PA8786101A1 - "DERIVADOS DE 6-CICLOAMINO-3-(PIRIDIN-4-IL) IMIDAZO[1,2-b]-PIRIDAZINA, SU PREPARACION Y SU APLICACION EN TERAPEUTICA" - Google Patents

"DERIVADOS DE 6-CICLOAMINO-3-(PIRIDIN-4-IL) IMIDAZO[1,2-b]-PIRIDAZINA, SU PREPARACION Y SU APLICACION EN TERAPEUTICA"

Info

Publication number
PA8786101A1
PA8786101A1 PA20088786101A PA8786101A PA8786101A1 PA 8786101 A1 PA8786101 A1 PA 8786101A1 PA 20088786101 A PA20088786101 A PA 20088786101A PA 8786101 A PA8786101 A PA 8786101A PA 8786101 A1 PA8786101 A1 PA 8786101A1
Authority
PA
Panama
Prior art keywords
group
groups
eventually replaced
piridin
imidazo
Prior art date
Application number
PA20088786101A
Other languages
English (en)
Inventor
Philippe Burnier
Pascal George
Adrien Tak Li
Frederic Puech
Matthieu Barrague
Zhongli Gao
Roy Vaz
Qiuxia Zhao
Cecile Enguehard
Alain Gueiffier
Garcia Antonio Almario
Original Assignee
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 filed Critical Sanofi Aventis
Publication of PA8786101A1 publication Critical patent/PA8786101A1/es

Links

Classifications

    • 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
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/20—Hypnotics; Sedatives
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/30—Drugs for disorders of the nervous system for treating abuse or dependence
    • 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
    • A61P35/00—Antineoplastic agents
    • A61P35/02—Antineoplastic agents specific for leukemia
    • 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

Landscapes

  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (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)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Psychiatry (AREA)
  • Oncology (AREA)
  • Addiction (AREA)
  • Hematology (AREA)
  • Anesthesiology (AREA)
  • Hospice & Palliative Care (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Abstract

LA INVENCIÓN SE REFIERE A DERIVADOS DE 6-CICLOAMINO-3-(PIRIDIN-4-IL)IMIDAZO[1,2-B]PIRIDAZINA, QUE RESPONDEN A LA FÓRMULA GENERAL ( I ) EN LA QUE : -R2 REPRESENTA UN GRUPO ARILO EVENTUALMENTE SUSTITUIDO CON UNO O VARIOS SUSTITUYENTES ELEGIDOS ENTRE ÁTOMOS DE HALÓGENO Y GRUPOS ALQUILO(C1-C6), ALCOXI(C1-C6), ALQUILTIO(C1-C6), FLUOROALQUILO(C1-C6), FLUOROALCOXI(C1-C6), -CN ; R3 REPRESENTA UN ÁTOMO DE HIDRÓGENO O UN GRUPO ALQUILO(C1-C3), -NR4R5, HIDROXILO O ALCOXI(C1-C4) ; -A REPRESENTA UN GRUPO ALQUILENO(C1-C7) EVENTUALMENTE SUSTITUIDO CON UNO O DOS GRUPOS RA ; B REPRESENTA UN GRUPO ALQUILENO(C1-C7) EVENTUALMENTE SUSTITUIDO CON UN GRUPO RB ; L REPRESENTA, O UN ÁTOMO DE NITRÓGENO EVENTUALMENTE SUSTITUIDO CON UN GRUPO RC O RD, O UN ÁTOMO DE CARBONO SUSTITUIDO CON UN GRUPO RE1 Y UN GRUPO RD O DOS GRUPOS RE2 ; ESTANDO LOS ÁTOMOS DE CARBONO DE A Y DE B O LOS GRUPOS RE2 EVENTUALMENTE SUSTITUIDOS CON UNO O VARIOS GRUPOS RF IDÉNTICOS O DIFERENTES UNO DE OTRO ; - R7 Y R8 REPRESENTAN, INDEPENDIENTEMENTE UNO DE OTRO, UN ÁTOMO DE HIDRÓGENO O UN GRUPO ALQUILO(C1-C6). PROCEDIMIENTO DE PREPARACIÓN Y APLICACIÓN EN TERAPÉUTICA.
PA20088786101A 2007-06-28 2008-06-27 "DERIVADOS DE 6-CICLOAMINO-3-(PIRIDIN-4-IL) IMIDAZO[1,2-b]-PIRIDAZINA, SU PREPARACION Y SU APLICACION EN TERAPEUTICA" PA8786101A1 (es)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US94678507P 2007-06-28 2007-06-28
FR0704661A FR2918061B1 (fr) 2007-06-28 2007-06-28 Derives de 6-cycloamino-3-(pyridin-4-yl)imidazo°1,2-b!- pyridazine,leur preparation et leur application en therapeutique.

