DK198282A - PENICILLIN OR CEPHALOSPORINE DERIVATIVES, THEIR PREPARATION AND USE AS PHARMACEUTICALS - Google Patents

PENICILLIN OR CEPHALOSPORINE DERIVATIVES, THEIR PREPARATION AND USE AS PHARMACEUTICALS Download PDF

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Publication number
DK198282A
DK198282A DK198282A DK198282A DK198282A DK 198282 A DK198282 A DK 198282A DK 198282 A DK198282 A DK 198282A DK 198282 A DK198282 A DK 198282A DK 198282 A DK198282 A DK 198282A
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DK
Denmark
Prior art keywords
penicillin
pharmaceuticals
preparation
cephalosporine derivatives
alkyl
Prior art date
Application number
DK198282A
Other languages
Danish (da)
Inventor
Rezso Bognar
Csaba Jaszberenyi
Erzsebet Farkas
Maria Punyiczki
Ferenc Hernadi
Katalin Eke
Ilona Petrikovics
Original Assignee
Chinoin Gyogyszer Es Vegyeszet
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 Chinoin Gyogyszer Es Vegyeszet filed Critical Chinoin Gyogyszer Es Vegyeszet
Publication of DK198282A publication Critical patent/DK198282A/en

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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
    • 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
    • C07D499/00Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring
    • C07D499/21Heterocyclic compounds containing 4-thia-1-azabicyclo [3.2.0] heptane ring systems, i.e. compounds containing a ring system of the formula:, e.g. penicillins, penems; Such ring systems being further condensed, e.g. 2,3-condensed with an oxygen-, nitrogen- or sulfur-containing hetero ring with a nitrogen atom directly attached in position 6 and 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
    • C07D499/44Compounds with an amino radical acylated by carboxylic acids, attached in position 6
    • C07D499/48Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical
    • C07D499/58Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical substituted in alpha-position to the carboxamido radical
    • C07D499/64Compounds with an amino radical acylated by carboxylic acids, attached in position 6 with a carbon chain, substituted by hetero atoms or by carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, attached to the carboxamido radical substituted in alpha-position to the carboxamido radical by nitrogen atoms

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  • 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)
  • Hydrogenated Pyridines (AREA)

Description

H, alkyl eller eventuelt med halogen, OH, alkoxy eller alkyl 4 substitueret phenyl, Q er 0, S eller Se, R er H, alkyl 5 5 eller -COOR , R er alkyl, benzyl, benzhydryl eller eventuelt som R^· substitueret phenyl, R6 er phenyl, alkyl, cyclo-alkyl, alkenyl, naphthyl, heteroaryl, heterocyclyl eller adamantyl, hvorhos phenyl eventuelt er substitueret med halogen, alkyl, nitro, alkoxycarbonyl, CF3, dialkylamino, OH, COOh eller SO^H, alkyl eventuelt er substitueret med alkoxycarbonyl, OH, dialkylamino eller alkoxy, og heterocyclyl eventuelt er substitueret med én eller flere phenyl-grupper og/eller er substitueret, R er H, eller -N(R R ) er en fortrinsvis substitueret heterocyclisk gruppe med 4-8 led og eventuelt yderligere N-, O- og/eller S-atomer og eventuelt kondenseret med en eller flére phenylgrupper, Z er OH, n er 0 eller 1, og t er 0-2, eller farmakologisk acceptable salte eller biologisk aktive estre deraf fremstilles ved en række fremgangsmåder.H, alkyl or optionally with halogen, OH, alkoxy or alkyl 4 substituted phenyl, Q is 0, S or Se, R is H, alkyl 5 or -COOR, R is alkyl, benzyl, benzhydryl or optionally substituted with R phenyl, R6 is phenyl, alkyl, cycloalkyl, alkenyl, naphthyl, heteroaryl, heterocyclyl or adamantyl, wherein phenyl is optionally substituted with halogen, alkyl, nitro, alkoxycarbonyl, CF3, dialkylamino, OH, COOh or SO3H, alkyl optionally is substituted by alkoxycarbonyl, OH, dialkylamino or alkoxy, and heterocyclyl is optionally substituted by one or more phenyl groups and / or is substituted, R is H, or -N (RR) is a preferably substituted 4-8 membered heterocyclic group and optionally additional N, O and / or S atoms and optionally condensed with one or more phenyl groups, Z is OH, n is 0 or 1, and t is 0-2, or pharmacologically acceptable salts or biologically active esters thereof are prepared. by a variety of methods.

