Trioxogrisan derivatives
The invention comprises compounds of formula where R is an alkyl radical, a benzyl radical or a phenyl radical which may be substituted by methyl, methoxy or nitro radicals or by halogen atoms. The compounds may be substituted at positions 4, 5, 6, 7, 31, 51 and/or 61 by halogen, methyl or methoxy...
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creator | MORLEY JOHN SELWYN |
description | The invention comprises compounds of formula where R is an alkyl radical, a benzyl radical or a phenyl radical which may be substituted by methyl, methoxy or nitro radicals or by halogen atoms. The compounds may be substituted at positions 4, 5, 6, 7, 31, 51 and/or 61 by halogen, methyl or methoxy radicals e.g. at positions 4 and/or 6 by methoxy radicals, at positions 5 and/or 7 by chlorine or bromine atoms, and at positions 31, 51 and/or 61 by methyl radicals. The compounds may be prepared by reacting a compound of formula which may be substituted as above, with a sulphenyl halide or thiocyanate of formula RSX where X is chlorine, bromine, iodine or the thiocyanate radical. Examples are given. Benzylsulphenyl bromide is prepared by reacting benzyl mercaptan with N-bromosuccinimide; t-butylsulphenyl chloride is prepared by reacting sulphenyl chloride with bis-t-butyl disulphide; o-methoxphenylsulphenyl chloride is prepared by reacting o-methoxythiophenol with N-chlorosuccinimide; and isopropylsulphenyl chloride is prepared by reacting propane-2-thiol with N-chlorosuccinimide. |
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The compounds may be substituted at positions 4, 5, 6, 7, 31, 51 and/or 61 by halogen, methyl or methoxy radicals e.g. at positions 4 and/or 6 by methoxy radicals, at positions 5 and/or 7 by chlorine or bromine atoms, and at positions 31, 51 and/or 61 by methyl radicals. The compounds may be prepared by reacting a compound of formula <FORM:0921665/IV(a)/2> which may be substituted as above, with a sulphenyl halide or thiocyanate of formula RSX where X is chlorine, bromine, iodine or the thiocyanate radical. Examples are given. Benzylsulphenyl bromide is prepared by reacting benzyl mercaptan with N-bromosuccinimide; t-butylsulphenyl chloride is prepared by reacting sulphenyl chloride with bis-t-butyl disulphide; o-methoxphenylsulphenyl chloride is prepared by reacting o-methoxythiophenol with N-chlorosuccinimide; and isopropylsulphenyl chloride is prepared by reacting propane-2-thiol with N-chlorosuccinimide.</description><language>eng</language><subject>CHEMISTRY ; HETEROCYCLIC COMPOUNDS ; METALLURGY ; ORGANIC CHEMISTRY</subject><creationdate>1963</creationdate><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19630320&DB=EPODOC&CC=GB&NR=921665A$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25542,76290</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&date=19630320&DB=EPODOC&CC=GB&NR=921665A$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>MORLEY JOHN SELWYN</creatorcontrib><title>Trioxogrisan derivatives</title><description>The invention comprises compounds of formula <FORM:0921665/IV(a)/1> where R is an alkyl radical, a benzyl radical or a phenyl radical which may be substituted by methyl, methoxy or nitro radicals or by halogen atoms. The compounds may be substituted at positions 4, 5, 6, 7, 31, 51 and/or 61 by halogen, methyl or methoxy radicals e.g. at positions 4 and/or 6 by methoxy radicals, at positions 5 and/or 7 by chlorine or bromine atoms, and at positions 31, 51 and/or 61 by methyl radicals. The compounds may be prepared by reacting a compound of formula <FORM:0921665/IV(a)/2> which may be substituted as above, with a sulphenyl halide or thiocyanate of formula RSX where X is chlorine, bromine, iodine or the thiocyanate radical. Examples are given. Benzylsulphenyl bromide is prepared by reacting benzyl mercaptan with N-bromosuccinimide; t-butylsulphenyl chloride is prepared by reacting sulphenyl chloride with bis-t-butyl disulphide; o-methoxphenylsulphenyl chloride is prepared by reacting o-methoxythiophenol with N-chlorosuccinimide; and isopropylsulphenyl chloride is prepared by reacting propane-2-thiol with N-chlorosuccinimide.</description><subject>CHEMISTRY</subject><subject>HETEROCYCLIC COMPOUNDS</subject><subject>METALLURGY</subject><subject>ORGANIC CHEMISTRY</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1963</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZJAIKcrMr8hPL8osTsxTSEktyixLLMksSy3mYWBNS8wpTuWF0twMcm6uIc4euqkF-fGpxQWJyal5qSXx7k6WRoZmZqaOxgQVAABl5SGS</recordid><startdate>19630320</startdate><enddate>19630320</enddate><creator>MORLEY JOHN SELWYN</creator><scope>EVB</scope></search><sort><creationdate>19630320</creationdate><title>Trioxogrisan derivatives</title><author>MORLEY JOHN SELWYN</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_GB921665A3</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1963</creationdate><topic>CHEMISTRY</topic><topic>HETEROCYCLIC COMPOUNDS</topic><topic>METALLURGY</topic><topic>ORGANIC CHEMISTRY</topic><toplevel>online_resources</toplevel><creatorcontrib>MORLEY JOHN SELWYN</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>MORLEY JOHN SELWYN</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>Trioxogrisan derivatives</title><date>1963-03-20</date><risdate>1963</risdate><abstract>The invention comprises compounds of formula <FORM:0921665/IV(a)/1> where R is an alkyl radical, a benzyl radical or a phenyl radical which may be substituted by methyl, methoxy or nitro radicals or by halogen atoms. The compounds may be substituted at positions 4, 5, 6, 7, 31, 51 and/or 61 by halogen, methyl or methoxy radicals e.g. at positions 4 and/or 6 by methoxy radicals, at positions 5 and/or 7 by chlorine or bromine atoms, and at positions 31, 51 and/or 61 by methyl radicals. The compounds may be prepared by reacting a compound of formula <FORM:0921665/IV(a)/2> which may be substituted as above, with a sulphenyl halide or thiocyanate of formula RSX where X is chlorine, bromine, iodine or the thiocyanate radical. Examples are given. Benzylsulphenyl bromide is prepared by reacting benzyl mercaptan with N-bromosuccinimide; t-butylsulphenyl chloride is prepared by reacting sulphenyl chloride with bis-t-butyl disulphide; o-methoxphenylsulphenyl chloride is prepared by reacting o-methoxythiophenol with N-chlorosuccinimide; and isopropylsulphenyl chloride is prepared by reacting propane-2-thiol with N-chlorosuccinimide.</abstract><oa>free_for_read</oa></addata></record> |
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subjects | CHEMISTRY HETEROCYCLIC COMPOUNDS METALLURGY ORGANIC CHEMISTRY |
title | Trioxogrisan derivatives |
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