AR059594A1 - Derivados de 2,4-diaminopirimidinas - Google Patents

Derivados de 2,4-diaminopirimidinas

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Publication number
AR059594A1
AR059594A1 ARP070100726A ARP070100726A AR059594A1 AR 059594 A1 AR059594 A1 AR 059594A1 AR P070100726 A ARP070100726 A AR P070100726A AR P070100726 A ARP070100726 A AR P070100726A AR 059594 A1 AR059594 A1 AR 059594A1
Authority
AR
Argentina
Prior art keywords
piperazin
benzo
ylamino
trifluoromethyl
phenylamino
Prior art date
Application number
ARP070100726A
Other languages
English (en)
Inventor
Ingelheim Internati Boehringer
Harald Engelhardt
Stephan Karl Zahn
Heinz Stadtmueller
Anke Baum
Flavio Solca
Martin Steegmaier
Jens Juergen Quant
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
Application filed by Boehringer Ingelheim Int filed Critical Boehringer Ingelheim Int
Publication of AR059594A1 publication Critical patent/AR059594A1/es

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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D498/02—Heterocyclic 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
    • C07D498/04—Ortho-condensed systems
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00—Antineoplastic agents
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/02—Immunomodulators
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic 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
    • C07D487/04—Ortho-condensed systems

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Veterinary Medicine (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Immunology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)

