http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S61257977-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bb4ee28d43b5e8d4a3c5141fa9bcfeb0
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-54
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-56
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D239-553
filingDate 1986-05-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4a3afa274abc464d8ffc2fbf1089665b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_74d49a58435feeb795aac6682d55745f
publicationDate 1986-11-15-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S61257977-A
titleOfInvention Fluorine-containing heterocyclic compound
abstract NEW MATERIAL:A fluorine-containing heterocyclic compound shown by the formula I (Rf is fluoroalkyl; R 1 and R 2 are alkyl; X is O or S; Y is F, fluoroalkyl or dialkylamino). n EXAMPLE: A compound shown by the formula II. n USE: An intermediate for a fluoro compound showing physiological activity such as antiviral activity, etc. n PREPARATION: A fluoroacylurea shown by the formula III (Rf 1 and Rf 2 are preferably ≤5C fluoroalkyl like Rf) or a fluoroacylthiourea is subjected to a ring formation reaction of dehydrofluorination by the action of especially a base (e.g., tertiary amine such as triethylamine, etc.) to give a compound shown by the formula I. Preferably the compound shown by the formula III is produced by reacting a fluoroacylcarboxylic acid fluoride shown by the formula IV with an N,N'-dialkylurea or N,N'-dialkylthiourea shown by the formula V under dehydrofluorination condition. n COPYRIGHT: (C)1986,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7884202-B2
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http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007153876-A
priorityDate 1986-05-09-04:00^^<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: 37.