AU7561091A - Heterocyclic n-substituted derivatives, their preparation and thepharmaceutical compositions containing them - Google Patents
Heterocyclic n-substituted derivatives, their preparation and thepharmaceutical compositions containing themInfo
- Publication number
- AU7561091A AU7561091A AU75610/91A AU7561091A AU7561091A AU 7561091 A AU7561091 A AU 7561091A AU 75610/91 A AU75610/91 A AU 75610/91A AU 7561091 A AU7561091 A AU 7561091A AU 7561091 A AU7561091 A AU 7561091A
- Authority
- AU
- Australia
- Prior art keywords
- alkyl
- phenyl
- carbonyl
- alkoxy
- halogen
- 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.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D235/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings
- C07D235/02—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, condensed with other rings condensed with carbocyclic rings or ring systems
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/415—1,2-Diazoles
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
-
- 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
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/04—Inotropic agents, i.e. stimulants of cardiac contraction; Drugs for heart failure
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P9/00—Drugs for disorders of the cardiovascular system
- A61P9/12—Antihypertensives
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/12—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/56—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with only hydrogen atoms or radicals containing only hydrogen and carbon atoms, attached to ring carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/70—One oxygen atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D233/00—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings
- C07D233/54—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members
- C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D233/84—Sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/70—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
- C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
- C07D403/10—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings linked by a carbon chain containing aromatic rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D491/00—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00
- C07D491/02—Heterocyclic compounds containing in the condensed ring system both one or more rings having oxygen atoms as the only ring hetero atoms and one or more rings having nitrogen atoms as the only ring hetero atoms, not provided for by groups C07D451/00 - C07D459/00, C07D463/00, C07D477/00 or C07D489/00 in which the condensed system contains two hetero rings
- C07D491/10—Spiro-condensed systems
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Cardiology (AREA)
- Heart & Thoracic Surgery (AREA)
- Hospice & Palliative Care (AREA)
- Ophthalmology & Optometry (AREA)
- Biomedical Technology (AREA)
- Neurology (AREA)
- Neurosurgery (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Plural Heterocyclic Compounds (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Cephalosporin Compounds (AREA)
- Paints Or Removers (AREA)
- Organic Insulating Materials (AREA)
Abstract
Heterocyclic N-substituted derivatives of formula (I) and their salts are new. R1, R2 = H, 1-6C alkyl, 1-4C alkoxy, NH2, NH2CH2-, COOH, (1-4C alkoxy)carbonyl, CN, tetrazolyl, methyltetrazolyl, methylsulphonylamino, trifluoromethyl sulphonylamino(methyl), N-cyanoacetamide, N-hydroxy- acetamide, N-((4-carboxy)-1, 3-thiazol-2-yl) acetamido, ureido, 2-cyanoguanidinocarbonyl, 2-cyano-guanidino-methyl, imidazol-1-yl-carbonyl, 3-cyano-2-methyl isothioureidomethyl, with the proviso that R1 and R2 are not both H. R3 = H, 1-6C alkyl (optionally substituted by one or more halogen, 2-6C alkenyl, 3-7C cycloalkyl, Ph, phenyl-(1-3C alkyl) or (2-3C alkenyl)phenyl; the Ph groups are optionally substituted by at least 1 halogen, 1-4C alkyl, halogen-(1-4C alkyl), polyhalogeno-(1-4C alkyl), OH or 1-4C alkoxy. R4, R5 = 1-6C alkyl, Ph, phenyl-(1-3C alkyl), the alkyl, phenyl and phenylalkyl groups being optionally substituted by one or more halogen, perfluoro-(1-4C alkyl), OH or 1-4C alkoxy. Or R4 and R5 together form =CR7R8, (CH2)n or (CH2)pY(CH2)q. R7 = H, 1-4C alkyl or Ph; R8 = 1-4C alkyl or Ph. Y = O, S, C (substituted by 1-4C alkyl, Ph or phenyl-(1-3C alkyl) or NR6. R6 = H, 1-4C alkyl, phenyl-(1-3C alkyl), 1-4C alkylcarbonyl, halogeno-(1-4C(alkyl)carbonyl, polyhalo-(1-4C alkyl)carbonyl, -COPh, alpha-aminoacyl or an N-protecting group. Or R4 and R5 together form indane or adamantane. p + q = m; n = 2-11; m = 2-5; X = O or S. z and t = 0 or one is 0 and the other is 1. Specifically claimed is 2-n-butyl-4- spirocyclopentane -1-((2'-(5-tetrazolyl) biphenyl-4-yl)methyl) -2-imidazolin-5-one.
