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ES2185790T3 - Sintesis en un solo recipiente de derivados de 2-oxazolidinona. - Google Patents

Sintesis en un solo recipiente de derivados de 2-oxazolidinona.

Info

Publication number
ES2185790T3
ES2185790T3 ES96926465T ES96926465T ES2185790T3 ES 2185790 T3 ES2185790 T3 ES 2185790T3 ES 96926465 T ES96926465 T ES 96926465T ES 96926465 T ES96926465 T ES 96926465T ES 2185790 T3 ES2185790 T3 ES 2185790T3
Authority
ES
Spain
Prior art keywords
formula compound
formula
synthesis
single container
oxazolidinone 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 - Lifetime
Application number
ES96926465T
Other languages
English (en)
Inventor
Rajnikant Patel
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
AstraZeneca AB
Original Assignee
AstraZeneca AB
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 AstraZeneca AB filed Critical AstraZeneca AB
Application granted granted Critical
Publication of ES2185790T3 publication Critical patent/ES2185790T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D263/00Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D263/16Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member 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
    • C07D263/18Oxygen atoms
    • C07D263/20Oxygen atoms attached in position 2
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/06Antimigraine agents
    • 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
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06Esters of carbamic acids
    • C07C271/08Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/20Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by nitrogen atoms not being part of nitro or nitroso groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06Esters of carbamic acids
    • C07C271/08Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms
    • C07C271/22Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms with the nitrogen atoms of the carbamate groups bound to hydrogen atoms or to acyclic carbon atoms to carbon atoms of hydrocarbon radicals substituted by carboxyl groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D413/00Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/06Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Engineering & Computer Science (AREA)
  • Public Health (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Indole Compounds (AREA)

Abstract

LA INVENCION ACTUAL PROPORCIONA UN PROCESO MEJORADO PARA LA PREPARACION DE (S) 1H INDOL FORMACION DE UN CARBAMATO DE FORMULA (III), A PARTIR DE CLORHIDRATO DE METIL 4 DEL COMPUESTO DE FORMULA (III) PARA LOGRAR EL COMPUESTO DE FORMULA (IV); C) REDUCCION DEL GRUPO ESTER DE METILO EN EL COMPUESTO DE FORMULA (IV) PARA OBTENER EL COMPUESTO DE FORMULA (V); D) CIERRE DEL ANILLO DEL COMPUESTO DE FORMULA (V) PARA OBTENER EL COMPUESTO DE FORMULA (VI); E) FORMACION DE SAL DE DIAZONIO A PARTIR DEL COMPUESTO DE FORMULA (VI) SEGUIDA DE REDUCCION PARA OBTENER EL COMPUESTO DE FORMULA (VII); F) REACCION DE FISCHER DEL COMPUESTO DE FORMULA (VII) PARA OBTENER (S) [2 -(DIMETILAMINO)ETIL] OLIDINONA.
ES96926465T 1995-08-07 1996-08-02 Sintesis en un solo recipiente de derivados de 2-oxazolidinona. Expired - Lifetime ES2185790T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9516145.1A GB9516145D0 (en) 1995-08-07 1995-08-07 Improved chemical synthesis

Publications (1)

Publication Number Publication Date
ES2185790T3 true ES2185790T3 (es) 2003-05-01

Family

ID=10778867

Family Applications (2)

Application Number Title Priority Date Filing Date
ES02008427T Expired - Lifetime ES2261545T3 (es) 1995-08-07 1996-08-02 Procedimiento para la purificacion de (s)-4-((3-(dimetilamino)etil)-1h-indol-5-il)metil)-2-oxazolidinona.
ES96926465T Expired - Lifetime ES2185790T3 (es) 1995-08-07 1996-08-02 Sintesis en un solo recipiente de derivados de 2-oxazolidinona.

Family Applications Before (1)

Application Number Title Priority Date Filing Date
ES02008427T Expired - Lifetime ES2261545T3 (es) 1995-08-07 1996-08-02 Procedimiento para la purificacion de (s)-4-((3-(dimetilamino)etil)-1h-indol-5-il)metil)-2-oxazolidinona.

