http://rdf.ncbi.nlm.nih.gov/pubchem/patent/CO-4810291-A1
Outgoing Links
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| filingDate | 1998-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d03db768286027fd83c384c52e4f91e5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_87206b3f39341287017be658c08eb9b9 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_820fec6ecd73fde5ae7927a6c712151c http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fd7851c044cf4ae6b909df7ae2ee9b6f http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_fc7868146b48f2d1c1acad964f40573d http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_d4bbf48cfb8517a39575fdefb65225ef http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_532b26a180919e3dfbed087e020dc925 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_37c8196acfdb43e2ea15ea3ee53c35bc http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_5b5290ea9028774f0f50079daa718895 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f302455451539d824717c3a04f9c44d5 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_1606dfaa0b672ba4b41c13b4d90faf55 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_b543f609b28f01c2b55946c5a44baabd http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_8bc5f0f7e5c1839df8253335574e2945 http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_f072cdbc15f65e6997b7654bfccf505a |
| publicationDate | 1999-06-30-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| publicationNumber | CO-4810291-A1 |
| titleOfInvention | FUNGICIDE COMPOSITIONS AND METHODS AND COMPOUNDS AND METHODS FOR THE PREPARATION OF THESE |
| abstract | The acylated aminosalicylamide compound of formula I: Wherein: a. m is 1 or 2; b. n is 1-4; c. X is hydrogen H, halogen, C1-C4 alkyl, C2-C4 alkenyl, cyclopropyl, cyano, NO2, C1-C4 haloalkyl, hydroxy, C1-C3 alkoxy, C1-C3 alkylthio, C1-C3 alkylsulfonyl, alkylsulfinyl C1-C3, SCO C1-C2 alkyl, Nhalkyl C1-C3, N (alkyl) 2 C1-C3, NHCO C1-C3 alkyl, NHC (O), N-alkyl C1-C3 alkyl, NHCONHH C1-C3 alkyl or NHCON (alkyl) 2 C1-C2, C (O) Rx, C (O) ORx or C (O) NRxRx, in which Rx is H or C1-C4 alkyl; d. Y is selected from the group consisting of O, S, NOH, NH or NOC1-3 alkyl. and. Z is selected from the group consisting of H, C1-C2 alkyl, CH3, NH2 or Me2 N, and f. R1 -R6 are defined as follows: (i) each of R1 -R6 is independently selected from the group consisting of: (1). H, halogen and cyano, (2) C1-C8 alkyl (straight or branched chain), C2-C8 alkenyl (straight or branched chain), C2-C8 alkenyl (straight or branched chain), C3-C8 cycloalkyl and C4 cycloalkenyl C8, each of the above groups being optimally substituted with one or more of: OR7, SR7, SOR7a, SO2 R7a, NR8 R8a, halogen, - 2-cyano, (C3-C8) cycloalkyl, Si (C1-C4 alkyl) 3, C (O) OR7a, aryl, or heterocycle (3). C1-C8 alkoxycarbonyl, aryloxycarbonyl, (alxoxythio) carbonyl, (alkylo) carbonyl, C1-C7, CONH-C1-C7-alkyl, CONHaryl, aryl-C1-C3-alkylaryl, CON-C1-C4, and COR11, (4). Aryl or heterocycle, which may be the same or different, provided that not more than two of the R1-R6 can be aryl or heterocycle, (5). C1-C8 alkoxy (straight or branched chain), C3-C8 alkenyloxy, C3-C8 alkynyloxy, C3-C8 cycloalkoxy, C1-C8 haloalkoxy (straight or branched chain), C3-C8 alkoxyalkoxy, C3-C8 alkylthio (straight or