http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102304082-B

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a3d7e466c44c7b54e2a48e4bf62665ef
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D213-61
filingDate 2011-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_54f77225cf4069bacdc2f8bee4fa9b1d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aac9c0d3b9457b71a6f5e29e2015f272
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_518b36266fcd9856f253b06d7f6a1fc2
publicationDate 2013-05-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102304082-B
titleOfInvention Synthesis method of 2-chloro-4-(piperidylmethyl)pyridine
abstract The invention relates to a synthesis method of 2-chloro-4-(piperidylmethyl)pyridine, belonging to the field of medicine synthesis. The method comprises the following steps: dropwisely adding a nitrite water solution into acid and 2-amino-4-methylpyridine to react, thereby obtaining a white solid product; adding POCl3 into the white solid to obtain a compound 2-chloro-4-methylpyridine; dropwisely adding SO2Cl2 into the compound 2-chloro-4-methylpyridine while adding a free-radical initiator batch by batch, and distilling under reduced pressure to obtain a compound 2-chloro-4-chloromethylpyridine; and condensing the 2-chloro-4-chloromethylpyridine and piperidine to obtain the 2-chloro-4-(piperidylmethyl)pyridine. Compared with the traditional synthesis method of 2-chloro-4-(piperidylmethyl)pyridine, the synthesis method provided by the invention has the advantages of simpler steps (only three steps) and lower cost of raw materials, and the total yield is higher than 32%. Generally, the invention can greatly lower the synthesis cost of lafutidine.
priorityDate 2011-09-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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