FI104897B - Menetelmä terapeuttisesti käyttökelpoisten 3-[(2-kinolinyyli)etenyyli] fenyyli-1-hydroksialkyylifenyylialkyylitiokarboksyylihappojohdannaisten valmistamiseksi - Google Patents
Menetelmä terapeuttisesti käyttökelpoisten 3-[(2-kinolinyyli)etenyyli] fenyyli-1-hydroksialkyylifenyylialkyylitiokarboksyylihappojohdannaisten valmistamiseksi Download PDFInfo
- Publication number
- FI104897B FI104897B FI914796A FI914796A FI104897B FI 104897 B FI104897 B FI 104897B FI 914796 A FI914796 A FI 914796A FI 914796 A FI914796 A FI 914796A FI 104897 B FI104897 B FI 104897B
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- Finland
- Prior art keywords
- phenyl
- phe
- acid
- quinolinyl
- mmol
- Prior art date
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic 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
- C07D215/16—Heterocyclic 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 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
- C07D215/18—Halogen atoms or nitro radicals
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic 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
- C07D215/16—Heterocyclic 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 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
- C07D215/20—Oxygen atoms
- C07D215/22—Oxygen atoms attached in position 2 or 4
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- 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
- A61K31/435—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
- A61K31/44—Non condensed pyridines; Hydrogenated derivatives thereof
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/10—Expectorants
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
- A61P13/02—Drugs for disorders of the urinary system of urine or of the urinary tract, e.g. urine acidifiers
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
-
- 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
- A61P27/00—Drugs for disorders of the senses
- A61P27/02—Ophthalmic agents
- A61P27/14—Decongestants or antiallergics
-
- 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
- A61P27/16—Otologicals
-
- 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]
-
- 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]
- A61P29/02—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID] without antiinflammatory effect
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P37/00—Drugs for immunological or allergic disorders
- A61P37/08—Antiallergic 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic 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
- C07D215/12—Heterocyclic 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D215/00—Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
- C07D215/02—Heterocyclic 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
- C07D215/16—Heterocyclic 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 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
- C07D215/20—Oxygen atoms
- C07D215/24—Oxygen atoms attached in position 8
