ATE381335T1 - 2-cyanopyrrolopyrimidine und deren pharmazeutische verwendung - Google Patents

2-cyanopyrrolopyrimidine und deren pharmazeutische verwendung

Info

Publication number
ATE381335T1
ATE381335T1 AT04708332T AT04708332T ATE381335T1 AT E381335 T1 ATE381335 T1 AT E381335T1 AT 04708332 T AT04708332 T AT 04708332T AT 04708332 T AT04708332 T AT 04708332T AT E381335 T1 ATE381335 T1 AT E381335T1
Authority
AT
Austria
Prior art keywords
cyanopyrrolopyrimidines
pharmaceutical use
pharmaceutical
Prior art date
Application number
AT04708332T
Other languages
English (en)
Inventor
Francis Buxton
Takeru Ehara
Pamposh Ganju
Allan Hallett
Ozamu Irie
Atsuko Iwasaki
Takanori Kanazawa
Keiichi Masuya
Kazuhiko Nonomura
Junichi Sakaki
Christopher Snell
Chuanheng Song
Keiko Tanabe
Naoki Teno
Ichiro Umemura
Fumiaki Yokokawa
Original Assignee
Novartis Pharma 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
Priority claimed from GB0302748A external-priority patent/GB0302748D0/en
Priority claimed from GB0304642A external-priority patent/GB0304642D0/en
Priority claimed from GB0304641A external-priority patent/GB0304641D0/en
Application filed by Novartis Pharma Gmbh filed Critical Novartis Pharma Gmbh
Application granted granted Critical
Publication of ATE381335T1 publication Critical patent/ATE381335T1/de

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
    • A61P25/02—Drugs for disorders of the nervous system for peripheral neuropathies
    • 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
    • A61P25/04—Centrally acting analgesics, e.g. opioids
    • 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]
AT04708332T 2003-02-06 2004-02-05 2-cyanopyrrolopyrimidine und deren pharmazeutische verwendung ATE381335T1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
GB0302748A GB0302748D0 (en) 2003-02-06 2003-02-06 Organic compounds
GB0304642A GB0304642D0 (en) 2003-02-28 2003-02-28 Organic compounds
GB0304641A GB0304641D0 (en) 2003-02-28 2003-02-28 Organic compounds

Publications (1)

Publication Number Publication Date
ATE381335T1 true ATE381335T1 (de) 2008-01-15

Family

ID=32854008

Family Applications (1)

Application Number Title Priority Date Filing Date
AT04708332T ATE381335T1 (de) 2003-02-06 2004-02-05 2-cyanopyrrolopyrimidine und deren pharmazeutische verwendung

Country Status (17)

Country Link
US (1) US20060247251A1 (de)
EP (1) EP1592426B1 (de)
JP (1) JP4499667B2 (de)
AR (1) AR043692A1 (de)
AT (1) ATE381335T1 (de)
AU (1) AU2004210422B2 (de)
BR (1) BRPI0407327A (de)
CA (1) CA2514287A1 (de)
DE (1) DE602004010785T2 (de)
ES (1) ES2297378T3 (de)
HK (1) HK1084883A1 (de)
MX (1) MXPA05008348A (de)
PE (1) PE20050068A1 (de)
PL (1) PL378135A1 (de)
PT (1) PT1592426E (de)
TW (1) TW200420566A (de)
WO (1) WO2004069256A1 (de)

