PL3040333T3 - Krystaliczne postacie 5-(2,6-di-4-morfolinylo-4-pirymidynylo)-4-trifluorometylopirydyno-2-aminy, inhibitora pik3 - Google Patents

Krystaliczne postacie 5-(2,6-di-4-morfolinylo-4-pirymidynylo)-4-trifluorometylopirydyno-2-aminy, inhibitora pik3

Info

Publication number
PL3040333T3
PL3040333T3 PL16151719T PL16151719T PL3040333T3 PL 3040333 T3 PL3040333 T3 PL 3040333T3 PL 16151719 T PL16151719 T PL 16151719T PL 16151719 T PL16151719 T PL 16151719T PL 3040333 T3 PL3040333 T3 PL 3040333T3
Authority
PL
Poland
Prior art keywords
pyridmidinyl
trifluoromethylpyridin
morpholinyl
amine
crystalline forms
Prior art date
Application number
PL16151719T
Other languages
English (en)
Inventor
John Vincent Calienni
Marilyn De La Cruz
Dietmar Flubacher
Baoqing Gong
Prasad Koteswara Kapa
Piotr H. Karpinski
Hui Liu
Pascal Michel
Rasmus Mose
Maria Caterina Testa
Liladhar Murlidhar Waykole
Original Assignee
Novartis Ag
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=44773179&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PL3040333(T3) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Novartis Ag filed Critical Novartis Ag
Publication of PL3040333T3 publication Critical patent/PL3040333T3/pl

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • 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
    • A61K31/535Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P13/00Drugs for disorders of the urinary system
    • A61P13/08Drugs for disorders of the urinary system of the prostate
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • 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
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/72Nitrogen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02Boron compounds
    • C07F5/025Boronic and borinic acid compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F5/00Compounds containing elements of Groups 3 or 13 of the Periodic Table
    • C07F5/02Boron compounds
    • C07F5/04Esters of boric acids
    • 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)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Engineering & Computer Science (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Oncology (AREA)
  • Urology & Nephrology (AREA)
  • Hematology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Pyridine Compounds (AREA)
PL16151719T 2010-10-01 2011-09-29 Krystaliczne postacie 5-(2,6-di-4-morfolinylo-4-pirymidynylo)-4-trifluorometylopirydyno-2-aminy, inhibitora pik3 PL3040333T3 (pl)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US38872110P 2010-10-01 2010-10-01
US201161494915P 2011-06-09 2011-06-09
PCT/US2011/053808 WO2012044727A2 (en) 2010-10-01 2011-09-29 Manufacturing process for pyrimidine derivatives
EP16151719.8A EP3040333B1 (en) 2010-10-01 2011-09-29 Crystalline forms of 5-(2,6-di-4-morpholinyl-4-pyridmidinyl)-4-trifluoromethylpyridin-2-amine, a pik3 inhibitor
EP11767362.4A EP2621908A2 (en) 2010-10-01 2011-09-29 Manufacturing process for pyrimidine derivatives

Publications (1)

Publication Number Publication Date
PL3040333T3 true PL3040333T3 (pl) 2019-03-29

Family

ID=44773179

Family Applications (1)

Application Number Title Priority Date Filing Date
PL16151719T PL3040333T3 (pl) 2010-10-01 2011-09-29 Krystaliczne postacie 5-(2,6-di-4-morfolinylo-4-pirymidynylo)-4-trifluorometylopirydyno-2-aminy, inhibitora pik3

Country Status (30)

