http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1121447-A
Outgoing Links
| Predicate | Object |
|---|---|
| assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_97a285d8ecd0184a7e5d89a1e4e07997 |
| classificationCPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D257-04 |
| classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D257-04 |
| filingDate | 1966-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_69b4533b10e4efb40fed956dd4b6da32 |
| publicationDate | 1968-07-24-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | GB-1121447-A |
| titleOfInvention | Tetrazole derivatives and a process for the preparation |
| abstract | The invention comprises compounds of formula <FORM:1121447/C2/1> wherein R1 is a fluorine, chlorine, bromine or iodine atom or a trifluoromethyl, trifluoromethoxy, trifluoromethylthio, C1- 6 alkyl, C1- 6 alkoxy, nitro, methylsulphonyl, di-(C1- 6 alkyl)-amino or C1- 6 alkylthio group and R2 and R3 are each hydrogen atoms or one of the groups R1, R2 being hydrogen only when R3 is hydrogen, pharmaceutically acceptable salts thereof, and their preparation by reaction of a compound of formula <FORM:1121447/C2/2> with an azide or with hydrazoic acid. o-Cyano-N-substituted anilines of the second formula above are prepared from the corresponding N-substituted anthranilic acids by conversion to an alkyl ester or acid chloride, reaction with ammonia to form the corresponding amide, and dehydration of this with phosphorous oxychloride and phosphorous pentachloride. N-(2-R2-3-R1-6-R3)-anthranilic acids are prepared by (a) reaction of o-chloro-benzoic acid with an N-substituted aniline, or (b) reaction of a substituted phenol with 2,4-dichloro-quinazoline to form a 2,4-di-(substituted phenoxy)-quinazoline, heating this to form a 113-bis-(substituted phenoxy) - tetrahydroquinazoline-2,4-dione, and subjecting this to hydrolysis. 2,4-Dichloroquinazoline is prepared by reaction of 2,4-dihydroxyquinazoline with phosphorus oxychloride and phosphorus pentachloride. 2,6-Dichloro-3-methyl-phenol is prepared by reaction of m-cresyl acetate with aluminium chloride to form 4-hydroxy-2-methyl-acetophenone, reacting this with a hypochlorite to form 3,5-dichloro-4-hydroxy-2-methyl-benzoic acid, and decarboxylating this by heating. The compounds of the invention have anti-inflammatory activity and may be used in pharmaceutical compositions in combination with a carrier. |
| isCitedBy | http://rdf.ncbi.nlm.nih.gov/pubchem/patent/WO-2008142073-A1 |
| priorityDate | 1965-04-12-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 57.