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PE20081703A1 - Nuevos derivados triciclicos, su procedimiento de preparacion y las composiciones farmaceuticas que los contienen - Google Patents

Nuevos derivados triciclicos, su procedimiento de preparacion y las composiciones farmaceuticas que los contienen

Info

Publication number
PE20081703A1
PE20081703A1 PE2008000167A PE2008000167A PE20081703A1 PE 20081703 A1 PE20081703 A1 PE 20081703A1 PE 2008000167 A PE2008000167 A PE 2008000167A PE 2008000167 A PE2008000167 A PE 2008000167A PE 20081703 A1 PE20081703 A1 PE 20081703A1
Authority
PE
Peru
Prior art keywords
methyl
nitrobenzenosulfonamide
biphenyl
carbonyl
chloro
Prior art date
Application number
PE2008000167A
Other languages
English (en)
Inventor
Patrick Casara
Diguarher Thierry Le
Oliver Geneste
John Hickman
Original Assignee
Servier Lab
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 Servier Lab filed Critical Servier Lab
Publication of PE20081703A1 publication Critical patent/PE20081703A1/es

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
    • 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
    • A61K31/4985Pyrazines or piperazines ortho- or peri-condensed with heterocyclic ring systems
    • 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
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • 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

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)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Epidemiology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Hematology (AREA)
  • Oncology (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)

Abstract

REFERIDA A UN COMPUESTO TRICICLICO DE FORMULA (I), DONDE A ES UN CICLO AROMATICO O NO AROMATICO QUE CONTIENE 5, 6 O 7 ESLABONES QUE PUEDE CONTENER 1 O 2 HETEROATOMOS TALES COMO O, S Y N. n Y n' SON 0, 1 O 2 DONDE LA SUMA DE n Y n' ESTA ENTRE 0 Y 4; R3 ES ARILO O HETEROARILO; X ES UN ALQUILENO C1-C6 OPCIONALMENTE SUSTITUIDO CON OXIGENO, CICLOALQUILENO, ARILENO, HETEROARILENO O SO2; R1 Y R2 SON H O UN COMPUESTO DE FORMULA (II); Y ES C=O O CH2; R5 ES H; R6 ES H O UN GRUPO -NR7R7' O -CH2-NR7R7'; R7 Y R7' SON H, ALQUILO C1-C6, ENTRE OTROS. SON COMPUESTOS PREFERIDOS: N-({(4aR)-3-[(4'-CLORO[1,1'-BIFENIL]-2-IL)METIL]-2,3,4,4a,5,6-HEXAHIDRO-1H-PIRAZINO[1,2-a]QUINOLIN-8-IL}CARBONIL)-4-({(1R)-3-(DIMETILAMINO)-1-[(FENILSULFANIL)-METIL]PROPIL}AMINO)-3-NITROBENCENOSULFONAMIDA, N-({(4aR)-3-[(4'-CLORO[1,1'-BIFENIL]-2-IL)METIL]-2,3,4,4a,5,6-HEXAHIDRO-1H-PIRAZINO[1,2-a]QUINOLIN-8-IL}CARBONIL)-4-({(1R)-3-((1R,5S)-3-AZABICICLO[3.1.0]HEX-3-IL)-1-[(FENILSULFANIL)-METIL]PROPIL}AMINO)-3-NITROBENCENOSULFONAMIDA, N-({(10aß)-2-[(4'-CLORO[1,1'-BIFENIL]-2-IL)METIL]-1,2,3,4,10,10a-HEXAHIDROPIRAZINO[1,2-a]INDOL-8-IL}CARBONIL)-4-({(1R)-3-(DIMETILAMINO)-1-[(FENILSULFANIL)METIL]PROPIL}AMINO)-3-NITROBENCENOSULFONAMIDA. TAMBIEN ESTA REFERIDA A UN PROCEDIMIENTO DE PREPARACION Y A UNA COMPOSICION FARMACEUTICA. DICHOS COMPUESTOS TIENEN ACTIVIDAD PRO-APOPTOTICA Y SON UTILES EN EL TRATAMIENTO DEL CANCER
PE2008000167A 2007-02-02 2008-01-23 Nuevos derivados triciclicos, su procedimiento de preparacion y las composiciones farmaceuticas que los contienen PE20081703A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR0700741A FR2912145B1 (fr) 2007-02-02 2007-02-02 Nouveaux derives tricycliques,leur procede de preparation et les compositions pharmaceutiques qui les contiennent

Publications (1)

Publication Number Publication Date
PE20081703A1 true PE20081703A1 (es) 2009-01-14

Family

ID=38219469

Family Applications (1)

