SG10201801402XA - Processes of making and crystalline forms of a mdm2 inhibitor - Google Patents

Processes of making and crystalline forms of a mdm2 inhibitor

Info

Publication number
SG10201801402XA
SG10201801402XA SG10201801402XA SG10201801402XA SG10201801402XA SG 10201801402X A SG10201801402X A SG 10201801402XA SG 10201801402X A SG10201801402X A SG 10201801402XA SG 10201801402X A SG10201801402X A SG 10201801402XA SG 10201801402X A SG10201801402X A SG 10201801402XA
Authority
SG
Singapore
Prior art keywords
processes
making
crystalline forms
mdm2 inhibitor
mdm2
Prior art date
Application number
SG10201801402XA
Inventor
Matthew Bio
Sebastien Caille
Brian Cochran
Yuanqing Fang
Brian Fox
Brian Lucas
Lawrence Mcgee
Filisaty Vounatsos
Sean Wiedemann
Sarah Wortman
Original Assignee
Amgen Inc
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=SG10201801402X(A) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Amgen Inc filed Critical Amgen Inc
Publication of SG10201801402XA publication Critical patent/SG10201801402XA/en

Links

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
    • 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
    • C07D211/04Heterocyclic 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
    • 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
SG10201801402XA 2013-06-10 2014-06-09 Processes of making and crystalline forms of a mdm2 inhibitor SG10201801402XA (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201361833196P 2013-06-10 2013-06-10

Publications (1)

Publication Number Publication Date
SG10201801402XA true SG10201801402XA (en) 2018-04-27

Family

ID=51063849

Family Applications (2)

Application Number Title Priority Date Filing Date
SG10201801402XA SG10201801402XA (en) 2013-06-10 2014-06-09 Processes of making and crystalline forms of a mdm2 inhibitor
SG11201509896VA SG11201509896VA (en) 2013-06-10 2014-06-09 Processes of making and crystalline forms of a mdm2 inhibitor

Family Applications After (1)

Application Number Title Priority Date Filing Date
SG11201509896VA SG11201509896VA (en) 2013-06-10 2014-06-09 Processes of making and crystalline forms of a mdm2 inhibitor

Country Status (37)

Country Link
US (10) US9376386B2 (en)
EP (2) EP3805232A1 (en)
JP (4) JP6998655B2 (en)
KR (3) KR20160018576A (en)
CN (3) CN110003092A (en)
AP (1) AP2015008891A0 (en)
AR (2) AR096582A1 (en)
AU (4) AU2014278428B2 (en)
BR (2) BR122020003153B1 (en)
CA (4) CA3115609C (en)
CL (3) CL2015003589A1 (en)
CR (2) CR20210290A (en)
CY (1) CY1123661T1 (en)
DK (1) DK3008039T3 (en)
EA (3) EA031254B1 (en)
ES (1) ES2851023T3 (en)
HR (1) HRP20202065T1 (en)
HU (1) HUE053047T2 (en)
IL (4) IL297860A (en)
JO (2) JOP20200296A1 (en)
LT (1) LT3008039T (en)
MA (3) MA38714A1 (en)
MX (2) MX2015016856A (en)
MY (1) MY194848A (en)
NZ (1) NZ714821A (en)
PE (2) PE20210153A1 (en)
PH (1) PH12015502705A1 (en)
PL (1) PL3008039T3 (en)
PT (1) PT3008039T (en)
RS (1) RS61192B1 (en)
SG (2) SG10201801402XA (en)
SI (1) SI3008039T1 (en)
TN (1) TN2015000521A1 (en)
TW (3) TWI698428B (en)
UA (1) UA121301C2 (en)
UY (1) UY35605A (en)
WO (1) WO2014200937A1 (en)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JO2998B1 (en) 2010-06-04 2016-09-05 Amgen Inc Piperidinone derivatives as mdm2 inhibitors for the treatment of cancer
CA2850166C (en) 2011-09-27 2019-12-03 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
JP6377123B2 (en) 2013-03-14 2018-08-22 アムジエン・インコーポレーテツド Heteroaryl morpholinone compounds as MDM2 inhibitors for the treatment of cancer
JOP20200296A1 (en) 2013-06-10 2017-06-16 Amgen Inc Processes of Making and Crystalline Forms of a MDM2 Inhibitor
EP4039256A1 (en) 2013-11-11 2022-08-10 Amgen Inc. Combination therapy including an mdm2 inhibitor and dasatinib or nilotinib for the treatment of chronic myeloid leukemia
WO2017201449A1 (en) 2016-05-20 2017-11-23 Genentech, Inc. Protac antibody conjugates and methods of use
US20210186946A1 (en) * 2018-04-30 2021-06-24 Kartos Therapeutics, Inc. Methods of Treating Cancer
CN112804994A (en) * 2018-05-25 2021-05-14 卡托斯医疗公司 Method for treating myeloproliferative tumors
CA3110525A1 (en) * 2018-08-31 2020-03-05 Amgen, Inc. Processes for preparing a mdm2 inhibitor
CN110963958A (en) 2018-09-30 2020-04-07 上海长森药业有限公司 MDM2 inhibitor, and preparation method, pharmaceutical composition and application thereof
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
JP2023539867A (en) 2020-08-27 2023-09-20 大塚製薬株式会社 Biomarkers for cancer treatment using MDM2 antagonists
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
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

