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HUT40798A - Process for producing new, heterocyclic imidazol derivatives and pharmaceutically acceptable acid additional salts thereof - Google Patents

Process for producing new, heterocyclic imidazol derivatives and pharmaceutically acceptable acid additional salts thereof

Info

Publication number
HUT40798A
HUT40798A HU862332A HU233286A HUT40798A HU T40798 A HUT40798 A HU T40798A HU 862332 A HU862332 A HU 862332A HU 233286 A HU233286 A HU 233286A HU T40798 A HUT40798 A HU T40798A
Authority
HU
Hungary
Prior art keywords
alkyl
heterocyclic
pharmaceutically acceptable
acceptable acid
producing new
Prior art date
Application number
HU862332A
Other languages
English (en)
Inventor
Ikuo Ueda
Youichi Shiokawa
Kazuhiko Take
Hiromichi Itani
Original Assignee
Fujisawa Pharmaceutical Co
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 GB858514080A external-priority patent/GB8514080D0/en
Priority claimed from GB858530878A external-priority patent/GB8530878D0/en
Application filed by Fujisawa Pharmaceutical Co filed Critical Fujisawa Pharmaceutical Co
Publication of HUT40798A publication Critical patent/HUT40798A/hu

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D471/00—Heterocyclic 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
    • C07D471/02—Heterocyclic 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
    • C07D471/04—Ortho-condensed systems
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Detergent Compositions (AREA)
  • Lubricants (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
HU862332A 1985-06-04 1986-06-03 Process for producing new, heterocyclic imidazol derivatives and pharmaceutically acceptable acid additional salts thereof HUT40798A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GB858514080A GB8514080D0 (en) 1985-06-04 1985-06-04 Imidazopyridine compounds
GB858530878A GB8530878D0 (en) 1985-12-16 1985-12-16 Imidazopyridine compounds

Publications (1)

Publication Number Publication Date
HUT40798A true HUT40798A (en) 1987-02-27

Family

ID=26289330

Family Applications (1)

Application Number Title Priority Date Filing Date
HU862332A HUT40798A (en) 1985-06-04 1986-06-03 Process for producing new, heterocyclic imidazol derivatives and pharmaceutically acceptable acid additional salts thereof

Country Status (15)

Country Link
US (1) US4725601A (hu)
EP (1) EP0204285B1 (hu)
KR (1) KR870000332A (hu)
CN (1) CN86104313A (hu)
AT (1) ATE71625T1 (hu)
AU (1) AU593802B2 (hu)
CA (1) CA1257264A (hu)
DE (1) DE3683403D1 (hu)
DK (1) DK250386A (hu)
ES (1) ES8800943A1 (hu)
FI (1) FI862210A (hu)
GR (1) GR861379B (hu)
HU (1) HUT40798A (hu)
IL (1) IL78923A0 (hu)
NO (1) NO862208L (hu)

