ES2622480T3 - Formas cristalinas del compuesto 4-(6-cloro-2,3-metilenodioxianilino)-7-[2-(4-metilpiperazin-1-il)etoxi]-5-tetrahidropiran-4-iloxiquinazolina - Google Patents

Formas cristalinas del compuesto 4-(6-cloro-2,3-metilenodioxianilino)-7-[2-(4-metilpiperazin-1-il)etoxi]-5-tetrahidropiran-4-iloxiquinazolina Download PDF

Info

Publication number
ES2622480T3
ES2622480T3 ES05818127.2T ES05818127T ES2622480T3 ES 2622480 T3 ES2622480 T3 ES 2622480T3 ES 05818127 T ES05818127 T ES 05818127T ES 2622480 T3 ES2622480 T3 ES 2622480T3
Authority
ES
Spain
Prior art keywords
compound
azd0530
approximately
crystalline
yloxyquinazoline
Prior art date
Legal status (The legal status 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 status listed.)
Expired - Lifetime
Application number
ES05818127.2T
Other languages
English (en)
Spanish (es)
Inventor
James Gair Ford
James Francis Mccabe
Anne O'kearney-Mcmullan
Philip O'keefe
Simon Mark Pointon
Lyn Powell
Mark Purdie
Jane Withnall
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AstraZeneca AB
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
Application filed by AstraZeneca AB filed Critical AstraZeneca AB
Application granted granted Critical
Publication of ES2622480T3 publication Critical patent/ES2622480T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/14Heterocyclic 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 three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic 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
    • C07D405/02Heterocyclic 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
    • C07D405/12Heterocyclic 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • 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
    • A61P35/00Antineoplastic agents
    • A61P35/04Antineoplastic agents specific for metastasis

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
ES05818127.2T 2004-12-17 2005-12-14 Formas cristalinas del compuesto 4-(6-cloro-2,3-metilenodioxianilino)-7-[2-(4-metilpiperazin-1-il)etoxi]-5-tetrahidropiran-4-iloxiquinazolina Expired - Lifetime ES2622480T3 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB0427697.8A GB0427697D0 (en) 2004-12-17 2004-12-17 Chemical process
GB0427697 2004-12-17
PCT/GB2005/004807 WO2006064217A2 (en) 2004-12-17 2005-12-14 PROCESS FOR THE PREPARATION OF 4-(6-CHLORO-2, 3-METHYLENEDIOXYANILINO)-7-[2-(4-METHYLPIPERAZIN-l-YL) ETHOXY]-5-TETRAHYDROPYRAN-4-YLOXYQUINAZOLINE , THEIR INTERMEDIATES AND CRYSTALLINE SALTS THEREOF

Publications (1)

Publication Number Publication Date
ES2622480T3 true ES2622480T3 (es) 2017-07-06

Family

ID=34090249

Family Applications (1)

Application Number Title Priority Date Filing Date
ES05818127.2T Expired - Lifetime ES2622480T3 (es) 2004-12-17 2005-12-14 Formas cristalinas del compuesto 4-(6-cloro-2,3-metilenodioxianilino)-7-[2-(4-metilpiperazin-1-il)etoxi]-5-tetrahidropiran-4-iloxiquinazolina

Country Status (16)

Country Link
US (1) US8304417B2 (https=)
EP (1) EP1871769B1 (https=)
JP (2) JP5161584B2 (https=)
KR (6) KR20080094847A (https=)
CN (1) CN101115744B (https=)
AU (2) AU2005315458B2 (https=)
BR (1) BRPI0519085A2 (https=)
CA (2) CA2590735C (https=)
ES (1) ES2622480T3 (https=)
GB (1) GB0427697D0 (https=)
IL (1) IL183525A0 (https=)
MX (1) MX2007007210A (https=)
NO (1) NO20072755L (https=)
NZ (1) NZ555468A (https=)
WO (1) WO2006064217A2 (https=)
ZA (1) ZA200704532B (https=)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB0412074D0 (en) * 2004-05-29 2004-06-30 Astrazeneca Ab Combination product
WO2009068906A2 (en) * 2007-11-26 2009-06-04 Astrazeneca Ab Combinations comprising zd4054 and a src family kinase inhibitor 172
CN103275072B (zh) * 2013-05-22 2016-01-20 苏州明锐医药科技有限公司 塞卡替尼的制备方法
US11241434B2 (en) 2013-06-13 2022-02-08 Yale Uninversity Compositions and methods for improving cognition in a subject
US10660957B2 (en) * 2013-06-13 2020-05-26 Yale University Compositions and methods for treating an Aβ-modulated disease or disorder or improving cognition in a subject
US10369152B2 (en) 2015-02-13 2019-08-06 The Brigham And Women's Hospital, Inc. Methods and compositions for the treatment or prevention of abnormal bone formation in a soft tissue
PT3930715T (pt) 2019-02-27 2024-08-02 Astrazeneca Ab Saracatinib para uso no tratamento de fibrose pulmonar idiopática
CN116332789A (zh) * 2023-03-10 2023-06-27 上海康鹏科技股份有限公司 一种4-氨基-2-氟苯甲酰胺的制备方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA73993C2 (uk) * 2000-06-06 2005-10-17 Астразенека Аб Хіназолінові похідні для лікування пухлин та фармацевтична композиція
CA2419301C (en) 2000-08-21 2009-12-08 Astrazeneca Ab Quinazoline derivatives
DE60229046D1 (de) 2001-04-19 2008-11-06 Astrazeneca Ab Chinazolin derivate
RU2350618C2 (ru) 2002-11-04 2009-03-27 Астразенека Аб ПРОИЗВОДНЫЕ ХИНАЗОЛИНА В КАЧЕСТВЕ ИНГИБИТОРОВ Src ТИРОЗИНКИНАЗЫ
GB0226434D0 (en) 2002-11-13 2002-12-18 Astrazeneca Ab Combination product
GB0307333D0 (en) 2003-03-29 2003-05-07 Astrazeneca Ab Therapeutic agent
GB0309850D0 (en) 2003-04-30 2003-06-04 Astrazeneca Ab Quinazoline derivatives
GB0310401D0 (en) * 2003-05-07 2003-06-11 Astrazeneca Ab Therapeutic agent