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
GB1016828A (en) 1961-11-13 1966-01-12 Mcneilab Inc Substituted morpholines and process for preparing same
US3518236A (en) * 1967-07-20 1970-06-30 Uniroyal Inc Acceleration of sulfur-vulcanization of rubber with sulfinic acids and derivatives
DE3246148A1 (en) 1982-12-14 1984-06-14 Troponwerke GmbH & Co KG, 5000 Köln Pyrazolo[4,3-b][1,4]-oxazines, process for their preparation and their use as medicaments
JP2604472B2 (en) 1989-07-12 1997-04-30 株式会社クラレ Polymerizable composition
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
CN1091768C (en) 1996-02-13 2002-10-02 艾博特公司 Novel benzo-1,3-dioxolyl- and benzofuranyl substituted pyrrolidine derivatives as endothelin antagonists
US6159990A (en) 1997-06-18 2000-12-12 Synaptic Pharmaceutical Corporation Oxazolidinones as α1A receptor antagonists
TR200000993T2 (en) 1997-08-04 2000-12-21 Abbott Laboratories 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
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 (en) * 1999-10-26 2001-05-03 Merck Patent Gmbh Process for the preparation of N- (4,5-bismethanesulfonyl-2-methyl-benzoyl) guanidine, hydrochloride
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 (en) 2001-01-30 2004-04-28 Bristol-Myers Squibb Company Sulfonamide lactam inhibitors of fxa and their use and pharmaceutical compositions containing them
EP1408986B1 (en) 2001-05-08 2008-09-24 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
ATE389400T1 (en) 2001-12-18 2008-04-15 Hoffmann La Roche CIS-2,4,5-TRIPHENYL-IMIDAZOLINE AND THEIR USE IN THE TREATMENT OF TUMORS
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
ES2314660T3 (en) 2004-05-18 2009-03-16 F. Hoffmann-La Roche Ag NEW CIS-IMIDAZOLINAS.
US7893278B2 (en) 2004-06-17 2011-02-22 Hoffman-La Roche Inc. CIS-imidazolines
JP2007297283A (en) 2004-07-28 2007-11-15 Santen Pharmaceut Co Ltd Novel cinnamic acid related compound
KR20070073791A (en) 2004-10-18 2007-07-10 암젠 인코포레이티드 Thiadiazole compounds and methods of use
BRPI0607863B8 (en) 2005-02-18 2021-05-25 Mitsubishi Pharma Corp 3-{(2s,4s)-4-[4-(3-methyl-1-phenyl-1h-pyrazol-5-yl)piperazin-1-yl]pyrrolidin-2-ylcarbonyl crystalline salt }thiazolidine and its preparation process
TWI314552B (en) 2005-03-16 2009-09-11 Hoffmann La Roche Novel cis-2,4,5-triaryl-imidazolines,their use as anti-cancer medicaments and their manufacture process
ME01224B (en) 2005-04-04 2013-06-20 Eisai R&D Man Co Ltd Dihydropyridine compounds for neurodegenerative diseases and dementia
JP5284779B2 (en) 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 Novel salts of conjugated psychotropic drugs and methods for their preparation
US7893268B2 (en) 2005-07-27 2011-02-22 University Of Toledo Epithiolone analogues
