http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-H08176150-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_01249be6ad92a1f01c99b5987ca16162 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-415 |
| filingDate | 1994-12-19^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fc687fbaf5db2ae60e78a19cbefa28d6 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_999651c94e031e10a7c3cda55c853768 |
| publicationDate | 1996-07-09^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | JP-H08176150-A |
| titleOfInvention | Process for producing 5-chloro-4- (2-imidazolin-2-ylamino) -2,1,3-benzothiadiazole or salt thereof |
| abstract | (57) [Summary] [Structure] 5-chloro-4- represented by the following formula [I] (2-Imidazolin-2-ylamino) -2,1,3- In the method for producing benzothiadiazole, the following formula [I I]] 4-amino-5-chloro-2,1,3- Benzothiadiazole is reacted with 2-chloro-2-imidazoline · sulfate represented by the following formula [III]. Embedded image According to the present invention, 4-amino-5-chloro- 2,1,3-Benzidithiadiazole and 2-chloro-2- By reacting imidazoline / sulfate with an organic solvent, 5-chloro-4- (2-imidazolin-2-ylamino) -2,1,3-benzothiadiazole can be industrially advantageously produced. . |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-106496219-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CZ-301889-B6 http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107778307-B http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-107778307-A http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CN-109535148-A |
| priorityDate | 1994-12-19^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
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