JP7318889B2 - 化合物 - Google Patents

化合物 Download PDF

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Publication number
JP7318889B2
JP7318889B2 JP2019559413A JP2019559413A JP7318889B2 JP 7318889 B2 JP7318889 B2 JP 7318889B2 JP 2019559413 A JP2019559413 A JP 2019559413A JP 2019559413 A JP2019559413 A JP 2019559413A JP 7318889 B2 JP7318889 B2 JP 7318889B2
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Japan
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alkyl
trifluoromethyl
pyrido
methyl
cycloalkyl
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Japanese (ja)
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JP2020505454A5 (https=
JP2020505454A (ja
Inventor
エー. ワード、ステファン
ジェイ. テイラー,マーク
エム. オネイル,ポール
デイヴィッド ホン,ウェイチィァン
ベナユード,ファリッド
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Eisai R&D Management Co Ltd
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Eisai R&D Management Co Ltd
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Priority to JP2023004747A priority Critical patent/JP2023052427A/ja
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    • 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
    • C07D471/04Ortho-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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P33/00Antiparasitic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/70Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
    • C07D239/72Quinazolines; Hydrogenated quinazolines
    • C07D239/86Quinazolines; Hydrogenated quinazolines with hetero atoms directly attached in position 4
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04Ortho-condensed systems
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02ATECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
    • Y02A50/00TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE in human health protection, e.g. against extreme weather
    • Y02A50/30Against vector-borne diseases, e.g. mosquito-borne, fly-borne, tick-borne or waterborne diseases whose impact is exacerbated by climate change

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  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Tropical Medicine & Parasitology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Plural Heterocyclic Compounds (AREA)
JP2019559413A 2017-01-17 2018-01-17 化合物 Active JP7318889B2 (ja)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2023004747A JP2023052427A (ja) 2017-01-17 2023-01-16 化合物

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GBGB1700814.5A GB201700814D0 (en) 2017-01-17 2017-01-17 Compounds
GB1700814.5 2017-01-17
PCT/IB2018/000216 WO2018134685A2 (en) 2017-01-17 2018-01-17 Compounds

Related Child Applications (1)

Application Number Title Priority Date Filing Date
JP2023004747A Division JP2023052427A (ja) 2017-01-17 2023-01-16 化合物

Publications (3)

Publication Number Publication Date
JP2020505454A JP2020505454A (ja) 2020-02-20
JP2020505454A5 JP2020505454A5 (https=) 2021-03-11
JP7318889B2 true JP7318889B2 (ja) 2023-08-01

Family

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Family Applications (2)

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JP2019559413A Active JP7318889B2 (ja) 2017-01-17 2018-01-17 化合物
JP2023004747A Withdrawn JP2023052427A (ja) 2017-01-17 2023-01-16 化合物

Family Applications After (1)

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JP2023004747A Withdrawn JP2023052427A (ja) 2017-01-17 2023-01-16 化合物

Country Status (5)

Country Link
US (2) US11518760B2 (https=)
EP (1) EP3571204A2 (https=)
JP (2) JP7318889B2 (https=)
GB (1) GB201700814D0 (https=)
WO (1) WO2018134685A2 (https=)