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
FR9003563 | 1990-03-20 | ||
FR9003563A FR2659967B1 (en) | 1990-03-20 | 1990-03-20 | N-SUBSTITUTED IMIDAZOLINONE DERIVATIVES, THEIR PREPARATION, THE PHARMACEUTICAL COMPOSITIONS CONTAINING SAME. |
FR9010144A FR2665702B1 (en) | 1990-08-08 | 1990-08-08 | N-SUBSTITUTED HETEROCYCLIC DERIVATIVES, THEIR PREPARATION, THE PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME. |
FR9010144 | 1990-08-08 |
Publications (2)
Publication Number | Publication Date |
---|---|
AU7561091A true AU7561091A (en) | 1991-10-21 |
AU641005B2 AU641005B2 (en) | 1993-09-09 |
Family
ID=26227935
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU75610/91A Expired AU641005B2 (en) | 1990-03-20 | 1991-03-20 | Heterocyclic N-substituted derivatives, their preparation and thepharmaceutical compositions containing them |
Country Status (30)
Country | Link |
---|---|
EP (1) | EP0454511B1 (en) |
JP (2) | JP2868313B2 (en) |
KR (1) | KR0175310B1 (en) |
AT (1) | ATE167475T1 (en) |
AU (1) | AU641005B2 (en) |
CA (1) | CA2057913C (en) |
CZ (2) | CZ287064B6 (en) |
DE (2) | DE69129606T2 (en) |
DK (1) | DK0454511T3 (en) |
ES (1) | ES2119764T3 (en) |
FI (1) | FI103407B1 (en) |
HK (1) | HK1008918A1 (en) |
HU (3) | HU223141B1 (en) |
IE (1) | IE910913A1 (en) |
IL (3) | IL97612A (en) |
LU (2) | LU90279I2 (en) |
LV (1) | LV10439B (en) |
MX (1) | MX9203586A (en) |
MY (1) | MY115638A (en) |
NL (2) | NL980039I2 (en) |
NO (3) | NO301977B1 (en) |
NZ (1) | NZ237476A (en) |
PL (3) | PL165945B1 (en) |
PT (1) | PT97078B (en) |
RU (1) | RU2099331C1 (en) |
SG (1) | SG49053A1 (en) |
SK (2) | SK280096B6 (en) |
TW (1) | TW201738B (en) |
UA (1) | UA42669A (en) |
WO (1) | WO1991014679A1 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU651021B2 (en) * | 1991-12-20 | 1994-07-07 | Rhone-Poulenc Agro | Fungicidal 2-amidazolin-5-one and 2-amidazoline-5-thione derivatives |
Families Citing this family (82)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DK0443983T3 (en) * | 1990-02-19 | 1996-03-18 | Ciba Geigy Ag | acrylic Compounds |
AU656551B2 (en) * | 1990-12-14 | 1995-02-09 | Smithkline Beecham Corporation | Angiotensin II receptor blocking compositions |
FR2673427B1 (en) * | 1991-03-01 | 1993-06-18 | Sanofi Elf | N-SUBSTITUTED DIAZOTATED HETEROCYCLIC DERIVATIVES BY A BIPHENYLMETHYL GROUP, THEIR PREPARATION, THE PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME. |
AU1625192A (en) * | 1991-05-31 | 1992-12-03 | Zeneca Limited | Heterocyclic derivatives |
IL102183A (en) * | 1991-06-27 | 1999-11-30 | Takeda Chemical Industries Ltd | Biphenyl substituted heterocyclic compounds their production and pharmaceutical compositions comprising them |
WO1993004045A1 (en) * | 1991-08-19 | 1993-03-04 | E.I. Du Pont De Nemours And Company | Angiotensin ii receptor blocking imidazolinone derivatives |
AU2494792A (en) * | 1991-08-19 | 1993-03-16 | E.I. Du Pont De Nemours And Company | Angiotensin ii receptor blocking imidazolinone derivatives |
US5182288A (en) * | 1991-11-13 | 1993-01-26 | Ortho Pharmaceutical Corporation | Substituted n-biphenylyl lactams |
IL104755A0 (en) * | 1992-02-17 | 1993-06-10 | Ciba Geigy Ag | Treatment of glaucoma |
US5326776A (en) * | 1992-03-02 | 1994-07-05 | Abbott Laboratories | Angiotensin II receptor antagonists |
