BE2016C002I2 - - Google Patents

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Publication number
BE2016C002I2
BE2016C002I2 BE2016C002C BE2016C002C BE2016C002I2 BE 2016C002 I2 BE2016C002 I2 BE 2016C002I2 BE 2016C002 C BE2016C002 C BE 2016C002C BE 2016C002 C BE2016C002 C BE 2016C002C BE 2016C002 I2 BE2016C002 I2 BE 2016C002I2
Authority
BE
Belgium
Application number
BE2016C002C
Original Assignee
Astellas Pharma Inc
Wakunaga Pharma 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
Priority claimed from AU2002952355A external-priority patent/AU2002952355A0/en
Priority claimed from AU2003904813A external-priority patent/AU2003904813A0/en
Application filed by Astellas Pharma Inc, Wakunaga Pharma Co Ltd filed Critical Astellas Pharma Inc
Publication of BE2016C002I2 publication Critical patent/BE2016C002I2/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D501/00—Heterocyclic compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D501/14—Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16—Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/20—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/24—7-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids with hydrocarbon radicals, substituted by hetero atoms or hetero rings, attached in position 3
    • C07D501/38—Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof
    • C07D501/46—Methylene radicals, substituted by nitrogen atoms; Lactams thereof with the 2-carboxyl group; Methylene radicals substituted by nitrogen-containing hetero rings attached by the ring nitrogen atom; Quaternary compounds thereof with the 7-amino radical acylated by carboxylic acids containing hetero rings
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/33—Heterocyclic compounds
    • A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/542—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/545—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
    • A61K31/546—Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine containing further heterocyclic rings, e.g. cephalothin
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00—Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • A61P31/04—Antibacterial agents
    • Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00—Technologies relating to chemical industry
    • Y02P20/50—Improvements relating to the production of bulk chemicals
    • Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Public Health (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Epidemiology (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Cephalosporin Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
BE2016C002C 2002-10-30 2016-01-21 BE2016C002I2 (fr)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AU2002952355A AU2002952355A0 (en) 2002-10-30 2002-10-30 Cephem compounds
AU2003904813A AU2003904813A0 (en) 2003-09-04 Cephem Compounds

Publications (1)

Publication Number Publication Date
BE2016C002I2 true BE2016C002I2 (fr) 2023-03-07

Family

ID=32231625

Family Applications (1)

Application Number Title Priority Date Filing Date
BE2016C002C BE2016C002I2 (fr) 2002-10-30 2016-01-21

Country Status (19)

