ES8606358A1 - Un procedimiento para la preparacion de monohidrato de bis- hidrobromuro de ceftazidima cristalino - Google Patents

Un procedimiento para la preparacion de monohidrato de bis- hidrobromuro de ceftazidima cristalino

Info

Publication number
ES8606358A1
ES8606358A1 ES541505A ES541505A ES8606358A1 ES 8606358 A1 ES8606358 A1 ES 8606358A1 ES 541505 A ES541505 A ES 541505A ES 541505 A ES541505 A ES 541505A ES 8606358 A1 ES8606358 A1 ES 8606358A1
Authority
ES
Spain
Prior art keywords
relating
salts
ceftazidime
crystalline
crystalline ceftazidime
Prior art date
Legal status (The legal status 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 status listed.)
Expired
Application number
ES541505A
Other languages
English (en)
Other versions
ES541505A0 (es
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Eli Lilly and Co
Original Assignee
Eli Lilly and Co
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 Eli Lilly and Co filed Critical Eli Lilly and Co
Publication of ES541505A0 publication Critical patent/ES541505A0/es
Publication of ES8606358A1 publication Critical patent/ES8606358A1/es
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic 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
    • C07D501/14Compounds having a nitrogen atom directly attached in position 7
    • C07D501/16Compounds having a nitrogen atom directly attached in position 7 with a double bond between positions 2 and 3
    • C07D501/207-Acylaminocephalosporanic or substituted 7-acylaminocephalosporanic acids in which the acyl radicals are derived from carboxylic acids
    • C07D501/247-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
    • C07D501/38Methylene 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
    • C07D501/46Methylene 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D501/00Heterocyclic 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Communicable Diseases (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Oncology (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Cephalosporin Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

PROCEDIMIENTO PARA LA PREPARACION DE MONOHIDRATO DE BIS-HIDROBROMURO DE CEFTAZIDIMA CRISTALINO. COMPRENDE: A) HACER REACCIONAR A (A) CON ACIDO FORMICO AL 98% Y ACIDO BROMHIDRICO AL 48%, PARA SEPARAR AL GRUPO T-BUTILO PROTECTOR DEL CARBOXI Y AL GRUPO TRITILO PROTECTOR DEL AMINO Y FORMAR UNA SAL DE BIS-HIDROBROMURO DE (A); B) FILTRAR A LA MEZCLA DE A), PARA AISLAR LA SAL CRISTALINA Y SEPARAR EL TRIFENILCARBINOL INSOLUBLE; C) DILUIR AL FILTRADO CON ACETONA, METIL ETILCETONA O CICLOHEXANO; D) ENFRIAR A LA DILUCION ENTRE 10 Y 20JC PARA CRISTALIZAR AL A-MONOHIDRATO DE BIS-HIDROBROMURO DE (A); E) FILTRAR A LA DILUCION CON LA SAL CRISTALINA Y AGUAS MADRES, PARA SEPARAR A LAS AGUAS MADRES; F) LAVAR A LA SAL CRISTALINA CON AGUA Y G) SECAR A VACIO Y A TEMPERATURA AMBIENTE A LA SAL CRISTALINA. SIENDO (A) CEFTAZIDIMA O (6R, 7R)-7-((Z)-2-(2-TRITILAMINO-1,3-TIAZOL-4-IL)-2-T-BUTILOXICARBONILPROP-2-OXIMINO)ACETAMIDO)-3-(1-PIRIDINIOMETIL)-3-CEFEM-4-CARBOXILATO.
ES541505A 1984-03-26 1985-03-22 Un procedimiento para la preparacion de monohidrato de bis- hidrobromuro de ceftazidima cristalino Expired ES8606358A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US06/593,441 US4537959A (en) 1984-03-26 1984-03-26 Crystalline cephalosporin antibiotic salt

Publications (2)

Publication Number Publication Date
ES541505A0 ES541505A0 (es) 1986-04-16
ES8606358A1 true ES8606358A1 (es) 1986-04-16

Family

ID=24374724

Family Applications (1)

Application Number Title Priority Date Filing Date
ES541505A Expired ES8606358A1 (es) 1984-03-26 1985-03-22 Un procedimiento para la preparacion de monohidrato de bis- hidrobromuro de ceftazidima cristalino

Country Status (16)

