AR057704A1 - Inhibidores macrociclicos del virus de la hepatitis c, composicion farmaceutica y proceso de preparacion del compuesto - Google Patents
Inhibidores macrociclicos del virus de la hepatitis c, composicion farmaceutica y proceso de preparacion del compuestoInfo
- Publication number
- AR057704A1 AR057704A1 ARP060103310A ARP060103310A AR057704A1 AR 057704 A1 AR057704 A1 AR 057704A1 AR P060103310 A ARP060103310 A AR P060103310A AR P060103310 A ARP060103310 A AR P060103310A AR 057704 A1 AR057704 A1 AR 057704A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- optionally substituted
- alkoxy
- cycloalkyl
- pyridyl
- Prior art date
Links
Classifications
-
- 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
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Veterinary Medicine (AREA)
- Pharmacology & Pharmacy (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Communicable Diseases (AREA)
- Oncology (AREA)
- Virology (AREA)
- Molecular Biology (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Reivindicacion 1: Un compuesto que posee la formula (1) un N-oxido, sal, o estereoisomero del mismo, donde cada línea punteada (representada por - - - - -) representa un doble enlace opcional; X es N, CH y cuando X posee un doble enlace es C; R1 es - OR11, -NH-SO2R12; R2 es hidrogeno, y cuando X es C o CH, R2 también puede ser alquilo C1-6; R3 es hidrogeno, alquilo C1-6, alcoxi C1-6-alquilo C1-6, o cicloalquilo C3-7; n es 3, 4, 5, o 6; W es un heterociclo del grupo de formulas (2); Q es N o CR4; R4 es hidrogeno; fenilo sustituido opcionalmente con alquilo C1-6 o por alcoxi C1-6; tiazolilo sustituido opcionalmente con alquilo C1-6; o piridilo; R5 es fenilo sustituido opcionalmente con alquilo C1-6 o por alcoxi C1-6; tiazolilo sustituido opcionalmente con alquilo C1-6; o piridilo; uno de R6, R7 es fenilo sustituido opcionalmente con alquilo C1-6 o con alcoxi C1-6; tiazolilo sustituido opcionalmente con alquilo C1-6; o piridilo; mientras que el otro de R6, R7 es hidrogeno; fenilo sustituido opcionalmente con alquilo C1-6 o con alcoxi C1-6; tiazolilo sustituido opcionalmente con alquilo C1-6; o piridilo; uno de R8, R9, R10 es fenilo sustituido opcionalmente con alquilo C1-6 o con alcoxi C1-6; tiazolilo sustituido opcionalmente con alquilo C1-6; o piridilo; mientras que los otros dos de R8, R9, R10 de manera independiente son hidrogeno; fenilo sustituido opcionalmente con alquilo C1-6 o con alcoxi C1-6; tiazolilo sustituido opcionalmente con alquilo C1-6; o piridilo; R11 es hidrogeno; arilo; Het; cicloalquilo C3-7 sustituido opcionalmente con alquilo C1-6; o alquilo C1-6 sustituido opcionalmente con cicloalquilo C3-7, arilo o con Het; R12 es arilo; Het; cicloalquilo C3-7 sustituido opcionalmente con alquilo C1-6; o alquilo C1-6 sustituido opcionalmente con cicloalquilo C3-7, arilo o con Het; cada arilo como grupo o parte de un grupo es fenilo, sustituido opcionalmente con uno, dos o tres sustituyentes seleccionados de halo, hidroxi, nitro, ciano, carboxilo, alquilo C1-6, alcoxi C1-6, alcoxi C1-6-alquilo C1-6, alquilcarbonilo C1-6, amino, mono- o di-alquilamino C1-6, azido, mercapto, polihaloalquilo C1-6, polihaloalcoxi C1-6, cicloalquilo C3-7, pirrolidinilo, piperidinilo, piperazinilo, 4-alquil C1-6-piperazinilo, 4-alquilcarbonil C1-6-piperazinilo, morfolinilo; donde los grupos morfolinilo y piperidilo pueden ser sustituidos opcionalmente con uno o dos alquilo radicales C1-6; y cada Het como grupo o parte de un grupo es un anillo heterocíclico de 5 o 6 miembros saturado, parcialmente no saturado o