[go: up one dir, main page]

PE20240886A1 - Compuestos espirociclicos - Google Patents

Compuestos espirociclicos

Info

Publication number
PE20240886A1
PE20240886A1 PE2024000416A PE2024000416A PE20240886A1 PE 20240886 A1 PE20240886 A1 PE 20240886A1 PE 2024000416 A PE2024000416 A PE 2024000416A PE 2024000416 A PE2024000416 A PE 2024000416A PE 20240886 A1 PE20240886 A1 PE 20240886A1
Authority
PE
Peru
Prior art keywords
alkyl
ccl
independently
formula
pharmaceutically acceptable
Prior art date
Application number
PE2024000416A
Other languages
English (en)
Inventor
James Michael Smith
Graeme Richard Robb
Piotr Antoni Raubo
Bernard Christophe Barlaam
Iain Alexander Cumming
Original Assignee
Astrazeneca Ab
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 Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of PE20240886A1 publication Critical patent/PE20240886A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D519/00Heterocyclic compounds containing more than one system of two or more relevant hetero rings condensed among themselves or condensed with a common carbocyclic ring system not provided for in groups C07D453/00 or C07D455/00
    • 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
    • A61K31/437Heterocyclic 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 five-membered ring having nitrogen as a ring hetero atom, e.g. indolizine, beta-carboline
    • 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
    • C07D487/10Spiro-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
    • A61K31/435Heterocyclic 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
    • A61K31/438The ring being spiro-condensed with carbocyclic or heterocyclic ring systems
    • 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
    • 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
    • C07D471/20Spiro-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)

Abstract

La presente invencion se refiere a compuestos espirociclicos de Formula (I) y sales farmaceuticamente aceptables de estos, tambien a procesos y productos intermedios usados para su preparacion, a composiciones farmaceuticas que los contienen y a su uso en el tratamiento de trastornos proliferativos celulares como el cancer de pancreas, colorrectal, de utero, entre otros. En particular, la invencion se refiere a un compuesto de Formula (I), o una sal farmaceuticamente aceptable de este, en donde: el anillo que contiene X e Y es un pirrol y X es NH e Y es CH o X es CH e Y es NH; Z se selecciona entre CH, CF, CCl o, si Q no es N, N; Q se selecciona entre CH, CF, CCl o, si Z no es N, N; m es 0, 1 o 2; n es 0, 1 o 2; p es 1 o 2; R1 se selecciona, en cada caso, independientemente entre F, Cl, CN, entre otros; R2 se selecciona, en cada caso, independientemente entre F, Cl, Me, entre otros; R3 es H, Me, alquilo C1-C3 o fluoroalquilo C1-C3; R4 es H, Me o alquilo C1-C3; R5 es H, Me, alquilo C1-C3, entre otros.
PE2024000416A 2021-09-13 2022-09-12 Compuestos espirociclicos PE20240886A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US202163243267P 2021-09-13 2021-09-13
PCT/EP2022/075248 WO2023036974A1 (en) 2021-09-13 2022-09-12 Spirocyclic compounds

Publications (1)

Publication Number Publication Date
PE20240886A1 true PE20240886A1 (es) 2024-04-24

Family

ID=83688613

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2024000416A PE20240886A1 (es) 2021-09-13 2022-09-12 Compuestos espirociclicos

Country Status (19)

Country Link
US (2) US11939344B2 (es)
EP (1) EP4402143A1 (es)
JP (1) JP7406674B2 (es)
KR (1) KR102624567B1 (es)
CN (1) CN117916241A (es)
AR (1) AR127050A1 (es)
AU (1) AU2022343903A1 (es)
CA (1) CA3230648A1 (es)
CL (1) CL2024000714A1 (es)
CO (1) CO2024002844A2 (es)
CR (1) CR20240160A (es)
DO (1) DOP2024000041A (es)
EC (1) ECSP24028270A (es)
IL (1) IL311254A (es)
MX (1) MX2024003076A (es)
PE (1) PE20240886A1 (es)
TW (1) TW202330538A (es)
WO (1) WO2023036974A1 (es)
ZA (1) ZA202400595B (es)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2023327684A1 (en) 2022-08-15 2025-03-20 Astrazeneca Ab Mta-cooperative prmt5 inhibitors for use in the treatment of cancer
WO2024170488A1 (en) 2023-02-13 2024-08-22 Astrazeneca Ab Prmt5 inhibitor for use in cancer therapy
WO2024188999A1 (en) 2023-03-13 2024-09-19 Astrazeneca Ab Crystalline form
WO2024255863A1 (zh) * 2023-06-16 2024-12-19 中山优理生物医药有限公司 一种氨基吡啶类化合物、其制备方法、包含其药物组合物及其应用
WO2025059579A1 (en) 2023-09-15 2025-03-20 Ideaya Biosciences, Inc. Methods of treating mat2a related diseases
WO2025064750A1 (en) 2023-09-20 2025-03-27 Ideaya Biosciences, Inc. Combination therapy with a parg inhibitor
WO2025072544A1 (en) 2023-09-27 2025-04-03 Ideaya Biosciences, Inc. Sulfonamino indazole compounds as inhibitors of parg