Country Link
US (1) US4537959A (es)
EP (1) EP0157538A3 (es)
JP (1) JPS60215689A (es)
KR (1) KR870000829B1 (es)
AU (1) AU575137B2 (es)
CA (1) CA1228851A (es)
DK (1) DK131785A (es)
ES (1) ES8606358A1 (es)
GR (1) GR850708B (es)
HU (1) HU194253B (es)
IL (1) IL74671A0 (es)
NZ (1) NZ211509A (es)
PH (1) PH21943A (es)
PT (1) PT80133B (es)
SU (1) SU1356963A3 (es)
ZA (1) ZA852042B (es)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3313818A1 (de) * 1983-04-16 1984-10-18 Hoechst Ag, 6230 Frankfurt Neue kristallmodifikation von ceftazidim
GB8406218D0 (en) * 1984-03-09 1984-04-11 Glaxo Group Ltd Process
US4616080A (en) * 1984-07-02 1986-10-07 Eli Lilly And Company Simplified process of forming crystalline ceftazidime pentahydrate
US4910301A (en) * 1985-08-05 1990-03-20 Bristol-Myers Company Cefepime cephalosporin salts
US5244891A (en) * 1985-08-05 1993-09-14 Bristol-Myers Squibb Company Injectable compositions of cefepime dihydrochloride hydrate
US4954624A (en) * 1986-10-07 1990-09-04 Sandoz Ltd. Process for the production of cephalosporin derivatives
AT387390B (de) * 1986-10-07 1989-01-10 Biochemie Gmbh Verfahren zur herstellung des antibiotikums (6r,7r)-7-(2-(2-amino-4-thiazolyl)-2-(2-carboxy
US5021564A (en) * 1987-02-02 1991-06-04 Eli Lilly And Company Process for preparing ceftazidime pentahydrate
DE3706020A1 (de) * 1987-02-25 1988-09-08 Hoechst Ag Kristallisierte cephem-saeureadditionssalze und verfahren zu ihrer herstellung
EP0321562B1 (en) * 1987-06-25 1993-11-24 Banyu Pharmaceutical Co., Ltd. Crystalline cephalosporin compounds, process for their preparation, and intermediates for their preparation
GB8802622D0 (en) * 1988-02-05 1988-03-02 Glaxo Group Ltd Chemical compound
DE10158488A1 (de) 2001-11-28 2003-06-12 Wolff Cellulosics Gmbh & Co Kg Lösungsverzögerte Celluloseether und ein Verfahren zu ihrer Herstellung
CN102924483B (zh) * 2012-10-31 2015-06-17 海南合瑞制药股份有限公司 一种头孢他啶晶体化合物、其制备方法及其无菌混合粉形式的药物组合物

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR228726A1 (es) * 1978-05-26 1983-04-15 Glaxo Group Ltd Procedimiento para la preparacion del antibiotico(6r,7r)-7-((z)-2-(2-aminotiazol-4-il)-2-(2-carboxiprop-2-oxiimino)acetamido)-3-(1-piridiniometil)cef-3-em-4-carboxilato
BE885488A (fr) * 1979-10-02 1981-04-01 Glaxo Group Ltd Bischlorhydrate de cephalosporine et sa preparation
US4329453A (en) * 1979-10-02 1982-05-11 Glaxo Group Limited Cephalosporin antibiotic
DE3313818A1 (de) * 1983-04-16 1984-10-18 Hoechst Ag, 6230 Frankfurt Neue kristallmodifikation von ceftazidim
DE3313816A1 (de) * 1983-04-16 1984-10-18 Hoechst Ag, 6230 Frankfurt Neue kristallmodifikation von ceftazidim

Also Published As

Publication number Publication date
KR850006425A (ko) 1985-10-05
US4537959A (en) 1985-08-27
GR850708B (es) 1985-07-19
KR870000829B1 (ko) 1987-04-23
PT80133B (en) 1987-03-23
PH21943A (en) 1988-04-15
DK131785A (da) 1985-09-27
ES541505A0 (es) 1986-04-16
EP0157538A3 (en) 1986-10-08
IL74671A0 (en) 1985-06-30
AU575137B2 (en) 1988-07-21
EP0157538A2 (en) 1985-10-09
JPS60215689A (ja) 1985-10-29
NZ211509A (en) 1987-11-27
PT80133A (en) 1985-04-01
ZA852042B (en) 1986-10-29
SU1356963A3 (ru) 1987-11-30
HUT36798A (en) 1985-10-28
HU194253B (en) 1988-01-28
CA1228851A (en) 1987-11-03
AU4025085A (en) 1985-10-03
DK131785D0 (da) 1985-03-22

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