SK285052B6 - Spôsob prípravy (S)-4-{[3-[2-(dimetylamino)etyl]-1H-indol-5- yl]metyl}-2-oxazolidinónu a medziprodukty na tento spôsob - Google Patents

Spôsob prípravy (S)-4-{[3-[2-(dimetylamino)etyl]-1H-indol-5- yl]metyl}-2-oxazolidinónu a medziprodukty na tento spôsob Download PDF

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Publication number
SK285052B6
SK285052B6 SK154-98A SK15498A SK285052B6 SK 285052 B6 SK285052 B6 SK 285052B6 SK 15498 A SK15498 A SK 15498A SK 285052 B6 SK285052 B6 SK 285052B6
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SK
Slovakia
Prior art keywords
formula
compound
methyl
carried out
sodium
Prior art date
Application number
SK154-98A
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English (en)
Slovak (sk)
Other versions
SK15498A3 (en
Inventor
Rajnikant Patel
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
Publication of SK15498A3 publication Critical patent/SK15498A3/sk
Publication of SK285052B6 publication Critical patent/SK285052B6/sk

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Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/08—Heterocyclic 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
    • C07D263/16—Heterocyclic 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
    • C07D263/18—Oxygen atoms
    • C07D263/20—Oxygen atoms attached in position 2
    • 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
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/06—Antimigraine 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06—Esters of carbamic acids
    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10—Esters 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
    • C07C271/20—Esters 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C271/00—Derivatives of carbamic acids, i.e. compounds containing any of the groups, the nitrogen atom not being part of nitro or nitroso groups
    • C07C271/06—Esters of carbamic acids
    • C07C271/08—Esters of carbamic acids having oxygen atoms of carbamate groups bound to acyclic carbon atoms
    • C07C271/10—Esters 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
    • C07C271/22—Esters 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic 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
    • C07D413/06—Heterocyclic 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)
SK154-98A 1995-08-07 1996-08-02 Spôsob prípravy (S)-4-{[3-[2-(dimetylamino)etyl]-1H-indol-5- yl]metyl}-2-oxazolidinónu a medziprodukty na tento spôsob SK285052B6 (sk)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
GBGB9516145.1A GB9516145D0 (en) 1995-08-07 1995-08-07 Improved chemical synthesis
PCT/GB1996/001885 WO1997006162A1 (fr) 1995-08-07 1996-08-02 Synthese en un seul creuset de derives de 2-oxazolidinone

Publications (2)

Publication Number Publication Date
SK15498A3 SK15498A3 (en) 1998-06-03
SK285052B6 true SK285052B6 (sk) 2006-05-04

Family

ID=10778867

Family Applications (1)

Application Number Title Priority Date Filing Date
SK154-98A SK285052B6 (sk) 1995-08-07 1996-08-02 Spôsob prípravy (S)-4-{[3-[2-(dimetylamino)etyl]-1H-indol-5- yl]metyl}-2-oxazolidinónu a medziprodukty na tento spôsob

Country Status (34)

Country Link
US (2) US6084103A (fr)
EP (2) EP0843672B1 (fr)
JP (6) JP3729503B2 (fr)
KR (1) KR100670704B1 (fr)
CN (3) CN1142904C (fr)
AR (2) AR006515A1 (fr)
AT (2) ATE325121T1 (fr)
AU (1) AU718413B2 (fr)
BR (1) BR9609830A (fr)
CA (2) CA2227039C (fr)
CZ (2) CZ293050B6 (fr)
DE (2) DE69636107T2 (fr)
DK (2) DK0843672T3 (fr)
ES (2) ES2261545T3 (fr)
GB (1) GB9516145D0 (fr)
HK (2) HK1047094B (fr)
HU (1) HU229966B1 (fr)
IL (4) IL123171A (fr)
IN (2) IN185148B (fr)
MX (1) MX9801044A (fr)
MY (1) MY117571A (fr)
NO (2) NO311690B1 (fr)
NZ (1) NZ315040A (fr)
PL (1) PL188805B1 (fr)
PT (2) PT843672E (fr)
RO (2) RO121816B1 (fr)
RU (1) RU2167875C2 (fr)
SI (2) SI1227095T1 (fr)
SK (1) SK285052B6 (fr)
TR (1) TR199800182T1 (fr)
TW (1) TW358811B (fr)
UA (1) UA53625C2 (fr)
WO (1) WO1997006162A1 (fr)
ZA (1) ZA966711B (fr)

Families Citing this family (19)

* 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
ES2204302B2 (es) 2002-08-07 2005-03-01 Laboratorios Vita, S.A. Procedimiento para la obtencion de un compuesto farmaceuticamente activo.
WO2005075467A2 (fr) * 2004-02-06 2005-08-18 Ciba Specialty Chemicals Holding Inc. Formes cristallines de zolmitriptan
WO2006055964A2 (fr) * 2004-11-19 2006-05-26 Teva Pharmaceutical Industries Ltd. Formes cristallines de zolmitriptan
JP4935675B2 (ja) 2005-08-25 2012-05-23 宇部興産株式会社 光学活性（Ｓ又はＲ）−α−アミノ酸及び光学活性（Ｒ又はＳ）−α−アミノ酸エステルの製造方法
WO2007083320A2 (fr) * 2006-01-19 2007-07-26 Matrix Laboratories Ltd Conversion d'un sel de diazonium aromatique en arylhydrazine
WO2008007390A2 (fr) * 2006-07-10 2008-01-17 Natco Pharma Limited Procédé amélioré de purification de zolmitriptan
WO2008018090A2 (fr) * 2006-08-09 2008-02-14 Matrix Laboratories Ltd Procédé de préparation amélioré de 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
US9193767B2 (en) 2011-03-30 2015-11-24 Brown University Enopeptins, uses thereof, and methods of synthesis thereto
WO2013057739A2 (fr) * 2011-09-02 2013-04-25 Emcure Pharmaceuticals Limited Procédé de préparation amélioré de 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 (fr) * 2014-09-04 2016-03-10 Brown University Analogues d'enopeptine s et leurs procédés d'utilisation

