http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-2057169-A2

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assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_220502f4465d0df4f6e058e25e45d626
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D491-22
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P35-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61P7-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D491-22
filingDate 2007-06-29-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ac0b6dd766a443cb47b0ee76c47133c3
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_87340c2a85c16683f8d795f3186013c8
publicationDate 2009-05-13-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-2057169-A2
titleOfInvention Compositions and methods of making a chlorin e6 derivative as a photoactive agent
abstract An improved two stage reaction process for production of mono-L-aspartyl chlorin e6. In a first stage, the activation reaction between chlorin e6 and a carbodiimide produces a previously unknown anhydride in an activation reaction product. This reaction product is purified to remove a significant proportion of the precursors of di-L-aspartyl chlorin e6. The purified activation reaction product contains a higher concentration of the previously unknown anhydride. This purified reaction product is used in a second stage: a coupling reaction of the purified activation reaction product with aspartate. The coupling reaction produces a coupling reaction product that has significantly reduced di-L-aspartyl chlorin e6 concentration. This reduced di-L-aspartyl chlorin e6 concentration facilitates purification of mono-L-aspartyl chlorin e6 from the coupling reaction mixture.
priorityDate 2006-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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