CA2856309C - Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors - Google Patents

Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors Download PDF

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Publication number
CA2856309C
CA2856309C CA2856309A CA2856309A CA2856309C CA 2856309 C CA2856309 C CA 2856309C CA 2856309 A CA2856309 A CA 2856309A CA 2856309 A CA2856309 A CA 2856309A CA 2856309 C CA2856309 C CA 2856309C
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alkyl
aryl
cycloalkyl
heterocyclyl
heteroaryl
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CA2856309A
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English (en)
French (fr)
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CA2856309A1 (en
Inventor
Changyou Zhou
Bo REN
Hexiang Wang
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BeOne Medicines Ltd
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Beigene Ltd
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    • 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
    • C07D487/06Peri-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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • 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
    • A61K31/55Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
    • A61K31/551Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole having two nitrogen atoms, e.g. dilazep
    • A61K31/55131,4-Benzodiazepines, e.g. diazepam or clozapine
    • A61K31/55171,4-Benzodiazepines, e.g. diazepam or clozapine condensed with five-membered rings having nitrogen as a ring hetero atom, e.g. imidazobenzodiazepines, triazolam
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/12Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains three hetero rings
    • C07D471/16Peri-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/22Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed systems contains four or more hetero rings
    • 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
    • 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
    • C07D487/12Heterocyclic 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 three hetero rings
    • C07D487/14Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Rheumatology (AREA)
  • Engineering & Computer Science (AREA)
  • Pain & Pain Management (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Immunology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen- Or Sulfur-Containing Heterocyclic Ring Compounds With Rings Of Six Or More Members (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
CA2856309A 2011-12-31 2011-12-31 Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors Active CA2856309C (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/CN2011/085148 WO2013097225A1 (en) 2011-12-31 2011-12-31 Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors

Publications (2)

Publication Number Publication Date
CA2856309A1 CA2856309A1 (en) 2013-07-04
CA2856309C true CA2856309C (en) 2016-06-07

Family

ID=48696280

Family Applications (1)

Application Number Title Priority Date Filing Date
CA2856309A Active CA2856309C (en) 2011-12-31 2011-12-31 Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors

Country Status (29)

Country Link
US (4) US9260440B2 (en:Method)
EP (2) EP3315500B1 (en:Method)
JP (1) JP6034877B2 (en:Method)
KR (1) KR101716012B1 (en:Method)
CN (2) CN106220635B (en:Method)
AU (1) AU2011384858B2 (en:Method)
BR (1) BR112014012628B8 (en:Method)
CA (1) CA2856309C (en:Method)
CY (1) CY1119804T1 (en:Method)
DK (1) DK2797921T3 (en:Method)
EA (1) EA027533B1 (en:Method)
ES (1) ES2645814T3 (en:Method)
HR (1) HRP20171883T1 (en:Method)
HU (1) HUE035153T2 (en:Method)
IL (1) IL233365A (en:Method)
IN (1) IN2014DN06169A (en:Method)
LT (1) LT2797921T (en:Method)
ME (1) ME02855B (en:Method)
MX (1) MX353578B (en:Method)
NO (1) NO2797921T3 (en:Method)
NZ (1) NZ624063A (en:Method)
PL (1) PL2797921T3 (en:Method)
PT (1) PT2797921T (en:Method)
RS (1) RS56616B1 (en:Method)
SG (1) SG11201401726VA (en:Method)
SI (1) SI2797921T1 (en:Method)
SM (1) SMT201700543T1 (en:Method)
WO (1) WO2013097225A1 (en:Method)
ZA (1) ZA201405560B (en:Method)

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WO2013097225A1 (en) 2011-12-31 2013-07-04 Beigene, Ltd. Fused tetra or penta-cyclic dihydrodiazepinocarbazolones as parp inhibitors
DK2822656T3 (en) 2012-03-07 2017-01-30 Inst Of Cancer Research: Royal Cancer Hospital (The) 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use
CA2922469A1 (en) 2013-09-11 2015-03-19 Institute Of Cancer Research: Royal Cancer Hospital (The) 3-aryl-5-substituted-isoquinolin-1-one compounds and their therapeutic use
AU2016312011B2 (en) * 2015-08-25 2021-02-04 Beigene, Ltd. Process for preparing Parp inhibitor, crystalline forms, and uses thereof
CN113717170A (zh) 2016-04-01 2021-11-30 里科瑞尔姆Ip控股有限责任公司 雌激素受体调节剂
WO2018059437A1 (en) 2016-09-27 2018-04-05 Beigene, Ltd. Treatment cancers using combination comprising parp inhibitors
WO2018157794A1 (en) * 2017-02-28 2018-09-07 Beigene, Ltd. Crystalline forms of salts of fused tera or penta-cyclic dihydrodiazepinocarazolones, and uses thereof
CN106883232B (zh) 2017-03-31 2019-01-22 苏州康润医药有限公司 一种氮杂非那烯-3-酮的衍生物及其制备方法与应用
EP3654985A4 (en) * 2017-07-17 2021-04-07 BeiGene, Ltd. TREATMENT OF CANCERS USING A COMBINATION INCLUDING PARP INHIBITORS, TEMOZOLOMIDE AND / OR RADIATION THERAPY
CN112292133A (zh) * 2018-06-01 2021-01-29 百济神州有限公司 在胃癌治疗中的parp抑制剂维持疗法
CN111171031B (zh) * 2019-05-10 2021-04-09 百济神州(苏州)生物科技有限公司 一种含parp抑制剂倍半水合物产物的制备方法
CN111171002B (zh) * 2019-05-16 2021-04-06 百济神州(苏州)生物科技有限公司 一种parp抑制剂中间体的制备方法
CA3141770A1 (en) 2019-05-31 2020-12-03 Beigene, Ltd. Parp inhibitor pellet preparation and preparation process therefor
US11278532B2 (en) 2019-08-06 2022-03-22 Recurium Ip Holdings, Llc Estrogen receptor modulators for treating mutants
WO2021046014A1 (en) 2019-09-03 2021-03-11 Teva Czech Industries S.R.O Solid state forms of pamiparib and process for preparation thereof
WO2024229406A1 (en) 2023-05-04 2024-11-07 Revolution Medicines, Inc. Combination therapy for a ras related disease or disorder
US20250049810A1 (en) 2023-08-07 2025-02-13 Revolution Medicines, Inc. Methods of treating a ras protein-related disease or disorder
WO2025080946A2 (en) 2023-10-12 2025-04-17 Revolution Medicines, Inc. Ras inhibitors
WO2025171296A1 (en) 2024-02-09 2025-08-14 Revolution Medicines, Inc. Ras inhibitors

