http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-8103020-A1

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filingDate 1981-04-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f38620f4633b89b9dd5ed2aa209cdc0b
publicationDate 1981-10-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber WO-8103020-A1
titleOfInvention Triazine synthesis
abstract A process for the synthesis of substituted 1,3,5-triazine compounds of the general formula: (FORMULA) wherein R<s1>s and R<s2>s, which may be the same or different, are selected from the group consisting of hydrogen, halogen, alkoxycarbonyl, alkyl, substituted alkyl, aryl, substituted aryl, heteroaryl, substituted heteroaryl, alkylamino, dialkylamino, arylamino, alkyl-arylamino, alkylthio, arylthio, alkoxy and aryloxy (provided that R<s1>s and R<s2>s are not both halogen); and R<s3>s is selected from the group consisting of halogen, alkylamino, dialkylamino, arylamino, alkyl-arylamino and N-heteroaryl; comprises reaction of a substituted halomethyleneiminium salt with a substituted N-cyanoamidine, N-cyanoguanidine, N-cyanocarbamimidate or N-cyanocarbamidothioate. Substituted 1,3,5-triazine compounds having fungal germination inhibition properties are also disclosed. The following compounds 1) 2-chloro-4-phenyl-1,3,5-triazine, 2) 2-chloro-4-phenoxymethyl-6-phenyl-1,3,5-triazine, 3) 2-N-methylphenylamino-4-phenyl-1,3,5-triazin, 4) 2-chloro-4-cyanomethyl-6-phenyl-1,3,5-triazine are also disclosed and claimed.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-7015227-B2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2006505514-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2021054856-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2002193952-A
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