IN2014CN04310A - - Google Patents

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Publication number
IN2014CN04310A
IN2014CN04310A IN4310CHN2014A IN2014CN04310A IN 2014CN04310 A IN2014CN04310 A IN 2014CN04310A IN 4310CHN2014 A IN4310CHN2014 A IN 4310CHN2014A IN 2014CN04310 A IN2014CN04310 A IN 2014CN04310A
Authority
IN
India
Prior art keywords
nrr
compounds
hydrogen
methoxy
alkyl
Prior art date
Application number
Inventor
Dirk Brohm
Melanie Heroult
Marie Pierre Collin
Walter Hübsch
Mario Lobell
Klemens Lustig
Sylvia Grünewald
Ulf Bömer
Verena VÖHRINGER
Original Assignee
Bayer Pharma AG
Bayer Ip Gmbh
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 Bayer Pharma AG, Bayer Ip Gmbh filed Critical Bayer Pharma AG
Publication of IN2014CN04310A publication Critical patent/IN2014CN04310A/en

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic 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
    • C07D487/04Ortho-condensed systems
    • 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
    • A61K31/53Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with three nitrogens as the only ring hetero atoms, e.g. chlorazanil, melamine
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/5355Non-condensed oxazines and containing further heterocyclic rings
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/541Non-condensed thiazines containing further heterocyclic rings
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/02Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
    • C07D409/04Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D409/00Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Treatment Of Liquids With Adsorbents In General (AREA)

Abstract

This invention relates to novel substituted 5 (1 benzothiophen 2 yl) pyrrolo[2 1 f][1 2 4]triazin 4 amine derivatives of formula (I) wherein R is hydrogen chloro methyl or methoxy R is hydrogen or methoxy with the proviso that at least one of R and R is other than hydrogen G represents chloro (C C) alkyl (C C) alkoxycarbonyl 5 membered aza heteroaryl or the group CH OR  CH NRR or C(=0) NRR and G represents chloro cyano (C C) alkyl or the group  CRR OH  CH NRR  C(=0) NRR or CH OR having protein tyrosine kinase inhibitory activities to processes for the preparation of such compounds to pharmaceutical compositions containing such compounds and to the use of such compounds or compositions for treating proliferative disorders in particular cancer and tumor diseases.
IN4310CHN2014 2011-12-15 2012-12-10 IN2014CN04310A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP11193841 2011-12-15
PCT/EP2012/074977 WO2013087578A1 (en) 2011-12-15 2012-12-10 Disubstituted benzothienyl-pyrrolotriazines and their use as fgfr kinase inhibitors

Publications (1)

Publication Number Publication Date
IN2014CN04310A true IN2014CN04310A (en) 2015-09-04

Family

ID=47326168

Family Applications (1)

Application Number Title Priority Date Filing Date
IN4310CHN2014 IN2014CN04310A (en) 2011-12-15 2012-12-10

Country Status (43)

Country Link
US (4) US20140336173A1 (en)
EP (1) EP2791140B1 (en)
JP (1) JP6050829B2 (en)
KR (1) KR102057444B1 (en)
CN (1) CN104245700B (en)
AR (1) AR089207A1 (en)
AU (3) AU2012350750B2 (en)
BR (1) BR112014014531B1 (en)
CA (1) CA2859133C (en)
CL (1) CL2014001547A1 (en)
CO (1) CO7030961A2 (en)
CR (1) CR20140288A (en)
CU (2) CU24426B1 (en)
CY (1) CY1118112T1 (en)
DK (1) DK2791140T3 (en)
DO (1) DOP2014000127A (en)
EA (1) EA029556B1 (en)
EC (1) ECSP14004722A (en)
ES (1) ES2591203T3 (en)
GT (1) GT201400113A (en)
HK (1) HK1205123A1 (en)
HR (1) HRP20161130T1 (en)
HU (1) HUE029582T2 (en)
IL (1) IL232611A (en)
IN (1) IN2014CN04310A (en)
JO (1) JO3295B1 (en)
LT (1) LT2791140T (en)
ME (1) ME02517B (en)
MX (1) MX367158B (en)
MY (1) MY178660A (en)
PE (1) PE20141855A1 (en)
PH (1) PH12014501355B1 (en)
PL (1) PL2791140T3 (en)
PT (1) PT2791140T (en)
RS (1) RS55144B1 (en)
SG (1) SG11201402325QA (en)
SI (1) SI2791140T1 (en)
TN (1) TN2014000255A1 (en)
TW (1) TWI567076B (en)
UA (1) UA116768C2 (en)
UY (1) UY34484A (en)
WO (1) WO2013087578A1 (en)
ZA (1) ZA201405140B (en)

