http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-105732549-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_88d060800d601726cfb561f20f5edc44
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-68
filingDate 2014-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b9aac0f2b008f982aad87544036e89e8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_86965acea8210aa4c76d55a5fd48fd80
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d6401c40019a191dd00a8a4612ca94c4
publicationDate 2016-07-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-105732549-A
titleOfInvention Method for preparing furbenicillin sodium intermediate
abstract The invention relates to a method for preparing a furbenicillin sodium intermediate. The furbenicillin sodium intermediate is alpha-[[[(2-furoyl)animo]carbonyl]animo]sodium phenylacetate. Alpha-isocyanate furoyl ester is prepared through the steps of oximation, rearrangement and condensation by using furfural as a raw material. Alpha-[[[(2-furoyl)animo]carbonyl]animo]phenylacetic acid is prepared by the reaction of alpha-isocyanate furoyl ester and D-phenylglycine, and then by alkalization, alpha-[[[(2-furoyl)animo]carbonyl]animo]sodium phenylacetate is prepared.
priorityDate 2014-12-10-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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