CA2814581C - Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt - Google Patents

Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt Download PDF

Info

Publication number
CA2814581C
CA2814581C CA2814581A CA2814581A CA2814581C CA 2814581 C CA2814581 C CA 2814581C CA 2814581 A CA2814581 A CA 2814581A CA 2814581 A CA2814581 A CA 2814581A CA 2814581 C CA2814581 C CA 2814581C
Authority
CA
Canada
Prior art keywords
cancer
peaks
tosylate salt
triazol
pyrido
Prior art date
Legal status (The legal status 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 status listed.)
Active
Application number
CA2814581A
Other languages
English (en)
French (fr)
Other versions
CA2814581A1 (en
Inventor
Bing Wang
Daniel Chu
Yongbo Liu
Shichun Peng
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Medivation Technologies LLC
Original Assignee
Medivation Technologies LLC
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=44903424&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=CA2814581(C) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Medivation Technologies LLC filed Critical Medivation Technologies LLC
Publication of CA2814581A1 publication Critical patent/CA2814581A1/en
Application granted granted Critical
Publication of CA2814581C publication Critical patent/CA2814581C/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • 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
    • C07D471/06Peri-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
    • A61K31/495Heterocyclic 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
    • A61K31/5025Pyridazines; Hydrogenated pyridazines ortho- or peri-condensed with heterocyclic 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
    • A61P35/00Antineoplastic agents
    • A61P35/02Antineoplastic agents specific for leukemia
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/13Crystalline forms, e.g. polymorphs

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Epidemiology (AREA)
  • Oncology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
CA2814581A 2010-10-21 2011-10-20 Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt Active CA2814581C (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US40547610P 2010-10-21 2010-10-21
US61/405,476 2010-10-21
PCT/US2011/057039 WO2012054698A1 (en) 2010-10-21 2011-10-20 Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt

Publications (2)

Publication Number Publication Date
CA2814581A1 CA2814581A1 (en) 2012-04-26
CA2814581C true CA2814581C (en) 2019-02-12

Family

ID=44903424

Family Applications (1)

Application Number Title Priority Date Filing Date
CA2814581A Active CA2814581C (en) 2010-10-21 2011-10-20 Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt

Country Status (24)

Country Link
US (3) US8735392B2 (OSRAM)
EP (2) EP3757106A1 (OSRAM)
JP (6) JP2013540158A (OSRAM)
KR (4) KR20210028747A (OSRAM)
CN (1) CN103282365B (OSRAM)
AR (1) AR083502A1 (OSRAM)
AU (2) AU2011317040B2 (OSRAM)
BR (1) BR112013009117A2 (OSRAM)
CA (1) CA2814581C (OSRAM)
CY (1) CY1123356T1 (OSRAM)
DK (1) DK2630146T3 (OSRAM)
ES (1) ES2816600T3 (OSRAM)
HU (1) HUE051535T2 (OSRAM)
IL (2) IL225789B (OSRAM)
MX (1) MX362563B (OSRAM)
NZ (1) NZ609490A (OSRAM)
PL (1) PL2630146T3 (OSRAM)
PT (1) PT2630146T (OSRAM)
RU (1) RU2598606C3 (OSRAM)
SG (2) SG189939A1 (OSRAM)
SI (1) SI2630146T1 (OSRAM)
TW (2) TWI557123B (OSRAM)
WO (1) WO2012054698A1 (OSRAM)
ZA (1) ZA201302810B (OSRAM)

