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filingDate 1969-03-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d22968f8bcf3ac20d9e62297205b4231
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publicationDate 1971-07-21-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1240224-A
titleOfInvention Improvements in or relating to hydroxylamine derivatives
abstract 1,240,224. Hydroxamic acid derivatives. RICHTER GEDEON VEGYESZETI GYAR RT. 25 March, 1969 [30 March, 1968], No. 15666/69. Heading C2C. Novel hydroxamic -acid derivatives of the formula wherein Ac is an acyl radical of a carboxylic acid containing one or more basic nitrogen atoms, with the exception of the amino acids leucine, valine and alanine, and of 4 - phenyl - 1,2,5,6 - tetrahydropyridinoalkanoic acids, and X is an unsubstituted or substituted aralkyl radical and the pharmaceutically acceptable acid addition salts thereof -are prepared either by reacting an O - substituted hydroxylamine of the formula H 2 N-O-X with an acid of the formula AcOH or reactive derivative thereof or by reacting an N-acylated (hydroxylamine of the formula AcNHOH with an aralkyl halide of the formula X-Hal. If desired the basic nitrogen atom in the above starting materials may be protected and the protective groups removed at the end of the above processes to give the desired products. N - (tert. - Butyloxycarbonyl) - L - prolyl- O - benzyl - hydroxylamine is obtained either by reacting O - benzyl - hydroxylamine with N- (tert. - butyloxycarbonyl) - L - proline pentachlorophenyl ester or by reacting benzyl chloride with N - tert. - butyloxycarbonyl - L - proline hydroxamic acid. N - (tert. - Butyloxycarbonyl) - L - prolyl - 0- p - nitro - benzyl - hydroxylamine, N - (tert. - butyloxycarbonyl) - L - seryl - 0 - p - chlorobenzyl - hydroxylamine, N - (tert. - butyloxycarbonyl) - L - seryl - O - benzyl - hydroxylamine, N - carbobenzoxy - L - phenylalanyl - O - benzylhydroxylamine, N - carbobenzoxy - glycylglycyl- O - benzyl - hydroxylamine, and N - carbobenzoxy- L - seryl - O - benzyl - hydroxylamine are prepared by reacting the appropriate o-substituted hydroxylamine with the corresponding amino acid or amino acid ester. Pharmaceutical compositions, suitable for oral, parenteral or rectal administration, contain the above-novel compounds or pharmaceutically acceptable acid addition salts thereof and suitable carriers or diluents. The compounds possess hypotensive activity and some of them also show sedative or hypnotic effects.
priorityDate 1968-03-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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