Families Citing this family (30)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB201700814D0 (en) 2017-01-17 2017-03-01 Liverpool School Tropical Medicine Compounds
KR102767739B1 (ko) 2018-06-27 2025-02-12 브리스톨-마이어스 스큅 컴퍼니 T 세포 활성화제로서 유용한 치환된 나프티리디논 화합물
CN112585139B (zh) 2018-06-27 2023-12-01 百时美施贵宝公司 用作t细胞激活剂的萘啶酮化合物
CN109627207A (zh) * 2018-12-17 2019-04-16 天津药明康德新药开发有限公司 一种3-(二氟甲氧基)哌啶盐酸盐的制备方法
CN109651171A (zh) * 2019-01-13 2019-04-19 苏州鹏旭医药科技有限公司 依拉戈利及其钠盐的中间体及其盐的制备方法和应用
WO2020167624A1 (en) 2019-02-13 2020-08-20 Ptc Therapeutics, Inc. Pyrrolo[2,3-d]pyrimidine compounds for treating familial dysautonomia
SG11202108519TA (en) 2019-02-13 2021-09-29 Ptc Therapeutics Inc Thioeno[3,2-b] pyridin-7-amine compounds for treating familial dysautonomia
MX2021010319A (es) * 2019-03-01 2021-12-10 Revolution Medicines Inc Compuestos biciclicos de heteroarilo y usos de estos.
CA3139018A1 (en) 2019-05-31 2020-12-03 Chiesi Farmaceutici S.P.A. Amino quinazoline derivatives as p2x3 inhibitors
JP7797204B2 (ja) * 2019-05-31 2026-01-13 キエシ・フアルマチエウテイチ・ソチエタ・ペル・アチオニ P2x3阻害剤としてのピリドピリミジン誘導体
AR119821A1 (es) 2019-08-28 2022-01-12 Bristol Myers Squibb Co Compuestos de piridopirimidinonilo sustituidos útiles como activadores de células t
CN115209955A (zh) * 2019-12-12 2022-10-18 Ptc医疗公司 治疗家族性自主神经功能障碍的化合物
BR112022012179A2 (pt) 2019-12-23 2022-09-06 Bristol Myers Squibb Co Compostos de quinazolina substituída úteis como ativadores de célula t
CA3162979A1 (en) 2019-12-23 2021-07-01 Upender Velaparthi Substituted piperazine derivatives useful as t cell activators
AR120823A1 (es) 2019-12-23 2022-03-23 Bristol Myers Squibb Co Compuestos bicíclicos sustituidos útiles como activadores de células t
TW202208355A (zh) 2020-05-04 2022-03-01 美商安進公司 作為骨髓細胞觸發受體2促效劑之雜環化合物及使用方法
WO2022058896A1 (en) * 2020-09-15 2022-03-24 Cadila Healthcare Limited Inhibitors of low molecular weight protein tyrosine phosphatase for management of metabolic disorder
US20230357239A1 (en) 2020-09-18 2023-11-09 Bayer Aktiengesellschaft Pyrido[2,3-d]pyrimidin-4-amines as sos1 inhibitors
GB202100635D0 (en) 2021-01-18 2021-03-03 Liverpool School Tropical Medicine Compounds and methods for treating or preventing dirofilaria infection in a mammal
WO2022171018A1 (zh) * 2021-02-09 2022-08-18 苏州泽璟生物制药股份有限公司 取代苯并或吡啶并嘧啶胺类抑制剂及其制备方法和应用
WO2022187411A1 (en) 2021-03-02 2022-09-09 Kumquat Biosciences Inc. Heterocycles and uses thereof
EP4074317A1 (en) 2021-04-14 2022-10-19 Bayer AG Phosphorus derivatives as novel sos1 inhibitors
AU2023255692A1 (en) 2022-04-20 2024-10-03 Kumquat Biosciences Inc. Macrocyclic heterocycles and uses thereof
CN115160294B (zh) * 2022-06-27 2023-09-29 中山大学 一种G9a/GLP共价抑制剂及其制备方法及应用
WO2024056782A1 (en) 2022-09-16 2024-03-21 Bayer Aktiengesellschaft Sulfone-substituted pyrido[3,4-d]pyrimidine derivatives for the treatment of cancer
EP4602049A1 (en) 2022-10-13 2025-08-20 Bayer Aktiengesellschaft Sos1 inhibitors
TW202430519A (zh) * 2022-11-28 2024-08-01 大陸商上海美悅生物科技發展有限公司 螺雜環取代的嘧啶類化合物及其製備方法和用途
AU2024288001A1 (en) * 2023-07-11 2026-01-15 Tay Therapeutics Limited Compounds comprising a naphthyridine or pyridopyrimidine core as ptc read-through agents
TW202543612A (zh) * 2024-01-05 2025-11-16 美商露點治療股份有限公司 噻吩并吡啶化合物及其用途
CN119161336B (zh) * 2024-07-24 2025-09-05 四川大学 一种作为Blimp1抑制剂的小分子化合物及其用途

