http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102718739-B

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http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b9dccff33aeb9f1de0fd4f63d6dd8043
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D317-46
filingDate 2012-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2013-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ca8af6a7349a23d15b827d5449dc68e4
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_e968c7672d2c500443ee6b852b1e1614
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8c5a604ab8b4bd0479005bc58dbaac31
publicationDate 2013-12-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-102718739-B
titleOfInvention Method for preparing (2S)-2-[[(9H-fluorene-9-yl methoxy) carbonyl] amino]-3-(2,2-dimethyl-1,3-benzo dioxol-5-yl)propionate
abstract The invention discloses a method for preparing (2S)-2-[[(9H-fluorene-9-yl methoxy) carbonyl] amino]-3-(2,2-dimethyl-1,3-benzo dioxol-5-yl)propionate, which mainly aims to solve the technical problems of complicated steps and high operating difficulty in existing synthetic routes. The invention has the technical scheme that levodopa reacts with Fmoc N-hydroxysuccinimide este to obtain Fmoc acyl levodopa; and the Fmoc acyl levodopa reacts with 2,2-dimethoxypropane to obtain (2S)-2-[[(9H-fluoren-9-yl methoxy) carbonyl] amino]-3-(2,2-dimethyl-1,3- benzo dioxol-5-yl)propionate. The solvent used in the reaction of the Fmoc acyl levodopa and the 2,2-dimethoxypropane to obtain the (2S)-2-[[(9H-fluoren-9-yl methoxy) carbonyl] amino]-3-(2,2-dimethyl-1,3- benzo dioxol-5-yl)propionate is tetrahydrofuran; and the catalyst is pyridinium p-toluenesulfonate. The resultant obtained by the method is applied in the field of peptide synthesis as a non-natural amino acid protecting reagent.
priorityDate 2012-06-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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