http://rdf.ncbi.nlm.nih.gov/pubchem/patent/DE-2065977-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D263-48
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-48
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-06
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filingDate 1970-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_01e40418bb2685180194f1ce1bf68fa7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b0151a92a1f25214b5835cd03311b5af
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_bd31b3ea2babc29ea3dc34fa2e85a993
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_431f47030348c5ffe1e56ef9de616414
publicationDate 1977-08-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber DE-2065977-A1
titleOfInvention PROCESS FOR THE PREPARATION OF 4,5-BIS-TRIFLUOROMETHYLIMINO DERIVATIVES FROM SULFUR-FREE HETEROCYCLIC FUENRINGS WITH TWO RING HETEROATOMES
abstract Prepn. of heterocycles of formula (I) comprises reacting carbonic or carboxylic acid derivs. of formula (II) with perfluoro-2,5-diazahexa-2,4-diene (III) in presence of an HF acceptor at -50 to 120 degrees C. In the formulae Z is O, R-N= or R'R"C=; X and Y = O, NR'" or NR1V, but not both O; and R, R', R", R'" and R1V are each H, is not >8C alkyl, alkenyl or alkynyl (all opt. substd. by halo, CN, lower alkoxy or alkylthio), opt. lower alkyl substd. cycloalkyl, carbalkoxy, aralkyl with 1-2C in the alkyl part, is not >14C aryl (opt. substd. by halo, CN, NO2, lower alkyl, haloalkyl, alkoxy or alkylthio), 5-7 membered heterocycles, or residues which join Z with X or Y to form a 5-7 membered ring (the heterocycles may be fused with a benzene ring which may be partially hydrogenated, and they may be substd. by halo, CN, NO2, or lower alkyl. (I) have antifungal, insecticidal and acaricidal activities and are useful in plant protection, veterinary medicine, hygienic applications and in preservation of stored goods. In an example N,N'-dimethylurea and (III) were reacted to give 1,3-dimethyl-4,5-bis-(trifluoromethylimino)-imidazol-2-one.
priorityDate 1970-12-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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