http://rdf.ncbi.nlm.nih.gov/pubchem/patent/ES-2637336-T3

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filingDate 2007-07-27-04:00^^<http://www.w3.org/2001/XMLSchema#date>
grantDate 2017-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
inventor http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_ecee64f68a853298771650c567aa45f8
http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_4c95f9bfe9b983165a1406713248ad6d
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publicationDate 2017-10-11-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber ES-2637336-T3
titleOfInvention Derivatives of 1- (acetyl) -piperidine and 1- (acetyl) -piperazine as fungicides for use in plant protection
abstract A compound selected from formula 1, an N-oxide and its salt, ** Formula ** wherein R1 is ** Formula ** or where when R4 is attached to a ring member carbon, said R4 is selected from R4a ; each R4a is independently C1-C2 alkyl, trifluoromethyl, Cl, Br, I or methoxy; A is CH2; W is O; X is ** Formula ** and the ring comprising X is saturated, and where the bond of X1 or X2 that is identified with "t" is connected to the carbon atom identified with "q" of formula 1, the bond that is identified with "u" is connected to the carbon atom that is identified with "r" of formula 1, and the link that is identified with "v" is connected to G; each R2 is independently ethyl, methoxy, cyano or hydroxy; G is selected from ** Formula ** where the link that projects to the left is attached to X, and the link that projects to the right is linked to Z1; and G is not substituted; each R3a H; J is selected from ** Formula ** where the link shown projected to the left is attached to Z1; each R5 is independently H, halogen, cyano, hydroxy, amino, nitro, -CHO, -C (> = O) OH, -C (> = O) NH2, -NR25R26, C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C1-C6 halogenoalkyl, C2-C6 halogenoalkenyl, C2-C6 halogenoalkynyl, C3-C8 cycloalkyl, C3-C8 halocycloalkyl, C4-C10 alkylcycloalkyl, C4-C10 cycloalkylalkyl, C6-cycloalkyl-C4-cycloalkyl-C6-cycloalkyl-C6-cycloalkyl-C6-cycloalkyl-C6-cycloalkyl-C6-cycloalkyl-C6-cycloalkyl-C6-cycloalkyl-C4-cycloalkyl-C4-alkyl alkylcycloalkylalkyl C5-C10 cycloalkenyl C3-C8 halocycloalkenyl C3-C8 alkoxyalkyl C2-C6, cycloalkoxyalkyl C4-C10 alkoxyalkoxyalkyl C3-C8 alkylthioalkyl C2-C6 alkylsulfinylalkyl, C2-C6 alkylsulfonylalkyl, C2-C6 alkylaminoalkyl, C2-C6, C3-C8 dialkylaminoalkyl, C2-C6 halogenoalkylaminoalkyl, C4-C10 cycloalkylaminoalkyl, C2-C6 alkylcarbonyl, C2-C6 alkylcarbonyl, C4-C8 cycloalkylcarbonyl, C2-C6 alkoxycarbonyl C4-C6-C6-alkyloxycarbonyl, C4-C6-C6-alkylalkyl C3-C8 dialkylaminocarbonyl, cycloal C4-C8 alkylaminocarbonyl, C1-C6 alkoxy, C1-C6 halogenoalkoxy, C3-C8 cycloalkoxy, C3-C8 halogenocycloalkoxy, C4-C10 cycloalkylalkoxy, C2-C6 alkynyloxy, C2-C6 alkyloxy, C2-C6 alkyloxy C2-C6 alkoxyalkoxy, C2-C6 alkylcarbonyloxy, C2-C6 halogenoalkylcarbonyloxy, C4-C6 cycloalkylcarbonyloxy, C1-C6 alkylcarbonyloxyC1-C6 alkyl, C3-C6-C1-C6-C6 alkyl haloalkyl alkyl , C1-C6 alkylsulfonyl, C1-C6 halogenoalkylsulfonyl, C3-C8 cycloalkylsulfonyl, C3-C10 trialkylsilyl, C1-C6 alkylsulfonylamino, C1-C6 halogenoalkylsulfonylamino or -Z2Q; each R25 is independently H, C1-C6 alkyl, C1-C6 haloalkyl, C3-C8 cycloalkyl, C2-C6 alkylcarbonyl, C2-C6 halogenoalkylcarbonyl, C2-C6 alkoxycarbonyl or C2-C6 alkoxycarbonyl; each R26 is independently C1-C6 alkyl, C1-C6 haloalkyl, C3-C8 cycloalkyl, C2-C6 alkylcarbonyl, C2-C6 halogenoalkylcarbonyl, C2-C6 alkoxycarbonyl, C2-C6 alkoxycarbonyl or -Z4Q; each Q is independently selected from ** Formula ** each R7 is independently C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C4-C10 cycloalkylalkyl, C4-C10 alkylcycloalkyl, C5-C10 alkylcycloalkyl, C1-C6 halogenoalkyl, C2-C6 halogenoalkenyl, C2-C6 halogenoalkyl, C3-C6 halocycloalkyl, halogen, hydroxy, amino, cyano, nitro, C1-C4 alkoxy, C1-C4 halogenoalkoxy, C1-C4 alkylsulfinyl, C1-C4 alkylsulfonyl, C1-C4 halogenoalkylthio, C1-C4 halogenoalkylsulfinyl, C1-C4 halogenoalkylsulfonyl, C1-C4 alkylamino, C2-C8 dialkylamino, C2-C4 cycloalkylamino, C1-C4 alkoxycarbonyl, C-C4-alkyl, C2-C6 alkoxycarbonyl, C2-C6 alkylcarbonyloxy, C2-C6 alkylcarbonylthio, C2-C6 alkylaminocarbonyl, C3-C8 dialkylaminocarbonyl or C3-C6 trialkylsilyl; or R5 and R7 are considered together with the atoms that connect R5 and R7 to form a ring of 5 to 7 members containing as members of the ring of 2 to 7 carbon atoms and 1 to 3 heteroatoms selected from up to 1 O, up to 1 S, up to 1 Si and up to 1 N, the ring optionally substituted in ring members other than the atoms joining R5 and R7 with up to 4 substituents selected from R8; each R8 is independently C1-C6 alkyl, C2-C6 alkenyl, C2-C6 alkynyl, C3-C6 cycloalkyl, C4-C10 cycloalkylalkyl, C4-C10 alkylcycloalkyl, C5-C10 alkylcycloalkylalkyl, C1-C6 halogenoalkyl-C2-haloalkenyl, C6 C2-C6, C3-C6 halogenocycloalkyl, halogen, hydroxy, amino, cyano, nitro, C1-C4 alkoxy, C1-C4 halogenoalkoxy, C1-C4 alkylthio, C1-C4 alkylsulfinyl, C1-C4 alkylsulphonyl, C1-C4 halogenoalkyl, halogenoalkylsulfinyl C1-C4, halogenoalkylsulfonyl C1-C4, alkylamino C1-C4, dialkylamino C2-C8, cycloalkylamino C3-C6, alkoxyalkyl C2-C4, hydroxyalkyl C1-C4, alkylcarbonyl C2-C4, alkoxycarbonyl C2-C6, alkylcarbonyloxyC2 C2-C6, C2-C6 alkylaminocarbonyl, C3-C8 dialkylaminocarbonyl or C3-C6 trialkylsilyl; Each Z1 and Z2 is a direct link; each Z4 is independently C (> = O) or S (O) 2; n is 0, 1 or 2; k is 0, 1 or 2; p is 0, 1 or 2; and x is an integer from 0 to 5.
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Total number of triples: 410.