CY1112092T1 - Διεργασια για την κατασκευη ενωσεων καρβαπενεμης - Google Patents

Διεργασια για την κατασκευη ενωσεων καρβαπενεμης

Info

Publication number
CY1112092T1
CY1112092T1 CY20111101043T CY111101043T CY1112092T1 CY 1112092 T1 CY1112092 T1 CY 1112092T1 CY 20111101043 T CY20111101043 T CY 20111101043T CY 111101043 T CY111101043 T CY 111101043T CY 1112092 T1 CY1112092 T1 CY 1112092T1
Authority
CY
Cyprus
Prior art keywords
organic solvents
carbapenem
pharmaceutically acceptable
formula
organic solvent
Prior art date
Application number
CY20111101043T
Other languages
English (en)
Inventor
Raymond Cvetovich
Robert Wenslow
John M Williams
Daniel Sidler
Louis Crocker
Hsien-Hsin Tung
Brian K Johnson
Joseph Ii Kukura
Ulf Dolling
Original Assignee
Merck Sharp & Dohme Corp.
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 Sharp & Dohme Corp. filed Critical Merck Sharp & Dohme Corp.
Publication of CY1112092T1 publication Critical patent/CY1112092T1/el

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Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D477/00Heterocyclic 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
    • C07D477/10Heterocyclic 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
    • C07D477/12Heterocyclic 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
    • C07D477/16Heterocyclic 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
    • C07D477/20Sulfur atoms
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D477/00Heterocyclic 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
    • C07D477/02Preparation

Landscapes

  • Organic Chemistry (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Animal Behavior & Ethology (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Oncology (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Communicable Diseases (AREA)
  • General Chemical & Material Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Molecular Biology (AREA)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Η παρούσα εφεύρεση αφορά διεργασία για την ελάττωση των επιπέδων των οργανικών διαλυτών σε φαρμακευτικώς αποδεκτά επίπεδα σε θερμικώς ασταθή στερεά κρυσταλλικής καρβαπενέμης που αντιπροσωπεύονται από τον τύπο (I), ή ένα άλας αυτών, όπου τα R1 και R2 είναι τα ίδια ή διαφορετικά, και επιλέγονται από Η, αλκυλ, αρυλ, και ετεροαρυλ, που περιλαμβάνει πλύση ενός στερεού καρβαπενέμης που περιέχει οργανικό διαλύτη με οργανικό διαλύτη που περιέχει νερό, και χρήση κενού ή/και αδρανούς αερίου (ενυδατωμένου ή ξηρού) σε χαμηλή θερμοκρασία ώστε να παραχθεί ένωση του τύπου (I) που περιέχει φαρμακευτικώς αποδεκτά επίπεδα οργανικών διαλυτών, όπου η περιεκτικότητα σε νερό του στερεού κρυσταλλικής καρβαπενέμης, διορθώνοντας για τους οργανικούς διαλύτες, διατηρείται περίπου στο 13% έως περίπου 25% κατά τη διάρκεια της διεργασίας.
CY20111101043T 2001-09-26 2011-10-31 Διεργασια για την κατασκευη ενωσεων καρβαπενεμης CY1112092T1 (el)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US32513001P 2001-09-26 2001-09-26
EP02775896A EP1474426B8 (en) 2001-09-26 2002-09-20 Process for making carbapenem compounds

Publications (1)

Publication Number Publication Date
CY1112092T1 true CY1112092T1 (el) 2015-11-04

Family

ID=23266556

Family Applications (1)

Application Number Title Priority Date Filing Date
CY20111101043T CY1112092T1 (el) 2001-09-26 2011-10-31 Διεργασια για την κατασκευη ενωσεων καρβαπενεμης

Country Status (22)

Country Link
US (1) US7022841B2 (el)
EP (1) EP1474426B8 (el)
JP (1) JP4480396B2 (el)
KR (1) KR100628676B1 (el)
CN (2) CN100338064C (el)
AT (1) ATE518864T1 (el)
AU (1) AU2002341747B2 (el)
BR (1) BRPI0212411B8 (el)
CA (1) CA2461565C (el)
CY (1) CY1112092T1 (el)
DK (1) DK1474426T3 (el)
EA (1) EA008168B1 (el)
ES (1) ES2368997T3 (el)
HU (1) HU230700B1 (el)
IL (1) IL160413A0 (el)
MX (1) MXPA04002797A (el)
NZ (1) NZ531174A (el)
PL (1) PL218808B1 (el)
PT (1) PT1474426E (el)
RS (1) RS52410B (el)
UA (1) UA78524C2 (el)
WO (1) WO2003027067A2 (el)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
USRE40794E1 (en) 2001-09-26 2009-06-23 Merck & Co., Inc. Crystalline forms of carbapenem antibiotics and methods of preparation
CN1608066A (zh) * 2001-11-16 2005-04-20 兰贝克赛实验室有限公司 结晶亚胺培南的制备方法
MX2007006018A (es) * 2004-11-30 2007-06-07 Astellas Pharma Inc Suspension farmaceutica oral novedosa de cristal de cefdinir.
CN100457760C (zh) * 2005-10-20 2009-02-04 上海交通大学 尔他培南钠盐的制备方法
US8293894B2 (en) * 2006-11-20 2012-10-23 Orchid Chemicals & Pharmaceuticals Limited Process for the preparation of carbapenem antibiotic
CN101367812B (zh) * 2007-06-28 2011-04-27 山东轩竹医药科技有限公司 被巯基吡咯烷甲酰胺基环戊烯酸取代的培南衍生物
CN101372490B (zh) * 2007-08-15 2011-02-09 山东轩竹医药科技有限公司 含有巯基氮杂环乙烯基氮杂环的培南衍生物
EP2505190A1 (en) 2008-06-11 2012-10-03 Ranbaxy Laboratories Limited Polymorphic forms of ertapenem monosodium salt and process for it's preparation
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
CN102363617B (zh) * 2011-11-09 2013-09-18 上海希迈医药科技有限公司 一种厄他培南单钠盐结晶体及其制备方法
EP2834242A4 (en) * 2012-04-04 2016-01-06 Hospira Inc IMPROVED PROCESS FOR THE PREPARATION OF CARBAPENEM ANTIBIOTICS
WO2015087245A1 (en) 2013-12-11 2015-06-18 Unimark Remedies Ltd. Process for preparation of ertapenem and salts thereof
CN113416193B (zh) 2021-08-23 2021-12-17 凯莱英医药集团(天津)股份有限公司 厄他培南钠新晶型及其制备方法

