AU2017378060B2 - 7-phenylethylamino-4H-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant IDH1 and IDH2 inhibitors - Google Patents

7-phenylethylamino-4H-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant IDH1 and IDH2 inhibitors Download PDF

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AU2017378060B2
AU2017378060B2 AU2017378060A AU2017378060A AU2017378060B2 AU 2017378060 B2 AU2017378060 B2 AU 2017378060B2 AU 2017378060 A AU2017378060 A AU 2017378060A AU 2017378060 A AU2017378060 A AU 2017378060A AU 2017378060 B2 AU2017378060 B2 AU 2017378060B2
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ethyl
compound
phenyl
oxazin
mutant
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AU2017378060A1 (en
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Renato Alejandro BAUER
Serge Louis Boulet
Timothy Paul Burkholder
Raymond Gilmour
Patric James Hahn
Zoran Rankovic
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Eli Lilly and Co
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Eli Lilly and Co
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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D498/00Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D498/04Ortho-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
    • A61K31/535Heterocyclic 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
    • A61K31/5365Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • 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

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
AU2017378060A 2016-12-16 2017-12-08 7-phenylethylamino-4H-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant IDH1 and IDH2 inhibitors Active AU2017378060B2 (en)

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AU2020260493A AU2020260493B2 (en) 2016-12-16 2020-10-29 7-phenylethylamino-4H-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant IDH1 and IDH2 inhibitors

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US201662435283P 2016-12-16 2016-12-16
US62/435,283 2016-12-16
PCT/US2017/065246 WO2018111707A1 (en) 2016-12-16 2017-12-08 7-phenylethylamino-4h-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant idh1 and idh2 inhibitors

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AU2020260493A Division AU2020260493B2 (en) 2016-12-16 2020-10-29 7-phenylethylamino-4H-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant IDH1 and IDH2 inhibitors

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AU2017378060A1 AU2017378060A1 (en) 2019-05-30
AU2017378060B2 true AU2017378060B2 (en) 2020-09-03

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AU2020260493A Active AU2020260493B2 (en) 2016-12-16 2020-10-29 7-phenylethylamino-4H-pyrimido[4,5-d][1,3]oxazin-2-one compounds as mutant IDH1 and IDH2 inhibitors

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US (3) US11001596B2 (https=)
EP (2) EP3555105B1 (https=)
JP (1) JP6793836B2 (https=)
KR (1) KR102276022B1 (https=)
CN (2) CN115109075B (https=)
AU (2) AU2017378060B2 (https=)
CA (1) CA3045303C (https=)
CL (1) CL2019001551A1 (https=)
CO (1) CO2019005287A2 (https=)
CR (1) CR20190252A (https=)
CY (1) CY1123577T1 (https=)
DK (1) DK3555105T3 (https=)
DO (1) DOP2019000163A (https=)
EA (1) EA036112B1 (https=)
EC (1) ECSP19042682A (https=)
ES (2) ES2941631T3 (https=)
HR (1) HRP20201882T1 (https=)
HU (1) HUE052067T2 (https=)
IL (1) IL267236B (https=)
JO (1) JOP20190142B1 (https=)
LT (1) LT3555105T (https=)
MA (2) MA47399B1 (https=)
MD (1) MD3555105T2 (https=)
MX (1) MX385562B (https=)
MY (1) MY197313A (https=)
NZ (1) NZ754115A (https=)
PE (1) PE20190977A1 (https=)
PH (1) PH12019501328B1 (https=)
PL (1) PL3555105T3 (https=)
PT (1) PT3555105T (https=)
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SA (1) SA519401897B1 (https=)
SI (1) SI3555105T1 (https=)
TN (1) TN2019000158A1 (https=)
UA (1) UA123640C2 (https=)
WO (1) WO2018111707A1 (https=)
ZA (1) ZA201903125B (https=)

