http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H024784-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_9ceaa82521cd0ffe561313badc619f1c |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D277-68 |
| filingDate | 1988-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_abd8548748fedfd409c53e10278c71d8 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_3c549e8e5c16c968e6db5641df757fab http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_81aac1eac7c5f110e822a20a07010c2f |
| publicationDate | 1990-01-09-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H024784-A |
| titleOfInvention | Production of 5-amino-6-fluoro-2-benzothiazolone |
| abstract | PURPOSE: To simply obtain the subject benzothiazolone of high purity useful as the raw material of a herbicide, a benzothiazole derivative by hydrolyzing a specified benzothiazole. n CONSTITUTION: Hydrolysis of 2-alkoxy-5-amino-6-fluoro-2-benzothiazole of formula I is carried out to provide the objective 5-amino-6-fluoro-2-benzothiazolone of formula II. In addition, the hydrolysis is recommended to be carried out, e.g., by reacting hydrochloric acid in ethanol solvent at 50-100°C. n COPYRIGHT: (C)1990,JPO&Japio |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-6363916-B2 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/US-5356864-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0588183-A1 |
| priorityDate | 1988-06-23-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 27.