TWI791153B - Mdm2抑制劑之製備方法及結晶型 - Google Patents

Mdm2抑制劑之製備方法及結晶型 Download PDF

Info

Publication number
TWI791153B
TWI791153B TW109118829A TW109118829A TWI791153B TW I791153 B TWI791153 B TW I791153B TW 109118829 A TW109118829 A TW 109118829A TW 109118829 A TW109118829 A TW 109118829A TW I791153 B TWI791153 B TW I791153B
Authority
TW
Taiwan
Prior art keywords
chlorophenyl
mixture
added
compound
water
Prior art date
Application number
TW109118829A
Other languages
English (en)
Chinese (zh)
Other versions
TW202035370A (zh
Inventor
馬修 比歐
西貝斯汀 凱爾
布萊恩 可琪瑞
方淵清
布萊恩 M 福斯
布萊恩 S 盧卡斯
羅倫斯 R 麥克奇
飛利薩提 沃那索斯
尚恩 衛德曼
沙拉 沃特曼
Original Assignee
美商安美基公司
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=51063849&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=TWI791153(B) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by 美商安美基公司 filed Critical 美商安美基公司
Publication of TW202035370A publication Critical patent/TW202035370A/zh
Application granted granted Critical
Publication of TWI791153B publication Critical patent/TWI791153B/zh

Links

Images

Classifications

    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/451Non condensed piperidines, e.g. piperocaine having a carbocyclic group directly attached to the heterocyclic ring, e.g. glutethimide, meperidine, loperamide, phencyclidine, piminodine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D211/00Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings
    • C07D211/04Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D211/68Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having one double bond between ring members or between a ring member and a non-ring member
    • C07D211/72Heterocyclic compounds containing hydrogenated pyridine rings, not condensed with other rings with only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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, directly attached to ring carbon atoms
    • C07D211/74Oxygen atoms
    • C07D211/76Oxygen atoms attached in position 2 or 6
    • 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
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/44Non condensed pyridines; Hydrogenated derivatives thereof
    • A61K31/445Non condensed piperidines, e.g. piperocaine
    • A61K31/45Non condensed piperidines, e.g. piperocaine having oxo groups directly attached to the heterocyclic ring, e.g. cycloheximide
    • 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
    • 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
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/02Sulfonic acids having sulfo groups bound to acyclic carbon atoms
    • C07C309/03Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton
    • C07C309/04Sulfonic acids having sulfo groups bound to acyclic carbon atoms of an acyclic saturated carbon skeleton containing only one sulfo group
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/25Sulfonic acids having sulfo groups bound to carbon atoms of rings other than six-membered aromatic rings of a carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C309/00Sulfonic acids; Halides, esters, or anhydrides thereof
    • C07C309/01Sulfonic acids
    • C07C309/28Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C309/33Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton of six-membered aromatic rings being part of condensed ring systems
    • C07C309/34Sulfonic acids having sulfo groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton of six-membered aromatic rings being part of condensed ring systems formed by two rings
    • C07C309/35Naphthalene sulfonic acids
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C313/00Sulfinic acids; Sulfenic acids; Halides, esters or anhydrides thereof; Amides of sulfinic or sulfenic acids, i.e. compounds having singly-bound oxygen atoms of sulfinic or sulfenic groups replaced by nitrogen atoms, not being part of nitro or nitroso groups
    • C07C313/02Sulfinic acids; Derivatives thereof
    • 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
    • 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
    • C07D491/04Ortho-condensed systems
    • C07D491/044Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring
    • C07D491/048Ortho-condensed systems with only one oxygen atom as ring hetero atom in the oxygen-containing ring the oxygen-containing ring being five-membered
    • 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
    • C07D498/04Ortho-condensed systems
    • 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)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Hydrogenated Pyridines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Enzymes And Modification Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Epoxy Compounds (AREA)
TW109118829A 2013-06-10 2014-06-10 Mdm2抑制劑之製備方法及結晶型 TWI791153B (zh)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US201361833196P 2013-06-10 2013-06-10
US61/833,196 2013-06-10