Families Citing this family (27)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10388493B2 (en) 2011-09-16 2019-08-20 Lam Research Corporation Component of a substrate support assembly producing localized magnetic fields
UY34484A (en) * 2011-12-15 2013-07-31 Bayer Ip Gmbh BENZOTIENILO-PIRROLOTRIAZINAS DISUSTITUIDAS AND ITS USES
DK3023100T3 (en) 2013-07-18 2019-05-27 Taiho Pharmaceutical Co Ltd ANTITUM MEDICINE FOR INTERMITTING ADMINISTRATION OF FGFR HARMFUL
JP6084292B2 (en) 2013-07-18 2017-02-22 大鵬薬品工業株式会社 FGFR inhibitor resistant cancer therapeutics
JP6434506B2 (en) * 2013-10-21 2018-12-05 ジェノスコ Substituted pyrimidine compounds and their use as SYK inhibitors
MX2017007656A (en) * 2014-12-11 2017-10-11 Bayer Pharma AG Use of pan fgfr inhibitors and method of identifying patients with cancer eligible for treatment with a pan fgfr inhibitor.
EP3268490B1 (en) * 2015-03-09 2020-07-08 Bayer Pharma Aktiengesellschaft Substituted 2,3-dihydroimidazo[1,2-c]quinazoline-containing combinations
SG11201804901WA (en) 2015-12-22 2018-07-30 SHY Therapeutics LLC Compounds for the treatment of cancer and inflammatory disease
JP7085985B2 (en) 2016-03-04 2022-06-17 大鵬薬品工業株式会社 Preparations and compositions for the treatment of malignant tumors
US11883404B2 (en) 2016-03-04 2024-01-30 Taiho Pharmaceuticals Co., Ltd. Preparation and composition for treatment of malignant tumors
EP3436461B1 (en) 2016-03-28 2023-11-01 Incyte Corporation Pyrrolotriazine compounds as tam inhibitors
CN107513068A (en) * 2016-06-16 2017-12-26 中国科学院上海药物研究所 A kind of new compound and its preparation and application with FGFR inhibitory activity
EP3554506B1 (en) 2016-12-16 2021-04-28 Cystic Fibrosis Foundation Bycyclic heteroaryl derivatives as cftr potentiators
CA3066939A1 (en) 2017-06-21 2018-12-27 SHY Therapeutics LLC Compounds that interact with the ras superfamily for the treatment of cancers, inflammatory diseases, rasopathies, and fibrotic disease
WO2019034076A1 (en) * 2017-08-15 2019-02-21 南京明德新药研发股份有限公司 Fgfr inhibitor and medical application thereof
WO2019034075A1 (en) * 2017-08-15 2019-02-21 南京明德新药研发股份有限公司 Fgfr and egfr inhibitor
WO2019081346A1 (en) * 2017-10-25 2019-05-02 Bayer Pharma Aktiengesellschaft Process for preparing benzothiophen-2yl boronate
WO2019105734A1 (en) 2017-11-28 2019-06-06 Bayer Consumer Care Ag Combinations of copanlisib
CN111867594A (en) 2018-03-19 2020-10-30 大鹏药品工业株式会社 Pharmaceutical composition comprising sodium alkyl sulfate
WO2019180141A1 (en) 2018-03-23 2019-09-26 Bayer Aktiengesellschaft Combinations of rogaratinib
GEP20237531B (en) * 2019-01-31 2023-08-25 Bayer Ag Monohydrate of rogaratinib hydrochloride and solid states thereof
US20220177475A1 (en) * 2019-02-15 2022-06-09 Cspc Zhongqi Pharmaceutical Technology (Shijiazhuang) Co., Ltd Fgfr inhibitor compound in solid form and preparation method therefor
WO2020170355A1 (en) * 2019-02-20 2020-08-27 大鵬薬品工業株式会社 Method for treating fgfr1 mutated tumor
CN109928976A (en) * 2019-02-26 2019-06-25 泰州亿腾景昂药业有限公司 A kind of method of industrialized production EOC317
WO2021089005A1 (en) * 2019-11-08 2021-05-14 石药集团中奇制药技术(石家庄)有限公司 Use of fgfr inhibitor
CN111004234A (en) * 2019-11-28 2020-04-14 湖南农业大学 C3-site halogenation method of 2-phenylimidazo [1,2- α ] pyridine compound
CN117402161A (en) * 2022-07-06 2024-01-16 上海科恩泰生物医药科技有限公司 Sulfoxide imine compound with FGFR inhibition effect, pharmaceutical composition containing sulfoxide imine compound and application of sulfoxide imine compound

