[go: up one dir, main page]
More Web Proxy on the site http://driver.im/

PE20212247A1 - Compuestos de 3-((3-aminofenil)amino)piperidina-2,6-diona sustituida, composiciones de estos y metodos de tratamiento con estos - Google Patents

Compuestos de 3-((3-aminofenil)amino)piperidina-2,6-diona sustituida, composiciones de estos y metodos de tratamiento con estos

Info

Publication number
PE20212247A1
PE20212247A1 PE2021000924A PE2021000924A PE20212247A1 PE 20212247 A1 PE20212247 A1 PE 20212247A1 PE 2021000924 A PE2021000924 A PE 2021000924A PE 2021000924 A PE2021000924 A PE 2021000924A PE 20212247 A1 PE20212247 A1 PE 20212247A1
Authority
PE
Peru
Prior art keywords
substituted
alkyl
amino
unsubstituted
aminophenyl
Prior art date
Application number
PE2021000924A
Other languages
English (en)
Inventor
Massimo Ammirante
Sogoie Bahmanyar
Matthew D Correa
Virginia Grant
Joshua Hansen
Evan J Horn
Timothy S Kercher
Christopher Mayne
Mark A Nagy
Rama Krishna Narla
Surendra Nayak
Stephen Norris
Patrick Papa
Veronique Plantevin-Krenitsky
John J Sapienza
Brandon W Whitefield
Shuichan Su
Original Assignee
Celgene Corp
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 Celgene Corp filed Critical Celgene Corp
Publication of PE20212247A1 publication Critical patent/PE20212247A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/92Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with a hetero atom directly attached to the ring nitrogen atom
    • C07D211/94Oxygen atom, e.g. piperidine N-oxide
    • 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
    • A61K31/495Heterocyclic 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
    • A61K31/496Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
    • 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
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/28Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D233/30Oxygen or sulfur atoms
    • 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
    • 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
    • C07D401/14Heterocyclic 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 three or more hetero rings
    • 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
    • C07D491/10Spiro-condensed systems
    • C07D491/107Spiro-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring

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)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

La invencion se refiere a compuestos derivados de 3-((3-aminofenil)amino)piperidina-2,6-diona de formula (IA); en donde RN es H; cada R1 se selecciona de halogeno, CN y C1-3 alquilo; cada R2 y R3 se selecciona independientemente de H y C1-3 alquilo, o R2 y R3 y el carbono al que estan unidos forman un C3-6 cicloalquilo sustituido o no sustituido; cada R4 es C1-3 alquilo sustituido o no sustituido, o dos grupos R4, junto con el mismo atomo de carbono o atomo o atomos de carbono adyacentes a los que estan unidos, forman un C3-6 cicloalquilo sustituido o no sustituido, o dos grupos R4 junto con los atomos de carbono no adyacentes a los que estan unidos forman un heterociclilo de 4-7 miembros sustituido o no sustituido; X es N; L es -O(C1-6 alquilo)- o -(C1-9 alquilo)-; n es 0-4; m es 0-8. Un compuesto seleccionado es formiato de 2-(4-(2-(4-(3-(6-ciano-5-(trifluorometil)piridin-3-il)-5,5-dimetil-4- oxo-2-tioxoimidazolidin-1-il)fenoxi)etil)piperazin-1-il)-N-(3-((2,6-dioxopiperidin-3- il)amino)fenil)acetamida. Dichos compuestos son mediadores de los receptores androgenico (AR), siendo utiles para el tratamiento de enfermedades mediadas por AR, tal como el cancer de prostata.
PE2021000924A 2018-12-19 2019-12-18 Compuestos de 3-((3-aminofenil)amino)piperidina-2,6-diona sustituida, composiciones de estos y metodos de tratamiento con estos PE20212247A1 (es)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US201862782298P 2018-12-19 2018-12-19
US201962879900P 2019-07-29 2019-07-29
PCT/US2019/067088 WO2020132014A1 (en) 2018-12-19 2019-12-18 Substituted 3-((3-aminophenyl)amino)piperidine-2,6-dione compounds, compositions thereof, and methods of treatment therewith

