JP2013501061A5 - - Google Patents
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- JP2013501061A5 JP2013501061A5 JP2012523705A JP2012523705A JP2013501061A5 JP 2013501061 A5 JP2013501061 A5 JP 2013501061A5 JP 2012523705 A JP2012523705 A JP 2012523705A JP 2012523705 A JP2012523705 A JP 2012523705A JP 2013501061 A5 JP2013501061 A5 JP 2013501061A5
- Authority
- JP
- Japan
- Prior art keywords
- methyl
- hydroxy
- chloro
- independently selected
- ring
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
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- 150000003839 salts Chemical class 0.000 claims description 44
- -1 cyano, hydroxy, amino Chemical group 0.000 claims description 39
- 150000001875 compounds Chemical class 0.000 claims description 19
- 239000007787 solid Substances 0.000 claims description 3
- CWXUCLFBQRJEAG-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-(2-fluorophenyl)-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C(=CC=CC=2)F)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 CWXUCLFBQRJEAG-UHFFFAOYSA-O 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims 42
- 229910052736 halogen Inorganic materials 0.000 claims 39
- 150000002367 halogens Chemical class 0.000 claims 39
- 125000000753 cycloalkyl group Chemical group 0.000 claims 26
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims 26
- 125000005119 alkyl cycloalkyl group Chemical group 0.000 claims 25
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 claims 25
- 125000004093 cyano group Chemical group *C#N 0.000 claims 23
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 claims 23
- 125000005120 alkyl cycloalkyl alkyl group Chemical group 0.000 claims 20
- 125000006448 cycloalkyl cycloalkyl group Chemical group 0.000 claims 19
- 229910052717 sulfur Inorganic materials 0.000 claims 17
- 125000004122 cyclic group Chemical group 0.000 claims 15
- 150000001721 carbon Chemical group 0.000 claims 14
- 125000004432 carbon atom Chemical group C* 0.000 claims 14
- 125000005842 heteroatom Chemical group 0.000 claims 14
- 125000004434 sulfur atom Chemical group 0.000 claims 14
- 125000000217 alkyl group Chemical group 0.000 claims 13
- 229910052760 oxygen Inorganic materials 0.000 claims 9
- 125000003545 alkoxy group Chemical group 0.000 claims 8
- 125000005112 cycloalkylalkoxy group Chemical group 0.000 claims 7
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims 7
- 125000003342 alkenyl group Chemical group 0.000 claims 6
- 125000003302 alkenyloxy group Chemical group 0.000 claims 6
- 125000005136 alkenylsulfinyl group Chemical group 0.000 claims 6
- 125000005137 alkenylsulfonyl group Chemical group 0.000 claims 6
- 125000004644 alkyl sulfinyl group Chemical group 0.000 claims 6
- 125000004390 alkyl sulfonyl group Chemical group 0.000 claims 6
- 125000004414 alkyl thio group Chemical group 0.000 claims 6
- 125000000304 alkynyl group Chemical group 0.000 claims 6
- 125000005133 alkynyloxy group Chemical group 0.000 claims 6
- 125000005134 alkynylsulfinyl group Chemical group 0.000 claims 6
- 125000005139 alkynylsulfonyl group Chemical group 0.000 claims 6
- 229910052799 carbon Inorganic materials 0.000 claims 6
- 125000001651 cyanato group Chemical group [*]OC#N 0.000 claims 6
- 125000000392 cycloalkenyl group Chemical group 0.000 claims 6
- 125000000000 cycloalkoxy group Chemical group 0.000 claims 6
- 125000005149 cycloalkylsulfinyl group Chemical group 0.000 claims 6
- 125000005144 cycloalkylsulfonyl group Chemical group 0.000 claims 6
- 125000004663 dialkyl amino group Chemical group 0.000 claims 6
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 claims 6