Also Published As

Publication number Publication date
ZA200704532B (en) 2008-07-30
CN101115744A (zh) 2008-01-30
KR20080094847A (ko) 2008-10-24
US8304417B2 (en) 2012-11-06
EP1871769A2 (en) 2008-01-02
KR20080094846A (ko) 2008-10-24
KR20110114727A (ko) 2011-10-19
US20090099196A1 (en) 2009-04-16
CA2675642A1 (en) 2006-06-22
EP1871769B1 (en) 2017-02-22
JP5161584B2 (ja) 2013-03-13
KR20080094849A (ko) 2008-10-24
AU2005315458B2 (en) 2009-03-12
AU2005315458A1 (en) 2006-06-22
CA2590735C (en) 2009-11-10
BRPI0519085A2 (pt) 2008-12-23
NZ555468A (en) 2010-12-24
WO2006064217A3 (en) 2006-12-21
WO2006064217A2 (en) 2006-06-22
WO2006064217A8 (en) 2007-07-05
MX2007007210A (es) 2007-11-07
IL183525A0 (en) 2007-09-20
AU2009200622A1 (en) 2009-03-12
KR20070090004A (ko) 2007-09-04
JP2008524183A (ja) 2008-07-10
CA2590735A1 (en) 2006-06-22
CN101115744B (zh) 2012-02-01
JP2009143920A (ja) 2009-07-02
NO20072755L (no) 2007-07-02
KR20080094848A (ko) 2008-10-24
GB0427697D0 (en) 2005-01-19

Similar Documents

Publication Publication Date Title
ES2639052T3 (es) Forma polimórfica de hidrocloruro de pridopidina
JP4159988B2 (ja) N−[2−(ジエチルアミノ)エチル]−5−[(5−フルオロ−1,2−ジヒドロ−2−オキソ−3h−インドール−3−イリデン)メチル]−2,4−ジメチル−1h−ピロール−3−カルボキシアミドのリンゴ酸塩を含む結晶、その製法およびその組成物
ES2483801T3 (es) Forma cristalina de compuesto de pirmido[6,1-a]isoquinolin-4-ona
ES2637829T3 (es) Cristales multicomponentes que comprenden dasatinib y agentes de formación de cocristales seleccionados
ES2982834T3 (es) Sal hidrobromuro cristalina de 5-MeO-DMT
BR112017007953B1 (pt) Forma cristalina ii do bissulfato inibidor de jak quinase, seu uso e seu método de preparação, e composição farmacêutica
CA2963581C (en) Crystal form of bisulfate of jak inhibitor and preparation method therefor
ES2622480T3 (es) Formas cristalinas del compuesto 4-(6-cloro-2,3-metilenodioxianilino)-7-[2-(4-metilpiperazin-1-il)etoxi]-5-tetrahidropiran-4-iloxiquinazolina
US12448366B2 (en) Solid forms of pralsetinib
BRPI0509595B1 (pt) Processos para a preparação de cristais de forma a e de material de padrão c de bissulfato de atazanavir
ES2597652T3 (es) Síntesis optimizada de ácidos biliares puros, cristalinos, no polimórficos, con tamaño de partícula definido
CZ2016276A3 (cs) Pevné formy volné báze ibrutinibu
ES2716633T3 (es) Formas cristalinas de fosfato de cabozantinib e hidrocloruro de cabozantinib
ES2605786T3 (es) Formas sólidas de clorhidrato de (1R,4R)-6'-fluor-N,N-dimetil-4-fenil-4',9'-dihidro-3'H-espiro[ciclohexano-1,1'-pirano[3,4b]indol]-4-amina
ES2536276T3 (es) Sal maleato de 11-(2-pirrolidin-1-il-etoxi)-14,19-dioxa-5,7,26-triaza-tetraciclo[19.3.1.1(2,6).1(8,12)]heptacosa-1(25),2(26),3,5,8,10,12(27),16,21,23-deceno
KR20240054327A (ko) Bcl-2 저해제의 고체 형태, 제조 방법 및 이의 용도
ES2815924T3 (es) Forma D1 cristalina altamente estable de la sal de monoetanolamina de eltrombopag
ES2716420T3 (es) Clorhidrato de eliglustat cristalino
CZ201769A3 (cs) Pevné formy venetoclaxu
EP3212193B1 (en) Crystalline forms of pemetrexed diacid and manufacturing processes therefor
ES2645567T3 (es) Modificaciones cristalinas de N-alfa-(2,4,6-triisopropilfenilsulfonil)-3-hidroxiamidino-(L)-fenilalanin-4-etoxicarbonil-piperazida y/o sales de la misma
ES2671126T3 (es) Formas sólidas estables de enclomifeno y citrato de enclomifeno
ES2222332T3 (es) Seudopolimorfo de hidrocloruro de (-)-cis-2-(2-clorofenil)-5,7-dihidroxi-8(4r-(3s-hidroxi-1-metil)piperidinil)-4h-1-benzopiran-4-ona.
US20260109685A1 (en) Solid forms of pralsetinib
BG106139A (bg) Полиморфи на кристален (2-бензхидрил-1-азабицикло/2.2.2/окт-3-ил)-(5-изопропил-2-метоксибензил)-амин цитрат като nk-1-рецепторни антагонисти