Publications (1)

Publication Number Publication Date
PE20212247A1 true PE20212247A1 (es) 2021-11-24

Family

ID=71098067

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2021000924A PE20212247A1 (es) 2018-12-19 2019-12-18 Compuestos de 3-((3-aminofenil)amino)piperidina-2,6-diona sustituida, composiciones de estos y metodos de tratamiento con estos

Country Status (16)

Country Link
US (3) US11149007B2 (es)
EP (1) EP3897636A4 (es)
JP (2) JP7494181B2 (es)
KR (1) KR20210118816A (es)
CN (1) CN113453681B (es)
AU (1) AU2019403207A1 (es)
BR (1) BR112021011968A2 (es)
CA (1) CA3124130A1 (es)
CL (1) CL2021001665A1 (es)
CO (1) CO2021007973A2 (es)
IL (1) IL284223A (es)
MX (1) MX2021007473A (es)
PE (1) PE20212247A1 (es)
SG (1) SG11202106507RA (es)
TW (1) TWI820276B (es)
WO (1) WO2020132014A1 (es)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20212247A1 (es) * 2018-12-19 2021-11-24 Celgene Corp Compuestos de 3-((3-aminofenil)amino)piperidina-2,6-diona sustituida, composiciones de estos y metodos de tratamiento con estos
MX2021007475A (es) 2018-12-19 2021-08-05 Celgene Corp Compuestos de 3-((3-aminofenil)amino)piperidina-2,6-diona sustituida, composiciones de estos y metodos de tratamiento con estos.
MX2022007678A (es) 2019-12-19 2022-09-19 Arvinas Operations Inc Compuestos y metodos para la degradacion dirigida del receptor de androgenos.
IL297762A (en) 2020-05-09 2022-12-01 Arvinas Operations Inc Methods for producing a bifunctional compound, ultrapure forms of the bifunctional compound, and dosage forms including it
CA3182325A1 (en) 2020-06-24 2021-12-30 Matthew D. Alexander Cereblon binding compounds, compositions thereof, and methods of treatment therewith
WO2021262815A1 (en) * 2020-06-24 2021-12-30 Celgene Corporation Cereblon binding compounds, compositions thereof, and methods of treatment therewith
CN115955979A (zh) * 2020-06-24 2023-04-11 新基公司 Cereblon结合化合物、其组合物及其用于治疗的方法
CA3186548A1 (en) 2020-07-21 2022-01-27 Song Hee Lee Compound for androgen receptor degradation, and pharmaceutical use thereof
WO2022061348A1 (en) 2020-09-16 2022-03-24 Biotheryx, Inc. Sos1 protein degraders, pharmaceutical compositions thereof, and their therapeutic applications
WO2022087335A1 (en) 2020-10-23 2022-04-28 Biotheryx, Inc. Kras protein degraders, pharmaceutical compositions thereof, and their therapeutic applications
US20240124418A1 (en) 2020-12-14 2024-04-18 Biotheryx, Inc. Pde4 degraders, pharmaceutical compositions, and therapeutic applications
WO2022272074A1 (en) * 2021-06-25 2022-12-29 Celgene Corporation Cereblon binding compounds, compositions thereof, and methods of treatment therewith
WO2022272053A1 (en) * 2021-06-25 2022-12-29 Celgene Corporation Cereblon binding compounds, compositions thereof, and methods of treatment therewith
WO2024102706A1 (en) * 2022-11-09 2024-05-16 Bristol-Myers Squibb Company Combination therapy with substituted 3-((3-aminophenyl)amino)piperidine-2,6-dione compounds

