AR068130A1 - Derivados de tiadiazinona - Google Patents

Derivados de tiadiazinona

Info

Publication number
AR068130A1
AR068130A1 ARP080103757A ARP080103757A AR068130A1 AR 068130 A1 AR068130 A1 AR 068130A1 AR P080103757 A ARP080103757 A AR P080103757A AR P080103757 A ARP080103757 A AR P080103757A AR 068130 A1 AR068130 A1 AR 068130A1
Authority
AR
Argentina
Prior art keywords
nha
naa
hal
mono
so2naa
Prior art date
Application number
ARP080103757A
Other languages
English (en)
Inventor
Dieter Dorsch
Frank Stieber
Oliver Schadt
Andree Blaukat
Original Assignee
Merck Patent Gmbh
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 Merck Patent Gmbh filed Critical Merck Patent Gmbh
Publication of AR068130A1 publication Critical patent/AR068130A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/10Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a carbon chain containing aromatic rings
    • 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
    • A61P37/00Drugs for immunological or allergic disorders
    • 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
    • C07D417/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/14Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings

Abstract

Los compuestos de la formula (1) donde R1 es Ar1 o Het1; Het es un heterociclo saturado, insaturado o aromático monocíclico con 1 a 4 átomos de N, O y/o S, que puede no estar sustituido o que puede estar mono-, di- o trisustituido con B, Ar1 es fenilo naftilo o bifenilo no sustituido o mono-, di- o trisustituido con Hal, A, OH, OA, CN, CONH2, CONHA, CONAA', SO2NH2, SO2NHA, SO2NAA', NH2, NHA, NAA', SOA, SO2A, OCH2O y/u OCH2CH2O, Het1 es un heterociclo aromático mono- o bicíclico con 1 a 4 átomos de N, O y/o S que puede no estar sustituido o que puede estar mono- di- o trisustituido con Hal, A, OH, OA, CN, CONH2, CONHA, CONAA', SO2NH2, SO2NHA, SO2NAA', NH2, NHA, NAA', SOA, SO2A, OCH2O y/u OCH2CH2O, Q está ausente o es alquileno C1-4; B es OA, A, CONH2, CONHA, CONAA', SO2NH2, SO2NHA, SO2NAA', NH2, NHA, NAA', SOA, SO2A, O(CH2)nR2, CONA(CH2)nR2, CONH(CH2)nR2, Hal, CN, NA(CH2)nR2,NH(CH2)nR2, N=CH-N(CH3)2, o como en los restos de formulas (2); R2 es H, OH, OA, NH2, NHA, NAA', o como en los restos de formulas (3), A, A' son en cada caso, de modo independiente entre sí, alquilo no ramificado o ramificado C1-10, en donde 1-7 átomos de H pueden estar reemplazados por F, Cl y/o Br, alquilo cíclico C3-7 o cicloalquilalquileno C4-10, Hal es F, Cl, Br o I, n es 0, 1, 2 o 3, así como sus derivados, solvatos, sales, tautomeros y estereoisomeros de utilidad farmacéutica, incluyendo sus mezclas en todas las proporciones. Son inhibidores de las tirosina quinasas, en especial de la Met-quinasa, y pueden utilizarse, por ejemplo, para el tratamiento de tumores
ARP080103757A 2007-08-30 2008-08-29 Derivados de tiadiazinona AR068130A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DE102007041115A DE102007041115A1 (de) 2007-08-30 2007-08-30 Thiadiazinonderivate

Publications (1)

Publication Number Publication Date
AR068130A1 true AR068130A1 (es) 2009-11-04

Family

ID=39952448

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080103757A AR068130A1 (es) 2007-08-30 2008-08-29 Derivados de tiadiazinona

Country Status (17)

Country Link
US (1) US8211886B2 (es)
EP (1) EP2181111B1 (es)
JP (1) JP5524840B2 (es)
KR (1) KR20100065171A (es)
CN (1) CN101784544B (es)
AR (1) AR068130A1 (es)
AU (1) AU2008295193B2 (es)
BR (1) BRPI0816058A2 (es)
CA (1) CA2698062C (es)
DE (1) DE102007041115A1 (es)
EA (1) EA017393B1 (es)
ES (1) ES2426356T3 (es)
HK (1) HK1146276A1 (es)
IL (1) IL204127A (es)
MX (1) MX2010002096A (es)
WO (1) WO2009030333A1 (es)
ZA (1) ZA201002218B (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20130315895A1 (en) 2010-07-01 2013-11-28 Takeda Pharmaceutical Company Limited COMBINATION OF A cMET INHIBITOR AND AN ANTIBODY TO HGF AND/OR cMET
ES2764299T3 (es) 2014-12-09 2020-06-02 Inst Nat Sante Rech Med Anticuerpos monoclonales humanos contra AXL
WO2016135041A1 (en) 2015-02-26 2016-09-01 INSERM (Institut National de la Santé et de la Recherche Médicale) Fusion proteins and antibodies comprising thereof for promoting apoptosis