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Veterinary Medicine (AREA)
- Public Health (AREA)
- General Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pulmonology (AREA)
- Ophthalmology & Optometry (AREA)
- Rheumatology (AREA)
- Pain & Pain Management (AREA)
- Heart & Thoracic Surgery (AREA)
- Cardiology (AREA)
- Immunology (AREA)
- Urology & Nephrology (AREA)
- Endocrinology (AREA)
- Reproductive Health (AREA)
- Epidemiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Plural Heterocyclic Compounds (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
- Quinoline Compounds (AREA)
- Steroid Compounds (AREA)
- Nitrogen Condensed Heterocyclic Rings (AREA)
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US59688790A | 1990-10-12 | 1990-10-12 | |
US59688790 | 1990-10-12 | ||
US74188891A | 1991-08-08 | 1991-08-08 | |
US74188891 | 1991-08-08 |
Publications (3)
Publication Number | Publication Date |
---|---|
FI914796A0 FI914796A0 (fi) | 1991-10-11 |
FI914796A FI914796A (fi) | 1992-04-13 |
FI104897B true FI104897B (fi) | 2000-04-28 |
Family
ID=27082671
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI914796A FI104897B (fi) | 1990-10-12 | 1991-10-11 | Menetelmä terapeuttisesti käyttökelpoisten 3-[(2-kinolinyyli)etenyyli] fenyyli-1-hydroksialkyylifenyylialkyylitiokarboksyylihappojohdannaisten valmistamiseksi |
FI20000250A FI20000250A (fi) | 1990-10-12 | 2000-02-07 | Lämpöeristeen asennustuki 3-((2-kinolinyyli)etenyyli)fenyyli-1-hydroksialkyylifenyylialkyylitiokarboksyylihappojohdannaiset |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
FI20000250A FI20000250A (fi) | 1990-10-12 | 2000-02-07 | Lämpöeristeen asennustuki 3-((2-kinolinyyli)etenyyli)fenyyli-1-hydroksialkyylifenyylialkyylitiokarboksyylihappojohdannaiset |
Country Status (27)
Country | Link |
---|---|
EP (1) | EP0480717B1 (fr) |
JP (1) | JP2501385B2 (fr) |
KR (1) | KR100227716B1 (fr) |
CN (1) | CN1046711C (fr) |
AT (1) | ATE165088T1 (fr) |
CA (1) | CA2053209C (fr) |
CY (1) | CY2094B1 (fr) |
CZ (1) | CZ281274B6 (fr) |
DE (2) | DE69129257T2 (fr) |
DK (1) | DK0480717T3 (fr) |
ES (1) | ES2114882T3 (fr) |
FI (2) | FI104897B (fr) |
HK (1) | HK1027473A1 (fr) |
HR (1) | HRP930751B1 (fr) |
HU (2) | HU222344B1 (fr) |
IE (1) | IE913609A1 (fr) |
IL (3) | IL99726A (fr) |
LU (1) | LU90284I2 (fr) |
LV (1) | LV12187B (fr) |
MX (1) | MX9101551A (fr) |
NL (1) | NL990009I2 (fr) |
NO (1) | NO914004D0 (fr) |
NZ (1) | NZ240194A (fr) |
PT (1) | PT99213B (fr) |
SI (1) | SI9111647B (fr) |
SK (1) | SK279944B6 (fr) |
YU (1) | YU48742B (fr) |
Families Citing this family (91)
Publication number | Priority date | Publication date | Assignee | Title |
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US5270324A (en) * | 1992-04-10 | 1993-12-14 | Merck Frosst Canada, Inc. | Fluorinated hydroxyalkylquinoline acids as leukotriene antagonists |
CA2111372C (fr) * | 1992-12-22 | 2007-01-16 | Robert N. Young | Acides heterocycliques diaryliques condenses en 5,6, antagonistes de la leucotriene |
US5472964A (en) * | 1992-12-22 | 1995-12-05 | Merck Frosst Canada, Inc. | Diaryl 5,6-fused heterocyclic acids as leukotriene antagonists |
