ES2097002T3 - Procedimiento para convertir loracarbef dihidrato en loracarbef monohidrato. - Google Patents

Procedimiento para convertir loracarbef dihidrato en loracarbef monohidrato.

Info

Publication number
ES2097002T3
ES2097002T3 ES94303945T ES94303945T ES2097002T3 ES 2097002 T3 ES2097002 T3 ES 2097002T3 ES 94303945 T ES94303945 T ES 94303945T ES 94303945 T ES94303945 T ES 94303945T ES 2097002 T3 ES2097002 T3 ES 2097002T3
Authority
ES
Spain
Prior art keywords
loracarbef
converting
procedure
dihydrate
monohydrate
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 - Lifetime
Application number
ES94303945T
Other languages
English (en)
Inventor
Edward Francis Plocharczyk
Erin Eckert Strouse
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
Application granted granted Critical
Publication of ES2097002T3 publication Critical patent/ES2097002T3/es
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • 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
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D463/00—Heterocyclic compounds containing 1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D463/10—Heterocyclic compounds containing 1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring 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
    • C07D463/14—Heterocyclic compounds containing 1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. carbacephalosporins; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring 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 hetero atoms directly attached in position 7
    • C07D463/16—Nitrogen atoms
    • C07D463/18—Nitrogen atoms further acylated by radicals derived from carboxylic acids or by nitrogen or sulfur analogues thereof
    • C07D463/20—Nitrogen atoms further acylated by radicals derived from carboxylic acids or by nitrogen or sulfur analogues thereof with the acylating radicals further substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen
    • C07D463/22—Nitrogen atoms further acylated by radicals derived from carboxylic acids or by nitrogen or sulfur analogues thereof with the acylating radicals further substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen further substituted by nitrogen 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

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)
  • Nitrogen Condensed Heterocyclic Rings (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Steroid Compounds (AREA)
  • Hydrogenated Pyridines (AREA)

Abstract

UN PROCESO PARA LA PREPARACION DE LA ESTRUCTURA DE MONOHIDRATO CRISTALINO DEL COMPUESTO DE LA FORMULA (I) QUE CONSISTE EN EXPONER LA ESTRUCTURA DE DIHIDRATO CRISTALINO DEL COMPUESTO DE LA FORMULA (I) A UNA TEMPERATURA DE ENTRE 50 (GRADOS) APROXIMADAMENTE Y 65 (GRADOS) C Y A UNA HUMEDAD RELATIVA DE ENTRE EL 60 APROXIMADAMENTE Y EL 100% APROXIMADAMENTE.
ES94303945T 1993-06-04 1994-06-01 Procedimiento para convertir loracarbef dihidrato en loracarbef monohidrato. Expired - Lifetime ES2097002T3 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US08/071,550 US5374719A (en) 1993-06-04 1993-06-04 Process for converting loracarbef dihydrate to loracarbef monohydrate

Publications (1)

Publication Number Publication Date
ES2097002T3 true ES2097002T3 (es) 1997-03-16

Family

ID=22102051

Family Applications (1)

Application Number Title Priority Date Filing Date
ES94303945T Expired - Lifetime ES2097002T3 (es) 1993-06-04 1994-06-01 Procedimiento para convertir loracarbef dihidrato en loracarbef monohidrato.

Country Status (29)

Country Link
US (1) US5374719A (es)
EP (1) EP0627430B1 (es)
JP (1) JP3442479B2 (es)
KR (1) KR100311699B1 (es)
CN (1) CN1042424C (es)
AT (1) ATE146472T1 (es)
AU (1) AU678000B2 (es)
BR (1) BR9402149A (es)
CA (1) CA2125001C (es)
CO (1) CO4230100A1 (es)
CZ (1) CZ283468B6 (es)
DE (1) DE69401163T2 (es)
DK (1) DK0627430T3 (es)
ES (1) ES2097002T3 (es)
FI (1) FI108132B (es)
GR (1) GR3022111T3 (es)
HU (1) HU217066B (es)
IL (1) IL109871A (es)
MY (1) MY110724A (es)
NO (1) NO306302B1 (es)
NZ (1) NZ260653A (es)
PE (1) PE13195A1 (es)
PH (1) PH30304A (es)
PL (1) PL174539B1 (es)
RU (1) RU2124013C1 (es)
TW (1) TW252980B (es)
UA (1) UA27812C2 (es)
YU (1) YU33394A (es)
ZA (1) ZA943827B (es)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5550231A (en) * 1993-06-15 1996-08-27 Eli Lilly And Company Loracarbef hydrochloride C1-C3 alcohol solvates and uses thereof
US5580977A (en) * 1995-03-01 1996-12-03 Eli Lilly And Company Process for preparing loracarbef monohydrate
US20070225285A1 (en) * 2005-11-04 2007-09-27 Amira Pharmaceuticals, Inc. 5-lipoxygenase-activating protein (flap) inhibitors

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3502663A (en) * 1969-04-21 1970-03-24 Lilly Co Eli Crystalline cephalosporin,method for its manufacture
US3531481A (en) * 1969-04-21 1970-09-29 Lilly Co Eli Method for manufacture of crystalline cephalosporin
DD273634A5 (de) * 1987-10-06 1989-11-22 ����@�����@�����@����k�� Verfahren zur herstellung eines kristallinen monohydrats eines 1-carbacephalosporins
CA2002596A1 (en) * 1988-11-14 1990-05-14 Thomas M. Eckrich Hydrates of b-lactam antibiotic
US4977257A (en) * 1988-11-14 1990-12-11 Eli Lilly And Company DMF solvates of a β-lactam antibiotic

Also Published As

Publication number Publication date
CN1097754A (zh) 1995-01-25
ZA943827B (en) 1995-12-01
HU217066B (hu) 1999-11-29
NO942048L (no) 1994-12-05
FI942633A (fi) 1994-12-05
GR3022111T3 (en) 1997-03-31
AU6451694A (en) 1994-12-08
CZ134294A3 (en) 1994-12-15
FI942633A0 (fi) 1994-06-03
CN1042424C (zh) 1999-03-10
UA27812C2 (uk) 2000-10-16
NO942048D0 (no) 1994-06-02
US5374719A (en) 1994-12-20
MY110724A (en) 1999-01-30
DE69401163T2 (de) 1997-04-30
PL303676A1 (en) 1994-12-12
JP3442479B2 (ja) 2003-09-02
ATE146472T1 (de) 1997-01-15
RU94019424A (ru) 1996-04-20
TW252980B (es) 1995-08-01
AU678000B2 (en) 1997-05-15
KR950000701A (ko) 1995-01-03
JPH06345763A (ja) 1994-12-20
CO4230100A1 (es) 1995-10-19
DK0627430T3 (da) 1997-06-02
IL109871A0 (en) 1994-10-07
RU2124013C1 (ru) 1998-12-27
BR9402149A (pt) 1994-12-27
IL109871A (en) 1998-08-16
NO306302B1 (no) 1999-10-18
HU9401675D0 (en) 1994-09-28
DE69401163D1 (de) 1997-01-30
KR100311699B1 (ko) 2001-12-28
FI108132B (fi) 2001-11-30
PH30304A (en) 1997-02-20
CA2125001C (en) 2004-08-03
CZ283468B6 (cs) 1998-04-15
EP0627430B1 (en) 1996-12-18
PE13195A1 (es) 1995-05-24
CA2125001A1 (en) 1994-12-05
EP0627430A1 (en) 1994-12-07
PL174539B1 (pl) 1998-08-31
YU33394A (sh) 1996-10-18
HUT67743A (en) 1995-04-28
NZ260653A (en) 1995-12-21

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