JP2025084856A5 - - Google Patents

Info

Publication number
JP2025084856A5
JP2025084856A5 JP2025029906A JP2025029906A JP2025084856A5 JP 2025084856 A5 JP2025084856 A5 JP 2025084856A5 JP 2025029906 A JP2025029906 A JP 2025029906A JP 2025029906 A JP2025029906 A JP 2025029906A JP 2025084856 A5 JP2025084856 A5 JP 2025084856A5
Authority
JP
Japan
Prior art keywords
formula
compound
forming
acid
preparing
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.)
Pending
Application number
JP2025029906A
Other languages
English (en)
Japanese (ja)
Other versions
JP2025084856A (ja
Filing date
Publication date
Priority claimed from JP2020084989A external-priority patent/JP6891322B2/ja
Application filed filed Critical
Publication of JP2025084856A publication Critical patent/JP2025084856A/ja
Publication of JP2025084856A5 publication Critical patent/JP2025084856A5/ja
Pending legal-status Critical Current

Links

JP2025029906A 2013-06-10 2025-02-27 製造方法及びmdm2阻害剤の結晶形 Pending JP2025084856A (ja)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201361833196P 2013-06-10 2013-06-10
US61/833,196 2013-06-10
JP2020084989A JP6891322B2 (ja) 2013-06-10 2020-05-14 製造方法及びmdm2阻害剤の結晶形
JP2021087378A JP7263439B2 (ja) 2013-06-10 2021-05-25 製造方法及びmdm2阻害剤の結晶形
JP2023064715A JP2023089126A (ja) 2013-06-10 2023-04-12 製造方法及びmdm2阻害剤の結晶形

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
JP2023064715A Division JP2023089126A (ja) 2013-06-10 2023-04-12 製造方法及びmdm2阻害剤の結晶形

Publications (2)

Publication Number Publication Date
JP2025084856A JP2025084856A (ja) 2025-06-03
JP2025084856A5 true JP2025084856A5 (https=) 2025-08-08

Family

ID=51063849

Family Applications (5)

Application Number Title Priority Date Filing Date
JP2016519576A Active JP6998655B2 (ja) 2013-06-10 2014-06-09 製造方法及びmdm2阻害剤の結晶形
JP2020084989A Active JP6891322B2 (ja) 2013-06-10 2020-05-14 製造方法及びmdm2阻害剤の結晶形
JP2021087378A Active JP7263439B2 (ja) 2013-06-10 2021-05-25 製造方法及びmdm2阻害剤の結晶形
JP2023064715A Pending JP2023089126A (ja) 2013-06-10 2023-04-12 製造方法及びmdm2阻害剤の結晶形
JP2025029906A Pending JP2025084856A (ja) 2013-06-10 2025-02-27 製造方法及びmdm2阻害剤の結晶形

Family Applications Before (4)

Application Number Title Priority Date Filing Date
JP2016519576A Active JP6998655B2 (ja) 2013-06-10 2014-06-09 製造方法及びmdm2阻害剤の結晶形
JP2020084989A Active JP6891322B2 (ja) 2013-06-10 2020-05-14 製造方法及びmdm2阻害剤の結晶形
JP2021087378A Active JP7263439B2 (ja) 2013-06-10 2021-05-25 製造方法及びmdm2阻害剤の結晶形
JP2023064715A Pending JP2023089126A (ja) 2013-06-10 2023-04-12 製造方法及びmdm2阻害剤の結晶形

Country Status (38)