US5438141A (en) * | 1993-05-21 | 1995-08-01 | Merck Frosst Canada, Inc. | Heteroaryl and haloaryl quinoline derivatives of cyclopropaneacetic acid as leukotriene antagonists |
ES2080656B1 (es) * | 1993-07-19 | 1996-10-16 | Merck Frosst Canada Inc | Acidos de hidroxialquilquinolina fluorados como antagonistas del leucotrieno. |
CA2130723C (fr) * | 1993-09-03 | 2006-01-31 | Wilhelm Quittmann | Methode pour l'obtention de derives de l'acide y-mercaptocarboxylique |
DE4339724C1 (de) * | 1993-11-22 | 1995-01-19 | Siemens Ag | Gasarmatur |
TW448160B (en) * | 1993-12-28 | 2001-08-01 | Merck & Co Inc | Novel dicyclohexylamine salt and process for the preparation of leukotriene antagonists |
CA2145735A1 (fr) * | 1994-04-21 | 1995-10-22 | Paul Hanselmann | Methode de preparation de 5-oxaspiro[2.4]heptan-6-one et nouveaux produits intermediaires intervenant dans le processus |
US5523477A (en) * | 1995-01-23 | 1996-06-04 | Merck & Co., Inc. | Process for the preparation of 1-(thiomethyl)-cyclopropaneacetic acid |
US5750539A (en) * | 1995-06-07 | 1998-05-12 | Merck Frosst Canada | Heteroaryl diol acids as leukotriene antagonists |
US5714488A (en) * | 1995-10-03 | 1998-02-03 | Abbott Laboratories | Bis-heteroarylylmethoxyphenyl ketone derivatives as inhibitors of leukotriene biosynthesis |
US5668150A (en) * | 1996-07-26 | 1997-09-16 | Abbott Laboratories | Non-symmetrical bis-heteroarylmethoxyphenylalkyl carboxylates as inhibitors of leukotriene biosynthesis |
FR2751969B1 (fr) * | 1996-08-01 | 1998-12-04 | Centre Nat Rech Scient | Composes activateurs du canal cftr, et compositions pharmaceutiques les contenant |
US6262066B1 (en) | 1998-07-27 | 2001-07-17 | Schering Corporation | High affinity ligands for nociceptin receptor ORL-1 |
US6221880B1 (en) | 1998-10-09 | 2001-04-24 | Schering Corporation | Composition and method for treating allergic diseases |
IT1320162B1 (it) | 2000-02-09 | 2003-11-18 | Rotta Research Lab | Derivati della tirosina ad attivita' anti leucotrienica, procedimentoper la loro preparazione e loro uso farmaceutico. |
JP4308667B2 (ja) * | 2002-02-06 | 2009-08-05 | デルマー ケミカルズ インコーポレーテッド | 1−(メルカプトメチル)−シクロプロパン酢酸の調製方法 |
CA2371048C (fr) | 2002-02-06 | 2011-01-04 | Delmar Chemicals Inc. | Procede de preparation d'acide 1-(mercaptomethyl)cyclopropylacetique |
AU2003209043A1 (en) * | 2002-02-07 | 2003-09-02 | Dr. Reddy's Laboratories Ltd. | Novel anhydrous amorphous forms of montelukast sodium salt |
CA2528228C (fr) | 2003-06-06 | 2011-09-20 | Morepen Laboratories Limited | Une methode de preparation d'un sel sodique de montelukast sous forme amorphe |
US7553853B2 (en) | 2003-10-10 | 2009-06-30 | Synthon Bv | Solid-state montelukast |
US20070225325A1 (en) * | 2004-01-28 | 2007-09-27 | Pliva-Istrazivanje I Razvoj D.O.O. | Solid Forms of Montelukast Acid |
KR20060117356A (ko) * | 2004-01-30 | 2006-11-16 | 테바 파마슈티컬 인더스트리즈 리미티드 | 몬테루카스트 유리산 다형체 |
EP1760077A1 (fr) * | 2004-01-30 | 2007-03-07 | Teva Pharmaceutical Industries Ltd. | Formes polymorphes du l'acide libre montelukast |
