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MX2017005893A - Sintesis de copanlisib y su sal diclorhidrato. - Google Patents

Sintesis de copanlisib y su sal diclorhidrato.

Info

Publication number
MX2017005893A
MX2017005893A MX2017005893A MX2017005893A MX2017005893A MX 2017005893 A MX2017005893 A MX 2017005893A MX 2017005893 A MX2017005893 A MX 2017005893A MX 2017005893 A MX2017005893 A MX 2017005893A MX 2017005893 A MX2017005893 A MX 2017005893A
Authority
MX
Mexico
Prior art keywords
copanlisib
synthesis
dihydrochloride salt
dihydrochloride
hydrates
Prior art date
Application number
MX2017005893A
Other languages
English (en)
Other versions
MX366904B (es
Inventor
Lender Andreas
Lovis Kai
Georg Peters Jan-
Rubenbauer Philipp
Götz Daniel
Grossbach Danja
Josef Mais Franz-
Schirmer Heiko
Stiehl Juergen
Seyfried Martin
Zweifel Theodor
Marty Maurus
Weingärtner Günter
Original Assignee
Bayer Pharma 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
Application filed by Bayer Pharma AG filed Critical Bayer Pharma AG
Publication of MX2017005893A publication Critical patent/MX2017005893A/es
Publication of MX366904B publication Critical patent/MX366904B/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D487/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/20Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D233/22Radicals substituted by oxygen atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D233/00Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
    • C07D233/04Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D233/20Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with substituted hydrocarbon radicals, directly attached to ring carbon atoms
    • C07D233/24Radicals substituted by nitrogen atoms not forming part of a nitro radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D295/00Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms
    • C07D295/04Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms
    • C07D295/08Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms
    • C07D295/084Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings
    • C07D295/088Heterocyclic compounds containing polymethylene-imine rings with at least five ring members, 3-azabicyclo [3.2.2] nonane, piperazine, morpholine or thiomorpholine rings, having only hydrogen atoms directly attached to the ring carbon atoms with substituted hydrocarbon radicals attached to ring nitrogen atoms substituted by singly bound oxygen or sulfur atoms with the ring nitrogen atoms and the oxygen or sulfur atoms attached to the same carbon chain, which is not interrupted by carbocyclic rings to an acyclic saturated chain
    • 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)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

La presente invención se relaciona con un nuevo método para preparar copanlisib, diclorhidrato de copanlisib, o hidratos de diclorhidrato de copanlisib, con nuevos compuestos intermediarios, y con el uso de dichos nuevos compuestos intermediarios en la preparación de copanlisib, diclorhidrato de copanlisib, o hidratos de diclorhidrato de copanlisib. La presente invención también se relaciona con hidratos de diclorhidrato de copanlisib como compuestos.
MX2017005893A 2014-11-07 2015-11-05 Síntesis de copanlisib y su sal diclorhidrato. MX366904B (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
EP14192203.9A EP3018127A1 (en) 2014-11-07 2014-11-07 Synthesis of copanlisib and its dihydrochloride salt
PCT/EP2015/075789 WO2016071435A2 (en) 2014-11-07 2015-11-05 Synthesis of copanlisib and its dihydrochloride salt

Publications (2)

Publication Number Publication Date
MX2017005893A true MX2017005893A (es) 2017-06-30
MX366904B MX366904B (es) 2019-07-30

Family

ID=51866061

Family Applications (1)

Application Number Title Priority Date Filing Date
MX2017005893A MX366904B (es) 2014-11-07 2015-11-05 Síntesis de copanlisib y su sal diclorhidrato.

