(O)R10, -S(O)R10, -S(O)2R10 o -S(O)2NR11R12, en donde R10, R11 y R12 son de modo independiente, H, alquilo C1-6, cicloalquilo C3-8, arilo, o heterociclilo o R10 y R11 o R11 y R12 se combinan con el o los átomos a los que están unidos para formar un anillo heterociclilo de 5 o 6 miembros, en donde los restos anteriores de alquilo, alquenilo, alquinilo, arilo, cicloalquilo o heterociclilo provistos en R1, R2, R7, R8, R9, R10, R11 y R12 están opcional e independientemente sustituidos con 1-3 sustituyentes seleccionados de alquilamina, amino, arilo, cicloalquilo, heterociclilo, alquilo C1-6, haloalquilo C1-6, hidroxialquilo C1-6, alcoxi C1-6, alquil C1-6-amina, dialquil C1-6-amina, alquenilo C2-6, o alquinilo C2-6, en donde cada uno de los cuales puede estar interrumpido por uno o varios heteroátomos, carboxilo, ciano, halo, hidroxi, nitro, oxo, -C(O)OH, -C(O)2-alquilo C1-6, C(O)2-cicloalquilo C3-8, -C(O)2-arilo, -CO)2-heterociclilo , alquilen C1-6-arilo, -C(O)2- alquilen C1-6- heterociclilo, -C(O)2-alquilen C1-6-cicloalquilo, -C(O)-alquilo C1-6), -C(O)-cicloalquilo C3-8, -C(O)-arilo, -C(O)-heterociclilo, -C(O)-alquilen C1-6-arilo, -C(O)-alquilen C1-6-heterociclilo y -C(O)-alquil C1-6-cicloalquilo, en donde cada uno de los sustituyentes opcionales anteriores también puede estar opcionalmente sustituido con 1-5 sustituyentes seleccionados de amino, ciano, halo, hidroxi, nitro, alquil C1-6-amina, dialquil C1-6-amina, alquilo C1-6, alcoxi C1-6, alquenilo C1-6 e hidroxialquilo C1-6, en donde cada alquilo está opcionalmente sustituido con uno o varios sustituyentes de halo, o una de sus sales, hidratos, tautomeros o estereoisomeros farmacéuticamente aceptables.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US81557806P | 2006-06-22 | 2006-06-22 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR061581A1 true AR061581A1 (es) | 2008-09-03 |
Family
ID=38833773
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP070102753A AR061581A1 (es) | 2006-06-22 | 2007-06-22 | Compuestos de pirro[1,2-b]piridazinona,composiciones farmaceuticas que los contienen y usos para tratar hepatitis c. |
Country Status (14)
Country | Link |
---|---|
US (3) | US7462611B2 (es) |
EP (1) | EP2038286B1 (es) |
JP (2) | JP5306194B2 (es) |
KR (1) | KR101384266B1 (es) |
CN (2) | CN101501039B (es) |
AR (1) | AR061581A1 (es) |
BR (1) | BRPI0713684A2 (es) |
CA (1) | CA2656000C (es) |
IL (1) | IL196106A0 (es) |
MX (1) | MX2008016519A (es) |
NZ (1) | NZ573875A (es) |
PA (1) | PA8733401A1 (es) |
TW (1) | TWI395749B (es) |
WO (1) | WO2007150001A1 (es) |
Families Citing this family (18)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU2005316396A1 (en) | 2004-12-17 | 2006-06-22 | Anadys Pharmaceuticals, Inc. | Pyridazinone compounds |
CN101501039B (zh) * | 2006-06-22 | 2012-02-22 | 安那迪斯药品股份有限公司 | 吡咯并[1,2-b]哒嗪酮化合物 |
UA100120C2 (en) * | 2007-04-03 | 2012-11-26 | Анадис Фармасьютикалз, Инк. | 5,6-dihydro-1h-pyridin-2-one compounds |
MX2009011930A (es) | 2007-05-04 | 2009-11-18 | Vertex Pharma | Terapia de combinacion para el tratamiento de infeccion de virus de hepatitis c. |
WO2009111337A1 (en) | 2008-03-03 | 2009-09-11 | Irm Llc | Compounds and compositions as tlr activity modulators |
JP2011516610A (ja) * | 2008-04-15 | 2011-05-26 | インターミューン・インコーポレーテッド | C型肝炎ウイルス複製の新規な阻害剤 |
TWI480272B (zh) | 2008-10-09 | 2015-04-11 | Anadys Pharmaceuticals Inc | 藉由5,6-二氫-1h-吡啶-2-酮與一或多種其他抗病毒化合物的組合物抑制c型肝炎病毒的方法 |
RU2012121847A (ru) * | 2009-10-28 | 2013-12-10 | Анадис Фармасьютикалз, Инк. | Дейтерированные соединения 5, 6-дигидро-1н-пиридин-2-она |
EA201200650A1 (ru) | 2009-10-30 | 2012-12-28 | Бёрингер Ингельхайм Интернациональ Гмбх | Курсы комбинированного лечения вируса гепатита с, включающие bi201335, интерферон-альфа и рибавирин |
TW201121968A (en) * | 2009-11-09 | 2011-07-01 | Intermune Inc | Novel inhibitors of hepatitis C virus replication |