EP2311814A1 (en) 2005-12-01 2011-04-20 F. Hoffmann-La Roche AG 2,4,5-triphenyl imidazoline derivatives as inhibitors of the interaction between P53 and MDM2 proteins for use as anticancer agents
BRPI0706621A2 (en) 2006-01-18 2011-04-05 Amgen Inc compound, pharmaceutical composition, methods for treating a kinase-mediated disorder in a mammal and for treating a proliferation-related disorder in a mammal, and, use of the compound
US20070213341A1 (en) 2006-03-13 2007-09-13 Li Chen Spiroindolinone derivatives
CA2656398A1 (en) 2006-06-30 2008-01-10 Schering Corporation Substituted piperidines that increase p53 activity and the uses thereof
EP2046328A4 (en) 2006-07-19 2009-10-28 Univ Georgia Res Found Pyridinone diketo acids: inhibitors of hiv replication in combination therapy
US20080045560A1 (en) 2006-08-15 2008-02-21 Wyeth Pyrrolidine and related derivatives useful as PR modulators
US7618989B2 (en) 2006-08-15 2009-11-17 Wyeth Tricyclic oxazolidone 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
EP2139882B1 (en) 2007-03-23 2013-12-25 Amgen Inc. 3- substituted quinoline or quinoxaline derivatives and their use as phosphatidylinositol 3-kinase (pi3k) inhibitors
PT2137186E (en) 2007-03-23 2016-03-30 Amgen Inc Heterocyclic compounds and their uses
CA2680783C (en) 2007-03-23 2012-04-24 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
EA018708B1 (en) 2007-07-09 2013-10-30 Астразенека Аб MORPHOLINO PYRIMIDINE DERIVATIVES USED IN DISEASES LINKED TO mTOR KINASE AND/OR PI3K
AU2008276521B2 (en) 2007-07-17 2011-11-03 Amgen Inc. Heterocyclic modulators of PKB
US7919504B2 (en) 2007-07-17 2011-04-05 Amgen Inc. Thiadiazole modulators of PKB
TW200911798A (en) 2007-08-02 2009-03-16 Amgen Inc PI3 kinase modulators and methods of use
JP5324586B2 (en) 2007-10-09 2013-10-23 エフ.ホフマン−ラ ロシュ アーゲー Chiral cis-imidazoline
EP2231661A1 (en) 2007-12-19 2010-09-29 Amgen, Inc. Inhibitors of pi3 kinase
US7776875B2 (en) 2007-12-19 2010-08-17 Hoffman-La Roche Inc. Spiroindolinone derivatives
WO2009082038A2 (en) 2007-12-26 2009-07-02 Eisai R & D Management Co., Ltd. Ampa receptor antagonists and zonisamide for epilepsy
JP2011514364A (en) 2008-03-21 2011-05-06 クロリオン ファーマ,インコーポレーテッド Substituted pyrrolidine and piperidine compounds, derivatives thereof, and methods for treating pain
WO2009155121A2 (en) 2008-05-30 2009-12-23 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
AR073578A1 (en) 2008-09-15 2010-11-17 Priaxon Ag PIRROLIDIN-2-ONAS
PE20110367A1 (en) 2008-09-18 2011-06-13 Hoffmann La Roche DERIVATIVES OF 4-CYANO-4-PHENYL-PYRROLIDIN-2-CARBOXAMIDES SUBSTITUTED AS INHIBITORS OF THE INTERACTION p53-MDM2
EP2387570A1 (en) 2009-01-15 2011-11-23 Amgen, Inc Fluoroisoquinoline substituted thiazole compounds and methods of use
