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PE20210400A1 - Degradadores selectivos del receptor de estrogeno - Google Patents

Degradadores selectivos del receptor de estrogeno

Info

Publication number
PE20210400A1
PE20210400A1 PE2020002017A PE2020002017A PE20210400A1 PE 20210400 A1 PE20210400 A1 PE 20210400A1 PE 2020002017 A PE2020002017 A PE 2020002017A PE 2020002017 A PE2020002017 A PE 2020002017A PE 20210400 A1 PE20210400 A1 PE 20210400A1
Authority
PE
Peru
Prior art keywords
cancer
benzopyrano
azetidin
quinolin
fluoromethyl
Prior art date
Application number
PE2020002017A
Other languages
English (en)
Inventor
Jolie Anne Bastian
Jeffrey Daniel Cohen
Almudena Rubio
Daniel Sall
Original Assignee
Lilly Co Eli
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=67470734&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20210400(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Lilly Co Eli filed Critical Lilly Co Eli
Publication of PE20210400A1 publication Critical patent/PE20210400A1/es

Links

Classifications

    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/4353Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/436Heterocyclic 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 ortho- or peri-condensed with heterocyclic ring systems the heterocyclic ring system containing a six-membered ring having oxygen as a ring hetero atom, e.g. rapamycin
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D491/00Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
    • C07D491/02Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/052Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being six-membered
    • 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
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4709Non-condensed quinolines 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
    • A61K31/435Heterocyclic 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
    • A61K31/47Quinolines; Isoquinolines
    • A61K31/4738Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/4741Quinolines; Isoquinolines ortho- or peri-condensed with heterocyclic ring systems condensed with ring systems having oxygen as a ring hetero atom, e.g. tubocuraran derivatives, noscapine, bicuculline
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K45/00Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
    • A61K45/06Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00Medicinal preparations characterised by special physical form
    • A61K9/0012Galenical forms characterised by the site of application
    • A61K9/0053Mouth and digestive tract, i.e. intraoral and peroral administration
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/12Heterocyclic 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 linked by a chain containing hetero atoms as chain links

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Epidemiology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Nutrition Science (AREA)
  • Physiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Steroid Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Finger-Pressure Massage (AREA)
  • Orthopedics, Nursing, And Contraception (AREA)

Abstract

Se proporcionan compuestos de formula (I), donde R1 o R2 se selecciona de Cl, F, -CF3, o -CH3, y el otro es hidrogeno. Son compuestos preferidos: 5-(4-{2-[3-(fluorometil)azetidin-1-il]etoxi}fenil)-8-(trifluorometil)-5H-[1]benzopirano[4,3-c]quinolin-2-ol; 5-(4-{2-[3-(fluorometil)azetidin-1-il]etoxi}fenil)-7-(trifluorometil)-5H-[1]benzopirano[4,3-c]quinolin-2-ol; 8-cloro-5-(4-{2-[3-(fluorometil)azetidin-1-il]etoxi}fenil)-5H-[1]benzopirano[4,3-c]quinolin-2-ol; entre otros. Dichos compuestos son degradadores selectivos del receptor de estrogeno (SERD) y son utiles en el tratamiento de tipos de cancer, tales como cancer de mama, cancer de ovario, cancer de endometrio, cancer de prostata, cancer de utero, cancer gastrico y cancer de pulmon, asi como mutaciones debido a una resistencia emergente.
PE2020002017A 2018-07-12 2019-07-11 Degradadores selectivos del receptor de estrogeno PE20210400A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201862697100P 2018-07-12 2018-07-12
PCT/US2019/041334 WO2020014435A1 (en) 2018-07-12 2019-07-11 Selective estrogen receptor degraders

Publications (1)

Publication Number Publication Date
PE20210400A1 true PE20210400A1 (es) 2021-03-02

Family

ID=67470734

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2020002017A PE20210400A1 (es) 2018-07-12 2019-07-11 Degradadores selectivos del receptor de estrogeno

Country Status (37)