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5324483B1 (en) 1992-10-08 1996-09-24 Warner Lambert Co Apparatus for multiple simultaneous synthesis
US8455477B2 (en) * 2008-08-05 2013-06-04 Merck Sharp & Dohme Corp. Therapeutic compounds
CN109415336B (zh) 2016-04-06 2023-08-29 密执安大学评议会 Mdm2蛋白质降解剂
CA3112591A1 (en) 2018-10-08 2020-04-16 The Regents Of The University Of Michigan Small molecule mdm2 protein degraders

Also Published As

Publication number Publication date
AR127050A1 (es) 2023-12-13
KR102624567B1 (ko) 2024-01-11
CN117916241A (zh) 2024-04-19
KR20230091198A (ko) 2023-06-22
IL311254A (en) 2024-05-01
WO2023036974A1 (en) 2023-03-16
CR20240160A (es) 2024-05-30
JP2023549418A (ja) 2023-11-24
ECSP24028270A (es) 2024-05-31
US20240270757A1 (en) 2024-08-15
AU2022343903A1 (en) 2024-05-02
JP7406674B2 (ja) 2023-12-27
MX2024003076A (es) 2024-03-27
ZA202400595B (en) 2024-09-25
US11939344B2 (en) 2024-03-26
DOP2024000041A (es) 2024-04-15
TW202330538A (zh) 2023-08-01
EP4402143A1 (en) 2024-07-24
CL2024000714A1 (es) 2024-09-27
US20230357279A1 (en) 2023-11-09
CA3230648A1 (en) 2023-03-16
CO2024002844A2 (es) 2024-03-18

Similar Documents

Publication Publication Date Title
PE20240886A1 (es) Compuestos espirociclicos
ECSP034475A (es) Derivados de 4-fenil-piridin como antagonistas del receptor de neuroquinina-1
AR106755A2 (es) Inhibidores pirrólicos de la proteína quinasa erk, síntesis e intermediarios de los mismos
PE20181298A1 (es) Inhibidores de bromodominio bivalentes y usos de los mismos
AR044402A1 (es) Compuestos heterociclicos y su uso como inmunodepresores. composiciones farmaceuticas que los contienen.
AR088919A2 (es) Derivados de pirazol, composiciones que contienen dichos compuestos y uso
AR036106A1 (es) Compuestos azaindoles inhibidores de quinasa selectivos, composiciones farmaceuticas y el uso de dicha composicion para la fabricacion de un medicamento
AR046297A1 (es) Inhibidores de la dpp - iv metodos para prepararlos y composiciones farmaceuticas que los contienen como agente activo
AR062666A1 (es) Benzotriazoles como moduladores de quinasas
PE20242071A1 (es) Compuestos moduladores de diacilglicerol quinasa
AR065863A1 (es) Derivados de imidazolidinona
UY29312A1 (es) Piperazin-1-carboxamidas n,4,sustituidas y sus derivados, composiciones que los contienen, procedimientos de preparación y aplicaciones
PE20181017A1 (es) Compuestos heteroarilo y su uso como farmacos terapeuticos
CO2023000056A2 (es) Derivados de amidopirimidona
PE20211769A1 (es) Compuestos heteroaromaticos como inhibidores de vanina
CO2020001326A2 (es) Nuevos compuestos heterocíclicos como inhibidores de cdk8/19
PE20190964A1 (es) Inhibidores de dopamina-b-hidroxilasa penetrantes de la barrera hematoencefalica
PE20240894A1 (es) Compuesto inductor de la degradacion de plk1 novedoso
MX389378B (es) Derivados de amino-imidazopiridina novedosos como inhibidores de cinasa de janus y uso farmacéutico de estos.
ECSP088257A (es) Derivados de amida
AR053835A1 (es) Tetrahidropiridoazepin - 8 - onas como moduladores del receptor de dopamina d2 y compuestos relacionados para el tratamiento de la esquizofrenia y otros trastornos del snc, composiciones farmaceuticas que los contienen y su empleo en la preparacion de medicamentos.
AR046753A1 (es) Derivados de benzoxazina y usos de los mismos
AR066150A1 (es) Compuestos de benzotriazollilfenol sililados sustituidos
AR118641A1 (es) Compuestos, composiciones y métodos
AR088639A1 (es) Composicion farmaceutica oftalmica, compuestos antimicrobianos a base de carbolina