http://rdf.ncbi.nlm.nih.gov/pubchem/patent/EP-0102925-A2

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filingDate 1983-08-26-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_00ccbc07a1f771a5543fec98cf4cbb8f
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_425c3a60b8a414ba8beadf643c661b00
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publicationDate 1984-03-14-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber EP-0102925-A2
titleOfInvention N-phenylsulfonyl-N'-pyrimidinyl- and -triazinyl urea
abstract R 1 Wasserstoff, Halogen, Nitro, Amino, C 1 -C 5 -Alkyl, C 1 -C 4 -Halogenalkyl oder einen Rest -Q-R 7 , -CO-OR 8 oder -(CO) n -NR 9 R 10 , R 2 Wasserstoff, C 1 -C 4 -Alkyl, C,-C 4 -Alkoxy, C 1 -C 4 -Alkylthio, C 1 -C 4 -Halogenalkyl, C 1 -C 4 -Halogenalkoxy, Halogen oder Alkoxyalkyl mit höchstens 4 Kohlenstoffatomen, R 3 einfach durch C 1 -C 4 -Alkoxy oder einfach oder mehrfach durch Fluor, Brom, Hydroxyl, Cyan, Nitro, -(Y) m --CO-(Z) n -R 8 , -SO 2 -NR 11 R 12 , -S(O) p -C 1 -C 3 -Halogenalkyl oder -S(O) p -C 1 -C 3 -Alkyl substituiertes C 2 -C 10 -Alkenyl, das zusätzlich ein- oder mehrfach durch Chlor substituiert sein kann, R 4 C 1 -C 3 -Alkyl, C 1 -C 3 -Halogenalkyl, C 1 -C 3 -Alkoxy oder C 1 -C 3 -Halogenalkoxy, R 5 Wasserstoff, Halogen, -NR 13 R 14 , C 1 -C 3 -Alkyl, C 1 -C 3 -Halogenalkyl, C l -C 3 -Alkoxy oder C 1 -C 2 -Halogenalkoxy, R 6 Wasserstoff, C 1 -C 3 -Alkyl oder C 1 -C 3 -Alkoxy, X Sauerstoff oder Schwefel und E Stickstoff oder die Methingruppe bedeuten, wobei R 7 für gegebenenfalls durch Halogen oder C 1 -C 3 -Alkoxy substituiertes C l -C 4 -Alkyl oder C 3 -C 5 -Alkenyl, R 8 für C l -C 4 -Alkyl, C,-C 4 -Halogenalkyl oder C 2 -C 6 -Alkoxyalkyl, R 9 , R 10 , R 11 , R, 2 , R 13 und R 14 unabhängig voneinander für Wasserstoff oder C l -C 3 -Alkyl, Q für Sauerstoff, Schwefel, die Sulfinyl- oder Sulfonylbrücke, Y für Sauerstoff, Schwefel oder -NR 16 -, Z für Sauerstoff, Schwefel oder -NR 17 -, m,nfür Null oder eins und p für Null, eins oder zwei stehen, wobei R, 6 und R 17 Wasserstoff oder C 1 -C 3 -Alkyl darstellen. N-phenylsulfonyl-N'-pyrimidinyl-and-triazinyl-ureas of the general formula and the salts of these compounds with amines, alkali or alkaline earth metal bases or with quaternary ammonium bases have good pre- and postemergent-selective herbicidal and growth-regulating properties. In this formula: R 1 is hydrogen, halogen, nitro, amino, C 1 -C 5 alkyl, C 1 -C 4 haloalkyl or a radical -QR 7 , -CO-OR 8 or - (CO) n -NR 9 R 10 , R 2 is hydrogen, C 1 -C 4 alkyl, C, -C 4 alkoxy, C 1 -C 4 alkylthio, C 1 -C 4 haloalkyl, C 1 -C 4 haloalkoxy, halogen or alkoxyalkyl having at most 4 Carbon atoms, R 3 simply by C 1 -C 4 alkoxy or single or multiple by fluorine, bromine, hydroxyl, cyan, nitro, - (Y) m --CO- (Z) n -R 8 , -SO 2 -NR 11 R 12 , -S (O) p -C 1 -C 3 haloalkyl or -S (O) p -C 1 -C 3 alkyl substituted C 2 -C 10 alkenyl, which are additionally substituted one or more times by chlorine can, R 4 is C 1 -C 3 alkyl, C 1 -C 3 haloalkyl, C 1 -C 3 alkoxy or C 1 -C 3 haloalkoxy, R 5 is hydrogen, halogen, -NR 13 R 14 , C 1 -C 3 alkyl, C 1 -C 3 haloalkyl, C l -C 3 alkoxy or C 1 -C 2 haloalkoxy, R 6 is hydrogen, C 1 -C 3 alkyl or C 1 -C 3 alkoxy, X oxygen or sulfur and E is nitrogen or the methine group, where R 7 is optionally substituted by halogen or C 1 -C 3 -alkoxy-substituted C l -C 4 alkyl or C 3 -C 5 alkenyl, R 8 is C 1 -C 4 -alkyl, C, -C 4 -haloalkyl or C 2 -C 6 -alkoxyalkyl, R 9 , R 10 , R 11 , R, 2 , R 13 and R 14 independently of one another are hydrogen or C 1 -C 3 -alkyl, Q for oxygen, sulfur, the sulfinyl or sulfonyl bridge, Y for oxygen, sulfur or -NR 16 -, Z for oxygen, sulfur or -NR 17 -, m, n for zero or one and p stands for zero, one or two, where R, 6 and R 17 represent hydrogen or C 1 -C 3 alkyl.
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