AR091259A1 - Formas solidas de un compuesto antiviral - Google Patents

Formas solidas de un compuesto antiviral

Info

Publication number
AR091259A1
AR091259A1 ARP130101956A AR091259A1 AR 091259 A1 AR091259 A1 AR 091259A1 AR P130101956 A ARP130101956 A AR P130101956A AR 091259 A1 AR091259 A1 AR 091259A1
Authority
AR
Argentina
Prior art keywords
solid forms
antiviral compound
aza
methyl
compound
Prior art date
Application number
Other languages
English (en)
Inventor
William Scott Robert
Wang Fang
Shi Bing
Mogalian Erik
Original Assignee
Gilead Sciences Inc
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 Gilead Sciences Inc filed Critical Gilead Sciences Inc
Publication of AR091259A1 publication Critical patent/AR091259A1/es

Links

Classifications

    • 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
    • C07D403/14—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 three or more hetero rings
    • 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
    • A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
    • A61K31/381—Heterocyclic compounds having sulfur as a ring hetero atom having five-membered rings
    • 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
    • A61K31/41—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
    • A61K31/4184—1,3-Diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • 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
    • A61K31/70—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
    • A61K31/7056—Compounds having saccharide radicals and heterocyclic rings having nitrogen as a ring hetero atom, e.g. nucleosides, nucleotides containing five-membered rings with nitrogen as a ring hetero atom
    • 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
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/08—Bridged systems
    • 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
    • C07D487/08—Bridged systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00—Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13—Crystalline forms, e.g. polymorphs

Abstract

Reivindicación 1: El solvato con diacetona del éster metílico del ácido (1-{3-[6-(9,9-difluoro-7-{2-[5-(2-metoxicarbonilamino-3-metil-butiril)-5-aza-espiro[2.4]hept-6-il]-3H-imidazol-4-il}-9H-fluoren-2-il)-1H-benzimidazol-2-il]-2-aza-biciclo[2.2.1]heptano-2-carbonil}-2-metil-propil)carbámico cristalino (Forma I del compuesto de fórmula (1)) caracterizado porque tiene un difractograma de rayos X en polvo que comprende los siguientes picos: 6,8, 12,5, y 19,8 º2q ± 0,2 º2q, determinados con un difractómetro usando radiación Cu-Ka con una longitud de onda de 1,54178 Å.
ARP130101956 2012-06-05 2013-06-03 Formas solidas de un compuesto antiviral AR091259A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201261655934P 2012-06-05 2012-06-05
US201361759295P 2013-01-31 2013-01-31
US13/800,374 US8969588B2 (en) 2012-06-05 2013-03-13 Solid forms of an antiviral compound

Publications (1)

Publication Number Publication Date
AR091259A1 true AR091259A1 (es) 2015-01-21

Family

ID=49670993

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP130101956 AR091259A1 (es) 2012-06-05 2013-06-03 Formas solidas de un compuesto antiviral

Country Status (20)

Country Link
US (4) US8969588B2 (es)
EP (1) EP2855478B1 (es)
JP (2) JP2015518891A (es)
KR (1) KR20150028971A (es)
CN (2) CN105524050A (es)
AR (1) AR091259A1 (es)
AU (1) AU2013271768B2 (es)
BR (1) BR112014030400A2 (es)
CA (1) CA2875507A1 (es)
ES (1) ES2694759T3 (es)
HK (1) HK1205127A1 (es)
IL (1) IL236004A0 (es)
IN (1) IN2014MN02644A (es)
MX (1) MX2014014563A (es)
PT (1) PT2855478T (es)
RU (1) RU2014150437A (es)
SG (1) SG11201408013WA (es)
TW (1) TW201408661A (es)
UY (1) UY34844A (es)
WO (1) WO2013184698A1 (es)

