MXPA04002797A - Procedimiento para elaborar compuestos de carbapenemo. - Google Patents
Procedimiento para elaborar compuestos de carbapenemo.Info
- Publication number
- MXPA04002797A MXPA04002797A MXPA04002797A MXPA04002797A MXPA04002797A MX PA04002797 A MXPA04002797 A MX PA04002797A MX PA04002797 A MXPA04002797 A MX PA04002797A MX PA04002797 A MXPA04002797 A MX PA04002797A MX PA04002797 A MXPA04002797 A MX PA04002797A
- Authority
- MX
- Mexico
- Prior art keywords
- organic solvents
- pharmaceutically acceptable
- formula
- organic solvent
- levels
- Prior art date
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
-
- 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
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
La presente invencion describe un procedimiento para reducir los niveles de solventes organicos a niveles farmaceuticamente aceptables en solidos de carbapenemo cristalino, termicamente inestable representado por la formula I, o una sal del mismo en donde R1 y R2, son los mismos o diferentes, y se seleccionan de H, alquilo, arilo y heteroarilo, comprendiendo el lavado del solido de carbapenemo que contiene solvente organico con un solvente organico que contiene agua; y usando vacio y/o gas inerte (hidratado o seco) a temperatura baja para reducir a un compuesto de formula 1 que contienen niveles farmaceuticamente aceptables de solventes organicos, en donde el contenido de agua del solido de carbapenemo cristalino, justo para los solventes organicos, se mantiene en cerca de 13% a cerca de 25% durante el procedimiento.
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 (1)
| Publication Number | Publication Date |
|---|---|
| MXPA04002797A true MXPA04002797A (es) | 2004-07-02 |
Family
ID=23266556
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| MXPA04002797A MXPA04002797A (es) | 2001-09-26 | 2002-09-20 | Procedimiento para elaborar compuestos de carbapenemo. |
Country Status (22)
| Country | Link |
|---|---|
| US (1) | US7022841B2 (es) |
| EP (1) | EP1474426B8 (es) |
| JP (1) | JP4480396B2 (es) |
| KR (1) | KR100628676B1 (es) |
| CN (2) | CN100387599C (es) |
| AT (1) | ATE518864T1 (es) |
| AU (1) | AU2002341747B2 (es) |
| BR (1) | BRPI0212411B8 (es) |
| CA (1) | CA2461565C (es) |
| CY (1) | CY1112092T1 (es) |
| DK (1) | DK1474426T3 (es) |
| EA (1) | EA008168B1 (es) |
| ES (1) | ES2368997T3 (es) |
| HU (1) | HU230700B1 (es) |
| IL (1) | IL160413A0 (es) |
| MX (1) | MXPA04002797A (es) |
| NZ (1) | NZ531174A (es) |
| PL (1) | PL218808B1 (es) |
| PT (1) | PT1474426E (es) |
| RS (1) | RS52410B (es) |
| UA (1) | UA78524C2 (es) |
| WO (1) | WO2003027067A2 (es) |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7145002B2 (en) * | 2001-09-26 | 2006-12-05 | Merck & Co. Inc. | Crystalline forms of carbapenem antibiotics and methods of preparation |
| JP2005509037A (ja) * | 2001-11-16 | 2005-04-07 | ランバクシー ラボラトリーズ リミテッド | 結晶イミペネム製造方法 |
| 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 |
| IN2013MU03862A (es) | 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)
| 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 |
| ES2180977T3 (es) * | 1996-04-26 | 2003-02-16 | Sankyo Co | Un derivado de 1-metilcarbapenem. |
| 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 |
| AU749234B2 (en) * | 1998-03-02 | 2002-06-20 | Merck Sharp & Dohme Corp. | 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 |
| US7145002B2 (en) * | 2001-09-26 | 2006-12-05 | Merck & Co. Inc. | Crystalline forms of carbapenem antibiotics and methods of preparation |
-
2002
- 2002-09-20 UA UA20040403037A patent/UA78524C2/uk unknown
- 2002-09-20 EP EP02775896A patent/EP1474426B8/en not_active Expired - Lifetime
- 2002-09-20 HU HU0500329A patent/HU230700B1/hu unknown
- 2002-09-20 MX MXPA04002797A patent/MXPA04002797A/es active IP Right Grant
- 2002-09-20 RS YU22404A patent/RS52410B/en unknown
- 2002-09-20 ES ES02775896T patent/ES2368997T3/es not_active Expired - Lifetime
- 2002-09-20 CN CNB2006100043356A patent/CN100387599C/zh not_active Expired - Lifetime
- 2002-09-20 IL IL16041302A patent/IL160413A0/xx unknown
- 2002-09-20 PT PT02775896T patent/PT1474426E/pt unknown
- 2002-09-20 AT AT02775896T patent/ATE518864T1/de active
- 2002-09-20 NZ NZ531174A patent/NZ531174A/en not_active IP Right Cessation
- 2002-09-20 EA EA200400474A patent/EA008168B1/ru unknown
- 2002-09-20 US US10/485,134 patent/US7022841B2/en not_active Expired - Lifetime
- 2002-09-20 DK DK02775896.0T patent/DK1474426T3/da active
- 2002-09-20 CA CA002461565A patent/CA2461565C/en not_active Expired - Lifetime
- 2002-09-20 JP JP2003530658A patent/JP4480396B2/ja not_active Expired - Lifetime
- 2002-09-20 KR KR1020047004533A patent/KR100628676B1/ko active IP Right Grant
- 2002-09-20 CN CNB028184319A patent/CN100338064C/zh not_active Expired - Lifetime
- 2002-09-20 WO PCT/US2002/029879 patent/WO2003027067A2/en active IP Right Grant
- 2002-09-20 PL PL371666A patent/PL218808B1/pl unknown
- 2002-09-20 BR BRPI0212411A patent/BRPI0212411B8/pt not_active IP Right Cessation
- 2002-09-20 AU AU2002341747A patent/AU2002341747B2/en not_active Expired
-
2011
- 2011-10-31 CY CY20111101043T patent/CY1112092T1/el unknown
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Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FG | Grant or registration | ||
| HC | Change of company name or juridical status | ||
| GB | Transfer or rights | ||
| HC | Change of company name or juridical status |