AR082875A1 - (s)-(4-fluorofenil)(4-((5-metil-1h-pirazol-3-il)amino)quinazolin-2-il)metanol opticamente activo, composiciones farmaceuticas que lo contienen, metodo para prepararlo y uso del mismo como agentes anticancer o antiinflamatorio - Google Patents

(s)-(4-fluorofenil)(4-((5-metil-1h-pirazol-3-il)amino)quinazolin-2-il)metanol opticamente activo, composiciones farmaceuticas que lo contienen, metodo para prepararlo y uso del mismo como agentes anticancer o antiinflamatorio

Info

Publication number
AR082875A1
AR082875A1 ARP110103206A ARP110103206A AR082875A1 AR 082875 A1 AR082875 A1 AR 082875A1 AR P110103206 A ARP110103206 A AR P110103206A AR P110103206 A ARP110103206 A AR P110103206A AR 082875 A1 AR082875 A1 AR 082875A1
Authority
AR
Argentina
Prior art keywords
quinazolin
amino
methyl
optically active
fluorophenil
Prior art date
Application number
ARP110103206A
Other languages
English (en)
Original Assignee
Ambit Biosciences Corp
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 Ambit Biosciences Corp filed Critical Ambit Biosciences Corp
Publication of AR082875A1 publication Critical patent/AR082875A1/es

Links

Classifications

    • 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
    • A61K31/495—Heterocyclic 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
    • A61K31/505—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/517—Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00—Drugs for disorders of the urinary system
    • A61P13/12—Drugs for disorders of the urinary system of the kidneys
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01D—SEPARATION
    • B01D15/00—Separating processes involving the treatment of liquids with solid sorbents; Apparatus therefor
    • B01D15/08—Selective adsorption, e.g. chromatography
    • B01D15/26—Selective adsorption, e.g. chromatography characterised by the separation mechanism
    • B01D15/38—Selective adsorption, e.g. chromatography characterised by the separation mechanism involving specific interaction not covered by one or more of groups B01D15/265 - B01D15/36
    • B01D15/3833—Chiral chromatography
    • 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
    • C07D403/02—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 two hetero rings
    • C07D403/12—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 two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Analytical Chemistry (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Urology & Nephrology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

Reivindicación 1: Un compuesto caracterizado porque es el (S)-(4-fluorofenil)(4-((5-metil-1H-pirazol-3-il)amino)quinazolin-2-il)metanol ópticamente activo o una variante isotópica de este; o una sal, solvato, hidrato o profármaco de este aceptables desde el punto de vista farmacéutico.
ARP110103206A 2010-09-01 2011-09-01 (s)-(4-fluorofenil)(4-((5-metil-1h-pirazol-3-il)amino)quinazolin-2-il)metanol opticamente activo, composiciones farmaceuticas que lo contienen, metodo para prepararlo y uso del mismo como agentes anticancer o antiinflamatorio AR082875A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US37928010P 2010-09-01 2010-09-01
US37928610P 2010-09-01 2010-09-01

Publications (1)

Publication Number Publication Date
AR082875A1 true AR082875A1 (es) 2013-01-16

Family

ID=45698050

Family Applications (2)

Application Number Title Priority Date Filing Date
ARP110103206A AR082875A1 (es) 2010-09-01 2011-09-01 (s)-(4-fluorofenil)(4-((5-metil-1h-pirazol-3-il)amino)quinazolin-2-il)metanol opticamente activo, composiciones farmaceuticas que lo contienen, metodo para prepararlo y uso del mismo como agentes anticancer o antiinflamatorio
ARP110103205A AR082874A1 (es) 2010-09-01 2011-09-01 Una pirazolilaminoquinazolina opticamente activa, y composiciones farmaceuticas y metodos de uso

Family Applications After (1)

Application Number Title Priority Date Filing Date
ARP110103205A AR082874A1 (es) 2010-09-01 2011-09-01 Una pirazolilaminoquinazolina opticamente activa, y composiciones farmaceuticas y metodos de uso

Country Status (9)

Country Link
US (5) US8912324B2 (es)
EP (2) EP2611796B1 (es)
JP (2) JP5932794B2 (es)
AR (2) AR082875A1 (es)
AU (2) AU2011296074B2 (es)
CA (2) CA2809994A1 (es)
ES (2) ES2579942T3 (es)
TW (2) TW201305143A (es)
WO (2) WO2012030917A1 (es)

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ES2579942T3 (es) * 2010-09-01 2016-08-17 Ambit Biosciences Corporation Pirazolilaminoquinazolina ópticamente activa y composiciones farmacéuticas y métodos de uso de la misma
US9611253B2 (en) 2012-02-29 2017-04-04 Ambit Biosciences Corporation Solid forms comprising optically active pyrazolylaminoquinazoline, compositions thereof, and uses therewith
WO2016024232A1 (en) 2014-08-11 2016-02-18 Acerta Pharma B.V. Therapeutic combinations of a btk inhibitor, a pi3k inhibitor, a jak-2 inhibitor and/or a cdk 4/6 inhibitor
HRP20211813T1 (hr) 2014-08-11 2022-03-04 Acerta Pharma B.V. Terapeutske kombinacije inhibitora btk i inhibitora bcl-2
TW201618775A (zh) 2014-08-11 2016-06-01 艾森塔製藥公司 Ｂｔｋ抑制劑、ｐｉ３ｋ抑制劑、ｊａｋ－２抑制劑、ｐｄ－１抑制劑及／或ｐｄ－ｌ１抑制劑之治療組合物
CN117858709A (zh) * 2022-08-08 2024-04-09 石药集团中奇制药技术（石家庄）有限公司 一种含有三环杂芳基的化合物的用途
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Also Published As

Publication number Publication date
JP2013536854A (ja) 2013-09-26
US8703943B2 (en) 2014-04-22
US20120053193A1 (en) 2012-03-01
EP2611796A1 (en) 2013-07-10
US20140194449A1 (en) 2014-07-10
ES2581840T3 (es) 2016-09-07
WO2012030913A1 (en) 2012-03-08
TW201305143A (zh) 2013-02-01
US9295672B2 (en) 2016-03-29
AU2011296074A1 (en) 2013-03-28
ES2579942T3 (es) 2016-08-17
CA2809993A1 (en) 2012-03-08
AU2011296078B2 (en) 2015-06-18
US20150353528A1 (en) 2015-12-10
CA2809994A1 (en) 2012-03-08
EP2611796B1 (en) 2016-04-20
US20150141443A1 (en) 2015-05-21
EP2611795B1 (en) 2016-05-04
AU2011296074B2 (en) 2015-06-18
US8912324B2 (en) 2014-12-16
AU2011296078A1 (en) 2013-03-28
US20120053194A1 (en) 2012-03-01
JP2013536853A (ja) 2013-09-26
JP5933554B2 (ja) 2016-06-15
TW201302732A (zh) 2013-01-16
US8952020B2 (en) 2015-02-10
EP2611795A1 (en) 2013-07-10
AR082874A1 (es) 2013-01-16
JP5932794B2 (ja) 2016-06-08
WO2012030917A1 (en) 2012-03-08

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