Publications (2)

Publication Number Publication Date
TW202035370A TW202035370A (zh) 2020-10-01
TWI791153B true TWI791153B (zh) 2023-02-01

Family

ID=51063849

Family Applications (3)

Application Number Title Priority Date Filing Date
TW109118829A TWI791153B (zh) 2013-06-10 2014-06-10 Mdm2抑制劑之製備方法及結晶型
TW107134691A TWI698428B (zh) 2013-06-10 2014-06-10 Mdm2抑制劑之製備方法及結晶型
TW103120104A TWI649306B (zh) 2013-06-10 2014-06-10 Mdm2抑制劑之製備方法及結晶型

Family Applications After (2)

Application Number Title Priority Date Filing Date
TW107134691A TWI698428B (zh) 2013-06-10 2014-06-10 Mdm2抑制劑之製備方法及結晶型
TW103120104A TWI649306B (zh) 2013-06-10 2014-06-10 Mdm2抑制劑之製備方法及結晶型

Country Status (38)

Country Link
US (10) US9376386B2 (enExample)
EP (2) EP3008039B1 (enExample)
JP (5) JP6998655B2 (enExample)
KR (4) KR20160018576A (enExample)
CN (3) CN110627708A (enExample)
AP (1) AP2015008891A0 (enExample)
AR (3) AR096582A1 (enExample)
AU (5) AU2014278428B2 (enExample)
BR (2) BR112015031004B1 (enExample)
CA (4) CA2914723C (enExample)
CL (3) CL2015003589A1 (enExample)
CR (2) CR20210290A (enExample)
CY (1) CY1123661T1 (enExample)
DK (1) DK3008039T3 (enExample)
EA (3) EA031254B1 (enExample)
ES (1) ES2851023T3 (enExample)
HR (1) HRP20202065T1 (enExample)
HU (1) HUE053047T2 (enExample)
IL (4) IL297860A (enExample)
JO (2) JOP20200296A1 (enExample)
LT (1) LT3008039T (enExample)
MA (3) MA38714A1 (enExample)
MX (2) MX2015016856A (enExample)
MY (2) MY205257A (enExample)
NZ (1) NZ714821A (enExample)
PE (2) PE20160113A1 (enExample)
PH (2) PH12020550916A1 (enExample)
PL (1) PL3008039T3 (enExample)
PT (1) PT3008039T (enExample)
RS (1) RS61192B1 (enExample)
SG (2) SG11201509896VA (enExample)
SI (1) SI3008039T1 (enExample)
SM (1) SMT202100013T1 (enExample)
TN (1) TN2015000521A1 (enExample)
TW (3) TWI791153B (enExample)
UA (2) UA129695C2 (enExample)
UY (2) UY35605A (enExample)
WO (1) WO2014200937A1 (enExample)

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
WO2013049250A1 (en) 2011-09-27 2013-04-04 Amgen Inc. Heterocyclic compounds as mdm2 inhibitors for the treatment of cancer
US11407721B2 (en) 2013-02-19 2022-08-09 Amgen Inc. CIS-morpholinone and other compounds as MDM2 inhibitors for the treatment of cancer
US9758495B2 (en) 2013-03-14 2017-09-12 Amgen Inc. Heteroaryl acid morpholinone compounds as MDM2 inhibitors for the treatment of cancer
JOP20200296A1 (ar) * 2013-06-10 2017-06-16 Amgen Inc عمليات صنع وأشكال بلورية من mdm2 مثبط
KR102305351B1 (ko) 2013-11-11 2021-09-24 암젠 인크 암의 치료를 위한, mdm2 억제제 및 하나 이상의 추가적 약제학적 활성 제제를 포함하는 조합 요법
JP2019522633A (ja) 2016-05-20 2019-08-15 ジェネンテック, インコーポレイテッド Protac抗体コンジュゲート及び使用方法
IL319432A (en) * 2018-04-30 2025-05-01 Kartos Therapeutics Inc Methods of treating cancer
WO2019224803A2 (en) * 2018-05-25 2019-11-28 Kartos Therapeutics, Inc. Methods of treating myeloproliferative neoplasms
WO2020047424A1 (en) * 2018-08-31 2020-03-05 Amgen, Inc. Processes for preparing a 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
WO2021236474A1 (en) * 2020-05-22 2021-11-25 Merck Sharp & Dohme Corp. Novel processes for preparing conjugates of the il-2 protein
CN116194088A (zh) 2020-08-27 2023-05-30 大冢制药株式会社 使用mdm2拮抗剂治疗癌症的生物标志物
GB202103080D0 (en) 2021-03-04 2021-04-21 Otsuka Pharma Co Ltd Cancer biomarkers
CA3227793A1 (en) * 2021-08-05 2023-02-09 Yong Moon Choi Phenylcarbamate crystalline form and method for manufacturing the same
US12054449B2 (en) 2021-08-05 2024-08-06 Bio-Pharm Solutions Co., Ltd. Phenylcarbamate crystalline form and method for manufacturing the same
US20250134877A1 (en) * 2021-09-09 2025-05-01 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

