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filingDate 1979-04-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1980-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_eb33333c4e1a1c7c07eed109bcf9b710
publicationDate 1980-10-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-4229349-A
titleOfInvention Production of semi-synthetic β-lactam antibiotics
abstract In the production of a semi-synthetic β-lactam antibiotic by reacting an amino compound of the formula ##STR1## in which X is the remaining members of a ring of a β-lactam antibiotic, and n R is a hydrogen atom or a methoxy group, n with an activated carboxylic acid derivative of the formula ##STR2## in which R 1 is an organic radical, n B is an optionally substituted phenyl, cyclohexadienyl or heterocyclyl radical and n R 2 is a lower alkyl radical, n the improvement which comprises effecting the reaction in an acetone/water mixture which contains acetone and water in a volume ratio of about 0.5:1 to 3:1. Advantageously the reaction is carried out at about -10° to +10° C. in the presence of an organic base employing about 1.1 to 1.2 mols of the amino compound per mol of the activated carboxylic acid derivative.
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