JP2012518037A (en) 2009-02-18 2012-08-09 アムジエン・インコーポレーテツド Indole / benzimidazole compounds as mTOR kinase inhibitors
WO2010108074A2 (en) 2009-03-20 2010-09-23 Amgen Inc. Inhibitors of pi3 kinase
US8076482B2 (en) 2009-04-23 2011-12-13 Hoffmann-La Roche Inc. 3,3′-spiroindolinone derivatives
UY32582A (en) 2009-04-28 2010-11-30 Amgen Inc 3 KINASE PHOSPHINOSITI INHIBITORS AND / OR MAMMAL OBJECTIVE
MX2011012037A (en) 2009-05-13 2012-02-28 Amgen Inc Heteroaryl compounds as pikk inhibitors.
EA201270051A1 (en) 2009-06-25 2012-05-30 Амген Инк. HETEROCYCLIC COMPOUNDS AND THEIR APPLICATIONS
JP2012531435A (en) 2009-06-25 2012-12-10 アムジエン・インコーポレーテツド 4H-pyrido [1,2-a] pyrimidin-4-one derivatives as PI3K inhibitors
TW201111362A (en) 2009-06-25 2011-04-01 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
IN2012DN01693A (en) 2009-08-26 2015-06-05 Novartis Ag
CA2777107A1 (en) 2009-10-09 2011-04-14 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
WO2011100434A2 (en) * 2010-02-10 2011-08-18 Chistopher Su-Yan Own Aberration-correcting dark-field electron microscopy
IT1399923B1 (en) 2010-05-11 2013-05-09 Cbb Net S A PROCEDURE FOR THE PREPARATION OF SALTS OF THE ACID (R) ALPHA-LIPOIC THEIR FORMULATION AND USE IN PHARMACEUTICAL COMPOSITIONS IN THE FORM OF TABLETS THAT CONTAIN THEM
JO2998B1 (en) 2010-06-04 2016-09-05 Amgen Inc Piperidinone derivatives as mdm2 inhibitors for the treatment of cancer
US8809349B2 (en) 2011-01-10 2014-08-19 Infinity Pharmaceuticals, Inc. Processes for preparing isoquinolinones and solid forms of isoquinolinones
CN102153557B (en) 2011-01-21 2013-03-20 中国科学院上海有机化学研究所 Chiral center nitrogen heterocyclic carbine precursor salt with quadrol skeleton, synthetic method and application
JP6025713B2 (en) * 2011-04-28 2016-11-16 大塚化学株式会社 New production method of azodicarbonamide
TW201309651A (en) 2011-06-29 2013-03-01 Otsuka Pharma Co Ltd Method for producing fine particles of aripiprazole anhydride crystals B
CA2850166C (en) 2011-09-27 2019-12-03 Amgen Inc. Heterocyclic compounds as mdm2 inhibitors for the treatment of cancer
CN103373951B (en) * 2012-04-28 2016-03-09 上海医药工业研究院 A kind of preparation method of lapatinib intermediate
MX362896B (en) 2013-02-19 2019-02-22 Amgen Inc Cis-morpholinone and other compounds as mdm2 inhibitors for the treatment of cancer.
AU2014223547B2 (en) 2013-02-28 2017-11-16 Amgen Inc. A benzoic acid derivative MDM2 inhibitor for the treatment of cancer
JP6377123B2 (en) 2013-03-14 2018-08-22 アムジエン・インコーポレーテツド Heteroaryl morpholinone compounds as MDM2 inhibitors for the treatment of cancer
JOP20200296A1 (en) 2013-06-10 2017-06-16 Amgen Inc Processes of Making and Crystalline Forms of a MDM2 Inhibitor

