http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106432182-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_a7645b337960b4895ea9079b72f1215c
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D401-02
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-02
filingDate 2016-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_610ef116c9626a1e324440cf24e6ab85
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_56c7b543c266eab828086e76a50e293d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d5f32683449db0063b19293a6be84271
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4e813169e41c251e3702c1d8a28de4b7
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_abca9c5d679104da75ce02d2a94ca2bd
publicationDate 2017-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CN-106432182-A
titleOfInvention The synthetic method of tedizolid intermediate
abstract The invention provides a method for synthesizing a tedizolid intermediate. The synthetic method of tedizolid intermediate comprises the following steps: step A: make the cyano group in compound (I) and alcohol generation addition reaction, generate the acid salt of compound (II) or compound (II); Step B: use Hydrazine group or methylhydrazine group replace the alkoxyl group on the acid salt of described compound (II) or compound (II), generate compound (III); Step C: make compound (III) and sodium nitrite under acidic condition The following reaction generates tedizolid intermediate (IV). The overall reaction is The invention solves the problems of explosive and highly toxic reaction reagents, difficulty in separating by-products of methyl isomerism, and the like.
priorityDate 2016-09-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-104447740-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2015095097-A2
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2013050341-A1
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102177156-A
http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102015693-A
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID465335447
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID163686323

Total number of triples: 22.