KR101890400B1 - 항바이러스성 화합물로서의 축합된 이미다졸릴이미다졸 - Google Patents

항바이러스성 화합물로서의 축합된 이미다졸릴이미다졸 Download PDF

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KR101890400B1
KR101890400B1 KR1020137015198A KR20137015198A KR101890400B1 KR 101890400 B1 KR101890400 B1 KR 101890400B1 KR 1020137015198 A KR1020137015198 A KR 1020137015198A KR 20137015198 A KR20137015198 A KR 20137015198A KR 101890400 B1 KR101890400 B1 KR 101890400B1
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mmol
tert
butyl
methyl
naphtho
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KR20140096239A (ko
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엘리자베스 엠 베이컨
제로미 제이 코텔
애슐리 앤 캐타나
데릴 가토
에반 에스 크리고우스키
존 오 링크
제임스 테일러
친 비엣 트란
마틴 테레사 알레잔드라 트레조
정-유 양
쉴라 지펠
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길리애드 파마셋 엘엘씨
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04—Ortho-condensed systems
    • C07D491/044—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/052—Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
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    • 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
    • A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4164—1,3-Diazoles
    • A61K31/4188—1,3-Diazoles condensed with other heterocyclic ring systems, e.g. biotin, sorbinil
    • A—HUMAN NECESSITIES
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    • A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
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    • A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
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    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7042—Compounds having saccharide radicals and heterocyclic rings
    • A61K31/7052—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides
    • A61K31/706—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom
    • A61K31/7064—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines
    • A61K31/7068—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid
    • A61K31/7072—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing six-membered rings with nitrogen as a ring hetero atom containing condensed or non-condensed pyrimidines having oxo groups directly attached to the pyrimidine ring, e.g. cytidine, cytidylic acid having two oxo groups directly attached to the pyrimidine ring, e.g. uridine, uridylic acid, thymidine, zidovudine
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    • A61K47/60—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient the non-active ingredient being chemically bound to the active ingredient, e.g. polymer-drug conjugates the non-active ingredient being a modifying agent the modifying agent being an organic macromolecular compound, e.g. an oligomeric, polymeric or dendrimeric molecule obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyureas or polyurethanes the organic macromolecular compound being a polyoxyalkylene oligomer, polymer or dendrimer, e.g. PEG, PPG, PEO or polyglycerol
    • A—HUMAN NECESSITIES
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    • 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
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    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
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    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12—Antivirals
    • A61P31/14—Antivirals for RNA viruses
    • A—HUMAN NECESSITIES
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/12—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
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  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Steroid Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
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  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Peptides Or Proteins (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Pyrrole Compounds (AREA)
  • Furan Compounds (AREA)
KR1020137015198A 2011-11-16 2012-11-16 항바이러스성 화합물로서의 축합된 이미다졸릴이미다졸 Active KR101890400B1 (ko)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201161560654P 2011-11-16 2011-11-16
US61/560,654 2011-11-16
PCT/US2012/065681 WO2013075029A1 (en) 2011-11-16 2012-11-16 Condensed imidazolylimidazoles as antiviral compounds

Related Child Applications (1)

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KR1020187023418A Division KR102036469B1 (ko) 2011-11-16 2012-11-16 항바이러스성 화합물로서의 축합된 이미다졸릴이미다졸

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KR20140096239A KR20140096239A (ko) 2014-08-05
KR101890400B1 true KR101890400B1 (ko) 2018-08-21

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KR1020137015198A Active KR101890400B1 (ko) 2011-11-16 2012-11-16 항바이러스성 화합물로서의 축합된 이미다졸릴이미다졸
KR1020217010778A Ceased KR20210043734A (ko) 2011-11-16 2012-11-16 항바이러스성 화합물로서의 축합된 이미다졸릴이미다졸
KR1020197030548A Ceased KR20190121406A (ko) 2011-11-16 2012-11-16 항바이러스성 화합물로서의 축합된 이미다졸릴이미다졸
KR1020207027928A Active KR102241651B1 (ko) 2011-11-16 2012-11-16 항바이러스성 화합물로서의 축합된 이미다졸릴이미다졸
KR1020187023418A Active KR102036469B1 (ko) 2011-11-16 2012-11-16 항바이러스성 화합물로서의 축합된 이미다졸릴이미다졸

