SG165416A1 - Chemical process - Google Patents

Chemical process

Info

Publication number
SG165416A1
SG165416A1 SG201006940-9A SG2010069409A SG165416A1 SG 165416 A1 SG165416 A1 SG 165416A1 SG 2010069409 A SG2010069409 A SG 2010069409A SG 165416 A1 SG165416 A1 SG 165416A1
Authority
SG
Singapore
Prior art keywords
manufacture
processes
relates
quinazoline derivatives
quinazoline
Prior art date
Application number
SG201006940-9A
Other languages
English (en)
Inventor
Joergen Blixt
Michael David Golden
Philip John Hogan
David Michael Glanville Martin
Francis Joseph Montgomery
Zakariya Patel
John David Pittam
George Joseph Sependa
Christopher John Squire
Nicholas Cartwright Alexander Wright
Original Assignee
Astrazeneca Ab
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=35395001&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=SG165416(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of SG165416A1 publication Critical patent/SG165416A1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/12Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/08Drugs for skeletal disorders for bone diseases, e.g. rachitism, Paget's disease
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P27/00Drugs for disorders of the senses
    • A61P27/02Ophthalmic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00Drugs for disorders of the cardiovascular system
    • A61P9/10Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/06Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members
    • C07D211/08Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms
    • C07D211/10Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms
    • C07D211/16Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having no double bonds between ring members or between ring members and non-ring members with hydrocarbon or substituted hydrocarbon radicals directly attached to ring carbon atoms with radicals containing only carbon and hydrogen atoms attached to ring carbon atoms with acylated ring nitrogen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/86Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • C07D239/94Nitrogen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Rheumatology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Cardiology (AREA)
  • Ophthalmology & Optometry (AREA)
  • Pain & Pain Management (AREA)
  • Vascular Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Dermatology (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
SG201006940-9A 2005-09-30 2006-09-27 Chemical process SG165416A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB0519879.1A GB0519879D0 (en) 2005-09-30 2005-09-30 Chemical process

Publications (1)

Publication Number Publication Date
SG165416A1 true SG165416A1 (en) 2010-10-28

Family

ID=35395001

Family Applications (1)

Application Number Title Priority Date Filing Date
SG201006940-9A SG165416A1 (en) 2005-09-30 2006-09-27 Chemical process

Country Status (31)

Country Link
US (8) US8163926B2 (de)
EP (2) EP1943240B1 (de)
JP (2) JP5213715B2 (de)
KR (1) KR101307641B1 (de)
CN (3) CN102503933B (de)
AR (1) AR055671A1 (de)
AT (2) ATE481399T1 (de)
AU (1) AU2006296367B2 (de)
BR (1) BRPI0616715A2 (de)
CA (2) CA2745829C (de)
CY (2) CY1110275T1 (de)
DE (2) DE602006010428D1 (de)
DK (2) DK2053048T3 (de)
ES (2) ES2335435T3 (de)
GB (1) GB0519879D0 (de)
HR (2) HRP20100019T1 (de)
IL (2) IL190172A (de)
ME (2) ME01466B (de)
MY (2) MY145540A (de)
NO (1) NO342152B1 (de)
NZ (2) NZ566566A (de)
PL (2) PL2053048T3 (de)
PT (2) PT1943240E (de)
RS (2) RS51263B (de)
RU (1) RU2448102C2 (de)
SG (1) SG165416A1 (de)
SI (2) SI1943240T1 (de)
TW (2) TWI424991B (de)
UY (1) UY29824A1 (de)
WO (1) WO2007036713A2 (de)
ZA (1) ZA200802416B (de)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
SI1474420T1 (sl) * 2002-02-01 2012-06-29 Astrazeneca Ab Spojine kinazolina
GB0519879D0 (en) * 2005-09-30 2005-11-09 Astrazeneca Ab Chemical process
CL2007003158A1 (es) * 2006-11-02 2008-05-16 Astrazeneca Ab Procedimiento de preparacion de compuestos derivados de quinazolina o sus sales farmaceuticamente aceptables; compuestos intermediarios; procedimiento de preparacion.
EP2404595B1 (de) * 2011-09-01 2015-08-05 Symrise AG Verfahren zur Herstellung von Indanon-Derivaten
BR112015003101B1 (pt) * 2012-08-15 2022-06-14 Glaxo Group Limited Processo para a preparação de um composto
CN104098544A (zh) * 2013-04-07 2014-10-15 浙江九洲药物科技有限公司 一种凡德他尼的制备方法
CN106397401B (zh) * 2016-08-30 2018-11-13 山东罗欣药业集团股份有限公司 一种抗癌药物的晶体化合物及其制备方法