Families Citing this family (29)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ES2726998T3 (es) 2003-05-30 2019-10-11 Gilead Pharmasset Llc Análogos de nucleósidos fluorados modificados
RS55249B8 (sr) 2009-05-13 2021-06-30 Gilead Pharmasset Llc Antiviralna jedinjenja
TWI510480B (zh) 2011-05-10 2015-12-01 Gilead Sciences Inc 充當離子通道調節劑之稠合雜環化合物
SG10201602044WA (en) 2011-09-16 2016-04-28 Gilead Pharmassett Llc Methods For Treating HCV
US9056860B2 (en) 2012-06-05 2015-06-16 Gilead Pharmasset Llc Synthesis of antiviral compound
TW201446286A (zh) * 2013-01-31 2014-12-16 Gilead Pharmasset Llc 抗病毒化合物之固態分散調製劑
CA2852867C (en) 2013-01-31 2016-12-06 Gilead Pharmasset Llc Combination formulation of two antiviral compounds
CN104211565A (zh) * 2013-05-31 2014-12-17 浙江九洲药业股份有限公司 一种抗丙型肝炎药物中间体的制备方法
MX2016002185A (es) 2013-08-27 2016-06-06 Gilead Pharmasset Llc Formulacion combinada de dos compuestos antivirales.
CN104513223B (zh) * 2014-11-20 2017-07-14 上海众强药业有限公司 芴乙酮衍生物的制备方法
JP2018505201A (ja) 2015-02-13 2018-02-22 サンド・アクチエンゲゼルシヤフト レジパスビルおよびソホスブビルを含む医薬組成物
WO2016145269A1 (en) 2015-03-12 2016-09-15 Teva Pharmaceuticals International Gmbh Solid state forms ledipasvir and processes for preparation of ledipasvir
CN104788361B (zh) * 2015-04-21 2017-06-30 杭州科巢生物科技有限公司 5‑氮杂螺[2.4]庚烷‑6‑甲酸衍生物的合成方法
WO2016193919A1 (en) 2015-06-05 2016-12-08 Mylan Laboratories Limited Polymorphic form of ledipasvir
CN104961733B (zh) * 2015-07-06 2019-04-09 上海众强药业有限公司 雷迪帕韦晶型及其制备方法
CN106608870A (zh) * 2015-10-26 2017-05-03 广东东阳光药业有限公司 一种制备雷迪帕韦杂质的方法
WO2017072596A1 (en) * 2015-10-26 2017-05-04 Optimus Drugs (P) Ltd An improved process for the preparation of ledipasvir
CN105237517B (zh) * 2015-10-30 2017-10-27 南京正大天晴制药有限公司 结晶的雷迪帕韦化合物及其制备方法
WO2017072714A1 (en) 2015-10-30 2017-05-04 Lupin Limited Stable ledipasvir premix and process of preparation thereof
CN105237384B (zh) * 2015-11-06 2017-06-30 上海万溯化学有限公司 一种多取代芴衍生物的制备方法
WO2017197036A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Spirocyclic degronimers for target protein degradation
WO2017197055A1 (en) 2016-05-10 2017-11-16 C4 Therapeutics, Inc. Heterocyclic degronimers for target protein degradation
EP3455218A4 (en) 2016-05-10 2019-12-18 C4 Therapeutics, Inc. C3 CARBON-BASED GLUTARIMIDE DEGRONIMERS FOR TARGET PROTEIN REDUCTION
CN106008316B (zh) * 2016-06-17 2018-04-27 成都百事兴科技实业有限公司 一种合成雷迪帕韦手性中间体的方法
CN111202744A (zh) * 2016-12-26 2020-05-29 上海博志研新药物技术有限公司 一种雷迪帕韦和索非布韦复方片剂及其制备方法和应用
US10392370B2 (en) 2017-03-13 2019-08-27 Optimus Drugs Pvt Ltd Process for the preparation of Daclatasvir dihydrochloride and its intermediates
CN109053400A (zh) * 2018-08-24 2018-12-21 江苏工程职业技术学院 一种雷迪帕韦关键中间体的制备方法
US11378965B2 (en) 2018-11-15 2022-07-05 Toyota Research Institute, Inc. Systems and methods for controlling a vehicle based on determined complexity of contextual environment
CN109678686A (zh) * 2018-12-19 2019-04-26 江苏工程职业技术学院 一种抗丙肝药物雷迪帕韦关键中间体的制备方法