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011153509A1 (en) * 2010-06-04 2011-12-08 Amgen Inc. Piperidinone derivatives as mdm2 inhibitors for the treatment of cancer

Family Cites Families (92)

* 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
US5334720A (en) 1991-03-07 1994-08-02 Fisons Corporation Diphenyl-1-(aminoalkyl)-2-piperidinone and -2-pyrrolidinone derivatives having anticonvulsant properties
WO1995023135A1 (en) 1991-03-07 1995-08-31 Fisons Corporation Diphenyl-2-piperidinone and -2-pyrrolidinone derivatives having anti-convulsant and neuroprotective activity
DE69527072T2 (de) 1994-08-19 2003-02-13 Abbott Laboratories, Abbott Park Endothelin antagoniste
EP0885215B1 (en) 1996-02-13 2006-04-19 Abbott Laboratories Novel benzo-1,3-dioxolyl- and benzofuranyl substituted pyrrolidine derivatives as endothelin antagonists
WO1999006397A2 (en) 1997-08-04 1999-02-11 Abbott Laboratories Pyrrolidine-3-carboxylic acid derivatives and their use as endothelin antagonists
US6159990A (en) 1997-06-18 2000-12-12 Synaptic Pharmaceutical Corporation Oxazolidinones as α1A receptor antagonists
AU1910299A (en) 1997-12-18 1999-07-05 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
US7052545B2 (en) * 2001-04-06 2006-05-30 California Institute Of Technology High throughput screening of crystallization of materials
US7195670B2 (en) * 2000-06-27 2007-03-27 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
DE60229059D1 (de) 2001-05-08 2008-11-06 Univ Yale Proteomimetische verbindungen und verfahren
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
RU2305095C2 (ru) 2001-12-18 2007-08-27 Ф.Хоффманн-Ля Рош Аг Цис-2,4,5-трифенилимидазолины и фармацевтическая композиция на их основе
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
MXPA06013246A (es) 2004-05-18 2007-02-08 Hoffmann La Roche Nuevas imidazolinas cis.
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
CN101389335A (zh) 2004-10-18 2009-03-18 安姆根有限公司 噻二唑化合物和使用方法
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
WO2006097261A1 (en) 2005-03-16 2006-09-21 F.Hoffmann-La Roche Ag Cis-2,4,5-triaryl-imidazolines and their use as anti-cancer medicaments
EP1871368B1 (en) 2005-04-04 2011-06-08 Eisai R&D Management Co., Ltd. Dihydropyridine compounds for neurodegenerative diseases and dementia
CA2610838A1 (en) * 2005-06-07 2006-12-14 Ramot At Tel Aviv University Ltd. Novel salts of conjugated psychotropic drugs and processes of preparing same
WO2007015929A2 (en) * 2005-07-27 2007-02-08 University Of Toledo Epothilone analogues
JP4870778B2 (ja) 2005-12-01 2012-02-08 エフ.ホフマン−ラ ロシュ アーゲー 抗ガン剤として使用されるp53およびmdm2タンパク質間の相互作用の阻害剤としての2,4,5−トリフェニルイミダゾリン誘導体
US7514566B2 (en) 2006-01-18 2009-04-07 Amgen, Inc. Thiazole compounds and methods of use
US20070213341A1 (en) 2006-03-13 2007-09-13 Li Chen Spiroindolinone derivatives
WO2008005268A1 (en) 2006-06-30 2008-01-10 Schering Corporation Substituted piperidines that increase p53 activity and the uses thereof
US20100092427A1 (en) 2006-07-19 2010-04-15 The University Of Georgia Research Foundation Pyridinone Diketo Acids: Inhibitors of HIV Replication in Combination Therapy
WO2008021338A2 (en) 2006-08-15 2008-02-21 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
SI2139882T1 (sl) 2007-03-23 2014-03-31 Amgen Inc. 3-substituirani kinolinski ali kinoksalinski derivati in njihoba uporaba kot inhibitorji fosfatidilinozitol 3-kinaze (pi3k)
CA2680783C (en) 2007-03-23 2012-04-24 Amgen Inc. Heterocyclic compounds and their uses