Families Citing this family (52)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PT2767537T (pt) 2008-08-06 2017-07-17 Medivation Technologies Inc Inibidores de di-hidropiridoftalazinona de poli(adp-ribose)polimerase (parp)
CN108524505A (zh) 2009-03-13 2018-09-14 安吉奥斯医药品有限公司 用于细胞增殖相关病症的方法和组合物
PT2448582T (pt) 2009-06-29 2017-07-10 Agios Pharmaceuticals Inc Compostos e composições terapêuticas
ES2594402T3 (es) 2009-10-21 2016-12-20 Agios Pharmaceuticals, Inc. Métodos y composiciones para trastornos relacionados con la proliferación celular
JP5883397B2 (ja) 2010-02-03 2016-03-15 ビオマリン プハルマセウトイカル インコーポレイテッド Pten欠損に関連した疾患の治療におけるポリ(adpリボース)ポリメラーゼ(parp)のジヒドロピリドフタラジノン阻害剤の使用
EP2533640B1 (en) 2010-02-08 2016-09-28 Medivation Technologies, Inc. Processes of synthesizing dihydropyridophthalazinone derivatives
NZ609490A (en) 2010-10-21 2015-06-26 Biomarin Pharm Inc Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt
SG194697A1 (en) 2011-05-03 2013-12-30 Agios Pharmaceuticals Inc Pyruvate kinase activators for use in therapy
CN102827170A (zh) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
CN102827073A (zh) 2011-06-17 2012-12-19 安吉奥斯医药品有限公司 治疗活性组合物和它们的使用方法
EP2742030B1 (de) * 2011-08-11 2016-07-27 Bayer Intellectual Property GmbH 1,2,4-triazolyl-substituierte ketoenole zum einsatz im pflanzenschutz
WO2013028495A1 (en) * 2011-08-19 2013-02-28 Biomarin Pharmaceutical Inc. Dihydropyridophthalazinone inhibitors of poly (adp-ribose) polymerase (parp) for the treatment of multiple myeloma
US9474779B2 (en) 2012-01-19 2016-10-25 Agios Pharmaceuticals, Inc. Therapeutically active compositions and their methods of use
NZ706999A (en) 2012-10-15 2018-12-21 Agios Pharmaceuticals Inc Inhibitors of mutant isocitrate dehydrogenase and therapeutical uses thereof
US9579324B2 (en) 2013-07-11 2017-02-28 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
US10376510B2 (en) 2013-07-11 2019-08-13 Agios Pharmaceuticals, Inc. 2,4- or 4,6-diaminopyrimidine compounds as IDH2 mutants inhibitors for the treatment of cancer
WO2015003355A2 (en) 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
WO2015003360A2 (en) 2013-07-11 2015-01-15 Agios Pharmaceuticals, Inc. Therapeutically active compounds and their methods of use
US20150031627A1 (en) 2013-07-25 2015-01-29 Agios Pharmaceuticals, Inc Therapeutically active compounds and their methods of use
JP6602779B2 (ja) 2014-02-13 2019-11-06 インサイト・コーポレイション Lsd1阻害剤としてのシクロプロピルアミン類
CN106164066B (zh) 2014-02-13 2020-01-17 因赛特公司 作为lsd1抑制剂的环丙胺
CN112159391A (zh) * 2014-03-14 2021-01-01 阿吉奥斯制药公司 治疗活性化合物的药物组合物
UA122962C2 (uk) * 2014-03-14 2021-01-27 Аджіос Фармасьютикалз, Інк. Спосіб лікування поширених солідних пухлин, які характеризуються наявністю мутантного алеля idh1
WO2016007722A1 (en) 2014-07-10 2016-01-14 Incyte Corporation Triazolopyridines and triazolopyrazines as lsd1 inhibitors
KR20170038850A (ko) * 2014-07-31 2017-04-07 메디베이션 테크놀로지즈, 인크. (2s,3s)-메틸 7-플루오로-2-(4-플루오로페닐)-3-(1-메틸-1h-1,2,4-트리아졸-5-일)-4-옥소-1,2,3,4-테트라하이드로퀴놀린-5-카르복실레이트의 공형성체 염 및 이의 제조 방법
CN107660205B (zh) 2015-04-03 2021-08-27 因赛特公司 作为lsd1抑制剂的杂环化合物