branched chain), C3-C8 alkenylthio, C3 -C8 alkynyl, C3-C8 cycloalkylthio, C1-C8 haloalkylthio, OR9, SR9, NR9 R10, aryloxy, heterocycloxy, arylthio or heterocyclotium, (6) . When any two of R1-R6 are on the same carbon, they can combine to form a CR12 R13 alkylene, ketone, NOH, NO C1-C3 alkyl, and (7). When either of two R1 AND # 8209; R6 are on the same carbon, they can combine to form a 3-8 membered ring that can contain oxygen, in addition to carbon, the ring being optimally substituted with one or more C1 AND #alkyl # 8209; C4, C2 alkenyl AND # 8209; C4, OR7, SR7, SOR7a, SO2 R7a, NR8 R8a, halogen, cyano or carboalkoxy C1 AND # 8209; C4; (ii) also in which: (1). R7 comprises H, C1 alkyl AND # 8209; C8, C3 alkenyl AND # 8209; C8, C3 alkynyl AND # 8209; C8, C3 cycloalkyl AND # 8209; C8, C3 cycloalkenyl AND # 8209; C8, C3 alkoxyalkyl AND # 8209; C8, CO C1 alkyl # 8209; C7, CON C1 alkyl AND # 8209; C6, CONaryl, CON (alkyl) 2 C1 AND # 8209; C4, aryl or heterocycle; R7a comprises C1-alkyl AND # 8209; C8, C3-C8 alkenyl, C3-alkynyl AND # 8209; C8, C3-cycloalkyl AND # 8209; C8, C5-cycloalkenyl AND # 8209; C8, alkoxyalkyl-C3 AND # 8209; C8, aryl and heterocycle , (2) R8 comprises C1-alkyl AND # 8209; C7, CO2-C1-alkyl AND # 8209; C6, COaryl, CON C1-alkyl AND # 8209; C6, CONCONHaryl, CON (alkyl) 2, C1 AND # 8209; C6, SO2 C1-alkyl AND # 8209; C6, SO2 aryl, SO2 NHalkyl C1 AND # 8209; C6, SO2 NHaryl or SO2 N (alkyl) 2 C1 AND # 8209; C7, (3) R8a comprises H, C1 alkyl AND # 8209; C8, aryl , heterocycle or CO alkyl C1 AND # 8209; C3, (4). R9 comprises H, C (O) H, CO alkyl C1 AND # 8209; C7, CO alkyl C2 AND # 8209; C7, COaryl, CONHalkyl C1 AND # 8209; C6, CONHaryl, CONalkyl2, SO2 C1 alkyl AND # 8209; C6, SO2 NHalkyl C1 AND # 8209; C6 or SO2 N (alkyl) 2 C1 AND # 8209; C4, (5). R10 is H or C1-alkyl AND # 8209; C4, (6). R11 comprises H, C1 alkyl AND # 8209; C8, C2 alkenyl AND # 8209; C8, C3 cycloalkyl AND # 8209; C8, aryl or heterocycle, and (7). R12 and R13 are the same or different and comprise H, C1 alkyl # 8209; C7, C1 haloalkyl AND # 8209; C6, C3-C8 cycloalkyl, aryl, heterocycle, cyano, carboalkoxy, C1 AND # 8209; C6, alkylAND # 8209 ; C1 AND # 8209 sulfonyl; C6, arylsulfonyl or C1 and # 8209 alkylsulfinyl; C6, or R12 and R13 being linked in a C3-C8 alkyl ring, (8). Each of the terms aryl and heterocycle include substituted and unsubstituted forms; (iii) R1 AND # 8209; R6 may be the same or different with the proviso that at least one of R1 AND # 8209; R6 must be different from hydrogen; (iv) R1 AND # 8209; R6 are independently cis or trans one or the other and the amide nitrogen, and when n = 2 the amide nitrogen is axial or equatorial, (v) R1 R6 are in any substitution pattern around the alicyclic ring in accordance with the chemical bonding rules; and any of the alicyclic rings contain 0AND # 8209; 2 endocyclic double bonds, where the ring size and substitution pattern are allowed according to the chemical bonding rules, since no heteroatom is attached to the bonded ring carbons double; and hydrates, salts and complexes of the above. |
| priorityDate | 1997-12-04-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
| type | http://data.epo.org/linked-data/def/patent/Publication |
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Total number of triples: 95.