FR2688781B1 (en) * | 1992-03-23 | 1994-07-01 | Sanofi Elf | IMIDAZOLINES N-SUBSTITUTED BY A BIPHENYLMETHYL GROUP, THEIR PREPARATION, THE PHARMACEUTICAL COMPOSITIONS CONTAINING THEM. |
EP0577025A3 (en) * | 1992-07-01 | 1998-02-04 | Hoechst Aktiengesellschaft | Angiotensin-ii-receptorantagonist for the treatment and prophylaxis of coronary heart diseases |
GB9218449D0 (en) | 1992-08-29 | 1992-10-14 | Boots Co Plc | Therapeutic agents |
ATE204276T1 (en) * | 1992-12-22 | 2001-09-15 | Takeda Chemical Industries Ltd | HETEROCYCLIC COMPOUNDS HAVING ANGIOTENSIN II ANTAGONISTIC ACTION AND THEIR APPLICATION |
FR2711367B1 (en) * | 1993-10-19 | 1995-12-01 | Roussel Uclaf | New process for the preparation of sulfur derivatives of imidazole and the new intermediates obtained. |
US5338740A (en) * | 1993-07-13 | 1994-08-16 | Pfizer Inc. | Angiotensin II receptor antagonists |
US5411641A (en) * | 1993-11-22 | 1995-05-02 | E. I. Du Pont De Nemours And Company | Electrochemical conversion of anhydrous hydrogen halide to halogen gas using a cation-transporting membrane |
TW442301B (en) * | 1995-06-07 | 2001-06-23 | Sanofi Synthelabo | Pharmaceutical compositions containing irbesartan |
US5994348A (en) * | 1995-06-07 | 1999-11-30 | Sanofi | Pharmaceutical compositions containing irbesartan |
ATE225657T1 (en) * | 1995-10-06 | 2002-10-15 | Novartis Erfind Verwalt Gmbh | ATI RECEPTOR ANTAGONISTS FOR PREVENTING AND TREATING POSTISCHEMIC NERVOUS FAILURE AND FOR PROTECTING ISCHEMIC KIDNEYS |
CA2196263C (en) * | 1996-02-09 | 2004-10-26 | Barry Jackson | Process for the preparation of 4-oxoimidazolinium salts |
DE69718146T2 (en) | 1996-02-29 | 2003-10-02 | Novartis Ag | AT1 RECEPTOR ANTAGONIST FOR EXCITING APOPTOSIS |
PT888286E (en) * | 1996-03-14 | 2002-04-29 | Warner Lambert Co | NEW AMINO CYCLIC ACIDS SUBSTITUTED AS PHARMACEUTICAL AGENTS |
HU218681B (en) | 1997-07-25 | 2000-10-30 | Sanofi-Synthelabo | Process for the preparation of 1,3-diaza-spiro(4,4)non-1-en-4-one derivatives and 1-cyano-1-acylamino-cyclopentane intermediates |
US6162922A (en) * | 1998-01-30 | 2000-12-19 | Bristol-Myers Squibb Co. | Method for preparing N-substituted heterocyclic derivatives using a phase-transfer catalyst |
AU757290B2 (en) * | 1998-03-25 | 2003-02-13 | Bristol-Myers Squibb Company | Imidazolone anorectic agents: II. phenyl derivatives |
FR2780403B3 (en) | 1998-06-24 | 2000-07-21 | Sanofi Sa | NOVEL FORM OF IRBESARTAN, METHODS FOR OBTAINING SAID FORM AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME |
US6638937B2 (en) | 1998-07-06 | 2003-10-28 | Bristol-Myers Squibb Co. | Biphenyl sulfonamides as dual angiotensin endothelin receptor antagonists |
CZ297795B6 (en) | 1998-12-23 | 2007-03-28 | Novartis Ag | Valsartan-containing tablets |
US6211217B1 (en) | 1999-03-16 | 2001-04-03 | Novartis Ag | Method for reducing pericardial fibrosis and adhesion formation |
SE9903028D0 (en) | 1999-08-27 | 1999-08-27 | Astra Ab | New use |
PE20020617A1 (en) | 2000-08-22 | 2002-08-05 | Novartis Ag | COMPOSITION INCLUDING AN AT1 RECEPTOR ANTAGONIST AND AN INSULIN SECRETION POTENTIAL OR AN INSULIN SENSITIZER |
US8168616B1 (en) | 2000-11-17 | 2012-05-01 | Novartis Ag | Combination comprising a renin inhibitor and an angiotensin receptor inhibitor for hypertension |
