EA200200898A1 - Способ получения циталопрама - Google Patents

Способ получения циталопрама

Info

Publication number
EA200200898A1
EA200200898A1 EA200200898A EA200200898A EA200200898A1 EA 200200898 A1 EA200200898 A1 EA 200200898A1 EA 200200898 A EA200200898 A EA 200200898A EA 200200898 A EA200200898 A EA 200200898A EA 200200898 A1 EA200200898 A1 EA 200200898A1
Authority
EA
Eurasian Patent Office
Prior art keywords
group
compound
formula
alkenyl
independently selected
Prior art date
Application number
EA200200898A
Other languages
English (en)
Other versions
EA005315B1 (ru
Inventor
Ханс Петерсен
Майкл Хэролд Рок
Халех Ахмадиан
Original Assignee
Х.Лундбекк А/С
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 Х.Лундбекк А/С filed Critical Х.Лундбекк А/С
Publication of EA200200898A1 publication Critical patent/EA200200898A1/ru
Publication of EA005315B1 publication Critical patent/EA005315B1/ru

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D307/00Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom
    • C07D307/77Heterocyclic compounds containing five-membered rings having one oxygen atom as the only ring hetero atom ortho- or peri-condensed with carbocyclic rings or ring systems
    • C07D307/87Benzo [c] furans; Hydrogenated benzo [c] furans
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/335Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin
    • A61K31/34Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide
    • A61K31/343Heterocyclic compounds having oxygen as the only ring hetero atom, e.g. fungichromin having five-membered rings with one oxygen as the only ring hetero atom, e.g. isosorbide condensed with a carbocyclic ring, e.g. coumaran, bufuralol, befunolol, clobenfurol, amiodarone
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • A61P25/24Antidepressants

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Medicinal Chemistry (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Neurology (AREA)
  • Engineering & Computer Science (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Neurosurgery (AREA)
  • Biomedical Technology (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Psychiatry (AREA)
  • Pain & Pain Management (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
  • Steroid Compounds (AREA)

Abstract

Настоящее изобретение относится к способу получения циталопрама, включающему взаимодействие соединения формулы (I) с соединением формулы (II), где Х представляет подходящую уходящую группу и R представляет -CH-O-Pg, -CH-NPgPg, -СО-N(СН), -CH(OR)(OR), -С(OR)(OR)(OR), -COOR, -CH-CO-NH, -CH=CHRили -CONHR, где Pg представляет защитную группу для спиртовой группы, Pgи Pgпредставляют защитные группы для аминогруппы, Rи Rнезависимо выбирают из алкильной, алкенильной, алкинильной и необязательно алкилзамещенной арильной или аралкильной групп или Rи Rвместе образуют цепь из 2-4 углеродных атомов, каждый из R, R, R, Rи Rнезависимо выбирают из алкила, алкенила, алкинила и необязательно алкилзамещенного арила или аралкила и Rпредставляет водород или метил, для образования соединения формулы (III), в которой R имеет определенные выше значения, с последующим превращением группы R в диметиламинометильную группу и выделением циталопрама в форме основания или его фармацевтически приемлемой соли.Отчет о международном поиске был опубликован 2002.01.31.
EA200200898A 2000-02-24 2001-02-22 Способ получения циталопрама EA005315B1 (ru)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DKPA200000296 2000-02-24
DKPA200000401 2000-03-13
PCT/DK2001/000123 WO2001043525A2 (en) 2000-02-24 2001-02-22 Method for the preparation of citalopram

Publications (2)

Publication Number Publication Date
EA200200898A1 true EA200200898A1 (ru) 2003-02-27
EA005315B1 EA005315B1 (ru) 2004-12-30

Family

ID=26068779

Family Applications (1)

Application Number Title Priority Date Filing Date
EA200200898A EA005315B1 (ru) 2000-02-24 2001-02-22 Способ получения циталопрама

Country Status (26)

Country Link
US (1) US6420574B2 (ru)
EP (1) EP1259501A2 (ru)
JP (1) JP2003523955A (ru)
KR (1) KR20020081355A (ru)
CN (1) CN1608057A (ru)
AR (1) AR029658A1 (ru)
AU (1) AU2001235358A1 (ru)
BE (1) BE1011177A6 (ru)
BG (1) BG107061A (ru)
BR (1) BR0108937A (ru)
CA (1) CA2401236A1 (ru)
EA (1) EA005315B1 (ru)
FR (1) FR2805812A1 (ru)
GR (1) GR1004073B (ru)
HR (1) HRP20020660A2 (ru)
HU (1) HUP0300212A2 (ru)
IE (1) IES20010163A2 (ru)
IL (1) IL151059A0 (ru)
IS (1) IS6487A (ru)
IT (1) ITMI20010386A1 (ru)
MX (1) MXPA02008228A (ru)
NL (1) NL1017415C1 (ru)
NO (1) NO20023928D0 (ru)
PL (1) PL363119A1 (ru)
SK (1) SK13672002A3 (ru)
WO (1) WO2001043525A2 (ru)