Country Link
US (4) US10654866B2 (es)
EP (2) EP3820873B1 (es)
JP (6) JP6995241B2 (es)
KR (3) KR102783756B1 (es)
CN (2) CN117379428A (es)
AR (1) AR115694A1 (es)
AU (2) AU2019299947B2 (es)
BR (1) BR122023025061A2 (es)
CA (1) CA3105501C (es)
CL (1) CL2021000045A1 (es)
CO (1) CO2021000043A2 (es)
CR (1) CR20210007A (es)
DK (1) DK3820873T3 (es)
EA (1) EA202092975A1 (es)
EC (1) ECSP21001770A (es)
ES (1) ES2933980T3 (es)
FI (1) FI3820873T3 (es)
HR (1) HRP20230009T1 (es)
HU (1) HUE060963T2 (es)
IL (3) IL289871B2 (es)
JO (1) JOP20210005A1 (es)
LT (1) LT3820873T (es)
MA (2) MA53124B1 (es)
MD (1) MD3820873T2 (es)
MX (2) MX2021000375A (es)
MY (1) MY198962A (es)
PE (1) PE20210400A1 (es)
PH (1) PH12021550049A1 (es)
PL (1) PL3820873T3 (es)
PT (1) PT3820873T (es)
RS (1) RS63809B1 (es)
SA (1) SA521421008B1 (es)
SG (1) SG11202100148TA (es)
SI (1) SI3820873T1 (es)
TW (1) TWI702219B (es)
UA (1) UA127507C2 (es)
WO (1) WO2020014435A1 (es)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113248494A (zh) 2015-10-01 2021-08-13 奥列马制药公司 四氢-1H-吡啶[3,4-b]吲哚类抗雌激素药物
TWI702219B (zh) * 2018-07-12 2020-08-21 美商美國禮來大藥廠 選擇性雌激素受體降解劑
SG11202100145YA (en) * 2018-07-12 2021-02-25 Lilly Co Eli Selective estrogen receptor degraders
AU2020311337A1 (en) 2019-07-07 2022-01-20 Olema Pharmaceuticals, Inc. Regimens of estrogen receptor antagonists
US12528768B2 (en) 2019-12-09 2026-01-20 Sanofi Crystalline form of a 7H-benzo[7]annulene-2-carboxylic acid derivative
TW202146007A (zh) * 2020-02-27 2021-12-16 法商賽諾菲公司 包含阿培利司(alpelisib)與6-(2,4-二氯苯基)-5-[4-[(3s)-1-(3-氟丙基)吡咯啶-3-基]氧苯基]-8,9-二氫-7h-苯并[7]輪烯-2-羧酸之組合
CN116782895A (zh) * 2020-11-23 2023-09-19 赛诺菲 包含阿贝西利和6-(2,4-二氯苯基)-5-[4-[(3s)-1-(3-氟丙基)吡咯烷-3-基]氧基苯基]-8,9-二氢-7h-苯并[7]轮烯-2-甲酸的组合
EP4294394A1 (en) * 2021-02-16 2023-12-27 Genentech, Inc. Treatment of breast cancer using combination therapies comprising gdc-9545 and abemaciclib or ribociclib
CN114957114A (zh) * 2021-02-26 2022-08-30 冷志 一种4-溴-3-氯-7-甲氧基喹啉的合成方法
CN117042771A (zh) * 2021-03-09 2023-11-10 伊莱利利公司 使用serd给药方案的组合治疗癌症的方法
TWI837605B (zh) * 2021-03-09 2024-04-01 美商美國禮來大藥廠 使用serd組合給藥方案治療癌症之方法
TWI894443B (zh) * 2021-03-16 2025-08-21 美商美國禮來大藥廠 選擇性雌激素受體降解劑
KR102743629B1 (ko) * 2022-02-01 2024-12-17 일라이 릴리 앤드 캄파니 선택적 에스트로겐 수용체 분해제의 제조 방법
TW202430176A (zh) 2022-10-17 2024-08-01 瑞典商阿斯特捷利康公司 用於治療癌症之組合療法
WO2024097206A1 (en) 2022-11-02 2024-05-10 Petra Pharma Corporation Allosteric chromenone inhibitors of phosphoinositide 3-kinase (pi3k) for the treatment of disease
CN120187416A (zh) 2022-11-11 2025-06-20 阿斯利康(瑞典)有限公司 用于治疗癌症的组合疗法
US20240180893A1 (en) 2022-11-17 2024-06-06 Astrazeneca Ab Methods of treatment of breast cancer
AU2024268541A1 (en) 2023-05-05 2025-11-20 Eli Lilly And Company Imlunestrant or salts thereof for use in treating and preventing central nervous system (cns) metastases in subjects having er+ breast cancer
CN121079090A (zh) 2023-05-11 2025-12-05 阿斯利康(瑞典)有限公司 用于治疗癌症的parp1抑制剂和选择性雌激素降解剂的组合