FR2831446B1 (en) * | 2001-10-26 | 2004-03-05 | Sanofi Synthelabo | USE OF IRBESARTAN FOR THE PREPARATION OF MEDICINES USEFUL FOR THE PREVENTION OR TREATMENT OF PULMONARY HYPERTENSION |
US7232828B2 (en) | 2002-08-10 | 2007-06-19 | Bethesda Pharmaceuticals, Inc. | PPAR Ligands that do not cause fluid retention, edema or congestive heart failure |
DE10335027A1 (en) | 2003-07-31 | 2005-02-17 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Use of telmisartan and simvastatin for treatment or prophylaxis of cardiovascular, cardiopulmonary and renal diseases e.g. hypertension combined with hyperlipidemia or atherosclerosis |
US7732162B2 (en) | 2003-05-05 | 2010-06-08 | Probiodrug Ag | Inhibitors of glutaminyl cyclase for treating neurodegenerative diseases |
GB0316546D0 (en) | 2003-07-15 | 2003-08-20 | Novartis Ag | Process for the manufacture of organic compounds |
EP2428516A1 (en) | 2003-11-19 | 2012-03-14 | Metabasis Therapeutics, Inc. | Novel phosphorus-containing thyromimetics |
GB0327839D0 (en) | 2003-12-01 | 2003-12-31 | Novartis Ag | Organic compounds |
GB0402262D0 (en) | 2004-02-02 | 2004-03-10 | Novartis Ag | Process for the manufacture of organic compounds |
US20080161321A1 (en) | 2004-03-17 | 2008-07-03 | David Louis Feldman | Use of Renin Inhibitors in Therapy |
JP4880591B2 (en) | 2004-06-04 | 2012-02-22 | テバ ファーマシューティカル インダストリーズ リミティド | Pharmaceutical composition comprising irbesartan |
WO2005122699A2 (en) * | 2004-06-16 | 2005-12-29 | Matrix Laboratories Ltd | An improved process for the preparation of n-substituted hetero cyclic derivatives |
SI21849A (en) | 2004-07-29 | 2006-02-28 | Krka, Tovarna Zdravil, D.D., Novo Mesto | Preparation of hydrochloride salts of tetrazole derivative |
TWI346108B (en) * | 2004-08-23 | 2011-08-01 | Bristol Myers Squibb Co | A method for preparing irbesartan and intermediates thereof |
EP1799199B1 (en) | 2004-10-08 | 2012-03-28 | Novartis AG | Use of renin inhibitors for the prevention or treatment of diastolic dysfunction or diastolic heart failure |
GB2419592A (en) | 2004-10-26 | 2006-05-03 | Cipla Ltd | Process for the preparation of irbesartan hydrochloride |
WO2006046593A1 (en) | 2004-10-27 | 2006-05-04 | Daiichi Sankyo Company, Limited | Benzene compound having 2 or more substituents |
FR2886642B1 (en) * | 2005-06-06 | 2008-05-30 | Sanofi Aventis Sa | IRBESARTAN ALKALINE-EARTH SALTS AND THEIR PREPARATION |
EP1749828A1 (en) | 2005-08-04 | 2007-02-07 | Farmaprojects S.L. | Process for preparing an angiotensin II receptor antagonist |
EP1948641A1 (en) | 2005-10-28 | 2008-07-30 | Alembic Limited | An improved process for preparation of irbesartan |
DE602006013261D1 (en) | 2006-01-09 | 2010-05-12 | Krka D D | Irbesartan containing solid preparation |
EP1908469A1 (en) | 2006-10-06 | 2008-04-09 | Boehringer Ingelheim Vetmedica Gmbh | Angiotensin II receptor antagonist for the treatment of systemic diseases in cats |
EP1918288A1 (en) | 2006-11-02 | 2008-05-07 | Cadila Pharmaceuticals Limited | A novel and improved process for the preparation of Irbesartan, an angiotensin-II receptor antagonist for the treatment of hypertension |
