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BE905219A - CEPHALOSPORIN SALTS AND INJECTABLE COMPOSITIONS. - Google Patents

CEPHALOSPORIN SALTS AND INJECTABLE COMPOSITIONS.

Info

Publication number
BE905219A
BE905219A BE07217010A BE217010A BE905219A BE 905219 A BE905219 A BE 905219A BE 07217010 A BE07217010 A BE 07217010A BE 217010 A BE217010 A BE 217010A BE 905219 A BE905219 A BE 905219A
Authority
BE
Belgium
Prior art keywords
injectable compositions
alpha
methyl
mixture
sulfuric acid
Prior art date
Application number
BE07217010A
Other languages
French (fr)
Original Assignee
Bristol Myers 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 Bristol Myers Co filed Critical Bristol Myers Co
Publication of BE905219A publication Critical patent/BE905219A/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/54Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame
    • A61K31/542Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one sulfur as the ring hetero atoms, e.g. sulthiame ortho- or peri-condensed with heterocyclic ring systems
    • A61K31/545Compounds containing 5-thia-1-azabicyclo [4.2.0] octane ring systems, i.e. compounds containing a ring system of the formula:, e.g. cephalosporins, cefaclor, or cephalexine
    • 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
    • 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)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Epidemiology (AREA)
  • Communicable Diseases (AREA)
  • Oncology (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • General Chemical & Material Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Cephalosporin Compounds (AREA)
  • Medicinal Preparation (AREA)

Abstract

Les sels d'addition cristallins des acides sulfurique, dinitrique, monochlorhydrate, dichlorhydrate et les di- et sesqui-orthosphosphate du 7-(alpha- (2-aminothiazol-4-yl) -alpha-(Z) -méthoxyiminoacétamidol)-3- ((1-méthyl-1-pyrrolidinio) méthyl)-3-céphem-4-carboxylate sont stables meme à des températures élevées. Ainsi, on prépare le sel d'addition cristallin de l'acide sulfurique en formant un mélange de (a) au moins un équivalent molaire d'acide sulfurique avec (b) un ion dipolaire en quantité telle qu'il soit présent dans le mélange à une concentration supérieure à 25 mg/ml, on provoque la cristallisation, on sépare les cristaux, on lave et on sèche.The crystalline addition salts of sulfuric, dinitric, monohydrochloride, dihydrochloride and the di- and sesqui-orthosphosphate of 7- (alpha- (2-aminothiazol-4-yl) -alpha- (Z) -methoxyiminoacetamidol) -3- ((1-methyl-1-pyrrolidinio) methyl) -3-cephem-4-carboxylate are stable even at elevated temperatures. Thus, the crystalline addition salt of sulfuric acid is prepared by forming a mixture of (a) at least one molar equivalent of sulfuric acid with (b) a dipolar ion in an amount such that it is present in the mixture. at a concentration above 25 mg / ml, crystallization is carried out, the crystals are separated, washed and dried.

BE07217010A 1985-08-05 1986-08-04 CEPHALOSPORIN SALTS AND INJECTABLE COMPOSITIONS. BE905219A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US76223585A 1985-08-05 1985-08-05

Publications (1)

Publication Number Publication Date
BE905219A true BE905219A (en) 1987-02-04

Family

ID=25064475

Family Applications (1)

Application Number Title Priority Date Filing Date
BE07217010A BE905219A (en) 1985-08-05 1986-08-04 CEPHALOSPORIN SALTS AND INJECTABLE COMPOSITIONS.

Country Status (34)

Country Link
JP (1) JPH0615548B2 (en)
KR (1) KR930003121B1 (en)
AR (1) AR243894A1 (en)
AT (1) AT390957B (en)
AU (1) AU597262B2 (en)
BE (1) BE905219A (en)
CA (1) CA1284994C (en)
CH (1) CH675581A5 (en)
CS (2) CS276849B6 (en)
CY (1) CY1614A (en)
DD (2) DD254941A5 (en)
DE (1) DE3626375A1 (en)
DK (1) DK162053C (en)
EG (1) EG18003A (en)
ES (1) ES2002112A6 (en)
FI (1) FI84484C (en)
FR (1) FR2585705B1 (en)
GB (1) GB2179936B (en)
GR (1) GR862055B (en)
HK (1) HK99691A (en)
HU (1) HU196602B (en)
IE (1) IE59222B1 (en)
IL (1) IL79608A (en)
IT (1) IT1197067B (en)
LU (2) LU88574I2 (en)
MY (1) MY102212A (en)
NL (1) NL8601991A (en)
OA (1) OA08672A (en)
PT (1) PT83134B (en)
SE (1) SE469633B (en)
SG (1) SG79791G (en)
SU (1) SU1516013A3 (en)
YU (1) YU45793B (en)
ZA (1) ZA865842B (en)