Families Citing this family (44)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4831041A (en) * 1986-11-26 1989-05-16 Fujisawa Pharmaceutical Co., Ltd. Imidazopyridine compounds and processes for preparation thereof
IL86269A0 (en) * 1987-05-08 1988-11-15 Byk Gulden Lomberg Chem Fab Imidazole derivatives,processes for the preparation thereof and pharmaceutical compositions containing the same
EP0370056A1 (de) * 1987-07-16 1990-05-30 Byk Gulden Lomberg Chemische Fabrik Gmbh Neue diazole
GB8722488D0 (en) * 1987-09-24 1987-10-28 Fujisawa Pharmaceutical Co Imidazopyridine compound
AT390438B (de) * 1987-10-08 1990-05-10 Yamanouchi Pharma Co Ltd Neue imidazo(1,2-a)pyridinderivate und deren herstellung und diese enthaltende pharmazeutische zubereitungen
SE8704248D0 (sv) * 1987-10-30 1987-10-30 Haessle Ab Medical use
EP0368158A1 (de) * 1988-11-07 1990-05-16 Byk Gulden Lomberg Chemische Fabrik GmbH Neue Imidazopyridine
DE3837809A1 (de) * 1988-11-08 1990-05-10 Merck Patent Gmbh Tetralinderivate
GB9201693D0 (en) * 1992-01-27 1992-03-11 Smithkline Beecham Intercredit Compounds
US5574042A (en) * 1992-11-02 1996-11-12 Fujisawa Pharmaceutical Co., Ltd Imidazo [1,2-a] pyridines and their pharmaceutical use
UA48122C2 (uk) * 1993-10-11 2002-08-15 Бік Гульден Ломберг Хеміше Фабрік Гмбх АЛКОКСІАЛКІЛКАРБАМАТИ ІМІДАЗО[1,2-а]ПІРИДИНІВ, СПОСІБ ЇХ ОДЕРЖАННЯ ТА ЛІКАРСЬКИЙ ЗАСІБ НА ЇХ ОСНОВІ
RU2138501C1 (ru) * 1994-07-28 1999-09-27 Бык Гульден Ломберг Хемише Фабрик Гмбх Имидазопиридиназолидиноны, их соли и лекарственное средство
CN1064360C (zh) * 1995-04-21 2001-04-11 新日本药品株式会社 稠合咪唑并[1,2－a]吡啶类
US6992188B1 (en) 1995-12-08 2006-01-31 Pfizer, Inc. Substituted heterocyclic derivatives
ES2200039T3 (es) * 1995-12-08 2004-03-01 Pfizer Inc. Derivados heterociclicos sustituidos como antagonistas de crf.
WO1997027192A1 (de) * 1996-01-26 1997-07-31 Byk Gulden Lomberg Chemische Fabrik Gmbh 3-methylimidazopyridine
AU1545297A (en) * 1996-01-26 1997-08-20 Byk Gulden Imidazopyridine halides
SE9700661D0 (sv) 1997-02-25 1997-02-25 Astra Ab New compounds
SE9704404D0 (sv) 1997-11-28 1997-11-28 Astra Ab New compounds
SE9801526D0 (sv) * 1998-04-29 1998-04-29 Astra Ab New compounds
SE9802793D0 (sv) 1998-08-21 1998-08-21 Astra Ab New compounds
SE9802794D0 (sv) * 1998-08-21 1998-08-21 Astra Ab New compounds
CA2311483A1 (en) * 2000-06-12 2001-12-12 Gregory N Beatch IMIDAZO [1,2-A] PYRIDINIC ETHERS AND USES THEREOF
SE0003186D0 (sv) * 2000-09-07 2000-09-07 Astrazeneca Ab New process
US6900324B2 (en) 2000-09-07 2005-05-31 Astrazeneca Ab Process for preparing a substituted imidazopyridine compound
UA80393C2 (uk) 2000-12-07 2007-09-25 Алтана Фарма Аг Фармацевтична композиція, яка містить інгібітор фде 4, диспергований в матриці
SE0102808D0 (sv) * 2001-08-22 2001-08-22 Astrazeneca Ab New compounds
DE10145457A1 (de) 2001-09-14 2003-04-03 Basf Ag Substituierte Imidazo[1,2-a]-5,6,7,8-tetrahydropyridin-8-one, Verfahren zu ihrer Herstellung, sowie deren Verwendung zur Herstellung von Imidazo[1,2,-a]pyridinen
MY140561A (en) 2002-02-20 2009-12-31 Nycomed Gmbh Dosage form containing pde 4 inhibitor as active ingredient
AR043002A1 (es) * 2003-02-18 2005-07-13 Altana Pharma Ag Imidazopirazinas 6-substituidos
JP4695588B2 (ja) 2003-02-26 2011-06-08 スージェン， インク． プロテインキナーゼ阻害剤としてのアミノヘテロアリール化合物
US7470791B2 (en) 2003-03-10 2008-12-30 Nycomed Gmbh Process for the preparation of roflumilast
SE0301904D0 (sv) * 2003-06-26 2003-06-26 Astrazeneca Ab Novel imidazopyridine compound II with therapeutic effect
CN1874772A (zh) 2003-11-03 2006-12-06 阿斯利康(瑞典)有限公司 治疗隐匿性胃食管反流的咪唑并[1,2－a]吡啶衍生物
JP2008523139A (ja) * 2004-12-14 2008-07-03 アストラゼネカ・アクチエボラーグ 置換アミノピリジン類及びその使用
CA2601250C (en) * 2005-03-16 2014-10-28 Nycomed Gmbh Taste masked dosage form containing roflumilast
CA2620223A1 (en) 2005-09-02 2007-03-08 Abbott Laboratories Novel imidazo based heterocycles
CN101326175B (zh) 2005-12-05 2012-07-18 辉瑞产品公司 C-met/hgfr抑制剂的多晶型物
BRPI0619424B1 (pt) 2005-12-05 2022-02-08 Pfizer Products Inc Uso de inibidores c-met/hgfrs para a fabricação de medicamentos
MX2008015747A (es) * 2006-06-06 2008-12-19 Schering Corp Imidazopirazinas como inhibidores de la proteina quinasa.
TW200815447A (en) * 2006-06-14 2008-04-01 Astrazeneca Ab Novel compounds IV
US20080051420A1 (en) * 2006-06-14 2008-02-28 Astrazeneca Ab New Compounds 317
FI20086158A0 (fi) 2008-12-03 2008-12-03 Mikael Dahlstroem Imidatsopyridiinijohdannaiset
JP5458813B2 (ja) * 2009-11-10 2014-04-02 オムロン株式会社 光電センサ

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
ZA81219B (en) * 1980-01-23 1982-01-27 Schering Corp Imidazo (1,2-a) pyridines ,process for their preparation and pharmaceutical compositions containing them
US4507294A (en) * 1982-03-08 1985-03-26 Schering Corp. Imidazo[1,2-a]pyrazines
DE3269604D1 (en) * 1981-06-26 1986-04-10 Schering Corp Novel imidazo(1,2-a)pyridines and pyrazines, processes for their preparation and pharmaceutical compositions containing them
AU7928787A (en) * 1986-10-07 1988-04-14 Yamanouchi Pharmaceutical Co., Ltd. Imidazopyridine derivatives
US4831041A (en) * 1986-11-26 1989-05-16 Fujisawa Pharmaceutical Co., Ltd. Imidazopyridine compounds and processes for preparation thereof

Also Published As

Publication number Publication date
EP0204285A1 (en) 1986-12-10
FI862210A (fi) 1986-12-05
FI862210A0 (fi) 1986-05-26
CN86104313A (zh) 1987-03-04
ES8800943A1 (es) 1987-12-01
AU5834586A (en) 1986-12-11
EP0204285B1 (en) 1992-01-15
AU593802B2 (en) 1990-02-22
ATE71625T1 (de) 1992-02-15
ES555653A0 (es) 1987-12-01
NO862208L (no) 1986-12-05
CA1257264A (en) 1989-07-11
DK250386D0 (da) 1986-05-28
NO862208D0 (no) 1986-06-03
IL78923A0 (en) 1986-09-30
GR861379B (en) 1986-08-28
DE3683403D1 (de) 1992-02-27
KR870000332A (ko) 1987-02-17
US4725601A (en) 1988-02-16
DK250386A (da) 1986-12-05

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