ATE278691T1 - Verbesserter prozess zur herstellung von carbapenemen - Google Patents

Verbesserter prozess zur herstellung von carbapenemen

Info

Publication number
ATE278691T1
ATE278691T1 AT02701042T AT02701042T ATE278691T1 AT E278691 T1 ATE278691 T1 AT E278691T1 AT 02701042 T AT02701042 T AT 02701042T AT 02701042 T AT02701042 T AT 02701042T AT E278691 T1 ATE278691 T1 AT E278691T1
Authority
AT
Austria
Prior art keywords
improved process
carbapenems
producing
producing carbapenems
improved
Prior art date
Application number
AT02701042T
Other languages
English (en)
Inventor
John M Williams
Renato Skerlj
Original Assignee
Merck & Co Inc
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 Merck & Co Inc filed Critical Merck & Co Inc
Application granted granted Critical
Publication of ATE278691T1 publication Critical patent/ATE278691T1/de

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D477/00—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring
    • C07D477/10—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, 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
    • C07D477/12—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, 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 with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached in position 6
    • C07D477/16—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached in position 4, 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 with hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, attached in position 6 with hetero atoms or carbon atoms 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 3
    • C07D477/20—Sulfur atoms
    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D477/00—Heterocyclic compounds containing 1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbapenicillins, thienamycins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulphur-containing hetero ring
    • C07D477/02—Preparation
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D487/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00
    • C07D487/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, not provided for by groups C07D451/00 - C07D477/00 in which the condensed system contains two hetero rings
    • C07D487/04—Ortho-condensed systems
    • 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)
  • Molecular Biology (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Animal Behavior & Ethology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Communicable Diseases (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Oncology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
AT02701042T 2001-01-16 2002-01-11 Verbesserter prozess zur herstellung von carbapenemen ATE278691T1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
US26193301P 2001-01-16 2001-01-16
US29344001P 2001-05-24 2001-05-24
PCT/US2002/000821 WO2002057266A1 (en) 2001-01-16 2002-01-11 Improved process for carbapenem synthesis

Publications (1)

Publication Number Publication Date
ATE278691T1 true ATE278691T1 (de) 2004-10-15

Family

ID=26948925

Family Applications (1)

Application Number Title Priority Date Filing Date
AT02701042T ATE278691T1 (de) 2001-01-16 2002-01-11 Verbesserter prozess zur herstellung von carbapenemen

Country Status (29)

Country Link
US (1) US7071330B2 (de)
EP (1) EP1353923B1 (de)
JP (1) JP4098626B2 (de)
KR (1) KR100827562B1 (de)
CN (1) CN1249065C (de)
AR (1) AR035728A1 (de)
AT (1) ATE278691T1 (de)
AU (1) AU2002234240B2 (de)
BR (1) BR0206372A (de)
CA (1) CA2433874C (de)
CZ (1) CZ301440B6 (de)
DE (1) DE60201498T2 (de)
DK (1) DK1353923T3 (de)
EA (1) EA006098B1 (de)
EG (1) EG23993A (de)
ES (1) ES2227423T3 (de)
HR (1) HRP20030566B1 (de)
HU (1) HUP0302764A3 (de)
IL (2) IL156507A0 (de)
MX (1) MXPA03006322A (de)
NZ (1) NZ527191A (de)
PL (1) PL362912A1 (de)
PT (1) PT1353923E (de)
RS (1) RS50494B (de)
SI (1) SI1353923T1 (de)
SK (1) SK287350B6 (de)
TW (1) TWI318627B (de)
UA (1) UA74870C2 (de)
WO (1) WO2002057266A1 (de)