Forbindelserne med formel (I) er farmaceutisk aktive, idet de har antibakterielle og β-lactamasehammende virkninger .The compounds of formula (I) are pharmaceutically active, having antibacterial and β-lactamase inhibitory effects.

DK198282A 1981-05-04 1982-05-03 PENICILLIN OR CEPHALOSPORINE DERIVATIVES, THEIR PREPARATION AND USE AS PHARMACEUTICALS DK198282A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
HU115481 1981-05-04
HU115481 1981-05-04

Publications (1)

Publication Number Publication Date
DK198282A true DK198282A (en) 1982-11-05

Family

ID=10953073

Family Applications (1)

Application Number Title Priority Date Filing Date
DK198282A DK198282A (en) 1981-05-04 1982-05-03 PENICILLIN OR CEPHALOSPORINE DERIVATIVES, THEIR PREPARATION AND USE AS PHARMACEUTICALS

Country Status (17)

Country Link
JP (1) JPS5813590A (en)
AU (1) AU8321282A (en)
BE (1) BE893057A (en)
BG (1) BG37227A1 (en)
DE (1) DE3215941A1 (en)
DK (1) DK198282A (en)
ES (1) ES511884A0 (en)
FI (1) FI821551L (en)
FR (1) FR2509311A1 (en)
GB (1) GB2101586A (en)
GR (1) GR78166B (en)
IL (1) IL65602A0 (en)
IT (1) IT1156467B (en)
NL (1) NL8201810A (en)
NO (1) NO821456L (en)
PL (1) PL236277A1 (en)
SE (1) SE8202674L (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE3137376C2 (en) * 1981-09-19 1986-02-27 Degussa Ag, 6000 Frankfurt Process for the preparation of 1,5-alkylene-3-aryl-hydantoin derivatives
AU577105B2 (en) * 1985-04-02 1988-09-15 T.P.O. :Pharmachim: Acylaminic penicillin derivatives

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1476312A (en) * 1974-06-03 1977-06-10 Beecham Group Ltd Penicillins and cephalosporins
CA1074298A (en) * 1974-09-20 1980-03-25 E.R. Squibb And Sons 3-heterothio-7-ureido cephalosporins
CA1075679A (en) * 1975-07-30 1980-04-15 E.R. Squibb And Sons 3-heterothio-7-thioureido cephalosporins
JPS5239694A (en) * 1975-08-29 1977-03-28 Toyama Chem Co Ltd Producing novel penicillins and cephalosporins
US4063019A (en) * 1976-03-30 1977-12-13 E. R. Squibb & Sons, Inc. [[[(2,4-Dioxo-1-imidazolidinyl)amino]carbonyl]amino]-acetylcephalosporin derivatives
PT67170B (en) * 1976-11-06 1979-03-21 Merck Patent Gmbh LACTAME METHOD FOR THE PRODUCTION THEREOF AND MEDIUM CONTAINING THESE COMPOUNDS
ES477520A1 (en) * 1978-02-25 1979-06-01 Thomae Gmbh Dr K Penicillins, their salts, process for their preparation and pharmaceutical compositions containing them.
DE2828261A1 (en) * 1978-06-28 1980-01-10 Thomae Gmbh Dr K NEW PENICILLINE, ITS SALTS, METHOD FOR THE PRODUCTION THEREOF AND MEDICINAL PRODUCTS CONTAINING THESE COMPOUNDS

Also Published As

Publication number Publication date
GB2101586A (en) 1983-01-19
PL236277A1 (en) 1983-08-15
IT1156467B (en) 1987-02-04
AU8321282A (en) 1982-11-11
ES8307814A1 (en) 1983-08-16
BE893057A (en) 1982-08-30
FI821551A0 (en) 1982-05-03
BG37227A1 (en) 1985-04-15
FI821551L (en) 1982-11-05
ES511884A0 (en) 1983-08-16
GR78166B (en) 1984-09-26
SE8202674L (en) 1982-11-05
FR2509311A1 (en) 1983-01-14
DE3215941A1 (en) 1983-05-05
JPS5813590A (en) 1983-01-26
IL65602A0 (en) 1982-07-30
NO821456L (en) 1982-11-05
NL8201810A (en) 1982-12-01
IT8267577A0 (en) 1982-05-03

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