Country Status (46)

Country Link
US (1) US10494372B2 (es)
EP (2) EP3018127A1 (es)
JP (1) JP6691115B2 (es)
KR (1) KR102566834B1 (es)
CN (1) CN107278204B (es)
AR (1) AR102570A1 (es)
AU (1) AU2015341788B2 (es)
BR (1) BR112017009470B1 (es)
CA (1) CA2966800C (es)
CL (1) CL2017001131A1 (es)
CO (1) CO2017004532A2 (es)
CR (1) CR20170184A (es)
CU (1) CU24489B1 (es)
CY (1) CY1121602T1 (es)
DK (1) DK3215493T3 (es)
DO (1) DOP2017000112A (es)
EA (1) EA035558B1 (es)
EC (1) ECSP17027755A (es)
ES (1) ES2721778T3 (es)
HR (1) HRP20190720T1 (es)
HU (1) HUE042866T2 (es)
IL (1) IL251874A0 (es)
JO (1) JO3644B1 (es)
LT (1) LT3215493T (es)
MA (1) MA40895B1 (es)
ME (1) ME03358B (es)
MX (1) MX366904B (es)
MY (1) MY189852A (es)
NI (1) NI201700054A (es)
NZ (1) NZ731287A (es)
PE (1) PE20170897A1 (es)
PH (1) PH12017500833A1 (es)
PL (1) PL3215493T3 (es)
PT (1) PT3215493T (es)
RS (1) RS58579B1 (es)
SA (1) SA517381462B1 (es)
SG (1) SG11201703702RA (es)
SI (1) SI3215493T1 (es)
SV (1) SV2017005433A (es)
TN (1) TN2017000179A1 (es)
TR (1) TR201905217T4 (es)
TW (1) TWI697495B (es)
UA (1) UA122398C2 (es)
UY (1) UY36392A (es)
WO (1) WO2016071435A2 (es)
ZA (1) ZA201703867B (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2168583A1 (en) 2008-09-24 2010-03-31 Bayer Schering Pharma Aktiengesellschaft Use of substituted 2,3-dihydroimidazo[1,2-c]quinazolines for the treatment of myeloma
EP2508525A1 (en) 2011-04-05 2012-10-10 Bayer Pharma Aktiengesellschaft Substituted 2,3-dihydroimidazo[1,2-c]quinazoline salts
EA037577B1 (ru) 2013-04-08 2021-04-16 Байер Фарма Акциенгезельшафт ПРИМЕНЕНИЕ 2-АМИНО-N-[7-МЕТОКСИ-8-(3-МОРФОЛИН-4-ИЛПРОПОКСИ)-2,3-ДИГИДРОИМИДАЗО[1,2-c]ХИНАЗОЛИН-5-ИЛ]ПИРИМИДИН-5-КАРБОКСАМИДА ИЛИ ЕГО ФИЗИОЛОГИЧЕСКИ ПРИЕМЛЕМОЙ СОЛИ ИЛИ ГИДРАТА И ФАРМАЦЕВТИЧЕСКОЙ КОМПОЗИЦИИ, СОДЕРЖАЩЕЙ УКАЗАННОЕ СОЕДИНЕНИЕ, ДЛЯ ЛЕЧЕНИЯ ИЛИ ПРОФИЛАКТИКИ НЕХОДЖКИНСКОЙ ЛИМФОМЫ (НХЛ)
JP6867295B2 (ja) 2015-03-09 2021-04-28 バイエル ファーマ アクチエンゲゼルシャフト 置換2,3−ジヒドロイミダゾ[1,2−c]キナゾリンを含んでいる組合せ
CA3016584A1 (en) 2016-03-08 2017-09-14 Bayer Pharma Aktiengesellschaft 2-amino-n-[7-methoxy-2,3-dihydroimidazo-[1,2-c]quinazolin-5-yl]pyrimidine-5-carboxamides
US10925880B2 (en) 2016-09-23 2021-02-23 Bayer Pharma Aktiengesellschaft Combination of PI3K-inhibitors
WO2018215282A1 (en) 2017-05-26 2018-11-29 Bayer Pharma Aktiengesellschaft Combination of bub1 and pi3k inhibitors
EP3645005A1 (en) 2017-06-28 2020-05-06 Bayer Consumer Care AG Combination of a pi3k-inhibitor with an androgen receptor antagonist
FI3678644T3 (fi) 2017-09-08 2023-07-28 Bayer Pharma AG Kopanlisibin formulaatioita
EP3498266A1 (en) 2017-12-15 2019-06-19 Bayer Consumer Care AG Formulations of copanlisib
WO2023139125A1 (en) 2022-01-18 2023-07-27 Synthon B.V. Improved process for preparation of copanlisib
WO2023218032A1 (en) 2022-05-13 2023-11-16 Synthon B.V. Solid forms of copanlisib salts

