AU1543797A - Process for preparing purine derivatives - Google Patents

Process for preparing purine derivatives

Info

Publication number
AU1543797A
AU1543797A AU15437/97A AU1543797A AU1543797A AU 1543797 A AU1543797 A AU 1543797A AU 15437/97 A AU15437/97 A AU 15437/97A AU 1543797 A AU1543797 A AU 1543797A AU 1543797 A AU1543797 A AU 1543797A
Authority
AU
Australia
Prior art keywords
preparing
purine derivatives
intermediates
preparing purine
purin
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.)
Abandoned
Application number
AU15437/97A
Inventor
Humberto B. Arzeno
Steven D. Axt
Colin C. Beard
Charles A. Dvorak
Paul R. Fatheree
Lawrence E. Fisher
Yeun-Kwei Han
Eric R Humphreys
Jan P. Lund
Sam Linh Nguyen
Douglas Leslie Wren
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.)
F Hoffmann La Roche AG
Original Assignee
F Hoffmann La Roche 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 F Hoffmann La Roche AG filed Critical F Hoffmann La Roche AG
Publication of AU1543797A publication Critical patent/AU1543797A/en
Abandoned legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • C07D473/02Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6
    • C07D473/18Heterocyclic compounds containing purine ring systems with oxygen, sulphur, or nitrogen atoms directly attached in positions 2 and 6 one oxygen and one nitrogen atom, e.g. guanine
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D473/00Heterocyclic compounds containing purine ring systems
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/495Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with two or more nitrogen atoms as the only ring heteroatoms, e.g. piperazine or tetrazines
    • A61K31/505Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim
    • A61K31/519Pyrimidines; Hydrogenated pyrimidines, e.g. trimethoprim ortho- or peri-condensed with heterocyclic rings
    • A61K31/52Purines, e.g. adenine

Landscapes

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

Abstract

Process and novel intermediates for preparing the L-monovaline ester of 2-(2-amino-1,6-dihydro-6-oxo-purin-9-yl)methoxy-1,3-propanediol and its pharmaceutically acceptable salts. The present process and intermediates provide for reduced impurities in the mono-valine ester end-product, also eliminating the costly and time consuming purification step and allowing the use of starting materials of lower purity, which, in turn, reduces overall production costs. These products are of value as antiviral agents with improved absorption.
AU15437/97A 1996-01-26 1997-01-21 Process for preparing purine derivatives Abandoned AU1543797A (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US59207996A 1996-01-26 1996-01-26
US592079 1996-01-26
PCT/EP1997/000262 WO1997027198A1 (en) 1996-01-26 1997-01-21 Process for preparing purine derivatives

Publications (1)

Publication Number Publication Date
AU1543797A true AU1543797A (en) 1997-08-20

Family

ID=24369197

Family Applications (1)

Application Number Title Priority Date Filing Date
AU15437/97A Abandoned AU1543797A (en) 1996-01-26 1997-01-21 Process for preparing purine derivatives

Country Status (10)

Country Link
JP (1) JP4094667B2 (en)
KR (1) KR100491941B1 (en)
CN (1) CN1064683C (en)
AT (1) ATE222909T1 (en)
AU (1) AU1543797A (en)
CA (1) CA2243650C (en)
DE (1) DE69714971T3 (en)
ES (1) ES2180923T5 (en)
MX (1) MX9805935A (en)
WO (1) WO1997027198A1 (en)

Families Citing this family (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US6703394B2 (en) 1996-02-16 2004-03-09 Medivir Ab Acyclic nucleoside derivatives
US5869493A (en) 1996-02-16 1999-02-09 Medivir Ab Acyclic nucleoside derivatives
WO2005023827A1 (en) * 2003-09-11 2005-03-17 F. Hoffmann-La Roche Ag Process for preparing antiviral nucleoside derivatives
ZA200702234B (en) * 2006-03-21 2008-07-30 Cipla Ltd Preparation of ester of purine derivatives
WO2012163373A1 (en) * 2011-05-31 2012-12-06 Pharmathen S.A. Process for the preparation of 2-amino-9-((2-phenyl-1,3-dioxan-5-yloxy)methyl)-1h-purin-6(9h)-one compound useful in the preparation of valganciclovir

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4816447A (en) * 1981-08-26 1989-03-28 Merck & Co., Inc. Anti-viral guanine compounds
NL8202626A (en) * 1982-06-29 1984-01-16 Stichting Rega V Z W DERIVATIVES OF 9- (2-HYDROXYETHOXYMETHYL) GUANINE.
AP160A (en) * 1987-08-15 1991-11-18 The Wellcome Foundation Ltd Therapeutic acyclic nucleosides.
DE68922903T2 (en) * 1988-12-19 1995-11-23 Wellcome Found Antiviral pyrimidine and purine compounds, processes for their preparation and pharmaceutical preparations containing them.
JP3225545B2 (en) * 1991-09-18 2001-11-05 味の素株式会社 Method for producing acyclic nucleosides
PE32296A1 (en) * 1994-07-28 1996-08-07 Hoffmann La Roche L-MONOVALINE ESTER DERIVED FROM 2- (2-AMINO-1,6-DIHYDRO-6-OXO-PURIN-9-IL) METOXI-1,3-PROPANDIOL AND ITS PHARMACEUTICALLY ACCEPTABLE SALTS

Also Published As

Publication number Publication date
CA2243650A1 (en) 1997-07-31
ATE222909T1 (en) 2002-09-15
ES2180923T5 (en) 2005-10-16
CA2243650C (en) 2006-08-15
ES2180923T3 (en) 2003-02-16
CN1212693A (en) 1999-03-31
JP2000503977A (en) 2000-04-04
DE69714971T3 (en) 2005-12-15
JP4094667B2 (en) 2008-06-04
WO1997027198A1 (en) 1997-07-31
KR100491941B1 (en) 2005-08-05
CN1064683C (en) 2001-04-18
MX9805935A (en) 1998-11-30
DE69714971D1 (en) 2002-10-02
DE69714971T2 (en) 2003-05-28
KR19990081991A (en) 1999-11-15

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