ES208018A1 - Improvements in or relating to the preparation of esters and amides of penicillin g and penicillin x - Google Patents

Improvements in or relating to the preparation of esters and amides of penicillin g and penicillin x

Info

Publication number
ES208018A1
ES208018A1 ES0208018A ES208018A ES208018A1 ES 208018 A1 ES208018 A1 ES 208018A1 ES 0208018 A ES0208018 A ES 0208018A ES 208018 A ES208018 A ES 208018A ES 208018 A1 ES208018 A1 ES 208018A1
Authority
ES
Spain
Prior art keywords
benzyl
penicillin
penicillinate
benzyl penicillin
anhydride
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
ES0208018A
Other languages
Spanish (es)
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.)
Glaxo Laboratories Ltd
Original Assignee
Glaxo 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 Glaxo Laboratories Ltd filed Critical Glaxo Laboratories Ltd
Publication of ES208018A1 publication Critical patent/ES208018A1/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

Abstract

An intermediate in the preparation of esters and amides of penicillin G and X, has the formula <FORM:0727481/IV (b)/1> where R1 is hydrogen or hydroxyl and R2 is alkyl, aralkyl or aryl. It is prepared by reacting a penicillin salt with a chloroformic ester in an inert solvent. For salts with metals e.g. sodium or potassium penicillin, preferred solvents are water-miscible e.g. acetone, dioxan and tetrahydrofuran and may contain up to 30 per cent of water. For salts with organic bases e.g. salts of tertiary amines such as triethylamine and N-ethylpiperidine, specified solvents are chloroform, ethyl acetate, acetone or ether. It is preferred that R2 be 1 to 4 carbon alkyl e.g. methyl, ethyl, propyl or butyl, or a benzyl group. Esters are produced by reacting a compound of the above general formula with a hydroxylic compound in an inert solvent under basic conditions i.e. in the presence of a tertiary amine such as pyridine, dimethyl aniline or triethylamine or by the use of a hydroxylic compound which itself contains a tertiary amino group. Amides are produced by reacting compounds of the above general formula with a primary or secondary amine. The said intermediate product need not be isolated. The preparation of the following is described: (a) methylbenzylpenicillinate (b) phenylbenzyl penicillinate (3) 2-diethyl aminoethyl benzyl penicillinate (d) benzyl penicillin cyclohexylamide (e) benzyl penicillin 2 : 2-dimethyl cyclohexylamide (f) benzylpenicillin p-toluidide (g) benzyl penicillin morphalide (h) benzyl penicillin - diethylaminoethylamide (i) benzyl penicillin ethanolamide (j) benzyl penicillin carbethoxyanhydride (k) benzyl penicillin p - amidobenzoic acid (l) benzyl penicillin carbobenzyloxy anhydride (m) furfuryl benzyl penicillinate (n) benzyl penicillin carboisobutyloxyanhydride (o) benzyl penicillin carboisopropyloxy anhydride (p) benzyl penicillin carbomethoxy anhydride (q) 3-morpholinoprop - 2 - yl benzyl penicillinate (r) N-ethyl diethanolamine bis-benzyl-penicillinate.
ES0208018A 1952-02-29 1953-02-27 Improvements in or relating to the preparation of esters and amides of penicillin g and penicillin x Expired ES208018A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB538452A GB727481A (en) 1952-02-29 1952-02-29 Improvements in or relating to the preparation of esters and amides of penicillin g and penicillin x

Publications (1)

Publication Number Publication Date
ES208018A1 true ES208018A1 (en) 1953-11-01

Family

ID=9795130

Family Applications (1)

Application Number Title Priority Date Filing Date
ES0208018A Expired ES208018A1 (en) 1952-02-29 1953-02-27 Improvements in or relating to the preparation of esters and amides of penicillin g and penicillin x

Country Status (2)

Country Link
ES (1) ES208018A1 (en)
GB (1) GB727481A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1578730A (en) * 1976-06-24 1980-11-05 Beecham Group Ltd Esters of penicillin antibiotics

Also Published As

Publication number Publication date
GB727481A (en) 1955-04-06

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