Also Published As

Publication number Publication date
AU2018260844B2 (en) 2020-08-13
EP3008039B1 (en) 2020-11-11
CN110003092A (en) 2019-07-12
IL281807A (en) 2021-05-31
TW202035370A (en) 2020-10-01
CA3201958A1 (en) 2014-12-18
US9801867B2 (en) 2017-10-31
US20160289190A1 (en) 2016-10-06
IL297860A (en) 2023-01-01
TW201922705A (en) 2019-06-16
US20220280496A1 (en) 2022-09-08
US20160287570A1 (en) 2016-10-06
EA202091612A1 (en) 2020-10-05
CR20160010A (en) 2016-02-04
CL2021000566A1 (en) 2021-09-03
US9757367B2 (en) 2017-09-12
AR096582A1 (en) 2016-01-20
TWI698428B (en) 2020-07-11
MX2015016856A (en) 2016-04-07
IL242622A0 (en) 2016-02-01
NZ753956A (en) 2020-12-18
EA201891642A1 (en) 2019-08-30
US20140364455A1 (en) 2014-12-11
TWI791153B (en) 2023-02-01
UA121301C2 (en) 2020-05-12
AU2018260844A1 (en) 2018-11-22
NZ714821A (en) 2020-10-30
SI3008039T1 (en) 2021-03-31
BR112015031004A2 (en) 2020-05-12
AU2014278428B2 (en) 2018-11-15
CN110627708A (en) 2019-12-31
JOP20200296A1 (en) 2017-06-16
KR20230019216A (en) 2023-02-07
US9623018B2 (en) 2017-04-18
CY1123661T1 (en) 2022-03-24
JO3768B1 (en) 2021-01-31
WO2014200937A1 (en) 2014-12-18
DK3008039T3 (en) 2021-01-04
RS61192B1 (en) 2021-01-29
TW201536743A (en) 2015-10-01
PH12015502705B1 (en) 2016-03-14
IL242622B (en) 2019-06-30
HUE053047T2 (en) 2021-06-28
AR119727A2 (en) 2022-01-05
JP2020147573A (en) 2020-09-17
EP3008039A1 (en) 2016-04-20
MA53572A1 (en) 2021-10-29
US20160289243A1 (en) 2016-10-06
JP2021130685A (en) 2021-09-09
AU2022271425A1 (en) 2022-12-22
IL266504A (en) 2019-07-31
JP2016528179A (en) 2016-09-15
IL281807B2 (en) 2023-04-01
JP6891322B2 (en) 2021-06-18
AU2014278428A1 (en) 2015-11-26
PL3008039T3 (en) 2021-04-19
CN105358530A (en) 2016-02-24
AU2020267169A1 (en) 2020-12-03
KR20160018576A (en) 2016-02-17
MA38714A1 (en) 2017-10-31
TN2015000521A1 (en) 2017-04-06
AU2020267169B2 (en) 2022-08-25
US20230301974A1 (en) 2023-09-28
PE20210153A1 (en) 2021-01-26
KR20210121270A (en) 2021-10-07
US20160289178A1 (en) 2016-10-06
US20180092898A1 (en) 2018-04-05
CA3115609C (en) 2023-08-08
SG11201509896VA (en) 2016-01-28
US20160264526A1 (en) 2016-09-15
UY35605A (en) 2015-01-30
TWI649306B (en) 2019-02-01
CA2914723A1 (en) 2014-12-18
US20200281912A1 (en) 2020-09-10
CA3115609A1 (en) 2014-12-18
JP2023089126A (en) 2023-06-27
MA43288A1 (en) 2020-04-30
JP7263439B2 (en) 2023-04-24
MA43288B1 (en) 2020-10-28
PE20160113A1 (en) 2016-03-03
MY194848A (en) 2022-12-19
HRP20202065T1 (en) 2021-02-19
US9376386B2 (en) 2016-06-28
EP3805232A1 (en) 2021-04-14
ES2851023T3 (en) 2021-09-02
BR112015031004B1 (en) 2022-09-20
PT3008039T (en) 2021-01-13
LT3008039T (en) 2021-01-25
MX2019012007A (en) 2019-11-11
CL2015003589A1 (en) 2016-06-17
CR20210290A (en) 2021-07-23
US9855259B2 (en) 2018-01-02
PH12015502705A1 (en) 2016-03-14
IL281807B (en) 2022-12-01
CA2914723C (en) 2021-06-15
EA031254B1 (en) 2018-12-28
AP2015008891A0 (en) 2015-11-30
BR122020003153B1 (en) 2022-09-27
CA3200532A1 (en) 2014-12-18
JP6998655B2 (en) 2022-02-04
CL2019000056A1 (en) 2019-05-03
EA201592305A1 (en) 2016-05-31
IL266504B (en) 2021-04-29

Similar Documents

Publication Publication Date Title
IL281807A (en) Processes of making and crystalline forms of a mdm2 inhibitor
IL268452A (en) Processes and intermediates for making a jak inhibitor
GB201313840D0 (en) Method of Manufacturing a Component
GB201313841D0 (en) Method of Manufacturing a Component
GB201313839D0 (en) Method of Manufacturing a Component
ZA201702252B (en) A selective inhibitor of prosphatidylinositol 3-kinase-gamma
SI3293176T1 (en) Crystal form of a pde4 inhibitor
HK1222339A1 (en) Inhibitors of metallo-ss-lactamase-enzymes --
GB201315841D0 (en) A substrate and a method of manufacturing a substrate
ZA201506677B (en) Firelog and method of making a firelog
SG11201508998PA (en) Methods of forming a substrate opening
EP2959896A4 (en) Inhibitor of tprotein phosphorylation
GB201320897D0 (en) Methods of manufacturing a polyolefin product and a case