Country Link
US (3) US9181215B2 (pl)
EP (2) EP2621908A2 (pl)
JP (3) JP5998145B2 (pl)
KR (2) KR20130119928A (pl)
CN (3) CN104987321A (pl)
AR (1) AR083213A1 (pl)
AU (4) AU2011308856B2 (pl)
BR (1) BR112013007123B1 (pl)
CA (1) CA2813333C (pl)
CL (2) CL2013000850A1 (pl)
CO (1) CO6700837A2 (pl)
DK (1) DK3040333T3 (pl)
EC (1) ECSP13012596A (pl)
ES (1) ES2699951T3 (pl)
GT (1) GT201300080A (pl)
HU (1) HUE041326T2 (pl)
IL (3) IL225113A (pl)
LT (1) LT3040333T (pl)
MX (1) MX354482B (pl)
MY (1) MY160785A (pl)
NZ (1) NZ608285A (pl)
PE (1) PE20140002A1 (pl)
PH (2) PH12013500579A1 (pl)
PL (1) PL3040333T3 (pl)
PT (1) PT3040333T (pl)
RU (2) RU2576619C2 (pl)
SG (1) SG188439A1 (pl)
SI (1) SI3040333T1 (pl)
TW (1) TWI540133B (pl)
WO (1) WO2012044727A2 (pl)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PE20141381A1 (es) 2011-07-01 2014-10-21 Novartis Ag Terapia de combinacion que comprende un inhibidor de cdk4/6 y un inhibidor de pi3k para el uso en el tratamiento de cancer
AU2012313888B2 (en) 2011-09-27 2016-03-31 Novartis Ag 3-pyrimidin-4-yl-oxazolidin-2-ones as inhibitors of mutant IDH
UY34632A (es) 2012-02-24 2013-05-31 Novartis Ag Compuestos de oxazolidin- 2- ona y usos de los mismos
MX360703B (es) * 2012-10-23 2018-11-14 Novartis Ag Proceso mejorado para la elaboración de 5-(2, 6-di-4-morfolinil-4-pirimidinil)-4-trifluoro-metil-piridin-2-amin a.
US9296733B2 (en) 2012-11-12 2016-03-29 Novartis Ag Oxazolidin-2-one-pyrimidine derivative and use thereof for the treatment of conditions, diseases and disorders dependent upon PI3 kinases
KR20150131224A (ko) 2013-03-14 2015-11-24 노파르티스 아게 돌연변이 idh의 억제제로서의 3-피리미딘-4-일-옥사졸리딘-2-온
US9318944B2 (en) 2013-04-29 2016-04-19 Rockwell Automation Technologies, Inc. Methods and apparatus for active front end filter capacitor degradation detection
US9294005B2 (en) 2013-10-01 2016-03-22 Rockwell Automation Technologies, Inc. Method and apparatus for detecting AFE filter capacitor degradation
WO2015055071A1 (zh) * 2013-10-16 2015-04-23 上海璎黎药业有限公司 稠合杂环化合物、其制备方法、药物组合物和用途
RU2688665C2 (ru) * 2014-04-22 2019-05-22 Университет Базель Новый способ получения производных триазина, пиримидина и пиридина
CN105085476B (zh) * 2014-11-24 2018-03-09 苏州晶云药物科技有限公司 5‑[2,6‑二(4‑吗啉基)‑4‑嘧啶基]‑4‑(三氟甲基)‑2‑吡啶胺二盐酸盐的晶型及其制备方法
AU2015366357B2 (en) 2014-12-17 2018-07-19 Shanghai Haiyan Pharmaceutical Technology Co. Ltd. 2-morpholin-4,6-disubstituted pyrimidine derivative, and preparation method and pharmaceutical use thereof
US9481665B2 (en) * 2015-03-13 2016-11-01 Yong Xu Process for preparing PI3K inhibitor buparsilib
CN107787226A (zh) 2015-03-25 2018-03-09 诺华股份有限公司 药物组合
CN105001151B (zh) * 2015-08-28 2017-07-14 苏州明锐医药科技有限公司 布帕尼西中间体及其制备方法
CN106543140A (zh) * 2015-09-21 2017-03-29 苏州晶云药物科技有限公司 5-[2,6-二(4-吗啉基)-4-嘧啶基]-4-(三氟甲基)-2-吡啶胺盐酸盐的晶型及其制备方法
MY196817A (en) * 2015-12-16 2023-05-03 Genentech Inc Process for the preparation of tricyclic pi3k inhibitor compounds and methods for using the same for the treatment of cancer
CN106905294A (zh) * 2016-07-08 2017-06-30 苏州科睿思制药有限公司 5‑[2,6‑二(4‑吗啉基)‑4‑嘧啶基]‑4‑(三氟甲基)‑2‑吡啶胺的晶型及其制备方法
CN107793394A (zh) * 2017-08-03 2018-03-13 上海厚璞生物科技有限公司 一种生产选择性pi3k抑制剂的系列关键中间体
CN110016142B (zh) * 2019-04-30 2021-08-03 合肥工业大学 一种含嘧啶硼酸结构的硅油及其制备方法

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6124476A (en) 1998-04-17 2000-09-26 Symyx Technologies, Inc. Catalyst ligands, catalyst compositions, catalyst metal complexes and processes for cross-coupling aromatic boron compounds with aromatic halogens or perfluoroalkylsulfonates
CN1735598A (zh) * 2002-11-11 2006-02-15 拜耳医药保健股份公司 作为ip受体拮抗剂的苯基或杂芳基氨基烷烃衍生物
ATE527250T1 (de) 2002-11-21 2011-10-15 Novartis Ag 2,4,6-trisubstituierten pyrimidinen als phosphotidylinositol (pi) 3-kinase inhibitoren und deren verwendung zur behandlung von krebs
JO2660B1 (en) * 2006-01-20 2012-06-17 نوفارتيس ايه جي Pi-3 inhibitors and methods of use
JP5534811B2 (ja) 2006-08-24 2014-07-02 アストラゼネカ アクチボラグ 増殖性疾患の治療に有用なモルホリノピリミジン誘導体
AU2008213808B2 (en) 2007-02-06 2011-11-10 Novartis Ag PI 3-kinase inhibitors and methods of their use
WO2009066084A1 (en) * 2007-11-21 2009-05-28 F. Hoffmann-La Roche Ag 2 -morpholinopyrimidines and their use as pi3 kinase inhibitors
MX2011012201A (es) 2009-05-15 2011-12-08 Novartis Ag Combinacion de un inhibidor de cinasa de fosfoinositida-3 y un compuesto anti-diabetico.

