http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-102120734-B
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_24c6c2c562cbff40a65d618fb81fcb53 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-82 |
| filingDate | 2011-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 2013-08-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_293e23c74b5e1bf73112f011cf265625 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_c8cd3038ac8c7d49323deeac7b926a4c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_98c51697af55695dade7b7d555f7d575 |
| publicationDate | 2013-08-07-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CN-102120734-B |
| titleOfInvention | Method for preparing 2-(N-alkyl)aminobenzothiazole derivatives by using active alcohol as alkylating reagent |
| abstract | The invention relates to a method for preparing 2-(N-alkyl)aminobenzothiazole derivatives by using active alcohol as alkylating reagent. The method is as follows: commercial or easily synthesized 2-aminobenzothiazole compounds used as the starting raw material perform alkylation reaction with alcohol in the presence of the catalytic amounts of copper salt and alkali to obtain the 2-(N-alkyl)aminobenzothiazole derivatives. The method uses environmentally friendly alcohol as alkylating reagent; only one byproduct-water is generated, which can not damage the environment; the reaction has high atom economy, the requirements of green chemistry can be met and the method has wide application prospect. |
| priorityDate | 2011-01-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 142.