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ES2354249T3 (es) 2000-12-01 2011-03-11 Eisai Inc. Derivados de azafenantridona y su uso como inhibidores de parp.
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US6906096B2 (en) 2002-06-28 2005-06-14 Irm Llc 4,7-Disubstituted indoles and methods of making
CA2512683C (en) 2003-01-09 2010-03-16 Pfizer Inc. Tricyclic compounds protein kinase inhibitors for enhancing the efficacy of anti-neoplastic agents and radiation therapy
JP4824566B2 (ja) 2003-05-28 2011-11-30 エーザイ インコーポレーテッド Parpを阻害するための化合物、方法、および医薬組成物
CA2648369A1 (en) 2006-04-04 2007-10-11 Pfizer Products Inc. Polymorphic forms of (2r,z)-2-amino-2-cyclohexyl-n-(5-(1-methyl-1h-pyrazol-4?l)-1-oxo-2,6-dihydro-1h-[1,2]diazepino[4,5,6-cd]indol-8-yl)acetamide
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US9637488B2 (en) 2015-01-29 2017-05-02 Fuqiang Ruan Heterocyclic compounds as inhibitors of class I PI3KS
AU2016312011B2 (en) 2015-08-25 2021-02-04 Beigene, Ltd. Process for preparing Parp inhibitor, crystalline forms, and uses thereof
WO2018059437A1 (en) 2016-09-27 2018-04-05 Beigene, Ltd. Treatment cancers using combination comprising parp inhibitors
WO2018157794A1 (en) 2017-02-28 2018-09-07 Beigene, Ltd. Crystalline forms of salts of fused tera or penta-cyclic dihydrodiazepinocarazolones, and uses thereof
EP3654985A4 (en) 2017-07-17 2021-04-07 BeiGene, Ltd. TREATMENT OF CANCERS USING A COMBINATION INCLUDING PARP INHIBITORS, TEMOZOLOMIDE AND / OR RADIATION THERAPY

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Publication number Publication date
US20170305921A1 (en) 2017-10-26
KR101716012B1 (ko) 2017-03-13
PT2797921T (pt) 2017-11-14
EA201491303A1 (ru) 2014-10-30
MX353578B (es) 2018-01-19
WO2013097225A1 (en) 2013-07-04
BR112014012628A2 (pt) 2017-06-13
AU2011384858B2 (en) 2016-05-05
CN106220635B (zh) 2019-03-08
JP6034877B2 (ja) 2016-11-30
EP2797921A1 (en) 2014-11-05
US20190016731A1 (en) 2019-01-17
NZ624063A (en) 2016-09-30
LT2797921T (lt) 2017-11-27
EP3315500A1 (en) 2018-05-02
PL2797921T3 (pl) 2018-02-28
US20160159811A1 (en) 2016-06-09
IL233365A0 (en) 2014-08-31
US9260440B2 (en) 2016-02-16
SG11201401726VA (en) 2014-10-30
ZA201405560B (en) 2017-02-22
BR112014012628B8 (pt) 2023-01-17
DK2797921T3 (en) 2017-10-02
US10501467B2 (en) 2019-12-10
AU2011384858A1 (en) 2014-05-29
EA027533B1 (ru) 2017-08-31
CA2856309A1 (en) 2013-07-04
HUE035153T2 (en) 2018-05-02
SI2797921T1 (en) 2018-01-31
NO2797921T3 (en:Method) 2018-02-03
RS56616B1 (sr) 2018-02-28
HK1192233A1 (zh) 2014-08-15
SMT201700543T1 (it) 2018-01-11
EP2797921A4 (en) 2015-10-21
EP3315500B1 (en) 2020-03-18
HRP20171883T1 (hr) 2018-01-12
KR20140107353A (ko) 2014-09-04
US20150175617A1 (en) 2015-06-25
MX2014007840A (es) 2014-08-21
ME02855B (me) 2018-04-20
ES2645814T3 (es) 2017-12-07
EP2797921B1 (en) 2017-09-06
CN103703004A (zh) 2014-04-02
JP2015503526A (ja) 2015-02-02
IN2014DN06169A (en:Method) 2015-08-21
CN106220635A (zh) 2016-12-14
US9617273B2 (en) 2017-04-11
US10112952B2 (en) 2018-10-30
BR112014012628B1 (pt) 2021-02-09
CY1119804T1 (el) 2018-06-27
CN103703004B (zh) 2016-06-29
IL233365A (en) 2016-08-31

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