Country Status (34)

Country Link
US (2) US6084103A (es)
EP (2) EP0843672B1 (es)
JP (6) JP3729503B2 (es)
KR (1) KR100670704B1 (es)
CN (3) CN1092657C (es)
AR (2) AR006515A1 (es)
AT (2) ATE325121T1 (es)
AU (1) AU718413B2 (es)
BR (1) BR9609830A (es)
CA (2) CA2227039C (es)
CZ (2) CZ293050B6 (es)
DE (2) DE69624825T2 (es)
DK (2) DK0843672T3 (es)
ES (2) ES2261545T3 (es)
GB (1) GB9516145D0 (es)
HK (1) HK1047094B (es)
HU (1) HU229966B1 (es)
IL (4) IL156733A (es)
IN (2) IN185148B (es)
MX (1) MX9801044A (es)
MY (1) MY117571A (es)
NO (2) NO311690B1 (es)
NZ (1) NZ315040A (es)
PL (1) PL188805B1 (es)
PT (2) PT1227095E (es)
RO (2) RO121816B1 (es)
RU (1) RU2167875C2 (es)
SI (2) SI0843672T1 (es)
SK (1) SK285052B6 (es)
TR (1) TR199800182T1 (es)
TW (1) TW358811B (es)
UA (1) UA53625C2 (es)
WO (1) WO1997006162A1 (es)
ZA (1) ZA966711B (es)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AU5851400A (en) * 1999-07-09 2001-01-30 Chugai Seiyaku Kabushiki Kaisha Process for the preparation of aniline derivatives
GB9928578D0 (en) * 1999-12-03 2000-02-02 Zeneca Ltd Pharmaceutical formulations
ES2204302B2 (es) * 2002-08-07 2005-03-01 Laboratorios Vita, S.A. Procedimiento para la obtencion de un compuesto farmaceuticamente activo.
US20070173536A1 (en) * 2004-02-06 2007-07-26 Ciba Specialty Chemicals Holding Inc. Crystalline forms of zolmitriptan
WO2006055964A2 (en) * 2004-11-19 2006-05-26 Teva Pharmaceutical Industries Ltd. Zolmitriptan crystal forms
CN101248184B (zh) 2005-08-25 2013-01-16 宇部兴产株式会社 光学活性(S或R)-α-氨基酸及光学活性(S或R)-α-氨基酸酯的制造方法
ATE510836T1 (de) * 2006-01-19 2011-06-15 Matrix Lab Ltd Umwandlung eines aromatischen diazoniumsalzes in ein arylhydrazin
WO2008007390A2 (en) * 2006-07-10 2008-01-17 Natco Pharma Limited An improved process for purification of zolmitriptan
WO2008018090A2 (en) * 2006-08-09 2008-02-14 Matrix Laboratories Ltd An improved process for the preparation of zolmitriptan
CZ301538B6 (cs) * 2007-02-26 2010-04-07 Zentiva, A. S. Zpusob prípravy zolmitriptanu
CZ2007158A3 (cs) * 2007-02-26 2008-10-22 Zentiva, A. S. Zpusob prípravy zolmitriptanu
JP2010540613A (ja) * 2007-10-03 2010-12-24 ジェネリクス・(ユーケー)・リミテッド ゾルミトリプタン、その塩、及びその溶媒和物の調製方法
CN101230047B (zh) * 2008-02-04 2010-08-04 江苏中威药业有限公司 一种4-取代手性噁唑烷酮类化合物的制备方法
US8906949B2 (en) 2010-05-21 2014-12-09 Sanovel Ilac Sanayi Ve Ticaret Anonim Sirketi Orally disintegrating tablets of zolmitriptan and process for preparing the same
CN101948443B (zh) * 2010-08-17 2012-08-22 河南师范大学 一种简单、高效合成4-取代噁唑烷酮衍生物的方法
EP2691396B1 (en) 2011-03-30 2016-08-10 Brown University Enopeptins, uses thereof, and methods of synthesis thereto
WO2013057739A2 (en) * 2011-09-02 2013-04-25 Emcure Pharmaceuticals Limited An improved process for preparation of zolmitriptan
CN102964270B (zh) * 2012-11-21 2015-01-07 合肥星宇化学有限责任公司 一种亚硫酸钠还原重氮盐合成肼的方法
CN103275075B (zh) * 2013-06-24 2015-01-07 成都天台山制药有限公司 佐米曲普坦及其制备方法
WO2016037072A2 (en) * 2014-09-04 2016-03-10 Brown University Enopeptin analogas and methods of use thereof

