http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S63216889-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_b9822bceff022feda91b10019125e70f |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-40 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-403 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D495-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P35-00 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D209-00 |
| filingDate | 1987-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1437f4405d66d7548bdb74495c5fd6a5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4b466a633772259ebd6ee737b1d55300 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_202d48f90d70811a7f24b245aac00325 |
| publicationDate | 1988-09-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-S63216889-A |
| titleOfInvention | 5-thiabenz(cd)indoles |
| abstract | NEW MATERIAL:The compound of formula I [X is H or arenesulfonyl; S-x-y are group of formula II (R is H or lower alkyl), etc.]. n USE: A synthetic raw material for antibiotic substance chuanghsinmycins and carcinostatic agent. n PREPARATION: The compound of formula I can be produced e.g. by adding acetyl chloride to 4-(cyanomethylthio)indole of formula III in a solvent in argon stream to effect 3-acetylation reaction, reacting the reaction product with p- toluenesulfonylhydrazine, etc., dissolving the resultant compound of formula IV (Ts is p-toluenesulfonyl) in diglyme, etc., adding sodium hydride to the solution and thermally refluxing the mixture to effect cyclization reaction. n COPYRIGHT: (C)1988,JPO&Japio |
| priorityDate | 1987-03-06-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 26.