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8724912D0 (en) * 1987-10-23 1987-11-25 Wellcome Found Indole derivatives
CA2064815C (fr) * 1990-06-07 1999-11-16 Alan Duncan Robertson Composes heterocycliques therapeutiques
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
US6025374A (en) * 1994-12-06 2000-02-15 Merck Sharp & Dohme, Ltd. Azetidine, pyrrolidine and piperidine derivatives as 5HT1 receptor agonists

Also Published As

Publication number Publication date
EP1227095A3 (fr) 2003-11-19
MX9801044A (es) 1998-05-31
GB9516145D0 (en) 1995-10-04
DK1227095T3 (da) 2006-07-31
CN1244579C (zh) 2006-03-08
JP2002037786A (ja) 2002-02-06
IL156733A0 (en) 2004-02-08
PT843672E (pt) 2003-03-31
DE69636107T2 (de) 2007-05-03
EP1227095B1 (fr) 2006-05-03
NZ315040A (en) 2000-01-28
PL324881A1 (en) 1998-06-22
NO980522D0 (no) 1998-02-06
NO20005187D0 (no) 2000-10-16
IL123171A0 (en) 1998-09-24
JP2006077025A (ja) 2006-03-23
EP1227095A2 (fr) 2002-07-31
AR046236A2 (es) 2005-11-30
IN189756B (fr) 2003-04-19
HU229966B1 (hu) 2015-03-30
DE69624825D1 (de) 2002-12-19
CA2572508A1 (fr) 1997-02-20
KR19990036165A (ko) 1999-05-25
JPH11513023A (ja) 1999-11-09
WO1997006162A1 (fr) 1997-02-20
CA2572508C (fr) 2010-03-30
ES2185790T3 (es) 2003-05-01
IL148030A (en) 2010-05-17
CN1092657C (zh) 2002-10-16
CA2227039C (fr) 2007-12-04
AU6663496A (en) 1997-03-05
EP0843672B1 (fr) 2002-11-13
JP3739678B2 (ja) 2006-01-25
CZ35298A3 (cs) 1998-06-17
SK15498A3 (en) 1998-06-03
SI1227095T1 (sl) 2006-08-31
TW358811B (en) 1999-05-21
RO119618B1 (ro) 2005-01-28
ES2261545T3 (es) 2006-11-16
NO311691B1 (no) 2002-01-07
NO980522L (no) 1998-02-06
RU2167875C2 (ru) 2001-05-27
JP2002308858A (ja) 2002-10-23
CN1403455A (zh) 2003-03-19
CN1142904C (zh) 2004-03-24
HK1047094A1 (en) 2003-02-07
BR9609830A (pt) 1999-03-09
MY117571A (en) 2004-07-31
DE69624825T2 (de) 2003-09-04
US6160123A (en) 2000-12-12
AU718413B2 (en) 2000-04-13
CA2227039A1 (fr) 1997-02-20
RO121816B1 (ro) 2008-05-30
CN1201460A (zh) 1998-12-09
JP2006225406A (ja) 2006-08-31
JP2002097178A (ja) 2002-04-02
AR006515A1 (es) 1999-09-08
DE69636107D1 (de) 2006-06-08
ZA966711B (en) 1997-02-18
SI0843672T1 (en) 2003-04-30
CZ301603B6 (cs) 2010-04-28
NO311690B1 (no) 2002-01-07
CN1317480A (zh) 2001-10-17
IL123171A (en) 2003-10-31
HK1047094B (zh) 2006-10-13
HUP9900188A2 (hu) 1999-05-28
EP0843672A1 (fr) 1998-05-27
ATE325121T1 (de) 2006-06-15
HK1009129A1 (en) 1999-05-28
IL148030A0 (en) 2002-09-12
DK0843672T3 (da) 2003-02-17
US6084103A (en) 2000-07-04
PT1227095E (pt) 2006-08-31
NO20005187L (no) 1998-02-06
IL156733A (en) 2007-07-04
HUP9900188A3 (en) 1999-11-29
PL188805B1 (pl) 2005-04-29
JP3729503B2 (ja) 2005-12-21
CZ293050B6 (cs) 2004-01-14
KR100670704B1 (ko) 2007-07-11
TR199800182T1 (xx) 1998-05-21
UA53625C2 (uk) 2003-02-17
JP4634286B2 (ja) 2011-02-16
IN185148B (fr) 2000-11-25
ATE227723T1 (de) 2002-11-15

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MK4A Expiry of patent

Expiry date: 20160802