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FI64154C - Foerfarande foer framstaellning av en terapeutiskt verkande 5-etyl-isoxazol-4-karboxylsyra-(4-trifluormetyl)-anilid - Google Patents

Foerfarande foer framstaellning av en terapeutiskt verkande 5-etyl-isoxazol-4-karboxylsyra-(4-trifluormetyl)-anilid Download PDF

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Publication number
FI64154C
FI64154C FI793899A FI793899A FI64154C FI 64154 C FI64154 C FI 64154C FI 793899 A FI793899 A FI 793899A FI 793899 A FI793899 A FI 793899A FI 64154 C FI64154 C FI 64154C
Authority
FI
Finland
Prior art keywords
formula
anilide
trifluoromethyl
methylisoxazole
iii
Prior art date
Application number
FI793899A
Other languages
English (en)
Finnish (fi)
Other versions
FI793899A (fi
FI64154B (fi
Inventor
Friedrich-Johannes Kaemmerer
Rudolf Schleyerbach
Original Assignee
Hoechst Ag
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 by Hoechst Ag filed Critical Hoechst Ag
Publication of FI793899A publication Critical patent/FI793899A/fi
Publication of FI64154B publication Critical patent/FI64154B/fi
Application granted granted Critical
Publication of FI64154C publication Critical patent/FI64154C/fi

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D261/00—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings
    • C07D261/02—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings
    • C07D261/06—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members
    • C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two 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, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D261/18—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen
    • 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
    • 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
    • A61P37/00—Drugs for immunological or allergic disorders
    • A61P37/08—Antiallergic agents

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Biomedical Technology (AREA)
  • Immunology (AREA)
  • Pain & Pain Management (AREA)
  • Rheumatology (AREA)
  • Pulmonology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Chemical And Physical Treatments For Wood And The Like (AREA)
  • Lubricants (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
FI793899A 1978-12-16 1979-12-13 Foerfarande foer framstaellning av en terapeutiskt verkande 5-etyl-isoxazol-4-karboxylsyra-(4-trifluormetyl)-anilid FI64154C (fi)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19782854439 DE2854439A1 (de) 1978-12-16 1978-12-16 Ein isoxazolderivat, verfahren zu seiner herstellung, diese verbindung enthaltende mittel und verwendung
DE2854439 1978-12-16

Publications (3)

Publication Number Publication Date
FI793899A FI793899A (fi) 1980-06-17
FI64154B FI64154B (fi) 1983-06-30
FI64154C true FI64154C (fi) 1983-10-10

Family

ID=6057414

Family Applications (1)

Application Number Title Priority Date Filing Date
FI793899A FI64154C (fi) 1978-12-16 1979-12-13 Foerfarande foer framstaellning av en terapeutiskt verkande 5-etyl-isoxazol-4-karboxylsyra-(4-trifluormetyl)-anilid

Country Status (25)

Country Link
US (2) US4284786A (fr)
EP (1) EP0013376B1 (fr)
JP (1) JPS5583767A (fr)
AR (2) AR222680A1 (fr)
AT (1) ATE1067T1 (fr)
AU (1) AU529341B2 (fr)
BG (1) BG60764B2 (fr)
CA (1) CA1129867A (fr)
DE (2) DE2854439A1 (fr)
DK (1) DK149886C (fr)
EG (1) EG13926A (fr)
ES (2) ES486750A1 (fr)
FI (1) FI64154C (fr)
GR (1) GR72731B (fr)
HU (1) HU178015B (fr)
IE (1) IE49126B1 (fr)
IL (1) IL58951A (fr)
LU (1) LU90466I2 (fr)
MX (2) MX6174E (fr)
NL (1) NL990037I2 (fr)
NO (1) NO148925C (fr)
NZ (1) NZ192400A (fr)
PH (1) PH16627A (fr)
PT (1) PT70596A (fr)
ZA (1) ZA796793B (fr)

