IL103568A0 - Quinoline derivatives,process for their preparation and their therapeutic applications - Google Patents

Quinoline derivatives,process for their preparation and their therapeutic applications

Info

Publication number
IL103568A0
IL103568A0 IL103568A IL10356892A IL103568A0 IL 103568 A0 IL103568 A0 IL 103568A0 IL 103568 A IL103568 A IL 103568A IL 10356892 A IL10356892 A IL 10356892A IL 103568 A0 IL103568 A0 IL 103568A0
Authority
IL
Israel
Prior art keywords
group
alkoxy
aryl
independently
preparation
Prior art date
Application number
IL103568A
Original Assignee
Synthelabo
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=9418349&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=IL103568(A0) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Synthelabo filed Critical Synthelabo
Publication of IL103568A0 publication Critical patent/IL103568A0/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/06Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • 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
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/12Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom with substituted hydrocarbon radicals attached to ring carbon atoms

Abstract

Compounds corresponding to the formula (I) <IMAGE> in which, R1 represents either a 1H-tetrazol-5-yl group or a CO2H group, R2 represents either a (C1-7)alkyl group or a (C2-6)alkenyl group, R3 and R4 represent, each independently of the other, either a hydrogen atom, or a halogen atom, or a cyano group, or a (C1-7)alkyl group, or a (C3-7)cycloalkyl(C1-4)alkyl group, or an aryl group, or an aryl(C1-4)alkyl group, or an aryl(C2-4)alkenyl group, or a group -(CH2)mCOR5 in which m = 0 to 4 and R5 represents a hydrogen atom, an OH group, a (C1-6)alkoxy group or a group NR7R8, R7 and R8 representing, each independently of the other, a hydrogen atom or a (C1-4)alkyl group, or R3 and R4 represents, each independently of the other, a group -(CH2)n-R6 in which n = 1 to 4 and R6 represents an OH group, a (C1-6)alkoxy group, a (C1-4)alkoxy(C1-4)alkoxy group or a (C3-7)cycloalkyl(C1-4)alkoxy group, and their pharmaceutically acceptable organic or inorganic salts. Application in therapeutics.
IL103568A 1991-10-28 1992-10-27 Quinoline derivatives,process for their preparation and their therapeutic applications IL103568A0 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
FR9113240A FR2683819B1 (en) 1991-10-28 1991-10-28 QUINOLEIN DERIVATIVES, THEIR PREPARATION PROCESS AND THEIR THERAPEUTIC APPLICATION.

Publications (1)

Publication Number Publication Date
IL103568A0 true IL103568A0 (en) 1993-03-15

Family

ID=9418349

Family Applications (1)

Application Number Title Priority Date Filing Date
IL103568A IL103568A0 (en) 1991-10-28 1992-10-27 Quinoline derivatives,process for their preparation and their therapeutic applications

Country Status (18)

Country Link
EP (1) EP0540400B1 (en)
JP (1) JPH05239053A (en)
KR (1) KR930007935A (en)
CN (1) CN1073171A (en)
AT (1) ATE126798T1 (en)
AU (1) AU651740B2 (en)
CA (1) CA2081537A1 (en)
CZ (1) CZ324292A3 (en)
DE (1) DE69204252T2 (en)
FI (1) FI924869A (en)
FR (1) FR2683819B1 (en)
HU (1) HUT62883A (en)
IL (1) IL103568A0 (en)
MX (1) MX9206169A (en)
NO (1) NO924138L (en)
NZ (1) NZ244892A (en)
PL (1) PL296369A1 (en)
ZA (1) ZA928297B (en)