Families Citing this family (19)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003016312A1 (en) * 2001-08-13 2003-02-27 Eisai Co., Ltd. Process for preparation of carbapenem antibiotics
WO2003026572A2 (en) * 2001-09-26 2003-04-03 Merck & Co., Inc. Crystalline forms of ertapenem sodium
WO2003027067A2 (en) * 2001-09-26 2003-04-03 Merck & Co., Inc. Process for making carbapenem compounds
HUP0402112A2 (hu) * 2001-11-16 2005-02-28 Ranbaxy Laboratories Limited Eljárás kristályos imipenem előállítására
CN101172962B (zh) * 2002-11-13 2010-09-08 株式会社钟化 经口给药用碳青霉素烯化合物的合成中间体
DE102005025899A1 (de) * 2005-06-06 2006-12-07 Basf Ag Verfahren zur Aufbereitung eines Alkoxycarbonylaminotriazin enthaltenden Reaktionsgemisches
AU2006290416B2 (en) * 2005-09-15 2012-04-12 Orchid Chemicals And Pharmaceuticals Limited An improved process for the preparation of beta-lactam antibiotic
TW200801004A (en) * 2006-03-28 2008-01-01 Kaneka Corp Improved process for producing carbapenem compound
WO2008062279A2 (en) * 2006-11-20 2008-05-29 Orchid Chemicals & Pharmaceuticals Limited An improved process for the preparation of carbapenem antibiotic
CN101357920B (zh) * 2007-06-22 2011-01-12 山东轩竹医药科技有限公司 含有巯基吡咯烷甲酰胺基三嗪的培南化合物
CN101367807B (zh) * 2007-06-28 2011-01-12 山东轩竹医药科技有限公司 被巯基吡咯烷甲酰胺基吡啶取代的培南衍生物
CN101875665B (zh) 2009-04-30 2013-02-06 石药集团中奇制药技术（石家庄）有限公司 一种厄他培南中间体、含其的组合物及其制备方法
US20130079322A1 (en) * 2010-05-21 2013-03-28 Xuanzhu Pharama Co., Ltd. Crystalline of carbapenem derivative or its hydrate, preparation methods and uses thereof
US8822445B2 (en) 2010-06-03 2014-09-02 Xuanzhu Pharma Co., Ltd. Crystalline form of carbapenem derivative or its hydrates and preparation methods and uses thereof
WO2012038979A2 (en) * 2010-09-24 2012-03-29 Sequent Anti Biotics Private Limited A process for preparation of ertapenem
CN102558182B (zh) 2010-12-31 2015-02-11 石药集团中奇制药技术（石家庄）有限公司 一种厄他培南钠晶型及其制备方法
WO2013121279A2 (en) * 2012-02-14 2013-08-22 Aurobindo Pharma Limited Process to prepare ertapenem
WO2014097221A1 (en) * 2012-12-21 2014-06-26 Ranbaxy Laboratories Limited Process for the purification of biapenem
ES2731242T3 (es) * 2014-03-27 2019-11-14 Johnson Matthey Plc Procedimiento de preparación de un antibiótico carbapenem

Family Cites Families (26)

