DE1670042

1,226,797. 2,4-Amino- and -alkylamino - 6- chloro-s-triazines. AGRIPAT S.A. 19 March, 1968 [20 March, 1967], No. 13160/68. Heading C2C. Compounds of the general formula wherein R 1 and R 2 represent C 1-4 alkyl radicals and R 3 and R 4 represent hydrogen or C 1-4 alkyl radicals, are produced from cy...

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1. Verfasser: SAUL, GEORGE A., MOBILE, ALA. (V.ST.A.)
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description 1,226,797. 2,4-Amino- and -alkylamino - 6- chloro-s-triazines. AGRIPAT S.A. 19 March, 1968 [20 March, 1967], No. 13160/68. Heading C2C. Compounds of the general formula wherein R 1 and R 2 represent C 1-4 alkyl radicals and R 3 and R 4 represent hydrogen or C 1-4 alkyl radicals, are produced from cyanuric chloride, an amine R 1 R 3 NH and an amine R 2 R 4 NH by adding sequentially to a solution of cyanuric chloride in an inert, substantially anhydrous, organic solvent, per mole of cyanuric chloride (a) about 1 mole of an amine R 1 R 3 NH, (b) about 1 mole of anhydrous ammonia, (c) about 1 mole of an amine R 2 R 4 NH, and (d) about 1 mole of anhydrous ammonia, and thereafter recovering the product from the reaction mixture. In a modification of the process, products wherein the moieties R 1 R 3 N- and R 2 R 4 N- are identical are obtained by omitting steps (c) and (d) and employing about 2 moles of the amine in step (a) and about 2 moles of ammonia in step (b). In the first process, minor amounts of the corresponding symmetrical 2,4-bis-(alkylamino) - 6 - chloro - s - triazines are obtained, together with some of the corresponding 2- amino - 4 - alkylamino - 6 - chloro - s - triazines. In a comparative Example (4), ammonia is added to a trichloroethylene solution of cyanuric chloride, and isopropylamine is added at the reaction mixture to give 2-amino-4-isopropylamino - 6 - chloro - a - triazine.
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Compounds of the general formula wherein R 1 and R 2 represent C 1-4 alkyl radicals and R 3 and R 4 represent hydrogen or C 1-4 alkyl radicals, are produced from cyanuric chloride, an amine R 1 R 3 NH and an amine R 2 R 4 NH by adding sequentially to a solution of cyanuric chloride in an inert, substantially anhydrous, organic solvent, per mole of cyanuric chloride (a) about 1 mole of an amine R 1 R 3 NH, (b) about 1 mole of anhydrous ammonia, (c) about 1 mole of an amine R 2 R 4 NH, and (d) about 1 mole of anhydrous ammonia, and thereafter recovering the product from the reaction mixture. In a modification of the process, products wherein the moieties R 1 R 3 N- and R 2 R 4 N- are identical are obtained by omitting steps (c) and (d) and employing about 2 moles of the amine in step (a) and about 2 moles of ammonia in step (b). In the first process, minor amounts of the corresponding symmetrical 2,4-bis-(alkylamino) - 6 - chloro - s - triazines are obtained, together with some of the corresponding 2- amino - 4 - alkylamino - 6 - chloro - s - triazines. In a comparative Example (4), ammonia is added to a trichloroethylene solution of cyanuric chloride, and isopropylamine is added at the reaction mixture to give 2-amino-4-isopropylamino - 6 - chloro - a - triazine.</description><language>eng</language><subject>AGRICULTURE ; ANIMAL HUSBANDRY ; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES ; FISHING ; FORESTRY ; HUMAN NECESSITIES ; HUNTING ; PEST REPELLANTS OR ATTRACTANTS ; PLANT GROWTH REGULATORS ; PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF ; TRAPPING</subject><creationdate>1975</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&amp;date=19750403&amp;DB=EPODOC&amp;CC=DE&amp;NR=1670042C3$$EHTML$$P50$$Gepo$$Hfree_for_read</linktohtml><link.rule.ids>230,308,776,881,25543,76293</link.rule.ids><linktorsrc>$$Uhttps://worldwide.espacenet.com/publicationDetails/biblio?FT=D&amp;date=19750403&amp;DB=EPODOC&amp;CC=DE&amp;NR=1670042C3$$EView_record_in_European_Patent_Office$$FView_record_in_$$GEuropean_Patent_Office$$Hfree_for_read</linktorsrc></links><search><creatorcontrib>SAUL, GEORGE A., MOBILE, ALA. (V.ST.A.)</creatorcontrib><title>DE1670042</title><description>1,226,797. 