SI3307271T1 (sl) 2015-06-11 2023-11-30 Agios Pharmaceuticals, Inc. Postopki za uporabo aktivatorjev piruvat kinaze
EA035534B1 (ru) 2015-08-12 2020-06-30 Инсайт Корпорейшн Соли ингибитора lsd1
HUE057263T2 (hu) 2015-10-15 2022-04-28 Servier Lab Kombinációs terápia rosszindulató betegségek kezelésére
EP3362065B1 (en) 2015-10-15 2024-04-03 Les Laboratoires Servier Combination therapy comprising ivosidenib, cytarabine and daunorubicin or idarubicin for treating acute myelogenous leukemia
EP3368041A4 (en) * 2015-10-26 2019-07-17 Medivation Technologies LLC TREATMENT OF SMALL CELL LUNG CANCER WITH A PARP INHIBITOR
AU2017227929B2 (en) 2016-02-29 2022-06-30 F. Hoffmann-La Roche Ag Dosage form compositions comprising an inhibitor of Bruton's tyrosine kinase
MX2020003361A (es) 2017-10-13 2020-07-29 Merck Patent Gmbh Combinacion de un inhibidor parp y un antagonista de union al eje pd-1.
TW201938165A (zh) 2017-12-18 2019-10-01 美商輝瑞股份有限公司 治療癌症的方法及組合療法
US11368702B2 (en) 2018-06-04 2022-06-21 Lg Electronics, Inc. Method and device for processing video signal by using affine motion prediction
US10980788B2 (en) 2018-06-08 2021-04-20 Agios Pharmaceuticals, Inc. Therapy for treating malignancies
US10942500B2 (en) * 2018-06-11 2021-03-09 Purdue Research Foundation System architecture and method of processing data therein
US10382772B1 (en) * 2018-07-02 2019-08-13 Tencent America LLC Method and apparatus for video coding
EP4339899A3 (en) 2018-07-13 2024-05-22 Magic Leap, Inc. Systems and methods for display binocular deformation compensation
US10968200B2 (en) 2018-08-31 2021-04-06 Incyte Corporation Salts of an LSD1 inhibitor and processes for preparing the same
WO2020095184A1 (en) 2018-11-05 2020-05-14 Pfizer Inc. Combinations for treating cancer
CN115175912B (zh) * 2019-10-10 2025-04-11 住友制药瑞士有限公司 N-(4-(1-(2,6-二氟苄基)-5-((二甲基氨基)甲基)-3-(6-甲氧基-3-哒嗪基)-2,4-二氧代-1,2,3,4-四氢噻吩并[2,3-d]嘧啶-6-基)苯基)-n′-甲氧基脲的结晶溶剂化形式
US20240209061A1 (en) 2020-03-09 2024-06-27 Pfizer Inc. Fusion proteins and uses thereof
MX2023005641A (es) 2020-11-13 2023-05-24 Pfizer Forma de dosificacion en capsula de gelatina blanda de talazoparib.
WO2022123427A1 (en) 2020-12-07 2022-06-16 Pfizer Inc. Methods of identifying a tumor that is sensitive to treatment with talazoparib and methods of treatment thereof
AU2022244439A1 (en) 2021-03-24 2023-09-28 Astellas Pharma Inc. Combination of talazoparib and an anti-androgen for the treatment of ddr gene mutated metastatic castration-sensitive prostate cancer
WO2023131894A1 (en) 2022-01-08 2023-07-13 Pfizer Inc. Genomic loss of heterozygosity as a predictive biomarker for treatment with talazoparib and methods of treatment thereof
WO2023201338A1 (en) 2022-04-15 2023-10-19 Ideaya Biosciences, Inc. Combination therapy comprising a mat2a inhibitor and a parp inhibitor
CN119451954A (zh) 2022-06-01 2025-02-14 伊迪亚生物科学有限公司 作为DNA聚合酶θ抑制剂的噻二唑基衍生物及其用途
TWI883565B (zh) 2022-10-02 2025-05-11 美商輝瑞大藥廠 用於治療轉移性去勢抵抗性前列腺癌之他拉唑帕尼及恩雜魯胺之組合
TW202425976A (zh) 2022-12-17 2024-07-01 美商輝瑞大藥廠 用於治療轉移性去勢抵抗性前列腺癌之他拉唑帕尼及恩雜魯胺之組合
WO2025210510A1 (en) 2024-04-04 2025-10-09 Pfizer Inc. Tmprss2-erg and rb1 as predictive biomarkers for treatment with a parp inhibitor

