首页> 外国专利> SAOSOM HERBICIDER ANVAENDBARA 6-AMINO-S-TRIAZINE-2,4- (1H, 3H) DIONER SAMT FOERFARANDE FOER FRAMSTAELLNING AV DESSA

SAOSOM HERBICIDER ANVAENDBARA 6-AMINO-S-TRIAZINE-2,4- (1H, 3H) DIONER SAMT FOERFARANDE FOER FRAMSTAELLNING AV DESSA

机译:作为除草剂,使用6-氨基-S-三嗪-2,4-(1H,3H)二酮及其制备方法

摘要

1435585 6-Amino-s-triazin-2,4[1H,3H]-dione derivatives E I DU PONT DE NEMOURS & CO 23 May 1973 [24 May 1972 5 April 1973 (2)] 24677/73 Headings A5E E1C5J E1C5P E1C5M E1C14A E1C15D3 E1A3B ElA3Cand E1A5B3 Novel compounds have the Formula I wherein R 1 is selected from (a) alkyl of 2 to 8 carbon atoms, alkenyl of 3 to 6 carbon atoms, alkynyl of 3 to 6 carbon atoms, cycloalkyl of 4 to 8 carbon atoms, cycloalkenyl of 5 to 8 carbon atoms, cycloalkylmethyl of 4 to 9 carbon atoms, cycloalkenylmethyl of 6 to 9 carbon atoms, bicycloalkyl or bicycloalkenyl of 7 to 10 carbon atoms and bicycloalkylmethyl or bicycloalkenylmethyl of 8 to 11 carbon atoms, trimethylcyclohexyl and tetramethylcyclohexyl; (b) the above alkyl groups substituted with one methoxy, ethoxy, methylthio or ethylthio group; (c) the above cycloalkyl groups substituted with one alkyl group of 2 to 4 carbon atoms, 1 or 2 methyl groups, 1 or 2 chlorine or bromine atoms, one methoxy or one ethoxy group; and (d) a group of Formula wherein Q is hydrogen, fluorine, chlorine, bromine, alkyl of 1 to 4 carbon atoms, alkoxy of alkylthio of 1 or 2 carbon atoms, nitro or a trifluoromethyl group; Y is hydrogen, chlorine or methyl; and Z is hydrogen or chlorine; R 2 is hydrogen, alkyl of 1 to 3 carbon atoms or a cation selected from NaSP+/SP, LiSP+/SP, KSP+/SP, (Ca/2)SP+/SP, ammonium and dimethylammonium; R 2 is hydrogen, methyl or ethyl; R 4 is alkyl of 1 to 4 carbon atoms, alkenyl of 3 or 4 carbon atoms, alkynyl of 3 or 4 carbon atoms, or methoxy; and X is oxygen or sulphur; provided that when X is sulphur, neither R 2 nor R 3 is hydrogen. The compounds of Formula I are prepared, for example, by reaction of a corresponding 6- methylthio compound with an amine of Formula R 3 R 4 NH or, in the case of a 4-thio derivative, by reaction of P 2 S 5 with the corresponding 2,4-dione derivative. The compounds of Formula I in which R 2 is alkyl [=RSP1/SP 2 ] are also obtained by cyclization, in the presence of a base (an alkali metal C 1-4 alkoxide), of a compound of Formula CH 3 O-CO-NRSP1/SP 2 -C(NR 3 R 4 )=N-CX-NHR 1 These latter starting materials are themselves obtained by reacting methoxycarbonyl-cyanamide with an alkylating agent of Formula RSP1/SP 2 -Q [Q = chloride, bromide, iodide or -O-SO 2 ORSP1/SP 2 ] to form N-methoxycarbonyl-N-alkylcyanamide, reacting the latter with an amine of Formula R 3 R 4 NH to form a compound of Formula CH 3 O-CO-NRSP1/SP 2 -C(NR 3 R 4 )=NH and then reacting this intermediate with an isocyanate or isothiocyanate of Formula R 1 NCX. The compounds of Formula I are herbicides.
机译:1435585 6-氨基-s-三嗪-2,4 [1H,3H]-二酮衍生物EI DU PONT DE NEMOURS&CO 1973年5月23日[1972年5月24日1973年4月5日(2)] 24677/73标题A5E E1C5J E1C5P E1C5M E1C14A E1C15D3 E1A3B E1A3B和E1A5B3新型化合物具有式I,其中R 1选自(a)2至8个碳原子的烷基,3至6个碳原子的烯基,3至6个碳原子的炔基,4至8个碳原子的环烷基,5至8个碳原子的环烯基,4至9个碳原子的环烷基甲基,6至9个碳原子的环烯基甲基,7至10个碳原子的双环烷基或双环烯基和8至11个碳原子的双环烷基甲基或双环烯基甲基,三甲基环己基和四甲基环己基; (b)被一个甲氧基,乙氧基,甲硫基或乙硫基取代的上述烷基; (c)上述环烷基被一个具有2-4个碳原子的烷基,1或2个甲基,1或2个氯或溴原子,一个甲氧基或一个乙氧基取代的环烷基; (d)式中的基团,其中Q是氢,氟,氯,溴,1-4个碳原子的烷基,1-4个碳原子的烷硫基的烷氧基,硝基或三氟甲基; Y是氢,氯或甲基; Z为氢或氯; R 2是氢,1-3个碳原子的烷基或选自Na + ,Li + ,K + ,(Ca / 2) + ,铵和二甲基铵; R 2为氢,甲基或乙基; R 4为1-4个碳原子的烷基,3或4个碳原子的烯基,3或4个碳原子的炔基或甲氧基; X是氧或硫;前提是当X是硫时,R 2和R 3都不是氢。式I的化合物例如通过使相应的6-甲硫基化合物与式R 3 R 4 NH的胺反应或在4-硫代衍生物的情况下通过使P 2 S 5与胺反应而制备。相应的2,4-二酮衍生物。 R 2为烷基[= R 1 2]的式I化合物也可通过在碱(碱金属C 1-4醇盐)的存在下环化获得。式CH 3 O-CO-NR 1 2 -C(NR 3 R 4)= N-CX-NHR 1的分子式这些后继的原料本身是通过使甲氧基羰基-氰胺与烷基化剂式R 1 2 -Q [Q =氯化物,溴化物,碘化物或-O-SO 2 OR 1 2]形成N-甲氧基羰基-N-烷基氰酰胺,使后者与式R 3 R 4 NH的胺形成式CH 3 O-CO-NR 1 2 -C(NR 3 R 4)= NH的化合物,然后使该中间体与式R 1 NCX的异氰酸酯或异硫氰酸酯。式I化合物是除草剂。

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