FR1453897A - Thiophene and thienopyridazine derivatives - Google Patents

Thiophene and thienopyridazine derivatives

Info

Publication number
FR1453897A
FR1453897A FR20979A FR20979A FR1453897A FR 1453897 A FR1453897 A FR 1453897A FR 20979 A FR20979 A FR 20979A FR 20979 A FR20979 A FR 20979A FR 1453897 A FR1453897 A FR 1453897A
Authority
FR
France
Prior art keywords
thienopyridazine
thiophene
derivatives
thienopyridazine derivatives
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.)
Expired
Application number
FR20979A
Other languages
French (fr)
Inventor
Max Fernand Robba
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 filed Critical
Priority to FR20979A priority Critical patent/FR1453897A/en
Application granted granted Critical
Publication of FR1453897A publication Critical patent/FR1453897A/en
Expired legal-status Critical Current

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
    • C07D495/04—Ortho-condensed systems
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/22—Radicals substituted by doubly bound hetero atoms, or by two hetero atoms other than halogen singly bound to the same carbon atom
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/24—Radicals substituted by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D495/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms
    • C07D495/12—Heterocyclic compounds containing in the condensed system at least one hetero ring having sulfur atoms as the only ring hetero atoms in which the condensed system contains three hetero rings
    • C07D495/14—Ortho-condensed systems

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
FR20979A 1965-06-16 1965-06-16 Thiophene and thienopyridazine derivatives Expired FR1453897A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
FR20979A FR1453897A (en) 1965-06-16 1965-06-16 Thiophene and thienopyridazine derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR20979A FR1453897A (en) 1965-06-16 1965-06-16 Thiophene and thienopyridazine derivatives

Publications (1)

Publication Number Publication Date
FR1453897A true FR1453897A (en) 1966-07-22

Family

ID=8582160

Family Applications (1)

Application Number Title Priority Date Filing Date
FR20979A Expired FR1453897A (en) 1965-06-16 1965-06-16 Thiophene and thienopyridazine derivatives

Country Status (1)

Country Link
FR (1) FR1453897A (en)

Cited By (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2463145A1 (en) * 1979-08-07 1981-02-20 Sanofi Sa Sedative and muscle relaxant thieno pyridazine(s) - prepd. from benzoyl thienaldehyde and hydrazine hydrate
FR2478640A1 (en) * 1980-03-24 1981-09-25 Sanofi Sa Antiinflammatory phenyl thieno pyridazinone(s) - prepd. by reaction of hydrazine hydrate and benzoyl thiophene carboxylic acid
WO1991012251A1 (en) * 1990-02-19 1991-08-22 Chugai Seiyaku Kabushiki Kaisha Novel fused heterocyclic compound and antiasthmatic agent prepared therefrom
WO1999029695A1 (en) * 1997-12-05 1999-06-17 Astrazeneca Uk Limited Novel compounds
WO2001023375A2 (en) * 1999-09-28 2001-04-05 Bayer Corporation Substituted pyridines and pyridazines with angiogenesis inhibiting activity
US6579882B2 (en) 1998-06-04 2003-06-17 Abbott Laboratories Cell adhesion-inhibiting antiinflammatory compounds
US6689883B1 (en) 1999-09-28 2004-02-10 Bayer Pharmaceuticals Corporation Substituted pyridines and pyridazines with angiogenesis inhibiting activity
US7977333B2 (en) 2000-04-20 2011-07-12 Bayer Healthcare Llc Substituted pyridines and pyridazines with angiogenesis inhibiting activity
EP2994128A4 (en) * 2013-05-10 2016-11-23 Nimbus Apollo Inc Acc inhibitors and uses thereof
US9988399B2 (en) 2013-05-10 2018-06-05 Gilead Apollo, Llc Bicyclic compounds as ACC inhibitors and uses thereof
US10208044B2 (en) 2013-05-10 2019-02-19 Gilead Apollo, Llc ACC inhibitors and uses thereof
US10208063B2 (en) 2013-05-10 2019-02-19 Gilead Apollo, Llc ACC inhibitors and uses thereof
EP4279074A1 (en) * 2022-05-19 2023-11-22 Georg-August-Universität Göttingen Stiftung Öffentlichen Rechts, Universitätsmedizin Azolo compounds for treatment of fibrotic diseases

