CO6270255A2 - Proceso e intermediarios para preparar inhibidores de integrasas - Google Patents

Proceso e intermediarios para preparar inhibidores de integrasas

Info

Publication number
CO6270255A2
CO6270255A2 CO10037836A CO10037836A CO6270255A2 CO 6270255 A2 CO6270255 A2 CO 6270255A2 CO 10037836 A CO10037836 A CO 10037836A CO 10037836 A CO10037836 A CO 10037836A CO 6270255 A2 CO6270255 A2 CO 6270255A2
Authority
CO
Colombia
Prior art keywords
compound
formula
salt
prepare
prepared
Prior art date
Application number
CO10037836A
Other languages
English (en)
Spanish (es)
Inventor
Eric D Dowdy
Steffen Pfeiffer
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 CO6270255A2 publication Critical patent/CO6270255A2/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C07D215/54Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3
    • C07D215/56Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen attached in position 3 with oxygen atoms in position 4
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/14Antivirals for RNA viruses
    • A61P31/18Antivirals for RNA viruses for HIV
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01Preparation of ethers
    • C07C41/18Preparation of ethers by reactions not forming ether-oxygen bonds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C41/00Preparation of ethers; Preparation of compounds having groups, groups or groups
    • C07C41/01Preparation of ethers
    • C07C41/18Preparation of ethers by reactions not forming ether-oxygen bonds
    • C07C41/30Preparation of ethers by reactions not forming ether-oxygen bonds by increasing the number of carbon atoms, e.g. by oligomerisation
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/15Preparation of carboxylic acids or their salts, halides or anhydrides by reaction of organic compounds with carbon dioxide, e.g. Kolbe-Schmitt synthesis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C51/00Preparation of carboxylic acids or their salts, halides or anhydrides
    • C07C51/347Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups
    • C07C51/377Preparation of carboxylic acids or their salts, halides or anhydrides by reactions not involving formation of carboxyl groups by splitting-off hydrogen or functional groups; by hydrogenolysis of functional groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/30Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • C07C67/343Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton by increase in the number of carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Virology (AREA)
  • Molecular Biology (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • AIDS & HIV (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Quinoline Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)
CO10037836A 2007-09-11 2010-04-05 Proceso e intermediarios para preparar inhibidores de integrasas CO6270255A2 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US97139507P 2007-09-11 2007-09-11

Publications (1)

Publication Number Publication Date
CO6270255A2 true CO6270255A2 (es) 2011-04-20

Family

ID=39887255

Family Applications (1)

Application Number Title Priority Date Filing Date
CO10037836A CO6270255A2 (es) 2007-09-11 2010-04-05 Proceso e intermediarios para preparar inhibidores de integrasas

Country Status (20)

Country Link
US (4) US20090099366A1 (cg-RX-API-DMAC7.html)
EP (1) EP2190804B1 (cg-RX-API-DMAC7.html)
JP (2) JP5202635B2 (cg-RX-API-DMAC7.html)
KR (1) KR101488550B1 (cg-RX-API-DMAC7.html)
CN (1) CN101821223B (cg-RX-API-DMAC7.html)
AP (1) AP2785A (cg-RX-API-DMAC7.html)
AR (1) AR068403A1 (cg-RX-API-DMAC7.html)
AU (1) AU2008298943B2 (cg-RX-API-DMAC7.html)
BR (1) BRPI0816694A2 (cg-RX-API-DMAC7.html)
CA (1) CA2698245C (cg-RX-API-DMAC7.html)
CO (1) CO6270255A2 (cg-RX-API-DMAC7.html)
EA (1) EA019431B1 (cg-RX-API-DMAC7.html)
ES (1) ES2562080T3 (cg-RX-API-DMAC7.html)
MX (1) MX2010002783A (cg-RX-API-DMAC7.html)
NZ (1) NZ583647A (cg-RX-API-DMAC7.html)
PT (1) PT2190804E (cg-RX-API-DMAC7.html)
TW (1) TWI419867B (cg-RX-API-DMAC7.html)
UA (1) UA101956C2 (cg-RX-API-DMAC7.html)
WO (1) WO2009036161A1 (cg-RX-API-DMAC7.html)
ZA (1) ZA201002066B (cg-RX-API-DMAC7.html)