Families Citing this family (28)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR022329A1 (es) 1999-01-29 2002-09-04 Lundbeck & Co As H Metodo para la preparacion de 5-cianoftalida
NZ514671A (en) * 1999-04-14 2003-10-31 H Method for the preparation of citalopram
ITMI991581A1 (it) * 1999-06-25 2001-01-15 Lundbeck & Co As H Metodo per la preparazione di citalopram
DK1228056T3 (da) 1999-10-25 2005-01-24 Lundbeck & Co As H Fremgangsmåde til fremstilling af citalopram
AR026063A1 (es) 1999-11-01 2002-12-26 Lundbeck & Co As H Metodo para la preparacion de 5-carboxiftalida.
US6310222B1 (en) 1999-11-01 2001-10-30 Sumika Fine Chemicals Co., Ltd. Production method of 5-phthalancarbonitrile compound, intermediate therefor and production method of the intermediate
JP2003519136A (ja) 1999-12-28 2003-06-17 ハー・ルンドベック・アクチエゼルスカベット シタロプラムの製造方法
DE69912652T2 (de) 1999-12-30 2004-06-09 H. Lundbeck A/S Verfahren zur herstellung von citalopram
SI1254129T1 (en) * 2000-01-14 2004-02-29 H. Lundbeck A/S Method for the preparation of 5-cyanophthalide
US6433196B1 (en) * 2000-02-17 2002-08-13 Sumika Fine Chemicals Co., Ltd. Production method of citalopram, intermediate therefor and production method of the intermediate
NL1017417C1 (nl) * 2000-03-03 2001-03-16 Lundbeck & Co As H Werkwijze voor de bereiding van Citalopram.
NL1017500C1 (nl) 2000-03-13 2001-04-26 Lundbeck & Co As H Werkwijze voor de bereiding van Citalopram.
EP1265881A1 (en) * 2000-03-13 2002-12-18 H. Lundbeck A/S Stepwise alkylation of 5-substituted 1-(4-fluorophenyl)-1,3-dihydroisobenzofurans
NZ521201A (en) * 2000-03-13 2004-02-27 H Method for the preparation of citalopram
MXPA02008653A (es) 2000-03-14 2003-02-24 Lundbeck & Co As H Metodo para la preparacion de citalopram.
JP2003527388A (ja) * 2000-03-16 2003-09-16 ハー・ルンドベック・アクチエゼルスカベット 5−シアノ−1−(4−フルオロフェニル)−1,3−ジヒドロイソベンゾフランの製造方法
AR032455A1 (es) 2000-05-12 2003-11-12 Lundbeck & Co As H Metodo para la preparacion de citalopram, un intermediario empleado en el metodo, un metodo para la preparacion del intermediario empleado en el metodo y composicion farmaceutica antidepresiva
CA2354877C (en) 2000-08-18 2006-05-02 H. Lundbeck A/S Method for the preparation of citalopram
NL1017525C1 (nl) 2000-12-22 2001-04-26 Lundbeck & Co As H Werkwijze voor de bereiding van zuiver Citalopram
AR034759A1 (es) * 2001-07-13 2004-03-17 Lundbeck & Co As H Metodo para la preparacion de escitalopram
CA2465186A1 (en) * 2001-11-08 2003-05-15 Sepracor, Inc. Methods for treating depression and other cns disorders using enantiomerically enriched desmethyl- and didesmethyl-metabolites of citalopram
AR040970A1 (es) 2002-08-12 2005-04-27 Lundbeck & Co As H Metodo para la separacion de intermediarios que pueden ser utilizados para la preparacion de escitalopram
US20050154052A1 (en) * 2003-03-24 2005-07-14 Hetero Drugs Limited Novel crystalline forms of (s)-citalopram oxalate
WO2005047274A1 (en) * 2003-11-12 2005-05-26 Dr. Reddy's Laboratories, Inc. Preparation of escitalopram
TWI339651B (en) 2004-02-12 2011-04-01 Lundbeck & Co As H Method for the separation of intermediates which may be used for the preparation of escitalopram
GB0601286D0 (en) 2006-01-23 2006-03-01 Sandoz Ag Asymmetric synthesis
NZ580738A (en) * 2007-05-18 2012-02-24 Cipla Ltd Process for the preparation of escitalopram
WO2009111031A2 (en) * 2008-03-04 2009-09-11 Intra-Cellular Therapies, Inc. Methods of treating vasomotor symptoms

