UY25779A1 - Procedimiento para la preparación de una forma anhidra de clorhidrato de valaciclovir - Google Patents

Procedimiento para la preparación de una forma anhidra de clorhidrato de valaciclovir

Info

Publication number
UY25779A1
UY25779A1 UY25779A UY25779A UY25779A1 UY 25779 A1 UY25779 A1 UY 25779A1 UY 25779 A UY25779 A UY 25779A UY 25779 A UY25779 A UY 25779A UY 25779 A1 UY25779 A1 UY 25779A1
Authority
UY
Uruguay
Prior art keywords
valacyclovir
hydrochloride
crystalline form
valacyclovir hydrochloride
anhydrous crystalline
Prior art date
Application number
UY25779A
Other languages
English (en)
Spanish (es)
Inventor
Peter Gregory Varlashkin
Richard Augustus Winnike
David James Whatrup
Jane Muse Partin
David Michael Skinner
Philip George Lake
Gregory Alan Conway
William Bayne Grubb Iii
Barry Howard Carter
Original Assignee
Wellcome Found
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
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=10768347&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=UY25779(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Wellcome Found filed Critical Wellcome Found
Publication of UY25779A1 publication Critical patent/UY25779A1/es

Links

Classifications

    • 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
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/12Antivirals
    • A61P31/20Antivirals for DNA viruses
    • A61P31/22Antivirals for DNA viruses for herpes viruses

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Virology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Engineering & Computer Science (AREA)
  • Biotechnology (AREA)
  • Molecular Biology (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Peptides Or Proteins (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Saccharide Compounds (AREA)
UY25779A 1995-01-20 1999-10-29 Procedimiento para la preparación de una forma anhidra de clorhidrato de valaciclovir UY25779A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GBGB9501178.9A GB9501178D0 (en) 1995-01-20 1995-01-20 Guanine derivative

Publications (1)

Publication Number Publication Date
UY25779A1 true UY25779A1 (es) 2000-08-21

Family

ID=10768347

Family Applications (1)

Application Number Title Priority Date Filing Date
UY25779A UY25779A1 (es) 1995-01-20 1999-10-29 Procedimiento para la preparación de una forma anhidra de clorhidrato de valaciclovir

Country Status (40)

Country Link
US (1) US6107302A (enExample)
EP (1) EP0804436B1 (enExample)
JP (1) JP3176633B2 (enExample)
KR (1) KR100376074B1 (enExample)
CN (1) CN1049893C (enExample)
AP (1) AP662A (enExample)
AR (1) AR002270A1 (enExample)
AT (1) ATE302777T1 (enExample)
AU (1) AU702794B2 (enExample)
BG (1) BG63393B1 (enExample)
BR (1) BR9606768A (enExample)
CA (1) CA2210799C (enExample)
CY (1) CY2531B1 (enExample)
CZ (1) CZ297065B6 (enExample)
DE (1) DE69635106T2 (enExample)
DK (1) DK0804436T3 (enExample)
EA (1) EA000364B1 (enExample)
EE (1) EE03528B1 (enExample)
ES (1) ES2248806T3 (enExample)
FI (1) FI973063L (enExample)
GB (1) GB9501178D0 (enExample)
GE (1) GEP20001940B (enExample)
HR (1) HRP960024B1 (enExample)
HU (1) HU222993B1 (enExample)
IL (1) IL116831A (enExample)
IN (1) IN182468B (enExample)
IS (1) IS2268B (enExample)
NO (1) NO315558B1 (enExample)
NZ (1) NZ298851A (enExample)
OA (1) OA10499A (enExample)
PL (1) PL182175B1 (enExample)
RO (1) RO118693B1 (enExample)
RS (1) RS49518B (enExample)
SI (1) SI0804436T1 (enExample)
SK (1) SK285329B6 (enExample)
TR (1) TR199700656T1 (enExample)
UA (1) UA46001C2 (enExample)
UY (1) UY25779A1 (enExample)
WO (1) WO1996022291A1 (enExample)
ZA (1) ZA96449B (enExample)

Families Citing this family (61)

