http://rdf.ncbi.nlm.nih.gov/pubchem/patent/GB-1215507-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/F24H1-103
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07C251-72
http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D249-06
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D249-06
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/F24H1-10
filingDate 1968-08-20-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_dc51d83d03d1b3f65c5229db7010f09d
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f4c32fc73bd226e1d683986816e57645
publicationDate 1970-12-09-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber GB-1215507-A
titleOfInvention Process for the production of 2-aryl-1,2,3-triazoles
abstract 1,215,507. 2 - Aryl - 1,2,3 - triazole derivatives. FARBENFABRIKEN BAYER A.G. 20 Aug., 1968 [23 Aug., 1967], No. 39821/68. Heading C2C. The invention comprises a process of preparing 2 - aryl - 1,2,3 - triazoles of the Formula VI where R is an optionally substituted aryl or arylene radical (which term covers tolane and stilbene radicals as well as diarylene-alkane radicals) or a 3-phthalimide radical, R 1 is an optionally substituted aryl or alkyl radical, or a nitro group, R 2 is H or an optionally substituted alkyl or aryl radical and n is 1 or 2 by cyclizing an α-oximino-aryl hydrazone of the Formula VIII or an O-acyl derivative thereof by heating in urea at a temperature of 100‹ to 210‹ C. Examples include compounds of the Formula VI where R is a carboxylic acid substituted aryl radical; a sulphonic acid substituted aryl radical where R 1 may be aryl substituted by an alkoxy group; an acylamino substituted aryl or alkaryl radical; an aryl or alkaryl radical where R 1 is NO 2 ; or a nitro substituted aryl radical. The preparation of certain compounds of the Formula VIII is described; α-oximinopropiophenone - (3 - sulphophenyl) - hydrazine from phenylhydrazine - 3 - sulphonic acid and α- oximinopropiophenone; the disodium salt of 4,41 - bis - (α - oximinoacetophenone - hydrazono)- 1,2 - diphenyl - ethane - 2,2<SP>1</SP>- disulphonic acid from 4,4<SP>1</SP>-dihydrazino - 1,2 - diphenyl - ethane- 2,2<SP>1</SP> - disulphonic acid, oximinoacetophenone and saturated sodium chloride solution; oximinoacetophenone - hydrazono - 4 - benzoic acid from 4 - hydrazino - benzoic acid hydrochloride and oximinoacetophenone; and oximinoacetophenone - hydrazono - 4 - phenylacetic acid from 4-hydrazinophenyl-acetic acid and oximinoacetophenone.
priorityDate 1967-08-23-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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Total number of triples: 44.