completamente no saturado de 1 a 4 heteroátomos, cada uno seleccionado de manera independiente de nitrogeno, oxígeno y azufre, y estando sustituido opcionalmente con uno, dos o tres sustituyentes cada uno seleccionado de manera independiente del grupo que consiste en halo, hidroxi, nitro, ciano, carboxilo, alquilo C1-6, alcoxi C1-6, alcoxi C1-6-alquilo C1-6, alquilcarbonilo C1-6 amino, mono- o di-alquilamino C1- 6, azido, mercapto, polihaloalquilo C1-6, polihaloalcoxi C1-6, cicloalquilo C3-7, pirrolidinilo, piperidinilo, piperazinilo, 4-alquil C1-6-piperazinilo, 4-alquil C1-6-carbonil-piperazinilo, morfolinilo; donde los grupos morfolinilo y piperidilo pueden estar sustituidos opcionalmente con uno o dos alquilo radicales C1-6.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP05107072 | 2005-07-29 |
Publications (1)
Publication Number | Publication Date |
---|---|
AR057704A1 true AR057704A1 (es) | 2007-12-12 |
Family
ID=35583505
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
ARP060103310A AR057704A1 (es) | 2005-07-29 | 2006-07-28 | Inhibidores macrociclicos del virus de la hepatitis c, composicion farmaceutica y proceso de preparacion del compuesto |
Country Status (15)
Country | Link |
---|---|
US (2) | US8183277B2 (es) |
EP (1) | EP1913015B1 (es) |
JP (1) | JP5230416B2 (es) |
CN (1) | CN101273052B (es) |
AR (1) | AR057704A1 (es) |
BR (1) | BRPI0614696A2 (es) |
DK (1) | DK1913015T3 (es) |
ES (1) | ES2449540T3 (es) |
MX (1) | MX2008001402A (es) |
MY (1) | MY142972A (es) |
PL (1) | PL1913015T3 (es) |
RU (1) | RU2436787C2 (es) |
SI (1) | SI1913015T1 (es) |
TW (1) | TWI412535B (es) |
WO (1) | WO2007014924A1 (es) |
Families Citing this family (45)
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MY140680A (en) | 2002-05-20 | 2010-01-15 | Bristol Myers Squibb Co | Hepatitis c virus inhibitors |
ES2342944T3 (es) | 2004-01-30 | 2010-07-19 | Medivir Ab | Inhibidores de ns-3 serina proteasa de vhc. |
ATE524475T1 (de) | 2005-07-29 | 2011-09-15 | Tibotec Pharm Ltd | Makrocyclische inhibitoren des hepatitis-c-virus |
JP5230416B2 (ja) | 2005-07-29 | 2013-07-10 | テイボテク・フアーマシユーチカルズ | C型肝炎ウイルスの大員環状阻害剤 |
PE20070211A1 (es) | 2005-07-29 | 2007-05-12 | Medivir Ab | Compuestos macrociclicos como inhibidores del virus de hepatitis c |
US7741281B2 (en) | 2005-11-03 | 2010-06-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
WO2008008776A2 (en) | 2006-07-11 | 2008-01-17 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
CA2656816A1 (en) | 2006-08-04 | 2008-02-14 | Enanta Pharmaceuticals, Inc. | Tetrazolyl macrocyclic hepatitis c serine protease inhibitors |
US8343477B2 (en) | 2006-11-01 | 2013-01-01 | Bristol-Myers Squibb Company | Inhibitors of hepatitis C virus |
US7772180B2 (en) | 2006-11-09 | 2010-08-10 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US8003604B2 (en) | 2006-11-16 | 2011-08-23 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US7763584B2 (en) | 2006-11-16 | 2010-07-27 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US7888464B2 (en) | 2006-11-16 | 2011-02-15 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US8383583B2 (en) | 2007-10-26 | 2013-02-26 | Enanta Pharmaceuticals, Inc. | Macrocyclic, pyridazinone-containing hepatitis C serine protease inhibitors |
US8426360B2 (en) * | 2007-11-13 | 2013-04-23 | Enanta Pharmaceuticals, Inc. | Carbocyclic oxime hepatitis C virus serine protease inhibitors |
CN102026544A (zh) | 2007-11-14 | 2011-04-20 | 益安药业 | 大环四唑基丙型肝炎病毒丝氨酸蛋白酶抑制剂 |
US8263549B2 (en) | 2007-11-29 | 2012-09-11 | Enanta Pharmaceuticals, Inc. | C5-substituted, proline-derived, macrocyclic hepatitis C serine protease inhibitors |