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001032632A2 (en) 1999-11-01 2001-05-10 Eli Lilly And Company Pharmaceutically active 4-substituted pyrimidine derivatives
JP2007513996A (ja) 2003-12-16 2007-05-31 ファイザー・プロダクツ・インク PDE2インヒビターとしてのピリド[2,3−d]ピリミジン−2,4−ジアミン類
WO2009001060A2 (en) 2007-06-27 2008-12-31 Summit Corporation Plc Use of compounds for preparing anti-tuberculosis agents
JP2013500255A (ja) 2009-07-21 2013-01-07 プレジデント アンド フェロウズ オブ ハーバード カレッジ 自食作用の強力な小分子阻害剤、およびそれの使用方法
CN106083742A (zh) 2016-05-31 2016-11-09 广东工业大学 一种2,4‑二胺基喹唑啉衍生物及其制备方法和应用

Family Cites Families (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1470356A1 (de) 1964-01-15 1970-04-30 Thomae Gmbh Dr K Neue Thieno[3,2-d]pyrimidine und Verfahren zu ihrer Herstellung
US6262059B1 (en) * 1995-06-07 2001-07-17 Cell Pathways, Inc. Method of treating a patient having precancerous lesions with quinazoline derivatives
US6103903A (en) 1998-02-26 2000-08-15 Neurogen Corporation 4-(4-piperidylmethyhlamino) substituted heteroaryl fused pyridines: GABA brain receptor ligands
WO2003055890A1 (en) 2001-12-21 2003-07-10 Bayer Pharmaceuticals Corporation Thienopyrimidine derivative compounds as inhibitors of prolylpeptidase, inducers of apoptosis and cancer treatment agents
WO2007063934A1 (ja) * 2005-12-02 2007-06-07 Mitsubishi Tanabe Pharma Corporation 脂環式複素環化合物
US8027888B2 (en) * 2006-08-31 2011-09-27 Experian Interactive Innovation Center, Llc Online credit card prescreen systems and methods
WO2010042489A2 (en) * 2008-10-06 2010-04-15 Emory University Aminoquinoline derived heat shock protein 90 inhibitors, methods of preparing same, and methods for their use
FR2959510B1 (fr) * 2010-04-28 2013-04-26 Centre Nat Rech Scient Derives de pyrido[3,2-d]pyrimidine, leurs procedes de preparation et leurs utilisations therapeutiques
WO2012097258A2 (en) * 2011-01-15 2012-07-19 The Regents Of The University Of California Formulations for the prevention and treatment of wolbachia-related disease
EP2532661A1 (en) 2011-06-10 2012-12-12 Syngenta Participations AG Novel insecticides
CN103087077B (zh) 2011-11-03 2016-05-18 上海希迈医药科技有限公司 噻吩并嘧啶和呋喃并嘧啶类衍生物、其制备方法及其在医药上的应用
CN103204816B (zh) 2012-01-16 2016-04-27 中国人民解放军军事医学科学院毒物药物研究所 哌嗪基嘧啶类衍生物及其制备方法和用途
HK1246679A1 (zh) 2015-01-09 2018-09-14 Abbvie Inc. 丝虫病的治疗
US9670205B2 (en) 2015-03-04 2017-06-06 Gilead Sciences, Inc. Toll like receptor modulator compounds
JP2020511400A (ja) 2016-12-09 2020-04-16 ワッカー ケミー アクチエンゲゼルシャフトWacker Chemie AG ヒドリドシランの製造方法
GB201700814D0 (en) * 2017-01-17 2017-03-01 Liverpool School Tropical Medicine Compounds
CN110128419A (zh) 2019-05-17 2019-08-16 南开大学 一类二氟吡唑杂环甲酰胺类衍生物及其制备方法和用途
GB202100635D0 (en) 2021-01-18 2021-03-03 Liverpool School Tropical Medicine Compounds and methods for treating or preventing dirofilaria infection in a mammal
KR102682408B1 (ko) 2021-05-12 2024-07-05 에이치케이이노엔 주식회사 신규한 벤조티아졸 유도체, 이의 제조방법 및 이의 간질환 예방 또는 치료 용도
CN118510778A (zh) 2022-01-12 2024-08-16 百济神州有限公司 作为DNA聚合酶θ抑制剂的噻唑并吡啶基酰胺衍生物
US20250122221A1 (en) 2022-01-13 2025-04-17 Nanjing Zaiming Pharmaceutical Co., Ltd. Six-membered cyclothiazole compound and use thereof