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1143703A (ru) 1965-03-18
GB1526331A (en) * 1976-01-14 1978-09-27 Kefalas As Phthalanes
GB8419963D0 (en) 1984-08-06 1984-09-12 Lundbeck & Co As H Intermediate compound and method
US5296007A (en) 1986-11-17 1994-03-22 Ensci Inc. Process for removing sulfur from coal
GB8814057D0 (en) 1988-06-14 1988-07-20 Lundbeck & Co As H New enantiomers & their isolation
DE19626659A1 (de) 1996-07-03 1998-01-08 Basf Ag Verfahren zur Herstellung von Phthaliden
DE19627697A1 (de) 1996-07-10 1998-01-15 Basf Ag Verfahren zur Herstellung von Phthaliden
KR100357975B1 (ko) 1997-07-08 2002-10-25 하. 룬트벡 아크티에 셀스카브 시탈로프램의 제조방법
UA62985C2 (en) 1997-11-10 2004-01-15 Lunnbeck As H A method for the preparation of citalopram
CN1286687A (zh) 1997-11-11 2001-03-07 H·隆德贝克有限公司 制备西酞普兰的方法
DE69904853T2 (de) 1998-10-20 2003-09-04 Lundbeck As Valby H Verfahren zur herstellung von citalopram
CA2356188C (en) 1998-12-23 2006-05-23 H. Lundbeck A/S Method for the preparation of 5-cyanophthalide
AR022329A1 (es) 1999-01-29 2002-09-04 Lundbeck & Co As H Metodo para la preparacion de 5-cianoftalida
NZ514671A (en) 1999-04-14 2003-10-31 H Method for the preparation of citalopram
ITMI991581A1 (it) 1999-06-25 2001-01-15 Lundbeck & Co As H Metodo per la preparazione di citalopram
ITMI991579A1 (it) 1999-06-25 2001-01-15 Lundbeck & Co As H Metodo per la preparazione di citalopram
ES2229774T3 (es) 1999-10-25 2005-04-16 H. Lundbeck A/S Metodo para la preparacion de citalopram.
US6310222B1 (en) 1999-11-01 2001-10-30 Sumika Fine Chemicals Co., Ltd. Production method of 5-phthalancarbonitrile compound, intermediate therefor and production method of the intermediate

Also Published As

Publication number Publication date
HUP0300212A2 (hu) 2003-06-28
ITMI20010386A1 (it) 2002-08-26
WO2001043525A3 (en) 2002-01-31
CN1608057A (zh) 2005-04-20
EA005315B1 (ru) 2004-12-30
MXPA02008228A (es) 2004-04-05
BE1011177A6 (fr) 2001-07-03
JP2003523955A (ja) 2003-08-12
KR20020081355A (ko) 2002-10-26
NO20023928L (no) 2002-08-19
EP1259501A2 (en) 2002-11-27
US20010027256A1 (en) 2001-10-04
IS6487A (is) 2002-07-29
FR2805812A1 (fr) 2001-09-07
AR029658A1 (es) 2003-07-10
AU2001235358A1 (en) 2001-06-25
GR20010100098A (el) 2001-10-31
SK13672002A3 (sk) 2003-03-04
BR0108937A (pt) 2003-06-17
IL151059A0 (en) 2003-04-10
NL1017415C1 (nl) 2001-05-18
NO20023928D0 (no) 2002-08-19
IES20010163A2 (en) 2002-03-06
WO2001043525A2 (en) 2001-06-21
PL363119A1 (en) 2004-11-15
BG107061A (en) 2003-05-30
US6420574B2 (en) 2002-07-16
HRP20020660A2 (en) 2004-12-31
CA2401236A1 (en) 2001-06-21
GR1004073B (el) 2002-11-26

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Legal Events

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MM4A Lapse of a eurasian patent due to non-payment of renewal fees within the time limit in the following designated state(s)

Designated state(s): AM AZ BY KZ KG MD TJ TM RU