CA2681136C (en) 2007-03-23 2012-05-22 Amgen Inc. Heterocyclic compounds and their uses
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
ES2385692T3 (es) 2007-07-09 2012-07-30 Astrazeneca Ab Derivados de morfolino pirimidina usados en enfermedades relacionadas con mTOR quinasa y/o PI3K
US7919504B2 (en) 2007-07-17 2011-04-05 Amgen Inc. Thiadiazole modulators of PKB
US7897619B2 (en) 2007-07-17 2011-03-01 Amgen Inc. Heterocyclic modulators of PKB
ES2401557T3 (es) 2007-08-02 2013-04-22 Amgen, Inc Moduladores de Pl3 cinasas y métodos de uso
KR101203020B1 (ko) 2007-10-09 2012-11-20 에프. 호프만-라 로슈 아게 카이랄 시스-이미다졸린
US7776875B2 (en) 2007-12-19 2010-08-17 Hoffman-La Roche Inc. Spiroindolinone derivatives
US7820665B2 (en) 2007-12-19 2010-10-26 Amgen Inc. Imidazopyridazine inhibitors of PI3 kinase for cancer treatment
US20100256191A1 (en) 2007-12-26 2010-10-07 Eisai R&D Management Co., Ltd. Ampa receptor antagonists and zonisamide for epilepsy
US20110105488A1 (en) 2008-03-21 2011-05-05 Chlorion Pharma, Inc. Substituted pyrrolidine and piperidine compounds, derivatives thereof, and methods for treating pain
US8415376B2 (en) 2008-05-30 2013-04-09 Amgen Inc. Inhibitors of PI3 kinase
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
TW201011009A (en) 2008-09-15 2010-03-16 Priaxon Ag Novel pyrrolidin-2-ones
AU2009294673B2 (en) 2008-09-18 2014-08-14 F. Hoffmann-La Roche Ag Substituted pyrrolidine-2-carboxamides
EP2387570A1 (en) 2009-01-15 2011-11-23 Amgen, Inc Fluoroisoquinoline substituted thiazole compounds and methods of use
MX2011008674A (es) 2009-02-18 2011-11-04 Amgen Inc Compuestos de indol/bencimidazol como inhibidores de quinasa mtor.
US8729074B2 (en) 2009-03-20 2014-05-20 Amgen Inc. Inhibitors of PI3 kinase
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
CA2760778A1 (en) 2009-05-13 2010-11-18 Amgen Inc. Heteroaryl compounds as pikk inhibitors
EP2445902A2 (en) 2009-06-25 2012-05-02 Amgen, Inc Heterocyclic compounds and their uses as inhibitors of pi3k activity
EA201270013A1 (ru) 2009-06-25 2012-06-29 Амген Инк. Гетероциклические соединения и их применение
CA2765823A1 (en) 2009-06-25 2010-12-29 Amgen Inc. Tricyclic heterocyclic compounds as mediators of p13k activity
JP2012531435A (ja) 2009-06-25 2012-12-10 アムジエン・インコーポレーテツド PI3K阻害剤としての4H−ピリド[1,2−a]ピリミジン−4−オン誘導体
CA2771936A1 (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
JP2013519980A (ja) * 2010-02-10 2013-05-30 モチイ,インコーポレイテッド(ディービーエー ヴォクサ) 収差補正暗視野電子顕微鏡
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
EP2663309B1 (en) * 2011-01-10 2017-03-15 Infinity Pharmaceuticals, Inc. Processes for preparing isoquinolinones and solid forms of isoquinolinones
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
WO2012147953A1 (ja) * 2011-04-28 2012-11-01 大塚化学株式会社 アゾジカルボンアミドの新規製造法
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
WO2013049250A1 (en) 2011-09-27 2013-04-04 Amgen Inc. Heterocyclic compounds as mdm2 inhibitors for the treatment of cancer
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
JP6417338B2 (ja) 2013-02-19 2018-11-07 アムジエン・インコーポレーテツド 癌の治療のためのmdm2阻害剤としてのシス−モルホリノン及び他の化合物
EP2961735B1 (en) 2013-02-28 2017-09-27 Amgen Inc. A benzoic acid derivative mdm2 inhibitor for the treatment of cancer
US9758495B2 (en) 2013-03-14 2017-09-12 Amgen Inc. Heteroaryl acid morpholinone compounds as MDM2 inhibitors for the treatment of cancer
JOP20200296A1 (ar) 2013-06-10 2017-06-16 Amgen Inc عمليات صنع وأشكال بلورية من mdm2 مثبط