Families Citing this family (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI1564210T1 (sl) 2002-11-20 2010-01-29 Japan Tobacco Inc 4-oksokinolinske spojine in njihova uporaba kot inhibitorji HIV integraze
CA2847871C (en) * 2005-12-30 2016-07-26 Gilead Sciences, Inc. Methods for improving the pharmacokinetics of hiv integrase inhibitors
AU2007223260C1 (en) 2006-03-06 2011-02-03 Japan Tobacco Inc. Method for producing 4-oxoquinoline compound
WO2007102499A1 (ja) * 2006-03-06 2007-09-13 Japan Tobacco Inc. 4-オキソキノリン化合物の製造方法
HRP20090213B1 (hr) 2006-09-12 2016-12-02 Gilead Sciences, Inc. Postupak i međuprodukti u pripravi inhibitora integraze
JP5547066B2 (ja) * 2007-06-29 2014-07-09 ギリアード サイエンシーズ, インコーポレイテッド 治療用組成物およびその使用
JP5547067B2 (ja) * 2007-06-29 2014-07-09 ギリアード サイエンシーズ, インコーポレイテッド 治療組成物およびその使用
AR068403A1 (es) * 2007-09-11 2009-11-18 Gilead Sciences Inc Proceso e intermediarios para la preparacion de inhibidores de integrasa
WO2011004389A2 (en) 2009-06-18 2011-01-13 Matrix Laboratories Ltd An improved process for the preparation of elvitegravir
CN102212032B (zh) * 2011-04-20 2013-07-31 复旦大学 一种5-羟基喹诺酮类衍生物及其制备方法和用途
US9089574B2 (en) 2011-11-30 2015-07-28 Emory University Antiviral JAK inhibitors useful in treating or preventing retroviral and other viral infections
AU2013296289B2 (en) * 2012-08-03 2017-10-05 Gilead Sciences, Inc. Process and intermediates for preparing integrase inhibitors
CZ304984B6 (cs) * 2012-10-12 2015-03-11 Zentiva, K.S. Zlepšený způsob výroby a nové intermediáty syntézy elvitegraviru
CZ304983B6 (cs) * 2012-10-12 2015-03-11 Zentiva, K.S. Způsob výroby a nové intermediáty syntézy elvitegraviru
AU2013361401C1 (en) 2012-12-21 2018-08-09 Gilead Sciences, Inc. Polycyclic-carbamoylpyridone compounds and their pharmaceutical use
NO2865735T3 (cg-RX-API-DMAC7.html) 2013-07-12 2018-07-21
EP3019503B1 (en) 2013-07-12 2017-09-06 Gilead Sciences, Inc. Polycyclic-carbamoylpyridone compounds and their use for the treatment of hiv infections
NO2717902T3 (cg-RX-API-DMAC7.html) 2014-06-20 2018-06-23
TW201613936A (en) 2014-06-20 2016-04-16 Gilead Sciences Inc Crystalline forms of(2R,5S,13aR)-8-hydroxy-7,9-dioxo-n-(2,4,6-trifluorobenzyl)-2,3,4,5,7,9,13,13a-octahydro-2,5-methanopyrido[1',2':4,5]pyrazino[2,1-b][1,3]oxazepine-10-carboxamide
TWI744723B (zh) 2014-06-20 2021-11-01 美商基利科學股份有限公司 多環型胺甲醯基吡啶酮化合物之合成
TWI695003B (zh) 2014-12-23 2020-06-01 美商基利科學股份有限公司 多環胺甲醯基吡啶酮化合物及其醫藥用途
PT3466490T (pt) 2015-04-02 2020-12-24 Gilead Sciences Inc Compostos de carbamoilpiridona policíclicos e sua utilização farmacêutica
CN111733133B (zh) * 2020-07-22 2020-12-01 华夏源(上海)生命科技有限公司 一种促进表皮干细胞分化和生长的方法
CN111944761B (zh) * 2020-08-23 2021-03-26 泉州伟业生物医学科技有限公司 促进表皮干细胞分化和生长的方法

