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AR120896A1 - COMPUESTO DE PIRIDAZINIL-TIAZOLCARBOXAMIDA COMO INHIBIDORES DE DGKz - Google Patents

COMPUESTO DE PIRIDAZINIL-TIAZOLCARBOXAMIDA COMO INHIBIDORES DE DGKz

Info

Publication number
AR120896A1
AR120896A1 ARP200103641A ARP200103641A AR120896A1 AR 120896 A1 AR120896 A1 AR 120896A1 AR P200103641 A ARP200103641 A AR P200103641A AR P200103641 A ARP200103641 A AR P200103641A AR 120896 A1 AR120896 A1 AR 120896A1
Authority
AR
Argentina
Prior art keywords
alkyl
group
halogen
methyl
optionally substituted
Prior art date
Application number
ARP200103641A
Other languages
English (en)
Inventor
Kozo Miyasaka
Akihiko Nakamura
Yoshinori Iwai
Hiroshi Tomiyama
Osamu Ikeda
Kazuo Kurosawa
Keiichiro Okuyama
Yohei Seki
Hideyuki Watanabe
Original Assignee
Astellas Pharma Inc
Kotobuki Pharmaceutical Co Ltd
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 Astellas Pharma Inc, Kotobuki Pharmaceutical Co Ltd filed Critical Astellas Pharma Inc
Publication of AR120896A1 publication Critical patent/AR120896A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero 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
    • A61K31/495Heterocyclic 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
    • A61K31/50Pyridazines; Hydrogenated pyridazines
    • A61K31/501Pyridazines; Hydrogenated pyridazines not condensed 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
    • A61K31/535Heterocyclic 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53771,4-Oxazines, e.g. morpholine not condensed and containing further heterocyclic rings, e.g. timolol
    • 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
    • A61K31/53751,4-Oxazines, e.g. morpholine
    • A61K31/53861,4-Oxazines, e.g. morpholine spiro-condensed or forming part of bridged 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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
    • C07D471/02Heterocyclic 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 two hetero rings
    • C07D471/10Spiro-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
    • C07D487/02Heterocyclic 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
    • 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
    • C07D498/10Spiro-condensed systems

Landscapes

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

Abstract

Compuestos derivados de piridazinil-tiazolcarboxamida con actividad inhibitoria de DGKz, composición farmacéutica e inhibidor de DGKz que comprende a uno de éstos compuestos y el uso de los mismos para el tratamiento del cáncer relacionado con la activación de células inmunitarias o del cáncer que ofrece resistencia a un tratamiento con anticuerpos anti PD1 / anticuerpos anti PD-L1. Reivindicación 1: Un compuesto de fórmula (1) o una sal de este, caracterizado por que: R¹ es un grupo de fórmula seleccionado del grupo de fórmulas (2), R² es un alquilo C₁₋₆, un cicloalquilo C₃₋₅, un -O-(alquilo C₁₋₆), metanosulfonilo, un halógeno-alquilo C₁₋₆ o un halógeno, R³ es I) un fenilo opcionalmente sustituido con un grupo que se selecciona del grupo que consiste en un alquilo C₁₋₆, un halógeno-alquilo C₁₋₆, un cicloalquilo C₃₋₅, un -O-(alquilo C₁₋₆), un -O-(halógeno-alquilo C₁₋₆), ciano, nitro, metanosulfonilo y un halógeno, II) un cicloalquilo C₃₋₈ opcionalmente sustituido con un grupo que se selecciona del grupo que consiste en alquilo C₁₋₆ y un halógeno, III) un piridilo opcionalmente sustituido con un grupo que se selecciona del grupo que consiste en un alquilo C₁₋₆, un halógeno alquilo C₁₋₆, un cicloalquilo C₃₋₅, un -O-(alquilo C₁₋₆), un -O-(halógeno alquilo C₁₋₆), ciano, nitro, metanosulfonilo y un halógeno, IV) un pirazolilo opcionalmente sustituido con un grupo que se selecciona del grupo que consiste en un alquilo C₁₋₆ y un halógeno, o V) un pirrolidinilo opcionalmente sustituido con un alquilo C₁₋₆, R⁴ es H o F, L es un enlace, CO, SO₂, O ó NH, X es CH₂, O ó N-metilo, Y es CH₂ u O, Rᵃ es H o metilo, Rᵇ es H, metilo, etilo o -(CH₂)₂O-CH₃, Rᶜ es H, metilo u oxetanilo, Rᵈ es H, metilo, -(CH₂)₂OH, -(CH₂)₂O-CH₃ u oxetanilo, m es 1 ó 2, y n es 1 ó 2.
ARP200103641A 2019-12-25 2020-12-23 COMPUESTO DE PIRIDAZINIL-TIAZOLCARBOXAMIDA COMO INHIBIDORES DE DGKz AR120896A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2019233673 2019-12-25

