[go: up one dir, main page]

PE20131143A1 - Nuevas aminopirazoloquinazolinas - Google Patents

Nuevas aminopirazoloquinazolinas

Info

Publication number
PE20131143A1
PE20131143A1 PE2013000125A PE2013000125A PE20131143A1 PE 20131143 A1 PE20131143 A1 PE 20131143A1 PE 2013000125 A PE2013000125 A PE 2013000125A PE 2013000125 A PE2013000125 A PE 2013000125A PE 20131143 A1 PE20131143 A1 PE 20131143A1
Authority
PE
Peru
Prior art keywords
alkyl
aminopyrazoloquinazolines
new
dihydropirazolo
pyrazole
Prior art date
Application number
PE2013000125A
Other languages
English (en)
Inventor
Matthias Treu
Original Assignee
Boehringer Ingelheim Int
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=43037625&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=PE20131143(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Boehringer Ingelheim Int filed Critical Boehringer Ingelheim Int
Publication of PE20131143A1 publication Critical patent/PE20131143A1/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
    • A61K31/517Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with carbocyclic ring systems, e.g. quinazoline, perimidine
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/16Drugs for disorders of the alimentary tract or the digestive system for liver or gallbladder disorders, e.g. hepatoprotective agents, cholagogues, litholytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • A61P37/02Immunomodulators
    • 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
    • C07D493/00Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system
    • C07D493/12Heterocyclic compounds containing oxygen atoms as the only ring hetero atoms in the condensed system in which the condensed system contains three hetero rings
    • C07D493/14Ortho-condensed systems
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D495/00Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/12Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D495/14Ortho-condensed systems
    • 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
    • C07D498/12Heterocyclic 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 three hetero rings
    • C07D498/14Ortho-condensed systems

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)
  • Immunology (AREA)
  • Communicable Diseases (AREA)
  • Rheumatology (AREA)
  • Pain & Pain Management (AREA)
  • Oncology (AREA)
  • Pulmonology (AREA)
  • Gastroenterology & Hepatology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

SE REFIERE A NUEVAS AMINOPIRAZOLOQUINAZOLINAS DE FORMULA (I) DONDE R1 ES H, ALQUILO C1-C6, ALQUENILO C2-C6, ALQUINILO C2-C6 ENTRE OTROS; R2 ES H, ALQUILO C1-C6, ALQUENILO C2-C6, ALQUINILO C2-C6, CICLOALQUILO C3-C10, ENTRE OTROS; R3 ES (II) , (III) DONDE A ES UN ARILO C6-C10 Y HETEROARILO C5-C12; B ES UN HETEROARILO NO AROMATICO C5-C7 CON AL MENOS UN HETEROATOMO SELECCIONADO DEL GRUPO N, S Y O, R4 Y R5 ESTAN SELECCIONADOS DEL GRUPO Ra y Rb, Ra ES UN ALQUILO C1-C6, ALQUENILO C2-C6 ENTRE OTROS; Rb ES HALOGENO, -CN, -NO2 ENTRE OTROS; m es 0,1,2,y3; n ES 0 Y 1; X ES -CH2- Y -CH2-CH2- ENTRE OTROS. SON COMPUESTOS PREFERIDOS (5S)-N-[1-(2-METOXIETIL) PIRAZOL-3-IL]-5,8-DIMETIL-9-FENIL-5,6-DIHIDROPIRAZOLO[3,4-H]-QUINAZOLIN-2-AMINA, N-[1-(2-DIMETILAMINOETIL)PIRAZOL-3-IL]-5,8-DIMETIL-9-FENIL-5,6-DIHIDROPIRAZOLO[3,4-H]-QUINAZOLIN-2-AMINA, ENTRE OTROS. SE REFIERE TAMBIEN A UNA FORMULACION FARMACEUTICA. DICHOS COMPUESTOS SON UTILES PARA EL TRATAMIENTO DE CARCINOMAS BRONQUIALES NO MICROCITICOS Y CARCINOMAS HEPATOCITICOS.
PE2013000125A 2010-07-23 2011-07-22 Nuevas aminopirazoloquinazolinas PE20131143A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP10170683 2010-07-23

Publications (1)

Publication Number Publication Date
PE20131143A1 true PE20131143A1 (es) 2013-10-23

Family

ID=43037625

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2013000125A PE20131143A1 (es) 2010-07-23 2011-07-22 Nuevas aminopirazoloquinazolinas

Country Status (23)