Country Link
US (10) US9376386B2 (https=)
EP (2) EP3805232B1 (https=)
JP (5) JP6998655B2 (https=)
KR (4) KR20160018576A (https=)
CN (3) CN105358530A (https=)
AP (1) AP2015008891A0 (https=)
AR (3) AR096582A1 (https=)
AU (5) AU2014278428B2 (https=)
BR (2) BR122020003153B1 (https=)
CA (4) CA2914723C (https=)
CL (3) CL2015003589A1 (https=)
CR (2) CR20210290A (https=)
CY (1) CY1123661T1 (https=)
DK (1) DK3008039T3 (https=)
EA (3) EA202091612A1 (https=)
ES (1) ES2851023T3 (https=)
HR (1) HRP20202065T1 (https=)
HU (1) HUE053047T2 (https=)
IL (4) IL297860A (https=)
JO (2) JO3768B1 (https=)
LT (1) LT3008039T (https=)
MA (3) MA38714A1 (https=)
MX (2) MX2015016856A (https=)
MY (2) MY205257A (https=)
NZ (1) NZ714821A (https=)
PE (2) PE20160113A1 (https=)
PH (2) PH12020550916A1 (https=)
PL (1) PL3008039T3 (https=)
PT (1) PT3008039T (https=)
RS (1) RS61192B1 (https=)
SG (2) SG10201801402XA (https=)
SI (1) SI3008039T1 (https=)
SM (1) SMT202100013T1 (https=)
TN (1) TN2015000521A1 (https=)
TW (3) TWI791153B (https=)
UA (2) UA129695C2 (https=)
UY (2) UY35605A (https=)
WO (1) WO2014200937A1 (https=)

Families Citing this family (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO2998B1 (ar) 2010-06-04 2016-09-05 Amgen Inc مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان
MX352672B (es) 2011-09-27 2017-12-04 Amgen Inc Compuestos heterocíclicos como inhibidores de mdm2 para el tratamiento del cáncer.
US11407721B2 (en) 2013-02-19 2022-08-09 Amgen Inc. CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer
AU2014236812B2 (en) 2013-03-14 2018-03-01 Amgen Inc. Heteroaryl acid morpholinone compounds as MDM2 inhibitors for the treatment of cancer
CN105358530A (zh) 2013-06-10 2016-02-24 美国安进公司 制备mdm2抑制剂的方法及其结晶形式
HRP20220718T1 (hr) 2013-11-11 2022-09-30 Amgen Inc. Kombinacijska terapija uključujući inhibitor mdm2 i jedan ili više dodatnih farmaceutski aktivnih sredstava za liječenje raka
EP3458101B1 (en) 2016-05-20 2020-12-30 H. Hoffnabb-La Roche Ag Protac antibody conjugates and methods of use
IL308399B2 (en) * 2018-04-30 2025-08-01 Kartos Therapeutics Inc Methods of treating cancer
CN112804994A (zh) * 2018-05-25 2021-05-14 卡托斯医疗公司 治疗骨髓增殖性肿瘤的方法
IL315550A (en) 2018-08-31 2024-11-01 Amgen Inc A process for preparing an MDM2 inhibitor
CN110963958B (zh) 2018-09-30 2025-10-10 上海长森药业有限公司 一种mdm2抑制剂,及其制备方法、药物组合物和应用
GB201919219D0 (en) 2019-12-23 2020-02-05 Otsuka Pharma Co Ltd Cancer biomarkers
US20230272001A1 (en) * 2020-05-22 2023-08-31 Merck Sharp & Dohme Llc Novel processes for preparing conjugates of the il-2 protein
CA3181715A1 (en) 2020-08-27 2022-03-03 Otsuka Pharmaceutical Co., Ltd. Biomarkers for cancer therapy using mdm2 antagonists
GB202103080D0 (en) 2021-03-04 2021-04-21 Otsuka Pharma Co Ltd Cancer biomarkers
US12054449B2 (en) 2021-08-05 2024-08-06 Bio-Pharm Solutions Co., Ltd. Phenylcarbamate crystalline form and method for manufacturing the same
EP4382509A4 (en) * 2021-08-05 2025-08-27 Bio Pharm Solutions Co Ltd CRYSTALLINE FORM OF PHENYLCARBAMATE AND PROCESS FOR ITS PREPARATION
WO2023039161A1 (en) * 2021-09-09 2023-03-16 Kartos Therapeutics Methods of treating cancer dependent on myc gene expresssion
WO2023056069A1 (en) 2021-09-30 2023-04-06 Angiex, Inc. Degrader-antibody conjugates and methods of using same
CN115925589A (zh) * 2022-12-26 2023-04-07 诚达药业股份有限公司 一种脂肪族亚磺酸钙盐及其制备方法
WO2024240858A1 (en) 2023-05-23 2024-11-28 Valerio Therapeutics Protac molecules directed against dna damage repair system and uses thereof

