MA32633B1 - Formes cristallines d'un derive 2-thiazolyl-4-quinolinyl-oxy, un inhibiteur puissant du vhc - Google Patents

Formes cristallines d'un derive 2-thiazolyl-4-quinolinyl-oxy, un inhibiteur puissant du vhc

Info

Publication number
MA32633B1
MA32633B1 MA33699A MA33699A MA32633B1 MA 32633 B1 MA32633 B1 MA 32633B1 MA 33699 A MA33699 A MA 33699A MA 33699 A MA33699 A MA 33699A MA 32633 B1 MA32633 B1 MA 32633B1
Authority
MA
Morocco
Prior art keywords
vhc
crystalline forms
quinolinyloxy
thiazolyl
derivative
Prior art date
Application number
MA33699A
Other languages
Arabic (ar)
English (en)
Inventor
Thilo Berkenbusch
Carl Alan Busacca
Burkhard Jaeger
Richard J Varsolona
Original Assignee
Boehringer Ingelheim Int
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=41268627&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=MA32633(B1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Boehringer Ingelheim Int filed Critical Boehringer Ingelheim Int
Publication of MA32633B1 publication Critical patent/MA32633B1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Virology (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Molecular Biology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Peptides Or Proteins (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

La présente invention concerne de nouvelles formes cristallines du composé (1) suivant, et de son sel de sodium. L'invention concerne également des procédés de préparation de ceux-ci, des compositions pharmaceutiques de ceux-ci, et leur utilisation dans le traitement de l'infection par le virus de l'hépatite c (vhc).
MA33699A 2008-09-16 2011-03-14 Formes cristallines d'un derive 2-thiazolyl-4-quinolinyl-oxy, un inhibiteur puissant du vhc MA32633B1 (fr)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US9729108P 2008-09-16 2008-09-16
US15082609P 2009-03-09 2009-03-09
PCT/US2009/056772 WO2010033444A1 (fr) 2008-09-16 2009-09-14 Formes cristallines d'un dérivé 2-thiazolyl-4-quinolinyl-oxy, un inhibiteur puissant du vhc

Publications (1)

Publication Number Publication Date
MA32633B1 true MA32633B1 (fr) 2011-09-01

Family

ID=41268627

Family Applications (1)

Application Number Title Priority Date Filing Date
MA33699A MA32633B1 (fr) 2008-09-16 2011-03-14 Formes cristallines d'un derive 2-thiazolyl-4-quinolinyl-oxy, un inhibiteur puissant du vhc

Country Status (33)

Country Link
US (2) US8232293B2 (fr)
EP (2) EP2687526A1 (fr)
JP (2) JP5520301B2 (fr)
KR (1) KR101653550B1 (fr)
CN (1) CN102159571B (fr)
AR (1) AR073298A1 (fr)
AU (1) AU2009293494B2 (fr)
BR (1) BRPI0918513A2 (fr)
CA (1) CA2737055C (fr)
CL (1) CL2011000558A1 (fr)
CO (1) CO6351741A2 (fr)
CY (1) CY1115253T1 (fr)
DK (1) DK2331538T3 (fr)
EA (1) EA018603B1 (fr)
EC (1) ECSP11010878A (fr)
ES (1) ES2474992T3 (fr)
HR (1) HRP20140666T1 (fr)
IL (1) IL210345A (fr)
MA (1) MA32633B1 (fr)
ME (1) ME01831B (fr)
MX (1) MX2011002828A (fr)
MY (1) MY153093A (fr)
NZ (2) NZ602163A (fr)
PE (2) PE20130307A1 (fr)
PL (1) PL2331538T3 (fr)
PT (1) PT2331538E (fr)
RS (1) RS53292B (fr)
SG (1) SG189740A1 (fr)
SI (1) SI2331538T1 (fr)
TW (1) TWI471323B (fr)
UY (1) UY32119A (fr)
WO (1) WO2010033444A1 (fr)
ZA (1) ZA201100096B (fr)

