http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106674116-A

Outgoing Links

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_0ce58d6b1dbe1bc3bfad551a58ccb034
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D231-38
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filingDate 2016-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_04387f20d48b4ec5b7a519dd185ea3e2
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publicationDate 2017-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-106674116-A
titleOfInvention Synthetic method of 4-amino-1,3-dimethylpyrazole and pharmaceutically acceptable salt thereof
abstract The invention discloses a synthesis method of 4-amino-1,3-dimethylpyrazole and a pharmaceutically acceptable salt thereof. The method starts with methylhydrazine and 4,4-dimethoxy-2-butanone Raw materials, first synthesize 1,3-dimethylpyrazole, then add concentrated nitric acid for nitration to obtain 4-nitro-1,3-dimethylpyrazole, and then directly reduce it to a pharmaceutically acceptable salt, or first nitrate the nitro-1,3-dimethylpyrazole After reduction to the amino group, it is converted to 4-amino-1,3-dimethylpyrazole. The raw materials used in the synthesis method of the invention are low in price, low in cost and easy to obtain. Moreover, the present invention has short synthetic route, high yield, high chemical purity of the obtained product, all reactions do not need special production equipment, and the obtained intermediate and final product do not need column chromatography and crystallization purification.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-112574095-A
priorityDate 2016-12-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID5200289
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Total number of triples: 21.