http://rdf.ncbi.nlm.nih.gov/pubchem/patent/RU-2024516-C1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_620ecb9324409347c27e96b6071503ee |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P25-06 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-415 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-4184 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D401-12 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-08 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-04 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61P1-14 |
| filingDate | 1990-02-01-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1994-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b15e9b68b7f8a9ace710b8a354527227 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_7d07a62007bce9a0de301b347a4f4157 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_2da9be7dd184b4042785da613449dbc2 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_623d78af2c6a52c353483b3d9b829a8e http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4d7fd01f41ea0b38d98f8fc398cdd49d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1fcb69982561a67a65e3927f3277a7fd http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_6f720102abef8979ff42d427bf78135d |
| publicationDate | 1994-12-15-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | RU-2024516-C1 |
| titleOfInvention | Method of synthesis of tetrahydrobenzimidazole derivative or its pharmaceutically acceptable salt |
| abstract | FIELD: organic chemistry. SUBSTANCE: product of the formula (I), where Het - a residue of indole, 2,3-dihydroindole, benzoxazine, dihydrobenzoxazine, phenothiazine, tetrahydroquinoline, benzothiophene, pyrrole, tetrahydroisoquinoline, thiadiazole, pyridine, 2,3-dihydrobenzimidazole, benzofuran, pyrrolidine, pyrimidine, benzimidazole, benzothiazole, quinoline, indazole, cyclopentathiazole, dihydrocyclopentathiazole, carbazole, 2,3-dihydrobenzimidazole-2-one, tetrahydrobenzothiophene, indene, thiophene, indolysidine or furan which can be substituted with 1-3 substituents taken from the group consisting of the lower alkyl group, lower alkenyl group, lower alkinyl group, cycloalkyl-lower alkyl group, aralkyl group, lower alkoxy-group, nitro-group, hydroxyl-group, lower alkoxycarbonyl-group or halide atom. X 2 - bond linked with carbon atom of heterocyclic ring Het. Reagent 1: heterocyclic compound of the formula (II) where Het and X 2 - as indicated above. Reagent 2: compound of the formula (III), or its reactive derivative. Synthesized compounds are used as preparations usable as 3-HI 3 -receptor antagonists. EFFECT: improved method of synthesis. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EA-003276-B1 |
| priorityDate | 1989-02-02-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 176.