Abstract

Reivindicacion 1: Compuestos de la formula general (1) en donde significan X O o N, y Y -CH2- o C=O, y R1 y R1' en cada caso independientemente entre sí, hidrogeno o un radical eventualmente sustituido una o varias veces seleccionado del grupo constituido por alquiloC1-5, cicloalquilo C3-6, arilo, heterociclilo y heteroarilo, pudiendo ser el o los sustituyentes iguales o diferentes y se seleccionan del grupo constituido por halogeno, -ORa, -C(=O)Ra, -C(=O)ORa, -C(=O)NRaRa, -NRaRa, - NRaC(=O)Ra, -NRaC(=O)ORa, -NRaC(=O)NRaRa, -NRaSO2Ra, -N=CRaRa, -SRa, -SORa, -SO2Ra, -SO2NRaRa, -NRaSO2NRaRa, -OSO2NRaRa y pseudohalogeno, o eventualmente los R1' que se encuentran en el mismo átomo de C pueden formar conjuntamente un anillo cicloalquílico C3-7, o eventualmente R1 puede estar unido con un R1' formando un puente alquílico comun de 3-6 miembros, saturado o parcialmente insaturado, el cual puede contener eventualmente uno a dos heteroátomos, y R2 un radical heterociclilo eventualmente sustituido una o varias veces, pudiendo ser el/los sustituyentes iguales o diferentes y se seleccionan del grupo constituido por alquiloC1-5, alquenilo C2-5, alquinilo C2-5, cicloalquil C3-6-alquilo C0-3 y R3 hidrogeno o alquilo C1-3 o R2 y R3 forman conjuntamente un anillo heterociclilo eventualmente una o varias veces sustituido, el cual eventualmente puede contener uno a dos heteroátomos, pudiendo ser el/los sustituyentes iguales o distintos y se seleccionan del grupo constituido por alquilo C1-5, alquenilo C2-5, alquinilo C2-5 y cicloalquil C3-6-alquilo C0-3 o un sustituyente adecuado seleccionado del grupo constituido por halogeno, -ORa, -C(=O)Ra, -C(=O)ORa, -C(=O)NRaRa, -NRaRa, -NRaC(=O)Ra, -NRaC(=O)ORa, - NRaC(=O)NRaRa, -NRaSO2Ra, -N=CRaRa, -SRa, -SORa, -SO2Ra, -SO2NRaRa, -NRaSO2NRaRa, -OSO2NRaRa y pseudohalogeno, y R4 en cada caso independientemente entre sí un radical seleccionado del grupo constituido por halogeno, NO2, -ORa, -C(=O)Ra, -C(=O)ORa, - C(=O)NRaRa, -NRaRa, -NRaCORa, -NRaC(=O)ORa, -NRaC(=O)NRaRa, -NRaC(=O)ONRaRa, -NRaSO2Ra, -N=CRaRa, -SRa, -SORa, -SO2Ra, -SO2NRaRa, -NRaSO2NRaRa, -OSO2NRaRa y pseudohalogeno; y R5 hidrogeno, halogeno, alquilo C1-3, alquenilo C2-3, alquinilo C2-3, halogeno-alquilo C1-3, -ORa o pseudohalogeno, y R6 en cada caso independientemente entre sí, un radical seleccionado del grupo constituido por halogeno, alquilo C1-3, -ORa y pseudohalogeno, y Ra en cada caso independientemente entre sí, hidrogeno o un radical seleccionado del grupo constituido por alquilo C1-8 eventualmente sustituido, alquenilo C2-8, alquinilo C2-8, cicloalquilo C3-10, arilo, heterociclilo y heteroarilo, pudiendo ser el/los sustituyentes iguales o diferentes y se seleccionan del grupo constituido por halogeno, -NH2, -OH y pseudohalogeno; y m es 0, 1 o 2; y n en cada caso independientemente entre sí, 0, 1 o 2, eventualmente en forma de sus tautomeros, sus racematos, sus enantiomeros, sus diastereoisomeros y sus mezclas, así como eventualmente sus sales farmacologicamente tolerables, con la condicion de que están excluidos 2-(2-metoxi-4-piperazin-1-il-fenilamino)-4-(3,3-dimetil-5-oxo-2,3,4,5- benzo[°][1,4]oxazepin-6-ilamino-5-trifluormetil-pirimidina, 2-(2-metoxi-4- piperazin-l-il-fenilamino)-4-((S)-4-oxo-2,3,10,10a-tetrahidro-1H,4H-9-oxa-3a-aza-benzo[°]azulen-5-ilamino-5-trifluormetil-pirimidina, 2-[4-(4-etil-piperazin-1-il)-2-metoxi-fenilamino]-4-((S)-4-oxo-2,3,10,10a-tetrahidro-1H,4H-9-oxa-3a-aza- benzo[°]azulen-5-ilamino-5-trifluormetil-pirimidina, 2-[4-(4-metil-piperazin-1-il)-2-metoxi-fenilamino]-4-((S)-4-oxo-2,3,10,10a tetrahidro-1H,4H-9-oxa-3a-aza-benzo[°]azulen-5-ilamino-5-trifluormetil-pirimidina, 