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* Cited by examiner, † Cited by third party
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US1003580A (en) 1910-08-10 1911-09-19 Remington Typewriter Co Type-writing machine.
US6221877B1 (en) * 2000-04-12 2001-04-24 Regents Of The University Of California Substituted 4-phthalimidocarboxanilides as inhibitors of purine salvage phosphoribosyltransferases
IT1319674B1 (it) * 2000-12-01 2003-10-23 Erregierre Spa Processo per la preparazione dell'acido1-(aminometil)cicloesanacetico.
TW565582B (en) * 2001-04-13 2003-12-11 Kaneka Corp Diamine, acid dianhydride, and reactive group containing polyimide composition prepared therefrom and preparing them
RU2004107485A (ru) * 2001-08-15 2005-03-27 Е.И.Дюпон де Немур энд Компани (US) Орто-гетероциклические замещенные ариламиды для борьбы с беспозвоночными вредителями
RU2326881C9 (ru) 2002-09-30 2009-04-10 Байер Фармасьютикалс Корпорейшн Конденсированные производные азолпиримидина, обладающие свойствами ингибитора фосфатидилинозитол-3-киназы (pi3k)
AR064106A1 (es) 2006-12-05 2009-03-11 Bayer Schering Pharma Ag Derivados de 2,3-dihidroimidazo [1,2-c] quinazolina sustituida utiles para el tratamiento de enfermedades y trastornos hiper-proliferativos asociados con la angiogenesis
CA2713388C (en) 2008-01-14 2016-03-29 William Scott Sulfone substituted 2,3-dihydroimidazo [1,2-c] quinazoline derivatives useful for treating hyper-proliferative disorders and diseases associated with angiogenesis
EP2168583A1 (en) 2008-09-24 2010-03-31 Bayer Schering Pharma Aktiengesellschaft Use of substituted 2,3-dihydroimidazo[1,2-c]quinazolines for the treatment of myeloma
EP2508525A1 (en) * 2011-04-05 2012-10-10 Bayer Pharma Aktiengesellschaft Substituted 2,3-dihydroimidazo[1,2-c]quinazoline salts
JO3733B1 (ar) 2011-04-05 2021-01-31 Bayer Ip Gmbh استخدام 3,2-دايهيدروايميدازو[1, 2 -c]كوينازولينات مستبدلة
EA037577B1 (ru) 2013-04-08 2021-04-16 Байер Фарма Акциенгезельшафт ПРИМЕНЕНИЕ 2-АМИНО-N-[7-МЕТОКСИ-8-(3-МОРФОЛИН-4-ИЛПРОПОКСИ)-2,3-ДИГИДРОИМИДАЗО[1,2-c]ХИНАЗОЛИН-5-ИЛ]ПИРИМИДИН-5-КАРБОКСАМИДА ИЛИ ЕГО ФИЗИОЛОГИЧЕСКИ ПРИЕМЛЕМОЙ СОЛИ ИЛИ ГИДРАТА И ФАРМАЦЕВТИЧЕСКОЙ КОМПОЗИЦИИ, СОДЕРЖАЩЕЙ УКАЗАННОЕ СОЕДИНЕНИЕ, ДЛЯ ЛЕЧЕНИЯ ИЛИ ПРОФИЛАКТИКИ НЕХОДЖКИНСКОЙ ЛИМФОМЫ (НХЛ)
CA2932221C (en) 2013-12-03 2022-02-22 Bayer Pharma Aktiengesellschaft Combination of pi3k-inhibitors
EP3018131A1 (en) 2014-11-07 2016-05-11 Bayer Pharma Aktiengesellschaft Synthesis of copanlisib and its dihydrochloride salt
HK1250645A1 (zh) 2015-03-09 2019-01-11 Bayer Pharma Aktiengesellschaft 取代的2,3-二氢咪唑并[1,2-c]喹唑啉类化合物的用途
JP6867295B2 (ja) 2015-03-09 2021-04-28 バイエル ファーマ アクチエンゲゼルシャフト 置換2,3−ジヒドロイミダゾ[1,2−c]キナゾリンを含んでいる組合せ
BR112018015782A2 (pt) 2016-02-01 2019-01-02 Bayer Pharma AG biomarcadores de copanlisibe
AU2017215096A1 (en) 2016-02-01 2018-08-09 Bayer Pharma Aktiengesellschaft Copanlisib biomarkers
CA3016584A1 (en) 2016-03-08 2017-09-14 Bayer Pharma Aktiengesellschaft 2-amino-n-[7-methoxy-2,3-dihydroimidazo-[1,2-c]quinazolin-5-yl]pyrimidine-5-carboxamides
US10925880B2 (en) 2016-09-23 2021-02-23 Bayer Pharma Aktiengesellschaft Combination of PI3K-inhibitors