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2000071129A1 (en) * 1999-05-21 2000-11-30 Bristol-Myers Squibb Company Pyrrolotriazine inhibitors of kinases
PL354241A1 (en) 1999-09-17 2003-12-29 Abbott Gmbh & Co.Kgabbott Gmbh & Co.Kg Kinase inhibitors as therapeutic agents
JPWO2004096806A1 (en) * 2003-04-30 2006-07-13 大日本住友製薬株式会社 Condensed imidazole derivatives
DE10327439A1 (en) * 2003-06-18 2005-01-05 Boehringer Ingelheim Pharma Gmbh & Co. Kg Novel imidazopyridazinone and imidazopyridone derivatives, their production and their use as pharmaceuticals
CN102924458B (en) 2004-04-02 2014-11-05 Osi制药有限责任公司 6,6-bicyclic ring substituted heterobicyclic protein kinase inhibitors
UY28931A1 (en) 2004-06-03 2005-12-30 Bayer Pharmaceuticals Corp USED PIRROLOTRIAZINE DERIVATIVES TO TREAT HYPER-PROLIFERATIVE DISORDERS AND DISEASES ASSOCIATED WITH ANGIOGENESIS
TW200635927A (en) * 2004-12-22 2006-10-16 Bristol Myers Squibb Co Synthetic process
WO2007056170A2 (en) 2005-11-02 2007-05-18 Bayer Healthcare Ag Pyrrolo[2,1-f] [1,2,4] triazin-4-ylamines igf-1r kinase inhibitors for the treatment of cancer and other hyperproliferative diseases
EP2385053B1 (en) * 2005-11-17 2013-10-02 OSI Pharmaceuticals, Inc. Intermediates for the preparation of fused bicyclic mTOR inhibitors
US7514435B2 (en) 2005-11-18 2009-04-07 Bristol-Myers Squibb Company Pyrrolotriazine kinase inhibitors
PE20070855A1 (en) * 2005-12-02 2007-10-14 Bayer Pharmaceuticals Corp DERIVATIVES OF 4-AMINO-PYRROLOTRIAZINE SUBSTITUTE AS KINASE INHIBITORS
US8338594B2 (en) 2005-12-02 2012-12-25 Bayer Healthcare Llc Pyrrolotriazine derivatives useful for treating cancer through inhibition of aurora kinase
MX2008007103A (en) 2005-12-02 2008-09-12 Bayer Healthcare Llc Substituted 4-amino-pyrrolotriazine derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis.
EP1973917B1 (en) * 2005-12-29 2015-06-10 AbbVie Inc. Protein kinase inhibitors
US8124759B2 (en) 2007-05-09 2012-02-28 Abbott Laboratories Inhibitors of protein kinases
US8476282B2 (en) 2008-11-03 2013-07-02 Intellikine Llc Benzoxazole kinase inhibitors and methods of use
JP5656976B2 (en) 2009-04-29 2015-01-21 ローカス ファーマシューティカルズ インコーポレイテッド Pyrrolotriazine compounds
UY34484A (en) * 2011-12-15 2013-07-31 Bayer Ip Gmbh BENZOTIENILO-PIRROLOTRIAZINAS DISUSTITUIDAS AND ITS USES

Also Published As

Publication number Publication date
AU2017206140A1 (en) 2017-08-03
BR112014014531B1 (en) 2022-02-08
KR20140103328A (en) 2014-08-26
CN104245700B (en) 2016-11-16
ZA201405140B (en) 2017-04-26
CU20160039A7 (en) 2016-08-31
CA2859133A1 (en) 2013-06-20
US20140336173A1 (en) 2014-11-13
JO3295B1 (en) 2018-09-16
CY1118112T1 (en) 2017-06-28
ME02517B (en) 2017-02-20
MY178660A (en) 2020-10-20
MX367158B (en) 2019-08-07
IL232611A0 (en) 2014-06-30
JP6050829B2 (en) 2016-12-21
EA201400707A1 (en) 2014-11-28
AR089207A1 (en) 2014-08-06
LT2791140T (en) 2016-10-10
IL232611A (en) 2017-05-29
SG11201402325QA (en) 2014-09-26
US20220153745A1 (en) 2022-05-19
CR20140288A (en) 2014-07-14
CL2014001547A1 (en) 2014-10-24
AU2012350750B2 (en) 2017-08-03
PE20141855A1 (en) 2014-11-26
TW201339162A (en) 2013-10-01
CN104245700A (en) 2014-12-24
CO7030961A2 (en) 2014-08-21
US9206184B2 (en) 2015-12-08
US20130158000A1 (en) 2013-06-20
WO2013087578A1 (en) 2013-06-20
SI2791140T1 (en) 2016-10-28
UA116768C2 (en) 2018-05-10
HK1205123A1 (en) 2015-12-11
TWI567076B (en) 2017-01-21
JP2015500307A (en) 2015-01-05
DOP2014000127A (en) 2014-08-15
AU2012350750A1 (en) 2014-06-12
DK2791140T3 (en) 2016-09-19
PT2791140T (en) 2016-09-20
GT201400113A (en) 2015-08-25
CA2859133C (en) 2020-03-24
RS55144B1 (en) 2016-12-30
ES2591203T3 (en) 2016-11-25
BR112014014531A2 (en) 2019-08-06
ECSP14004722A (en) 2015-11-30
CU20140065A7 (en) 2014-11-27
NZ625073A (en) 2016-07-29
EA029556B1 (en) 2018-04-30
MX2014006905A (en) 2014-09-08
TN2014000255A1 (en) 2015-09-30
PH12014501355A1 (en) 2014-09-22
US20190016724A1 (en) 2019-01-17
HRP20161130T1 (en) 2016-11-18
UY34484A (en) 2013-07-31
HUE029582T2 (en) 2017-03-28
PH12014501355B1 (en) 2014-09-22
PL2791140T3 (en) 2017-08-31
AU2019204255A1 (en) 2019-07-04
CU24426B1 (en) 2019-06-04
EP2791140B1 (en) 2016-06-15
EP2791140A1 (en) 2014-10-22
KR102057444B1 (en) 2019-12-19

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