CA2679446C (en) | 2007-03-01 | 2016-05-17 | Probiodrug Ag | New use of glutaminyl cyclase inhibitors |
US9656991B2 (en) | 2007-04-18 | 2017-05-23 | Probiodrug Ag | Inhibitors of glutaminyl cyclase |
EP2170930B3 (en) | 2007-06-04 | 2013-10-02 | 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 |
EP2212295A2 (en) | 2007-10-16 | 2010-08-04 | Novartis AG | 4-phenyl-5-oxo-imidazole derivatives, pharmaceutical compositions and uses therof |
PT2065035E (en) | 2007-11-28 | 2010-10-04 | Lesvi Laboratorios Sl | Pharmaceutical formulations containing irbesartan |
JP2011522828A (en) | 2008-06-04 | 2011-08-04 | 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 | Guanylate cyclase agonists useful for the treatment of gastrointestinal disorders, inflammation, cancer, and other disorders |
WO2009149734A1 (en) * | 2008-06-13 | 2009-12-17 | Ratiopharm Gmbh | Process for the preparation of irbesartan and intermediate products |
AU2009270833B2 (en) | 2008-07-16 | 2015-02-19 | Bausch Health Ireland Limited | Agonists of guanylate cyclase useful for the treatment of gastrointestinal, inflammation, cancer and other disorders |
EP2194050A1 (en) | 2008-12-08 | 2010-06-09 | KRKA, tovarna zdravil, d.d., Novo mesto | A new process for the preparation of irbesartan |
WO2010093601A1 (en) | 2009-02-10 | 2010-08-19 | Metabasis Therapeutics, Inc. | Novel sulfonic acid-containing thyromimetics, and methods for their use |
MX2012002993A (en) | 2009-09-11 | 2012-04-19 | Probiodrug Ag | Heterocylcic derivatives as inhibitors of glutaminyl cyclase. |
HUP0900788A2 (en) | 2009-12-16 | 2011-11-28 | Sanofi Aventis | Process for producing 4-bromomethyl-biphenyl derivatives |
WO2011107530A2 (en) | 2010-03-03 | 2011-09-09 | Probiodrug Ag | Novel inhibitors |
JP5688745B2 (en) | 2010-03-10 | 2015-03-25 | プロビオドルグ エージー | Heterocyclic inhibitor of glutaminyl cyclase (QC, EC 2.3.2.5) |
EP2560953B1 (en) | 2010-04-21 | 2016-01-06 | Probiodrug AG | Inhibitors of glutaminyl cyclase |
US9616097B2 (en) | 2010-09-15 | 2017-04-11 | Synergy Pharmaceuticals, Inc. | Formulations of guanylate cyclase C agonists and methods of use |
ES2570167T3 (en) | 2011-03-16 | 2016-05-17 | Probiodrug Ag | Benzimidazole derivatives as glutaminyl cyclase inhibitors |
BR112014014527A2 (en) | 2011-12-15 | 2017-06-13 | Takeda Pharmaceuticals Usa Inc | combinations of azilsartan and chlorotalidone to treat hypertension in black patients |
PL223830B1 (en) | 2012-04-03 | 2016-11-30 | Univ Jagielloński | Derivatives of aromatic imidazolidinones and their use |
CA2905435A1 (en) | 2013-03-15 | 2014-09-25 | Synergy Pharmaceuticals Inc. | Compositions useful for the treatment of gastrointestinal disorders |
WO2014151206A1 (en) | 2013-03-15 | 2014-09-25 | Synergy Pharmaceuticals Inc. | Agonists of guanylate cyclase and their uses |
EP3004138B1 (en) | 2013-06-05 | 2024-03-13 | Bausch Health Ireland Limited | Ultra-pure agonists of guanylate cyclase c, method of making and using same |
EP3025711B1 (en) | 2013-07-23 | 2020-11-18 | Daiichi Sankyo Company, Limited | Medicine for preventing or treating hypertension |
EP3434284A4 (en) | 2016-03-24 | 2019-11-13 | Daiichi Sankyo Company, Limited | Medicine for treating renal disease |