Family Cites Families (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4415504A (en) 1981-09-21 1983-11-15 Tanabe Seiyaku Co., Ltd. p-Hydroxyphenylglycine.α-phenylethanesulfonate, process for production thereof and utilization thereof in resolution of p-hydroxyphenylglycine
JPS58225065A (ja) 1982-06-21 1983-12-27 Nippon Shinyaku Co Ltd 2−キノロン誘導体
US5328905A (en) 1987-07-20 1994-07-12 Duphar International Research B.V. 8,9-anellated-1,2,3,4-tetrahydro-β-carboline derivatives
GB9505538D0 (en) 1995-03-18 1995-05-03 Ciba Geigy Ag New compounds
ID19155A (id) 1996-12-13 1998-06-18 Tanabe Seiyaku Co Turunan-turunan piridin, pembuatannya dan intermediet untuk pembuatannya
DE19727410A1 (de) 1997-06-27 1999-01-07 Hoechst Schering Agrevo Gmbh 3-(5-Tetrazolylcarbonyl)-2-chinolone und diese enthaltende nutzpflanzenschützende Mittel
US6514983B1 (en) 1997-09-03 2003-02-04 Guilford Pharmaceuticals Inc. Compounds, methods and pharmaceutical compositions for treating neural or cardiovascular tissue damage
TW430656B (en) 1997-12-03 2001-04-21 Dainippon Ink & Chemicals Quinolinone derivative, method for preparing the same, and anti-allergic agent
CA2332239A1 (en) 1998-05-15 1999-11-25 Guilford Pharmaceuticals Inc. Fused tricyclic compounds which inhibit parp activity
DE19921567A1 (de) 1999-05-11 2000-11-16 Basf Ag Verwendung von Phthalazine-Derivaten
JP2001302669A (ja) 2000-04-18 2001-10-31 Meiji Seika Kaisha Ltd 三環性フタラジノン誘導体
JP2002284699A (ja) 2001-03-28 2002-10-03 Sumitomo Pharmaceut Co Ltd 視細胞変性疾患治療剤
AR036081A1 (es) 2001-06-07 2004-08-11 Smithkline Beecham Corp Compuesto de 1,2-dihidroquinolina, su uso para preparar una composicion farmaceutica, metodos para prepararlo y compuestos del acido 2-aminobenzoico n-alquilado de utilidad como intermediarios en dichos metodos
SE0102315D0 (sv) 2001-06-28 2001-06-28 Astrazeneca Ab Compounds
AU2003211381B9 (en) 2002-02-19 2009-07-30 Ono Pharmaceutical Co., Ltd. Fused pyridazine derivative compounds and drugs containing the compounds as the active ingredient
EP1340819A1 (en) 2002-02-28 2003-09-03 Institut National De La Sante Et De La Recherche Medicale (Inserm) Microsatellite markers
GB0221443D0 (en) 2002-09-16 2002-10-23 Glaxo Group Ltd Pyridine derivates
EP1400244A1 (en) 2002-09-17 2004-03-24 Warner-Lambert Company LLC New spirocondensed quinazolinones and their use as phosphodiesterase inhibitors
EP1582520A1 (en) 2002-11-12 2005-10-05 Mochida Pharmaceutical Co., Ltd. Novel parp inhibitors
NZ542680A (en) 2003-03-12 2008-08-29 Kudos Pharm Ltd Phthalazinone derivatives
JP4824566B2 (ja) 2003-05-28 2011-11-30 エーザイ インコーポレーテッド Parpを阻害するための化合物、方法、および医薬組成物
