GB835725A - Purification of phenoxymethyl penicillin - Google Patents

Purification of phenoxymethyl penicillin

Info

Publication number
GB835725A
GB835725A GB3577757A GB3577757A GB835725A GB 835725 A GB835725 A GB 835725A GB 3577757 A GB3577757 A GB 3577757A GB 3577757 A GB3577757 A GB 3577757A GB 835725 A GB835725 A GB 835725A
Authority
GB
United Kingdom
Prior art keywords
penicillin
extract
organic solvent
water
aqueous
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
GB3577757A
Inventor
William Norman Jones
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.)
Distillers Co Yeast Ltd
Distillers Co Ltd
Original Assignee
Distillers Co Yeast Ltd
Distillers Co 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 Distillers Co Yeast Ltd, Distillers Co Ltd filed Critical Distillers Co Yeast Ltd
Priority to GB3577757A priority Critical patent/GB835725A/en
Publication of GB835725A publication Critical patent/GB835725A/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
    • 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
    • C07D499/60Compounds 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 oxygen atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Preparation Of Compounds By Using Micro-Organisms (AREA)

Abstract

Phenoxymethyl penicillin is recovered from crude fermentation broths containing it by extracting the penicillin from the broth at a pH value below 3.5 and preferably pH 2.0 to 2.3 into a substantially water-immiscible organic solvent, treating the solution so obtained with active carbon, re-extracting the phenoxymethyl penicillin into an aqueous solution at a pH value between 6 and 8.5, and precipitating phenoxymethyl penicillin from the aqueous extract in the presence of a minor proportion of a water-miscible organic solvent by acidifying the extract. Suitable water-immiscible organic solvents are alkyl esters of organic acids such as butyl acetate and alkanols such as n-butanol. The broth is preferably clarified prior to the organic solvent extraction. The extract is treated with 0.2 to 1.0% w./v. carbon. After filtering off the carbon, the organic extract is treated with an aqueous phosphate or sodium bicarbonate or potassium bicarbonate buffer solution so that the final aqueous extract contains 10,000 to 100,000 m g./ml. of penicillin V. The water-miscible organic solvent is a ketone such as acetone or an alkanol such as ethanol or isopropanol and is used in quantities of 5 to 15%. Reference has been directed by the Comptroller to Specification 734,232.
GB3577757A 1957-11-18 1957-11-18 Purification of phenoxymethyl penicillin Expired GB835725A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
GB3577757A GB835725A (en) 1957-11-18 1957-11-18 Purification of phenoxymethyl penicillin

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
GB3577757A GB835725A (en) 1957-11-18 1957-11-18 Purification of phenoxymethyl penicillin

Publications (1)

Publication Number Publication Date
GB835725A true GB835725A (en) 1960-05-25

Family

ID=10381447

Family Applications (1)

Application Number Title Priority Date Filing Date
GB3577757A Expired GB835725A (en) 1957-11-18 1957-11-18 Purification of phenoxymethyl penicillin

Country Status (1)

Country Link
GB (1) GB835725A (en)

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