* Cited by examiner, † Cited by third party
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BE794554A (fr) * 1972-01-31 1973-07-26 Lilly Co Eli Nouveaux derives de penicilline et de cephalusporine
US3925372A (en) * 1973-02-23 1975-12-09 Lilly Co Eli Alpha-aminoacyl-3-halo cephalosporins
US3897424A (en) * 1973-07-23 1975-07-29 Lilly Co Eli Process for 7-{62 -amino-7-{60 -methoxy-cephalosporanic acid esters and related compounds
AR207327A1 (es) * 1974-02-06 1976-09-30 Lilly Co Eli Un procedimiento para preparar acidos 3-cefem 3-sulfonatos y sus esteres
US4001226A (en) * 1974-12-04 1977-01-04 Eli Lilly And Company 3-(substituted)carbonylamino cephem derivatives
US3992377A (en) * 1974-12-13 1976-11-16 Eli Lilly And Company 3-Thio-substituted cephalosporin antibiotics
US3985746A (en) * 1975-03-25 1976-10-12 E. R. Squibb & Sons, Inc. 7-(α-Cyanomethylthio)acetamido-3-cephem carboxylates
US4217453A (en) * 1978-07-24 1980-08-12 Merck & Co., Inc. 6-Amido-3-substituted-amino-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylic acid
US4656263A (en) * 1979-03-05 1987-04-07 Pfizer Inc. 6-β-substituted penicillanic acid compound free of the 6-α-epimer
US4299954A (en) * 1979-11-05 1981-11-10 Eli Lilly And Company Cephalosporin vinyl halides
US4414155A (en) 1980-01-14 1983-11-08 Merck & Co., Inc. Synthesis of thienamycin via esters of (3SR, 4RS)-3-[(SR)-1-hydroxyethyl]-β,2-dioxo-4-azetidinebutanoic acid
US4269772A (en) 1980-01-14 1981-05-26 Merck & Co., Inc. Synthesis of thienamycin via trans-3-carboxymethylene-4-carboxy-5-methyl-Δ2 -isoxazoline
US4369187A (en) * 1980-02-06 1983-01-18 Merck & Co., Inc. 3-Substituted-1-azabicyclo[3.2.0]hept-2-en-7-one-2-carboxylic acid
US4383946A (en) 1980-03-27 1983-05-17 Merck & Co., Inc. Process for the preparation of 1-carbapenems and intermediates via silyl-substituted dithioacetals
US4501741A (en) * 1983-04-12 1985-02-26 Eli Lilly And Company Cephalosporin antibiotics
US4783453A (en) * 1985-06-10 1988-11-08 Merck & Co., Inc. 2-aza-substituted 1-carbadethiapen-2-em-3-carboxylic acids
JPS6475488A (en) * 1987-09-17 1989-03-22 Sumitomo Pharma Production of beta-lactam compound
US5034384A (en) 1990-08-01 1991-07-23 Merck & Co., Inc. 2-(9-fluorenonyl)-carbapenem antibacterial agents
GB9202298D0 (en) 1992-02-04 1992-03-18 Ici Plc Antibiotic compounds
CA2091309A1 (en) 1992-03-26 1993-09-27 Frederic H. Jung Antibiotic compounds
HRP970281B1 (en) 1996-05-28 2002-04-30 Merck & Co Inc Carbapenem antibiotic, composition and method of preparation
UA62920C2 (en) 1996-05-28 2004-01-15 Merck & Co Inc Carbapeneme antibiotic, a composition and a method for the preparation
US6180783B1 (en) 1997-06-16 2001-01-30 Merck & Co., Inc. Stabilized carbapenem intermediates and improved process for carbapenem synthesis
US6063931A (en) 1997-07-09 2000-05-16 Merck & Co., Inc. Process for synthesizing carbapenem side chain intermediates
US5872250A (en) 1997-07-30 1999-02-16 Merck & Co., Inc. Process for synthesizing carbapenem antibiotics
CA2322658C (en) * 1998-03-02 2005-04-12 Merck & Co., Inc. Process for synthesizing carbapenem antibiotics

Also Published As

Publication number Publication date
HUP0302764A3 (en) 2005-11-28
CZ301440B6 (cs) 2010-03-03
BR0206372A (pt) 2003-12-23
KR20040007438A (ko) 2004-01-24
PT1353923E (pt) 2005-01-31
WO2002057266A1 (en) 2002-07-25
TWI318627B (en) 2009-12-21
CA2433874A1 (en) 2002-07-25
CN1486318A (zh) 2004-03-31
IL156507A (en) 2010-06-30
EA200300804A1 (ru) 2003-12-25
EP1353923A1 (de) 2003-10-22
YU55003A (sh) 2006-05-25
SK8972003A3 (en) 2003-10-07
US7071330B2 (en) 2006-07-04
AR035728A1 (es) 2004-07-07
KR100827562B1 (ko) 2008-05-07
CN1249065C (zh) 2006-04-05
HUP0302764A2 (hu) 2003-11-28
RS50494B (sr) 2010-03-02
HRP20030566A2 (en) 2005-06-30
MXPA03006322A (es) 2003-10-06
IL156507A0 (en) 2004-01-04
JP2004518672A (ja) 2004-06-24
DK1353923T3 (da) 2005-01-31
US20040063931A1 (en) 2004-04-01
HRP20030566B1 (en) 2011-08-31
PL362912A1 (en) 2004-11-02
AU2002234240B2 (en) 2006-04-27
EP1353923B1 (de) 2004-10-06
NZ527191A (en) 2004-04-30
UA74870C2 (en) 2006-02-15
CA2433874C (en) 2009-08-11
EG23993A (en) 2008-03-10
DE60201498T2 (de) 2005-11-17
SI1353923T1 (en) 2005-02-28
DE60201498D1 (de) 2004-11-11
JP4098626B2 (ja) 2008-06-11
EA006098B1 (ru) 2005-08-25
ES2227423T3 (es) 2005-04-01
CZ20031911A3 (cs) 2003-10-15
SK287350B6 (sk) 2010-08-09

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