http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104910155-A

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D471-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D471-04
filingDate 2015-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ae243c12ccc56f5a56d8725b6dd88b8f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e65ef6d343f20fc341c09c8d33886d73
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publicationDate 2015-09-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-104910155-A
titleOfInvention 3-Iodo-6-chloro-imidazo [1,2-a] pyridine synthetic method
abstract The present invention belongs to the field of organic synthesis, and in particular relates to a 3-iodo-6-chloro-imidazo [1,2-a] pyridine synthetic method. The synthetic method comprises the following steps: 2-amino-5-chloropyridine, A chloroacetaldehyde aqueous solution, and N-iodosuccinimide are used as raw materials for continuous reaction under the action of a base in a suitable solvent at 40-150 DEG C to obtain a 3-iodo-6-chloro-imidazo [1,2-a] pyridine crude product, wherein the ratio of the number of moles of 2-amino-5-chloropyridine to chloroacetaldehyde aqueous solution is 1: 0.7-2.8, the ratio of the number of moles of 2-amino-5-chloropyridine to N-iodosuccinimide is 1: 1.0-3.1, and the 3-iodo-6-chloro-imidazo [1,2-a] pyridine crude product is purified to obtain a 3-iodo-6-chloro-imidazo [ 1,2-a] pyridine pure product. Reaction raw materials are relatively easy to obtain, and are reasonable in prices, the reaction are mild in conditions, easy to operate, and easy to control, post-processing is simple, product quality is stable, and purity is high.
priorityDate 2015-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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