Family Cites Families (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4302485A1 (de) 1993-01-29 1994-08-04 Merck Patent Gmbh Piperazinderivate
HU228769B1 (en) 1996-07-24 2013-05-28 Celgene Corp Substituted 2(2,6-dioxopiperidin-3-yl)phthalimides and -1-oxoisoindolines and their use for production of pharmaceutical compositions for mammals to reduce the level of tnf-alpha
FR2768729A1 (fr) 1997-09-19 1999-03-26 Rhodia Chimie Sa Procede d'acylation d'un compose aromatique et complexes catalytiques
FR2768728B1 (fr) 1997-09-19 1999-12-03 Rhodia Chimie Sa Procede d'acylation d'un compose aromatique
US7629360B2 (en) 1999-05-07 2009-12-08 Celgene Corporation Methods for the treatment of cachexia and graft v. host disease
EP1790640A4 (en) * 2004-09-09 2009-07-29 Chugai Pharmaceutical Co Ltd NEW IMIDAZOLIDINE DERIVATIVE AND APPLICATION THEREOF
WO2007044804A2 (en) 2005-10-11 2007-04-19 Chemocentryx, Inc. Piperidine derivatives and methods of use
WO2007136640A2 (en) * 2006-05-16 2007-11-29 Celgene Corporation Processes for the preparation of substituted 2-(2,6-dioxopiperidin-3-yl)isoindole-1,3-dione
EP2453908B1 (en) 2009-07-13 2018-03-14 President and Fellows of Harvard College Bifunctional stapled polypeptides and uses thereof
RU2434851C1 (ru) 2010-07-22 2011-11-27 Александр Васильевич Иващенко Циклические n, n'-диарилтиомочевины или n, n'-диарилмочевины - антагонисты андрогенных рецепторов, противораковое средство, способ получения и применения
US8765978B2 (en) 2010-12-16 2014-07-01 Transitions Optical, Inc. Method of making indeno-fused naphthol materials
EP2683694B1 (en) 2011-03-10 2016-04-27 Suzhou Kintor Pharmaceuticals, Inc. Androgen receptor antagonists and uses thereof
WO2012135284A2 (en) 2011-03-28 2012-10-04 Cornell University Targeted protein silencing using chimeras between antibodies and ubiquitination enzymes
KR102668696B1 (ko) 2012-01-12 2024-05-29 예일 유니버시티 E3 유비퀴틴 리가아제에 의한 표적 단백질 및 다른 폴리펩티드의 증진된 분해를 위한 화합물 및 방법
RS61242B1 (sr) 2012-09-04 2021-01-29 Shanghai hengrui pharmaceutical co ltd Derivati imidazolina, postupci njihove pripreme i njihove primene u medicini
WO2014063061A1 (en) 2012-10-19 2014-04-24 Dana-Farber Cancer Institute, Inc. Hydrophobically tagged small molecules as inducers of protein degradation
MX368833B (es) 2013-01-31 2019-10-18 Vertex Pharma Derivados de quinolina y quinazolina amidas como inhibidores de canales de sodio nav1.8 y el uso de los mismos en el tratamiento del dolor.
US20160058872A1 (en) 2014-04-14 2016-03-03 Arvinas, Inc. Imide-based modulators of proteolysis and associated methods of use
RU2738833C9 (ru) 2014-04-14 2022-02-28 Арвинас, Оперэйшнз, Инк. Имидные модуляторы протеолиза и способы их применения
RU2557235C1 (ru) 2014-07-08 2015-07-20 Александр Васильевич Иващенко Замещенные 2-тиоксо-имидазолидин-4-оны и их спироаналоги, противораковый активный компонент, фармацевтическая композиция, лекарственный препарат, способ лечения рака простаты