Family Cites Families (11)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP1395563B1 (en) * 2001-05-22 2006-03-29 Eli Lilly And Company 2-substituted 1,2,3,4-tetrahydroquinolines and derivatives thereof, compositions and methods
US7329654B2 (en) * 2001-12-19 2008-02-12 Janssen Pharmaceutica N.V. Heteroatom containing tetracyclic derivatives as selective estrogen receptor modulators
MXPA04010433A (es) * 2002-04-19 2005-08-19 Signal Pharm Inc Compuestos benzopiranona, composiciones de estos y los metodos para el tratamiento con estos.
WO2005073204A1 (en) 2004-01-22 2005-08-11 Eli Lilly And Company Selective estrogen receptor modulators for the treatment of vasomotor symptoms
US20080221163A1 (en) * 2005-01-18 2008-09-11 Jeffrey Alan Dodge Selective Estrogen Receptor Modulators
JP6389517B2 (ja) 2013-06-19 2018-09-12 セラゴン ファーマシューティカルズ, インク. アゼチジンエストロゲン受容体調節因子及びその使用
CN112375077A (zh) * 2014-12-18 2021-02-19 豪夫迈·罗氏有限公司 四氢-吡啶并[3,4-b]吲哚雌激素受体调节剂及其用途
US9845291B2 (en) * 2014-12-18 2017-12-19 Genentech, Inc. Estrogen receptor modulators and uses thereof
WO2018108954A1 (en) 2016-12-12 2018-06-21 F. Hoffmann-La Roche Ag Process for the preparation of 2-(3-(fluoromethyl)azetidin-1-yl)ethan-1-ol
SG11202100145YA (en) * 2018-07-12 2021-02-25 Lilly Co Eli Selective estrogen receptor degraders
TWI702219B (zh) * 2018-07-12 2020-08-21 美商美國禮來大藥廠 選擇性雌激素受體降解劑

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JP2024169490A (ja) 2024-12-05
CL2021000045A1 (es) 2021-07-19
MA53126B1 (fr) 2023-02-28
MA53124B1 (fr) 2023-02-28
CN112638916B (zh) 2023-09-12
AU2019299947B2 (en) 2022-03-17
EP4155310A1 (en) 2023-03-29
IL289871A (en) 2022-03-01
EP3820873B1 (en) 2022-11-23
JP7746496B2 (ja) 2025-09-30
CN112638916A (zh) 2021-04-09
ES2933980T3 (es) 2023-02-15
SG11202100148TA (en) 2021-02-25
US20200017516A1 (en) 2020-01-16
CA3105501C (en) 2023-10-31
FI3820873T3 (fi) 2023-03-02
IL289871B (en) 2022-10-01
US20230234960A1 (en) 2023-07-27
PH12021550049A1 (en) 2021-09-20
EA202092975A1 (ru) 2021-04-14
EP3820873A1 (en) 2021-05-19
BR122023025061A2 (pt) 2024-02-20
CR20210007A (es) 2021-02-08
TWI702219B (zh) 2020-08-21
US10654866B2 (en) 2020-05-19
US11117902B2 (en) 2021-09-14
SA521421008B1 (ar) 2022-10-30
DK3820873T3 (da) 2022-12-12
AU2019299947A1 (en) 2021-01-07
KR20230005404A (ko) 2023-01-09
JP7009672B1 (ja) 2022-01-25
KR20210019065A (ko) 2021-02-19
US20210403480A1 (en) 2021-12-30
KR102783756B1 (ko) 2025-03-21
JP2022050591A (ja) 2022-03-30
MA53124A (fr) 2021-05-19
US11634426B2 (en) 2023-04-25
PT3820873T (pt) 2022-12-23
NZ771718A (en) 2024-05-31
LT3820873T (lt) 2023-01-10
PL3820873T3 (pl) 2023-02-13
IL289871B2 (en) 2023-02-01
UA127507C2 (uk) 2023-09-13
JP2025186400A (ja) 2025-12-23
HRP20230009T1 (hr) 2023-02-17
MA53126A (fr) 2021-05-19
TW202019935A (zh) 2020-06-01
HUE060963T2 (hu) 2023-04-28
AU2022203969B2 (en) 2024-02-15
JP7241211B2 (ja) 2023-03-16
RS63809B1 (sr) 2023-01-31
JP6995241B2 (ja) 2022-01-14
KR20230148386A (ko) 2023-10-24
CA3105501A1 (en) 2020-01-16
WO2020014435A1 (en) 2020-01-16
MD3820873T2 (ro) 2023-05-31
MY198962A (en) 2023-10-05
JP2021530484A (ja) 2021-11-11
JOP20210005A1 (ar) 2021-01-10
SI3820873T1 (sl) 2023-02-28
IL295598A (en) 2022-10-01
AU2022203969A1 (en) 2022-06-30
JP2022037102A (ja) 2022-03-08
KR102589886B1 (ko) 2023-10-17
IL295598B1 (en) 2023-05-01
IL280065A (en) 2021-03-01
CN117379428A (zh) 2024-01-12
BR112020025654A2 (pt) 2021-04-06
CO2021000043A2 (es) 2021-01-18
JP7557564B2 (ja) 2024-09-27
MX2021000375A (es) 2021-05-27
ECSP21001770A (es) 2021-02-26
IL295598B2 (en) 2023-09-01
AR115694A1 (es) 2021-02-17
KR102550538B1 (ko) 2023-07-04
US20200347073A1 (en) 2020-11-05
IL280065B (en) 2022-04-01
JP2023081954A (ja) 2023-06-13
MX2023006047A (es) 2023-06-02
US11993608B2 (en) 2024-05-28

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