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FR2538806B1 (fr) * 1982-12-30 1986-02-21 Bago Sa Labor Composes phenyl-3 methyl isoxazole-5 carboxy-4 anilides substitues, actifs therapeutiquement contre l'inflammation et la douleur
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DE3534440A1 (de) * 1985-09-27 1987-04-02 Hoechst Ag Arzneimittel gegen chronische graft-versus-host-krankheiten sowie gegen autoimmunerkrankungen, insbesondere systemischen lupus erythematodes
US4935434A (en) * 1988-01-26 1990-06-19 Bristol-Myers Company Antiarthritic isoxazole-4-carboxamides
FR2662692B1 (fr) * 1990-05-30 1995-04-28 Novapharme Derives heterocycliques doues d'activite anticonvulsivante, procede de preparation et composition pharmaceutique.
US5258397A (en) * 1988-11-30 1993-11-02 Novapharme 3-Isoxazoyl derivatives endowed with anticonvulsant activity, procedure for their preparation and their pharmaceutical compositions
DD297328A5 (de) 1989-08-18 1992-01-09 �������@���������k���Kk�� 5-methyl-isoxalol-4-carbonsaeureanilide und 2 hydroxyethyliden-cyanoessigsaeureanilide zur behandlung von augenerkrankungen
US5583150A (en) * 1989-08-18 1996-12-10 Alcon Laboratories, Inc. 5-methyl-isoxazole-4-carboxylic acid anilides and 2-hydroxyethylidene-cyano acetic anilides for the treatment of ocular diseases
US5001124A (en) * 1990-02-02 1991-03-19 Syntex (U.S.A.) Inc. 4-isoxazolecarboxamide derivatives
US5108999A (en) * 1990-02-02 1992-04-28 Syntex (U.S.A.) Inc. 4-isoxazolecarboxamide derivatives
RU2142937C1 (ru) * 1990-05-18 1999-12-20 Хехст АГ Амиды органических кислот, способ их получения и фармацевтическая композиция
US6133301A (en) * 1991-08-22 2000-10-17 Aventis Pharma Deutschland Gmbh Pharmaceuticals for the treatment of rejection reactions in organ transplantations
DE4127737A1 (de) * 1991-08-22 1993-02-25 Hoechst Ag Arzneimittel zur behandlung von abstossungsreaktionen bei organverpflanzungen
DE59407415D1 (de) * 1993-01-08 1999-01-21 Hoechst Ag Verwendung von Leflunomid zur Hemmung von Interleukin 8
DK0607774T3 (da) * 1993-01-08 1999-08-16 Hoechst Ag Anvendelse af leflunomid til inhibering af interleukin 1 alfa
EP0607776B1 (fr) * 1993-01-08 1998-12-09 Hoechst Aktiengesellschaft Utilisation de leflunomid pour inhiber le facteur alpha de necrose tumorale
DE59407413D1 (de) * 1993-01-08 1999-01-21 Hoechst Ag Verwendung von Leflunomid zur Hemmung von Interleukin 1 beta
TW314467B (fr) * 1993-03-31 1997-09-01 Hoechst Ag
DE4323636A1 (de) * 1993-07-15 1995-01-19 Hoechst Ag Arzneistoffzubereitungen aus umhüllten, schwerstwasserlöslichen Arzneistoffen für Inhalationsarzneiformen und Verfahren zu ihrer Herstellung
LT3589B (en) 1993-11-30 1995-12-27 Hoechst Ag Using of known combination for treatment of rejection reaction by transplantation of organs
US5700823A (en) * 1994-01-07 1997-12-23 Sugen, Inc. Treatment of platelet derived growth factor related disorders such as cancers
US5610173A (en) * 1994-01-07 1997-03-11 Sugen, Inc. Formulations for lipophilic compounds
US6335356B1 (en) 1994-01-07 2002-01-01 Sugen, Inc. Method of treating a patient by parenteral administration of a lipophilic compound
US5519042A (en) * 1994-01-13 1996-05-21 Hoechst Aktiengesellschaft Method of treating hyperproliferative vascular disease
US5624946A (en) * 1994-07-05 1997-04-29 Williams; James Use of leflunomide to control and reverse chronic allograft rejection
PT787491E (pt) * 1994-10-17 2000-11-30 Aventis Pharma Ltd Composicao para a profilaxia e para o tratamento de doencas alergicas de tipo i
US5721277A (en) * 1995-04-21 1998-02-24 Sugen, Inc. Compounds and methods for inhibiting hyper-proliferative cell growth
US6331555B1 (en) 1995-06-01 2001-12-18 University Of California Treatment of platelet derived growth factor related disorders such as cancers
DE19539638A1 (de) * 1995-10-25 1997-04-30 Hoechst Ag Die Verwendung von Isoxazol- und Crotonsäureamidderivaten zur Behandlung von Krebserkrankungen