Publications (1)

Publication Number Publication Date
PA8786101A1 true PA8786101A1 (es) 2009-01-23

Family

ID=39203151

Family Applications (1)

Application Number Title Priority Date Filing Date
PA20088786101A PA8786101A1 (es) 2007-06-28 2008-06-27 "DERIVADOS DE 6-CICLOAMINO-3-(PIRIDIN-4-IL) IMIDAZO[1,2-b]-PIRIDAZINA, SU PREPARACION Y SU APLICACION EN TERAPEUTICA"

Country Status (22)

Country Link
US (2) US8354405B2 (es)
EP (1) EP2170889B1 (es)
JP (1) JP5537424B2 (es)
KR (1) KR20100050492A (es)
CN (1) CN101765602A (es)
AR (1) AR069269A1 (es)
AU (1) AU2008281662A1 (es)
BR (1) BRPI0814807A2 (es)
CA (1) CA2691866A1 (es)
CL (1) CL2008001932A1 (es)
CO (1) CO6251269A2 (es)
EA (1) EA201070072A1 (es)
FR (1) FR2918061B1 (es)
MA (1) MA31572B1 (es)
MX (1) MX2009013948A (es)
NZ (1) NZ582677A (es)
PA (1) PA8786101A1 (es)
PE (1) PE20090556A1 (es)
TW (1) TW200911812A (es)
UY (1) UY31193A1 (es)
WO (1) WO2009016286A2 (es)
ZA (1) ZA200909186B (es)