EP3256470B1 (en) 2014-12-23 2023-07-26 Dana-Farber Cancer Institute, Inc. Methods to induce targeted protein degradation through bifunctional molecules
US9694084B2 (en) 2014-12-23 2017-07-04 Dana-Farber Cancer Institute, Inc. Methods to induce targeted protein degradation through bifunctional molecules
BR112017015497A2 (pt) 2015-01-20 2018-01-30 Arvinas, Inc. composto, e, composição
EP4414369A3 (en) 2015-03-18 2024-10-16 Arvinas, Inc. Compounds and methods for the enhanced degradation of targeted proteins
GB201506871D0 (en) 2015-04-22 2015-06-03 Glaxosmithkline Ip Dev Ltd Novel compounds
WO2017011371A1 (en) 2015-07-10 2017-01-19 Arvinas, Inc Mdm2-based modulators of proteolysis and associated methods of use
WO2017030814A1 (en) 2015-08-19 2017-02-23 Arvinas, Inc. Compounds and methods for the targeted degradation of bromodomain-containing proteins
TWI726969B (zh) * 2016-01-11 2021-05-11 比利時商健生藥品公司 用作雄性激素受體拮抗劑之經取代之硫尿囊素衍生物
EP3455218A4 (en) 2016-05-10 2019-12-18 C4 Therapeutics, Inc. C3 CARBON-BASED GLUTARIMIDE DEGRONIMERS FOR TARGET PROTEIN REDUCTION
CN110167556A (zh) 2016-07-08 2019-08-23 詹森药业有限公司 用于治疗癌症的硫代乙内酰脲雄性激素受体拮抗剂
TWI739888B (zh) 2016-10-07 2021-09-21 美商陶氏農業科學公司 農藥組合物及方法
EP3526202A4 (en) 2016-10-11 2020-04-29 Arvinas, Inc. COMPOUNDS AND METHODS FOR TARGETED DEGRADATION OF ANDROGEN RECEPTOR
US10925868B2 (en) 2016-11-10 2021-02-23 Dana-Farber Cancer Institute, Inc. Degradation of protein kinases by conjugation of protein kinase inhibitors with E3 ligase ligand and methods of use
WO2018098280A1 (en) 2016-11-22 2018-05-31 Dana-Farber Cancer Institute, Inc. Degradation of protein kinases by conjugation of protein kinase inhibitors with e3 ligase ligand and methods of use
EP3524603B1 (en) 2016-12-19 2022-06-08 Abbisko Therapeutics Co., Ltd. Fgfr4 inhibitor, preparation method therefor and pharmaceutical use thereof
CA3050309A1 (en) 2017-01-31 2018-08-09 Arvinas Operations, Inc. Cereblon ligands and bifunctional compounds comprising the same
WO2018237026A1 (en) 2017-06-20 2018-12-27 C4 Therapeutics, Inc. N / O-LINKED DEGRONS AND DEGRONIMERS FOR DEGRADATION OF PROTEINS
CN109422725A (zh) 2017-09-04 2019-03-05 北京美倍他药物研究有限公司 前列腺癌治疗药物
HUE064356T2 (hu) 2017-11-28 2024-03-28 Aarti Pharmalabs Ltd Eljárás enzalutamid elõállítására új intermedier felhasználásával
US20210380576A1 (en) 2017-12-05 2021-12-09 Dow Agrosciences Llc Pesticidal compositions and methods
KR20210018304A (ko) 2018-05-30 2021-02-17 장쑤 한서 파마슈티칼 그룹 캄파니 리미티드 트리사이클릭 유도체를 함유하는 억제제, 이를 위한 제조 방법, 및 이의 적용
CN109651256A (zh) 2018-11-20 2019-04-19 上海健康医学院 一种式(viii)的恩杂鲁胺的制备方法
MX2021007475A (es) 2018-12-19 2021-08-05 Celgene Corp Compuestos de 3-((3-aminofenil)amino)piperidina-2,6-diona sustituida, composiciones de estos y metodos de tratamiento con estos.
PE20212247A1 (es) * 2018-12-19 2021-11-24 Celgene Corp Compuestos de 3-((3-aminofenil)amino)piperidina-2,6-diona sustituida, composiciones de estos y metodos de tratamiento con estos

