http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-113912554-A

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filingDate 2021-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a10a1553560af059eaf2ceca1ab51d5a
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publicationDate 2022-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-113912554-A
titleOfInvention A kind of synthesis and refining process of erlotinib hydrochloride
abstract The erlotinib hydrochloride synthesis and purification process of the present invention comprises the following steps: 1. using 6,7-bis(2-methoxyethoxy)-quinazoline-4 ketone as a starting material, chlorination to obtain an intermediate (1): 4-chloro-6,7-two-(2-methoxyethoxy)-quinazoline; 2. the intermediate (1) is docked with 3-amino phenylacetylene, and the intermediate is free and refined through aftertreatment Body (2): N-(3-acetylene phenyl)-6,7-bis(2-methoxyethoxy)-4-quinolinamine; 3. make intermediate (2) salify with hydrogen chloride, and obtain Finished product erlotinib hydrochloride. The synthesis and purification process of the invention has the advantages of easy availability of raw materials, mild reaction conditions, avoiding the use of multiple types of highly toxic solvents, simple operation steps and suitable for industrial production, and the total yield of the products obtained by the process is higher, and the quality index is better than domestic standard.
priorityDate 2021-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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