http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H1036358-A
Outgoing Links
Predicate | Object |
---|---|
assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b0977255f940397ca6bbbb3f5cd7e1db |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-58 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D265-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C333-16 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D263-16 |
filingDate | 1996-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_35b7d571f86833ce930a15f9fdde6f22 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5d8f74b65fe2ea018bc369e28a76534c |
publicationDate | 1998-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-H1036358-A |
titleOfInvention | Method for producing 2-thioxo-1,3-O, N-heterocyclic compound |
abstract | (57) [Summary] [PROBLEMS] To safely and efficiently yield 2-thioxo-1,3- To produce an O, N-heterocyclic compound. SOLUTION: An amino alcohol compound is reacted with carbon disulfide in the presence of a base to form a dithiocarbamate, and then reacted with hydrogen peroxide in a water-soluble organic solvent, Chemical formula [3] (Wherein, R 1 is an alkylene group, a cycloalkylene group, R 2 represents a hydrogen atom, Represents an alkyl group or a substituted alkyl group. 2-) represented by Produce a thioxo-1,3-O, N-heterocyclic compound. |
priorityDate | 1996-07-22-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 114.