- 125000004665 trialkylsilyl group Chemical group 0.000 claims 6
- 125000001960 7 membered carbocyclic group Chemical group 0.000 claims 5
- 125000005109 alkynylthio group Chemical group 0.000 claims 5
- 125000005366 cycloalkylthio group Chemical group 0.000 claims 5
- 125000006456 halo alkyl cycloalkyl group Chemical group 0.000 claims 5
- 125000005347 halocycloalkyl group Chemical group 0.000 claims 5
- 125000004461 halocycloalkylalkyl group Chemical group 0.000 claims 5
- 125000000623 heterocyclic group Chemical group 0.000 claims 5
- 125000005108 alkenylthio group Chemical group 0.000 claims 4
- 125000004076 pyridyl group Chemical group 0.000 claims 4
- 125000006413 ring segment Chemical group 0.000 claims 4
- 230000000967 entomopathogenic effect Effects 0.000 claims 3
- NYPJDWWKZLNGGM-UHFFFAOYSA-N fenvalerate Aalpha Natural products C=1C=C(Cl)C=CC=1C(C(C)C)C(=O)OC(C#N)C(C=1)=CC=CC=1OC1=CC=CC=C1 NYPJDWWKZLNGGM-UHFFFAOYSA-N 0.000 claims 3
- 125000004692 haloalkylcarbonyl group Chemical group 0.000 claims 3
- 229910052739 hydrogen Inorganic materials 0.000 claims 3
- 229910052757 nitrogen Inorganic materials 0.000 claims 3
- 125000004433 nitrogen atom Chemical group N* 0.000 claims 3
- 125000000714 pyrimidinyl group Chemical group 0.000 claims 3
- ZMZDMBWJUHKJPS-UHFFFAOYSA-N thiocyanic acid Chemical compound SC#N ZMZDMBWJUHKJPS-UHFFFAOYSA-N 0.000 claims 3
- 239000005660 Abamectin Substances 0.000 claims 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- 125000004429 atom Chemical group 0.000 claims 2
- 239000003795 chemical substances by application Substances 0.000 claims 2
- 239000003085 diluting agent Substances 0.000 claims 2
- ZXQYGBMAQZUVMI-GCMPRSNUSA-N gamma-cyhalothrin Chemical compound CC1(C)[C@@H](\C=C(/Cl)C(F)(F)F)[C@H]1C(=O)O[C@H](C#N)C1=CC=CC(OC=2C=CC=CC=2)=C1 ZXQYGBMAQZUVMI-GCMPRSNUSA-N 0.000 claims 2
- 125000004438 haloalkoxy group Chemical group 0.000 claims 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims 2
- 229960000490 permethrin Drugs 0.000 claims 2
- XLNZEKHULJKQBA-UHFFFAOYSA-N terbufos Chemical compound CCOP(=S)(OCC)SCSC(C)(C)C XLNZEKHULJKQBA-UHFFFAOYSA-N 0.000 claims 2
- 125000000335 thiazolyl group Chemical group 0.000 claims 2
- CXBMCYHAMVGWJQ-CABCVRRESA-N (1,3-dioxo-4,5,6,7-tetrahydroisoindol-2-yl)methyl (1r,3r)-2,2-dimethyl-3-(2-methylprop-1-enyl)cyclopropane-1-carboxylate Chemical compound CC1(C)[C@H](C=C(C)C)[C@H]1C(=O)OCN1C(=O)C(CCCC2)=C2C1=O CXBMCYHAMVGWJQ-CABCVRRESA-N 0.000 claims 1
- AGMMRUPNXPWLGF-AATRIKPKSA-N (2,3,5,6-tetrafluoro-4-methylphenyl)methyl 2,2-dimethyl-3-[(e)-prop-1-enyl]cyclopropane-1-carboxylate Chemical compound CC1(C)C(/C=C/C)C1C(=O)OCC1=C(F)C(F)=C(C)C(F)=C1F AGMMRUPNXPWLGF-AATRIKPKSA-N 0.000 claims 1
- LZTIMERBDGGAJD-SNAWJCMRSA-N (2e)-2-(nitromethylidene)-1,3-thiazinane Chemical compound [O-][N+](=O)\C=C1/NCCCS1 LZTIMERBDGGAJD-SNAWJCMRSA-N 0.000 claims 1
- 125000004765 (C1-C4) haloalkyl group Chemical group 0.000 claims 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims 1
- 125000006650 (C2-C4) alkynyl group Chemical group 0.000 claims 1
- WCXDHFDTOYPNIE-RIYZIHGNSA-N (E)-acetamiprid Chemical compound N#C/N=C(\C)N(C)CC1=CC=C(Cl)N=C1 WCXDHFDTOYPNIE-RIYZIHGNSA-N 0.000 claims 1
- PGOOBECODWQEAB-UHFFFAOYSA-N (E)-clothianidin Chemical compound [O-][N+](=O)\N=C(/NC)NCC1=CN=C(Cl)S1 PGOOBECODWQEAB-UHFFFAOYSA-N 0.000 claims 1
- CFRPSFYHXJZSBI-DHZHZOJOSA-N (E)-nitenpyram Chemical compound [O-][N+](=O)/C=C(\NC)N(CC)CC1=CC=C(Cl)N=C1 CFRPSFYHXJZSBI-DHZHZOJOSA-N 0.000 claims 1