US8273709B2 (en) | 2007-12-14 | 2012-09-25 | Enanta Pharmaceuticals, Inc. | Triazole-containing macrocyclic HCV serine protease inhibitors |
US8283309B2 (en) | 2007-12-20 | 2012-10-09 | Enanta Pharmaceuticals, Inc. | Bridged carbocyclic oxime hepatitis C virus serine protease inhibitors |
US8202996B2 (en) | 2007-12-21 | 2012-06-19 | Bristol-Myers Squibb Company | Crystalline forms of N-(tert-butoxycarbonyl)-3-methyl-L-valyl-(4R)-4-((7-chloro-4-methoxy-1-isoquinolinyl)oxy)-N- ((1R,2S)-1-((cyclopropylsulfonyl)carbamoyl)-2-vinylcyclopropyl)-L-prolinamide |
MX2010008523A (es) | 2008-02-04 | 2010-08-31 | Idenix Pharmaceuticals Inc | Inhibidores macrociclicos de serina proteasa. |
US8372802B2 (en) | 2008-03-20 | 2013-02-12 | Enanta Pharmaceuticals, Inc. | Fluorinated macrocyclic compounds as hepatitis C virus inhibitors |
US8163921B2 (en) | 2008-04-16 | 2012-04-24 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US7964560B2 (en) | 2008-05-29 | 2011-06-21 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
CN102046648A (zh) | 2008-05-29 | 2011-05-04 | 百时美施贵宝公司 | 丙型肝炎病毒抑制剂 |
US8207341B2 (en) | 2008-09-04 | 2012-06-26 | Bristol-Myers Squibb Company | Process or synthesizing substituted isoquinolines |
UY32099A (es) | 2008-09-11 | 2010-04-30 | Enanta Pharm Inc | Inhibidores macrocíclicos de serina proteasas de hepatitis c |
US8563505B2 (en) | 2008-09-29 | 2013-10-22 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US8044087B2 (en) | 2008-09-29 | 2011-10-25 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US8283310B2 (en) | 2008-12-15 | 2012-10-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
TW201040181A (en) | 2009-04-08 | 2010-11-16 | Idenix Pharmaceuticals Inc | Macrocyclic serine protease inhibitors |
CA2769652A1 (en) | 2009-08-05 | 2011-02-10 | Idenix Pharmaceuticals, Inc. | Macrocyclic serine protease inhibitors useful against viral infections, particularly hcv |
WO2012092409A2 (en) | 2010-12-30 | 2012-07-05 | Enanta Phararmaceuticals, Inc | Macrocyclic hepatitis c serine protease inhibitors |
JP2014506255A (ja) | 2010-12-30 | 2014-03-13 | エナンタ ファーマシューティカルズ インコーポレイテッド | フェナントリジン大環状c型肝炎セリンプロテアーゼ阻害剤 |
US9353100B2 (en) | 2011-02-10 | 2016-05-31 | Idenix Pharmaceuticals Llc | Macrocyclic serine protease inhibitors, pharmaceutical compositions thereof, and their use for treating HCV infections |
US8957203B2 (en) | 2011-05-05 | 2015-02-17 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US10201584B1 (en) | 2011-05-17 | 2019-02-12 | Abbvie Inc. | Compositions and methods for treating HCV |
US8691757B2 (en) | 2011-06-15 | 2014-04-08 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
BR112015007879A2 (pt) | 2012-10-19 | 2017-07-04 | Bristol Myers Squibb Co | inibidores do vírus da hepatite c |
US9598433B2 (en) | 2012-11-02 | 2017-03-21 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
US9643999B2 (en) | 2012-11-02 | 2017-05-09 | Bristol-Myers Squibb Company | Hepatitis C virus inhibitors |
WO2014071007A1 (en) | 2012-11-02 | 2014-05-08 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
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EP2964664B1 (en) | 2013-03-07 | 2017-01-11 | Bristol-Myers Squibb Company | Hepatitis c virus inhibitors |
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KR100187990B1 (ko) | 1992-12-29 | 1999-06-01 | 스티븐 에프. 웨인스톡 | 레트로바이러스성 프로테아제 억제 화합물 제조용 합성 중간체 |
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DK0966465T3 (da) | 1997-03-14 | 2003-10-20 | Vertex Pharma | Inhibitorer af IMPDH-enzymer |