Families Citing this family (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5478832A (en) * 1992-05-08 1995-12-26 The Green Cross Corporation Quinoline compounds
IT1255461B (en) * 1992-07-28 1995-11-02 Luso Farmaco Inst ETHERS OF IMIDAZOLI ACTIVATED IN II ANTAGONIST
FR2699174B1 (en) * 1992-12-14 1995-01-20 Synthelabo Derivatives of 3- (quinoline-6-yl-methyl) -4H-imidazol-4-one, their preparation and their therapeutic use.
FR2710914B1 (en) * 1993-10-04 1995-11-24 Synthelabo 2- [2- (tetrazol-5-yl) phenyl] -1,2-dihydroquinoline derivatives, their preparation and their use as synthesis intermediates.
FR2716196B1 (en) * 1994-02-16 1996-04-05 Synthelabo 8- [2- (1H-tetrazol-5-yl) phenyl] quinoline derivatives, their preparation and their therapeutic use.
JPH09202774A (en) 1996-01-25 1997-08-05 Green Cross Corp:The 2-arylquinoline and its production
DE19706161A1 (en) * 1997-02-17 1998-08-20 Oswald Hartmut Prof Dr Med Use of cyanines, isocyanines and pseudoisocyanines as diuretics
KR100744826B1 (en) * 2006-04-05 2007-08-01 한국화학연구원 Quinolinone derivatives substituted with imidazole group
US7879802B2 (en) 2007-06-04 2011-02-01 Synergy Pharmaceuticals Inc. Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders
US8969514B2 (en) 2007-06-04 2015-03-03 Synergy Pharmaceuticals, Inc. Agonists of guanylate cyclase useful for the treatment of hypercholesterolemia, atherosclerosis, coronary heart disease, gallstone, obesity and other cardiovascular diseases
EP3239170B1 (en) 2008-06-04 2019-03-20 Synergy Pharmaceuticals Inc. Agonists of guanylate cyclase useful for the treatment of gastrointestinal disorders, inflammation, cancer and other disorders
EP3241839B1 (en) 2008-07-16 2019-09-04 Bausch Health Ireland Limited Agonists of guanylate cyclase useful for the treatment of gastrointestinal, inflammation, cancer and other disorders
US9616097B2 (en) 2010-09-15 2017-04-11 Synergy Pharmaceuticals, Inc. Formulations of guanylate cyclase C agonists and methods of use
CN103804349A (en) * 2012-11-01 2014-05-21 杨子娇 Compounds for treatment of glaucoma and their use
CA2905435A1 (en) 2013-03-15 2014-09-25 Synergy Pharmaceuticals Inc. Compositions useful for the treatment of gastrointestinal disorders
US9708367B2 (en) 2013-03-15 2017-07-18 Synergy Pharmaceuticals, Inc. Agonists of guanylate cyclase and their uses
JP6606491B2 (en) 2013-06-05 2019-11-13 シナジー ファーマシューティカルズ インコーポレイテッド Ultra high purity agonist of guanylate cyclase C, method for producing and using the same
CN108558750B (en) * 2018-07-11 2021-01-05 武汉工程大学 Process for synthesizing 3-nitroquinoline derivative by solvent-free method

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
IL94390A (en) * 1989-05-30 1996-03-31 Merck & Co Inc Di-substituted imidazo fused 6-membered nitrogen-containing heterocycles and pharmaceutical compositions containing them
MX9200299A (en) * 1991-02-07 1992-12-01 Roussel Uclaf NEW NITROGENATED BICYCLE DERIVATIVES, THEIR PROCEDURE FOR PREPARING THE NEW INTERMEDIATE COMPOUNDS OBTAINED THEIR APPLICATION AS MEDICINES AND THE PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM.
DE4117750A1 (en) * 1991-05-30 1992-12-24 Bayer Ag NEW 2-AMINO-5-CYANO-1,4-DIHYDROPYRIDINE, PROCESS FOR THEIR PREPARATION AND THEIR USE IN MEDICINAL PRODUCTS
EP0528762B1 (en) * 1991-08-15 1997-05-07 Novartis AG N-acyl-N-heterocyclyl- or naphthyl-alkyl amino acids as angiotensin II antagonists

Also Published As

Publication number Publication date
JPH05239053A (en) 1993-09-17
ZA928297B (en) 1993-05-07
CZ324292A3 (en) 1993-09-15
DE69204252D1 (en) 1995-09-28
PL296369A1 (en) 1993-05-31
NZ244892A (en) 1994-06-27
FI924869A (en) 1993-04-29
FI924869A0 (en) 1992-10-27
AU651740B2 (en) 1994-07-28
CA2081537A1 (en) 1993-04-29
HUT62883A (en) 1993-06-28
NO924138D0 (en) 1992-10-27
AU2734892A (en) 1993-04-29
CN1073171A (en) 1993-06-16
NO924138L (en) 1993-04-29
DE69204252T2 (en) 1996-04-18
MX9206169A (en) 1993-07-01
EP0540400A1 (en) 1993-05-05
FR2683819A1 (en) 1993-05-21
ATE126798T1 (en) 1995-09-15
EP0540400B1 (en) 1995-08-23
HU9203374D0 (en) 1993-01-28
FR2683819B1 (en) 1994-02-11
KR930007935A (en) 1993-05-20

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