Family Cites Families (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4870083A (en) 1987-11-24 1989-09-26 Merrell Dow Pharmaceuticals Inc. 1,4-Disubstituted-piperidinyl compounds useful as analgesics and muscle relaxants
JP2829744B2 (ja) 1989-05-31 1998-12-02 川研ファインケミカル株式会社 ピペリジンカルボン酸類の製造方法
AU8506791A (en) 1990-10-01 1992-04-28 Janssen Pharmaceutica N.V. Novel 4-piperidinylcarbonyl derivatives
HU225047B1 (en) 1991-03-28 2006-05-29 Eisai Co Ltd Heterocyclic-piperidin-derivatives, pharmaceutical compositions containing them and process for their production
US5710158A (en) 1991-05-10 1998-01-20 Rhone-Poulenc Rorer Pharmaceuticals Inc. Aryl and heteroaryl quinazoline compounds which inhibit EGF and/or PDGF receptor tyrosine kinase
SG64322A1 (en) 1991-05-10 1999-04-27 Rhone Poulenc Rorer Int Bis mono and bicyclic aryl and heteroaryl compounds which inhibit egf and/or pdgf receptor tyrosine kinase
US5624926A (en) 1993-02-18 1997-04-29 Kyowa Hakko Kogyo Co., Ltd. Piperidinyl-dioxoquinazolines as adenosine reuptake inhibitors
AU680004B2 (en) * 1993-05-26 1997-07-17 Syntex (U.S.A.) Inc. Novel 1-phenylalkanone 5-HT4 receptor ligands
DE4326344A1 (de) 1993-08-05 1995-02-09 Thomae Gmbh Dr K Carbonamide, diese Verbindungen enthaltende Arzneimittel und Verfahren zu ihrer Herstellung
ES2120170T3 (es) * 1994-01-13 1998-10-16 Merck Sharp & Dohme Antagonistas azaciclicos gem-disustituidos de taquiquininas.
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
NZ331191A (en) 1996-03-05 2000-03-27 Zeneca Ltd 4-anilinoquinazoline derivatives and pharmaceutical compositions thereof
EP0954315A2 (de) 1996-09-13 1999-11-10 Sugen, Inc. Verwendung von quinazolinderivate zur herstellung eines arzneimittels zur behandlung hyperproliferativer hautkrankheiten
GB9718972D0 (en) * 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
KR100881105B1 (ko) * 1999-11-05 2009-02-02 아스트라제네카 아베 Vegf 억제제로서의 퀴나졸린 유도체
GB0126879D0 (en) 2001-11-08 2002-01-02 Astrazeneca Ab Combination therapy
EA012926B1 (ru) 2001-12-20 2010-02-26 Оси Фармасьютикалз, Инк. Пирролопиримидиновые соединения, относящиеся к a-селективным антагонистам, их синтез и применение
SI1474420T1 (sl) 2002-02-01 2012-06-29 Astrazeneca Ab Spojine kinazolina
WO2003066602A1 (en) 2002-02-06 2003-08-14 Ube Industries, Ltd. Process for producing 4-aminoquinazoline compound
GB0218526D0 (en) 2002-08-09 2002-09-18 Astrazeneca Ab Combination therapy
AU2003249000B2 (en) 2002-08-09 2007-04-05 Astrazeneca Ab Combination of ZD6474, an inhibitor of the vasuclar endothelial growth factor receptor, with radiotherapy in the treatment of cancer
GB0223380D0 (en) 2002-10-09 2002-11-13 Astrazeneca Ab Combination therapy
KR20050100683A (ko) 2003-02-13 2005-10-19 아스트라제네카 아베 5-fu 또는/및 cpt-11과 zd6474의 병용 요법
EP1648465B1 (de) 2003-07-10 2010-08-25 AstraZeneca AB Verwendung des chinazolin-derivats zd6474 in kombination mit platinverbindungen und optional ionisierender strahlung bei der behandlung von erkrankungen im zusammenhang mit angiogenese und/oder erhöhter gefässpermeabilität
GB0318423D0 (en) 2003-08-06 2003-09-10 Astrazeneca Ab Chemical compounds
GB0519879D0 (en) * 2005-09-30 2005-11-09 Astrazeneca Ab Chemical process

