http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-103265551-A

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classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-22
filingDate 2013-06-08-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8538ef03d608088411210dc0817cb956
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publicationDate 2013-08-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-103265551-A
titleOfInvention Method for synthesizing camptothecin serving as active intermediate of anti-tumor medicament
abstract The invention discloses a novel synthetic method for camptothecin serving as an intermediate of anti-tumor medicament irinotecan hydrochloride and various functional medicament camptothecin derivatives. According to the technical scheme, the method mainly comprises the following steps of: (1) obtaining a compound 2 from a compound 1; (2) obtaining a compound 3 from the compound 2; (3) obtaining a compound 4 from the compound 3; (4) obtaining a compound 6 from a compound 5; (5) obtaining a compound 7 from the compound 6; (6) obtaining a compound 8 from the compound 7; (7) obtaining a compound 9 from the compound 8; (8) obtaining a compound 10 from the compounds 4 and 9; and (9) obtaining a compound 11 from the compound 10, namely (20S)-camptothecin. By adopting the technical scheme, the method can be used for efficiently completing full synthesis of the camptothecin with short route based on simple commercial raw materials by using common reagents and simple operation.
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