http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2313522-C1

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_10efc646a4dd605c2f09c493718f5b81
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-14
filingDate 2006-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2007-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c6dc23d0e54859eb70e22e73e3763e09
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4509a9942e22240712890e34e4698c98
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_14b2672061ab8ee720262f4f8974d52e
publicationDate 2007-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber RU-2313522-C1
titleOfInvention Method for preparing 5-amino-1,2,4-triazole-3-ylacetic acid monohydrate
abstract FIELD: organic chemistry, chemical technology. n SUBSTANCE: invention describes a method for synthesis of 5-amino-1,2,4-triazole-3-ylacetic acid. Method involves interaction of malonic acid with aminoguanidine hydrocarbonate in the ratio = 1.1:(1.0-1.3) at pH 0-1 in the presence of HCl. Then water is distilled off from the reaction mixture under vacuum followed by cyclization of formed malonic acid monoguanylhydrazide by effect with alkali and isolation of the end substance at acidification of the reaction mass to pH 3-4 and cooling. All process is carried out at temperature 80-100 0 C. Proposed process provides preparing the end substance with high yield for short period of time. n EFFECT: improved method of synthesis. n 2 cl, 1 dwg, 8 ex
priorityDate 2006-06-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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