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3879410A (en) * 1971-02-08 1975-04-22 Messrs Lab Guidotti & C S P A 4-Aryl-4-oxazolin-2-ones exhibiting myotonic and myorelaxing activity
GB1478108A (en) * 1975-10-30 1977-06-29 Nippon Chemipar Co Ltd 5-benzyl-2-oxazolidone derivatives and a process for producing the same
GB8724912D0 (en) * 1987-10-23 1987-11-25 Wellcome Found Indole derivatives
DK0486666T3 (da) * 1990-06-07 1998-03-30 Zeneca Ltd Terapeutisk heterocykliske forbindelser
GB9012672D0 (en) * 1990-06-07 1990-08-01 Wellcome Found Therapeutic heterocyclic compounds
GB9401436D0 (en) * 1994-01-26 1994-03-23 Wellcome Found Therapeutic heterocyclic compounds
GB9423682D0 (en) * 1994-11-23 1995-01-11 Merck Sharp & Dohme Therapeutic agents
CA2207201A1 (en) * 1994-12-06 1996-06-13 Caroline Henry Azetidine, pyrrolidine and piperidine derivatives as 5ht1 receptor agonists

Also Published As

Publication number Publication date
HK1047094B (en) 2006-10-13
DE69636107T2 (de) 2007-05-03
HK1047094A1 (en) 2003-02-07
EP1227095A2 (en) 2002-07-31
NZ315040A (en) 2000-01-28
DE69636107D1 (de) 2006-06-08
CA2572508C (en) 2010-03-30
ZA966711B (en) 1997-02-18
NO311690B1 (no) 2002-01-07
RO121816B1 (ro) 2008-05-30
CZ293050B6 (cs) 2004-01-14
CZ35298A3 (cs) 1998-06-17
CN1317480A (zh) 2001-10-17
PL324881A1 (en) 1998-06-22
SK15498A3 (en) 1998-06-03
PT843672E (pt) 2003-03-31
CN1244579C (zh) 2006-03-08
JP2002308858A (ja) 2002-10-23
ATE227723T1 (de) 2002-11-15
AU6663496A (en) 1997-03-05
NO980522D0 (no) 1998-02-06
GB9516145D0 (en) 1995-10-04
HUP9900188A2 (hu) 1999-05-28
US6084103A (en) 2000-07-04
JP2002037786A (ja) 2002-02-06
SK285052B6 (sk) 2006-05-04
CZ301603B6 (cs) 2010-04-28
JPH11513023A (ja) 1999-11-09
JP3729503B2 (ja) 2005-12-21
US6160123A (en) 2000-12-12
CN1092657C (zh) 2002-10-16
DE69624825D1 (de) 2002-12-19
NO20005187L (no) 1998-02-06
CN1142904C (zh) 2004-03-24
IN185148B (es) 2000-11-25
JP3739678B2 (ja) 2006-01-25
SI1227095T1 (sl) 2006-08-31
CN1201460A (zh) 1998-12-09
UA53625C2 (uk) 2003-02-17
AR046236A2 (es) 2005-11-30
NO20005187D0 (no) 2000-10-16
DK0843672T3 (da) 2003-02-17
DK1227095T3 (da) 2006-07-31
JP2006077025A (ja) 2006-03-23
SI0843672T1 (en) 2003-04-30
ES2261545T3 (es) 2006-11-16
EP0843672A1 (en) 1998-05-27
IL148030A (en) 2010-05-17
HU229966B1 (hu) 2015-03-30
IL123171A (en) 2003-10-31
HK1009129A1 (en) 1999-05-28
IL148030A0 (en) 2002-09-12
TR199800182T1 (xx) 1998-05-21
NO311691B1 (no) 2002-01-07
NO980522L (no) 1998-02-06
MY117571A (en) 2004-07-31
TW358811B (en) 1999-05-21
JP4634286B2 (ja) 2011-02-16
IL156733A (en) 2007-07-04
CA2572508A1 (en) 1997-02-20
ATE325121T1 (de) 2006-06-15
JP2002097178A (ja) 2002-04-02
WO1997006162A1 (en) 1997-02-20
RU2167875C2 (ru) 2001-05-27
JP2006225406A (ja) 2006-08-31
AU718413B2 (en) 2000-04-13
IL156733A0 (en) 2004-02-08
RO119618B1 (ro) 2005-01-28
HUP9900188A3 (en) 1999-11-29
BR9609830A (pt) 1999-03-09
IL123171A0 (en) 1998-09-24
CN1403455A (zh) 2003-03-19
CA2227039C (en) 2007-12-04
PL188805B1 (pl) 2005-04-29
PT1227095E (pt) 2006-08-31
CA2227039A1 (en) 1997-02-20
KR100670704B1 (ko) 2007-07-11
EP0843672B1 (en) 2002-11-13
IN189756B (es) 2003-04-19
EP1227095B1 (en) 2006-05-03
KR19990036165A (ko) 1999-05-25
MX9801044A (es) 1998-05-31
EP1227095A3 (en) 2003-11-19
AR006515A1 (es) 1999-09-08
DE69624825T2 (de) 2003-09-04

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