GB891586A - Antibacterial agents - Google Patents

Antibacterial agents

Info

Publication number
GB891586A
GB891586A GB37790/60A GB3779060A GB891586A GB 891586 A GB891586 A GB 891586A GB 37790/60 A GB37790/60 A GB 37790/60A GB 3779060 A GB3779060 A GB 3779060A GB 891586 A GB891586 A GB 891586A
Authority
GB
United Kingdom
Prior art keywords
acids
acid
group
isobutyramido
general formula
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
GB37790/60A
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.)
Beecham Research Laboratories Ltd
Original Assignee
Beecham Research Laboratories Ltd
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 Beecham Research Laboratories Ltd filed Critical Beecham Research Laboratories Ltd
Publication of GB891586A publication Critical patent/GB891586A/en
Expired legal-status Critical Current

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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

Relates to acids of the general formula <FORM:0891586/IV (b)/1> and non-toxic salts thereof, wherein R1 is a cyclopentyl, cyclohexyl, trifluoroethyl or tetrafluoropropyl group or an aliphatic group having from one to twenty carbon atoms inclusive and R2 and R3 are the same or different and each is a C1-C6\t alkyl group. Typical examples of acids of the above formula are 6-(a -methoxyisobutyramido)-, 6-(a -butoxyisobutyramido)-, 6-(a -isopropoxyisobutyramido)-, 6-(a -allyloxyisobutyramido)-, 6-(a -isobutoxyisobutyramido)-, 6-(a -ethoxyisobutyramido)-, 6-[a -(2,2,2-trifluorethoxy)isobutyramido]-, 6-(a -cyclohexyloxyisobutyramido)-, 6-[a -(2,2,3,3-tetrafluoropropoxy)isobutyramido]-, and 6-(a -allyloxy-a -ethylbutyramido)-penicillanic acid. The acids may be prepared by reacting 6-aminopenicillanic acid or a neutral salt thereof with an acid chloride of the general formula <FORM:0891586/IV (b)/2> or with its functional equivalent as an acylating agent for a primary amino group, such as the corresponding carboxylic acid bromides, acid anhydrides and mixed anhydrides with other carboxylic acids.
GB37790/60A 1959-11-04 1960-11-03 Antibacterial agents Expired GB891586A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US891586XA 1959-11-04 1959-11-04

Publications (1)

Publication Number Publication Date
GB891586A true GB891586A (en) 1962-03-14

Family

ID=22216010

Family Applications (1)

Application Number Title Priority Date Filing Date
GB37790/60A Expired GB891586A (en) 1959-11-04 1960-11-03 Antibacterial agents

Country Status (1)

Country Link
GB (1) GB891586A (en)

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