Publications (1)

Publication Number Publication Date
AR120896A1 true AR120896A1 (es) 2022-03-30

Family

ID=76574296

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP200103641A AR120896A1 (es) 2019-12-25 2020-12-23 COMPUESTO DE PIRIDAZINIL-TIAZOLCARBOXAMIDA COMO INHIBIDORES DE DGKz

Country Status (29)

Country Link
EP (1) EP4083038B1 (es)
JP (1) JP6948659B1 (es)
KR (1) KR20220119702A (es)
CN (3) CN115626919A (es)
AR (1) AR120896A1 (es)
AU (1) AU2020413997A1 (es)
BR (1) BR112022012637A2 (es)
CA (1) CA3165889A1 (es)
CL (1) CL2022001752A1 (es)
CO (1) CO2022009124A2 (es)
CR (1) CR20220328A (es)
DK (1) DK4083038T3 (es)
DO (1) DOP2022000137A (es)
EC (1) ECSP22057324A (es)
ES (1) ES2995459T3 (es)
FI (1) FI4083038T3 (es)
HR (1) HRP20241588T1 (es)
IL (1) IL294136A (es)
JO (1) JOP20220163A1 (es)
LT (1) LT4083038T (es)
MX (1) MX2022007993A (es)
PE (1) PE20230163A1 (es)
PH (1) PH12022551569A1 (es)
PL (1) PL4083038T3 (es)
PT (1) PT4083038T (es)
SA (1) SA522433129B1 (es)
TW (3) TW202136275A (es)
WO (1) WO2021132422A1 (es)
ZA (1) ZA202207543B (es)

Families Citing this family (14)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2023509881A (ja) 2019-12-24 2023-03-10 カルナバイオサイエンス株式会社 ジアシルグリセロールキナーゼ調節化合物
AR120896A1 (es) * 2019-12-25 2022-03-30 Astellas Pharma Inc COMPUESTO DE PIRIDAZINIL-TIAZOLCARBOXAMIDA COMO INHIBIDORES DE DGKz
JP2023522250A (ja) 2020-04-24 2023-05-29 バイエル・アクチエンゲゼルシヤフト 免疫活性化のためのdgkzeta阻害剤としての置換アミノチアゾール類
AR124172A1 (es) 2020-11-30 2023-02-22 Astellas Pharma Inc Compuesto de heteroarilcarboxamida
WO2022271684A1 (en) 2021-06-23 2022-12-29 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
EP4359411A1 (en) 2021-06-23 2024-05-01 Gilead Sciences, Inc. Diacylglyercol kinase modulating compounds
JP2024520593A (ja) 2021-06-23 2024-05-24 ギリアード サイエンシーズ, インコーポレイテッド ジアシルグリエルコール(diacylglyercol)キナーゼ調節化合物
CN117396478A (zh) 2021-06-23 2024-01-12 吉利德科学公司 二酰基甘油激酶调节化合物
CN114621214B (zh) * 2022-04-25 2024-04-26 宜春学院 一种抗菌席夫碱n-酰化物及其制备方法和应用
WO2024108100A1 (en) * 2022-11-18 2024-05-23 Incyte Corporation Heteroaryl fluoroalkenes as dgk inhibitors
WO2024151346A1 (en) * 2023-01-12 2024-07-18 Incyte Corporation Heteroaryl fluoroalkenes as dgk inhibitors
WO2024165468A1 (en) 2023-02-06 2024-08-15 Bayer Aktiengesellschaft Combination of ccr8 antibodies with dgk inhibitors in the treatment of cancer
WO2024199387A1 (zh) * 2023-03-30 2024-10-03 微境生物医药科技(上海)有限公司 作为DGKζ抑制剂的化合物
WO2024208198A1 (zh) * 2023-04-06 2024-10-10 微境生物医药科技(上海)有限公司 作为DGKζ抑制剂的噻唑类化合物