3,3-dimetil-6-{2-[4-(4-metil-piperazin- 1-il)-fenilamino]-5-trifluormetil-pirimidin-4-ilamino}-3,4-dihidro-2H-benzo[°][1,4]oxazepin-5-ona, 6-{2-[4-(4-etil-piperazin-1-il)-fenilamino]-5-trifluormetil-pirimidin-4-ilamino}-3,3-dimetil-3,4-dihidro-2H-benzo[°][1,4]oxazepin-5-ona; 3,3-dimetil-6- {2-[4-(4-prop-2-inil-piperazin-1-il)-fenilamino]5trifluometil-pirimidin-4-ilamino}-3,4-dihidro-2H-benzo[°][1,4]oxazepin-5-ona, 6-{2-[4-(4-isopropil-piperazin-1-il)-fenilamino]-5-trifluormetil-pirimidin-4iIamino}-3,3-dimetil-3,4-dihidro-2H- benzo[°][1,4]oxazepin-5-ona, (S)-3-metil-6-[2-(4-piperazin-1-il-fenilamino)-5-trifluormetil-pirimidin-4-ilamino]-3,4-dihidro-2H-benzo[°][1,4]oxazepin-5-ona, (S)-3-metil-6-{2[4-(4-metil-piperazin-1-iI)-fenilamino]-5-trifluormetiI-pirimidin-4-ilamino}- 3,4-dihidro-2H-benzo[°][1,4]oxazepin-5-ona, (S)-6-{2-[4-(4-isopropil-piperazin-1-il-fenilamino]-5-trifluormetil-pirimidin-4-ilamino}-3-metil-3,4-dihidro-2H-benzo[°][1,4]oxazepin-5-ona, (S)-3-metil-6-{2-[4-(4-prop-2-iniI-piperazin-1-il)-fenilamino]-5- trifluormetil- pirimidin-4-ilamino}-3,4-dihidro-2H-benzo[°][1,4]oxazepin-5-ona, (S)-3-etil-6-[2-(4-piperazin-1-il-fenilamino)-5-trifluormetil-pirimidin-4-ilamino]-3,4-dihidro-2H-benzo[°][1,4joxazepin-5-ona, (S)-6-[2-(4-piperazin-1-il-fenilamino)-5- trifluormetil-pirimidin-4-ilamino]-3-propil-3,4-dihidro-2H-benzo[°][1,4]oxazepin-5-ona, (S)-6-{2-[4-(4-prop-2-inil-piperazin-1-il)-fenilamino]-5-trifluormetil-pirimidin-4-ilamino}-1,2,3,11a-tetrahidro-10H-benzo[e]pirrolo[1,2-a][1,4}diazepin-5,11- diona, (S)-6-{2-[4-(4-etil-piperazin-1-il)-fenilamino]-5-trifluormetil-pirimidin-4-ilamino}-1,2,3,11a-tetrahidro-10H-benzo[e]pirrolo[1,2-a][1,4]diazepin-5,11-diona, (S)-6-{2-[4-(4-isobutil-piperazin-1-il)-fenilamino]-5-trifluormetil-pirimidin-4- ilamino}-1,2,3,11a-tetrahidro-10H-benzo[e]pirrolo[1,2-a][1,4]diazepin-5,11-diona, (S)-6-{2-[4-(4-metil-piperazin-1-il)-fenilamino]-5-trifluormetil-pirimidin-4-ilamino}-1,2,3,11a-tetrahidro-10H-benzo[e]pirrolo[1,2-a][1,4]diazepin-5,11-diona, 6-{2-[4- (4-etil-piperazin-1-il)-fenilamino]-5-trifluormetil-pirimidin-4-ilamino}-3,3-dimetil-3,4-dihidro-1H-benzo[e][1,4]diazepin-2,5-diona, 3,3-dimetiI-6-{2-[4-(4-metil-piperazin-1-il)-feniIamino]-5-trifluormetiI-pirimidin-4-ilamino} -3,4-dihidro-1H- benzo[e][1,4]diazepin-2,5-diona, 6-{2-[4-(4-isopropil-piperazin-1-il)-feniIamino]-5-trifluormetiI-pirimidin-4-ilamino}-3,3-dimetil-3,4-dihidro-1H-benzo[e][1,4]diazepin-2,5-diona, 3,3-dimetil-6-{2-[4-(4-prop-2-inil-piperazin-1-i1l-fenilamino]-5- trifluormetil-pirimidin-4-ilamino}-3,4-dihidro-1H-benzo[e][1,4]diazepin-2,5-diona, (S)-6-{2-[4-(4-isopropil-piperazin-1-il)-fenilamino]-5-trifluormetil-pirimidin-4-ilamino}-1,2,3,11a-tetrahidro-10H-benzo[e]pirrolo[1,2-a][1,4]diazepin-5,11-diona, (S)- 6-{2-[4-(4-isopropil-piperazin-1-il)-fenilamino]-5-trifluormetil-pirimidin-4-ilamino}-3-metil-3,4-dihidro-1H-benzo[e][1,4]diazepin-2,5-diona, (S)-3-metil-6-{2-[4-(4-metil-piperazin-1-il)-fenilamino]-5-trifluormetil-pirimidin-4-ilamino}-3,4-dihidro- 1H-benzo[e][1,4]diazepin-2,5-diona, (S)-3-metil-6-{2-[4-(4-prop-2-inil-piperazin-1-il)-fenilamino]-5-trifluormetil-pirimidin-4-ilamino}-3,4-dihidro-1H-benzo[e][1,4]diazepin-2,5-diona, (S)-6-{2-[4-(4-etil-piperazin-1-il)-fenilamino]-5-trifluormetil- pirimidin-4-ilamino}-3-metil-3,4-dihidro-1H-benzo[e][1,4]diazepin-2,5-diona y {(S)-2,5-dioxo-6-[2-(4-piperazin-1-il-fenilamino)-5-trifluormetil-pirimidin-4-ilamino]-2,3,4,5-tetrahidro-1H-benzo[e][1,4]diazepin-3-il}-metiléster del ácido acético.
ARP070100726A 2006-02-22 2007-02-21 Derivados de 2,4-diaminopirimidinas AR059594A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
EP06110303 2006-02-22