Family Cites Families (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US1564210A (en) * 1925-12-08 Obin d
DE3501247A1 (de) * 1985-01-16 1986-07-17 Bayer Ag, 5090 Leverkusen Aminoacrylsaeure-derivate
IL155677A0 (en) * 2000-12-14 2003-11-23 Procter & Gamble Cyclization process step in the making of quinolones and naphthyridines
TW200300349A (en) 2001-11-19 2003-06-01 Sankyo Co A 4-oxoqinoline derivative
US20050104233A1 (en) * 2002-05-31 2005-05-19 Shinji Kato Method of substituent introduction through halogen-metal exchange reaction
US6803469B2 (en) * 2002-08-05 2004-10-12 The Procter & Gamble Company Process for preparing quinolone antibiotic intermediates
TW200409759A (en) 2002-09-25 2004-06-16 Wyeth Corp Substituted 4-(indazol-3-yl)phenols
SI1564210T1 (sl) * 2002-11-20 2010-01-29 Japan Tobacco Inc 4-oksokinolinske spojine in njihova uporaba kot inhibitorji HIV integraze
EP1582523A1 (en) 2004-04-02 2005-10-05 Ludwig-Maximilians-Universität München Method of preparing organomagnesium compounds
EP1582524B1 (en) 2004-04-02 2008-08-13 Ludwig Maximilians Universität Method of preparing organomagnesium compounds
MY134672A (en) * 2004-05-20 2007-12-31 Japan Tobacco Inc Stable crystal of 4-oxoquinoline compound
US7531554B2 (en) 2004-05-20 2009-05-12 Japan Tobacco Inc. 4-oxoquinoline compound and use thereof as HIV integrase inhibitor
US8633219B2 (en) 2004-05-21 2014-01-21 Japan Tobacco Inc. Combination therapy
WO2007063869A1 (ja) 2005-11-30 2007-06-07 Japan Tobacco Inc. 高純度キノロン化合物の製造方法
US20090233964A1 (en) * 2005-12-30 2009-09-17 Gilead Sciences, Inc. Methods for improving the pharmacokinetics of hiv integrase inhibitors
AU2007223260C1 (en) 2006-03-06 2011-02-03 Japan Tobacco Inc. Method for producing 4-oxoquinoline compound
WO2007102499A1 (ja) 2006-03-06 2007-09-13 Japan Tobacco Inc. 4-オキソキノリン化合物の製造方法
TW200811153A (en) * 2006-06-23 2008-03-01 Japan Tobacco Inc 6-(heterocyclyl-substituted benzyl)-4-oxoquinoline compound and use thereof as HIV integrase inhibitor
HRP20090213B1 (hr) * 2006-09-12 2016-12-02 Gilead Sciences, Inc. Postupak i međuprodukti u pripravi inhibitora integraze
JP5547066B2 (ja) * 2007-06-29 2014-07-09 ギリアード サイエンシーズ, インコーポレイテッド 治療用組成物およびその使用
JP5547067B2 (ja) * 2007-06-29 2014-07-09 ギリアード サイエンシーズ, インコーポレイテッド 治療組成物およびその使用
AR068403A1 (es) * 2007-09-11 2009-11-18 Gilead Sciences Inc Proceso e intermediarios para la preparacion de inhibidores de integrasa

Also Published As

Publication number Publication date
AP2785A (en) 2013-10-31
CA2698245A1 (en) 2009-03-19
UA101956C2 (uk) 2013-05-27
US20120238758A1 (en) 2012-09-20
TW200927716A (en) 2009-07-01
AU2008298943A1 (en) 2009-03-19
EP2190804A1 (en) 2010-06-02
US8440831B2 (en) 2013-05-14
US20090099366A1 (en) 2009-04-16
CN101821223A (zh) 2010-09-01
KR101488550B1 (ko) 2015-02-02
NZ583647A (en) 2012-07-27
US20100292480A1 (en) 2010-11-18
US20130253200A1 (en) 2013-09-26
KR20100069675A (ko) 2010-06-24
AP2010005187A0 (en) 2010-04-30
TWI419867B (zh) 2013-12-21
JP2010539101A (ja) 2010-12-16
JP2013129659A (ja) 2013-07-04
JP5202635B2 (ja) 2013-06-05
US8153801B2 (en) 2012-04-10
PT2190804E (pt) 2016-03-15
AR068403A1 (es) 2009-11-18
AU2008298943B2 (en) 2013-10-10
EA019431B1 (ru) 2014-03-31
EP2190804B1 (en) 2015-11-18
MX2010002783A (es) 2010-03-31
CN101821223B (zh) 2014-07-09
EA201070256A1 (ru) 2010-12-30
HK1141785A1 (zh) 2010-11-19
CA2698245C (en) 2015-06-16
US8759525B2 (en) 2014-06-24
ZA201002066B (en) 2010-12-29
BRPI0816694A2 (pt) 2015-03-17
WO2009036161A1 (en) 2009-03-19
ES2562080T3 (es) 2016-03-02