- IQVNEKKDSLOHHK-FNCQTZNRSA-N (E,E)-hydramethylnon Chemical compound N1CC(C)(C)CNC1=NN=C(/C=C/C=1C=CC(=CC=1)C(F)(F)F)\C=C\C1=CC=C(C(F)(F)F)C=C1 IQVNEKKDSLOHHK-FNCQTZNRSA-N 0.000 claims 1
- ZFHGXWPMULPQSE-SZGBIDFHSA-N (Z)-(1S)-cis-tefluthrin Chemical compound FC1=C(F)C(C)=C(F)C(F)=C1COC(=O)[C@@H]1C(C)(C)[C@@H]1\C=C(/Cl)C(F)(F)F ZFHGXWPMULPQSE-SZGBIDFHSA-N 0.000 claims 1
- HOKKPVIRMVDYPB-UVTDQMKNSA-N (Z)-thiacloprid Chemical compound C1=NC(Cl)=CC=C1CN1C(=N/C#N)/SCC1 HOKKPVIRMVDYPB-UVTDQMKNSA-N 0.000 claims 1
- IAKOZHOLGAGEJT-UHFFFAOYSA-N 1,1,1-trichloro-2,2-bis(p-methoxyphenyl)-Ethane Chemical compound C1=CC(OC)=CC=C1C(C(Cl)(Cl)Cl)C1=CC=C(OC)C=C1 IAKOZHOLGAGEJT-UHFFFAOYSA-N 0.000 claims 1
- IYPPDGRZXQJRSZ-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-3-(2-methoxyphenyl)-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound COC1=CC=CC=C1C(C1=O)=C(O)[N+](CC=2SC(Cl)=NC=2)=C2N1C=CC=C2C IYPPDGRZXQJRSZ-UHFFFAOYSA-O 0.000 claims 1
- UKRUOLNZJLTUQS-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-3-(3-iodo-5-methoxyphenyl)-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound COC1=CC(I)=CC(C=2C(N3C=CC=C(C)C3=[N+](CC=3SC(Cl)=NC=3)C=2O)=O)=C1 UKRUOLNZJLTUQS-UHFFFAOYSA-O 0.000 claims 1
- KTWMWIRJXDVWAA-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-3-(3-iodophenyl)-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(I)C=CC=2)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 KTWMWIRJXDVWAA-UHFFFAOYSA-O 0.000 claims 1
- YHOYEVOTCXAULR-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-3-(3-methoxyphenyl)-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound COC1=CC=CC(C=2C(N3C=CC=C(C)C3=[N+](CC=3SC(Cl)=NC=3)C=2O)=O)=C1 YHOYEVOTCXAULR-UHFFFAOYSA-O 0.000 claims 1
- QFVHAVLVUZEIRR-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-3-[2-methoxy-5-(trifluoromethoxy)phenyl]-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound COC1=CC=C(OC(F)(F)F)C=C1C(C1=O)=C(O)[N+](CC=2SC(Cl)=NC=2)=C2N1C=CC=C2C QFVHAVLVUZEIRR-UHFFFAOYSA-O 0.000 claims 1
- PWQNAUPOEXRFFG-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-3-phenylpyrimido[2,1-a]isoquinolin-5-ium-4-one Chemical compound O=C1N2C=CC3=CC=CC=C3C2=[N+](CC=2SC(Cl)=NC=2)C(O)=C1C1=CC=CC=C1 PWQNAUPOEXRFFG-UHFFFAOYSA-O 0.000 claims 1
- ZMAXVJAJJZBJRG-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-9-methoxy-3-[3-(trifluoromethoxy)phenyl]pyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound COC1=CC=CN(C(C(C=2C=C(OC(F)(F)F)C=CC=2)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 ZMAXVJAJJZBJRG-UHFFFAOYSA-O 0.000 claims 1
- QCSHNCXBAFDJIE-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-9-methyl-3-[3-(trifluoromethoxy)phenyl]pyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(OC(F)(F)F)C=CC=2)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 QCSHNCXBAFDJIE-UHFFFAOYSA-O 0.000 claims 1
- ILMHMQLAHSPLFY-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-9-methyl-3-[3-(trifluoromethyl)phenyl]pyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(C=CC=2)C(F)(F)F)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 ILMHMQLAHSPLFY-UHFFFAOYSA-O 0.000 claims 1
- WPRMWWNDJUWKFX-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-9-methyl-3-[3-(trifluoromethylsulfanyl)phenyl]pyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(SC(F)(F)F)C=CC=2)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 WPRMWWNDJUWKFX-UHFFFAOYSA-O 0.000 claims 1
- AEYJISVUNNQUGD-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-9-methyl-3-[3-[3-(trifluoromethoxy)phenyl]phenyl]pyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(C=CC=2)C=2C=C(OC(F)(F)F)C=CC=2)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 AEYJISVUNNQUGD-UHFFFAOYSA-O 0.000 claims 1