UA85576C2 (ru) 2004-02-18 2009-02-10 Астразенека Аб Тетразольные соединения и их применение в качестве метаботропических антагонистов рецепторов глутамата
GB0612971D0 (en) 2006-06-30 2006-08-09 Angeletti P Ist Richerche Bio Therapeutic compounds
US8198448B2 (en) 2006-07-14 2012-06-12 Amgen Inc. Fused heterocyclic derivatives and methods of use
MX2009011816A (es) 2007-05-03 2009-11-19 Pfizer Ltd Derivados de piridina.
BRPI0721950A2 (pt) 2007-08-22 2015-09-29 4Sc Ag indolopiridinas como inibidores da proteína de fuso de cinesina
CN101998959B (zh) 2008-02-06 2013-08-28 生物马林药物股份有限公司 聚(adp-核糖)聚合酶(parp)的苯并噁唑甲酰胺抑制剂
PT2767537T (pt) 2008-08-06 2017-07-17 Medivation Technologies Inc Inibidores de di-hidropiridoftalazinona de poli(adp-ribose)polimerase (parp)
MX2011001563A (es) 2008-08-12 2011-03-04 Boehringer Ingelheim Int Procedimiento para la preparacion de compuestos de piperazina sustituidos con cloalquilo.
JP5883397B2 (ja) 2010-02-03 2016-03-15 ビオマリン プハルマセウトイカル インコーポレイテッド Pten欠損に関連した疾患の治療におけるポリ(adpリボース)ポリメラーゼ(parp)のジヒドロピリドフタラジノン阻害剤の使用
US20110190266A1 (en) 2010-02-04 2011-08-04 Daniel Chu 5,6,6a,7,8,9-HEXAHYDRO-2H-PYRIDOPHTHALAZINONE INHIBITORS OF POLY(ADP-RIBOSE)POLYMERASE (PARP)
EP2533640B1 (en) 2010-02-08 2016-09-28 Medivation Technologies, Inc. Processes of synthesizing dihydropyridophthalazinone derivatives
WO2011130661A1 (en) 2010-04-16 2011-10-20 Biomarin Pharmaceutical Inc. Methods of using dihydropyridophthalazinone inhibitors of poly (adp-ribose)polymerase (parp)
WO2011140009A1 (en) 2010-05-04 2011-11-10 Biomarin Pharmaceutical Inc. Methods of using semi-synthetic glycopeptides as antibacterial agents
NZ609490A (en) 2010-10-21 2015-06-26 Biomarin Pharm Inc Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt
WO2012166151A1 (en) 2011-06-03 2012-12-06 Biomarin Pharmaceutical Inc. Use of dihydropyridophthalazinone inhibitors of poly (adp-ribose) polymerase (parp) in the treatment of myelodysplastic syndrome (mds) and acute myeloid leukaemia (aml)
WO2013028495A1 (en) 2011-08-19 2013-02-28 Biomarin Pharmaceutical Inc. Dihydropyridophthalazinone inhibitors of poly (adp-ribose) polymerase (parp) for the treatment of multiple myeloma
US20130053365A1 (en) 2011-08-30 2013-02-28 Biomarin Pharmaceutical, Inc. Dihydropyridophthalazinone inhibitors of poly(adp-ribose)polymerase (parp)
CN105916846A (zh) 2013-11-07 2016-08-31 麦迪韦逊科技有限公司 用于合成经保护的n-烷基三唑甲醛的三唑中间体
KR20170038850A (ko) 2014-07-31 2017-04-07 메디베이션 테크놀로지즈, 인크. (2s,3s)-메틸 7-플루오로-2-(4-플루오로페닐)-3-(1-메틸-1h-1,2,4-트리아졸-5-일)-4-옥소-1,2,3,4-테트라하이드로퀴놀린-5-카르복실레이트의 공형성체 염 및 이의 제조 방법