Similar Documents

Publication Publication Date Title
CO6270255A2 (es) Proceso e intermediarios para preparar inhibidores de integrasas
CR20110013A (es) Derivados de Heteroarilo como Inhibidores de DGAT1
JO2892B1 (en) CYP inhibitors 17
AR092278A1 (es) Proceso de obtencion de derivados n-acilicos de bifenil-alanina e intermediarios relacionados
AR106141A1 (es) Métodos e intermediarios para la preparación de derivados de ácidos biliares
AR102362A1 (es) Compuestos de metil-piperidina útiles para inhibir la sintasa-1 de prostaglandina microsomal e2
UA114611C2 (uk) Пестицидні композиції і способи, що їх стосуються
ECSP099755A (es) Derivados de pirrolopiridina y su uso como inhibidores de bace
MX347476B (es) Compuestos de ácido dimetil-benzoico.
MX2014010009A (es) Composicion que comprende un compuesto de amina alcoxilada y un compuesto de acido carboxilico, el uso de la misma en emulsiones de agua en aceite y proceso que utiliza la composicion como o como parte de un fluido de perforacion.
AR063710A1 (es) Proceso para la preparacion de acido 6-(3-cloro-2-fluorbencil)-1-[(s)-1-hidroximetil-2-metilpropil]-7-metoxi-4-oxo-1, 4-dihidroquinolon-3-carboxilico como inhibidores de integrasa del hiv e intermediarios de sintesis del mismo y composiciones que lo comprenden.
NI200900164A (es) COMPUESTOS AMINO- 5 -[ -4- (DIFLUOROMETOXI) FENIL SUSTITUIDO] -5- FENILIMIDAZOLONA COMO INHIBIDORES DE Beta - SECRETASA.
EA201890752A1 (ru) Способ получения противогрибковых соединений
ES2531190T3 (es) Método para producir un compuesto de 4-oxoquinolina
CO6680645A2 (es) Inhibidores de oxadiazol de la producción de leucotrieno
MX2013012982A (es) Metodo para promover el crecimiento de plantas.
AR085052A1 (es) Metodos para producir un compuesto profarmaco inhibidor de la union al vih e intermediarios
PE20141382A1 (es) Inhibidor de la fosfoinositida-3-quinasa con un grupo de union a zinc
MX2013012978A (es) Metodo para promover el crecimiento de plantas.
MX2017008045A (es) Composiciones de polímero parcialmente fluorado curables.
MX2016010973A (es) Compuestos de aminocarbonilcarbamato.
ES2422733T3 (es) Pirimidilciclopentanos hidroxilados como inhibidores de proteínas cinasas AKT
MX384710B (es) Proceso para preparar 3-metilciclopentadecan-1,5-diona.
EA201270237A1 (ru) Способ получения 1-бензил-3-гидроксиметил-1н-индазола и его производных и необходимые промежуточные соединения, содержащие магний
AR075262A1 (es) Compuestos de 1,6-dihidro-2h-3-oxa-6-aza-as-indaceno, proceso para prepararlos, composicion farmaceutica que los comprende, sus usos como medicamentos, o en tratamientos o prevenciones de condiciones asociadas con un funcionamiento alterado de los sistemas regulados por la melatonina, sus usos para

Legal Events

Date Code Title Description
FG Application granted