Family Cites Families (93)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2483213A (en) * 1947-06-14 1949-09-27 American Cyanamid Co Alpha naphthalene sulfonic anhydride
CH436295A (de) 1961-11-13 1967-05-31 Mcneilab Inc Verfahren zur Herstellung neuer 3-Morpholinone
US3518236A (en) * 1967-07-20 1970-06-30 Uniroyal Inc Acceleration of sulfur-vulcanization of rubber with sulfinic acids and derivatives
DE3246148A1 (de) 1982-12-14 1984-06-14 Troponwerke GmbH & Co KG, 5000 Köln Pyrazolo(4.3-b)(1.4)oxazine, verfahren zu ihrer herstellung und ihre verwendung als arzneimittel
JP2604472B2 (ja) 1989-07-12 1997-04-30 株式会社クラレ 重合性組成物
WO1995023135A1 (en) 1991-03-07 1995-08-31 Fisons Corporation Diphenyl-2-piperidinone and -2-pyrrolidinone derivatives having anti-convulsant and neuroprotective activity
US5334720A (en) 1991-03-07 1994-08-02 Fisons Corporation Diphenyl-1-(aminoalkyl)-2-piperidinone and -2-pyrrolidinone derivatives having anticonvulsant properties
CA2195677C (en) 1994-08-19 2005-11-08 Martin Winn Endothelin antagonists
ES2259803T3 (es) 1996-02-13 2006-10-16 Abbott Laboratories Nuevos derivados de pirrolidina sustituidos con benzo-1,3-dioxolilo y benzofuranilo como antagonistas de endostelina.
US6159990A (en) 1997-06-18 2000-12-12 Synaptic Pharmaceutical Corporation Oxazolidinones as α1A receptor antagonists
NZ502395A (en) 1997-08-04 2002-08-28 Abbott Lab 4-Benzodioxolyl substituted pyrrolidine-3-carboxylic acid derivatives useful as endothelin antagonists
WO1999031507A1 (en) 1997-12-18 1999-06-24 Eli Lilly And Company Peptidomimetic template-based combinatorial libraries
US6770658B2 (en) 1998-09-09 2004-08-03 Inflazyme Pharmaceuticals Ltd. Substituted γ-phenyl-Δ-lactams and uses related thereto
US7214540B2 (en) * 1999-04-06 2007-05-08 Uab Research Foundation Method for screening crystallization conditions in solution crystal growth
US6630006B2 (en) * 1999-06-18 2003-10-07 The Regents Of The University Of California Method for screening microcrystallizations for crystal formation
US7195670B2 (en) * 2000-06-27 2007-03-27 California Institute Of Technology High throughput screening of crystallization of materials
US7052545B2 (en) * 2001-04-06 2006-05-30 California Institute Of Technology High throughput screening of crystallization of materials
DE19951418A1 (de) * 1999-10-26 2001-05-03 Merck Patent Gmbh Verfahren zur Herstellung von N-(4,5-Bismethansulfonyl-2-methyl-benzoyl) -guanidin, Hydrochlorid
WO2002017912A1 (en) 2000-08-31 2002-03-07 Abbott Laboratories Endothelin antagonists
AU2002228598A1 (en) * 2000-11-20 2002-06-03 Parallel Synthesis Technologies, Inc. Methods and devices for high throughput crystallization
HUP0304058A2 (hu) 2001-01-30 2004-04-28 Bristol-Myers Squibb Company Xa faktor szulfonamid-laktám inhibitorok és alkalmazásuk és ezeket tartalmazó gyógyszerkészítmények
CA2446380A1 (en) 2001-05-08 2002-11-14 Yale University Proteomimetic compounds and methods
WO2002094787A1 (en) 2001-05-23 2002-11-28 Ucb, S.A. 2-oxo-piperidinyl- and 2-oxo-azepanyl alkanoic acid derivativ es for the treatment of epilepsy and other neurological disorders
BR0215157A (pt) 2001-12-18 2004-10-19 Hoffmann La Roche Cis-2,4,5-trifenil-imidazolinas e seu uso no tratamento de tumores
US6860940B2 (en) * 2002-02-11 2005-03-01 The Regents Of The University Of California Automated macromolecular crystallization screening
US6916833B2 (en) * 2003-03-13 2005-07-12 Hoffmann-La Roche Inc. Substituted piperidines