Families Citing this family (31)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3194383B1 (en) 2014-09-19 2019-11-06 Forma Therapeutics, Inc. Quinolinone pyrimidines compositions as mutant-isocitrate dehydrogenase inhibitors
MA53352A (fr) 2014-09-19 2021-09-15 Forma Therapeutics Inc Dérivés de pyridin-2-(1h)-one-quinolinone en tant qu'inhibiteurs d'isocitrate déshydrogénase
MX372964B (es) 2014-09-19 2020-03-27 Forma Therapeutics Inc Derivados de fenil quinolinona como inhibidores de isocitrato deshidrogenasa mutante (mt-idh)
AU2015317327B9 (en) 2014-09-19 2020-04-09 Forma Therapeutics, Inc. Pyridinyl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US9624175B2 (en) 2015-04-21 2017-04-18 Forma Therapeutics, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
US10407419B2 (en) 2015-04-21 2019-09-10 Forma Therapeutics, Inc. Quinolinone five-membered heterocyclic compounds as mutant-isocitrate dehydrogenase inhibitors
EP3640251B1 (en) 2016-10-24 2021-12-08 Astrazeneca AB 6,7,8,9-tetrahydro-3h-pyrazolo[4,3-f]isoquinoline derivatives useful in the treatment of cancer
JP7291077B2 (ja) 2016-12-16 2023-06-14 ヤンセン ファーマシューティカ エヌ.ベー. Jakファミリーのキナーゼの低分子阻害物質
ES2941631T3 (es) * 2016-12-16 2023-05-24 Lilly Co Eli Compuestos de Pirido[4,3-d][1,3]oxazin-2-ona como inhibidores de IDH1 e IDH2 mutantes
JOP20190144A1 (ar) 2016-12-16 2019-06-16 Janssen Pharmaceutica Nv إيميدازو بيرولو بيريدين كمثبطات لعائلة jak الخاصة بإنزيمات الكيناز
PL3494116T3 (pl) 2017-01-30 2020-04-30 Astrazeneca Ab Modulatory receptora estrogenowego
US11013734B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Treating patients harboring an isocitrate dehydrogenase-1 (IDH-1) mutation
US20210196701A1 (en) 2018-05-16 2021-07-01 Forma Therapeutics, Inc. Inhibiting mutant idh-1
WO2019222551A1 (en) 2018-05-16 2019-11-21 Forma Therapeutics, Inc. Solid forms of ((s)-5-((1-(6-chloro-2-oxo-1,2-dihydroquinolin-3-yl)ethyl)amino)-1-methyl-6-oxo-1,6-dihydropyridine-2-carbonitrile
US11013733B2 (en) 2018-05-16 2021-05-25 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mlDH-1)
US11311527B2 (en) 2018-05-16 2022-04-26 Forma Therapeutics, Inc. Inhibiting mutant isocitrate dehydrogenase 1 (mIDH-1)
TW202016110A (zh) 2018-06-15 2020-05-01 比利時商健生藥品公司 Jak激酶家族之小分子抑制劑
CN115038700B (zh) * 2019-11-08 2025-07-25 内尔维亚诺医疗科学公司 偕二取代的杂环化合物及其作为idh抑制剂的用途
MX2022011846A (es) * 2020-03-23 2023-01-04 Lilly Co Eli Metodo para el tratamiento de sujetos resistentes al inhibidor idh1.
CN115443137B (zh) * 2020-03-23 2024-05-31 伊莱利利公司 使用突变idh抑制剂和bcl-2抑制剂的组合疗法
AU2021242260B2 (en) * 2020-03-23 2023-12-14 Eli Lilly And Company Combination therapy with a mutant IDH inhibitor
MX2022013258A (es) 2020-04-24 2022-11-14 Astrazeneca Ab Formulaciones farmaceuticas.
MX2022013391A (es) 2020-04-24 2022-11-30 Astrazeneca Ab Pauta posologica para el tratamiento del cancer.
US12559505B2 (en) 2020-06-28 2026-02-24 Wigen Biomedicine Technology (shanghai) Co., Ltd. IDH mutant inhibitor and use thereof
WO2022020281A1 (en) 2020-07-20 2022-01-27 Eli Lilly And Company Combination therapy with a mutant idh1 inhibitor, a deoxyadenosine analog, and a platinum agent
MX2023010642A (es) 2021-03-11 2023-11-28 Janssen Pharmaceutica Nv Lorpucitinib para uso en el tratamiento de trastornos mediados por jak.
CN113588768B (zh) * 2021-05-18 2022-07-05 国家卫生健康委科学技术研究所 一种以分子图像方式定量组织内内源性代谢物的质谱方法
US20240261294A1 (en) * 2021-06-09 2024-08-08 Eli Lilly And Company Method for treating idh inhibitor-resistant subjects
CA3217608A1 (en) 2021-06-15 2022-12-22 Yuli Xie Idh mutant inhibitor and use thereof
US11746115B2 (en) 2021-08-13 2023-09-05 Eli Lilly And Company Solid forms of 7-[[(1S)-1-[4-[(1S)-2-cyclopropyl-1-(4-prop-2-enoylpiperazin-1-yl)ethyl]phenyl]ethyl]amino]-1-ethyl-4H-pyrimido[4,5-d][1,3]oxazin-2-one
WO2023141087A1 (en) 2022-01-19 2023-07-27 Eli Lilly And Company Combination therapy with a mutant idh inhibitor