Country Link
US (2) US7129232B2 (fr)
EP (1) EP1556389B9 (fr)
JP (1) JP4448821B2 (fr)
KR (1) KR101023035B1 (fr)
AR (1) AR041729A1 (fr)
AT (1) ATE368042T1 (fr)
BE (1) BE2016C002I2 (fr)
BR (1) BRPI0315188B8 (fr)
CA (1) CA2504730C (fr)
DE (1) DE60315178T3 (fr)
DK (1) DK1556389T6 (fr)
ES (1) ES2290498T7 (fr)
FR (1) FR16C0004I2 (fr)
HU (1) HUS1600008I1 (fr)
LU (1) LU92943I2 (fr)
NL (1) NL300793I1 (fr)
PT (1) PT1556389E (fr)
TW (1) TWI319403B (fr)
WO (1) WO2004039814A1 (fr)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4251873B2 (ja) * 2001-05-01 2009-04-08 アステラス製薬株式会社 セフェム化合物
BRPI0315188B8 (pt) * 2002-10-30 2021-05-25 Astellas Pharma Inc composto e composição farmacêutica
AU2003902380A0 (en) * 2003-05-16 2003-06-05 Fujisawa Pharmaceutical Co., Ltd. Cephem compounds
JP4643577B2 (ja) * 2003-09-18 2011-03-02 アステラス製薬株式会社 セフェム化合物
EP2308562B1 (fr) * 2003-12-25 2015-02-25 Ono Pharmaceutical Co., Ltd. Composes cycliques d'azetidine et medicaments les renfermant
JP2009530228A (ja) * 2006-03-16 2009-08-27 アステラス製薬株式会社 セフェム化合物および抗菌薬としての利用
ITFE20060029A1 (it) * 2006-10-17 2008-04-18 Gruppo Kemon Spa Intermedi eterociclici primari per la colorazione ossidativa dei capelli a struttura pirazolica
CA2935651A1 (fr) 2007-10-09 2009-04-16 Gladius Pharmaceuticals Corporation Inhibiteurs de beta-lactamase a large spectre
MY173181A (en) 2011-05-13 2020-01-02 Array Biopharma Inc Pyrrolidinyl urea, pyrrolidinyl thiourea and pyrrolidinyl guanidine compounds as trka kinase inhibitors
SI3616695T1 (sl) 2011-09-09 2025-01-31 Merck Sharp & Dohme Llc Ceftolozan/tazobaktam za zdravljenje intrapulmonalnih okužb
EP2628730B1 (fr) * 2012-02-16 2017-12-06 Noxell Corporation Synthèse télescopique des sels de 5-amino-4-nitroso-1-alkyl-1h-pyrazole
US8809314B1 (en) 2012-09-07 2014-08-19 Cubist Pharmacueticals, Inc. Cephalosporin compound
WO2014052799A1 (fr) 2012-09-27 2014-04-03 Cubist Pharmaceuticals, Inc. Compositions antibiotiques à base d'arginine-tazobactame
US8476425B1 (en) 2012-09-27 2013-07-02 Cubist Pharmaceuticals, Inc. Tazobactam arginine compositions
US20140274999A1 (en) 2013-03-14 2014-09-18 Cubist Pharmaceuticals, Inc. Cephalosporin compositions and methods of manufacture
US9872906B2 (en) 2013-03-15 2018-01-23 Merck Sharp & Dohme Corp. Ceftolozane antibiotic compositions
UA121298C2 (uk) * 2013-03-15 2020-05-12 Мерк Шарп І Доум Корп. Антибіотична композиція на основі цефтолозану і тазобактаму
US20140274997A1 (en) 2013-03-15 2014-09-18 Cubist Pharmaceuticals, Inc. Cephalosporin pharmaceutical compositions
AU2014233637A1 (en) 2013-09-09 2015-03-26 Merck Sharp & Dohme Corp. Treating infections with ceftolozane/tazobactam in subjects having impaired renal function
US20160228448A1 (en) * 2013-09-27 2016-08-11 Merck Sharp & Dohme Corp. Solid Forms of Ceftolozane
US20150094293A1 (en) 2013-09-27 2015-04-02 Calixa Therapeutics, Inc. Solid forms of ceftolozane
US9120796B2 (en) 2013-10-02 2015-09-01 Cubist Pharmaceuticals, Inc. B-lactamase inhibitor picoline salt
LT3154959T (lt) 2014-05-15 2019-09-25 Array Biopharma, Inc. 1-((3s,4r)-4-(3-fluorfenil)-1-(2-metoksietil)pirolidin-3-il)-3-(4-metil-3-(2-metilpirimidin-5-il)-1-fenil-1h-pirazol-5-il)karbamidas kaip trka kinazės inhibitorius
CN106795175A (zh) 2014-08-15 2017-05-31 默沙东公司 头孢菌素化合物的合成
US10221196B2 (en) 2014-08-15 2019-03-05 Merck Sharp & Dohme Corp. Intermediates in the synthesis of cephalosporin compounds
WO2016028670A1 (fr) * 2014-08-18 2016-02-25 Merck Sharp & Dohme Corp. Formes salines de ceftolozane
WO2016100897A1 (fr) * 2014-12-18 2016-06-23 Merck Sharp & Dohme Corp. Composés dérivés de l'acide thiadiazolyl-oxyminoacétique
WO2016095860A1 (fr) * 2014-12-18 2016-06-23 Merck Sharp & Dohme Corp. Composés sous forme de dérivés d'acide pyrazolyl-carboxylique et de pyrazolyl-urée
US20160176897A1 (en) 2014-12-23 2016-06-23 Merck Sharp & Dohme Corp. 7-aminocephem derivative compounds
US10214543B2 (en) 2014-12-30 2019-02-26 Merck Sharp & Dohme Corp. Synthesis of cephalosporin compounds
ES2729026T3 (es) * 2015-06-29 2019-10-29 Sandoz Ag Procedimiento para la preparación de derivados de carbamoilamino pirazol
CN107922435B (zh) 2015-09-08 2022-05-17 桑多斯股份公司 由7-氨基头孢烷酸(7-aca)制备头孢洛扎的方法
KR20180066264A (ko) 2015-12-10 2018-06-18 나에자-알지엠 파마슈티칼스 유엘씨 세펨 화합물, 그의 제조 및 용도
CN109195967A (zh) 2016-06-06 2019-01-11 默沙东公司 头孢洛扎的固体形式和制备方法
CN107586305A (zh) * 2017-06-23 2018-01-16 浙江惠迪森药业有限公司 一种β‑内酰胺类化合物羧基及羟基保护基脱除方法
WO2019145784A2 (fr) * 2018-01-26 2019-08-01 Legochem Biosciences, Inc. Polythérapies pour agents pathogènes résistant aux médicaments multiples
CN109369535A (zh) * 2018-11-07 2019-02-22 浙江东邦药业有限公司 一种氨基甲酰氨基吡唑衍生化合物的制备方法