DE19702988A1 (de) * 1997-01-28 1998-07-30 Hoechst Ag Isoxazol- und Crotonsäureamidderivate und deren Verwendung als Arzneimittel und Diagnostika
US6316479B1 (en) 1997-05-19 2001-11-13 Sugen, Inc. Isoxazole-4-carboxamide compounds active against protein tryosine kinase related disorders
ATE207065T1 (de) * 1997-08-08 2001-11-15 Aventis Pharma Gmbh Kristallform von n-(4-trifluormethylphenyl)-5- methylisoxazol-4-carbonsäureamid
US7691890B2 (en) 1998-03-11 2010-04-06 James W. Williams Anti-viral uses of leflunomide products
US20050255071A1 (en) * 1998-12-10 2005-11-17 Aventis Pharma Deutschland Gmbh Preparation having improved therapeutic breadth comprising nucleotide synthesis inhibitors
DE19908527C2 (de) * 1999-02-26 2001-08-30 Aventis Pharma Gmbh Verfahren zur Kristallisation von N-(4-Trifluormethylphenyl)-5-methyl-isoxazol-4-carboxamid
US6566395B1 (en) 1999-05-25 2003-05-20 Biomedicines, Inc. Methods of treating proliferative disorders
DE19960443C2 (de) * 1999-12-15 2002-05-08 Aventis Pharma Gmbh Verfahren zur Auffindung von Nukleotidsyntheseinhibitoren mit weniger Nebenwirkungen
JP2003517011A (ja) * 1999-12-16 2003-05-20 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 レフルノミドの新規な製法及び新しい結晶形態
EP1473035A1 (fr) * 2000-02-15 2004-11-03 Teva Pharmaceutical Industries Ltd. Leflunomide d'une pureté elevée
AU2001234943A1 (en) * 2000-02-15 2001-08-27 Teva Pharmaceutical Industries Ltd. A method for synthesizing leflunomide
AU2001284891A1 (en) * 2000-08-14 2002-02-25 Teva Pharmaceutical Industries Ltd. Micronized leflunomide
PT1381356E (pt) 2001-04-05 2008-07-24 Aventis Pharma Inc Utilização de (4' -trifluorometilfenil) - amida do ácido (z) -2- ciano-3-hidroxi-but-2-enóico para tratamento da esclerose múltipla
GB0123571D0 (en) 2001-04-05 2001-11-21 Aventis Pharm Prod Inc Use of (Z)-2-cyano-3-hydroxy-but-2-enoic acid-(4'-trifluoromethylphenyl)-amide for treating multiple sclerosis
US20030139606A1 (en) * 2001-11-09 2003-07-24 Ray Anup Kumar Process for preparing 5-methylisoxazole-4-carboxylic- (4'-trifluoromethyl)-anilide
US20050158371A1 (en) * 2002-02-12 2005-07-21 Sumitomo Pharmaceuticals Co., Ltd. Novel external agent
EP2583678A3 (fr) 2004-06-24 2013-11-13 Novartis Vaccines and Diagnostics, Inc. Immunopotentiateurs de petites molécules et dosages pour leur détection
US20060024376A1 (en) * 2004-07-30 2006-02-02 The University Of Chicago Methods and compositions for reducing toxicity associated with leflunomide treatment
CN101242831A (zh) * 2005-08-31 2008-08-13 兴和株式会社 类风湿性关节炎的预防和/或治疗方法
WO2008093246A2 (fr) 2007-02-02 2008-08-07 Vegenics Limited Antagoniste de facteurs de croissance pour l'allo-immunité de greffe d'organe et l'artériosclérose
CN101817797B (zh) * 2009-02-26 2013-04-10 江苏亚邦爱普森药业有限公司 高纯度3-甲基-n-[4-(三氟甲基)苯基]-4-异噁唑甲酰胺的合成方法
US9138309B2 (en) 2010-02-05 2015-09-22 Allergan, Inc. Porous materials, methods of making and uses
US9205577B2 (en) * 2010-02-05 2015-12-08 Allergan, Inc. Porogen compositions, methods of making and uses
US11202853B2 (en) * 2010-05-11 2021-12-21 Allergan, Inc. Porogen compositions, methods of making and uses
JOP20190207A1 (ar) 2017-03-14 2019-09-10 Actelion Pharmaceuticals Ltd تركيبة صيدلانية تشتمل على بونيسيمود
EP3773579A4 (fr) 2018-03-26 2022-03-09 Clear Creek Bio, Inc. Compositions et procédés pour inhiber la dihydroorotate déshydrogénase
AU2021232637A1 (en) 2020-03-06 2022-09-22 Actelion Pharmaceuticals Ltd Methods of slowing brain volume loss
US20210300873A1 (en) 2020-03-20 2021-09-30 Clear Creek Bio, Inc. Stable polymorphic compositions of brequinar sodium and methods of use and manufacture thereof
US11951097B2 (en) 2021-10-11 2024-04-09 Vanda Pharmaceuticals Inc. Methods of treating multiple sclerosis
CA3220702A1 (fr) 2022-02-11 2023-08-17 Actelion Pharmaceuticals Ltd Methodes de ralentissement d'une augmentation du volume ventriculaire cerebral

