BR0314883A - Derivados de piridoindolona substituìdos em -3 por uma fenila, seu preparo e sua aplicação em terapêutica - Google Patents

Derivados de piridoindolona substituìdos em -3 por uma fenila, seu preparo e sua aplicação em terapêutica

Info

Publication number
BR0314883A
BR0314883A BR0314883-1A BR0314883A BR0314883A BR 0314883 A BR0314883 A BR 0314883A BR 0314883 A BR0314883 A BR 0314883A BR 0314883 A BR0314883 A BR 0314883A
Authority
BR
Brazil
Prior art keywords
group
phenyl
alkyl
preparation
conr
Prior art date
Legal status (The legal status 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 status listed.)
Pending
Application number
BR0314883-1A
Other languages
English (en)
Inventor
Bernard Bourrie
Pierre Casellas
Paola Ciapetti
Jean-Marie Derocq
Samir Jegham
Yvette Muneaux
Camille-Georges Wermuth
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
sanofi-aventis Deutschland GmbH
sanofi-aventis
Original Assignee
sanofi-aventis Deutschland GmbH
sanofi-aventis
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 sanofi-aventis Deutschland GmbH, sanofi-aventis filed Critical sanofi-aventis Deutschland GmbH
Publication of BR0314883A publication Critical patent/BR0314883A/pt
Pending legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D471/00Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04Ortho-condensed systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P35/00Antineoplastic agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

"DERIVADOS DE PIRIDOINDOLONA SUBSTITUìDOS EM -3 POR UMA FENILA, SEU PREPARO E SUA APLICAçãO EM TERAPêUTICA". A presente invenção refere-se a compostos que têm uma atividade anti-cancerígena, correspondendo à fórmula (I), na qual: R~ 1~, representa um átomo de hidrogênio, um grupo (C~ 1~-C~ 4~)alquila ou um grupamento (CH~ 2~)~ n~OH, (CH~ 2~)~ n~-O-tetrahidropiran-2-ila, (CH~ 2~)~ n~ NR<39>~ 6~R<39>~ 7~, (CH~ 2~)~ n~ CN, (CH~ 2~)~ n~ C0~ 2~(C~ 1~-C~ 4~)Alq ou (CH~ 2~)~ n~ CONR~ 6~R~ 7~; R~ 2~ representa um átomo de hidrogênio ou um grupo (C~ 1~-C~ 4~)alquila; ou R~ 1~, e R~ 2~ juntos formam um grupo (CH~ 2~)~ 3~; R~ 3~ representa uma fenila monossubstituída por um grupo hidroxila, hidroximetila, carbóxi, (C~ 1~-C~ 4~)alcanoíla, azido, (C~ 1~-C~ 4~)alcoxicarbonila, hidroxiiminometila, (C~ 1~-C~ 4~)alquisulfonila, trifluorometila, tiol, (C~ 1~-C~ 4~)alquiltio, ciano ou por um grupamento (CH~ 2~)~ m~NR<39>~ 7~R~ 10~, CONR~ 6~R~ 8~ ou O(CH~ 2~)~ n~R~ 9~; uma fenila substituída por de 2 a 5 substituintes idênticos ou diferentes escolhidos dentre um átomo de halogênio, um grupo (C~ 1~-C~ 4~)alquila, trifluorometila, hidroxila, hidroximetila, (C~ 1~-C~ 4~)alcóxi, carbóxi, (C~ 1~-C~ 4~)alcanoíla, azido, (C~ 1~-C~ 4~)alcoxicarbonila, hidroxiiminometila, tiol,(C~ 1~-C~ 4~)alquiltio, (C~ 1~-C~ 4~)alquilsulfonila, uma fenila, ciano ou por um grupamento (CH~ 2~)~ m~NR<39>~ 7~R~ 10~, CONR~ 6~R~ 8~ ou O(CH~ 2~)~ n~R~ 9~; ou R~ 3~ representa um grupo benzodioxolila não substituído ou substituído sobre a fenila por um átomo de halogênio; R~ 4~ e R~ 5~ são idênticos ou diferentes e representam, cada um independentemente, um átomo de hidrogênio ou de halogênio, ou um grupo hidroxila, (C~ 1~-C~ 4~)alquila, trifluorometila, fenila, ciano, (C~ 1~-C~ 4~)alcóxi, (C~ 1~-C~ 4~)alcoxicarbonila, (C~ 1~-C~ 4~)alquilsulfonila ou um grupamento 0-(CH~ 2~)~ n~NR~ 6~R~ 7~ ou (CH~ 2~)~ n~ NR~ 6~R~ 7~.
BR0314883-1A 2002-10-23 2003-10-21 Derivados de piridoindolona substituìdos em -3 por uma fenila, seu preparo e sua aplicação em terapêutica Pending BR0314883A (pt)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR0213264A FR2846329B1 (fr) 2002-10-23 2002-10-23 Derives de pyridoindolone substitues en -3 par un phenyle, leur preparation et leur application en therapeutique
PCT/FR2003/003110 WO2004041817A1 (fr) 2002-10-23 2003-10-21 Derives de pyridoindolone substitues en -3 par un phenyle, leur preparation et leur application en therapeutique.