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5023252A (en) 1985-12-04 1991-06-11 Conrex Pharmaceutical Corporation Transdermal and trans-membrane delivery of drugs
US5001139A (en) 1987-06-12 1991-03-19 American Cyanamid Company Enchancers for the transdermal flux of nivadipine
US4992445A (en) 1987-06-12 1991-02-12 American Cyanamid Co. Transdermal delivery of pharmaceuticals
US6482847B2 (en) * 2000-10-03 2002-11-19 Hoffmann-La Roche Inc. Amorphous form of cell cycle inhibitor having improved solubility and bioavailability
CA2537132A1 (en) * 2003-08-28 2005-03-10 Ranbaxy Laboratories Limited Amorphous valganciclovir hydrochloride
CN100448879C (zh) * 2004-07-22 2009-01-07 北京化工大学 一种无定型头孢呋辛酯的制备方法
US20100076047A1 (en) * 2007-08-20 2010-03-25 Sankar Reddy Budidet Amorphous 1-(9H-carbazol-4-yloxy)-3-[[2-(2-methoxyphenoxy)ethyl]amino]-2-propanol phosphate salt
KR20100031045A (ko) * 2008-09-11 2010-03-19 씨제이제일제당 (주) 아데포비어 디피복실의 정제방법
RS55249B8 (sr) 2009-05-13 2021-06-30 Gilead Pharmasset Llc Antiviralna jedinjenja
US20120135965A1 (en) * 2009-05-20 2012-05-31 Ranbaxy Laboratories Limited Amorphous fosamprenavir calcium
KR20120052231A (ko) * 2009-10-16 2012-05-23 이데미쓰 고산 가부시키가이샤 함플루오렌 방향족 화합물, 유기 일렉트로루미네선스 소자용 재료 및 그것을 사용한 유기 일렉트로루미네선스 소자
WO2011156757A1 (en) 2010-06-10 2011-12-15 Gilead Sciences, Inc. Combination of anti-hcv compounds with ribavirin for the treatment of hcv
EP2797586A1 (en) * 2011-12-29 2014-11-05 AbbVie Inc. Solid compositions comprising an hcv inhibitor
US9056860B2 (en) 2012-06-05 2015-06-16 Gilead Pharmasset Llc Synthesis of antiviral compound
CA2852867C (en) * 2013-01-31 2016-12-06 Gilead Pharmasset Llc Combination formulation of two antiviral compounds

Also Published As

Publication number Publication date
BR112014030400A2 (pt) 2016-06-07
US9139570B2 (en) 2015-09-22
JP2017128605A (ja) 2017-07-27
CA2875507A1 (en) 2013-12-12
HK1205127A1 (en) 2015-12-11
US8969588B2 (en) 2015-03-03
CN104379584A (zh) 2015-02-25
AU2013271768B2 (en) 2018-05-17
ES2694759T3 (es) 2018-12-27
TW201408661A (zh) 2014-03-01
EP2855478B1 (en) 2018-08-08
CN105524050A (zh) 2016-04-27
US20130324496A1 (en) 2013-12-05
EP2855478A1 (en) 2015-04-08
JP2015518891A (ja) 2015-07-06
US9682987B2 (en) 2017-06-20
KR20150028971A (ko) 2015-03-17
US20150141659A1 (en) 2015-05-21
US20170327488A1 (en) 2017-11-16
PT2855478T (pt) 2018-11-21
RU2014150437A (ru) 2016-08-10
MX2014014563A (es) 2015-07-06
US20150344488A1 (en) 2015-12-03
AU2013271768A1 (en) 2015-01-15
IN2014MN02644A (es) 2015-10-16
SG11201408013WA (en) 2015-01-29
WO2013184698A1 (en) 2013-12-12
IL236004A0 (en) 2015-02-01
UY34844A (es) 2013-12-31

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