MX2014001944A - Formas cristalinas de un inhibidor de la proteasa del virus de la hepatitis c. - Google Patents

Formas cristalinas de un inhibidor de la proteasa del virus de la hepatitis c.

Info

Publication number
MX2014001944A
MX2014001944A MX2014001944A MX2014001944A MX2014001944A MX 2014001944 A MX2014001944 A MX 2014001944A MX 2014001944 A MX2014001944 A MX 2014001944A MX 2014001944 A MX2014001944 A MX 2014001944A MX 2014001944 A MX2014001944 A MX 2014001944A
Authority
MX
Mexico
Prior art keywords
protease inhibitor
crystal forms
hcv protease
hcv
crystal
Prior art date
Application number
MX2014001944A
Other languages
English (en)
Inventor
Robert M Wenslow Jr
Juan D Arredondo
Gregory L Beutner
Jeremy Scott
Eric J Choi
Clinton Scott Shultz
Laura Artino
Original Assignee
Merck Sharp & Dohme
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
Application filed by Merck Sharp & Dohme filed Critical Merck Sharp & Dohme
Publication of MX2014001944A publication Critical patent/MX2014001944A/es

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C35/00—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring
    • C07C35/02—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic
    • C07C35/04—Compounds having at least one hydroxy or O-metal group bound to a carbon atom of a ring other than a six-membered aromatic ring monocyclic containing a three or four-membered rings
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C269/00—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C269/04—Preparation of derivatives of carbamic acid, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups from amines with formation of carbamate groups
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06—Esters of carbamic acids
    • C07C271/32—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of rings other than six-membered aromatic rings
    • C07C271/34—Esters of carbamic acids having oxygen atoms of carbamate groups bound to carbon atoms of rings other than six-membered aromatic rings with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00—Preparation of carboxylic acid esters
    • C07C67/14—Preparation of carboxylic acid esters from carboxylic acid halides
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/013—Esters of alcohols having the esterified hydroxy group bound to a carbon atom of a ring other than a six-membered aromatic ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C69/00—Esters of carboxylic acids; Esters of carbonic or haloformic acids
    • C07C69/02—Esters of acyclic saturated monocarboxylic acids having the carboxyl group bound to an acyclic carbon atom or to hydrogen
    • C07C69/12—Acetic acid esters
    • 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
    • C07D403/12—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 linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D498/16—Peri-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/08—Tripeptides
    • C07K5/0802—Tripeptides with the first amino acid being neutral
    • C07K5/0804—Tripeptides with the first amino acid being neutral and aliphatic
    • C07K5/0808—Tripeptides with the first amino acid being neutral and aliphatic the side chain containing 2 to 4 carbon atoms, e.g. Val, Ile, Leu
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07K—PEPTIDES
    • C07K5/00—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof
    • C07K5/04—Peptides containing up to four amino acids in a fully defined sequence; Derivatives thereof containing only normal peptide links
    • C07K5/12—Cyclic peptides with only normal peptide bonds in the ring
    • C07K5/126—Tetrapeptides
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K38/00—Medicinal preparations containing peptides

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Molecular Biology (AREA)
  • Medicinal Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Genetics & Genomics (AREA)
  • Biophysics (AREA)
  • Biochemistry (AREA)
  • Virology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Communicable Diseases (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Peptides Or Proteins (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
  • Cephalosporin Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

La presente invención se refiere a diversas formas de un compuesto inhibidor de HCV.
MX2014001944A 2011-08-19 2012-08-16 Formas cristalinas de un inhibidor de la proteasa del virus de la hepatitis c. MX2014001944A (es)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201161525462P 2011-08-19 2011-08-19
US201161533439P 2011-09-12 2011-09-12
US201161533915P 2011-09-13 2011-09-13
US201161539540P 2011-09-27 2011-09-27
PCT/US2012/051168 WO2013028465A1 (en) 2011-08-19 2012-08-16 Crystal forms of a hcv protease inhibitor

Publications (1)

Publication Number Publication Date
MX2014001944A true MX2014001944A (es) 2014-03-27

Family

ID=47746773

Family Applications (2)

Application Number Title Priority Date Filing Date
MX2014001945A MX2014001945A (es) 2011-08-19 2012-08-16 Procedimiento e intermedios para la preparacion de macrolactamas.
MX2014001944A MX2014001944A (es) 2011-08-19 2012-08-16 Formas cristalinas de un inhibidor de la proteasa del virus de la hepatitis c.

Family Applications Before (1)

Application Number Title Priority Date Filing Date
MX2014001945A MX2014001945A (es) 2011-08-19 2012-08-16 Procedimiento e intermedios para la preparacion de macrolactamas.

