http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-993739-A

Outgoing Links

Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_c7ad58d3c0b071069a8ee0cb8c8ba2e8
classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D487-04
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D487-04
filingDate 1963-10-18-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1965-06-02-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-993739-A
titleOfInvention 3-acylamino-pyrazolo-(1,5-a)-benzimidazoles
abstract The invention comprises 3-acylaminopyrazolo-(1,5-a)-benzimidazoles optionally substituted in the 4-position by the same acyl group present in the acylamino radical, said acyl group being derived from a carboxylic acid; and their production by acylating a 3-aminopyrazolo-(1,5-a)-benzimidazole. Suitable acylating agents are the anhydrides and chlorides of carboxylic acids such as acetic, propionic, butyric, valeric, capronic and benzoic. Examples prepare the pyrazolobenzimidazoles substituted as follows:-(1) 2-phenyl-3-acetylamino - 6 - sulphonic acid; (2) 2 - phenyl - 3-propionylamino - 6 - sulphonic acid; (3) 2-phenyl - 3 - benzoylamino - 6 - sulphonic acid; (4) 2 - methyl - 3 - acetylamino - 4 - acetyl; (5) 2 - phenyl - 3 - acetylamino; and (6) 2-methyl-3-acetylamino. The compounds of the invention exhibit central nervous system stimulation when perorally or parenterally administered to animals in a liquid or solid carrier.
priorityDate 1962-10-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

Incoming Links

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Total number of triples: 18.