Family Cites Families (18)

* Cited by examiner, † Cited by third party
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GR78245B (fr) * 1980-09-12 1984-09-26 Ciba Geigy Ag
US5194432A (en) 1985-11-22 1993-03-16 Fujisawa Pharmaceutical Co., Ltd. Cephem compounds
CA1293719C (fr) * 1986-09-22 1991-12-31 Takao Takaya Composes de cephem et procede de preparation
US5210080A (en) * 1987-09-07 1993-05-11 Fujisawa Pharmaceutical Co., Ltd. Cephem compounds
US5663163A (en) * 1987-09-07 1997-09-02 Fujisawa Pharmaceutical Co., Ltd. Cephem compounds and processes for preparation thereof
IE63094B1 (en) * 1987-09-14 1995-03-22 Fujisawa Pharmaceutical Co Cephem compound and a process for preparation thereof
US5173485A (en) * 1988-03-09 1992-12-22 Fujisawa Pharmaceutical Company, Ltd. Cephem compounds
GB8905301D0 (en) * 1989-03-08 1989-04-19 Fujisawa Pharmaceutical Co New cephem compound and a process for preparation thereof
US5215982A (en) * 1989-11-10 1993-06-01 Fujisawa Pharmaceutical Co., Ltd. Cephem compounds
KR910015587A (ko) * 1990-02-27 1991-09-30 후지사와 토모키치로 세펨 화합물
GB9023479D0 (en) * 1990-10-29 1990-12-12 Fujisawa Pharmaceutical Co New cephem compounds and processes for preparation thereof
JPH09110877A (ja) 1995-10-17 1997-04-28 Katayama Seiyakushiyo:Kk セフェム化合物、その製造法及びそれを含有する抗菌剤
AUPN955596A0 (en) 1996-04-30 1996-05-23 Fujisawa Pharmaceutical Co., Ltd. New compound
TW526202B (en) * 1998-11-27 2003-04-01 Shionogi & Amp Co Broad spectrum cephem having benzo[4,5-b]pyridium methyl group of antibiotic activity
JP4251873B2 (ja) * 2001-05-01 2009-04-08 アステラス製薬株式会社 セフェム化合物
BRPI0315188B8 (pt) * 2002-10-30 2021-05-25 Astellas Pharma Inc composto e composição farmacêutica
AU2003902380A0 (en) * 2003-05-16 2003-06-05 Fujisawa Pharmaceutical Co., Ltd. Cephem compounds
JP4643577B2 (ja) * 2003-09-18 2011-03-02 アステラス製薬株式会社 セフェム化合物

Also Published As

Publication number Publication date
ES2290498T7 (es) 2015-07-10
JP2006506459A (ja) 2006-02-23
EP1556389B3 (fr) 2015-04-01
ATE368042T1 (de) 2007-08-15
KR20050084897A (ko) 2005-08-29
DE60315178D1 (de) 2007-09-06
JP4448821B2 (ja) 2010-04-14
BR0315188A (pt) 2005-09-06
KR101023035B1 (ko) 2011-03-24
ES2290498T3 (es) 2008-02-16
US7129232B2 (en) 2006-10-31
EP1556389B1 (fr) 2007-07-25
HK1086566A1 (zh) 2006-09-22
EP1556389B9 (fr) 2015-09-09
TW200410977A (en) 2004-07-01
DK1556389T6 (da) 2015-05-11
FR16C0004I2 (fr) 2017-01-06
TWI319403B (en) 2010-01-11
BRPI0315188B8 (pt) 2021-05-25
CA2504730C (fr) 2011-04-12
NL300793I2 (fr) 2016-03-15
WO2004039814A1 (fr) 2004-05-13
CA2504730A1 (fr) 2004-05-13
AR041729A1 (es) 2005-05-26
US20070037786A1 (en) 2007-02-15
LU92943I2 (fr) 2016-03-14
HUS1600008I1 (hu) 2016-03-29
DK1556389T3 (da) 2007-11-26
EP1556389A1 (fr) 2005-07-27
DE60315178T2 (de) 2008-04-30
BRPI0315188B1 (pt) 2017-04-25
NL300793I1 (fr) 2016-03-15
US20040132994A1 (en) 2004-07-08
DE60315178T3 (de) 2015-06-18
FR16C0004I1 (fr) 2016-03-25
PT1556389E (pt) 2007-11-08

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