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UY32099A (es) 2008-09-11 2010-04-30 Enanta Pharm Inc Inhibidores macrocíclicos de serina proteasas de hepatitis c
AU2009293494B2 (en) 2008-09-16 2014-04-24 Boehringer Ingelheim International Gmbh Crystalline forms of a 2-thiazolyl- 4-quinolinyl-oxy derivative, a potent HCV inhibitor
AU2009293493B2 (en) 2008-09-17 2014-09-18 Boehringer Ingelheim International Gmbh Combination of HCV NS3 protease inhibitor with interferon and ribavirin
EP2408382A4 (fr) * 2009-03-13 2013-06-19 Univ Toledo Cage pliable peu invasive
JP2012520891A (ja) * 2009-03-19 2012-09-10 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 スルホニルキノリンの製造方法
US8633320B2 (en) 2009-05-05 2014-01-21 Boehringer Ingelheim International Gmbh Process for preparing bromo-substituted quinolines
PE20120322A1 (es) 2009-07-07 2012-04-14 Boehringer Ingelheim Int Composicion farmaceutica que comprende faldaprevir o una sal del mismo en un vehiculo auto-emulsionante
KR20120106942A (ko) 2009-10-30 2012-09-27 베링거 인겔하임 인터내셔날 게엠베하 Ｂｉ２０１３３５, 인터페론 알파 및 리바비린을 포함하는 ｈｃｖ 병용 치료요법을 위한 투여 용법
US8530497B2 (en) 2010-03-11 2013-09-10 Boehringer Ingelheim International Gmbh Crystalline salts of a potent HCV inhibitor
WO2012041771A1 (fr) * 2010-09-30 2012-04-05 Boehringer Ingelheim International Gmbh Thérapie combinée pour le traitement d'une infection par le vhc
KR20140003521A (ko) 2010-12-30 2014-01-09 이난타 파마슈티칼스, 인코포레이티드 페난트리딘 매크로사이클릭 ｃ형 간염 세린 프로테아제 억제제
CN103534256B (zh) 2010-12-30 2016-08-10 益安药业 大环丙型肝炎丝氨酸蛋白酶抑制剂
US10201584B1 (en) 2011-05-17 2019-02-12 Abbvie Inc. Compositions and methods for treating HCV
US8492386B2 (en) 2011-10-21 2013-07-23 Abbvie Inc. Methods for treating HCV
US8466159B2 (en) 2011-10-21 2013-06-18 Abbvie Inc. Methods for treating HCV
DE112012003510T5 (de) 2011-10-21 2015-03-19 Abbvie Inc. Verfahren zur Behandlung von HCV umfassend mindestens zwei direkt wirkende antivirale Wirkstoffe, Ribavirin aber nicht Interferon
CN104023726A (zh) 2011-10-21 2014-09-03 艾伯维公司 用于治疗hcv的一种或多种daa的联合治疗(例如，与abt-072或abt-333)
US20140037719A1 (en) 2012-01-12 2014-02-06 Boehringer Ingelheim International Gmbh Stabilized pharmaceutical formulations of a potent hcv inhibitor
JP2015509980A (ja) 2012-03-14 2015-04-02 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 Ｈｃｖ−ｈｉｖ同時感染患者集団のｈｃｖ感染症を治療するための併用療法
WO2013147749A1 (fr) 2012-03-27 2013-10-03 Boehringer Ingelheim International Gmbh Polythérapie orale pour le traitement d'une infection au vhc dans des populations de sous-génotypes de patients spécifiques
WO2013147750A1 (fr) 2012-03-27 2013-10-03 Boehringer Ingelheim International Gmbh Polythérapie orale pour le traitement d'une infection au vhc dans une sous-population de patients spécifiques
WO2013143581A1 (fr) 2012-03-28 2013-10-03 Boehringer Ingelheim International Gmbh Polythérapie pour le traitement d'une infection par le vhc dans une sous-population de sous-génotype de patients spécifique
UA119315C2 (uk) 2012-07-03 2019-06-10 Гіліад Фармассет Елелсі Інгібітори вірусу гепатиту с
WO2014138374A1 (fr) 2013-03-08 2014-09-12 Boehringer Ingelheim International Gmbh Polythérapie par voie orale pour le traitement d'une infection par le vhc chez une sous-population spécifique de patients
JP6511432B2 (ja) 2013-03-15 2019-05-15 ギリアード サイエンシーズ， インコーポレイテッド Ｃ型肝炎ウイルスの大環状二環式阻害剤
AU2014233705C1 (en) * 2013-03-15 2019-10-10 Boehringer Ingelheim International Gmbh Solid oral dosage formulation of HCV inhibitor in the amorphous state
WO2015103490A1 (fr) 2014-01-03 2015-07-09 Abbvie, Inc. Formes galéniques antivirales solides
JP7129703B2 (ja) 2016-04-28 2022-09-02 エモリー ユニバーシティー アルキン含有ヌクレオチド及びヌクレオシド治療組成物並びにそれらに関連した使用
WO2022107182A1 (fr) * 2020-11-18 2022-05-27 University Of Petra Composition de fentanyl et d'acides gras, et son procédé de préparation