Also Published As

Publication number Publication date
EA035558B1 (ru) 2020-07-07
KR102566834B1 (ko) 2023-08-16
JO3644B1 (ar) 2020-08-27
MY189852A (en) 2022-03-14
SA517381462B1 (ar) 2021-01-25
BR112017009470A2 (en) 2018-01-02
JP2017534631A (ja) 2017-11-24
CA2966800A1 (en) 2016-05-12
PL3215493T3 (pl) 2019-07-31
MX366904B (es) 2019-07-30
PT3215493T (pt) 2019-05-21
ZA201703867B (en) 2019-07-31
IL251874A0 (en) 2017-06-29
NZ731287A (en) 2023-01-27
AU2015341788A1 (en) 2017-05-18
CU24489B1 (es) 2020-12-17
CY1121602T1 (el) 2020-05-29
HUE042866T2 (hu) 2019-07-29
CL2017001131A1 (es) 2018-01-19
TR201905217T4 (tr) 2019-05-21
CA2966800C (en) 2023-02-21
KR20170082563A (ko) 2017-07-14
CO2017004532A2 (es) 2017-07-19
ECSP17027755A (es) 2017-06-30
SG11201703702RA (en) 2017-06-29
TW201625634A (zh) 2016-07-16
AU2015341788B2 (en) 2020-01-16
EP3215493B1 (en) 2019-01-23
MA40895A (fr) 2017-09-13
EP3215493A2 (en) 2017-09-13
DK3215493T3 (da) 2019-05-06
ME03358B (me) 2019-10-20
AR102570A1 (es) 2017-03-08
BR112017009470B1 (pt) 2022-11-01
CR20170184A (es) 2017-06-20
PE20170897A1 (es) 2017-07-12
DOP2017000112A (es) 2017-06-15
US20180282337A1 (en) 2018-10-04
HK1245774A1 (zh) 2018-08-31
EP3018127A1 (en) 2016-05-11
WO2016071435A2 (en) 2016-05-12
SV2017005433A (es) 2018-04-30
TWI697495B (zh) 2020-07-01
TN2017000179A1 (en) 2018-10-19
CN107278204A (zh) 2017-10-20
JP6691115B2 (ja) 2020-04-28
CU20170061A7 (es) 2017-10-05
HRP20190720T1 (hr) 2019-06-14
UA122398C2 (uk) 2020-11-10
EA201790983A1 (ru) 2017-10-31
NI201700054A (es) 2017-07-17
WO2016071435A3 (en) 2016-06-30
SI3215493T1 (sl) 2019-05-31
CN107278204B (zh) 2019-12-17
RS58579B1 (sr) 2019-05-31
PH12017500833A1 (en) 2017-10-18
LT3215493T (lt) 2019-04-25
UY36392A (es) 2016-06-30
ES2721778T3 (es) 2019-08-05
MA40895B1 (fr) 2019-07-31
US10494372B2 (en) 2019-12-03

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