CA2554927A1 (fr) | 2004-02-03 | 2005-08-18 | Chemagis Ltd. | Formes amorphes stables de montelukast sodique |
WO2005105751A1 (fr) * | 2004-04-21 | 2005-11-10 | Teva Pharmaceutical Industries Ltd. | Procedes de preparation de sodium montelukast |
US7829716B2 (en) | 2004-04-30 | 2010-11-09 | Synthon Pharmaceuticals, Inc. | Process for making montelukast and intermediates therefor |
US7501517B2 (en) | 2004-04-30 | 2009-03-10 | Synthon Ip, Inc. | Process for making montelukast and intermediates therefor |
WO2006008751A2 (fr) * | 2004-07-19 | 2006-01-26 | Matrix Laboratories Ltd | Procede de preparation de montelukast et de ses sels |
ATE539061T1 (de) | 2004-07-19 | 2012-01-15 | Matrix Lab Ltd | 2-ä(3s)-ä3-ä(2e)-(7-chlorchinolin-2- yl)ethenylüphenylü-3- halogenpropylübenzoesäuremethylester |
CA2574362A1 (fr) | 2004-07-23 | 2006-01-26 | Pliva-Istrazivanje I Razvoj D.O.O. | Nouvelle forme de derive de benzenesulfonamide |
WO2006021974A1 (fr) * | 2004-08-23 | 2006-03-02 | Morepen Laboratories Limited | Procede pour synthetiser un diol (viii), intermediaire du sodium de montelukast |
PL205637B1 (pl) * | 2004-10-22 | 2010-05-31 | Inst Farmaceutyczny | Sposób wytwarzania kwasu (R,E)-(1-{1-{3-[2-(7-chlorochinolin-2-ylo)etenylo]fenylo}-3-[2-(1-hydroksy-1-metyloetylo)fenylo] propylosulfanylometylo}cyklopropylo)octowego i/lub jego farmaceutycznie dopuszczalnych soli |
WO2006058545A1 (fr) * | 2004-11-30 | 2006-06-08 | Medichem, S.A. | Nouveau procede de preparation d'un antagoniste de leucotriene |
WO2006131782A1 (fr) * | 2005-06-07 | 2006-12-14 | Glade Organics Private Limited | Procede de preparation de methyl-2-(3-(2-(7-chloro-2-quinolinyl-ethenyl)-phenyl)-3-oxopropyl)benzoate |
EP1904448B1 (fr) | 2005-07-05 | 2011-02-02 | Teva Pharmaceutical Industries, Ltd. | Purification du montélukast |
EP1948612A2 (fr) * | 2005-11-16 | 2008-07-30 | Teva Pharmaceutical Industries Ltd | Procede de sechage de montelukast sodique par distillation azeotropique du solvant |
AR057909A1 (es) | 2005-11-18 | 2007-12-26 | Synthon Bv | Proceso para preparar montelukast y compuestos relacionados, que utiliza un compuesto intermediario derivado de un ester sulfonico. |
ES2403067T3 (es) | 2005-12-13 | 2013-05-13 | Msn Laboratories Limited | Un procedimiento mejorado para la preparación de montelukast y sus sales farmaceúticamente aceptables |
WO2007088545A2 (fr) | 2006-02-02 | 2007-08-09 | Chemagis Ltd. | Nouveau procédé pour la préparation de l'acide 1-[(mercaptométhyl)cyclopropane]acétique, un intermédiaire utile dans la préparation de montelukaste et des ses sels |
US7528254B2 (en) | 2006-02-27 | 2009-05-05 | Chemagis Ltd. | Process for preparing montelukast and salts thereof |
US20090099367A1 (en) * | 2006-03-06 | 2009-04-16 | Farmaprojects, S. A. | Process for preparing a leukotriene antagonist |
EP1996552A1 (fr) | 2006-03-17 | 2008-12-03 | Synthon B.V. | Sel d'amantadine de montélukast |
ATE524444T1 (de) | 2006-04-12 | 2011-09-15 | Glade Organics Private Ltd | Verbessertes verfahren zur herstellung von montelukast-natrium |