Cited By (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2463145A1 (en) * 1979-08-07 1981-02-20 Sanofi Sa Sedative and muscle relaxant thieno pyridazine(s) - prepd. from benzoyl thienaldehyde and hydrazine hydrate
FR2478640A1 (en) * 1980-03-24 1981-09-25 Sanofi Sa Antiinflammatory phenyl thieno pyridazinone(s) - prepd. by reaction of hydrazine hydrate and benzoyl thiophene carboxylic acid
WO1991012251A1 (en) * 1990-02-19 1991-08-22 Chugai Seiyaku Kabushiki Kaisha Novel fused heterocyclic compound and antiasthmatic agent prepared therefrom
WO1999029695A1 (en) * 1997-12-05 1999-06-17 Astrazeneca Uk Limited Novel compounds
US6342601B1 (en) 1997-12-05 2002-01-29 Astrazeneca Ab Compounds
US6770646B2 (en) 1997-12-05 2004-08-03 Astrazeneca Ab Substituted fused pyridazinone compounds; composition and use thereof
US6579882B2 (en) 1998-06-04 2003-06-17 Abbott Laboratories Cell adhesion-inhibiting antiinflammatory compounds
CN100374435C (en) * 1999-09-28 2008-03-12 拜尔药品公司 Substd. pyridines and pyridazines with angiogenesis inhibiting activity
US6689883B1 (en) 1999-09-28 2004-02-10 Bayer Pharmaceuticals Corporation Substituted pyridines and pyridazines with angiogenesis inhibiting activity
WO2001023375A3 (en) * 1999-09-28 2002-05-02 Bayer Ag Substituted pyridines and pyridazines with angiogenesis inhibiting activity
WO2001023375A2 (en) * 1999-09-28 2001-04-05 Bayer Corporation Substituted pyridines and pyridazines with angiogenesis inhibiting activity
JP4919567B2 (en) * 1999-09-28 2012-04-18 バイエル・コーポレーシヨン Substituted pyridines and pyridazines with anti-angiogenic activity
CZ304767B6 (en) * 1999-09-28 2014-10-08 Bayer Corporation Substituted pyridine and pyridazine, pharmaceutical composition containing thereof and their use
US7977333B2 (en) 2000-04-20 2011-07-12 Bayer Healthcare Llc Substituted pyridines and pyridazines with angiogenesis inhibiting activity
EP2994128A4 (en) * 2013-05-10 2016-11-23 Nimbus Apollo Inc Acc inhibitors and uses thereof
US9765089B2 (en) 2013-05-10 2017-09-19 Gilead Apollo, Llc ACC inhibitors and uses thereof
US9988399B2 (en) 2013-05-10 2018-06-05 Gilead Apollo, Llc Bicyclic compounds as ACC inhibitors and uses thereof
AU2014262546B2 (en) * 2013-05-10 2018-11-08 Gilead Apollo, Llc ACC inhibitors and uses thereof
US10208044B2 (en) 2013-05-10 2019-02-19 Gilead Apollo, Llc ACC inhibitors and uses thereof
US10208063B2 (en) 2013-05-10 2019-02-19 Gilead Apollo, Llc ACC inhibitors and uses thereof
EP4279074A1 (en) * 2022-05-19 2023-11-22 Georg-August-Universität Göttingen Stiftung Öffentlichen Rechts, Universitätsmedizin Azolo compounds for treatment of fibrotic diseases
WO2023222865A1 (en) * 2022-05-19 2023-11-23 Georg-August-Universität Göttingen Stiftung Öffentlichen Rechts, Universitätsmedizin Azolo compounds for treatment of fibrotic diseases

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