Family Cites Families (23)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5795964A (en) 1980-12-04 1982-06-15 Morishita Seiyaku Kk Preparation of 2-substituted-3(2h)-pyridazinone derivative
US4397854A (en) 1981-05-14 1983-08-09 Warner-Lambert Company Substituted 6-phenyl-3(2H)-pyridazinones useful as cardiotonic agents
DE4310699A1 (de) * 1993-04-01 1994-10-06 Merck Patent Gmbh Thiadiazinone
AU691673B2 (en) 1994-11-14 1998-05-21 Dow Agrosciences Llc Pyridazinones and their use as fungicides
US5635494A (en) 1995-04-21 1997-06-03 Rohm And Haas Company Dihydropyridazinones and pyridazinones and their use as fungicides and insecticides
GB9624482D0 (en) 1995-12-18 1997-01-15 Zeneca Phaema S A Chemical compounds
DE19604388A1 (de) 1996-02-07 1997-08-14 Merck Patent Gmbh Arylalkyl-diazinone
TR199801530T2 (xx) 1996-02-13 1998-11-23 Zeneca Limited VEGF �nhibit�rleri olarak kinazolin t�revleri.
JP4464466B2 (ja) 1996-03-05 2010-05-19 アストラゼネカ・ユーケイ・リミテッド 4―アニリノキナゾリン誘導体
GB9718972D0 (en) 1996-09-25 1997-11-12 Zeneca Ltd Chemical compounds
GB9714249D0 (en) 1997-07-08 1997-09-10 Angiogene Pharm Ltd Vascular damaging agents
WO1999025697A1 (fr) 1997-11-19 1999-05-27 Kowa Co., Ltd. Nouveaux derives de pyridazine et medicaments contenant ces composes comme principe actif
TWI241295B (en) 1998-03-02 2005-10-11 Kowa Co Pyridazine derivative and medicine containing the same as effect component
GB9900334D0 (en) 1999-01-07 1999-02-24 Angiogene Pharm Ltd Tricylic vascular damaging agents
GB9900752D0 (en) 1999-01-15 1999-03-03 Angiogene Pharm Ltd Benzimidazole vascular damaging agents
WO2001092224A1 (en) 2000-05-31 2001-12-06 Astrazeneca Ab Indole derivatives with vascular damaging activity
IL153484A0 (en) 2000-07-07 2003-07-06 Angiogene Pharm Ltd Colchinol derivatives as angiogenesis inhibitors
BR0112225A (pt) 2000-07-07 2003-05-06 Angiogene Pharm Ltd Composto, composição farmacêutica, uso de um composto, e, processo papa preparar um composto
EP1463509A1 (en) 2001-10-31 2004-10-06 MERCK PATENT GmbH Type 4 phosphodiesterase inhibitors and uses thereof
DE102005055355A1 (de) 2005-11-21 2007-10-31 Merck Patent Gmbh 3,6-Dihydro-2-oxo-6H-[1,3,4]thiadiazinderivate
DE102005055354A1 (de) 2005-11-21 2007-10-31 Merck Patent Gmbh Substituierte 5-Phenyl-3,6-dihydro-2-oxo-6H-[1,3,4]thiadiazine
DE102006037478A1 (de) * 2006-08-10 2008-02-14 Merck Patent Gmbh 2-(Heterocyclylbenzyl)-pyridazinonderivate
DE102007032507A1 (de) * 2007-07-12 2009-04-02 Merck Patent Gmbh Pyridazinonderivate

Also Published As

Publication number Publication date
CA2698062A1 (en) 2009-03-12
JP5524840B2 (ja) 2014-06-18
IL204127A (en) 2013-08-29
EA017393B1 (ru) 2012-12-28
EP2181111A1 (de) 2010-05-05
JP2010536896A (ja) 2010-12-02
US20100311733A1 (en) 2010-12-09
ZA201002218B (en) 2010-12-29
CN101784544B (zh) 2012-08-29
HK1146276A1 (en) 2011-05-20
CA2698062C (en) 2016-05-31
US8211886B2 (en) 2012-07-03
CN101784544A (zh) 2010-07-21
DE102007041115A1 (de) 2009-03-05
AU2008295193A1 (en) 2009-03-12
EA201000364A1 (ru) 2010-08-30
AU2008295193B2 (en) 2013-04-18
EP2181111B1 (de) 2013-06-26
MX2010002096A (es) 2010-03-26
KR20100065171A (ko) 2010-06-15
ES2426356T3 (es) 2013-10-22
BRPI0816058A2 (pt) 2015-03-31
WO2009030333A1 (de) 2009-03-12

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