Publications (1)

Publication Number Publication Date
BR0314883A true BR0314883A (pt) 2005-08-02

Family

ID=32088223

Family Applications (1)

Application Number Title Priority Date Filing Date
BR0314883-1A Pending BR0314883A (pt) 2002-10-23 2003-10-21 Derivados de piridoindolona substituìdos em -3 por uma fenila, seu preparo e sua aplicação em terapêutica

Country Status (33)

Country Link
US (2) US7390818B2 (pt)
EP (1) EP1556382B1 (pt)
JP (1) JP4488899B2 (pt)
KR (1) KR101051859B1 (pt)
CN (1) CN100345850C (pt)
AR (1) AR041689A1 (pt)
AT (1) ATE396994T1 (pt)
AU (1) AU2003296769B2 (pt)
BR (1) BR0314883A (pt)
CA (1) CA2502769C (pt)
CY (1) CY1109785T1 (pt)
DE (1) DE60321372D1 (pt)
DK (1) DK1556382T3 (pt)
EA (1) EA010833B1 (pt)
ES (1) ES2304546T3 (pt)
FR (1) FR2846329B1 (pt)
HK (1) HK1074446A1 (pt)
HR (1) HRP20050362B1 (pt)
IL (1) IL168133A (pt)
IS (1) IS2641B (pt)
MA (1) MA27455A1 (pt)
ME (1) ME00102B (pt)
MX (1) MXPA05004349A (pt)
NO (1) NO331297B1 (pt)
NZ (1) NZ539866A (pt)
PL (1) PL214867B1 (pt)
PT (1) PT1556382E (pt)
RS (1) RS51605B (pt)
SI (1) SI1556382T1 (pt)
TW (1) TWI325864B (pt)
UA (1) UA79317C2 (pt)
WO (1) WO2004041817A1 (pt)
ZA (1) ZA200503231B (pt)