Families Citing this family (13)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4883868A (en) * 1984-12-27 1989-11-28 Banyu Pharmaceutical Co., Ltd. 7-amino-3-(substituted isoindolinium)methyl-3-cephem derivatives
US4959469A (en) * 1984-12-27 1990-09-25 Banyu Pharmaceutical Company, Ltd. Crystalline cephalosporin compounds
US5244891A (en) * 1985-08-05 1993-09-14 Bristol-Myers Squibb Company Injectable compositions of cefepime dihydrochloride hydrate
US4910301A (en) * 1985-08-05 1990-03-20 Bristol-Myers Company Cefepime cephalosporin salts
US4808617A (en) * 1985-12-18 1989-02-28 Bristol-Myers Company Lyophilized or precipitated cephalosporin zwitterion and salt combination
EP0321562B1 (en) * 1987-06-25 1993-11-24 Banyu Pharmaceutical Co., Ltd. Crystalline cephalosporin compounds, process for their preparation, and intermediates for their preparation
JPH02101081A (en) * 1988-10-08 1990-04-12 Meiji Seika Kaisha Ltd Crystalline dihydrochloride of cephalosporin derivative and production thereof
CA2011116C (en) * 1989-03-06 1999-11-16 Murray A. Kaplan Lyophilized bmy-28142 dihydrochloride for parenteral use
CA2101571A1 (en) * 1992-09-08 1994-03-09 Elizabeth A. Garofalo Crystalline dihydrate of a cephalosporin dihydrate salt and injectable compositions thereof
EP0638573A1 (en) * 1993-08-10 1995-02-15 Lucky Ltd. Crystalline hydrates of cephalosporin and process for preparation thereof
EP1699804B1 (en) 2003-12-23 2008-02-06 Sandoz Gmbh Process for production of intermediates for use in cefalosporin synthesis
WO2008056221A2 (en) * 2006-11-06 2008-05-15 Orchid Chemicals & Pharmaceuticals Limited Crystalline sulfate salt of cephalosporin antibiotic
DE102012101680A1 (en) * 2012-02-29 2013-08-29 Aicuris Gmbh & Co. Kg Pharmaceutical preparation containing an antiviral dihydroquinazoline derivative

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS55151588A (en) * 1979-05-14 1980-11-26 Takeda Chem Ind Ltd Preparation of cephalosporin salt crystal
US4406899A (en) * 1982-03-04 1983-09-27 Bristol-Myers Company Cephalosporins
CA1213882A (en) * 1982-03-04 1986-11-12 Jun Okumura Cephalosporins
US4525473A (en) * 1983-03-30 1985-06-25 Bristol-Myers Company Cephalosporins
DE3419015A1 (en) * 1984-05-22 1985-11-28 Bayer Ag, 5090 Leverkusen METHOD FOR PRODUCING CEPHALOSPORINES
GB8424692D0 (en) * 1984-10-01 1984-11-07 Glaxo Group Ltd Chemical compounds
GB2165245B (en) * 1984-10-01 1988-05-25 Glaxo Group Ltd Chemical compounds

Also Published As

Publication number Publication date
DD268395A5 (en) 1989-05-31
CA1284994C (en) 1991-06-18
ATA211086A (en) 1990-01-15
DK162053C (en) 1992-02-10
FI84484C (en) 1991-12-10
AT390957B (en) 1990-07-25
IE862078L (en) 1987-02-05
JPS62103090A (en) 1987-05-13
GR862055B (en) 1986-12-24
IT8621409A0 (en) 1986-08-04
IL79608A0 (en) 1986-11-30
CY1614A (en) 1992-07-10
AU597262B2 (en) 1990-05-31
SE8603308D0 (en) 1986-08-04
NL8601991A (en) 1987-03-02
LU86540A1 (en) 1987-03-06
GB2179936A (en) 1987-03-18
ZA865842B (en) 1987-04-29
FI863155A0 (en) 1986-08-01
AR243894A1 (en) 1993-09-30
PT83134B (en) 1989-07-31
EG18003A (en) 1991-08-30
CS276717B6 (en) 1992-08-12
IT1197067B (en) 1988-11-25
DK371886A (en) 1987-02-06
PT83134A (en) 1986-09-01
FI84484B (en) 1991-08-30
IT8621409A1 (en) 1988-02-04
ES2002112A6 (en) 1988-07-16
DK162053B (en) 1991-09-09
YU137186A (en) 1987-12-31
HUT41802A (en) 1987-05-28
IE59222B1 (en) 1994-01-26
DK371886D0 (en) 1986-08-04
SE469633B (en) 1993-08-09
CS276849B6 (en) 1992-08-12
FI863155A (en) 1987-02-06
SU1516013A3 (en) 1989-10-15
OA08672A (en) 1989-03-31
FR2585705B1 (en) 1989-01-13
DD254941A5 (en) 1988-03-16
CH675581A5 (en) 1990-10-15
IL79608A (en) 1991-07-18
DE3626375A1 (en) 1987-02-12
HK99691A (en) 1991-12-13
SG79791G (en) 1991-11-15
LU88574I2 (en) 1995-03-01
KR880002530A (en) 1988-05-09
JPH0615548B2 (en) 1994-03-02
YU45793B (en) 1992-07-20
MY102212A (en) 1992-05-15
KR930003121B1 (en) 1993-04-19
SE8603308L (en) 1987-02-06
GB2179936B (en) 1989-04-26
GB8618989D0 (en) 1986-09-17
AU6069486A (en) 1987-02-12
HU196602B (en) 1988-12-28
FR2585705A1 (en) 1987-02-06

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Legal Events

Date Code Title Description
CCPA Application for a supplementary protection certificate

Free format text: 094C0018; 094C0018

CCPV Grant of a supplementary protection certificate

Free format text: 094C0018, EXPIRES 20080727

RE20 Patent expired

Owner name: *BRISTOL-MYERS SQUIBB CY

Effective date: 20060804

CCRE Expiry of a supplementary protection certificate

Free format text: PRODUCT NAME: CEFEPIME DICHLORHYDRATE MONOHYDRATE; NATIONAL REGISTRATION NO/DATE: 203 IS 240 F 12 19940606; FIRST REGISTRATION: FR 558 101.3 19930727

Spc suppl protection certif: 94C0018

Filing date: 19941205

Expiry date: 20060804

Extension date: 20080727