Publications (1)

Publication Number Publication Date
AR059594A1 true AR059594A1 (es) 2008-04-16

Family

ID=36997219

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ARP070100726A AR059594A1 (es) 2006-02-22 2007-02-21 Derivados de 2,4-diaminopirimidinas

Country Status (7)

Country Link
US (1) US7569561B2 (es)
EP (1) EP1989198B1 (es)
JP (1) JP5306830B2 (es)
AR (1) AR059594A1 (es)
CA (1) CA2638095C (es)
TW (1) TW200804364A (es)
WO (1) WO2007096351A1 (es)

Families Citing this family (19)

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Publication number Priority date Publication date Assignee Title
CL2007003049A1 (es) 2006-10-23 2008-05-16 Cephalon Inc Pharmacopeia Drug Compuestos derivados de 2,4-diaminopirimidina; composicion farmaceutica, utiles para tratar trastornos proliferativos.
JP5443342B2 (ja) * 2007-06-08 2014-03-19 ジヤンセン・フアーマシユーチカ・ナームローゼ・フエンノートシヤツプ ピペリジン／ピペラジン誘導体
WO2008148851A1 (en) * 2007-06-08 2008-12-11 Janssen Pharmaceutica N.V. Piperidine/piperazine derivatives
JO2972B1 (en) * 2007-06-08 2016-03-15 جانسين فارماسوتيكا ان. في Piperidine / piperazine derivatives
PE20090362A1 (es) * 2007-06-08 2009-04-04 Janssen Pharmaceutica Nv Derivados de piperidina/piperazina como moduladores de dgat
US9273077B2 (en) 2008-05-21 2016-03-01 Ariad Pharmaceuticals, Inc. Phosphorus derivatives as kinase inhibitors
LT2300013T (lt) 2008-05-21 2017-12-27 Ariad Pharmaceuticals, Inc. Fosforo dariniai kaip kinazių inhibitoriai
WO2009147170A2 (en) 2008-06-05 2009-12-10 Janssen Pharmaceutica Nv Drug combinations comprising a dgat inhibitor and a ppar-agonist
AR074210A1 (es) 2008-11-24 2010-12-29 Boehringer Ingelheim Int Derivados de pirimidina como inhibidores de ptk2-quinasa
TW201024281A (en) 2008-11-24 2010-07-01 Boehringer Ingelheim Int New compounds
WO2011018517A1 (en) 2009-08-14 2011-02-17 Boehringer Ingelheim International Gmbh Regioselective preparation of 2-amino-5-trifluoromethylpyrimidine derivatives
US8933227B2 (en) 2009-08-14 2015-01-13 Boehringer Ingelheim International Gmbh Selective synthesis of functionalized pyrimidines
CN103501612B (zh) 2011-05-04 2017-03-29 阿里亚德医药股份有限公司 抑制表皮生长因子受体导致的癌症中细胞增殖的化合物
EP2751110B1 (en) * 2011-10-14 2017-04-19 MedImmune Limited Asymmetrical bis-(5H-Pyrrolo[2,1-c][1,4]benzodiazepin-5-one) derivatives for the treatment of proliferative and autoimmune diseases
US20150166591A1 (en) 2012-05-05 2015-06-18 Ariad Pharmaceuticals, Inc. Methods and compositions for raf kinase mediated diseases
US9611283B1 (en) 2013-04-10 2017-04-04 Ariad Pharmaceuticals, Inc. Methods for inhibiting cell proliferation in ALK-driven cancers
JP7109013B2 (ja) 2019-03-19 2022-07-29 ボロノイ インコーポレイテッド ヘテロアリール誘導体、ヘテロアリール誘導体の生成方法、およびヘテロアリール誘導体を有効成分として含む医薬組成物
CN112341468A (zh) * 2020-11-19 2021-02-09 烟台大学 一种1,4-苯并二氮杂*类化合物及其制备与功能化方法
JPWO2023204308A1 (es) * 2022-04-22 2023-10-26

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ES2325440T3 (es) 2003-02-20 2009-09-04 Smithkline Beecham Corporation Compuestos de pirimidina.
GB0305929D0 (en) 2003-03-14 2003-04-23 Novartis Ag Organic compounds
US7521457B2 (en) * 2004-08-20 2009-04-21 Boehringer Ingelheim International Gmbh Pyrimidines as PLK inhibitors

Also Published As

Publication number Publication date
CA2638095C (en) 2014-07-08
US7569561B2 (en) 2009-08-04
CA2638095A1 (en) 2007-08-30
WO2007096351A1 (de) 2007-08-30
US20070207999A1 (en) 2007-09-06
EP1989198B1 (de) 2013-10-09
EP1989198A1 (de) 2008-11-12
TW200804364A (en) 2008-01-16
JP5306830B2 (ja) 2013-10-02
JP2009527532A (ja) 2009-07-30

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