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DK1033128T4 (da) 1993-09-28 2012-03-19 Scherer Gmbh R P Blød gelatinekapselfremstilling
AR022061A1 (es) 1998-08-10 2002-09-04 Boehringer Ingelheim Ca Ltd Peptidos inhibidores de la hepatitis c, una composicion farmaceutica que los contiene, el uso de los mismos para preparar una composicion farmaceutica, el uso de un producto intermedio para la preparacion de estos peptidos y un procedimiento para la preparacion de un peptido analogo de los mismos.
US6323180B1 (en) * 1998-08-10 2001-11-27 Boehringer Ingelheim (Canada) Ltd Hepatitis C inhibitor tri-peptides
US6608027B1 (en) 1999-04-06 2003-08-19 Boehringer Ingelheim (Canada) Ltd Macrocyclic peptides active against the hepatitis C virus
UA74546C2 (en) 1999-04-06 2006-01-16 Boehringer Ingelheim Ca Ltd Macrocyclic peptides having activity relative to hepatitis c virus, a pharmaceutical composition and use of the pharmaceutical composition
IL150524A0 (en) * 2000-01-07 2003-02-12 Transform Pharmaceuticals Inc High-throughput formation, identification, and analysis of diverse solid-forms
UY28240A1 (es) * 2003-03-27 2004-11-08 Boehringer Ingelheim Pharma Fases cristalinas de un potente inhibidor de la hcv
CL2004001161A1 (es) 2003-05-21 2005-04-08 Boehringer Ingelheim Int Compuestos describe compuestos derivados de quinolina; composicion farmaceutica; y su uso para tratar una enfermedad causada por el virus de la hepatitis c.
EP1753775B1 (fr) 2004-05-25 2012-12-26 Boehringer Ingelheim International GmbH Processus de preparation d'inhibiteurs de protease hcv acyclique
AU2009293494B2 (en) 2008-09-16 2014-04-24 Boehringer Ingelheim International Gmbh Crystalline forms of a 2-thiazolyl- 4-quinolinyl-oxy derivative, a potent HCV inhibitor
US8530497B2 (en) 2010-03-11 2013-09-10 Boehringer Ingelheim International Gmbh Crystalline salts of a potent HCV inhibitor

Also Published As

Publication number Publication date
PE20110388A1 (es) 2011-07-01
PT2331538E (pt) 2014-05-12
PE20130307A1 (es) 2013-03-22
CO6351741A2 (es) 2011-12-20
WO2010033444A1 (fr) 2010-03-25
CA2737055C (fr) 2016-08-30
PL2331538T3 (pl) 2014-09-30
EP2687526A1 (fr) 2014-01-22
AU2009293494A1 (en) 2010-03-25
SG189740A1 (en) 2013-05-31
US20100093792A1 (en) 2010-04-15
RS53292B (sr) 2014-08-29
CL2011000558A1 (es) 2011-07-15
JP5520301B2 (ja) 2014-06-11
ECSP11010878A (es) 2011-07-29
CN102159571B (zh) 2014-10-01
KR101653550B1 (ko) 2016-09-02
TWI471323B (zh) 2015-02-01
MX2011002828A (es) 2011-04-05
JP2014062116A (ja) 2014-04-10
SI2331538T1 (sl) 2014-06-30
NZ591013A (en) 2012-09-28
CA2737055A1 (fr) 2010-03-25
AU2009293494B2 (en) 2014-04-24
ME01831B (me) 2014-12-20
JP2012502910A (ja) 2012-02-02
US20120270775A1 (en) 2012-10-25
ES2474992T3 (es) 2014-07-10
US8232293B2 (en) 2012-07-31
MY153093A (en) 2014-12-31
ZA201100096B (en) 2011-09-28
UY32119A (es) 2010-04-30
EP2331538B1 (fr) 2014-04-16
EP2331538A1 (fr) 2011-06-15
NZ602163A (en) 2013-06-28
HRP20140666T1 (hr) 2014-10-10
AR073298A1 (es) 2010-10-28
BRPI0918513A2 (pt) 2015-12-01
CN102159571A (zh) 2011-08-17
CY1115253T1 (el) 2017-01-04
TW201024292A (en) 2010-07-01
EA201100482A1 (ru) 2011-10-31
IL210345A0 (en) 2011-03-31
KR20110059841A (ko) 2011-06-07
EA018603B1 (ru) 2013-09-30
US8362035B2 (en) 2013-01-29
HK1156624A1 (en) 2012-06-15
DK2331538T3 (da) 2014-06-02
IL210345A (en) 2015-06-30
WO2010033444A8 (fr) 2010-06-17

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