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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_6cfc033f059d282fcd915bc8be2ae53f
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D239-553
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-553
filingDate 1977-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4798fb432f7b342142431f200f88773c
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_54af6e8db59d6e04a3ed0c29582622ef
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0751b17bbc91739766362931df4a1f15
publicationDate 1982-07-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CH-630907-A5
titleOfInvention Process for preparing derivatives of 1-carbamoyluracil.
abstract Compounds of the formula: <IMAGE> are prepared by reacting a uracil, which is optionally substituted in the 5 position by halogen, methyl or trifluoromethyl, with an amine HNRR' and phosgene. R denotes hydrogen or a hydrocarbon radical and R' denotes a hydrocarbon radical, or R and R' together represent a divalent hydrocarbon radical. Some of the products of the process are novel compounds; they are distinguished by having anti-tumour activity and can be administered per os. As compared with the previously known syntheses, the process has the advantage of consisting of one single and simple reaction step.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0240352-A2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/FR-2539412-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0240352-A3
priorityDate 1976-04-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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