http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0204264-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_5929f2d6f4dba84be8dd3a8ba633db12
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-06
filingDate 1986-05-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5f2d35660ec32e359b1cb487ea1946b2
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fb00f7d504d05b0a13f99f103010d175
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_9d8c69c706ffd321f128eb629445d5a6
publicationDate 1986-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0204264-A2
titleOfInvention Conversion of uracil derivatives to cytosine derivatives
abstract A process is disclosed for producing a 4-0-sulfonyluracil derivative of the formula[wherein R<sup>1</sup> is hydrogen, halogen, alkyl and alkoxy, R<sup>2</sup> is glycosyl having protected hydroxyls; and -SO<sub>2</sub>R<sup>3</sup> is an organic sulfonyl] which comprises reacting an uracil derivative of the formula[wherein R<sup>1</sup> and R<sup>2</sup> are the same above] with an organic sulfonylating agent of the formula R<sup>2</sup> S0<sub>2</sub>X [wherein R<sup>3</sup>S0<sub>2</sub> is an organic sulfonyl and X is halogen] in the presence of potassium carbonate. The obtained 4-0-sulfonyluracil is further subjected to amination. The processes are industrially advantageous and produce cytosine derivatives such as cytidine in high yield.
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0757056-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-101580528-B
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0630897-A2
priorityDate 1985-06-04-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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