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GB9501178D0 (en) * 1995-01-20 1995-03-08 Wellcome Found Guanine derivative
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WO2003040145A1 (en) * 2001-11-05 2003-05-15 Glaxo Group Limited Anhydrous crystal form of valaciclovir hydrochloride
MX242714B (es) * 2001-11-14 2006-12-15 Teva Pharma Sintesis y purificacion de valaciclovir.
AU2003240213A1 (en) * 2002-06-24 2004-01-06 Ranbaxy Laboratories Limited Process for the preparation of robust formulations of valacyclovir hydrochloride tablets
US7407955B2 (en) * 2002-08-21 2008-08-05 Boehringer Ingelheim Pharma Gmbh & Co., Kg 8-[3-amino-piperidin-1-yl]-xanthines, the preparation thereof and their use as pharmaceutical compositions
US20050043329A1 (en) * 2002-09-06 2005-02-24 Shlomit Wizel Crystalline forms of valacyclovir hydrochloride
US20050059684A1 (en) * 2002-10-16 2005-03-17 Ben-Zion Dolitzky Method for reducing residual alcohols in crystalline valacyclovir hydrochloride
US20050070711A1 (en) * 2002-10-16 2005-03-31 Igor Lifshitz Method for reducing residual alcohols in crystalline valacyclovir hydrochloride
AU2003289995A1 (en) * 2002-12-09 2004-06-30 Texcontor Etablissement Anhydrous crystalline form of valacyclovir hydrochloride
EP1633753A1 (en) * 2003-05-30 2006-03-15 EOS Eczacibasi Ozgun Kimyasal Urunler Sanayi Ve Ti Caret A.S. Novel crystalline forms of valacyclovir hydrochloride
CA2527708A1 (en) * 2003-06-02 2005-01-06 Teva Pharmaceutical Industries Ltd. Crystalline forms of valacyclovir hydrochloride
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US7846937B2 (en) * 2005-05-25 2010-12-07 Eli Lilly And Company Cyclopropanecarboxylate esters of acyclovir
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DE102005035891A1 (de) 2005-07-30 2007-02-08 Boehringer Ingelheim Pharma Gmbh & Co. Kg 8-(3-Amino-piperidin-1-yl)-xanthine, deren Herstellung und deren Verwendung als Arzneimittel
US20070112193A1 (en) * 2005-11-14 2007-05-17 Khunt Mayur D Valacyclovir process
PE20080251A1 (es) 2006-05-04 2008-04-25 Boehringer Ingelheim Int Usos de inhibidores de dpp iv
EP2540725A1 (de) 2006-05-04 2013-01-02 Boehringer Ingelheim International GmbH Polymorphe von 1-((4-Methyl-chinazolin-2-yl)methyl)-3-methyl-7-(2-butin-1-yl)-8-(3-(R)-amino-piperidin-1-yl)xanthin
EP1852108A1 (en) 2006-05-04 2007-11-07 Boehringer Ingelheim Pharma GmbH & Co.KG DPP IV inhibitor formulations
CN1903854B (zh) * 2006-08-09 2012-05-23 丽珠医药集团股份有限公司 一种合成盐酸伐昔洛韦的方法
US20080167325A1 (en) * 2006-12-27 2008-07-10 Bs Praveen Kumar Valacyclovir compositions
US20080281099A1 (en) * 2007-05-07 2008-11-13 Mayur Devjibhai Khunt Process for purifying valacyclovir hydrochloride and intermediates thereof
GB0710277D0 (en) * 2007-05-30 2007-07-11 Univ Birmingham Use of antivirals in the treatment of medical disorders
CN101784278A (zh) * 2007-08-17 2010-07-21 贝林格尔.英格海姆国际有限公司 用于治疗fab-相关的疾病的嘌呤衍生物
JPWO2009031576A1 (ja) * 2007-09-03 2010-12-16 味の素株式会社 バラシクロビル塩酸塩結晶の製造方法
US20090076039A1 (en) * 2007-09-14 2009-03-19 Protia, Llc Deuterium-enriched valacyclovir
PE20091730A1 (es) 2008-04-03 2009-12-10 Boehringer Ingelheim Int Formulaciones que comprenden un inhibidor de dpp4
PE20100156A1 (es) * 2008-06-03 2010-02-23 Boehringer Ingelheim Int Tratamiento de nafld
UY32030A (es) 2008-08-06 2010-03-26 Boehringer Ingelheim Int "tratamiento para diabetes en pacientes inapropiados para terapia con metformina"
BRPI0916997A2 (pt) 2008-08-06 2020-12-15 Boehringer Ingelheim International Gmbh Inibidor de dpp-4 e seu uso
AU2009281122C1 (en) * 2008-08-15 2016-04-21 Boehringer Ingelheim International Gmbh Purin derivatives for use in the treatment of fab-related diseases
JP2012502081A (ja) 2008-09-10 2012-01-26 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング 糖尿病及び関連症状の治療のための組み合わせ治療
US20200155558A1 (en) 2018-11-20 2020-05-21 Boehringer Ingelheim International Gmbh Treatment for diabetes in patients with insufficient glycemic control despite therapy with an oral antidiabetic drug
MX2011006713A (es) 2008-12-23 2011-07-13 Boehringer Ingelheim Int Formas salinas de compuesto organico.
TW201036975A (en) 2009-01-07 2010-10-16 Boehringer Ingelheim Int Treatment for diabetes in patients with inadequate glycemic control despite metformin therapy
KR20120107080A (ko) 2009-11-27 2012-09-28 베링거 인겔하임 인터내셔날 게엠베하 리나글립틴과 같은 dpp-iv 억제제를 사용한 유전자형 검사된 당뇨병 환자의 치료
CN107961377B (zh) 2010-05-05 2022-11-22 勃林格殷格翰国际有限公司 组合疗法
WO2011158252A1 (en) 2010-06-15 2011-12-22 Matrix Laboratories Ltd Process for the preparation of valacyclovir hydrochloride polymorphic form ii
KR20130093012A (ko) 2010-06-24 2013-08-21 베링거 인겔하임 인터내셔날 게엠베하 당뇨병 요법
US9034883B2 (en) 2010-11-15 2015-05-19 Boehringer Ingelheim International Gmbh Vasoprotective and cardioprotective antidiabetic therapy
CN102584825B (zh) * 2011-01-17 2014-04-02 四川科伦药物研究有限公司 一种合成盐酸伐昔洛韦的方法
EP3517539B1 (en) 2011-07-15 2022-12-14 Boehringer Ingelheim International GmbH Substituted dimeric quinazoline derivative, its preparation and its use in pharmaceutical compositions for the treatment of type i and ii diabetes
US20140296520A1 (en) * 2011-11-25 2014-10-02 Piramal Enterprises Limited Process for the preparation of valacyclovir hydrochloride
US9555001B2 (en) 2012-03-07 2017-01-31 Boehringer Ingelheim International Gmbh Pharmaceutical composition and uses thereof
EP3685839A1 (en) 2012-05-14 2020-07-29 Boehringer Ingelheim International GmbH Linagliptin for use in the treatment of albuminuria and kidney related diseases
WO2013171166A1 (en) 2012-05-14 2013-11-21 Boehringer Ingelheim International Gmbh A xanthine derivative as dpp-4 inhibitor for use in the treatment of sirs and/or sepsis
WO2013174767A1 (en) 2012-05-24 2013-11-28 Boehringer Ingelheim International Gmbh A xanthine derivative as dpp -4 inhibitor for use in modifying food intake and regulating food preference
JP6615109B2 (ja) 2014-02-28 2019-12-04 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング Dpp−4阻害薬の医学的使用
MX390363B (es) 2016-06-10 2025-03-20 Boehringer Ingelheim Int Combinacion de linagliptina y metformina
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* Cited by examiner, † Cited by third party
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AP55A (en) * 1987-08-15 1989-09-26 The Wellcome Foundation Ltd Therapeutic Acyclic Nucleosides
ATE199719T1 (de) * 1993-06-10 2001-03-15 Rolabo Sl Verfahren zur herstellung von aminosäureester von nukleosid analogen
GB9501178D0 (en) * 1995-01-20 1995-03-08 Wellcome Found Guanine derivative

