http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6341457-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_03d0f52bb4069f8a19d70dcfb697c67a
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D207-325
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-08
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-86
filingDate 1986-08-06-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4d5c11a3d1f34c70d652adfe407b0655
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_08703a65e84141d0765d9249b05f19fc
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3b4e36cd8db18de1dbe3dc7a249a8852
publicationDate 1988-02-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber JP-S6341457-A
titleOfInvention Production of heterocyclic derivative
abstract PURPOSE: To obtain the titled compound useful as a drug, agricultural chemical, dye or an intermediate for dye, by reacting an NH-containing heterocyclic compound with an aromatic sulfonic acid alkyl ester containing -O- bond in the presence of a specific amount of an alkali under a mild condition. n CONSTITUTION: An NH-containing heterocyclic compound such as pyrrole, indole, carbazole, etc., is reacted with an aromatic sulfonic acid alkyl ester containing an ether bond at the β-position in the presence of ≥an equimolar amount of an alkali based on the heterocyclic compound to give an N-substituted heterocyclic derivative (e.g. 1-phenoxyethyl-2-methylindole, etc.). n COPYRIGHT: (C)1988,JPO&Japio
isCitedBy http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-2007075972-A
priorityDate 1986-08-06-04:00^^<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/JP-S5989360-A
isDiscussedBy http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234881787
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID407208027
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID410031093
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID67859918
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID419559261
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID798
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226421593
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID19795561
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226393662
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID226398998
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID425240125
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID14178120
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID6854
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID56605938
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID420306702
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID3283
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234881795
http://rdf.ncbi.nlm.nih.gov/pubchem/compound/CID8027
http://rdf.ncbi.nlm.nih.gov/pubchem/substance/SID234881780

Total number of triples: 35.