http://rdf.ncbi.nlm.nih.gov/pubchem/patent/IT-1055503-B
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_bde8ecff5b221d2df08e4fde167a2c63 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C- |
| filingDate | 1966-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| grantDate | 1982-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1982-01-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | IT-1055503-B |
| titleOfInvention | PREPARATION PROCESS FOR AMINO 2 METHYL 6 HEPTANOL 6 DERIVATIVES |
| abstract | Medicaments containing the following salts of 2-amino-6-methylheptan-6-ol ('hepaminol') (I):- (a) camphorsulphonate, nicotinate, (b) p-aminohippurate, mono- and di-phosphates, (c) phthalamate, p-aminobenzoate, (d) succinate, glutamate, (e) glucuronate, salicylate. Salts (a) as myocardiotonics, (b) as diuretics, (c) as respiratory stimulants, (d) as psychostimulants and (e) as antifatigue and detoxicating agents. solutions of (I) (21.75g.) and succinic acid (17.7 g.) in 95% alc. (50 ml.) are mixed and evaporated at room temperature and 12 mm. press. Crystd. from EtOH (10 ml.) and acetone (40 ml.), the salt has m.p. 105 deg.; yield 70-80%. |
| priorityDate | 1966-11-19-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 36.