http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106632068-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D237-14
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D237-14
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_208a92c69ffeae6b8f69c6516390daf4
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publicationDate 2017-05-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-106632068-A
titleOfInvention Synthesis method of 4-bromine-6-chloropyridazine-3(2H)ketone
abstract The invention relates to a synthesis method of 4-bromine-6-chloropyridazine-3(2H)ketone. The synthesis method of the 4-bromine-6-chloropyridazine-3(2H)ketone comprises the following steps: continuously conducting reaction in a proper solvent and under the action of alkali at 0 to 100 DEG C for 6 to 25 hours by taking 3-amino-6-chloropyridazine, liquid bromine, concentrated sulfuric acid and sodium nitrite as raw materials to produce a 4-bromine-6-chloropyridazine-3(2H)ketone crude product, wherein the ratio of the 3-amino-6-chloropyridazine to the liquid bromine is 1:(0.8-3.2), and the ratio of the 3-amino-6-chloropyridazine to the sodium nitrite is 1:(1.0-2.1); performing purification to obtain a 4-bromine-6-chloropyridazine-3(2H)ketone pure product. According to the synthesis method of the 4-bromine-6-chloropyridazine-3(2H)ketone, the raw materials are easily available and the price is reasonable; meanwhile, heavy metal and corrosive gas are not used in the preparation reaction, the reaction is mild, special requirements on the reaction equipment are not needed, and the common corrosion-resistant equipment can perform production; in addition, the reaction condition is moderate.
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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