Country Status (11)

Country Link
US (3) US9238604B2 (es)
EP (3) EP2744331A4 (es)
JP (2) JP2014521750A (es)
KR (2) KR20140059236A (es)
CN (2) CN103874414A (es)
AU (2) AU2012299218A1 (es)
BR (2) BR112014003802A2 (es)
CA (2) CA2844386A1 (es)
MX (2) MX2014001945A (es)
RU (2) RU2014110400A (es)
WO (3) WO2013028470A1 (es)

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US8957203B2 (en) 2011-05-05 2015-02-17 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
BR112014003802A2 (pt) 2011-08-19 2017-06-13 Merck Sharp & Dohme composto, composto composição farmacêutica, uso de um composto, método para fabricar um composto, e, preparação de um medicamento
UA119315C2 (uk) 2012-07-03 2019-06-10 Гіліад Фармассет Елелсі Інгібітори вірусу гепатиту с
BR112015007879A2 (pt) 2012-10-19 2017-07-04 Bristol Myers Squibb Co inibidores do vírus da hepatite c
EP2914613B1 (en) 2012-11-02 2017-11-22 Bristol-Myers Squibb Company Hepatitis c virus inhibitors
US9643999B2 (en) 2012-11-02 2017-05-09 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
EP2914598B1 (en) 2012-11-02 2017-10-18 Bristol-Myers Squibb Company Hepatitis c virus inhibitors
EP2914614B1 (en) 2012-11-05 2017-08-16 Bristol-Myers Squibb Company Hepatitis c virus inhibitors
EP2764866A1 (en) 2013-02-07 2014-08-13 IP Gesellschaft für Management mbH Inhibitors of nedd8-activating enzyme
JP6342922B2 (ja) 2013-03-07 2018-06-13 ブリストル−マイヤーズ スクイブ カンパニーＢｒｉｓｔｏｌ−Ｍｙｅｒｓ Ｓｑｕｉｂｂ Ｃｏｍｐａｎｙ Ｃ型肝炎ウイルス阻害剤
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WO2015057611A1 (en) * 2013-10-18 2015-04-23 Merck Sharp & Dohme Corp. Methods and intermediates for preparing macrolactams
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EP4338739A3 (en) 2014-01-24 2024-05-29 Turning Point Therapeutics, Inc. Diaryl macrocycles as modulators of protein kinases
EP3151850A4 (en) * 2014-06-06 2017-11-29 AbbVie Inc. Crystal forms
ES2864839T3 (es) 2015-07-02 2021-10-14 Turning Point Therapeutics Inc Macrociclos de diarilo quirales como moduladores de proteína quinasas
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CN111057045A (zh) * 2019-12-18 2020-04-24 安徽红杉生物医药科技有限公司 Hcv ns3/4a蛋白酶抑制剂中间体及其合成方法、应用
CN112174982A (zh) * 2020-09-10 2021-01-05 上海希迈医药科技有限公司 一种洛普替尼晶型及其制备方法

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Also Published As

Publication number Publication date
EP2744331A1 (en) 2014-06-25
US20140243519A1 (en) 2014-08-28
RU2014110400A (ru) 2015-09-27
CN103874414A (zh) 2014-06-18
CA2844388A1 (en) 2013-02-28
CN103889439A (zh) 2014-06-25
US9073825B2 (en) 2015-07-07
BR112014003798A2 (pt) 2017-03-01
CA2844386A1 (en) 2013-02-28
WO2013028465A1 (en) 2013-02-28
EP2744331A4 (en) 2015-01-21
EP2744507A4 (en) 2015-01-28
US20140200343A1 (en) 2014-07-17
BR112014003802A2 (pt) 2017-06-13
JP2014524442A (ja) 2014-09-22
US9242917B2 (en) 2016-01-26
RU2014110399A (ru) 2015-09-27
KR20140059236A (ko) 2014-05-15
EP2744336B1 (en) 2017-07-05
US9238604B2 (en) 2016-01-19
AU2012299223A1 (en) 2014-02-27
MX2014001945A (es) 2014-03-27
WO2013028470A1 (en) 2013-02-28
KR20140053330A (ko) 2014-05-07
EP2744336A1 (en) 2014-06-25
US20140206605A1 (en) 2014-07-24
WO2013028471A1 (en) 2013-02-28
EP2744507A1 (en) 2014-06-25
AU2012299218A1 (en) 2014-02-20
JP2014521750A (ja) 2014-08-28
EP2744336A4 (en) 2014-12-31

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