http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106632016-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D213-75
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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-75
filingDate 2016-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4ad4a38ba1ff94af9ee114d915a0145b
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8f0797de794c422a403f049b1e5db3f9
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publicationDate 2017-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-106632016-A
titleOfInvention Synthesis method of 2-acetamido-5-bromopyridine
abstract The invention relates to a synthesis method of 2-acetamido-5-bromopyridine. 2-amino-5-bromopyridine and acetic anhydride are used as raw materials; the mol ratio of the 2-amino-5-bromopyridine to the acetic anhydride is 1: (0.85 to 3.6); in a proper solvent, the continuous reaction is performed at 45 to 115 DEG C to generate a coarse product of 2-acetamido-5-bromopyridine; after the purification, a pure product of the 2-acetamido-5-bromopyridine is obtained. The method has the advantages that the raw materials can be easily obtained; the price is reasonable; meanwhile, heavy metal and corrosive gas are not used in the preparation reaction; the reaction is mild; no special requirements exist on reaction equipment; the production can be performed by ordinary anti-corrosion equipment; in addition, the reaction conditions of the method are proper; no pollution can be caused on the environment.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-115010656-A
priorityDate 2016-11-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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