EA200400474A1 - Способ получения карбапенемовых соединений - Google Patents

Способ получения карбапенемовых соединений

Info

Publication number
EA200400474A1
EA200400474A1 EA200400474A EA200400474A EA200400474A1 EA 200400474 A1 EA200400474 A1 EA 200400474A1 EA 200400474 A EA200400474 A EA 200400474A EA 200400474 A EA200400474 A EA 200400474A EA 200400474 A1 EA200400474 A1 EA 200400474A1
Authority
EA
Eurasian Patent Office
Prior art keywords
organic solvents
carbapenem
pharmaceutically acceptable
formula
obtaining
Prior art date
Application number
EA200400474A
Other languages
English (en)
Other versions
EA008168B1 (ru
Inventor
Рэймонд Светович
Роберт Уэнслоу
Джон М. Уилльямс
Дэниел Сидлер
Луис Крокер
Хсиен-Хсин Танг
Брайан К. Джонсон
Джозеф II Кукура
Ульф Доллинг
Original Assignee
Мерк Энд Ко., Инк.
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 Мерк Энд Ко., Инк. filed Critical Мерк Энд Ко., Инк.
Publication of EA200400474A1 publication Critical patent/EA200400474A1/ru
Publication of EA008168B1 publication Critical patent/EA008168B1/ru

Links

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

Данное изобретение относится к способу снижения уровней органических растворителей до фармацевтически приемлемых уровней в твердых веществах термически нестабильных кристаллических карбапенемах, представляемых формулой I, или их солях, где Rи Rявляются одинаковыми или разными и выбраны из H, алкила, арила и гетероарила, включающему промывание твердого вещества карбапенема, содержащего органический растворитель, органическим растворителем, содержащим воду; и с использованием вакуума и/или инертного газа (гидратированного или сухого) при низкой температуре с получением соединения формулы I, содержащего фармацевтически приемлемые уровни органических растворителей, причем в течение данного процесса содержание воды в твердом веществе кристаллического карбапенема с поправкой на органические растворители поддерживают на уровне от примерно 13 до примерно 25%.
EA200400474A 2001-09-26 2002-09-20 Способ получения карбапенемовых соединений EA008168B1 (ru)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US32513001P 2001-09-26 2001-09-26
PCT/US2002/029879 WO2003027067A2 (en) 2001-09-26 2002-09-20 Process for making carbapenem compounds

Publications (2)

Publication Number Publication Date
EA200400474A1 true EA200400474A1 (ru) 2004-08-26
EA008168B1 EA008168B1 (ru) 2007-04-27

Family

ID=23266556

Family Applications (1)

Application Number Title Priority Date Filing Date
EA200400474A EA008168B1 (ru) 2001-09-26 2002-09-20 Способ получения карбапенемовых соединений

Country Status (22)

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

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2003026572A2 (en) * 2001-09-26 2003-04-03 Merck & Co., Inc. Crystalline forms of ertapenem sodium
PL368984A1 (en) * 2001-11-16 2005-04-04 Ranbaxy Laboratories Limited Process for the preparation of crystalline imipenem
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
US20110172201A1 (en) * 2008-06-11 2011-07-14 Ranbaxy Laboratories Limited Process for preparing a carbapenem antibiotic composition
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
US20150038726A1 (en) * 2012-04-04 2015-02-05 Hospira, Inc. Process for the preparation of carbapenem antibiotic
IN2013MU03862A (ru) 2013-12-11 2015-07-31 Unimark Remedies Ltd
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
CZ290002B6 (cs) * 1992-03-11 2002-05-15 Sankyo Company Limited Antimikrobiální karbapenemové deriváty, způsob výroby a farmaceutický prostředek
ZA938438B (en) * 1992-11-17 1994-06-20 Sankyo Co Crystalline carbapenem derivative
DE69714841T2 (de) * 1996-04-26 2003-05-28 Sankyo Co Ein 1-methylcarbapenem-derivat
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
JP3953274B2 (ja) 1998-03-02 2007-08-08 メルク エンド カムパニー インコーポレーテッド カルバペネム抗生物質の合成方法
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
WO2003026572A2 (en) * 2001-09-26 2003-04-03 Merck & Co., Inc. Crystalline forms of ertapenem sodium

Also Published As

Publication number Publication date
PL371666A1 (en) 2005-06-27
HUP0500329A3 (en) 2012-09-28
KR100628676B1 (ko) 2006-09-27
CY1112092T1 (el) 2015-11-04
EP1474426A2 (en) 2004-11-10
EP1474426B8 (en) 2011-10-12
CN1602312A (zh) 2005-03-30
JP2005508334A (ja) 2005-03-31
UA78524C2 (en) 2007-04-10
CA2461565A1 (en) 2003-04-03
HU230700B1 (hu) 2017-09-28
IL160413A0 (en) 2004-07-25
RS22404A (en) 2007-02-05
BR0212411A (pt) 2004-08-03
ES2368997T3 (es) 2011-11-24
MXPA04002797A (es) 2004-07-02
JP4480396B2 (ja) 2010-06-16
BRPI0212411B8 (pt) 2021-07-27
PL218808B1 (pl) 2015-01-30
DK1474426T3 (da) 2011-11-21
WO2003027067A2 (en) 2003-04-03
RS52410B (en) 2013-02-28
US7022841B2 (en) 2006-04-04
CA2461565C (en) 2009-09-15
CN100387599C (zh) 2008-05-14
BRPI0212411B1 (pt) 2015-10-27
KR20040039437A (ko) 2004-05-10
ATE518864T1 (de) 2011-08-15
AU2002341747B2 (en) 2007-10-18
NZ531174A (en) 2005-09-30
CN100338064C (zh) 2007-09-19
WO2003027067A3 (en) 2004-09-10
EP1474426A4 (en) 2005-01-05
EP1474426B1 (en) 2011-08-03
PT1474426E (pt) 2011-10-07
CN1821248A (zh) 2006-08-23
HUP0500329A2 (hu) 2005-07-28
EA008168B1 (ru) 2007-04-27
US20040176351A1 (en) 2004-09-09

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Legal Events

Date Code Title Description
PD4A Registration of transfer of a eurasian patent in accordance with the succession in title
PD4A Registration of transfer of a eurasian patent in accordance with the succession in title