JP7050893B2 (en) | 2017-07-07 | 2022-04-08 | ベーリンガー インゲルハイム フェトメディカ ゲーエムベーハー | Angiotensin II receptor blocker for the prevention or treatment of systemic diseases in cats |
ES2812698T3 (en) | 2017-09-29 | 2021-03-18 | Probiodrug Ag | Glutaminyl cyclase inhibitors |
Family Cites Families (12)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3340595A1 (en) * | 1983-11-10 | 1985-05-23 | Hoechst Ag, 6230 Frankfurt | IMIDAZOLINONES, METHOD FOR THEIR PRODUCTION AND THEIR USE IN PLANT PROTECTION |
DE3545597A1 (en) * | 1985-12-21 | 1987-07-02 | Celamerck Gmbh & Co Kg | NEW HERBICIDE EFFECTIVE IMIDAZOLINONES |
CA1334092C (en) * | 1986-07-11 | 1995-01-24 | David John Carini | Angiotensin ii receptor blocking imidazoles |
US4820843A (en) * | 1987-05-22 | 1989-04-11 | E. I. Du Pont De Nemours And Company | Tetrazole intermediates to antihypertensive compounds |
EP0303863A3 (en) * | 1987-08-17 | 1991-10-23 | American Cyanamid Company | Benzenesulfonyl carboxamide compounds, intermediate compounds and methods of preparation thereof and use of said compounds and intermediate compounds as herbicidal agents |
US5015651A (en) * | 1988-01-07 | 1991-05-14 | E. I. Du Pont De Nemours And Company | Treatment of hypertension with 1,2,4-angiotensin II antagonists |
CA1338238C (en) * | 1988-01-07 | 1996-04-09 | David John Carini | Angiotensin ii receptor blocking imidazoles and combinations thereof with diuretics and nsaids |
EP0407342A3 (en) * | 1989-07-06 | 1991-07-10 | Ciba-Geigy Ag | Pyrimidine derivatives |
EP0412594B1 (en) * | 1989-07-28 | 1996-01-03 | Merck & Co. Inc. | Substituted triazolinones, triazolinethiones, and triazolinimines as angiotensin II antagonists |
ATE113281T1 (en) * | 1989-08-02 | 1994-11-15 | Takeda Chemical Industries Ltd | PYRAZOLE DERIVATIVES, PROCESS FOR THEIR PRODUCTION AND APPLICATION. |
US5100897A (en) * | 1989-08-28 | 1992-03-31 | Merck & Co., Inc. | Substituted pyrimidinones as angiotensin ii antagonists |
IL99372A0 (en) * | 1990-09-10 | 1992-08-18 | Ciba Geigy Ag | Azacyclic compounds |
-
1991
- 1991-03-19 TW TW080102155A patent/TW201738B/zh not_active IP Right Cessation
- 1991-03-19 PT PT97078A patent/PT97078B/en not_active IP Right Cessation
- 1991-03-19 NZ NZ237476A patent/NZ237476A/en unknown
- 1991-03-19 IE IE091391A patent/IE910913A1/en not_active IP Right Cessation
- 1991-03-20 DE DE69129606T patent/DE69129606T2/en not_active Expired - Lifetime
- 1991-03-20 DK DK91400745T patent/DK0454511T3/en active
- 1991-03-20 JP JP3506471A patent/JP2868313B2/en not_active Expired - Lifetime
- 1991-03-20 HU HU9302497A patent/HU223141B1/en active IP Right Grant
- 1991-03-20 AT AT91400745T patent/ATE167475T1/en active
- 1991-03-20 PL PL91293015A patent/PL165945B1/en unknown
- 1991-03-20 RU SU5010343/04A patent/RU2099331C1/en active
- 1991-03-20 CA CA002057913A patent/CA2057913C/en not_active Expired - Lifetime
- 1991-03-20 WO PCT/FR1991/000224 patent/WO1991014679A1/en active IP Right Grant
- 1991-03-20 HU HU603/91A patent/HU221188B1/en unknown
- 1991-03-20 HU HU9302497A patent/HUT67648A/en active IP Right Revival
- 1991-03-20 CZ CS1991745A patent/CZ287064B6/en not_active IP Right Cessation
- 1991-03-20 UA UA5010343A patent/UA42669A/en unknown
- 1991-03-20 IL IL9761291A patent/IL97612A/en active Protection Beyond IP Right Term
- 1991-03-20 DE DE1999175029 patent/DE19975029I2/en active Active
