http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S54151968-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1374dd16777534b65ad4422333245af8 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D235-02 |
| filingDate | 1978-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_aaa5a7635cb4120b8648490ef868c472 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_568fb60bf49c58d4d71496648ab44a93 |
| publicationDate | 1979-11-29-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S54151968-A |
| titleOfInvention | Tetrahydronaphtho1,2-dimidazoline-2-thiones and their preparation |
| abstract | NEW MATERIAL:Tetrahydronaphtho[1, 2-d]imidazoline-2-thiones of formula I (ring A may be substituted with lower alkyl, lower alkoxy, halogen; condensed rings B and C may be either cis or trans). n EXAMPLE: Cis-3a,4,5,9b-tetrahydronaphtho[1,2-d]imidazoline-2-thione. n USE: Immunity controller, anti-inflammatory, central nervous system depressant, hypotensor, anthelmintics, or their intermediates. n PREPARATION: A compound of formula II (two amino groups on ring B may be either cis or trans) is made to react with 1W1.3 mole, per mole of the compound, of carbon disulfide to form their adduct, which is subjected to dehydrosulfurization to prepare the objective compound of formula I. n COPYRIGHT: (C)1979,JPO&Japio |
| priorityDate | 1978-05-17-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 17.