IN2012DN01251A - - Google Patents

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Publication number
IN2012DN01251A
IN2012DN01251A IN1251DEN2012A IN2012DN01251A IN 2012DN01251 A IN2012DN01251 A IN 2012DN01251A IN 1251DEN2012 A IN1251DEN2012 A IN 1251DEN2012A IN 2012DN01251 A IN2012DN01251 A IN 2012DN01251A
Authority
IN
India
Prior art keywords
group
integer
hydrogen atom
alkyl group
alkynyl
Prior art date
Application number
Inventor
Kazunari Tsuboike
Gen Mizuno
Hiroshi Nishida
Shigeyuki Kono
Akiko Toyota
Fumie Tanzawa
Kosaku Fujiwara
Original Assignee
Ube Industries
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 Ube Industries filed Critical Ube Industries
Publication of IN2012DN01251A publication Critical patent/IN2012DN01251A/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
    • A61K31/495Heterocyclic 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
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • 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

Landscapes

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

Abstract

Provided is a compound represented by the Formula (I) having a HER2 inhibitory action or a pharmacologically acceptable salt thereof, wherein T1 is a phenyl group, an indazolyl group, or a benzofuryl group, n is an integer of 0 to 3, R1 is a hydrogen atom, a halogen atom, a C1-4 alkyl group, a C2-6 alkenyl group, a C2-6 alkynyl group, or a C1-4 alkoxy group, m is an integer of 0 to 3, R2 is a hydroxy group or a C1-4 alkyl group optionally substituted with one or two C1-4 alkoxy groups, and R3 is a hydrogen atom, a C1-4 alkyl group, or a C2-6 alkynyl group.
IN1251DEN2012 2009-07-28 2010-07-27 IN2012DN01251A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP2009175619 2009-07-28
PCT/JP2010/062602 WO2011013656A1 (en) 2009-07-28 2010-07-27 Pyrrolo[2,3-d]pyrimidine derivative

Publications (1)

Publication Number Publication Date
IN2012DN01251A true IN2012DN01251A (en) 2015-05-15

Family

ID=43529310

Family Applications (1)

Application Number Title Priority Date Filing Date
IN1251DEN2012 IN2012DN01251A (en) 2009-07-28 2010-07-27

Country Status (10)

Country Link
US (1) US20120149902A1 (en)
EP (1) EP2511276A4 (en)
JP (1) JPWO2011013656A1 (en)
KR (1) KR20120065321A (en)
CN (1) CN102482281A (en)
AU (1) AU2010279188A1 (en)
CA (1) CA2768821A1 (en)
IN (1) IN2012DN01251A (en)
TW (1) TW201107328A (en)
WO (1) WO2011013656A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2015531361A (en) 2012-09-26 2015-11-02 バイエル・ファルマ・アクティエンゲゼルシャフト Substituted indazole-pyrrolopyrimidines useful for the treatment of hyperproliferative diseases
EP2900671A1 (en) * 2012-09-26 2015-08-05 Bayer Pharma Aktiengesellschaft Substituted indazol-pyrrolopyrimidines useful in the treatment of hyperproliferative diseases
US20190119284A1 (en) * 2016-04-19 2019-04-25 The Regents Of The University Of California ErbB Inhibitors and Uses Thereof
US20190185479A1 (en) * 2016-08-26 2019-06-20 Mitsubishi Tanabe Pharma Corporation Bicyclic nitrogenated heterocyclic compound
CN113277990A (en) * 2021-06-22 2021-08-20 仪征市海帆化工有限公司 Synthesis method of 1, 4-bis (p-toluenesulfonyl) triazacyclononane

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MX9800215A (en) * 1995-07-06 1998-03-31 Novartis Ag Pyrrolopyrimidines and processes for the preparation thereof.
GB9604361D0 (en) * 1996-02-29 1996-05-01 Pharmacia Spa 4-Substituted pyrrolopyrimidine compounds as tyrosine kinase inhibitors
WO1998007726A1 (en) * 1996-08-23 1998-02-26 Novartis Ag Substituted pyrrolopyrimidines and processes for their preparation
GB0119249D0 (en) * 2001-08-07 2001-10-03 Novartis Ag Organic compounds
TW200300350A (en) * 2001-11-14 2003-06-01 Bristol Myers Squibb Co C-5 modified indazolylpyrrolotriazines
MY145634A (en) * 2003-12-29 2012-03-15 Bristol Myers Squibb Co Pyrrolotriazine compounds as kinase inhibitors
ATE421510T1 (en) * 2005-03-28 2009-02-15 Bristol Myers Squibb Co COMPETITIVE ATP KINASE INHIBITORS

Also Published As

Publication number Publication date
KR20120065321A (en) 2012-06-20
JPWO2011013656A1 (en) 2013-01-07
CN102482281A (en) 2012-05-30
WO2011013656A1 (en) 2011-02-03
EP2511276A4 (en) 2012-12-19
CA2768821A1 (en) 2011-02-03
US20120149902A1 (en) 2012-06-14
AU2010279188A1 (en) 2012-02-23
EP2511276A1 (en) 2012-10-17
TW201107328A (en) 2011-03-01

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