Also Published As

Publication number Publication date
TR199700656T1 (xx) 1998-03-21
SI0804436T1 (sl) 2006-02-28
GEP20001940B (en) 2000-02-05
BR9606768A (pt) 1997-12-30
US6107302A (en) 2000-08-22
IL116831A (en) 1998-10-30
AU4453996A (en) 1996-08-07
HRP960024B1 (en) 2005-08-31
FI973063A7 (fi) 1997-09-18
BG63393B1 (bg) 2001-12-29
CN1049893C (zh) 2000-03-01
EA000364B1 (ru) 1999-06-24
OA10499A (en) 2002-04-10
HRP960024A2 (en) 1997-10-31
EP0804436B1 (en) 2005-08-24
NZ298851A (en) 1999-01-28
RS49518B (sr) 2006-10-27
NO973326L (no) 1997-09-16
DK0804436T3 (da) 2005-12-27
FI973063A0 (fi) 1997-07-18
ATE302777T1 (de) 2005-09-15
YU3396A (sh) 1998-12-23
GB9501178D0 (en) 1995-03-08
PL182175B1 (pl) 2001-11-30
CZ229497A3 (en) 1997-12-17
IL116831A0 (en) 1996-05-14
WO1996022291A1 (en) 1996-07-25
JPH11503718A (ja) 1999-03-30
IS4527A (is) 1997-07-15
FI973063L (fi) 1997-09-18
CA2210799A1 (en) 1996-07-25
IN182468B (enExample) 1999-04-17
AP662A (en) 1998-08-19
KR100376074B1 (ko) 2003-06-02
SK96597A3 (en) 1998-02-04
AU702794B2 (en) 1999-03-04
EP0804436A1 (en) 1997-11-05
CN1179159A (zh) 1998-04-15
SK285329B6 (sk) 2006-11-03
CA2210799C (en) 2008-06-10
BG101833A (bg) 1998-04-30
CY2531B1 (en) 2006-04-12
EE03528B1 (et) 2001-10-15
RO118693B1 (ro) 2003-09-30
CZ297065B6 (cs) 2006-08-16
EA199700124A1 (ru) 1997-12-30
ES2248806T3 (es) 2006-03-16
PL321326A1 (en) 1997-12-08
IS2268B (is) 2007-07-15
JP3176633B2 (ja) 2001-06-18
HU222993B1 (hu) 2004-01-28
HUP9801836A3 (en) 1999-06-28
NO315558B1 (no) 2003-09-22
MX9705462A (es) 1997-10-31
NO973326D0 (no) 1997-07-18
AR002270A1 (es) 1998-03-11
AP9701058A0 (en) 1997-10-31
DE69635106T2 (de) 2006-06-08
UA46001C2 (uk) 2002-05-15
KR19980701525A (ko) 1998-05-15
DE69635106D1 (de) 2005-09-29
EE9700175A (et) 1998-02-16
HUP9801836A2 (hu) 1999-05-28
ZA96449B (en) 1996-08-07

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Effective date: 20191029