Application Number Title Priority Date Filing Date
PE2008000167A PE20081703A1 (es) 2007-02-02 2008-01-23 Nuevos derivados triciclicos, su procedimiento de preparacion y las composiciones farmaceuticas que los contienen

Country Status (45)

Country Link
US (1) US20080188460A1 (es)
EP (1) EP1953161B1 (es)
JP (1) JP2008266296A (es)
KR (1) KR100997027B1 (es)
CN (1) CN101270120A (es)
AP (1) AP2009004945A0 (es)
AR (1) AR065131A1 (es)
AT (1) ATE440842T1 (es)
AU (1) AU2008200499A1 (es)
BR (1) BRPI0800988A2 (es)
CA (1) CA2619897C (es)
CL (1) CL2008000318A1 (es)
CO (1) CO6230990A2 (es)
CR (1) CR10953A (es)
CY (1) CY1109637T1 (es)
DE (1) DE602008000104D1 (es)
DK (1) DK1953161T3 (es)
EA (1) EA014672B1 (es)
EC (1) ECSP099546A (es)
ES (1) ES2332337T3 (es)
FR (1) FR2912145B1 (es)
GE (1) GEP20115186B (es)
GT (1) GT200900217A (es)
HR (1) HRP20090565T1 (es)
IL (1) IL200128A0 (es)
JO (1) JO2616B1 (es)
MA (1) MA29725B1 (es)
MX (1) MX2008001504A (es)
MY (1) MY144633A (es)
NI (1) NI200900147A (es)
NZ (1) NZ565643A (es)
PA (1) PA8768301A1 (es)
PE (1) PE20081703A1 (es)
PL (1) PL1953161T3 (es)
PT (1) PT1953161E (es)
RS (1) RS51133B (es)
SA (1) SA08290043B1 (es)
SG (1) SG144892A1 (es)
SI (1) SI1953161T1 (es)
SV (1) SV2009003348A (es)
TN (1) TN2009000307A1 (es)
TW (1) TW200838532A (es)
UA (1) UA90726C2 (es)
WO (1) WO2008110691A1 (es)
ZA (1) ZA200801103B (es)

Families Citing this family (10)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU2007293916B2 (en) 2006-09-07 2011-02-03 Emisphere Technologies, Inc. A process for the manufacture of SNAC (salcaprozate sodium)
FR2933983B1 (fr) * 2008-07-15 2010-08-27 Servier Lab Nouveaux derives tricycliques,leur procede de preparation et les compositions pharmaceutiques qui les contiennent.
US8546377B2 (en) * 2009-04-23 2013-10-01 Abbvie Inc. Modulators of 5-HT receptors and methods of use thereof
US8518933B2 (en) * 2009-04-23 2013-08-27 Abbvie Inc. Modulators of 5-HT receptors and methods of use thereof
ES2568262T3 (es) * 2009-04-23 2016-04-28 Abbvie Inc. Moduladores de receptores de 5-HT y sus métodos de uso
EP2475661B1 (en) * 2009-09-10 2013-10-23 Novartis AG Sulfonamides as inhibitors of bcl-2 family proteins for the treatment of cancer
CN102584744B (zh) * 2011-01-06 2015-07-01 上海药明康德新药开发有限公司 4-(4-((2-(4-氯苯基)-5,5-二甲基环己基-1-烯)甲基)哌嗪-1-基)苯甲酸的合成方法
CN104039797B (zh) 2011-10-12 2016-06-01 南京奥昭生物科技有限公司 作为细胞凋亡诱导剂的杂环分子
TWI620733B (zh) * 2013-05-21 2018-04-11 拜耳作物科學股份有限公司 製備特定肟類及肟醚類之改良方法
JOP20190239A1 (ar) 2017-04-19 2019-10-09 Neurocrine Biosciences Inc مركبات مثبطة لـ vmat2 وتركيبات منها

Family Cites Families (16)

