http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-2002010326-A1

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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D285-01
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07H21-00
classificationIPCAdditional http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-00
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07H21-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-01
filingDate 1997-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ea0e1d0e93d29c2e7904967e8de65dc9
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8885a09d31b8ad044cdb4396d90c8c18
publicationDate 2002-01-24-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber US-2002010326-A1
titleOfInvention Novel sulfurizing reagent 3-phenyl-1,2,4-dithiazoline-5-one
abstract In our research, 3-phenyl-1,2,4-dithiazoline-5-one is found to be a potential sulfur-transfer reagent. The efficiency and optimization of this new sulfur-transfer reagent was investigated by solid-phase syntheses of dinucleotide phosphorothioate and 25 mer oligonucleotide phosphorothioates at 1 μmol and 200 μmol scales. The results show that 3-phenyl-1,2,4-dithiazoline-5-one is a highly efficient sulfurizing reagent, and greater than 99.8% sulfur transfer efficiency can be achieved. In contrast to EDITH or Beaucage reagent, this novel sulfur-transfer reagent is highly stable in storage and in solution, highly soluble in CH 3 CN solvent, and can be synthesized at a low cost because of the single step reaction. Due to these advantages, 3-phenyl-1,2,4-dithiazoline-5-one can be considered as a better alternative to EDITH or Beaucage reagent, especially in large-scale preparation of oligonucleotide phosphorothioates.
priorityDate 1997-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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