Family Cites Families (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA1283906C (en) 1983-05-09 1991-05-07 Makoto Sunagawa .beta.-LACTAM COMPOUNDS AND PRODUCTION THEREOF
IE60588B1 (en) * 1986-07-30 1994-07-27 Sumitomo Pharma Carbapenem compound in crystalline form, and its production and use
JP3048196B2 (ja) * 1991-06-20 2000-06-05 第一製薬株式会社 カルバペネム誘導体
GB9202298D0 (en) * 1992-02-04 1992-03-18 Ici Plc Antibiotic compounds
HU218676B (hu) * 1992-03-11 2000-10-28 Sankyo Co. Ltd. Antimikrobiális karbapenemszármazékok, ilyen vegyületeket tartalmazó gyógyászati készítmények és eljárás ezek előállítására
ZA938438B (en) * 1992-11-17 1994-06-20 Sankyo Co Crystalline carbapenem derivative
CN1093861C (zh) * 1996-04-26 2002-11-06 三共株式会社 1-甲基碳青霉烯衍生物
US6180783B1 (en) 1997-06-16 2001-01-30 Merck & Co., Inc. Stabilized carbapenem intermediates and improved process for carbapenem synthesis
US5872250A (en) * 1997-07-30 1999-02-16 Merck & Co., Inc. Process for synthesizing carbapenem antibiotics
EP1060180B1 (en) * 1998-03-02 2006-03-29 Merck & Co., Inc. Process for synthesizing carbapenem antibiotics
TWI250160B (en) * 1999-07-06 2006-03-01 Sankyo Co Crystalline 1-methylcarbapenem compound
AR035728A1 (es) * 2001-01-16 2004-07-07 Merck & Co Inc Proceso perfeccionado para la sintesis de carbapenem
USRE40794E1 (en) * 2001-09-26 2009-06-23 Merck & Co., Inc. Crystalline forms of carbapenem antibiotics and methods of preparation

Also Published As

Publication number Publication date
DK1474426T3 (da) 2011-11-21
EP1474426B8 (en) 2011-10-12
PL371666A1 (en) 2005-06-27
US20040176351A1 (en) 2004-09-09
CA2461565A1 (en) 2003-04-03
BRPI0212411B8 (pt) 2021-07-27
CN1821248A (zh) 2006-08-23
US7022841B2 (en) 2006-04-04
HUP0500329A3 (en) 2012-09-28
HU230700B1 (hu) 2017-09-28
BRPI0212411B1 (pt) 2015-10-27
CN100338064C (zh) 2007-09-19
RS52410B (en) 2013-02-28
IL160413A0 (en) 2004-07-25
KR20040039437A (ko) 2004-05-10
ES2368997T3 (es) 2011-11-24
EA008168B1 (ru) 2007-04-27
UA78524C2 (en) 2007-04-10
CN1602312A (zh) 2005-03-30
JP2005508334A (ja) 2005-03-31
CN100387599C (zh) 2008-05-14
HUP0500329A2 (hu) 2005-07-28
EA200400474A1 (ru) 2004-08-26
RS22404A (en) 2007-02-05
CA2461565C (en) 2009-09-15
WO2003027067A3 (en) 2004-09-10
ATE518864T1 (de) 2011-08-15
EP1474426A2 (en) 2004-11-10
EP1474426A4 (en) 2005-01-05
WO2003027067A2 (en) 2003-04-03
PL218808B1 (pl) 2015-01-30
KR100628676B1 (ko) 2006-09-27
PT1474426E (pt) 2011-10-07
MXPA04002797A (es) 2004-07-02
JP4480396B2 (ja) 2010-06-16
EP1474426B1 (en) 2011-08-03
BR0212411A (pt) 2004-08-03
AU2002341747B2 (en) 2007-10-18
NZ531174A (en) 2005-09-30

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