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2001032632A2 (en) 1999-11-01 2001-05-10 Eli Lilly And Company Pharmaceutically active 4-substituted pyrimidine derivatives
JP2007513996A (ja) 2003-12-16 2007-05-31 ファイザー・プロダクツ・インク PDE2インヒビターとしてのピリド[2,3−d]ピリミジン−2,4−ジアミン類
WO2009001060A2 (en) 2007-06-27 2008-12-31 Summit Corporation Plc Use of compounds for preparing anti-tuberculosis agents
JP2013500255A (ja) 2009-07-21 2013-01-07 プレジデント アンド フェロウズ オブ ハーバード カレッジ 自食作用の強力な小分子阻害剤、およびそれの使用方法
CN106083742A (zh) 2016-05-31 2016-11-09 广东工业大学 一种2,4‑二胺基喹唑啉衍生物及其制备方法和应用

Non-Patent Citations (5)

* Cited by examiner, † Cited by third party
Title
CHAKRABORTI A K,3D-QSAR STUDIES ON THIENO[3,2-D]PYRIMIDINES AS PHOSPHODIESTERASE IV INHIBITORS,BIOORGANIC AND MEDICINAL CHEMISTRY LETTERS,NL,PERGAMON,2003年,VOL:13, NR:8,,PAGE(S):1403 - 1408,http://dx.doi.org/10.1016/S0960-894X(03)00172-0
DIEGO GONZALEZ CABRERA,2,4-DIAMINOTHIENOPYRIMIDINES AS ORALLY ACTIVE ANTIMALARIAL AGENTS,JOURNAL OF MEDICINAL CHEMISTRY,2014年01月28日,VOL:57, NR:3,,PAGE(S):1014 - 1022,http://dx.doi.org/10.1021/jm401760c
DIEGO GONZALEZ CABRERA,STRUCTURE-ACTIVITY RELATIONSHIP STUDIES OF ORALLY ACTIVE ANTIMALARIAL 2,4-DIAMINO-THIENOPYRIMIDINES,JOURNAL OF MEDICINAL CHEMISTRY,2015年09月08日,VOL:58, NR:18,,PAGE(S):7572 - 7579,http://dx.doi.org/10.1021/acs.jmedchem.5b01156
MARIA FONT,NEW INSIGHTS INTO THE STRUCTURAL REQUIREMENTS FOR PRO-APOPTOTIC AGENTS BASED ON 2,4-以下備考,EUROPEAN JOURNAL OF MEDICINAL CHEMISTRY,フランス,2011年05月24日,VOL:46, NR:9,,PAGE(S):3887 - 3899,http://dx.doi.org/10.1016/j.ejmech.2011.05.060,DIAMINOQUINAZOLINE, 2,4-DIAMINOPYRIDO[2,3-D]PYRIMIDINE AND 2,4-DIAMINOPYRIMIDINE DERIVATIVES
ODINGO JOSHUA,SYNTHESIS AND EVALUATION OF THE 2,4-DIAMINOQUINAZOLINE SERIES AS ANTI-TUBERCULAR AGENTS,BIOORGANIC & MEDICINAL CHEMISTRY,英国,PERGAMON,2014年10月22日,VOL:22, NR:24,,PAGE(S):6965 - 6979,http://dx.doi.org/10.1016/j.bmc.2014.10.007

Also Published As

Publication number Publication date
WO2018134685A2 (en) 2018-07-26
GB201700814D0 (en) 2017-03-01
WO2018134685A3 (en) 2018-11-15
US20230348460A1 (en) 2023-11-02
EP3571204A2 (en) 2019-11-27
US12545675B2 (en) 2026-02-10
JP2020505454A (ja) 2020-02-20
US20190345157A1 (en) 2019-11-14
US11518760B2 (en) 2022-12-06
JP2023052427A (ja) 2023-04-11

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