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SE0201980D0 (sv) 2002-06-24 2002-06-24 Astrazeneca Ab Novel compounds
GB0304640D0 (en) * 2003-02-28 2003-04-02 Novartis Ag Organic compounds
EP1797883A3 (de) * 2003-04-28 2007-08-01 Novartis AG Pharmezeutische Zusammensetzung einen Cathepsin S Inhibitor und ein Opioid enthaltend
EP1756109B1 (de) * 2004-05-03 2016-07-13 Janssen Pharmaceutica NV Neue indolderivate als selektive androgen rezeptor modulatoren (sarms)
US8501198B2 (en) 2004-06-07 2013-08-06 Qu Biologics Inc. Tissue targeted antigenic activation of the immune response to treat cancers
US9107864B2 (en) 2004-06-07 2015-08-18 Qu Biologics Inc. Tissue targeted antigenic activation of the immune response to treat cancers
AR077280A1 (es) 2009-06-29 2011-08-17 Incyte Corp Pirimidinonas como inhibidores de pi3k, y composiciones farmaceuticas que los comprenden
US8759359B2 (en) 2009-12-18 2014-06-24 Incyte Corporation Substituted heteroaryl fused derivatives as PI3K inhibitors
UY33304A (es) * 2010-04-02 2011-10-31 Amgen Inc Compuestos heterocíclicos y sus usos
WO2011130342A1 (en) 2010-04-14 2011-10-20 Incyte Corporation FUSED DERIVATIVES AS ΡI3Κδ INHIBITORS
US9062055B2 (en) 2010-06-21 2015-06-23 Incyte Corporation Fused pyrrole derivatives as PI3K inhibitors
CA2804709A1 (en) 2010-07-26 2012-02-02 Qu Biologics Inc. Immunogenic anti-inflammatory compositions
TWI501967B (zh) * 2010-12-16 2015-10-01 Janssen R&D Ireland 作為呼吸道融合病毒抗病毒劑之氮雜吲哚類
TWI515187B (zh) 2010-12-16 2016-01-01 健生科學愛爾蘭無限公司 作為呼吸道融合病毒抗病毒劑之吲哚類
TWI527814B (zh) 2010-12-16 2016-04-01 健生科學愛爾蘭無限公司 作為呼吸道融合病毒抗病毒劑之氮雜苯并咪唑類
ES2764848T3 (es) 2010-12-20 2020-06-04 Incyte Holdings Corp N-(1-(fenilo sustituido)etilo)-9H-purina-6-aminas como inhibidores de PI3K
WO2012125629A1 (en) 2011-03-14 2012-09-20 Incyte Corporation Substituted diamino-pyrimidine and diamino-pyridine derivatives as pi3k inhibitors
US9126948B2 (en) 2011-03-25 2015-09-08 Incyte Holdings Corporation Pyrimidine-4,6-diamine derivatives as PI3K inhibitors
PE20181272A1 (es) 2011-09-02 2018-08-03 Incyte Holdings Corp Heterociclilaminas como inhibidores de pi3k
CN103304525B (zh) * 2012-03-08 2015-08-05 深圳海王药业有限公司 一种制备达非那新中间体5-(卤代乙基)-2,3-二氢苯并呋喃的方法
AR090548A1 (es) 2012-04-02 2014-11-19 Incyte Corp Azaheterociclobencilaminas biciclicas como inhibidores de pi3k
KR20140145171A (ko) * 2012-04-17 2014-12-22 아스테라스 세이야쿠 가부시키가이샤 함질소 이환식 방향족 헤테로환 화합물
WO2013186333A1 (en) * 2012-06-15 2013-12-19 Janssen R&D Ireland 1,3 -dihydro- 2h-benzimidazol- 2 -one derivatives substituted with heterocycles as respiratory syncytial virus antiviral agents
SG11201503025WA (en) 2012-10-16 2015-06-29 Janssen Sciences Ireland Uc Rsv antiviral compounds
WO2014143638A1 (en) * 2013-03-14 2014-09-18 Novartis Ag 2-(1h-indol-4-ylmethyl)-3h-imidazo[4,5-b]pyridine-6-carbonitrile derivatives as complement factor b inhibitors useful for the treatment of ophthalmic diseases
WO2015066241A1 (en) 2013-10-30 2015-05-07 Novartis Ag 2-benzyl-benzimidazole complement factor b inhibitors and uses thereof
TWI671299B (zh) 2014-04-14 2019-09-11 愛爾蘭商健生科學愛爾蘭無限公司 作為ｒｓｖ抗病毒化合物之螺脲化合物
CN113855791A (zh) 2014-05-02 2021-12-31 Qu生物制药公司 抗微生物免疫调节
US10077277B2 (en) 2014-06-11 2018-09-18 Incyte Corporation Bicyclic heteroarylaminoalkyl phenyl derivatives as PI3K inhibitors
CR20210055A (es) 2015-02-27 2021-04-27 Incyte Corp SALES DE IHNIBIDOR DE PI3K Y PROCESOS DE PREPARACIÓN (Divisional 2017-0389)
US10537552B2 (en) 2015-05-05 2020-01-21 Carafe Drug Innovation, Llc Substituted 5-hydroxyoxindoles and their use as analgesics and fever reducers
WO2016183060A1 (en) 2015-05-11 2016-11-17 Incyte Corporation Process for the synthesis of a phosphoinositide 3-kinase inhibitor
US9988401B2 (en) 2015-05-11 2018-06-05 Incyte Corporation Crystalline forms of a PI3K inhibitor
TW201925179A (zh) * 2017-10-27 2019-07-01 西班牙商艾斯提夫製藥公司 治療疼痛及疼痛相關病症之新型烷氧基胺基衍生物
TW202024083A (zh) 2018-09-03 2020-07-01 德商拜耳廠股份有限公司 3,9-二氮雜螺[5.5]十一烷化合物

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CA2249739A1 (en) * 1996-03-15 1997-09-25 Novartis Ag Novel n-7-heterocyclyl pyrrolo[2,3-d]pyridines and their use
AU4710699A (en) * 1998-06-30 2000-01-17 Eli Lilly And Company Bicyclic sPLA2 inhibitors
GB0100622D0 (en) * 2001-01-10 2001-02-21 Vernalis Res Ltd Chemical compounds V111
GB0121033D0 (en) * 2001-08-30 2001-10-24 Novartis Ag Organic compounds
US20030144234A1 (en) * 2001-08-30 2003-07-31 Buxton Francis Paul Methods for the treatment of chronic pain and compositions therefor

Also Published As

Publication number Publication date
PT1592426E (pt) 2008-03-13
CA2514287A1 (en) 2004-08-19
WO2004069256A8 (en) 2004-10-14
BRPI0407327A (pt) 2006-01-10
WO2004069256A1 (en) 2004-08-19
EP1592426B1 (de) 2007-12-19
AU2004210422B2 (en) 2008-01-17
DE602004010785D1 (de) 2008-01-31
DE602004010785T2 (de) 2008-12-04
PE20050068A1 (es) 2005-03-11
HK1084883A1 (en) 2006-08-11
ES2297378T3 (es) 2008-05-01
EP1592426A1 (de) 2005-11-09
JP4499667B2 (ja) 2010-07-07
AR043692A1 (es) 2005-08-10
MXPA05008348A (es) 2005-11-04
JP2006516554A (ja) 2006-07-06
PL378135A1 (pl) 2006-03-06
US20060247251A1 (en) 2006-11-02
TW200420566A (en) 2004-10-16
AU2004210422A1 (en) 2004-08-19

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