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classificationCPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentcpc/C07D285-14
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http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-832
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N43-828
filingDate 1970-02-16-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationDate 1970-08-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber IE-34208-L
titleOfInvention Benzthiadiazoles
abstract 1303711 Benzothiadiazoles PHILIPS GLOEILAMPENFABRIEKEN NV 16 Feb 1970 [19 Feb 1969] 7314/70 Heading C2C [Also in Divisions A5 and Cl] Compounds of formula wherein X is the group -OCHR 1 COOR, in which R 1 is hydrogen or C 1-3 alkyl and R is hydrogen or C 1-10 alkyl, Y is chlorine or bromine, n is 0, 1, 2 or 3 and Z is hydrogen or C 1-3 -alkyl, are prepared by (a) etherification, (b) halogenation or (c) ester hydrolysis. The products have herbicidal, pesticidal and plant growth regulant activity (see Division A5). 6 - Hydroxy - benzothiadiazole starting materials are prepared by hydrolysis of their methyl ethers. 6 - Methoxy - benzothiadiazoles are prepared by (a) replacement of a chlorine atom by reaction with sodium methoxide, (b) chlorination or (c) reduction of an o-dinitro-benzene or an onitro-aniline to the corresponding diamine, followed by cyclization with thionyl chloride. 2 - Chloro - 4 - methoxy - 6 - nitro - aniline is prepared by reaction of 2-chloro-6-nitro-phenyl azide with sulphuric acid to give 2-chloro-4- hydroxy - 6 - nitro - aniline, followed by methylation. 2,3,5 - Trichloro - 6 - nitro - aniline is prepared by nitration of 2,3,5-trichloro-acetanilide. 2,4 - Dichloro - 5,6 - dinitro - anisole is prepared by nitration of 2,4-dichloro-anisole.n[GB1303711A]
priorityDate 1969-02-19-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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