- UVPMGXWDHDWRRW-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-9-methyl-3-[4-(trifluoromethylsulfanyl)phenyl]pyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=CC(SC(F)(F)F)=CC=2)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 UVPMGXWDHDWRRW-UHFFFAOYSA-O 0.000 claims 1
- MTBVLVGKIKBZRH-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-9-methyl-3-phenylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=CC=CC=2)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 MTBVLVGKIKBZRH-UHFFFAOYSA-O 0.000 claims 1
- ATRLXSMHGOZXRF-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-(2,4-difluorophenyl)-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C(=CC(F)=CC=2)F)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 ATRLXSMHGOZXRF-UHFFFAOYSA-O 0.000 claims 1
- XKIVTPJYLCAJBF-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-(2,6-difluorophenyl)-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C(=CC=CC=2F)F)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 XKIVTPJYLCAJBF-UHFFFAOYSA-O 0.000 claims 1
- AZCDZMPIQOBPTC-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-(3-ethenylphenyl)-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(C=C)C=CC=2)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 AZCDZMPIQOBPTC-UHFFFAOYSA-O 0.000 claims 1
- HBDAVFRJYIMHPW-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-(4-fluorophenyl)-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=CC(F)=CC=2)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 HBDAVFRJYIMHPW-UHFFFAOYSA-O 0.000 claims 1
- FHTSKDGMFJJSQS-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-[2-fluoro-5-(trifluoromethyl)phenyl]-2-hydroxy-9-methoxypyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound COC1=CC=CN(C(C(C=2C(=CC=C(C=2)C(F)(F)F)F)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 FHTSKDGMFJJSQS-UHFFFAOYSA-O 0.000 claims 1
- BVXAYHINJGGMNR-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-[2-fluoro-5-(trifluoromethyl)phenyl]-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C(=CC=C(C=2)C(F)(F)F)F)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 BVXAYHINJGGMNR-UHFFFAOYSA-O 0.000 claims 1
- UGRXMCZULHDFHG-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-[3-(2,4-dichlorophenyl)phenyl]-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(C=CC=2)C=2C(=CC(Cl)=CC=2)Cl)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 UGRXMCZULHDFHG-UHFFFAOYSA-O 0.000 claims 1
- VGGYDDAHAHCUOI-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-[3-(2,5-difluorophenyl)phenyl]-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(C=CC=2)C=2C(=CC=C(F)C=2)F)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 VGGYDDAHAHCUOI-UHFFFAOYSA-O 0.000 claims 1
- FUAJLWAQGIFTRB-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-[3-chloro-5-(trifluoromethoxy)phenyl]-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(OC(F)(F)F)C=C(Cl)C=2)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 FUAJLWAQGIFTRB-UHFFFAOYSA-O 0.000 claims 1
- DFPYRTFQQULOFO-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-[3-chloro-5-(trifluoromethyl)phenyl]-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(C=C(Cl)C=2)C(F)(F)F)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 DFPYRTFQQULOFO-UHFFFAOYSA-O 0.000 claims 1
- OZQHSJNQCXWLRC-UHFFFAOYSA-O 1-[(2-chloro-1,3-thiazol-5-yl)methyl]-3-[3-fluoro-5-(trifluoromethyl)phenyl]-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(C=C(F)C=2)C(F)(F)F)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 OZQHSJNQCXWLRC-UHFFFAOYSA-O 0.000 claims 1
