http://rdf.ncbi.nlm.nih.gov/pubchem/patent/KR-0130942-B1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_e58dd78098a9ff1f2ebd9a222bfcbc51
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H19-067
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-7068
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H19-06
filingDate 1994-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1998-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7079c41719dceebc005db4b567695fb4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0f62a0306fd8ce9b400746a297509d5c
publicationDate 1998-04-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber KR-0130942-B1
titleOfInvention Method for preparing 3'-azido-3'-deoxythymidine
abstract The present invention provides a method for preparing 3'-azido-3'-deoxythymidine of the general formula (I) below, which is useful as an antiviral or AIDS treatment. In the process of the present invention, in preparing a compound of general formula (I) from thymidine, a hydroxyl group in the 5'-position is protected by a trityl group (compound of general formula (III ')) or an unprotected thymidine ( Reacting the compound of formula (III)) with O-acetyl salicyloyl crawlide to obtain a compound of formula (II) or formula (II '); Reacting a compound of formula (II) or formula (II ′) with (PhO) 2 PON 3 or Ph 3 P-NH 3 -diethyl azodicarboxylate; And optionally removing the protecting group of the hydroxyl group at the 5'-position.n n n n n n n n (The compound in which 5′-position is —OR in the formula is (III ′).)n n n n n n n n (The compound whose 5'-position is -OR in the formula is (II ').)n n n n n n n n (Wherein R is a trityl group)
priorityDate 1994-07-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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