CL2017001130A1 - Síntesis de copanlisib y su sal diclorhidrato - Google Patents

Síntesis de copanlisib y su sal diclorhidrato

Info

Publication number
CL2017001130A1
CL2017001130A1 CL2017001130A CL2017001130A CL2017001130A1 CL 2017001130 A1 CL2017001130 A1 CL 2017001130A1 CL 2017001130 A CL2017001130 A CL 2017001130A CL 2017001130 A CL2017001130 A CL 2017001130A CL 2017001130 A1 CL2017001130 A1 CL 2017001130A1
Authority
CL
Chile
Prior art keywords
copanlisib
synthesis
dihydrochloride salt
new
compounds
Prior art date
Application number
CL2017001130A
Other languages
English (en)
Inventor
Jan Georg Peters
Juergen Stiehl
Kai Lovis
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 CL2017001130A1 publication Critical patent/CL2017001130A1/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
    • C07D233/24Radicals substituted by nitrogen atoms not forming part of a nitro radical
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D265/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/281,4-Oxazines; Hydrogenated 1,4-oxazines
    • C07D265/301,4-Oxazines; Hydrogenated 1,4-oxazines not condensed with other rings
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Epidemiology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Catalysts (AREA)
  • Pyridine Compounds (AREA)

Abstract

<p>LA PRESENTE INVENCIÓN SE RELACIONA CON UN NUEVO MÉTODO PARA PREPARAR COPANLISIB, Y DICLORHIDRATO DE COPANLISIB, CON NUEVOS COMPUESTOS INTERMEDIARIOS, Y CON EL USO DE DICHOS NUEVOS COMPUESTOS INTERMEDIARIOS PARA LA PREPARACIÓN DE COPANLISIB.</p>
CL2017001130A 2014-11-07 2017-05-05 Síntesis de copanlisib y su sal diclorhidrato CL2017001130A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP14192202.1A EP3018131A1 (en) 2014-11-07 2014-11-07 Synthesis of copanlisib and its dihydrochloride salt

Publications (1)

Publication Number Publication Date
CL2017001130A1 true CL2017001130A1 (es) 2018-01-19

Family

ID=51866060

Family Applications (1)

Application Number Title Priority Date Filing Date
CL2017001130A CL2017001130A1 (es) 2014-11-07 2017-05-05 Síntesis de copanlisib y su sal diclorhidrato

Country Status (34)

Country Link
US (1) US10035803B2 (es)
EP (2) EP3018131A1 (es)
JP (1) JP6691114B2 (es)
KR (1) KR102562286B1 (es)
CN (1) CN107074776B (es)
AR (1) AR102568A1 (es)
AU (1) AU2015341779B2 (es)
BR (1) BR112017009471B1 (es)
CA (1) CA2966796C (es)
CL (1) CL2017001130A1 (es)
CO (1) CO2017004533A2 (es)
DK (1) DK3215507T3 (es)
EA (1) EA031248B1 (es)
ES (1) ES2716730T3 (es)
HR (1) HRP20190527T8 (es)
HU (1) HUE042794T2 (es)
IL (1) IL251586B (es)
JO (1) JO3487B1 (es)
LT (1) LT3215507T (es)
MX (1) MX365111B (es)
MY (1) MY183123A (es)
NZ (1) NZ730843A (es)
PE (1) PE20170951A1 (es)
PL (1) PL3215507T3 (es)
PT (1) PT3215507T (es)
RS (1) RS58494B1 (es)
SG (1) SG11201702999XA (es)
SI (1) SI3215507T1 (es)
TR (1) TR201904346T4 (es)
TW (1) TWI697494B (es)
UA (1) UA118999C2 (es)
UY (1) UY36396A (es)
WO (1) WO2016071426A1 (es)
ZA (1) ZA201703866B (es)

Families Citing this family (9)

* 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
MX2015014171A (es) 2013-04-08 2015-12-16 Bayer Pharma AG Uso de 2,3-dihidroimidazo[1,2-c]quinazolinas sustituidas.
EP3018127A1 (en) 2014-11-07 2016-05-11 Bayer Pharma Aktiengesellschaft Synthesis of copanlisib and its dihydrochloride salt
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
CN105130998B (zh) * 2015-09-25 2017-07-28 苏州立新制药有限公司 库潘尼西的制备方法
EP3426657B1 (en) 2016-03-08 2022-07-13 Bayer Pharma Aktiengesellschaft 2 amino n [7 methoxy 2, 3-dihydroimidazo-[1, 2-c]quinazolin-5-yl]pyrimidine 5 carboxamides
JP2019532922A (ja) 2016-09-23 2019-11-14 バイエル ファーマ アクチエンゲゼルシャフト Pi3k−阻害剤の組み合わせ
CA3068324A1 (en) 2017-06-28 2019-01-03 Bayer Consumer Care Ag Combination of a pi3k-inhibitor with an androgen receptor antagonist