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2011153509A1 (en) * 2010-06-04 2011-12-08 Amgen Inc. Piperidinone derivatives as mdm2 inhibitors for the treatment of cancer

Also Published As

Publication number Publication date
JOP20200296A1 (ar) 2017-06-16
US20160289178A1 (en) 2016-10-06
CA2914723A1 (en) 2014-12-18
MA43288A1 (fr) 2020-04-30
TW202035370A (zh) 2020-10-01
EP3805232A1 (en) 2021-04-14
US20160287570A1 (en) 2016-10-06
CA3115609C (en) 2023-08-08
IL281807B2 (en) 2023-04-01
PH12015502705B1 (en) 2022-04-27
KR20210121270A (ko) 2021-10-07
CR20210290A (es) 2021-07-23
EA201891642A1 (ru) 2019-08-30
SG11201509896VA (en) 2016-01-28
TW201922705A (zh) 2019-06-16
JP7263439B2 (ja) 2023-04-24
EA202091612A1 (ru) 2020-10-05
IL281807B (en) 2022-12-01
US9757367B2 (en) 2017-09-12
WO2014200937A1 (en) 2014-12-18
KR20240159641A (ko) 2024-11-05
MX2015016856A (es) 2016-04-07
CL2019000056A1 (es) 2019-05-03
CR20160010A (es) 2016-02-04
EP3008039B1 (en) 2020-11-11
JO3768B1 (ar) 2021-01-31
CN110003092A (zh) 2019-07-12
US20140364455A1 (en) 2014-12-11
JP2020147573A (ja) 2020-09-17
UY35605A (es) 2015-01-30
CA3115609A1 (en) 2014-12-18
US20160289190A1 (en) 2016-10-06
MY205257A (en) 2024-10-09
AR119727A2 (es) 2022-01-05
DK3008039T3 (da) 2021-01-04
AR096582A1 (es) 2016-01-20
US20200281912A1 (en) 2020-09-10
JP2021130685A (ja) 2021-09-09
RS61192B1 (sr) 2021-01-29
TW201536743A (zh) 2015-10-01
KR20230019216A (ko) 2023-02-07
PT3008039T (pt) 2021-01-13
CN110627708A (zh) 2019-12-31
NZ753956A (en) 2020-12-18
AU2022271425A1 (en) 2022-12-22
SG10201801402XA (en) 2018-04-27
US20180092898A1 (en) 2018-04-05
SI3008039T1 (sl) 2021-03-31
AU2020267169A1 (en) 2020-12-03
MX379872B (es) 2025-03-11
UA121301C2 (uk) 2020-05-12
HRP20202065T1 (hr) 2021-02-19
LT3008039T (lt) 2021-01-25
PL3008039T3 (pl) 2021-04-19
AU2022271425B2 (en) 2024-06-13
AU2024216533A1 (en) 2024-09-19
MA53572A1 (fr) 2021-10-29
US9376386B2 (en) 2016-06-28
JP2025084856A (ja) 2025-06-03
BR112015031004A2 (pt) 2020-05-12
JP6998655B2 (ja) 2022-02-04