Families Citing this family (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2823975B1 (fr) 2001-04-27 2003-05-30 Sanofi Synthelabo Nouvelle utilisation de pyridoindolone
US7456193B2 (en) 2002-10-23 2008-11-25 Sanofi-Aventis Pyridoindolone derivatives substituted in the 3-position by a heterocyclic group, their preparation and their application in therapeutics
US8512727B2 (en) * 2003-03-03 2013-08-20 Alkermes Pharma Ireland Limited Nanoparticulate meloxicam formulations
US20100297252A1 (en) * 2003-03-03 2010-11-25 Elan Pharma International Ltd. Nanoparticulate meloxicam formulations
FR2869316B1 (fr) 2004-04-21 2006-06-02 Sanofi Synthelabo Derives de pyridoindolone substitues en -6, leur preparation et leur application en therapeutique.
FR2876377B1 (fr) * 2004-10-11 2007-03-16 Univ Claude Bernard Lyon Nouveaux derives de 9h-pyrido[2,3-b]indole, leur procede de preparation, ainsi que les compositions pharmaceutiques contenant de tels composes
FR2892416B1 (fr) * 2005-10-20 2008-06-27 Sanofi Aventis Sa Derives de 6-heteroarylpyridoindolone, leur preparation et leur application en therapeutique
FR2945950A1 (fr) 2009-05-27 2010-12-03 Elan Pharma Int Ltd Compositions de nanoparticules anticancereuses et procedes pour les preparer
HUE032426T2 (en) 2009-05-27 2017-09-28 Alkermes Pharma Ireland Ltd Inhibition of flake aggregation in nanoparticulate meloxicam formulations
FR2959133A1 (fr) 2010-04-22 2011-10-28 Sanofi Aventis Formulation pharmaceutique anticancereuse
CN107459481A (zh) * 2017-07-25 2017-12-12 广州大学 一种3‑(4‑甲氧基苯基)‑6‑甲氧基‑4‑氯‑5,7‑二溴喹啉的合成方法
US12122780B2 (en) * 2019-02-01 2024-10-22 Jiangsu Aosaikang Pharmaceutical Co., Ltd. Pyrimidinyl group-containing tricyclic compound serving as c-Met inhibitor
CN113329276B (zh) 2020-02-28 2022-10-28 华为技术有限公司 数据传输方法、装置、网关、芯片及存储介质
CN116171156A (zh) * 2020-07-31 2023-05-26 南京明德新药研发有限公司 含嘧啶基团的三并环类化合物的盐型、晶型及其制备方法
US20240132446A1 (en) * 2021-05-26 2024-04-25 Refined Technologies, Inc. Compositions and methods for removal of n-methyl-2-pyrrolidone (nmp) degradation products and other foulants from nmp purification systems

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1268772A (en) 1968-03-15 1972-03-29 Glaxo Lab Ltd NOVEL alpha-CARBOLINE DERIVATIVES, THE PREPARATION THEREOF AND COMPOSITIONS CONTAINING THE SAME
US4263304A (en) 1978-06-05 1981-04-21 Sumitomo Chemical Company, Limited 7 H-indolo[2,3-c]isoquinolines
SU833971A1 (ru) 1979-07-10 1981-05-30 Ленинградский Химико-Фармацевтическийинститут Способ получени 3-фенил-2-оксо- - КАРбОлиНОВ
FR2595701B1 (fr) 1986-03-17 1988-07-01 Sanofi Sa Derives du pyrido-indole, leur application a titre de medicaments et les compositions les renfermant
EP0755454B1 (en) 1994-04-13 2008-02-13 The Rockefeller University Aav-mediated delivery of dna to cells of the nervous system
DE19502753A1 (de) * 1995-01-23 1996-07-25 Schering Ag Neue 9H-Pyrido[3,4-b]indol-Derivate
FR2765581B1 (fr) * 1997-07-03 1999-08-06 Synthelabo Derives de 3-aryl-1,9-dihydro-2h-pyrido[2,3-b]indol-2-one, leur preparation et leur application en therapeutique
FR2765582B1 (fr) 1997-07-03 1999-08-06 Synthelabo Derives de 3-alkyl-1,9-dihydro-2h-pyrido[2,3-b]indol-2-one leur preparation et leur application en therapeutique
CA2326319A1 (en) 1998-04-02 1999-10-14 Neurogen Corporation Aminoalkyl substituted 5,6,7,8-tetrahydro-9h pyrimidino[2,3-b]indole and 5,6,7,8-tetrahydro-9h-pyrimidino[4,5-b]indole derivatives: crf1 specific ligands
IT1313592B1 (it) * 1999-08-03 2002-09-09 Novuspharma Spa Derivati di 1h-pirido 3,4-b indol-1-one.
US20020156016A1 (en) 2001-03-30 2002-10-24 Gerald Minuk Control of cell growth by altering cell membrane potentials
FR2823975B1 (fr) 2001-04-27 2003-05-30 Sanofi Synthelabo Nouvelle utilisation de pyridoindolone
FR2846330B1 (fr) 2002-10-23 2004-12-03 Sanofi Synthelabo Derives de pyridoindolone substitues en -3 par groupe heterocyclique, leur preparation et leur application en therapeutique
US7456193B2 (en) 2002-10-23 2008-11-25 Sanofi-Aventis Pyridoindolone derivatives substituted in the 3-position by a heterocyclic group, their preparation and their application in therapeutics
FR2869316B1 (fr) 2004-04-21 2006-06-02 Sanofi Synthelabo Derives de pyridoindolone substitues en -6, leur preparation et leur application en therapeutique.
FR2892416B1 (fr) 2005-10-20 2008-06-27 Sanofi Aventis Sa Derives de 6-heteroarylpyridoindolone, leur preparation et leur application en therapeutique

