http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CA-1243673-A

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Predicate Object
assignee http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_1e70c0aeade92d7571d955d3b90ea06e
classificationIPCInventive http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D409-00
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07D417-14
http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/A01N47-36
filingDate 1987-09-01-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 1988-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ecee64f68a853298771650c567aa45f8
publicationDate 1988-10-25-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber CA-1243673-A
titleOfInvention Herbicidal thiophenesulfonamides
abstract Title HERBICIDAL THIOPHENESULFONAMIDES Abstract of the Disclosure This invention relates to thiophenesulfonamides such as N-[(4,6-dimethylpyrimidin-2-yl)aminocarbonyl]-3-(isoxazol-3-yl)-2-thiophenesulfonamide which are useful as herbicides and plant growth regulants. More specifically the herbicides are of the formula: Ia Ib Ic wherein R is H or CH3; n is 0, 1 or 2; W is O or S; Q is a saturated 5- or 6- membered ring containing 1 heteroatom selected from sulfur, nitrogen or oxygen or an unsaturated 5- or 6- membered ring containing 1-3 heteroatoms selected from 0-1 sulfur, 0-1 oxygen or 0-3 nitrogen and Q may optionally be substituted by one or more groups selected from SH C1-C4 alkyl, C3-C4 alkenyl, C1-C3 haloalkyl, halogen, C1-C3 alkoxy, C1-C4 alkylthio, C3-C4 alkenylthio, C3-C4 alkenylthio, C3-C4 alkenyloxy, C1-C2 haloalkoxy, C1-C2 haloalkylthio, C3-C4 alkynylthio, C -C cyanoalkylthio, C1-C2 alkylcarbonylmeth-ylthio or C1-C2 alkoxycarbonylmethylthio; E is H, C1-C2 alkyl, C1-C2 alkoxy, halo-gen, NO2, C1-C2 haloalkyl, C1-C2 alkylthio, C1-C2 alkylsulfonyl, C1-C2 alkoxycarbonyl, C1-C2 diakylaminosulfamoyl; A is or X is H, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkyl, C1-C4 haloalkylthio, C1-C4 alkylthio, halogen, C2-C5 alkoxyalkyl, C2-C5, amino, C1-C3 alkylamino or di(C1-C3 alkyl)amino; Y is H, C1-C4 alkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 haloalkylthio, C1-C4 alkylthio, halogen, C2-C5 alkoxyalkyl, C2-C5 alkoxyalkoxy, amino, C1-C3 alkylamino, di(C1-C3 alkyl)amino, C3-C4 alkenyloxy, C3-C4 alkynyloxy, C2-C5 alkylthioalkyl, C2-C5 alkylsulfinylalkyl, C2-C5 alkylsulfonylalkyl, C1-C4 haloalkyl, C3-C5 cycloalky, C2-C4 alkynyl, C(O)RC, , , or N(OCH3)CH3; m is 2 or 3; L1 and L2 are independently O or S; Ra and Rb are independently C1-C2 alkyl; Rc is H or CH3; Z is CH or N; Y1 is O or CH2; X1 is CH3, OCH3, OC2H5 OR OCF2H; Y2 IS H OR CH3; X2 IS CH3, OCH3 OR SCH3; Y3 IS CH3, CH2CH3 OR CH2CF3; AND X3 IS CH3 OR OCH3; and their agriculturally suitable salts; provided that 1) when X is F, Cl, Br or I, then Z is CH and Y is OCF2H, OCH3 OC2G5, NH2, N(OCH3)CH3, NHCH3, N(CH3)2; 2) the total number of carbon atoms of Q must be less than or equal to 8; 3) when X or Y is OCF2H, then Z is CH; 4) when Q is a saturated 5- or 6- membered ring containing one nitrogen atom, it is bonded to the thiophene ring through carbon; and 5) when W is S, then R is H, A is A-1 and Y is CH3, OCH3, OC2H5, CH2OCH3, C2H5, CF3, SCH3, OCH2CH-CH2, OCH2C CH, OCH2CG2ICG3, CH(OCH3)2 or ;
priorityDate 1984-06-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
type http://data.epo.org/linked-data/def/patent/Publication

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