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US4087534A (en) * 1974-05-22 1978-05-02 David Ovadia N-haloalkylmio urazole pesticides
NL178596C (nl) * 1975-06-05 1986-04-16 Hoechst Ag Werkwijze voor het bereiden van een geneesmiddel met antiflogistische en/of analgetische werking, alsmede werkwijze voor het bereiden van daarin als geneeskrachtige verbindingen te gebruiken 5-methylisoxazool-4-carbonzuuraniliden.
DE2524959C2 (de) * 1975-06-05 1983-02-10 Hoechst Ag, 6000 Frankfurt 5-Methyl-isoxazol-4-carbonsäureanilide, Verfahren zu ihrer Herstellung, diese Verbindungen enthaltende Mittel
DE2654797A1 (de) * 1976-12-03 1978-06-08 Hoechst Ag Verfahren zur herstellung von isoxazolderivaten

Also Published As

Publication number Publication date
AR222680A1 (es) 1981-06-15
NO794094L (no) 1980-06-17
IL58951A (en) 1984-01-31
IE49126B1 (en) 1985-08-07
EP0013376A3 (en) 1980-09-17
CA1129867A (fr) 1982-08-17
JPH0133470B2 (fr) 1989-07-13
NO148925B (no) 1983-10-03
EG13926A (en) 1982-09-30
ES486758A1 (es) 1980-05-16
MX8403A (es) 1994-03-31
BG60764B2 (bg) 1996-02-29
DK534279A (da) 1980-06-17
FI793899A (fi) 1980-06-17
ZA796793B (en) 1980-11-26
IE792426L (en) 1980-06-16
MX6174E (es) 1984-12-04
NL990037I1 (nl) 2000-01-03
NO148925C (no) 1984-01-11
IL58951A0 (en) 1980-03-31
ES486750A1 (es) 1980-06-16
GR72731B (fr) 1983-12-01
FI64154B (fi) 1983-06-30
AR226894A1 (es) 1982-08-31
HU178015B (en) 1982-02-28
AU529341B2 (en) 1983-06-02
DE2962929D1 (en) 1982-07-08
JPS5583767A (en) 1980-06-24
PH16627A (en) 1983-12-05
EP0013376A2 (fr) 1980-07-23
DK149886B (da) 1986-10-20
EP0013376B1 (fr) 1982-05-19
NZ192400A (en) 1982-02-23
DK149886C (da) 1987-04-21
AU5385379A (en) 1980-06-19
DE2854439A1 (de) 1980-07-03
NL990037I2 (nl) 2000-01-03
ATE1067T1 (de) 1982-06-15
US4284786A (en) 1981-08-18
PT70596A (de) 1980-01-01
US4351841A (en) 1982-09-28
LU90466I2 (fr) 2000-01-03

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Legal Events

Date Code Title Description
SPCG Supplementary protection certificate granted

Spc suppl protection certif: L100

Extension date: 20041213

MA Patent expired

Owner name: AVENTIS PHARMA DEUTSCHLAND GMBH