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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_14effe3850d2129f863b969dac4f1db8
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D413-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-79
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-80
filingDate 1993-05-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1997-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3aebb696e2eff55dba278122c892dab3
publicationDate 1997-09-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2090558-C1
titleOfInvention 5,6-disubstituted 3-pyridylmethylammonium halogenides, method of their synthesis and methods of synthesis 5-(substituted methyl)-2,3-pyridine carboxylic acids
abstract FIELD: organic chemistry, chemical technology. SUBSTANCE: products: 5,6-disubstituted 3-pyridylmethylammonium halogenides of the formula (I) given in description where: Z and Z 1 - H; X - Cl, Br or J; Y and y 1 - OR 4 ; R 4 - H, C 1 -C 4 -alkyl; Q - RR 1 R 2 -N ⊕ -, or nitrogen-containing heterocycle, R, R 1 and R 2 - C 1 -C 4 -alkyl. Reagent 1: compound of the formula (II) given in description where: Z, Z 1 , Y and y 1 as indicated above. Method involves interaction with halogenating agent in medium of inert organic solvent in the presence of radical initiating agent followed by treatment of the formed reaction mixture with 1 mole trialkylamine. Synthesized compounds were used as semiproducts for synthesis of herbicides. EFFECT: improved method of synthesis. 1 tbl, 10 cl
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2549896-C2
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priorityDate 1992-10-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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