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EP1226237A2 (en) | 1999-08-31 | 2002-07-31 | Basf Aktiengesellschaft | Method of identifying inhibitors of cdc25 |
FR2803203B1 (fr) | 1999-12-31 | 2002-05-10 | Fournier Ind & Sante | Nouvelles formulations galeniques du fenofibrate |
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IL135550A0 (en) | 2000-04-09 | 2001-05-20 | Acktar Ltd | Method and apparatus for temperature controlled vapor deposition on a substrate |
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AR029851A1 (es) | 2000-07-21 | 2003-07-16 | Dendreon Corp | Nuevos peptidos como inhibidores de ns3-serina proteasa del virus de hepatitis c |
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JP2007524576A (ja) * | 2003-02-07 | 2007-08-30 | エナンタ ファーマシューティカルズ インコーポレイテッド | 大環状のc型肝炎セリンプロテアーゼ阻害剤 |
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US7125845B2 (en) * | 2003-07-03 | 2006-10-24 | Enanta Pharmaceuticals, Inc. | Aza-peptide macrocyclic hepatitis C serine protease inhibitors |
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ES2342944T3 (es) * | 2004-01-30 | 2010-07-19 | Medivir Ab | Inhibidores de ns-3 serina proteasa de vhc. |
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ATE524475T1 (de) | 2005-07-29 | 2011-09-15 | Tibotec Pharm Ltd | Makrocyclische inhibitoren des hepatitis-c-virus |
PE20070211A1 (es) | 2005-07-29 | 2007-05-12 | Medivir Ab | Compuestos macrociclicos como inhibidores del virus de hepatitis c |
JP5230416B2 (ja) | 2005-07-29 | 2013-07-10 | テイボテク・フアーマシユーチカルズ | C型肝炎ウイルスの大員環状阻害剤 |
-
2006
- 2006-07-28 JP JP2008523380A patent/JP5230416B2/ja not_active Expired - Fee Related
- 2006-07-28 WO PCT/EP2006/064818 patent/WO2007014924A1/en active Application Filing
- 2006-07-28 AR ARP060103310A patent/AR057704A1/es unknown
- 2006-07-28 PL PL06764266T patent/PL1913015T3/pl unknown
- 2006-07-28 SI SI200631753T patent/SI1913015T1/sl unknown
- 2006-07-28 RU RU2008107726/04A patent/RU2436787C2/ru not_active IP Right Cessation
- 2006-07-28 TW TW095127604A patent/TWI412535B/zh not_active IP Right Cessation
- 2006-07-28 BR BRPI0614696-1A patent/BRPI0614696A2/pt not_active IP Right Cessation
- 2006-07-28 CN CN200680035185.3A patent/CN101273052B/zh not_active Expired - Fee Related
- 2006-07-28 MX MX2008001402A patent/MX2008001402A/es active IP Right Grant
- 2006-07-28 US US11/995,560 patent/US8183277B2/en not_active Expired - Fee Related
- 2006-07-28 ES ES06764266.0T patent/ES2449540T3/es active Active
- 2006-07-28 MY MYPI20063672A patent/MY142972A/en unknown
- 2006-07-28 EP EP06764266.0A patent/EP1913015B1/en active Active
- 2006-07-28 DK DK06764266.0T patent/DK1913015T3/en active
-
2012
- 2012-04-20 US US13/451,660 patent/US8754116B2/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
PL1913015T3 (pl) | 2014-04-30 |
RU2436787C2 (ru) | 2011-12-20 |
JP2009502887A (ja) | 2009-01-29 |
EP1913015B1 (en) | 2013-12-11 |
RU2008107726A (ru) | 2009-09-10 |
MY142972A (en) | 2011-01-31 |
US20080262058A1 (en) | 2008-10-23 |
SI1913015T1 (sl) | 2014-05-30 |
TWI412535B (zh) | 2013-10-21 |
CN101273052A (zh) | 2008-09-24 |
US20120202859A1 (en) | 2012-08-09 |
WO2007014924A1 (en) | 2007-02-08 |
BRPI0614696A2 (pt) | 2011-04-12 |
EP1913015A1 (en) | 2008-04-23 |
ES2449540T3 (es) | 2014-03-20 |
CN101273052B (zh) | 2016-01-13 |
US8754116B2 (en) | 2014-06-17 |
TW200728317A (en) | 2007-08-01 |
JP5230416B2 (ja) | 2013-07-10 |
MX2008001402A (es) | 2008-04-04 |
US8183277B2 (en) | 2012-05-22 |
DK1913015T3 (en) | 2014-03-10 |
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