| Predicate |
Object |
| assignee |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_59e1d955a7b1560dc68cf7fd800e8fac |
| classificationCPCAdditional |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/Y02P20-55 |
| classificationCPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D233-84
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D235-28 |
| classificationIPCInventive |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D233-84
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-28 |
| filingDate |
2001-10-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor |
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5bce4779936b3cce4ebaff9014cdf206
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1cbfe02de90c62d2eea136a7d0cfe117 |
| publicationDate |
2003-07-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber |
EP-1326844-A2 |
| titleOfInvention |
Process for preparation of n-substituted 2-sulfanylimidazoles |
| abstract |
A convenient one step synthesis of N-substituted 2-sulfanylimidazole from an isothiocyanate, an α-aminocarbonyl compound and an alkyl halide or an activated aryl halide is described. Reaction of an isothiocyanate with an α-aminocarbonyl compound affords a thiourea acetal intermediate, which without isolation or purification affords the desired N-substituted 2-sulfanylimidazole upon treatment with an alkyl halide or an activated aryl halide. |
| priorityDate |
2000-10-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type |
http://data.epo.org/linked-data/def/patent/Publication |