US7425638B2 (en) 2003-06-17 2008-09-16 Hoffmann-La Roche Inc. Cis-imidazolines
BRPI0511328A (pt) 2004-05-18 2007-12-04 Hoffmann La Roche cis-imidazolinas
US7893278B2 (en) 2004-06-17 2011-02-22 Hoffman-La Roche Inc. CIS-imidazolines
JP2007297283A (ja) * 2004-07-28 2007-11-15 Santen Pharmaceut Co Ltd 新規桂皮酸関連化合物
EA012181B1 (ru) 2004-10-18 2009-08-28 Амген, Инк. Соединения тиадиазола и их применение
CN102372704B (zh) 2005-02-18 2014-10-08 田边三菱制药株式会社 脯氨酸衍生物的盐,其溶剂合物,及其生产方法
JP4955646B2 (ja) 2005-03-16 2012-06-20 エフ.ホフマン−ラ ロシュ アーゲー シス−2,4,5−トリアリール−イミダゾリン及びそれらの抗癌薬としての使用
US20060270709A1 (en) 2005-04-04 2006-11-30 Eisai Co. Ltd. Dihydropyridine compounds and compositions for headaches
JP5284779B2 (ja) * 2005-06-07 2013-09-11 ラモット・アット・テル・アビブ・ユニバーシテイ・リミテッド コンジュゲート化された向精神薬の新規な塩およびその調製方法
WO2007015929A2 (en) * 2005-07-27 2007-02-08 University Of Toledo Epothilone analogues
CN101316823B (zh) 2005-12-01 2013-05-22 霍夫曼-拉罗奇有限公司 用作抗癌剂的作为p53和MDM2蛋白之间相互作用的抑制剂的2,4,5-三苯基咪唑啉衍生物
MY149143A (en) 2006-01-18 2013-07-15 Amgen Inc Thiazole compounds as protien kinase b (pkb) inhibitors
US20070213341A1 (en) 2006-03-13 2007-09-13 Li Chen Spiroindolinone derivatives
CN101595107A (zh) 2006-06-30 2009-12-02 先灵公司 能提高p53活性的有取代哌啶及其用途
EP2046328A4 (en) 2006-07-19 2009-10-28 Univ Georgia Res Found PYRIDINONE DIKETOIC ACIDS: INHIBITORS OF HIV REPLICATION IN COMBINATION THERAPY
US7618989B2 (en) 2006-08-15 2009-11-17 Wyeth Tricyclic oxazolidone derivatives useful as PR modulators
US20080045560A1 (en) 2006-08-15 2008-02-21 Wyeth Pyrrolidine and related derivatives useful as PR modulators
TW200831080A (en) 2006-12-15 2008-08-01 Irm Llc Compounds and compositions as inhibitors of cannabinoid receptor 1 activity
GB0722769D0 (en) 2007-11-21 2008-01-02 Biolipox Ab New compounds
WO2008118454A2 (en) 2007-03-23 2008-10-02 Amgen Inc. Derivatives of quinoline or benzopyrazine and their uses for the treatment of (inter alia) inflammatory diseases, autoimmune diseases or various kinds of cancer
RS53151B (sr) 2007-03-23 2014-06-30 Amgen Inc. 3-supstituisani derivati hinolina ili hinoksalina i njihova upotreba kao inhibitora fosfatidilinozitol 3-kinaze (pi3k)
EA017389B1 (ru) 2007-03-23 2012-12-28 Амген Инк. Гетероциклические соединения и их применение
US7625895B2 (en) 2007-04-12 2009-12-01 Hoffmann-Le Roche Inc. Diphenyl-dihydro-imidazopyridinones
WO2008130614A2 (en) 2007-04-20 2008-10-30 University Of Pittsburg-Of The Commonwealth System Of Higher Education Selective and dual-action p53/mdm2/mdm4 antagonists
US7834179B2 (en) 2007-05-23 2010-11-16 Hoffmann-La Roche Inc. Spiroindolinone derivatives
WO2009004430A1 (en) 2007-06-29 2009-01-08 Pfizer Inc. N-benzyl oxazolidinones and related heterocycleic compounds as potentiators of glutamate receptors
CN101809002B (zh) 2007-07-09 2013-03-27 阿斯利康(瑞典)有限公司 用于与mtor激酶和/或pi3k相关的疾病中的吗啉代嘧啶衍生物
US7897619B2 (en) 2007-07-17 2011-03-01 Amgen Inc. Heterocyclic modulators of PKB
AU2008276512A1 (en) 2007-07-17 2009-01-22 Amgen Inc. Thiadiazole modulators of PKB
AU2008282728B2 (en) 2007-08-02 2012-04-19 Amgen Inc. Pl3 kinase modulators and methods of use
MX2010003868A (es) 2007-10-09 2010-04-27 Hoffmann La Roche Cis-imidazolinas quirales.
AU2008343813B2 (en) 2007-12-19 2012-04-12 Amgen Inc. Inhibitors of PI3 kinase
US7776875B2 (en) 2007-12-19 2010-08-17 Hoffman-La Roche Inc. Spiroindolinone derivatives
US20100256191A1 (en) 2007-12-26 2010-10-07 Eisai R&D Management Co., Ltd. Ampa receptor antagonists and zonisamide for epilepsy
