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filingDate 1988-12-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e3c7e5015ea160676e8f9def7bf7b49c
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publicationDate 1990-05-28-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-H02138177-A
titleOfInvention Preparation of noncyclic pyrimidine nucleotide
abstract PURPOSE: To obtain a substance in a high yield by a method in which a pyrimidine derivative, after being treated occasionally with hexamethyldisilazane, is reacted with 2-acetoxyethyl acetoxymethyl ether, etc., in the presence of CsI and an organic solvent. n CONSTITUTION: A compound of formula I (X is S or O; R 1 -R 3 are each H, CH 3 , F or OH; and R 2 can be NH 2 ), after being treated according to circumstances with hexamethyl silazane, is reacted with 2-acetoxyethyl acetoxymethyl ether or O-chloromethyl-1,3-di-O-benzyl glycerin in the presence of CsI and an organic solvent (example: acetonitrile) to obtain a compound of formula II [Z is 2-acetoxyethoxymethyl or 1,3-bis(benzyloxy)-2- propoxymethyl]. The compound of formula II are important as antiviral agents, anticancer drugs, and antibacterial agents and obtained inexpensively in a short time by the above-described method. n COPYRIGHT: (C)1990,JPO
priorityDate 1988-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
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Total number of triples: 27.