Also Published As

Publication number Publication date
ATE481399T1 (de) 2010-10-15
ATE448218T1 (de) 2009-11-15
US20160185754A1 (en) 2016-06-30
US20180118716A1 (en) 2018-05-03
US20220033377A1 (en) 2022-02-03
DK1943240T3 (da) 2010-03-01
US20190263782A1 (en) 2019-08-29
CN101277948B (zh) 2013-03-13
CN102503933B (zh) 2014-06-25
AU2006296367B2 (en) 2011-08-11
KR101307641B1 (ko) 2013-09-12
TWI424991B (zh) 2014-02-01
JP2013063998A (ja) 2013-04-11
TW200745036A (en) 2007-12-16
MY145540A (en) 2012-02-29
NZ566566A (en) 2011-08-26
IL190172A0 (en) 2008-08-07
CA2624045C (en) 2012-05-22
BRPI0616715A2 (pt) 2011-06-28
US20140378684A1 (en) 2014-12-25
RU2008116573A (ru) 2009-11-10
NZ593930A (en) 2013-02-22
PT2053048E (pt) 2010-11-10
NO20081267L (no) 2008-04-30
SI1943240T1 (sl) 2010-02-26
EP2053048A1 (de) 2009-04-29
CA2745829C (en) 2013-07-02
CY1110887T1 (el) 2015-06-10
CN102503898A (zh) 2012-06-20
JP5213715B2 (ja) 2013-06-19
IL227574A (en) 2015-08-31
GB0519879D0 (en) 2005-11-09
DE602006010428D1 (de) 2009-12-24
JP2009510039A (ja) 2009-03-12
SI2053048T1 (sl) 2010-12-31
US8163926B2 (en) 2012-04-24
HK1130478A1 (en) 2009-12-31
PL1943240T3 (pl) 2010-04-30
US20090203905A1 (en) 2009-08-13
ES2350513T3 (es) 2011-01-24
AU2006296367A1 (en) 2007-04-05
WO2007036713A3 (en) 2007-06-14
AR055671A1 (es) 2007-08-29
ME01466B (me) 2014-04-20
US8865899B2 (en) 2014-10-21
ES2335435T3 (es) 2010-03-26
JP5654546B2 (ja) 2015-01-14
IL190172A (en) 2014-05-28
CY1110275T1 (el) 2015-01-14
CN102503898B (zh) 2015-03-25
HRP20100620T1 (hr) 2010-12-31
RS51515B (sr) 2011-06-30
CN101277948A (zh) 2008-10-01
EP2053048B1 (de) 2010-09-15
HK1122553A1 (en) 2009-05-22
US10344015B2 (en) 2019-07-09
RU2448102C2 (ru) 2012-04-20
PT1943240E (pt) 2010-01-11
CN102503933A (zh) 2012-06-20
HRP20100019T1 (hr) 2010-02-28
PL2053048T3 (pl) 2011-03-31
DE602006017004D1 (de) 2010-10-28
UY29824A1 (es) 2007-04-30
RS51263B (sr) 2010-12-31
US9815816B2 (en) 2017-11-14
NO342152B1 (no) 2018-04-03
TW201018660A (en) 2010-05-16
CA2745829A1 (en) 2007-04-05
ZA200802416B (en) 2009-01-28
DK2053048T3 (da) 2010-11-29
KR20080049114A (ko) 2008-06-03
EP1943240A2 (de) 2008-07-16
EP1943240B1 (de) 2009-11-11
CA2624045A1 (en) 2007-04-05
US20240150317A1 (en) 2024-05-09
ME01531B (me) 2014-04-20
WO2007036713A2 (en) 2007-04-05
US20120095229A1 (en) 2012-04-19
MY149834A (en) 2013-10-31
TWI328580B (en) 2010-08-11
EP2053048B8 (de) 2011-09-21