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013046136A1 (en) * 2011-09-27 2013-04-04 Novartis Ag 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
WO2016171755A1 (en) * 2015-04-21 2016-10-27 Forma Therapeutics, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
WO2017213910A1 (en) * 2016-06-06 2017-12-14 Eli Lilly And Company Mutant idh1 inhibitors

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2014229283B2 (en) * 2013-03-14 2016-07-28 Novartis Ag 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant IDH
WO2014147586A1 (en) * 2013-03-22 2014-09-25 Novartis Ag 1-(2-(ethylamino)pyrimidin-4-yl)pyrrolidin-2-ones as inhibitors of mutant idh
CN107405687A (zh) * 2015-04-24 2017-11-28 哈利伯顿能源服务公司 制作陶瓷或金属间化合物零件的方法
ES2764523T3 (es) * 2015-07-27 2020-06-03 Lilly Co Eli Compuestos de 7-feniletilamino-4H-pirimido[4,5-D][1,3]oxazin-2-ona y su uso como inhibidores de IDH1 mutantes
ES2941631T3 (es) * 2016-12-16 2023-05-24 Lilly Co Eli Compuestos de Pirido[4,3-d][1,3]oxazin-2-ona como inhibidores de IDH1 e IDH2 mutantes

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2013046136A1 (en) * 2011-09-27 2013-04-04 Novartis Ag 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant idh
WO2016171755A1 (en) * 2015-04-21 2016-10-27 Forma Therapeutics, Inc. Fused-bicyclic aryl quinolinone derivatives as mutant-isocitrate dehydrogenase inhibitors
WO2017213910A1 (en) * 2016-06-06 2017-12-14 Eli Lilly And Company Mutant idh1 inhibitors

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JP2020502157A (ja) 2020-01-23
EP3555105A1 (en) 2019-10-23
JOP20190142B1 (ar) 2023-03-28
ZA201903125B (en) 2024-08-28
PH12019501328A1 (en) 2020-02-24
CL2019001551A1 (es) 2019-10-25
HUE052067T2 (hu) 2021-04-28
WO2018111707A1 (en) 2018-06-21
CR20190252A (es) 2019-08-26
DOP2019000163A (es) 2019-07-15
PH12019501328B1 (en) 2023-05-12
ECSP19042682A (es) 2019-06-30
KR102276022B1 (ko) 2021-07-13
SA519401897B1 (ar) 2022-07-28
EP3763717B1 (en) 2023-03-08
US11629156B2 (en) 2023-04-18
JOP20190142A1 (ar) 2019-06-13
JP6793836B2 (ja) 2020-12-02
ES2835281T3 (es) 2021-06-22
LT3555105T (lt) 2021-01-11
MA47399B1 (fr) 2021-02-26
MD3555105T2 (ro) 2021-01-31
IL267236B (en) 2020-08-31
HRP20201882T1 (hr) 2021-01-22
CY1123577T1 (el) 2022-03-24
UA123640C2 (uk) 2021-05-05
ES2941631T3 (es) 2023-05-24
AU2020260493A1 (en) 2020-11-26
MX385562B (es) 2025-03-18
CN110072867A (zh) 2019-07-30
CN115109075A (zh) 2022-09-27
RS61108B1 (sr) 2020-12-31
MA53881A (fr) 2022-04-27
EA036112B1 (ru) 2020-09-29
PE20190977A1 (es) 2019-07-09
US20200079791A1 (en) 2020-03-12
TN2019000158A1 (en) 2020-10-05
CO2019005287A2 (es) 2019-05-31
MA47399A (fr) 2019-10-23
EP3555105B1 (en) 2020-10-28
US20210230185A1 (en) 2021-07-29
MX2019006830A (es) 2019-08-22
CA3045303A1 (en) 2018-06-21
CN110072867B (zh) 2022-07-08
NZ754115A (en) 2021-07-30
CA3045303C (en) 2022-05-17
PL3555105T3 (pl) 2021-05-17
US11001596B2 (en) 2021-05-11
US20210206780A1 (en) 2021-07-08
SI3555105T1 (sl) 2020-12-31
KR20190077539A (ko) 2019-07-03
MY197313A (en) 2023-06-13
EA201991161A1 (ru) 2019-11-29
IL267236A (en) 2019-08-29
BR112019009648A2 (pt) 2019-09-10
AU2020260493B2 (en) 2021-09-09
EP3763717A1 (en) 2021-01-13
DK3555105T3 (da) 2020-11-09
CN115109075B (zh) 2024-09-20
US11649247B2 (en) 2023-05-16
PT3555105T (pt) 2020-12-21
AU2017378060A1 (en) 2019-05-30

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