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AR034321A1 - Un cristal anhidro de compuesto de beta-lactama y un procedimiento para su preparacion - Google Patents

Un cristal anhidro de compuesto de beta-lactama y un procedimiento para su preparacion

Info

Publication number
AR034321A1
AR034321A1 ARP020101581A ARP020101581A AR034321A1 AR 034321 A1 AR034321 A1 AR 034321A1 AR P020101581 A ARP020101581 A AR P020101581A AR P020101581 A ARP020101581 A AR P020101581A AR 034321 A1 AR034321 A1 AR 034321A1
Authority
AR
Argentina
Prior art keywords
beta
anhydrous crystal
tazobactam
formula
lactama
Prior art date
Application number
ARP020101581A
Other languages
English (en)
Inventor
Akihiro Shimabayashi
Shigetoshi Yaguchi
Original Assignee
Taiho Pharmaceutical Co Ltd
Otsuka Chemical Co Ltd
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=18981916&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=AR034321(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Application filed by Taiho Pharmaceutical Co Ltd, Otsuka Chemical Co Ltd filed Critical Taiho Pharmaceutical Co Ltd
Publication of AR034321A1 publication Critical patent/AR034321A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D499/00Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D499/87Compounds being unsubstituted in position 3 or with substituents other than only two methyl radicals attached in position 3, and with a carbon atom having three bonds to hetero atoms with at the most one bond to halogen, e.g. an ester or nitrile radical, directly attached in position 2
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D499/00Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04Antibacterial agents

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Other In-Based Heterocyclic Compounds (AREA)

Abstract

Un cristal anhidro de compuesto de beta-lactama representado por la fórmula (1). Un procedimiento para preparar el cristal anhidro de compuestos de beta-lactama representado por la fórmula (1), procedimiento que comprende los pasos de calentar una solución acuosa que contiene una sal de compuesto de beta-lactama representado por la fórmula (1) y ajustaNdo el pH de la solución acuosa a 3 o menos. El cristal anhidro de compuesto de beta-lactama(tazobactama)representado por la fórmula (1) muestra excelente estabilidad en almacenamiento y sustancialmente no se descompone incluso cuando se almacena a la temperatura común durante un tiempo prolongado. El cristal anhidro de tazobactama tiene una actividad farmacológica como la de la tazobactama conocida. Específicamente, el cristal anhidro de tazobactama presenta una actividad inhibitoria de beta- lactamasa cuando se une en forma irreversible a las beta-lactamasas producidas por microorganismos.
ARP020101581A 2001-05-01 2002-04-30 Un cristal anhidro de compuesto de beta-lactama y un procedimiento para su preparacion AR034321A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2001134187A JP3306473B1 (ja) 2001-05-01 2001-05-01 β−ラクタム化合物の無水結晶及びその製造法

Publications (1)

Publication Number Publication Date
AR034321A1 true AR034321A1 (es) 2004-02-18

Family

ID=18981916

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP020101581A AR034321A1 (es) 2001-05-01 2002-04-30 Un cristal anhidro de compuesto de beta-lactama y un procedimiento para su preparacion

Country Status (6)

Country Link
US (2) US7674898B2 (es)
JP (1) JP3306473B1 (es)
KR (1) KR100739103B1 (es)
CN (1) CN1247595C (es)
AR (1) AR034321A1 (es)
WO (1) WO2002090363A1 (es)

Families Citing this family (12)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
TW200523264A (en) * 2003-10-09 2005-07-16 Otsuka Chemical Co Ltd CMPB crystal and method for producing the same
TW200519119A (en) * 2003-10-10 2005-06-16 Otsuka Chemical Co Ltd PENAM crystal and process for producing the same
US7417143B2 (en) * 2004-04-07 2008-08-26 Orchid Chemicals & Pharmaceuticals Limited Process for the preparation of Tazobactam in pure form
US20150246931A1 (en) * 2012-09-06 2015-09-03 Hospira, Inc. Process for the preparation of tazobactam
US8476425B1 (en) 2012-09-27 2013-07-02 Cubist Pharmaceuticals, Inc. Tazobactam arginine compositions
CN105025901B (zh) * 2012-09-27 2019-04-19 默沙东公司 他唑巴坦精氨酸抗生素组合物
US9872906B2 (en) 2013-03-15 2018-01-23 Merck Sharp & Dohme Corp. Ceftolozane antibiotic compositions
US20140274990A1 (en) 2013-03-15 2014-09-18 Cubist Pharmaceuticals, Inc. Ceftolozane pharmaceutical compositions
DK2893929T3 (da) 2013-03-15 2025-07-07 Merck Sharp & Dohme Llc Antibiotisk ceftolozansammensætninger
AU2014233637A1 (en) 2013-09-09 2015-03-26 Merck Sharp & Dohme Corp. Treating infections with ceftolozane/tazobactam in subjects having impaired renal function
US8906898B1 (en) 2013-09-27 2014-12-09 Calixa Therapeutics, Inc. Solid forms of ceftolozane
CN104958302B (zh) * 2015-05-27 2016-11-16 济南康和医药科技有限公司 一种注射用头孢哌酮钠他唑巴坦钠药物组合物及其制备工艺

Family Cites Families (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4562073A (en) * 1982-12-24 1985-12-31 Taiho Pharmaceutical Company Limited Penicillin derivatives
JPS60214792A (ja) * 1984-04-06 1985-10-28 Taiho Yakuhin Kogyo Kk ペナム酸エステル誘導体
JP2602685B2 (ja) 1988-03-01 1997-04-23 大鵬薬品工業株式会社 2α−メチル−2β―(1,2,3−トリアゾール−1−イル)メチルペナム−3α−カルボン酸誘導体の製造法
JP2648750B2 (ja) * 1988-03-02 1997-09-03 大塚化学株式会社 β−ラクタム誘導体の製造方法
US4958020A (en) * 1989-05-12 1990-09-18 American Cyanamid Company Process for producing β-lactamase inhibitor
JPH03206093A (ja) * 1990-01-08 1991-09-09 Yoshitomi Pharmaceut Ind Ltd ペナムカルボン酸エステル
JPH03206038A (ja) * 1990-01-08 1991-09-09 Yoshitomi Pharmaceut Ind Ltd 抗菌剤
AU679800B2 (en) * 1993-11-06 1997-07-10 Taiho Pharmaceutical Co., Ltd. Crystalline penicillin derivative, and its production and use
JP3445664B2 (ja) * 1994-08-10 2003-09-08 大塚化学ホールディングス株式会社 アミノメチルペナム誘導体及びトリアゾリルメチルペナム誘導体の製造法

Also Published As

Publication number Publication date
KR100739103B1 (ko) 2007-07-13
JP3306473B1 (ja) 2002-07-24
WO2002090363A8 (fr) 2003-02-13
WO2002090363A1 (fr) 2002-11-14
US20090264642A1 (en) 2009-10-22
US7674898B2 (en) 2010-03-09
CN1505633A (zh) 2004-06-16
KR20030092117A (ko) 2003-12-03
US20040162277A1 (en) 2004-08-19
CN1247595C (zh) 2006-03-29
JP2002326993A (ja) 2002-11-15

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Legal Events

Date Code Title Description
FG Grant, registration
FD Application declared void or lapsed, e.g., due to non-payment of fee