Similar Documents

Publication Publication Date Title
TW200833667A (en) Chemical process
ATE447559T1 (de) 4-(phenylamino)-6-oxo-1,6-dihydropyridazine-3- carboxamid derivate als mek inhibitoren zur behandlung von hyperproliferativen erkrankungen
MY159522A (en) Administration of dipeptidyl peptidase inhibitors
UA95199C2 (en) Aqueous formulation of 3-(6-(1-(2,2-difluorobenzo[d][1,3]dioxol-5-yl) cyclopropanecarboxamido)-3-methylpyridin-2-yl)benzoic acid
NO20070453L (no) Kondenserte heterocykliske kinase inhibitorer
EP1954287A4 (de) Cetp-inhibitoren
CL2010000204A1 (es) Compuestos intermediarios derivados de 4 amino-3-metoxibenzamida; compuesto intermediario n-{4-[4-(ciclopropilmetil)piperazin-1-il]ciclohexil}acetamida; compuesto intermediario 2-cloro-7-etil-7,8-dihidro-5-metil-8-(1-metiletil)-6(5h)-pteridinona, útiles en la preparación de dihidropteridinonas sustituidas (divisional sol. 2077-05).
TW200800968A (en) Sulfoximine-substituted pyrimidines, processes for production thereof and use thereof as drugs
ATE457311T1 (de) Als inhibitoren von proteinkinasen geeignete aminopyridine und aminopyrimidine
ATE497961T1 (de) Als proteinkinaseinhibitoren geeignete verbindungen
CL2011002925A1 (es) Compuestos derivados de isoquinolin-1(2h)-ona, inhibidores selectivos de la actividad de poli (adp-ribosa) polimerasa parp-1; proceso para prepararlos; composicion farmaceutica; y su uso para tratar una enfermedad mediada por la proteina parp-1.
NZ579928A (en) Fluorinated derivatives of deferiprone
CY1116831T1 (el) ΧΡΗΣΗ 24-norUDCA
TW200640913A (en) 5-Substituted quinoline and isoquinoline derivatives, a process for their production and their use as anti-inflammatory agents
CY1110275T1 (el) Χημικη διαδικασια
ATE528309T1 (de) Als proteinkinaseinhibitoren geeignete verbindungen
EA201001773A1 (ru) Фумаратная соль 4-(3-хлор-2-фторанилино)-7-метокси-6-{[1-(n-метилкарбамоилметил)пиперидин-4-ил]окси}хиназолина
MX343273B (es) Intermediarios clave para la sintesis de rosuvastatina o de sales farmaceuticamente aceptables de la misma.
ATE425961T1 (de) Salze substituierter allophansaureester und deren verwendung in arzneimitteln
DE602006019830D1 (de) Tetrahydro- und dihydrochinazolinone
WO2010068920A3 (en) Diaminoquinazoline inhibitors of dihydrofolate reductase
NO20081266L (no) 4- (4-Brom-2-Fluoranilino) -6-Metoksy-7- (1-Metylpiperidin-4 -Ylmetoksy) kinazolinmonohydrate
TW200637803A (en) Processes for the preparation of aminoethoxybenzyl alcohols
TW200640868A (en) 5-Substituted quinoline and isoquinoline derivatives, a process for their production and their use as anti-inflammatory agents
UA91717C2 (en) Administration of 2-[[6-[(3r)-3-amino-l-piperidinyl]-3,4-dihydro-3-methyl-2,4-dioxo- l(2h)-pyrimaidinyl]methyl]-benzonitrile for the treatment of conditions mediated with dipeptidyl peptidase inhibitors