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FR2939134A1 (fr) * 2008-12-01 2010-06-04 Sanofi Aventis Derives de 6-cycloamino-3-(1h-pyrrolo°2,3-b!pyridin-4-yl) imidazo°1,2-b!-pyridazine, leur preparation et leur application en therapeutique
FR2940284B1 (fr) * 2008-12-19 2011-02-18 Sanofi Aventis Derives de 6-cycloamino-2,3-di-pyridinyl-imidazo°1,2-b!- pyridazine,leur preparation et leur application en therapeutique
FR2940285A1 (fr) * 2008-12-19 2010-06-25 Sanofi Aventis Derives de 6-cycloamino-2-thienyl-3-(pyridin-4-yl)imidazo °1,2-b!-pyridazine et 6-cycloamino-2-furanyl-3- (pyridin-4-yl)imidazo°1,2-b!-pyridazine, leur preparation et leur application en therapeutique
DK2491038T3 (da) * 2009-10-23 2016-07-18 Janssen Pharmaceutica Nv Disubstituerede octahydropyrrolo [3,4-c]pyrroler som orexin receptormodulatorer
EP2491031B1 (en) 2009-10-23 2013-08-07 Janssen Pharmaceutica N.V. Fused heterocyclic compounds as orexin receptor modulators
EP2491034B1 (en) 2009-10-23 2013-12-18 Janssen Pharmaceutica, N.V. Fused heterocyclic compounds as orexin receptor modulators
BR112012010041A2 (pt) 2009-10-30 2016-05-24 Janssen Pharmaceutica Nv derivados de imidazo [1,2-b] piridazina e seu uso como inibidores de pde10
AR080754A1 (es) 2010-03-09 2012-05-09 Janssen Pharmaceutica Nv Derivados de imidazo (1,2-a) pirazina y su uso como inhibidores de pde10
WO2011127202A2 (en) 2010-04-06 2011-10-13 Fred Hutchinson Cancer Research Center Methods for identifying and using inhibitors of casein kinase 1 epsilon isoform for inhibiting the growth and/or proliferation of myc-driven tumor cells
UY33597A (es) 2010-09-09 2012-04-30 Irm Llc Compuestos y composiciones como inhibidores de la trk
EP2651404B1 (en) 2010-12-14 2015-10-14 Electrophoretics Limited Casein kinase 1delta (ck1delta) inhibitors
TWI617559B (zh) 2010-12-22 2018-03-11 江蘇恆瑞醫藥股份有限公司 ２－芳基咪唑并［１，２－ｂ］嗒．２－苯基咪唑并［１，２－ａ］吡啶，和２－苯基咪唑并［１，２－ａ］吡衍生物
WO2012145581A1 (en) 2011-04-20 2012-10-26 Janssen Pharmaceutica Nv Disubstituted octahy-dropyrrolo [3,4-c] pyrroles as orexin receptor modulators
CN103619846B (zh) 2011-06-27 2016-08-17 詹森药业有限公司 1-芳基-4-甲基-[1,2,4]***[4,3-a]喹喔啉衍生物
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AU2013283426B2 (en) 2012-06-26 2018-02-22 Janssen Pharmaceutica Nv Combinations comprising PDE 2 inhibitors such as 1-aryl-4-methyl- [1,2,4] triazolo [4,3-a] quinoxaline compounds and PDE 10 inhibitors for use in the treatment of neurological or metabolic disorders
MX350418B (es) 2012-06-27 2017-09-06 4Sc Discovery Gmbh Inhibidores de bifluorodioxalano-amino-bencimidazol quinasa para el tratamiento de cáncer, inflamación autoinmune y trastornos del sistema nervioso central.
ES2607184T3 (es) 2012-07-09 2017-03-29 Janssen Pharmaceutica, N.V. Inhibidores de la enzima fosfodiesterasa 10
CZ2012538A3 (cs) * 2012-08-08 2014-02-19 Masarykova Univerzita Inhibitory pro léčbu B-buněčné chronické lymfocytární leukémie
WO2015077602A1 (en) 2013-11-22 2015-05-28 Fred Hutchinson Cancer Research Center Methods for identifying therapeutic targets and treating and monitoring cancers
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CN111068053A (zh) * 2014-02-03 2020-04-28 耶路撒冷希伯来大学的益生研究开发有限公司 使用酪蛋白激酶i抑制剂以消耗干细胞的用途
KR102559922B1 (ko) 2016-03-10 2023-07-25 얀센 파마슈티카 엔.브이. 오렉신-2 수용체 길항제를 사용한 우울증의 치료 방법
EP3597648B1 (en) 2017-03-14 2023-06-07 Daiichi Sankyo Company, Limited METHOD FOR PRODUCING 3, 6-DISUBSTITUTED IMIDAZO[1, 2-b]PYRIDAZINE DERIVATIVE
MA45614B1 (fr) 2017-03-20 2020-04-30 Forma Therapeutics Inc Compositions de pyrrolopyrrole en tant qu'activateurs de la pyruvate kinase (pkr)
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Also Published As

Publication number Publication date
UY31193A1 (es) 2009-01-30
JP2010531342A (ja) 2010-09-24
CL2008001932A1 (es) 2009-09-25
FR2918061B1 (fr) 2010-10-22
AR069269A1 (es) 2010-01-13
ZA200909186B (en) 2011-02-23
US20100179154A1 (en) 2010-07-15
BRPI0814807A2 (pt) 2015-02-03
FR2918061A1 (fr) 2009-01-02
WO2009016286A3 (fr) 2009-04-09
JP5537424B2 (ja) 2014-07-02
MX2009013948A (es) 2010-03-09
EP2170889A2 (fr) 2010-04-07
AU2008281662A1 (en) 2009-02-05
CN101765602A (zh) 2010-06-30
US8354405B2 (en) 2013-01-15
US20130012516A1 (en) 2013-01-10
WO2009016286A2 (fr) 2009-02-05
PE20090556A1 (es) 2009-06-01
US8846676B2 (en) 2014-09-30
EP2170889B1 (fr) 2016-08-17
MA31572B1 (fr) 2010-08-02
NZ582677A (en) 2011-12-22
CO6251269A2 (es) 2011-02-21
CA2691866A1 (fr) 2009-02-05
EA201070072A1 (ru) 2010-08-30
KR20100050492A (ko) 2010-05-13
TW200911812A (en) 2009-03-16

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