Also Published As

Publication number Publication date
EP3040333B1 (en) 2018-09-12
IL238046A (en) 2016-08-31
US9181215B2 (en) 2015-11-10
WO2012044727A3 (en) 2012-06-07
US9359326B2 (en) 2016-06-07
WO2012044727A2 (en) 2012-04-05
MX354482B (es) 2018-03-07
US20130225571A1 (en) 2013-08-29
ECSP13012596A (es) 2013-07-31
CL2013000850A1 (es) 2013-09-27
HK1220686A1 (en) 2017-05-12
EP3040333A1 (en) 2016-07-06
IL225113A (en) 2016-08-31
JP2013541536A (ja) 2013-11-14
ES2699951T3 (es) 2019-02-13
RU2015150728A (ru) 2019-01-15
RU2576619C2 (ru) 2016-03-10
MY160785A (en) 2017-03-15
PE20140002A1 (es) 2014-01-21
KR20180123586A (ko) 2018-11-16
TWI540133B (zh) 2016-07-01
RU2013120326A (ru) 2014-11-20
AU2011308856B2 (en) 2015-04-23
MX2013003507A (es) 2013-05-20
US20150232446A1 (en) 2015-08-20
CN104945373A (zh) 2015-09-30
IL233282A (en) 2016-08-31
US9452994B2 (en) 2016-09-27
EP2621908A2 (en) 2013-08-07
AU2011308856A1 (en) 2013-03-28
PH12013500579A1 (en) 2016-06-10
AU2015200938B2 (en) 2015-11-19
LT3040333T (lt) 2018-12-10
CA2813333A1 (en) 2012-04-05
AU2015200938A1 (en) 2015-03-12
KR20130119928A (ko) 2013-11-01
SG188439A1 (en) 2013-05-31
US20160251334A1 (en) 2016-09-01
PT3040333T (pt) 2018-12-04
PH12015501585A1 (en) 2015-09-21
AU2015200936A1 (en) 2015-03-12
JP2016106091A (ja) 2016-06-16
BR112013007123B1 (pt) 2021-11-09
AU2015246141B2 (en) 2016-07-07
CN103140479A (zh) 2013-06-05
CN104987321A (zh) 2015-10-21
CO6700837A2 (es) 2013-06-28
HUE041326T2 (hu) 2019-05-28
BR112013007123A2 (pt) 2016-06-14
SI3040333T1 (sl) 2019-01-31
AR083213A1 (es) 2013-02-06
JP2016128414A (ja) 2016-07-14
DK3040333T3 (da) 2019-01-02
CA2813333C (en) 2019-01-15
TW201215605A (en) 2012-04-16
CL2015001088A1 (es) 2015-07-10
IL233282A0 (en) 2014-08-31
JP5998145B2 (ja) 2016-09-28
GT201300080A (es) 2014-07-18
AU2015246141A1 (en) 2015-11-12
CN103140479B (zh) 2015-04-08
NZ608285A (en) 2014-06-27

Similar Documents

Publication Publication Date Title
HUE041326T2 (hu) 5-(2,6-di-4-morfolinil-4-piridmidinil)-4-trifluorometilpiridin-2-amin kristályformái, egy PIK3 inhibitor
IL295518B1 (en) Heterocyclic compounds used as pdk1 inhibitors
IL239081B (en) Benzoxazepine pi3k inhibitor compound
GB201004311D0 (en) New enzyme inhibitor compounds
GB201001075D0 (en) Crystalline forms
ZA201008019B (en) A crystalline form of posaconazole
PT2611779T (pt) Formas cristalinas de um inibidor do fator xa
GB0819182D0 (en) Crystalline forms
ZA201000829B (en) Oxadiazole- and oxazole-substituted benzamidazole-and indole-derivatives as dgat1 inhibitors
EP2519508A4 (en) METALLO ENZYME INHIBITOR COMPOUNDS
PL2527340T3 (pl) Związek piperazynowy wykazujący efekt hamowania pgds
SG11201400278TA (en) New enzyme inhibitor compounds
IL218967A (en) Phenyllaxadiazole derivatives as pgds barriers
PL2578595T3 (pl) Krystaliczna lewoizowalerylospiramycyna I
ZA201100694B (en) Salts of hiv inhibitor compounds
PL2085445T3 (pl) Zastosowanie linera
IL223584A0 (en) Crystalline form of a 3-phenoxymethylpyrrolidine compounds
ZA201104319B (en) Crystalline forms of a 3-carboxypropyl-aminotetralin compound
IL213935A0 (en) Novel heterocyclic compounds as metap-2 inhibitors
GB2461167B (en) Novel amidoxime derivatives
AP2717A (en) Mono-hydrochloric salts of an inhibitor of histonedeacetylase
GB201004308D0 (en) New inhibitor compounds
SI2307435T1 (sl) Soli spojin, inhibitorjev HIV
PL386893A1 (pl) Inhibitor parafin
AU2010904580A0 (en) Non-toxic locust-flight inhibitor