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7381401B2 (en) 2004-01-08 2008-06-03 The University Of Chicago T cell anergy is reversed by active Ras and regulated by diacylglycerol kinase
NZ556732A (en) * 2005-01-25 2011-11-25 Synta Pharmaceuticals Corp Pyrazine compounds for inflammation and immune-related uses
EP1983980A4 (en) * 2006-01-25 2010-05-05 Synta Pharmaceuticals Corp THIAZOL AND THIADIAZOL COMPOUNDS FOR USES IN RELATION TO INFLAMMATION AND IMMUNITY
KR20090004976A (ko) * 2006-04-19 2009-01-12 아스테라스 세이야쿠 가부시키가이샤 아졸카르복사미드 유도체
EP2078003B1 (en) * 2006-10-31 2017-03-08 Merck Sharp & Dohme Corp. Anilinopiperazine derivatives and methods of use thereof
CA3104654A1 (en) * 2018-06-27 2020-01-02 Bristol-Myers Squibb Company Substituted naphthyridinone compounds useful as t cell activators
AR120896A1 (es) * 2019-12-25 2022-03-30 Astellas Pharma Inc COMPUESTO DE PIRIDAZINIL-TIAZOLCARBOXAMIDA COMO INHIBIDORES DE DGKz
AR124172A1 (es) * 2020-11-30 2023-02-22 Astellas Pharma Inc Compuesto de heteroarilcarboxamida

Also Published As

Publication number Publication date
EP4083038B1 (en) 2024-10-30
TW202136275A (zh) 2021-10-01
ECSP22057324A (es) 2022-08-31
JP6948659B1 (ja) 2021-10-13
PH12022551569A1 (en) 2023-11-29
CL2022001752A1 (es) 2023-03-10
CA3165889A1 (en) 2021-07-01
PT4083038T (pt) 2024-12-02
CN113365994B (zh) 2024-08-09
JOP20220163A1 (ar) 2023-01-30
US20220315603A1 (en) 2022-10-06
ES2995459T3 (en) 2025-02-10
BR112022012637A2 (pt) 2022-09-06
LT4083038T (lt) 2024-12-27
DOP2022000137A (es) 2022-11-30
FI4083038T3 (fi) 2024-12-07
IL294136A (en) 2022-08-01
PL4083038T3 (pl) 2025-01-27
EP4083038A4 (en) 2023-12-20
CN113365994A (zh) 2021-09-07
JPWO2021132422A1 (ja) 2021-12-23
WO2021132422A1 (ja) 2021-07-01
AU2020413997A1 (en) 2022-06-09
PE20230163A1 (es) 2023-02-01
CN115590854B (zh) 2024-06-07
KR20220119702A (ko) 2022-08-30
CO2022009124A2 (es) 2022-07-19
ZA202207543B (en) 2023-12-20
DK4083038T3 (da) 2024-12-09
EP4083038A1 (en) 2022-11-02
HRP20241588T1 (hr) 2025-01-31
CR20220328A (es) 2022-08-30
TW202413375A (zh) 2024-04-01
CN115626919A (zh) 2023-01-20
SA522433129B1 (ar) 2024-11-11
TW202413376A (zh) 2024-04-01
MX2022007993A (es) 2022-07-21
CN115590854A (zh) 2023-01-13

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