Also Published As

Publication number Publication date
JP2024150772A (ja) 2024-10-23
SI2630146T1 (sl) 2020-12-31
HUE051535T2 (hu) 2021-03-01
RU2013123036A (ru) 2014-11-27
KR20190120458A (ko) 2019-10-23
RU2598606C3 (ru) 2021-12-20
CY1123356T1 (el) 2021-12-31
ES2816600T3 (es) 2021-04-05
AU2017201564B2 (en) 2019-05-09
WO2012054698A1 (en) 2012-04-26
TWI643858B (zh) 2018-12-11
US20120129865A1 (en) 2012-05-24
TW201307345A (zh) 2013-02-16
KR20210028747A (ko) 2021-03-12
US8735392B2 (en) 2014-05-27
MX362563B (es) 2019-01-25
BR112013009117A2 (pt) 2016-07-19
EP2630146A1 (en) 2013-08-28
KR20180069132A (ko) 2018-06-22
CA2814581A1 (en) 2012-04-26
JP2019034951A (ja) 2019-03-07
JP2017061526A (ja) 2017-03-30
KR20140009181A (ko) 2014-01-22
IL225789B (en) 2019-12-31
US10189837B2 (en) 2019-01-29
JP2022140637A (ja) 2022-09-26
TW201713656A (en) 2017-04-16
AU2011317040A1 (en) 2013-05-09
IL225789A0 (en) 2013-06-27
US20140228369A1 (en) 2014-08-14
US20180009806A1 (en) 2018-01-11
AU2017201564A1 (en) 2017-03-23
NZ609490A (en) 2015-06-26
AU2011317040B2 (en) 2016-12-08
JP2020169209A (ja) 2020-10-15
PL2630146T3 (pl) 2020-11-02
CN103282365B (zh) 2017-12-29
IL271497A (en) 2020-02-27
MX2013004195A (es) 2013-07-22
RU2598606C2 (ru) 2016-09-27
EP3757106A1 (en) 2020-12-30
EP2630146B1 (en) 2020-07-01
SG10201710578TA (en) 2018-02-27
AR083502A1 (es) 2013-02-27
TWI557123B (zh) 2016-11-11
DK2630146T3 (da) 2020-08-10
SG189939A1 (en) 2013-06-28
ZA201302810B (en) 2014-06-25
CN103282365A (zh) 2013-09-04
PT2630146T (pt) 2020-07-20
JP2013540158A (ja) 2013-10-31

Similar Documents

Publication Publication Date Title
CA2814581C (en) Crystalline (8s,9r)-5-fluoro-8-(4-fluorophenyl)-9-(1-methyl-1h-1,2,4-triazol-5-yl)-8,9-dihydro-2h-pyrido[4,3,2-de]phthalazin-3(7h)-one tosylate salt
CN111148745A (zh) Fgfr抑制剂的结晶形式及其制备方法
US20250051333A1 (en) Polymorph of kras inhibitor, preparation method therefor, and use thereof
CN102834097B (zh) 纯化的吡咯并喹啉基-吡咯烷-2,5-二酮组合物和用于制备且使用其的方法
KR20180067531A (ko) Pim 카이나제 저해제의 염
CA3104365A1 (en) Crystal form of compound for inhibiting the activity of cdk4/6 and use thereof
CN108884099B (zh) 一种咪唑并异吲哚类衍生物的游离碱的结晶形式及其制备方法
TW200806671A (en) Polymorphic forms of (2R,Z)-2-amino-2-cyclohexyl-N-(5-(1-methyl-1H-pyrazol-4-YL)-1-OXO-2,6-dihydro-1H-[1,2]diazepino[4,5,6-CD]indol-8-YL)acetamide
JP7141416B2 (ja) N-(2,6-ジエチルフェニル)-8-({4-[4-(ジメチルアミノ)ピペリジン-1-イル]-2-メトキシフェニル}アミノ)-1-メチル-4,5-ジヒドロ-1H-ピラゾロ[4,3-h]キナゾリン-3-カルボキサミドの新しい塩、その製造法、及びそれを含む製剤
TWI717859B (zh) 一種鴉片類物質受體激動劑的結晶形式及製備方法
CN121039114A (zh) 1,5-二氢-2,4-苯二氮䓬-3-酮衍生物枸橼酸盐的晶型、制备方法及其应用
HK40022862A (en) Salt of a compound inhibiting mps1 kinase, its preparation and formulations containing it
HK40022862B (en) Salt of a compound inhibiting mps1 kinase, its preparation and formulations containing it

Legal Events

Date Code Title Description
EEER Examination request

Effective date: 20161019