CA2718959A1 (en) 2008-03-21 2009-09-24 Chlorion Pharma, Inc. Substituted pyrrolidine and piperidine compounds, derivatives thereof, and methods for treating pain
JP5599783B2 (ja) 2008-05-30 2014-10-01 アムジエン・インコーポレーテツド Pi3キナーゼの阻害薬
GB0811643D0 (en) 2008-06-25 2008-07-30 Cancer Rec Tech Ltd New therapeutic agents
WO2010030704A2 (en) * 2008-09-10 2010-03-18 Achaogen, Inc. Antibacterial aminoglycoside analogs
AR073578A1 (es) 2008-09-15 2010-11-17 Priaxon Ag Pirrolidin-2-onas
AU2009294673B2 (en) 2008-09-18 2014-08-14 F. Hoffmann-La Roche Ag Substituted pyrrolidine-2-carboxamides
WO2010083246A1 (en) 2009-01-15 2010-07-22 Amgen Inc. Fluoroisoquinoline substituted thiazole compounds and methods of use
AU2010216239B2 (en) 2009-02-18 2012-06-14 Amgen Inc. Indole/benzimidazole compounds as mTOR kinase inhibitors
MX2011009796A (es) 2009-03-20 2011-12-14 Amgen Inc Inhibidores de la cinasa pi3.
US8076482B2 (en) 2009-04-23 2011-12-13 Hoffmann-La Roche Inc. 3,3′-spiroindolinone derivatives
UY32582A (es) 2009-04-28 2010-11-30 Amgen Inc Inhibidores de fosfoinositida 3 cinasa y/u objetivo mamífero
MX2011012037A (es) 2009-05-13 2012-02-28 Amgen Inc Compuestos de heteroarilo como inhibidores de pikk.
EA201270013A1 (ru) 2009-06-25 2012-06-29 Амген Инк. Гетероциклические соединения и их применение
CN102625799A (zh) 2009-06-25 2012-08-01 安姆根有限公司 杂环化合物及其用途
WO2010151735A2 (en) 2009-06-25 2010-12-29 Amgen Inc. Heterocyclic compounds and their uses
EP2445902A2 (en) 2009-06-25 2012-05-02 Amgen, Inc Heterocyclic compounds and their uses as inhibitors of pi3k activity
WO2011023677A1 (en) 2009-08-26 2011-03-03 Novartis Ag Tetra-substituted heteroaryl compounds and their use as mdm2 and/or mdm4 modulators
EP2486044A2 (en) * 2009-10-09 2012-08-15 Achaogen, Inc. Antibacterial aminoglycoside analogs
US8088815B2 (en) 2009-12-02 2012-01-03 Hoffman-La Roche Inc. Spiroindolinone pyrrolidines
US8440693B2 (en) 2009-12-22 2013-05-14 Novartis Ag Substituted isoquinolinones and quinazolinones
EP2534667A2 (en) * 2010-02-10 2012-12-19 Mochii, Inc. (d/b/a Voxa) Aberration-correcting dark-field electron microscopy
IT1399923B1 (it) * 2010-05-11 2013-05-09 Cbb Net S A Procedimento di preparazione di sali dell'acido (r) alfa-lipoico loro formulazione ed uso nelle composizioni farmaceutiche in forma di compresse che li contengono
JO2998B1 (ar) 2010-06-04 2016-09-05 Amgen Inc مشتقات بيبيريدينون كمثبطات mdm2 لعلاج السرطان
TWI674262B (zh) * 2011-01-10 2019-10-11 美商英菲尼提製藥股份有限公司 製備異喹啉酮之方法及異喹啉酮之固體形式
CN102153557B (zh) 2011-01-21 2013-03-20 中国科学院上海有机化学研究所 具有乙二胺骨架的多手性中心氮杂环卡宾前体盐、合成方法及用途
KR101921102B1 (ko) * 2011-04-28 2018-11-22 고꾸리츠 다이가꾸 호우징 오까야마 다이가꾸 아조디카본아미드의 신규 제조법
TW201309651A (zh) * 2011-06-29 2013-03-01 Otsuka Pharma Co Ltd 阿立哌唑(aripiprazole)無水物B形結晶微粒子之製造方法
MX352672B (es) 2011-09-27 2017-12-04 Amgen Inc Compuestos heterocíclicos como inhibidores de mdm2 para el tratamiento del cáncer.
CN103373951B (zh) * 2012-04-28 2016-03-09 上海医药工业研究院 一种拉帕替尼中间体的制备方法
US20160002185A1 (en) 2013-02-19 2016-01-07 Amgen Inc. Cis-morpholinone and other compounds as mdm2 inhibitors for the treatment of cancer
CA2902856C (en) 2013-02-28 2021-02-16 Amgen Inc. A benzoic acid derivative mdm2 inhibitor for the treatment of cancer
AU2014236812B2 (en) 2013-03-14 2018-03-01 Amgen Inc. Heteroaryl acid morpholinone compounds as MDM2 inhibitors for the treatment of cancer
CN105358530A (zh) 2013-06-10 2016-02-24 美国安进公司 制备mdm2抑制剂的方法及其结晶形式