- 1991-03-20 PL PL91304152A patent/PL166581B1/en unknown
- 1991-03-20 EP EP91400745A patent/EP0454511B1/en not_active Expired - Lifetime
- 1991-03-20 MY MYPI91000464A patent/MY115638A/en unknown
- 1991-03-20 SK SK745-91A patent/SK280096B6/en not_active IP Right Cessation
- 1991-03-20 PL PL91304153A patent/PL166403B1/en unknown
- 1991-03-20 AU AU75610/91A patent/AU641005B2/en not_active Expired
- 1991-03-20 KR KR1019910701647A patent/KR0175310B1/en not_active IP Right Cessation
- 1991-03-20 SG SG1996005558A patent/SG49053A1/en unknown
- 1991-03-20 IL IL11082091A patent/IL110820A/en not_active IP Right Cessation
- 1991-03-20 ES ES91400745T patent/ES2119764T3/en not_active Expired - Lifetime
- 1991-03-20 SK SK1256-98A patent/SK283197B6/en not_active IP Right Cessation
- 1991-11-19 FI FI915458A patent/FI103407B1/en active Protection Beyond IP Right Term
- 1991-11-19 NO NO914528A patent/NO301977B1/en not_active IP Right Cessation
-
1992
- 1992-06-26 MX MX9203586A patent/MX9203586A/en active IP Right Grant
-
1993
- 1993-02-25 LV LVP-93-147A patent/LV10439B/en unknown
-
1994
- 1994-08-30 IL IL11082094A patent/IL110820A0/en unknown
-
1996
- 1996-01-15 CZ CZ1996120A patent/CZ287225B6/en not_active IP Right Cessation
-
1997
- 1997-12-10 JP JP9339895A patent/JPH10279566A/en not_active Withdrawn
-
1998
- 1998-08-04 HK HK98109660A patent/HK1008918A1/en not_active IP Right Cessation
- 1998-08-21 LU LU90279C patent/LU90279I2/en unknown
- 1998-09-16 NO NO1998021C patent/NO1998021I1/en unknown
- 1998-12-02 NL NL980039C patent/NL980039I2/en unknown
-
1999
- 1999-03-05 NL NL990006C patent/NL990006I2/en unknown
- 1999-03-12 LU LU90371C patent/LU90371I2/en unknown
- 1999-12-09 NO NO1999025C patent/NO1999025I1/en unknown
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
AU651021B2 (en) * | 1991-12-20 | 1994-07-07 | Rhone-Poulenc Agro | Fungicidal 2-amidazolin-5-one and 2-amidazoline-5-thione derivatives |
Also Published As
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU7561091A (en) | Heterocyclic n-substituted derivatives, their preparation and thepharmaceutical compositions containing them | |
ATE204269T1 (en) | SUBSTITUTED BIPHENYL OR PHENYLPYRIDINE DERIVATIVES, METHOD FOR THE PRODUCTION THEREOF AND PHARMACEUTICAL COMPOSITIONS CONTAINING THEM | |
AU1070895A (en) | Indole-derived arylpiperazines as ligands for 5HT1-like receptors 5HT1B and 5HT1D | |
TW333532B (en) | Benzopyrans | |
PT873993E (en) | NEW HETEROCYCLIC COMPOUNDS PROCESS FOR THEIR PREPARATION AND THE PHARMACEUTICAL COMPOSITIONS THAT CONTAIN THEM | |
DE69416311D1 (en) | USE OF CEPHEM DERIVATIVES AS AN ANTIMETASTIC AGENT | |
ES2021556A6 (en) | Penam derivatives and salts thereof, and antibacterial agent comprising the same | |
KR910000141A (en) | Use of isooxazolin-3-one derivatives as antidepressants | |
NZ238644A (en) | 2-(1-oxo-alkoxy)alkanoic acid derivatives and pharmaceutical compositions thereof | |
BG106079A (en) | Cyclocarbamate derivatives as progesterone receptor modulators | |
DE69403896T2 (en) | 4-AMINO-2- (HETERO) ARYL-BUTANAMIDES CAN BE USED AS 5-HT1A ANTAGONISTS |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
HB | Alteration of name in register |
Free format text: SANOFI-SYNTHELABO |