http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0759429-A1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0efa077d881a96aeb1e29b21ef1bbb58
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-56
filingDate 1996-08-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_80c8555b30f4c90f10c62442ccc950f0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_75bf9f4884ae8c26dc0c5deddc145cf9
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_734fe184279ff10577e412eda124521d
publicationDate 1997-02-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0759429-A1
titleOfInvention Substituted trifluormethylpyridines useful as intermediates for herbicidal 1-(pyridyl)-pyrazoles
abstract R 1 Amino oder Hydrazino, im Falle von Ib zusätzlich Chlor oder Fluor; R 2 Halogen; R 3 C 1 -C 6 Alkyl, C 2 -C 6 Alkenyl oder C 2 -C 6 -Alkinyl, wobei diese Gruppen bis zu 6 Halogenatome tragen können, nC 3 -C 6 -Cycloalkyl, das bis zu 3 C 1 -C 3 -Alkylreste tragen kann, C 1 -C 6 -Cyanoalkyl, C 1 -C 4 -Alkoxy-C 2 -C 6 -alkyl, 3-Oxetanyl, Carboxyl-C 1 -C 6 -alkyl, C 1 -C 6 -Alkoxycarbonyl-C 1 -C 6 -Alkyl, C 1 -C 4 -Alkoxy-C 2 -C 4 -alkoxycarbonyl-C 1 -C 6 -alkyl, Aminocarbonyl-C 1 -C 6 -alkyl, C 1 -C 4 -Alkylaminocarbonyl-C 1 -C 6 -alkyl, C 1 -C 4 -Dialkylaminocarbonyl-C 1 -C 6 -alkyl, C 2 -C 4 -Alkenylaminocarbonyl-C 1 -C 6 -alkyl, C 3 -C 4 -Alkinylaminocarbonyl-C 1 -C 6 -alkyl, Aminocarbonyl-C 1 -C 6 -alkyl, C 1 -C 4 -Alkyl-C 3 -C 4 -alkenylaminocarbonyl-C 1 -C 6 -alkyl, C 1 -C 4 -Alkyl-C 3 -C 4 -alkinylaminocarbonyl-C 1 -C 6 -alkyl, C 3 -C 6 -(α-Alkylalkyliden)iminoxy-C 2 -C 6 -alkyl, Cyclopropylmethyl C 1 -C 6 -Alkylamino, C 1 -C 6 -Dialkylamino, α-C 1 -C 6 -Alkylidenimino- oder -(C 1 -C 4 -Alkyl)-C 2 -C 6 -alkylidenimino, und Halogen Fluor, Chlor, Brom oder Jod nund Verfahren zu deren Herstellung.Substituted trifluoromethylpyridines of the general formula Ia or Ib. in which the substituents have the following meaning: R 1 Amino or hydrazino, in the case of Ib additionally chlorine or fluorine; R 2 Halogen; R 3 C 1 -C 6 alkyl, C 2 -C 6 alkenyl or C 2 -C 6 alkynyl, where these groups can carry up to 6 halogen atoms, C 3 -C 6 cycloalkyl which can carry up to 3 C 1 -C 3 alkyl radicals, C 1 -C 6 cyanoalkyl, C 1 -C 4 alkoxy-C 2 -C 6 alkyl, 3-oxetanyl, Carboxyl-C 1 -C 6 -alkyl, C 1 -C 6 -alkoxycarbonyl-C 1 -C 6 -alkyl, C 1 -C 4 -alkoxy-C 2 -C 4 -alkoxycarbonyl-C 1 -C 6 -alkyl, Aminocarbonyl-C 1 -C 6 -alkyl, C 1 -C 4 -alkylaminocarbonyl-C 1 -C 6 -alkyl, C 1 -C 4 -dialkylaminocarbonyl-C 1 -C 6 -alkyl, C 2 -C 4 -alkenylaminocarbonyl- C 1 -C 6 -alkyl, C 3 -C 4 -alkynylaminocarbonyl-C 1 -C 6 -alkyl, aminocarbonyl-C 1 -C 6 -alkyl, C 1 -C 4 -alkyl-C 3 -C 4 -alkenylaminocarbonyl- C 1 -C 6 alkyl, C 1 -C 4 alkyl-C 3 -C 4 alkynylaminocarbonyl-C 1 -C 6 alkyl, C 3 -C 6 - (α-alkylalkylidene) iminoxy-C 2 -C 6 -alkyl, cyclopropylmethyl C 1 -C 6 -alkylamino, C 1 -C 6 -dialkylamino, α-C 1 -C 6 -alkylidenimino- or - (C 1 -C 4 -alkyl) -C 2 -C 6 -alkylidenimino, and Halogen fluorine, chlorine, bromine or iodine and methods of making them.n n n The compounds can be used as intermediates for herbicidal 1- (pyridyl) pyrazoles.
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http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID1519376
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Total number of triples: 996.