CU20170154A7 - Derivados de pirazol-3-il-amina sustituidos como inhibidores cdk - Google Patents

Derivados de pirazol-3-il-amina sustituidos como inhibidores cdk

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Publication number
CU20170154A7
CU20170154A7 CUP2017000154A CU20170154A CU20170154A7 CU 20170154 A7 CU20170154 A7 CU 20170154A7 CU P2017000154 A CUP2017000154 A CU P2017000154A CU 20170154 A CU20170154 A CU 20170154A CU 20170154 A7 CU20170154 A7 CU 20170154A7
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CU
Cuba
Prior art keywords
formula
derivatives
cdk inhibitors
pirazol
amina
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CUP2017000154A
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English (en)
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CU24496B1 (es
Inventor
Rajeev Goswami
Subhendu Mukherjee
Chetan Pandit
Ramulu Proddutoori
Susanta Samajdar
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Aurigene Discovery Tech Ltd
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Publication of CU20170154A7 publication Critical patent/CU20170154A7/es
Publication of CU24496B1 publication Critical patent/CU24496B1/es

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    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D231/38Nitrogen atoms
    • C07D231/40Acylated on said nitrogen atom
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    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
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    • A61K31/41Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
    • A61K31/4151,2-Diazoles
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/4427Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems
    • A61K31/4439Non condensed pyridines; Hydrogenated derivatives thereof containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. omeprazole
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    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/454Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a five-membered ring with nitrogen as a ring hetero atom, e.g. pimozide, domperidone
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    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/4523Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems
    • A61K31/4545Non condensed piperidines, e.g. piperocaine containing further heterocyclic ring systems containing a six-membered ring with nitrogen as a ring hetero atom, e.g. pipamperone, anabasine
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    • A61K31/47Quinolines; Isoquinolines
    • A61K31/472Non-condensed isoquinolines, e.g. papaverine
    • A61K31/4725Non-condensed isoquinolines, e.g. papaverine containing further heterocyclic rings
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    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
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    • 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
    • A61K31/4965Non-condensed pyrazines
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    • 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
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    • C07D401/04Heterocyclic 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 directly linked by a ring-member-to-ring-member bond
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    • C07D471/04Ortho-condensed systems

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

Abstract

<p>La presente invención proporciona derivados heterocíclicos sustituidos de la fórmula (I),</p> <p>ESPACIO PARA LA FÓRMULA</p> <p>que son terapéuticamente útiles, particularmente como inhibidores CDK transcripcionales selectivos incluyendo CDK7, CDK9, CDK12,CDK13, y CDK18, más concretamente CDK7 inhibidores transcripcionales. Estos compuestos son útiles en el tratamiento y prevención de enfermedades o trastornos asociados con las CDKs transcripcionales selectivas en un mamífero. La presente invención también proporciona preparación de los compuestos y formulaciones farmacéuticas que comprende al menos uno de los derivados heterocíclicos sustituidos de la fórmula (I) o una sal farmacéuticamente aceptable o un estereoisómero del mismo.</p>
CU2017000154A 2015-06-04 2016-06-03 Derivados de pirazol-3-il-amina sustituidos como inhibidores de cdk CU24496B1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
IN2803CH2015 2015-06-04
IN6214CH2015 2015-11-18
PCT/IB2016/053267 WO2016193939A1 (en) 2015-06-04 2016-06-03 Substituted heterocyclyl derivatives as cdk inhibitors

Publications (2)

Publication Number Publication Date
CU20170154A7 true CU20170154A7 (es) 2018-07-05
CU24496B1 CU24496B1 (es) 2021-01-12

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US (3) US10689347B2 (es)
EP (2) EP3302448B1 (es)
JP (3) JP6750806B2 (es)
KR (1) KR20180041112A (es)
CN (2) CN113773257A (es)
AU (3) AU2016272908B2 (es)
CA (1) CA2987552A1 (es)
CU (1) CU24496B1 (es)
DK (1) DK3302448T3 (es)
EA (1) EA037236B1 (es)
FI (1) FI3302448T3 (es)
HK (1) HK1255239A1 (es)
HR (1) HRP20240101T1 (es)
IL (2) IL255960B (es)
LT (1) LT3302448T (es)
MX (2) MX2017015521A (es)
MY (1) MY190459A (es)
PH (1) PH12017502179A1 (es)
SI (1) SI3302448T1 (es)
WO (1) WO2016193939A1 (es)

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KR20240022609A (ko) * 2021-06-16 2024-02-20 블루프린트 메디신즈 코포레이션 Cdk2 저해제로서의 치환된 피리미딜-피라졸
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