CA2914723C (en) 2021-06-15
AR132854A2 (es) 2025-08-06
CN105358530A (zh) 2016-02-24
US20220280496A1 (en) 2022-09-08
IL281807A (en) 2021-05-31
US9855259B2 (en) 2018-01-02
EA031254B1 (ru) 2018-12-28
UY40179A (es) 2023-04-14
US20230301974A1 (en) 2023-09-28
US20160264526A1 (en) 2016-09-15
US9801867B2 (en) 2017-10-31
CA3200532A1 (en) 2014-12-18
BR122020003153B1 (pt) 2022-09-27
AU2018260844A1 (en) 2018-11-22
JP6891322B2 (ja) 2021-06-18
KR20160018576A (ko) 2016-02-17
MA38714A1 (fr) 2017-10-31
TN2015000521A1 (en) 2017-04-06
JP2016528179A (ja) 2016-09-15
PH12015502705A1 (en) 2016-03-14
TWI698428B (zh) 2020-07-11
PE20210153A1 (es) 2021-01-26
PH12020550916A1 (en) 2024-03-25
MX2019012007A (es) 2019-11-11
SMT202100013T1 (it) 2021-03-15
BR112015031004B1 (pt) 2022-09-20
EA201592305A1 (ru) 2016-05-31
UA129695C2 (uk) 2025-07-09
IL266504A (en) 2019-07-31
IL297860A (en) 2023-01-01
AU2020267169B2 (en) 2022-08-25
CY1123661T1 (el) 2022-03-24
TWI649306B (zh) 2019-02-01
PE20160113A1 (es) 2016-03-03
CA3201958A1 (en) 2014-12-18
IL242622B (en) 2019-06-30
NZ714821A (en) 2020-10-30
CL2021000566A1 (es) 2021-09-03
CL2015003589A1 (es) 2016-06-17
AU2014278428B2 (en) 2018-11-15
HUE053047T2 (hu) 2021-06-28
AU2014278428A1 (en) 2015-11-26
ES2851023T3 (es) 2021-09-02
AP2015008891A0 (en) 2015-11-30
IL266504B (en) 2021-04-29
AU2018260844B2 (en) 2020-08-13
IL242622A0 (en) 2016-02-01
US9623018B2 (en) 2017-04-18
US20160289243A1 (en) 2016-10-06
MY194848A (en) 2022-12-19
JP2023089126A (ja) 2023-06-27
MA43288B1 (fr) 2020-10-28
EP3008039A1 (en) 2016-04-20

Similar Documents

Publication Publication Date Title
TWI791153B (zh) Mdm2抑制劑之製備方法及結晶型
US20250295647A1 (en) Processes of making and crystalline forms of a mdm2 inhibitor
HK40050580A (en) Crystalline synthetic intermediate useful in processes for making a mdm2 inhibitor
HK1226052B (en) Crystalline form of a mdm2 inhibitor
HK1226052A1 (en) Crystalline form of a mdm2 inhibitor
NZ753956B2 (en) Processes of making and crystalline forms of a mdm2 inhibitor