HUP0200013A2 - 3,6-disubstituted penam sulfone derivatives, process for their preparation and pharmaceutical compositions containing them - Google Patents

3,6-disubstituted penam sulfone derivatives, process for their preparation and pharmaceutical compositions containing them

Info

Publication number
HUP0200013A2
HUP0200013A2 HU0200013A HUP0200013A HUP0200013A2 HU P0200013 A2 HUP0200013 A2 HU P0200013A2 HU 0200013 A HU0200013 A HU 0200013A HU P0200013 A HUP0200013 A HU P0200013A HU P0200013 A2 HUP0200013 A2 HU P0200013A2
Authority
HU
Hungary
Prior art keywords
group
disubstituted
preparation
pharmaceutical compositions
compositions containing
Prior art date
Application number
HU0200013A
Other languages
Hungarian (hu)
Inventor
Panayota Bitha
Gerardo Delacruz Francisco
Zhong Li
Yang-I Lin
Original Assignee
American Cyanamid 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 American Cyanamid Co. filed Critical American Cyanamid Co.
Publication of HUP0200013A2 publication Critical patent/HUP0200013A2/en
Publication of HUP0200013A3 publication Critical patent/HUP0200013A3/en

Links

Classifications

    • 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
    • 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)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Cephalosporin Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

A találmány (I) és (II) általános képletű vegyületekre ésgyógyászatilag elfogadható sóira vonatkozik. Az (I) és (II) általánosképletben n értéke 0 vagy 1 és amikor n értéke 1, R jelentése 5- vagy 6-tagúheterociklusos gyűrű, hidroxilcsoport, halogénatom, oxo-, karbamoil-,alkoxi- vagy diszubsztituált aminocsoport; amikor n értéke 0,Rjelentése észter-, ciano- vagy amidcsoport; X jelentése =CH- vagy -NH- képletű csoport; R3 jelentése ciano-, metoxi- vagyacetamidocsoport; R1 jelentése hidrogénatom, alkilcsoport, negatívtöltés, egy kation, mégpedig nátrium-, kálium-, vagytetralkilammóniumion, aciloxialkil- vagy alkoxikarboniloxialkil-csoport és R2 jelentése hidrogénatom, acil-, triszubsztituált szilil-,karbamoil-, dialkil-aminokarbonil-csoport vagy egy aminosavmaradék. Atalálmány kiterjed, a fenti vegyületek előállítására, továbbá azezeket tartalmazó antibakteriális hatású gyógyszerkészítményekre is. ÓThe invention relates to compounds of formulas (I) and (II) and their pharmaceutically acceptable salts. In formulas (I) and (II), n is 0 or 1 and when n is 1, R is a 5- or 6-membered heterocyclic ring, hydroxyl group, halogen atom, oxo-, carbamoyl-, alkoxy- or disubstituted amino group; when n is 0, R is an ester, cyano or amide group; X is a group of formula =CH- or -NH-; R 3 is cyano, methoxy or acetamido; R1 is a hydrogen atom, an alkyl group, a negative charge, a cation, namely a sodium, potassium or tetraalkylammonium ion, an acyloxyalkyl or alkoxycarbonyloxyalkyl group and R2 is a hydrogen atom, an acyl, trisubstituted silyl, carbamoyl, dialkylaminocarbonyl group or an amino acid residue. The invention covers the production of the above compounds, as well as pharmaceutical preparations containing them with an antibacterial effect. HE

HU0200013A 1999-01-26 2000-01-26 3,6-disubstituted penam sulfone derivatives, process for their preparation and pharmaceutical compositions containing them HUP0200013A3 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US23772699A 1999-01-26 1999-01-26

Publications (2)

Publication Number Publication Date
HUP0200013A2 true HUP0200013A2 (en) 2002-05-29
HUP0200013A3 HUP0200013A3 (en) 2002-10-28

Family

ID=22894903

Family Applications (1)

Application Number Title Priority Date Filing Date
HU0200013A HUP0200013A3 (en) 1999-01-26 2000-01-26 3,6-disubstituted penam sulfone derivatives, process for their preparation and pharmaceutical compositions containing them

Country Status (20)

Country Link
EP (1) EP1144418A1 (en)
JP (1) JP2002535335A (en)
KR (1) KR20010101649A (en)
CN (1) CN1188417C (en)
AU (1) AU2624600A (en)
BG (1) BG105737A (en)
BR (1) BR0007729A (en)
CA (1) CA2355738A1 (en)
CZ (1) CZ20012691A3 (en)
EA (1) EA200100813A1 (en)
HK (1) HK1038747A1 (en)
HU (1) HUP0200013A3 (en)
ID (1) ID29400A (en)
IL (1) IL144116A0 (en)
NO (1) NO20013640D0 (en)
PL (1) PL349874A1 (en)
SK (1) SK10142001A3 (en)
TR (1) TR200102133T2 (en)
WO (1) WO2000043399A1 (en)
ZA (1) ZA200104323B (en)

Families Citing this family (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP5705751B2 (en) * 2009-03-10 2015-04-22 レール・リキード−ソシエテ・アノニム・プール・レテュード・エ・レクスプロワタシオン・デ・プロセデ・ジョルジュ・クロード Cyclic amino compounds for low-k silylation
CN109422765B (en) * 2017-09-05 2020-08-28 香港理工大学深圳研究院 C-class beta-lactamase inhibitor and preparation method and application thereof

Family Cites Families (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB2076812A (en) * 1980-05-22 1981-12-09 Ciba Geigy Ag Penam-dioxide compounds, processes for their manufacture, and their use
GR77151B (en) * 1982-01-11 1984-09-07 Prizer
US4562073A (en) * 1982-12-24 1985-12-31 Taiho Pharmaceutical Company Limited Penicillin derivatives
US4503040A (en) * 1984-02-27 1985-03-05 Pfizer Inc. 6-(Aminoacyloxymethyl)penicillanic acid 1,1-dioxides as beta-lactamase inhibitors
US4591459A (en) * 1984-12-03 1986-05-27 Pfizer Inc. Intermediates for 6-(aminoacyloxymethyl) penicillanic acid 1,1-dioxides
TW383308B (en) * 1993-08-24 2000-03-01 Hoffmann La Roche 2-beta-alkenyl penam sulfones as beta-lactamase inhibitors

Also Published As

Publication number Publication date
CA2355738A1 (en) 2000-07-27
SK10142001A3 (en) 2002-07-02
JP2002535335A (en) 2002-10-22
TR200102133T2 (en) 2001-12-21
CZ20012691A3 (en) 2002-06-12
BR0007729A (en) 2001-10-30
CN1337965A (en) 2002-02-27
HUP0200013A3 (en) 2002-10-28
BG105737A (en) 2002-05-31
WO2000043399A1 (en) 2000-07-27
HK1038747A1 (en) 2002-03-28
CN1188417C (en) 2005-02-09
ZA200104323B (en) 2002-08-26
NO20013640L (en) 2001-07-24
EA200100813A1 (en) 2003-02-27
KR20010101649A (en) 2001-11-14
IL144116A0 (en) 2002-05-23
PL349874A1 (en) 2002-09-23
ID29400A (en) 2001-08-30
EP1144418A1 (en) 2001-10-17
NO20013640D0 (en) 2001-07-24
AU2624600A (en) 2000-08-07

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