Similar Documents

Publication Publication Date Title
JP2025084856A5 (https=)
JP5752256B2 (ja) 2−メトキシメチル−1,4−ベンゼンジアミンの製造方法
JP2017520547A5 (https=)
JP2020097607A (ja) クロマノン誘導体の新規な製造方法
JP2011046751A (ja) ヒンバシンアナログの合成
JP2020525447A5 (https=)
WO2010004957A1 (ja) キラルなイリジウムアクア錯体およびそれを用いた光学活性ヒドロキシ化合物の製造方法
JP2010043053A (ja) 高純度のレバミピドの製造方法
JP2008539163A (ja) ヒドラゾン類の製造法
JP5039419B2 (ja) クロスカップリング化合物の製造方法
TW201326116A (zh) 2,6-二乙基-4-甲基苯醋酸之製造方法
JP6124015B2 (ja) ペンタフルオロスルファニル安息香酸の製造方法
JP2024096941A5 (https=)
CN100516022C (zh) 高纯度烯胺类的制备方法
JP4023255B2 (ja) ジカルボン酸の製造方法とそれに用いる触媒の製造方法
JP3817478B2 (ja) 3,3−ジフェニル−2,3−エポキシプロピオン酸エステルのエナンチオ選択的製造方法
JP2008517967A5 (https=)
JPH06771B2 (ja) オキセタン−3−カルボン酸の製法
US6403817B1 (en) Method for preparing prostaglandin E-type compound
JPS6254416B2 (https=)
JP2006124325A (ja) dl−1,2−ジフェニルエチレンジアミンの製造方法
JP2005289988A (ja) アミノ化合物の製造法
WO2001096273A1 (en) Process for the preparation of 1-substituted-cyclo-hexanecarbonyl halides
CN121064191A (zh) 一种奥格列龙半钙盐水合物的制备方法
TW565564B (en) Process for the production of N-phosphonomethylglycine