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
WO2003016304A1 (en) * 2001-08-15 2003-02-27 E. I. Du Pont De Nemours And Company Ortho-heterocyclic substituted aryl amides for controlling invertebrate pests
SI1549652T1 (sl) * 2002-09-30 2009-04-30 Bayer Healthcare Ag Kondenzirani azolpirimidinski derivati
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
JP5620275B2 (ja) * 2008-01-14 2014-11-05 バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングBayer Intellectual Property GmbH 超増殖性疾患及び脈管形成に関連する疾病を処理するために有用なスルホン置換された2,3−ジヒドロイミダゾ[1,2−c]キナゾリン誘導体類
PE20121471A1 (es) 2009-11-04 2012-11-01 Novartis Ag Derivados de sulfonamida heterociclicos utiles como inhibidores de mek
EP2508525A1 (en) * 2011-04-05 2012-10-10 Bayer Pharma Aktiengesellschaft Substituted 2,3-dihydroimidazo[1,2-c]quinazoline salts

Also Published As

Publication number Publication date
EP3215507A1 (en) 2017-09-13
EP3215507B1 (en) 2018-12-26
ZA201703866B (en) 2019-06-26
PT3215507T (pt) 2019-03-29
UY36396A (es) 2016-06-30
HRP20190527T8 (hr) 2020-02-21
TR201904346T4 (tr) 2019-04-22
DK3215507T3 (en) 2019-04-15
EP3018131A1 (en) 2016-05-11
NZ730843A (en) 2022-12-23
KR102562286B1 (ko) 2023-08-02
RS58494B1 (sr) 2019-04-30
IL251586A0 (en) 2017-06-29
TW201625633A (zh) 2016-07-16
EA201790982A1 (ru) 2017-10-31
KR20170078654A (ko) 2017-07-07
JP2017536352A (ja) 2017-12-07
CA2966796A1 (en) 2016-05-12
HUE042794T2 (hu) 2019-07-29
JP6691114B2 (ja) 2020-04-28
CN107074776A (zh) 2017-08-18
MX2017005891A (es) 2017-06-30
SG11201702999XA (en) 2017-05-30
US20170327505A1 (en) 2017-11-16
US10035803B2 (en) 2018-07-31
TWI697494B (zh) 2020-07-01
PL3215507T3 (pl) 2019-08-30
MY183123A (en) 2021-02-15
SI3215507T1 (sl) 2019-04-30
CA2966796C (en) 2022-12-06
IL251586B (en) 2019-05-30
CO2017004533A2 (es) 2017-07-19
CN107074776B (zh) 2021-02-02
JO3487B1 (ar) 2020-07-05
EA031248B1 (ru) 2018-12-28
AU2015341779A1 (en) 2017-05-11
UA118999C2 (uk) 2019-04-10
PE20170951A1 (es) 2017-07-13
LT3215507T (lt) 2019-04-10
ES2716730T3 (es) 2019-06-14
WO2016071426A1 (en) 2016-05-12
AU2015341779B2 (en) 2020-02-27
MX365111B (es) 2019-05-23
BR112017009471B1 (pt) 2023-02-28
AR102568A1 (es) 2017-03-08
BR112017009471A2 (pt) 2018-01-02
HRP20190527T1 (hr) 2019-05-17

Similar Documents

Publication Publication Date Title
CL2017001130A1 (es) Síntesis de copanlisib y su sal diclorhidrato
CL2017001131A1 (es) Síntesis de copanlisib y su sal diclorhidrato
CR20160098A (es) Polimorfo de los inhibidores de la syk
EA201692219A1 (ru) Способы получения противовирусных соединений
TW201613866A (en) Process for preparing fluorinated iminopyridine compounds
EA201692203A1 (ru) Соединения, ингибирующие tank-связывающую киназу
BR112016025427A2 (pt) processos de preparação de um inibidor de jak1 e formas do mesmo
EA201992183A3 (ru) Синтез полициклических карбамоилпиридоновых соединений
ES2897914T8 (es) Compuestos que contienen nitrógeno, adecuados para el uso en la producción de poliuretanos
BR112016017402A2 (pt) fusões anti-pcsk9~glp-1 e métodos para uso
BR112016026046A2 (pt) Uso de compostos de tienotriazolodiazepina
CL2016002336A1 (es) Uso de compuestos heterocíclicos para controlar nematodos
BR112016029510A2 (pt) métodos para a preparação de um composto, e, composto intermediário.
BR112017013286A2 (pt) composto de isoxazolina, e, uso de um composto de isoxazolina.
CL2017002255A1 (es) Procesos para preparar fluorocetólidos.
BR112018012325A2 (pt) métodos para a preparação de 5,6-di-hidro-6-fenilbenzo[f]isoquinolin-2-amina substituída
EA201690263A1 (ru) Улучшенные способы получения перампанеля
UY36284A (es) Método para la preparación de imidazopiridazinas sustituidas
UA31482S (uk) Сторінка документа для виїзду за кордон
UA31481S (uk) Сторінка документа для виїзду за кордон
TH1501004551A (th) กระบวนการซึ่งผสมผสานสำหรับการเตรียมของสารประกอบที่มีประโยชน์ในฐานะ เป็นส่วนประกอบของเชื้อเพลิง