MY142404A - A process for the preparation of racemic citalopram diol and/or s- or r- citalopram diols and the use of such diols for the preparation of racemic citalopram, ricitalopram and/or s-citalopram - Google Patents

A process for the preparation of racemic citalopram diol and/or s- or r- citalopram diols and the use of such diols for the preparation of racemic citalopram, ricitalopram and/or s-citalopram

Info

Publication number
MY142404A
MY142404A MYPI20034948A MYPI20034948A MY142404A MY 142404 A MY142404 A MY 142404A MY PI20034948 A MYPI20034948 A MY PI20034948A MY PI20034948 A MYPI20034948 A MY PI20034948A MY 142404 A MY142404 A MY 142404A
Authority
MY
Malaysia
Prior art keywords
diol
acid addition
free base
addition salt
citalopram
Prior art date
Application number
MYPI20034948A
Inventor
Eva Humble Rikke
Petersen Hans
Dancer Robert
Christiansen Brian
Original Assignee
H Lundbeck As
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 H Lundbeck As filed Critical H Lundbeck As
Publication of MY142404A publication Critical patent/MY142404A/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/32Separation; Purification; Stabilisation; Use of additives
    • C07C253/34Separation; Purification
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/275Nitriles; Isonitriles
    • A61K31/277Nitriles; Isonitriles having a ring, e.g. verapamil
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

THE PRESENT INVENTION RELATES TO A PROCESS FOR THE PREPARATION OF CERAMIC DIOL FREE BASE AND/OR ACID ADDITION SALT AND/OR R- OR S-DIOL FREE BASE AND/OR ACID ADDITION SALT COMPRISING A SEPARATION OF AN INITIAL NON-CERAMIC MIXTURE OF R-AND S-DIOL FREE BASE AND/OR ACID ADDITION SALT WITH MORE THAN 50OF ONE OF THE ENANTIOMERS INTO A FRACTION BEING ENRICHED WITH S-DIOL OF R-DIOL FREE BASE AND/OR ACID ADDITION SALT AND A FRACTION COMPRISING RS-DIOL FREE BASE AND/OR ACID ADDITION SALT WHEREIN THE RATIO OF R-DIOL:S-DIOL IS EQUAL TO 1:1 THAN IN THE INITIAL MIXTURE OF R- AND S-DIOL CHARACTERIZED IN THAT @i) RS-DIOL FREE BASE AND/OR ACID ADDITION SALT IS PRECIPITATED FROM A SOLUTION OF THE INITIAL NON-RACEMIC MIXTURE OF R- AND S-DIOL FREE BASE AND/OR ACID ADDITION SALT; OR @ R- OR S-DIOL FREE BASE AND/OR ACID ADDITION SALT IS DISSOLVED INTO A @ SOLVENT FROM THE INITIAL NON-RACEMIC MIXTURE OF R- AND S-DIOL FREE BASE AND/OR ACID ADDITION SALT IN SAID SOLVENT, LEAVING A RESIDUE COMPRISING RS-DIOL FREE BASE AND/OR ACID ADDITION SALT;@ii) THE RESIDUE/PRECIPITATE FORMED IS SEPARATED FROM THE FINAL SOLUTION PHASE;@iia) IF THE RESIDUE/PRECIPITATE IS CRYSTALLINE IT IS OPTIONALLE RECRYSTALLISED ONE OR MORE TIMES TO FORM RACEMIC DIOL;@iib) IF THE RESIDUE/PRECIPITATE IS NOT CRYSTALLINE, STEPS i) AND ii) ARE OPTIONALLY REPREATED UNTIL A CRYSTALLINE RESIDUE/PRECIPITATE IS OBTAINED AND THE CRYSTALLINE RESIDUE/PRECIPITATE IS OPTIONALLY RECRYSTALLINE ONE OR MORE TIMES TO FORM RECEMIC DIOL;@iii) THE FINAL SOLUTION PHASE IS OPTIONALLY SUBJECTED TO FURTHER PURIFICATION AND S-DIOL OR R-DIOL FREE BASE AND/OR ACID ADDITION SALT IS ISOLATED FROM THE FINAL SOLUTION PHASE;@THE FREE BASES OF THE DIOLS OBTAINED ARE OPTIONALLY CONVERTED TO ACID ADDITION SALTS THEREOF OR ACID ADDITION SALTS OF THE DIOLS OBTAINED ARE OPTIONALLY CONVERTED TO OTHER ACID ADDITION SALTS OR ACID ADDITION SALTS OF THE DIOLS
MYPI20034948A 2002-12-23 2003-12-22 A process for the preparation of racemic citalopram diol and/or s- or r- citalopram diols and the use of such diols for the preparation of racemic citalopram, ricitalopram and/or s-citalopram MY142404A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DKPA200202004 2002-12-23

Publications (1)

Publication Number Publication Date
MY142404A true MY142404A (en) 2010-11-30

Family

ID=35423357

Family Applications (1)

Application Number Title Priority Date Filing Date
MYPI20034948A MY142404A (en) 2002-12-23 2003-12-22 A process for the preparation of racemic citalopram diol and/or s- or r- citalopram diols and the use of such diols for the preparation of racemic citalopram, ricitalopram and/or s-citalopram

Country Status (17)

Country Link
KR (1) KR101076640B1 (en)
CN (1) CN100334071C (en)
AR (1) AR042655A1 (en)
BR (1) BR0317629A (en)
DK (1) DK1581483T3 (en)
EA (1) EA009061B1 (en)
ES (1) ES2385975T3 (en)
ME (1) MEP5708A (en)
MY (1) MY142404A (en)
PE (1) PE20050065A1 (en)
PT (1) PT1581483E (en)
RS (1) RS52152B (en)
SI (1) SI1581483T1 (en)
TW (1) TWI331605B (en)
UA (1) UA84859C2 (en)
UY (1) UY28146A1 (en)
ZA (1) ZA200504715B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
UA95199U (en) 2014-07-09 2014-12-10 PRECISION DISPOSER WITH ACCURATE DOSAGE FOR Bulk Products
CN110590602B (en) * 2019-09-25 2022-04-05 浙江海森药业股份有限公司 Resolution refining method of racemic citalopram diol

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8814057D0 (en) * 1988-06-14 1988-07-20 Lundbeck & Co As H New enantiomers & their isolation
AR034612A1 (en) * 2001-06-25 2004-03-03 Lundbeck & Co As H PROCESS FOR THE PREPARATION OF RACEMIC CITALOPRAM AND / OR OF THE S- OR R-CITALOPRAM THROUGH THE SEPARATION OF A MIXING OF R- AND S-CITALOPRAM

Also Published As

Publication number Publication date
TW200512202A (en) 2005-04-01
KR20050093801A (en) 2005-09-23
DK1581483T3 (en) 2012-07-23
UY28146A1 (en) 2004-07-30
EA009061B1 (en) 2007-10-26
UA84859C2 (en) 2008-12-10
CN1729164A (en) 2006-02-01
ME00034B (en) 2010-02-10
KR101076640B1 (en) 2011-10-27
BR0317629A (en) 2005-11-29
PT1581483E (en) 2012-07-24
MEP5708A (en) 2010-02-10
EA200501042A1 (en) 2005-12-29
AR042655A1 (en) 2005-06-29
CN100334071C (en) 2007-08-29
RS52152B (en) 2012-08-31
SI1581483T1 (en) 2012-09-28
ES2385975T3 (en) 2012-08-06
TWI331605B (en) 2010-10-11
RS20050488A (en) 2007-06-04
PE20050065A1 (en) 2005-02-18
ZA200504715B (en) 2006-08-30

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