US20060223999A1 (en) * | 2006-05-10 | 2006-10-05 | Chemagis Ltd. | Process for preparing montelukast and precursors thereof |
GB0614485D0 (en) * | 2006-07-21 | 2006-09-27 | Pliva Istrazivanje I Razvoj D | Process |
EP1886998A1 (fr) * | 2006-08-09 | 2008-02-13 | Esteve Quimica, S.A. | Procédés de purification du montelukast et ses sels d'amine |
GB0618703D0 (en) * | 2006-09-22 | 2006-11-01 | Almac Sciences Ltd | Synthesis of leikotriene compounds |
US7700776B2 (en) | 2006-10-24 | 2010-04-20 | Formosa Laboratories, Inc. | Compounds and preparation for montelukast sodium |
US8115004B2 (en) | 2006-11-20 | 2012-02-14 | Msn Laboratories Limited | Process for pure montelukast sodium through pure intermediates as well as amine salts |
US7271268B1 (en) | 2006-12-22 | 2007-09-18 | Formosa Laboratories Inc. | Process for preparation of [1-(mercaptomethyl)cyclopropyl]acetic acid and related derivatives |
EP1958936A1 (fr) * | 2007-02-14 | 2008-08-20 | Inke, S.A. | Procédé pour l'obtention de montelukast |
EP1988079A1 (fr) * | 2007-04-25 | 2008-11-05 | Lonza Ag | Processus de préparation d'alcools éthénylphényl actifs optiquement |
PL205444B1 (pl) | 2007-05-02 | 2010-04-30 | Zak & Lstrok Ady Farmaceutyczn | Sposób wytwarzania soli sodowej kwasu 1-(((1(R)-(3-(2-(7--chloro-2- chinolinylo)-etenylo)fenylo)-3-(2-(1-hydroksy-1- metyloetylo)fenylo)propylo)sulfanylo)metylo)-cyklopropanooctowego |
ES2320077B1 (es) | 2007-07-31 | 2010-02-26 | Moehs Iberica, S.L. | Proceso de preparacion de un antagonista de leucotrienos y de un intermedio del mismo. |
KR101072896B1 (ko) | 2007-10-09 | 2011-10-17 | 한미홀딩스 주식회사 | 이온성 액체 매개체를 이용한 몬테루카스트산의 제조 방법 |
EP2053043A1 (fr) | 2007-10-26 | 2009-04-29 | Inke, S.A. | Sel cristallin de montelukast |
DE102007061630B4 (de) | 2007-12-20 | 2013-07-04 | Formosa Laboratories, Inc. | Neue Verbindungen und Herstellung von Montelukast-Natrium |
CN101817818B (zh) * | 2008-03-06 | 2011-10-26 | 台耀化学股份有限公司 | 一种用于制备孟鲁司特钠的化合物 |
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TR200806298A2 (tr) | 2008-08-22 | 2010-03-22 | Bi̇lgi̇ç Mahmut | Farmasötik formülasyon |
KR101123292B1 (ko) | 2008-09-26 | 2012-03-19 | 주식회사 엘지생명과학 | 몬테루카스트 나트륨염의 제조방법 |
WO2010064109A2 (fr) | 2008-12-02 | 2010-06-10 | Mayuka Labs Private Limited | Procédé de préparation amélioré de montélukast sodique et ses intermédiaires |
WO2010107404A1 (fr) | 2009-03-16 | 2010-09-23 | Mahmut Bilgic | Combinaisons pharmaceutiques stables |
JP2012530140A (ja) | 2009-06-16 | 2012-11-29 | メルク・シャープ・アンド・ドーム・コーポレーション | グルココルチコイド受容体アゴニストとしての新規[3,2−c]ヘテロアリールステロイド、組成物およびこの使用 |
WO2011004298A1 (fr) | 2009-07-09 | 2011-01-13 | Alembic Limited | Montélukast à l'état hexaméthylène-diamine, et son utilisation pour l'élaboration de montélukast sodique |
EP2287154A1 (fr) | 2009-07-14 | 2011-02-23 | KRKA, D.D., Novo Mesto | Synthèse efficace pour la préparation de montelukast |
CN101638381B (zh) * | 2009-09-02 | 2012-08-29 | 鲁南制药集团股份有限公司 | 孟鲁司特钠中间体的合成方法 |
