http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-1474386-B1

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_3130c25007b4859641ec5a22fc903139
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D307-94
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C319-28
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C319-24
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C233-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C323-53
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D307-94
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C231-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C319-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C319-06
filingDate 2003-02-05-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2006-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_53c81f94858af898a7716399fca0b739
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f27c58795fb16d270d3ee1698b9ead02
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f78fcbaedc92255afc4b371c58eaf117
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_a1fd1013af62d34488cc1caa1af915ac
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_be2ecdca48dafd678be8ff87843eede0
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_69e4fb1127efaca6fd379300c8caf8ce
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6a1d56b3315d4113dbc8a8d53899685d
publicationDate 2006-12-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-1474386-B1
titleOfInvention Process for the preparation of 1-(mercaptomethyl)-cyclopropaneacetic acid
abstract A process for the preparation of highly pure 1-(mercaptomethyl)-cyclopropaneacetic acid is described. Treatment of 1-(hydroxymethyl)-cyclopropaneacetonitrile with an acid provides the corresponding imino ester and/or halo-amide, which when reacted with thiourea provides the corresponding amide-isothiuronium salt. Hydrolysis of the amide-isothiuronium salt followed by an in situ oxidation allows the facile isolation and purification of 1-[1-(carboxymethyl)-cyclopropanemethyldisulfanylmethyl]-cyclopropaneacetic acid (also known as 1-(mercaptomethyl)-cyclopropaneacetic acid disulfide). Reduction of the 1-(mercaptomethyl)-cyclopropaneacetic acid disulfide under mild conditions provides the 1-(mercaptomethyl)-cyclopropaneacetic acid with high purity.
priorityDate 2002-02-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

Predicate Subject
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231509524
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7909
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID128296525
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129766888
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231509541
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226942276
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9833939
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID247015108
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9793825
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231509561
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226394049
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID135792185
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID70297
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID248680478
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231509506
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID15970
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231509520
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID227856568
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID17989459
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231509519
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID227245350
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18674708
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231509528
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9964076
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID248009695
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226405837
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18674709
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID231509530
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9899067
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129465731
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67643801
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID18674711
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID246001583
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226926069
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129653032
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID7915
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID9964295
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87882594
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID129257365
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID57012192
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID87882595
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID4101437

Total number of triples: 67.