Also Published As

Publication number Publication date
MXPA05004349A (es) 2005-08-26
CA2502769A1 (en) 2004-05-21
HRP20050362B1 (hr) 2014-01-31
CN100345850C (zh) 2007-10-31
ATE396994T1 (de) 2008-06-15
CY1109785T1 (el) 2014-09-10
CA2502769C (en) 2011-03-15
HK1074446A1 (en) 2005-11-11
PT1556382E (pt) 2008-07-09
EA200500521A1 (ru) 2005-12-29
TW200413368A (en) 2004-08-01
RS20050362A (en) 2007-11-15
NO20051983D0 (no) 2005-04-22
FR2846329A1 (fr) 2004-04-30
PL376790A1 (pl) 2006-01-09
FR2846329B1 (fr) 2004-12-03
AU2003296769B2 (en) 2010-02-04
MEP22208A (en) 2010-06-10
DK1556382T3 (da) 2008-10-06
AR041689A1 (es) 2005-05-26
SI1556382T1 (sl) 2008-10-31
WO2004041817A1 (fr) 2004-05-21
NO20051983L (no) 2005-07-22
ME00102B (me) 2010-10-10
KR20050086421A (ko) 2005-08-30
MA27455A1 (fr) 2005-07-01
NZ539866A (en) 2008-01-31
AU2003296769A1 (en) 2004-06-07
UA79317C2 (en) 2007-06-11
JP2006511498A (ja) 2006-04-06
US8012991B2 (en) 2011-09-06
NO331297B1 (no) 2011-11-21
US20050288318A1 (en) 2005-12-29
CN1729190A (zh) 2006-02-01
RS51605B (en) 2011-08-31
US20080214538A1 (en) 2008-09-04
ES2304546T3 (es) 2008-10-16
EA010833B1 (ru) 2008-12-30
EP1556382A1 (fr) 2005-07-27
TWI325864B (en) 2010-06-11
HRP20050362A2 (en) 2005-12-31
IS2641B (is) 2010-08-15
IS7815A (is) 2005-04-20
IL168133A (en) 2010-05-31
EP1556382B1 (fr) 2008-05-28
US7390818B2 (en) 2008-06-24
DE60321372D1 (de) 2008-07-10
JP4488899B2 (ja) 2010-06-23
KR101051859B1 (ko) 2011-07-25
ZA200503231B (en) 2006-06-28
PL214867B1 (pl) 2013-09-30

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Legal Events

Date Code Title Description
B06F Objections, documents and/or translations needed after an examination request according [chapter 6.6 patent gazette]
B07D Technical examination (opinion) related to article 229 of industrial property law [chapter 7.4 patent gazette]
B08F Application dismissed because of non-payment of annual fees [chapter 8.6 patent gazette]

Free format text: REFERENTE A 12A ANUIDADE.

B08K Patent lapsed as no evidence of payment of the annual fee has been furnished to inpi [chapter 8.11 patent gazette]

Free format text: EM VIRTUDE DO ARQUIVAMENTO PUBLICADO NA RPI 2328 DE 18-08-2015 E CONSIDERANDO AUSENCIA DE MANIFESTACAO DENTRO DOS PRAZOS LEGAIS, INFORMO QUE CABE SER MANTIDO O ARQUIVAMENTO DO PEDIDO DE PATENTE, CONFORME O DISPOSTO NO ARTIGO 12, DA RESOLUCAO 113/2013.