http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1095866-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-32
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-32
filingDate 1966-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_31e7d8918fee3cc43624e7894fdd08f5
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d806bcc1874bd342a4a4b631768a0f29
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e2d8d9b12bb671c1773ca8f64d94a285
publicationDate 1967-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1095866-A
titleOfInvention Imidazolidin-2-one derivatives
abstract Novel compounds of the general formula II <FORM:1095866/C2/1> wherein R represents a hydrogen atom or an alkyl, substituted alkyl, aryl, substituted aryl, acyl, aroyl or a nitro group; R1 and R11 may be the same or different and represent hydrogen atoms or alkyl, hydroxyl, alkoxy, substituted alkoxy, aryloxy, substituted aryloxy, acyloxy or aroyloxy groups, and ester and ether derivatives thereof, are prepared by reacting 1 - R - 4 - R11 - 5 - imidazolidin - 2- ones with glyoxal in basic aqueous solution, preferably in molar proportions of 2:1. The substituted imidazolidin-2-one derivative may be prepared in situ from RNHCONH2 and glyoxal (R1 and R11 are hydroxyl groups). Preferred urea derivatives are isopropylurea and N-formylurea; preferred imidazolidin-2-one derivatives are the 4,5-dihydroxy, 4,5-dimethoxy and 1-formyl-4,5-dihydroxy compounds. The glyoxal is preferably in the form of its polymeric monohydrate, and the reaction medium may be rendered basic with Na2CO3 or NaHCO3.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-4837324-A
priorityDate 1966-03-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 29.