Also Published As

Publication number Publication date
JP2022514344A (ja) 2022-02-10
BR112021011968A2 (pt) 2021-09-08
IL284223A (en) 2021-08-31
US20230002321A1 (en) 2023-01-05
US11873283B2 (en) 2024-01-16
EP3897636A1 (en) 2021-10-27
JP7494181B2 (ja) 2024-06-03
AU2019403207A1 (en) 2021-07-15
EP3897636A4 (en) 2022-09-07
JP2024109765A (ja) 2024-08-14
CN113453681A (zh) 2021-09-28
MX2021007473A (es) 2021-08-05
KR20210118816A (ko) 2021-10-01
US11149007B2 (en) 2021-10-19
TWI820276B (zh) 2023-11-01
TW202039435A (zh) 2020-11-01
US20200199073A1 (en) 2020-06-25
US20240368083A1 (en) 2024-11-07
CN113453681B (zh) 2024-10-11
CL2021001665A1 (es) 2022-01-14
WO2020132014A1 (en) 2020-06-25
SG11202106507RA (en) 2021-07-29
CO2021007973A2 (es) 2021-09-09
CA3124130A1 (en) 2020-06-25

Similar Documents

Publication Publication Date Title
PE20212247A1 (es) Compuestos de 3-((3-aminofenil)amino)piperidina-2,6-diona sustituida, composiciones de estos y metodos de tratamiento con estos
AR085960A1 (es) 1,3-oxazinas como inhibidores de la bace1 y/o de la bace2
CL2020001919A1 (es) Inhibidores de endonucleasa cap-dependientes.
PE20190409A1 (es) Compuesto heterociclico
AR102426A1 (es) Compuestos de indolcarboxamida como inhibidores de btk
PH12014502866A1 (en) Fungicidal heterocyclic carboxamides
PE20190518A1 (es) Inhibidores de diacilglicerol aciltransferasa 2
PE20181298A1 (es) Inhibidores de bromodominio bivalentes y usos de los mismos
AR056691A1 (es) Derivados pirrolopirimidina como inhibidores de syk
TR201909160T4 (tr) Metabotropik glutamat reseptörü modülatörleri olarak etinil türevleri.
PE20181449A1 (es) Compuestos utiles como inhibidores de cinasa
AR086198A1 (es) Inhibidores sustituidos de acetil-coa carboxilasa y composiciones farmaceuticas que los contienen
PE20160995A1 (es) Inhibidores de syk
PE20151951A1 (es) Heteroarildihidropirimidinas unidas por puentes en 6 para el tratamiento y la profilaxis de infeccion por el virus de la hepatitis b
PE20151601A1 (es) Compuestos novedosos de pirimidina y piridina y su uso
AR054560A1 (es) Espiropiperidina como inhibidores de beta-secretasa para el tratamiento de la enfermedad de alzheimer
PE20131143A1 (es) Nuevas aminopirazoloquinazolinas
AR075635A1 (es) N-alcoxiamidas de 6-(fenil sustituido)-4-aminopicolinatos y 2-(fenil sustituido)-6-amino-4-pirimidina carboxilatos, su uso como herbicidas selectivos para las cosechas y proceso de preparacion de dichos compuestos
AR066155A1 (es) Compuestos de pirazol, simil tiroideo, composicion farmaceutica, proceso y uso en terapia
PE20080068A1 (es) Compuestos derivados de pirimidina como inhibidores de la quinasa aurora
RS54288B1 (en) SUBSTITUTED TRIAZOLOPYRIDINES AND THEIR USE AS TTK INHIBITORS
PE20180233A1 (es) Nuevos compuestos biciclicos como inhibidores duales de atx / ca
AR074021A1 (es) Compuestos heterociclicos fusionados como moduladores del canal ionico
PE20141380A1 (es) Imidazopiridazinas como inhibidores de quinasa akt
PE20170946A1 (es) 2-amino-6-(difluorometil)- 5,5-difluoro-6-fenil-3,4,5,6-tetrahidropiridinas como inhibidores de bace1