2,4-Amino- and -alkylamino - 6- chloro-s-triazines. AGRIPAT S.A. 19 March, 1968 [20 March, 1967], No. 13160/68. Heading C2C. Compounds of the general formula wherein R 1 and R 2 represent C 1-4 alkyl radicals and R 3 and R 4 represent hydrogen or C 1-4 alkyl radicals, are produced from cyanuric chloride, an amine R 1 R 3 NH and an amine R 2 R 4 NH by adding sequentially to a solution of cyanuric chloride in an inert, substantially anhydrous, organic solvent, per mole of cyanuric chloride (a) about 1 mole of an amine R 1 R 3 NH, (b) about 1 mole of anhydrous ammonia, (c) about 1 mole of an amine R 2 R 4 NH, and (d) about 1 mole of anhydrous ammonia, and thereafter recovering the product from the reaction mixture. In a modification of the process, products wherein the moieties R 1 R 3 N- and R 2 R 4 N- are identical are obtained by omitting steps (c) and (d) and employing about 2 moles of the amine in step (a) and about 2 moles of ammonia in step (b). In the first process, minor amounts of the corresponding symmetrical 2,4-bis-(alkylamino) - 6 - chloro - s - triazines are obtained, together with some of the corresponding 2- amino - 4 - alkylamino - 6 - chloro - s - triazines. In a comparative Example (4), ammonia is added to a trichloroethylene solution of cyanuric chloride, and isopropylamine is added at the reaction mixture to give 2-amino-4-isopropylamino - 6 - chloro - a - triazine.</description><subject>AGRICULTURE</subject><subject>ANIMAL HUSBANDRY</subject><subject>BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES</subject><subject>FISHING</subject><subject>FORESTRY</subject><subject>HUMAN NECESSITIES</subject><subject>HUNTING</subject><subject>PEST REPELLANTS OR ATTRACTANTS</subject><subject>PLANT GROWTH REGULATORS</subject><subject>PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF</subject><subject>TRAPPING</subject><fulltext>true</fulltext><rsrctype>patent</rsrctype><creationdate>1975</creationdate><recordtype>patent</recordtype><sourceid>EVB</sourceid><recordid>eNrjZOB0cTU0MzcwMDHiYWBNS8wpTuWF0twMCm6uIc4euqkF-fGpxQWJyal5qSXxcPXOxsZEKAEAyRoaXQ</recordid><startdate>19750403</startdate><enddate>19750403</enddate><creator>SAUL, GEORGE A., MOBILE, ALA. (V.ST.A.)</creator><scope>EVB</scope></search><sort><creationdate>19750403</creationdate><title>DE1670042</title><author>SAUL, GEORGE A., MOBILE, ALA. (V.ST.A.)</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-epo_espacenet_DE1670042C33</frbrgroupid><rsrctype>patents</rsrctype><prefilter>patents</prefilter><language>eng</language><creationdate>1975</creationdate><topic>AGRICULTURE</topic><topic>ANIMAL HUSBANDRY</topic><topic>BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES</topic><topic>FISHING</topic><topic>FORESTRY</topic><topic>HUMAN NECESSITIES</topic><topic>HUNTING</topic><topic>PEST REPELLANTS OR ATTRACTANTS</topic><topic>PLANT GROWTH REGULATORS</topic><topic>PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF</topic><topic>TRAPPING</topic><toplevel>online_resources</toplevel><creatorcontrib>SAUL, GEORGE A., MOBILE, ALA. (V.ST.A.)</creatorcontrib><collection>esp@cenet</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext_linktorsrc</fulltext></delivery><addata><au>SAUL, GEORGE A., MOBILE, ALA. (V.ST.A.)</au><format>patent</format><genre>patent</genre><ristype>GEN</ristype><title>DE1670042</title><date>1975-04-03</date><risdate>1975</risdate><abstract>1,226,797. 2,4-Amino- and -alkylamino - 6- chloro-s-triazines. AGRIPAT S.A. 19 March, 1968 [20 March, 1967], No. 13160/68. Heading C2C. Compounds of the general formula wherein R 1 and R 2 represent C 1-4 alkyl radicals and R 3 and R 4 represent hydrogen or C 1-4 alkyl radicals, are produced from cyanuric chloride, an amine R 1 R 3 NH and an amine R 2 R 4 NH by adding sequentially to a solution of cyanuric chloride in an inert, substantially anhydrous, organic solvent, per mole of cyanuric chloride (a) about 1 mole of an amine R 1 R 3 NH, (b) about 1 mole of anhydrous ammonia, (c) about 1 mole of an amine R 2 R 4 NH, and (d) about 1 mole of anhydrous ammonia, and thereafter recovering the product from the reaction mixture. In a modification of the process, products wherein the moieties R 1 R 3 N- and R 2 R 4 N- are identical are obtained by omitting steps (c) and (d) and employing about 2 moles of the amine in step (a) and about 2 moles of ammonia in step (b). In the first process, minor amounts of the corresponding symmetrical 2,4-bis-(alkylamino) - 6 - chloro - s - triazines are obtained, together with some of the corresponding 2- amino - 4 - alkylamino - 6 - chloro - s - triazines. In a comparative Example (4), ammonia is added to a trichloroethylene solution of cyanuric chloride, and isopropylamine is added at the reaction mixture to give 2-amino-4-isopropylamino - 6 - chloro - a - triazine.</abstract><oa>free_for_read</oa></addata></record>
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subjects AGRICULTURE
ANIMAL HUSBANDRY
BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES, AS HERBICIDES
FISHING
FORESTRY
HUMAN NECESSITIES
HUNTING
PEST REPELLANTS OR ATTRACTANTS
PLANT GROWTH REGULATORS
PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTSTHEREOF
TRAPPING
title DE1670042
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