Country Link
US (1) US8735386B2 (es)
EP (1) EP2595987B1 (es)
JP (1) JP5991974B2 (es)
KR (1) KR20130132394A (es)
CN (1) CN103097388A (es)
AP (1) AP2012006640A0 (es)
AR (1) AR082850A1 (es)
AU (1) AU2011281504A1 (es)
BR (1) BR112013000107A2 (es)
CA (1) CA2803467A1 (es)
CL (1) CL2012003745A1 (es)
CO (1) CO6670575A2 (es)
EA (1) EA201201661A1 (es)
EC (1) ECSP13012448A (es)
GE (1) GEP20156289B (es)
MA (1) MA34389B1 (es)
MX (1) MX2013000821A (es)
PE (1) PE20131143A1 (es)
PH (1) PH12013500152A1 (es)
SG (1) SG187548A1 (es)
TW (1) TW201217380A (es)
UY (1) UY33526A (es)
WO (1) WO2012010704A1 (es)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP2807166B1 (en) 2012-01-23 2016-04-06 Boehringer Ingelheim International GmbH 5,8-dihydro-6h-pyrazolo[3,4-h]quinazolines as igf-1r/ir inhibitors
US9376437B2 (en) 2013-03-13 2016-06-28 Oncoceutics, Inc 7-benzyl-4-(2-methylbenzyl)-2,4,6,7,8,9-hexahydroimidazo[1,2-a]pyrido[3,4-e]pyrimidin-5(1H)-one, salts thereof and methods of using the same in combination therapy
EP3546461B1 (en) * 2013-11-15 2021-08-11 Oncoceutics, Inc. 7-benzyl-4-(2-methylbenzyl)-2,4,6,7,8,9-hexahydroimidazo[1,2-a]pyrido[3,4-e]pyrimidin-5(1h)-one, salts thereof and methods of using the same in combination therapy
MX2021001096A (es) 2015-01-30 2023-01-17 Oncoceutics Inc 7-bencil-4-(2-metilbencilo)-2,4,6,7,8,9-hexahidroimidazo [1,2-a]pirido[3,4-e]pirimidin-5(1h)-ona, analogos y sales del mismo y su uso en terapia.
EP3294742B1 (en) 2015-05-13 2020-01-08 Boehringer Ingelheim International GmbH New (5,8-dimethyl-9-phenyl-5,8-dihydro-6h-pyrazolo[3,4-h)quinazolin-2-yl)-(1h-pyrazol-5-yl)-amines and theri derivatives as igf-1r/1r inhibitors.
CN113264935B (zh) * 2016-11-11 2022-09-20 上海海雁医药科技有限公司 吡啶胺取代的杂三环化合物及其中间体和医药上的用途
US11597725B2 (en) * 2017-05-26 2023-03-07 Jiangsu Atom Bioscience And Pharmaceutical Co., Ltd. URAT1 inhibitor for promoting uric acid excretion
CN107383019B (zh) * 2017-07-28 2019-10-15 江苏艾凡生物医药有限公司 吡唑并[4,3-h]喹唑啉类化合物及其用途
JP2021521282A (ja) * 2018-04-24 2021-08-26 上海海雁医薬科技有限公司Shanghai Haiyan Pharmaceutical Technology Co., Ltd. Cdk4/6阻害剤、その薬学的に許容可能な塩と結晶多形体、及びその応用
US11066404B2 (en) 2018-10-11 2021-07-20 Incyte Corporation Dihydropyrido[2,3-d]pyrimidinone compounds as CDK2 inhibitors
US12311048B2 (en) 2018-11-02 2025-05-27 Fount Bio, Inc. Crosslinked materials
WO2020160321A1 (en) * 2019-01-30 2020-08-06 Yale University Compounds, compositions, and methods for treating fibrosis
US11384083B2 (en) 2019-02-15 2022-07-12 Incyte Corporation Substituted spiro[cyclopropane-1,5′-pyrrolo[2,3-d]pyrimidin]-6′(7′h)-ones as CDK2 inhibitors
TW202100520A (zh) 2019-03-05 2021-01-01 美商英塞特公司 作為cdk2 抑制劑之吡唑基嘧啶基胺化合物
SG11202108752YA (en) * 2019-03-07 2021-09-29 BioNTech SE Process for the preparation of a substituted imidazoquinoline
WO2020205560A1 (en) 2019-03-29 2020-10-08 Incyte Corporation Sulfonylamide compounds as cdk2 inhibitors
JP7650817B2 (ja) * 2019-04-19 2025-03-25 ファウント バイオ, インコーポレイテッド 皮膚内への活性剤の送達および保持
US11447494B2 (en) 2019-05-01 2022-09-20 Incyte Corporation Tricyclic amine compounds as CDK2 inhibitors
WO2020223469A1 (en) 2019-05-01 2020-11-05 Incyte Corporation N-(1-(methylsulfonyl)piperidin-4-yl)-4,5-di hydro-1h-imidazo[4,5-h]quinazolin-8-amine derivatives and related compounds as cyclin-dependent kinase 2 (cdk2) inhibitors for treating cancer
AU2020328025A1 (en) 2019-08-14 2022-03-03 Incyte Corporation Imidazolyl pyrimidinylamine compounds as CDK2 inhibitors
CN119930611A (zh) 2019-10-11 2025-05-06 因赛特公司 作为cdk2抑制剂的双环胺
AU2021282596A1 (en) 2020-06-05 2023-01-19 Kinnate Biopharma Inc. Inhibitors of fibroblast growth factor receptor kinases
CN111960974A (zh) * 2020-08-28 2020-11-20 山东潍坊润丰化工股份有限公司 一种烯草酮中间体的合成方法
CN116761806B (zh) * 2021-02-08 2025-10-10 上海复星医药产业发展有限公司 5,6-二氢噻吩并[3,4-h]喹唑啉类化合物
US11981671B2 (en) 2021-06-21 2024-05-14 Incyte Corporation Bicyclic pyrazolyl amines as CDK2 inhibitors
US11976073B2 (en) 2021-12-10 2024-05-07 Incyte Corporation Bicyclic amines as CDK2 inhibitors