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EP2552892A1 (fr) | 2010-03-31 | 2013-02-06 | KRKA, D.D., Novo Mesto | Synthèse efficace pour la préparation de montélukast et nouvelle forme cristalline d'intermédiaires dans celle-ci |
KR100990046B1 (ko) * | 2010-07-30 | 2010-10-26 | 동국제약 주식회사 | 신규한 몬테루카스트 4-할로 벤질아민염 및 이를 이용한 몬테루카스트 나트륨염의 제조방법 |
HUP1000425A2 (en) | 2010-08-11 | 2012-03-28 | Richter Gedeon Nyrt | Process for the production of montelukast sodium |
TR201009398A2 (tr) | 2010-11-11 | 2012-05-21 | Bi̇lgi̇ç Mahmut | Fiziksel özellikleri geliştirilmiş tablet formülasyonları |
TR201009394A2 (tr) | 2010-11-11 | 2012-06-21 | Bi̇lgi̇ç Mahmut | Geliştirilmiş montelukast formülasyonları. |
US8471030B2 (en) | 2010-12-06 | 2013-06-25 | Orochem Technologies Inc. | Purification of montelukast using simulated moving bed |
EP2502910A1 (fr) | 2011-03-15 | 2012-09-26 | Laboratorios Lesvi, S.L. | Sel de camphre sulfonique d'un intermédiaire clef du Montélukast |
CN102690229B (zh) * | 2011-03-23 | 2016-06-08 | 上海相辉医药科技有限公司 | 一种孟鲁司特钠的合成及其制备中间体 |
KR20140108627A (ko) * | 2011-07-26 | 2014-09-12 | 썬 파마 어드밴스트 리서치 컴패니 리미티드 | 퀴놀린-, 퀸옥살린 또는 벤조티아졸계 시스테이닐 류코트리엔 길항물질 (ltc4) |
WO2013077829A1 (fr) | 2011-11-21 | 2013-05-30 | Mahmut Bilgic | Granulés pharmaceutiques hydrosolubles |
WO2014118796A1 (fr) | 2013-01-31 | 2014-08-07 | Melody Healthcare Pvt. Ltd. | Procédé in situ pour la préparation de montélukast sodique hautement pur |
CN104109122B (zh) * | 2013-04-16 | 2017-03-29 | 浙江奥翔药业股份有限公司 | 用于合成孟鲁司特的中间体化合物及其制备方法 |
CN104370810B (zh) * | 2013-08-13 | 2016-10-05 | 天津汉瑞药业有限公司 | 孟鲁司特钠化合物 |
CN103554017B (zh) * | 2013-10-25 | 2014-12-17 | 河北序能生物技术有限公司 | 一种孟鲁司特钠手性中间体的制备方法 |
CN103936671B (zh) * | 2014-05-06 | 2015-10-28 | 启东东岳药业有限公司 | 孟鲁司特钠中间体的制备方法 |
CN105294556A (zh) * | 2014-06-06 | 2016-02-03 | 上海迪赛诺化学制药有限公司 | 一种制备孟鲁司特酸的方法 |
CN105085391B (zh) | 2015-06-10 | 2017-08-22 | 广东默泰同创医药科技有限公司 | 用作白三烯受体拮抗剂的环丙基不饱和喹啉化合物及应用 |
CN105363019B (zh) * | 2015-12-16 | 2018-04-24 | 新乡医学院第一附属医院 | 一种治疗溶血性贫血的环孢素组合物及其应用 |
CN108530355B (zh) * | 2018-06-08 | 2019-09-10 | 福州华博立乐新材料科技有限公司 | 一种3-[2-(7-氯-2-喹啉基)乙烯基]苯甲醛的合成方法 |
CN108435257A (zh) * | 2018-06-08 | 2018-08-24 | 福州华博立乐新材料科技有限公司 | 一种用于合成3-[2-(7-氯-2-喹啉基)乙烯基]苯甲醛的催化剂 |
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DK282986A (da) * | 1985-06-18 | 1987-02-24 | Merck Frosst Canada Inc | Substitueret quinolin og farmaceutisk praeparat indeholdende en saadan forbindelse |
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IE59889B1 (en) * | 1986-02-14 | 1994-04-20 | Merck Frosst Canada Inc | 2-substituted quinoline dioic acids |
JPS62258362A (ja) * | 1986-05-02 | 1987-11-10 | Terumo Corp | アミド誘導体およびこれを含有する5−リポキシゲナ−ゼ作用阻害剤 |
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NZ233752A (en) * | 1989-05-24 | 1993-05-26 | Merck Frosst Canada Inc | Substituted quinoline derivatives, preparation and pharmaceutical compositions thereof |
WO1990015801A1 (fr) * | 1989-06-22 | 1990-12-27 | Pfizer Inc. | Sulfamides substitues et composes apparentes dans le traitement de l'asthme, de l'arthrite et des maladies apparentees |
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