http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-336690-A1
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_d629f98a51b15993f56f9e04fdea237f |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D285-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/A61K31-00 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D285-24 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A61K31-00 |
| filingDate | 1967-02-10-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationDate | 1968-01-16-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | ES-336690-A1 |
| titleOfInvention | A PROCEDURE FOR THE PREPARATION OF 3-CYCLOPENTENYL-2H - 1,2,4-BENZOTIADIAZINE - 1,1 - BIOXIDES. |
| abstract | Novel 3 - cyclopentenyl - 2H - 1,2,4 - benzothiadiazine - 1,1 - dioxides having a chloro, bromo, trifluoromethyl, nitro or methyl substituent in each of the 6- and 7-positions thereof, with the proviso that when one of the said positions is substituted by nitro or methyl the other is substituted by chloro, bromo or trifluoromethyl, and their tautomers and non- toxic salts are prepared (i) by subjecting a compound of the general formula wherein A together with the-C = C- double bond represents a phenylene radical having in the 5-position thereof a substituent X and in the 4-position thereof a substituent Y, where X and Y are each chloro, bromo, trifluoromethyl, nitro or methyl, with the proviso that when one of X and Y is nitro or methyl the other is chloro, bromo or trifluoromethyl Q is (H, H), (H, | | | # RCO), (RCO, RCO) or RCOR1, wherein R is cyclopentenyl and R1 is alkyl T is hydrogen or RCO and Z is hydrogen, benzyl, cyclopentenyl or alkyl, to a condensation reaction, optionally in the presence of a second reactant of the formula R-C#B, wherein B represents from one to three functional groups, in the case when in the first formula above Q is (H, H) and T is hydrogen, followed optionally by conversion to a non-toxic salt of the product or (ii) by subjecting a corresponding 3,4-dihydro-1,2,4- benzothiadiazine - 1,1 - dioxide to dehydrogenation or dehydrohalogenation to introduce a double bond between the atoms in the 3- and 4-positions. Ethyl ortho-3-cyclopentene-1-carboxylate is prepared by reacting an imino ester hydrochloride of cyclopentene with ethanol. 2 - (2- and 3 - Cyclopentene - 1 - carboxamido)- 4,5 - dichlorobenzenesulphonamides are prepared by reacting 2- or 3-cyclopentene-1-carboxylic acid with oxalyl chloride and then 2-amino-4,5- dichloro-benzenesulphonamide. Pharmaceutical compositions having antihypertensive activity comprise as active ingredient a novel 3-cyclopentenyl-2H-1,2,4- benzothiadiazine - 1,1 - dioxide as defined above in admixture with a therapeutically acceptable carrier. |
| priorityDate | 1966-02-11-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 45.