CA2784646A1 (en) * | 2009-12-18 | 2011-06-23 | Boehringer Ingelheim International Gmbh | Hcv combination therapy |
WO2012158271A1 (en) | 2011-04-06 | 2012-11-22 | Anadys Pharmaceuticals, Inc. | Bridged polycyclic compounds as antiviral agents |
KR20140037193A (ko) | 2011-06-07 | 2014-03-26 | 애나디스 파마슈티칼스, 인코포레이티드 | 혈청 요산을 낮추기 위한 [1,2,4]티아디아진 1,1-다이옥사이드 화합물 |
US9646817B2 (en) | 2011-06-23 | 2017-05-09 | Brooks Automation, Inc. | Semiconductor cleaner systems and methods |
CN102796105B (zh) * | 2012-08-15 | 2014-08-06 | 苏州施亚生物科技有限公司 | 2,5,6,7-四氢吡咯并[3,4-c]哒嗪-3-酮及其衍生物以及它们的合成方法 |
MX2015008827A (es) * | 2013-01-14 | 2015-10-14 | Hoffmann La Roche | Nuevo proceso para la preparacion de metil ester del acido n-(4-nitro-2-sulfamoil-fenil)-malonamico y metil ester del acido n-(4-amino-2-sulfamoil-fenil)-malonamico. |
CN103553986B (zh) * | 2013-11-19 | 2015-04-22 | 郑州西格玛化工有限公司 | 一种制备3,4-二氨基苯磺酰胺的方法 |
WO2021030278A1 (en) * | 2019-08-12 | 2021-02-18 | Aligos Therapeutics, Inc. | Bicyclic compounds |
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CN101501039B (zh) | 2006-06-22 | 2012-02-22 | 安那迪斯药品股份有限公司 | 吡咯并[1,2-b]哒嗪酮化合物 |
UA100120C2 (en) | 2007-04-03 | 2012-11-26 | Анадис Фармасьютикалз, Инк. | 5,6-dihydro-1h-pyridin-2-one compounds |
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2007
- 2007-06-21 CN CN2007800300269A patent/CN101501039B/zh not_active Expired - Fee Related
- 2007-06-21 US US11/766,697 patent/US7462611B2/en not_active Expired - Fee Related
- 2007-06-21 MX MX2008016519A patent/MX2008016519A/es active IP Right Grant
- 2007-06-21 CA CA2656000A patent/CA2656000C/en not_active Expired - Fee Related
- 2007-06-21 NZ NZ573875A patent/NZ573875A/en not_active IP Right Cessation
- 2007-06-21 JP JP2009516735A patent/JP5306194B2/ja not_active Expired - Fee Related
- 2007-06-21 TW TW096122375A patent/TWI395749B/zh not_active IP Right Cessation
- 2007-06-21 CN CN2011104533590A patent/CN102584649A/zh active Pending
- 2007-06-21 KR KR1020097001479A patent/KR101384266B1/ko active IP Right Grant
- 2007-06-21 WO PCT/US2007/071826 patent/WO2007150001A1/en active Application Filing
- 2007-06-21 BR BRPI0713684-6A patent/BRPI0713684A2/pt not_active IP Right Cessation
- 2007-06-21 EP EP07798903.6A patent/EP2038286B1/en not_active Not-in-force
- 2007-06-22 AR ARP070102753A patent/AR061581A1/es unknown
- 2007-06-22 PA PA20078733401A patent/PA8733401A1/es unknown
-
2008
- 2008-11-06 US US12/266,190 patent/US7582754B2/en not_active Expired - Fee Related
- 2008-12-22 IL IL196106A patent/IL196106A0/en not_active IP Right Cessation
-
2009
- 2009-08-21 US US12/545,547 patent/US7842838B2/en not_active Expired - Fee Related
-
2013
- 2013-02-01 JP JP2013018431A patent/JP5670487B2/ja not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
US20090105473A1 (en) | 2009-04-23 |
CA2656000A1 (en) | 2007-12-27 |
US20080031852A1 (en) | 2008-02-07 |
EP2038286A1 (en) | 2009-03-25 |
KR20090063203A (ko) | 2009-06-17 |
IL196106A0 (en) | 2009-09-01 |
JP5306194B2 (ja) | 2013-10-02 |
TWI395749B (zh) | 2013-05-11 |
CN101501039A (zh) | 2009-08-05 |
CN101501039B (zh) | 2012-02-22 |
CA2656000C (en) | 2016-09-06 |
US20090312570A1 (en) | 2009-12-17 |
MX2008016519A (es) | 2009-01-30 |
TW200817405A (en) | 2008-04-16 |
WO2007150001A8 (en) | 2008-02-28 |
PA8733401A1 (es) | 2008-11-19 |
EP2038286A4 (en) | 2010-05-12 |
JP2009544575A (ja) | 2009-12-17 |
NZ573875A (en) | 2011-11-25 |
JP5670487B2 (ja) | 2015-02-18 |
US7582754B2 (en) | 2009-09-01 |
JP2013136599A (ja) | 2013-07-11 |
KR101384266B1 (ko) | 2014-04-24 |
US7842838B2 (en) | 2010-11-30 |
EP2038286B1 (en) | 2017-03-08 |
WO2007150001A1 (en) | 2007-12-27 |
US7462611B2 (en) | 2008-12-09 |
AU2007260827A1 (en) | 2007-12-27 |
CN102584649A (zh) | 2012-07-18 |
BRPI0713684A2 (pt) | 2012-10-30 |
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