* Cited by examiner, † Cited by third party
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US3899490A (en) * 1968-01-12 1975-08-12 Pfizer Hexahydro pyrazinoquinolines
DE2362539C2 (de) * 1973-12-17 1986-05-07 Merck Patent Gmbh, 6100 Darmstadt 2-Acyl-4-oxo-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a]isochinoline, Verfahren zu ihrer Herstellung und diese Verbindungen enthaltende Arzneimittel
US5688950A (en) * 1996-04-23 1997-11-18 Neurogen Corporation Tricyclic aminoalkylcarboxamides; novel dopamine D3 receptor subtype specific ligands
JP2000169475A (ja) * 1998-07-24 2000-06-20 Dai Ichi Seiyaku Co Ltd ピラゾ―ル誘導体およびその塩
US6180629B1 (en) * 1998-08-14 2001-01-30 Cell Pathways, Inc. [4,5]-Fused-1,3-disubstituted-1,2-diazine-6-one derivatives with nitrogen containing substitutents in position one for the treatment of neoplasia
US6190629B1 (en) 1999-04-16 2001-02-20 Cbl Technologies, Inc. Organic acid scrubber and methods
US7919493B2 (en) * 2000-04-12 2011-04-05 Pharma Mar, S.A. Anititumoral ecteinascidin derivatives
KR100539139B1 (ko) * 2000-07-31 2005-12-26 에프. 호프만-라 로슈 아게 피페라진 유도체
JP2005515176A (ja) * 2001-11-03 2005-05-26 アストラゼネカ アクチボラグ 抗腫瘍剤としてのキナゾリン誘導体
US7094895B2 (en) * 2001-12-21 2006-08-22 King Pharmaceuticals Research & Development, Inc. Tyrosyl derivatives and their use as P2X7 receptor modulators
FR2841243B1 (fr) * 2002-06-19 2004-08-20 Servier Lab Nouveaux derives de 3-(4-oxo-4h-chromen-2yl)-(1h)-quinolein- 4-ones, leur procede de preparation et les compositions pharmaceutiques qui les contiennent
WO2004055163A2 (en) * 2002-12-12 2004-07-01 Cytovia, Inc. Substituted 1-benzoyl-3-cyano-pyrrolo[1,2-a]quinolines
WO2005049593A2 (en) * 2003-11-13 2005-06-02 Abbott Laboratories N-acylsulfonamide apoptosis promoters
ES2564804T3 (es) * 2004-02-12 2016-03-29 Mitsubishi Tanabe Pharma Corporation Compuesto de indazol y uso farmacéutico del mismo
US7790712B2 (en) * 2005-03-17 2010-09-07 Boehringer Ingelheim Pharmaceutical, Inc. Substituted [1,4]diazepino[1,2-A]indoles and azepino[1,2-A]indoles as anti-cytokine inhibitors
WO2009102864A1 (en) * 2008-02-12 2009-08-20 Stanford University Hedgehog pathway antagonists and methods of use

Also Published As

Publication number Publication date
ECSP099546A (es) 2009-08-28
TN2009000307A1 (fr) 2010-12-31
GEP20115186B (en) 2011-03-25
IL200128A0 (en) 2010-04-15
KR100997027B1 (ko) 2010-11-25
AU2008200499A1 (en) 2008-08-21
CO6230990A2 (es) 2010-12-20
EP1953161A1 (fr) 2008-08-06
CR10953A (es) 2009-09-09
KR20080072574A (ko) 2008-08-06
AP2009004945A0 (en) 2009-08-31
ZA200801103B (en) 2008-12-31
DK1953161T3 (da) 2009-11-30
GT200900217A (es) 2011-09-14
EP1953161B1 (fr) 2009-08-26
HRP20090565T1 (hr) 2009-12-31
DE602008000104D1 (de) 2009-10-08
CA2619897C (fr) 2011-06-14
JP2008266296A (ja) 2008-11-06
AR065131A1 (es) 2009-05-20
PA8768301A1 (es) 2008-11-19
CY1109637T1 (el) 2014-08-13
NZ565643A (en) 2009-05-31
JO2616B1 (ar) 2011-11-01
FR2912145A1 (fr) 2008-08-08
ES2332337T3 (es) 2010-02-02
MX2008001504A (es) 2009-02-24
CA2619897A1 (fr) 2008-08-02
CL2008000318A1 (es) 2008-08-08
TW200838532A (en) 2008-10-01
NI200900147A (es) 2010-02-15
MA29725B1 (fr) 2008-09-01
UA90726C2 (ru) 2010-05-25
SA08290043B1 (ar) 2011-06-22
EA200800235A1 (ru) 2008-08-29
US20080188460A1 (en) 2008-08-07
PT1953161E (pt) 2009-10-26
EA014672B1 (ru) 2010-12-30
SG144892A1 (en) 2008-08-28
BRPI0800988A2 (pt) 2008-11-25
CN101270120A (zh) 2008-09-24
RS51133B (sr) 2010-10-31
MY144633A (en) 2011-10-14
ATE440842T1 (de) 2009-09-15
SV2009003348A (es) 2010-02-01
PL1953161T3 (pl) 2010-01-29
SI1953161T1 (sl) 2009-12-31
FR2912145B1 (fr) 2009-03-06
WO2008110691A1 (fr) 2008-09-18

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