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KR1020217010778A Ceased KR20210043734A (ko) 2011-11-16 2012-11-16 항바이러스성 화합물로서의 축합된 이미다졸릴이미다졸
KR1020197030548A Ceased KR20190121406A (ko) 2011-11-16 2012-11-16 항바이러스성 화합물로서의 축합된 이미다졸릴이미다졸
KR1020207027928A Active KR102241651B1 (ko) 2011-11-16 2012-11-16 항바이러스성 화합물로서의 축합된 이미다졸릴이미다졸
KR1020187023418A Active KR102036469B1 (ko) 2011-11-16 2012-11-16 항바이러스성 화합물로서의 축합된 이미다졸릴이미다졸

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US (14) US20130164260A1 (https=)
EP (4) EP3431477B1 (https=)
JP (5) JP6082749B2 (https=)
KR (5) KR101890400B1 (https=)
CN (2) CN105837584B (https=)
AP (1) AP2013006877A0 (https=)
AU (1) AU2012318253B8 (https=)
BR (1) BR112013012091A2 (https=)
CA (2) CA2815082C (https=)
CL (1) CL2013001428A1 (https=)
CO (1) CO6791562A2 (https=)
CR (1) CR20130231A (https=)
CY (2) CY1116987T1 (https=)
DK (2) DK2635588T3 (https=)
EA (4) EA037883B1 (https=)
EC (2) ECSP13012790A (https=)
ES (3) ES2843023T3 (https=)
HR (2) HRP20150725T1 (https=)
HU (2) HUE027733T2 (https=)
IL (5) IL226345A (https=)
LT (1) LT2907816T (https=)
MA (1) MA34727B1 (https=)
MD (2) MD4403C1 (https=)
ME (1) ME02196B (https=)
MX (4) MX346729B (https=)
MY (2) MY173045A (https=)
PE (2) PE20141163A1 (https=)
PH (2) PH12013500976A1 (https=)
PL (3) PL2635588T3 (https=)
PT (3) PT2907816T (https=)
RS (2) RS57638B1 (https=)
SG (1) SG10201700947UA (https=)
SI (3) SI2635588T1 (https=)
SM (2) SMT201800470T1 (https=)
UA (2) UA110354C2 (https=)
WO (1) WO2013075029A1 (https=)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20150008908A (ko) * 2012-05-16 2015-01-23 길리어드 파마셋 엘엘씨 항바이러스성 화합물

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CA2841095A1 (en) 2011-07-09 2013-01-17 Sunshine Lake Pharma Co., Ltd. Spiro compounds as hepatitis c virus inhibitors
EP2709613B2 (en) 2011-09-16 2020-08-12 Gilead Pharmasset LLC Methods for treating hcv
CN105837584B (zh) 2011-11-16 2018-07-13 吉利德制药有限责任公司 作为抗病毒化合物的缩合的咪唑基咪唑
US9326973B2 (en) 2012-01-13 2016-05-03 Bristol-Myers Squibb Company Hepatitis C virus inhibitors
EP2950786B1 (en) 2013-01-31 2019-11-27 Gilead Pharmasset LLC Combination formulation of two antiviral compounds
JP5614568B1 (ja) 2013-02-07 2014-10-29 保土谷化学工業株式会社 ジアザトリフェニレン環構造を有する化合物および有機エレクトロルミネッセンス素子
WO2014185995A1 (en) * 2013-05-16 2014-11-20 Gilead Pharmasset Llc Hepatitis c treatments with sofosbuvir
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US20150023913A1 (en) 2013-07-02 2015-01-22 Bristol-Myers Squibb Company Hepatitis C Virus Inhibitors
WO2015005901A1 (en) * 2013-07-09 2015-01-15 Bristol-Myers Squibb Company Combinations of hepatitis c virus inhibitors
US9775831B2 (en) 2013-07-17 2017-10-03 Bristol-Myers Squibb Company Combinations comprising biphenyl derivatives for use in the treatment of HCV
US20150064252A1 (en) 2013-08-27 2015-03-05 Gilead Pharmasset Llc Solid dispersion formulation of an antiviral compound
PT3038601T (pt) 2013-08-27 2020-06-30 Gilead Pharmasset Llc Formulação combinada de dois compostos antivirais
CN104418784B (zh) * 2013-09-04 2019-02-19 浙江九洲药业股份有限公司 一种抗病毒药物中间体的拆分方法
JP6568541B2 (ja) 2013-12-23 2019-08-28 ギリアド ファーマセット エルエルシー 大環状ｈｃｖ ｎｓ３阻害トリペプチドの結晶形態
TWI721947B (zh) * 2014-06-11 2021-03-21 美商基利法瑪席特有限責任公司 抗病毒化合物的固態形式
TW202014413A (zh) * 2014-06-11 2020-04-16 美商基利法瑪席特有限責任公司 製備抗病毒化合物之方法
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