Family Cites Families (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL123581A (en) * 1995-10-02 2001-09-13 Hoffmann La Roche History of pyrimidine as receptor antagonists - 5HT2C, the process for their preparation and drugs containing them
BRPI0410563B8 (pt) 2003-05-22 2021-05-25 Nerviano Medical Sciences Srl compostos de pirazol-quinazolina, seus processos de preparação e composições farmacêuticas
CN1897950A (zh) * 2003-10-14 2007-01-17 惠氏公司 稠合芳基和杂芳基衍生物及其使用方法

Also Published As

Publication number Publication date
CA2803467A1 (en) 2012-01-26
MA34389B1 (fr) 2013-07-03
US8735386B2 (en) 2014-05-27
US20120238542A1 (en) 2012-09-20
PH12013500152A1 (en) 2013-02-18
AU2011281504A1 (en) 2013-01-10
JP5991974B2 (ja) 2016-09-14
GEP20156289B (en) 2015-05-25
SG187548A1 (en) 2013-03-28
ECSP13012448A (es) 2013-03-28
AP2012006640A0 (en) 2012-12-31
MX2013000821A (es) 2013-05-30
CL2012003745A1 (es) 2013-05-31
CN103097388A (zh) 2013-05-08
WO2012010704A1 (en) 2012-01-26
AR082850A1 (es) 2013-01-16
KR20130132394A (ko) 2013-12-04
EA201201661A1 (ru) 2013-07-30
CO6670575A2 (es) 2013-05-15
EP2595987B1 (en) 2018-04-18
EP2595987A1 (en) 2013-05-29
UY33526A (es) 2012-02-29
BR112013000107A2 (pt) 2016-05-17
TW201217380A (en) 2012-05-01
JP2013532652A (ja) 2013-08-19

Similar Documents

Publication Publication Date Title
PE20131143A1 (es) Nuevas aminopirazoloquinazolinas
EA201992884A2 (ru) Арильные, гетероарильные и гетероциклические соединения для лечения заболеваний
AR090760A1 (es) Compuestos de benzotiazol y su uso contra el virus de hiv
NZ754039A (en) Primary carboxamides as btk inhibitors
BR112014006660A2 (pt) novos derivados de dihidroquinolina-2-ona bicíclicos
EA201592126A1 (ru) 6-мостиковые гетероарилдигидропиримидины для лечения и профилактики заражения вирусом гепатита b
PE20181024A1 (es) Derivados de ciclohexano sustituido con amido
MX376833B (es) Oxiesteroles y metodos de uso de los mismos.
MX2013006847A (es) Compuesto heterociclico fusionado y su uso para el control de plagas.
EA201792259A1 (ru) Бензимидазольные и имидазопиридиновые карбоксимидамидные соединения
BR112012013349A2 (pt) novos compostos tricíclicos
ECSP12012103A (es) Inhibidores de virus flaviviridae.
AR074021A1 (es) Compuestos heterociclicos fusionados como moduladores del canal ionico
MX387736B (es) Derivados de fenoximetilo.
EA201501122A8 (ru) Новые агонисты соматостатиновых рецепторов подтипа 4 (sstr4)
ECSP12011684A (es) Inhibidores de los virus flaviviridae.
ECSP11010830A (es) Derivados de heteroarilo como inhibidores de dgat1
AR079205A1 (es) Morfolinotiazoles como moduladores alostericos positivos alfa 7
EA201890899A1 (ru) Модуляторы фарнезоидного x-рецептора
CU20140072A7 (es) Derivados de dihidro-oxazina y dihidro-pirido-oxazina
MX382122B (es) Oxiesteroles y metodos de uso de los mismos.
EA201791058A1 (ru) Морфолин- и 1,4-оксазепан-амиды в качестве агонистов соматостатинового рецептора подтипа 4 (sstr4)
EA201791226A1 (ru) Композиции, содержащие 2-((1-(2-(4-фторфенил)-2-оксоэтил)пиперидин-4-ил)метил)изоиндолин-1-он для лечения шизофрении
BR112013018732A2 (pt) novos derivados de amida de aril-benzocicloalquila
EA202091400A1 (ru) Производные пиррола в качестве ингибиторов асс

Legal Events

Date Code Title Description
FD Application declared void or lapsed