- XTZNXRSVHFJPDH-UHFFFAOYSA-O 2-hydroxy-9-methyl-1-[(2-methyl-1,3-thiazol-5-yl)methyl]-3-[3-(trifluoromethoxy)phenyl]pyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound S1C(C)=NC=C1C[N+]1=C2C(C)=CC=CN2C(=O)C(C=2C=C(OC(F)(F)F)C=CC=2)=C1O XTZNXRSVHFJPDH-UHFFFAOYSA-O 0.000 claims 1
- WIFKODFBSAFJME-UHFFFAOYSA-O 2-hydroxy-9-methyl-1-[(2-methyl-1,3-thiazol-5-yl)methyl]-3-[3-(trifluoromethyl)phenyl]pyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound S1C(C)=NC=C1C[N+]1=C2C(C)=CC=CN2C(=O)C(C=2C=C(C=CC=2)C(F)(F)F)=C1O WIFKODFBSAFJME-UHFFFAOYSA-O 0.000 claims 1
- VDDJSYRATMZQBR-UHFFFAOYSA-O 3-(2-fluorophenyl)-2-hydroxy-9-methyl-1-(pyrimidin-5-ylmethyl)pyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C(=CC=CC=2)F)=C2O)=O)C1=[N+]2CC1=CN=CN=C1 VDDJSYRATMZQBR-UHFFFAOYSA-O 0.000 claims 1
- CEZXNCUECFDITC-UHFFFAOYSA-O 3-(2-fluorophenyl)-2-hydroxy-9-methyl-1-[(2-methyl-1,3-thiazol-5-yl)methyl]pyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound S1C(C)=NC=C1C[N+]1=C2C(C)=CC=CN2C(=O)C(C=2C(=CC=CC=2)F)=C1O CEZXNCUECFDITC-UHFFFAOYSA-O 0.000 claims 1
- XGFCWLPGLGQYEM-UHFFFAOYSA-O 3-(3-bromophenyl)-1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(Br)C=CC=2)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 XGFCWLPGLGQYEM-UHFFFAOYSA-O 0.000 claims 1
- BVGAGXQZNPHZPI-UHFFFAOYSA-O 3-[3-(6-chloropyridin-3-yl)-5-(trifluoromethoxy)phenyl]-1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(C=C(OC(F)(F)F)C=2)C=2C=NC(Cl)=CC=2)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 BVGAGXQZNPHZPI-UHFFFAOYSA-O 0.000 claims 1
- YWFZLTOWZHETPA-UHFFFAOYSA-O 3-[3-bromo-5-(trifluoromethoxy)phenyl]-1-[(2-chloro-1,3-thiazol-5-yl)methyl]-2-hydroxy-9-methylpyrido[1,2-a]pyrimidin-5-ium-4-one Chemical compound CC1=CC=CN(C(C(C=2C=C(OC(F)(F)F)C=C(Br)C=2)=C2O)=O)C1=[N+]2CC1=CN=C(Cl)S1 YWFZLTOWZHETPA-UHFFFAOYSA-O 0.000 claims 1
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| UA110924C2 (uk) | 2009-08-05 | 2016-03-10 | Е. І. Дю Пон Де Немур Енд Компані | Мезоіонні пестициди |
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| KR20140018866A (ko) * | 2010-12-27 | 2014-02-13 | 스미또모 가가꾸 가부시끼가이샤 | 절지동물 해충 방제 조성물 및 절지동물 해충의 방제 방법 |
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| TWI528899B (zh) * | 2010-12-29 | 2016-04-11 | 杜邦股份有限公司 | 中離子性殺蟲劑 |
| WO2012106495A1 (en) * | 2011-02-03 | 2012-08-09 | E. I. Du Pont De Nemours And Company | Mesoionic pesticides |
| KR20140025429A (ko) | 2011-04-06 | 2014-03-04 | 바스프 에스이 | 동물 해충을 퇴치하기 위한 치환된 피리미디늄 화합물 |
| TWI572587B (zh) | 2011-12-15 | 2017-03-01 | 杜邦股份有限公司 | 丙二酸二鹽及用以製備丙二醯基二鹵化物之方法 |
| WO2013150115A1 (en) | 2012-04-05 | 2013-10-10 | Basf Se | N- substituted hetero - bicyclic compounds and derivatives for combating animal pests |
| MX2014015265A (es) | 2012-06-14 | 2015-08-12 | Basf Se | Metodos plaguicidas que utilizan compuestos de 3-piridiltiazol sustituido y derivados para combatir plagas de animales. |
| JP2014024830A (ja) * | 2012-06-21 | 2014-02-06 | Sumitomo Chemical Co Ltd | ウンカ類の防除方法 |
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| AU2014283346A1 (en) | 2013-06-17 | 2016-01-07 | Basf Se | Substituted pyrimidinium compounds and derivatives for combating animal pests |
| BR112017005140A2 (pt) | 2014-10-06 | 2018-01-23 | Basf Se | compostos, mistura, composição, métodos para a proteção de culturas e para o combate ou controle de praga de invertebrados, método não terapêutico para o tratamento de animais infestados ou infectados por parasitas e semente |
| CN107531700B (zh) * | 2015-04-21 | 2020-03-03 | 日本化药株式会社 | 介离子化合物 |
| AU2016363632A1 (en) | 2015-12-03 | 2018-06-07 | Bayer Cropscience Aktiengesellschaft | Mesoionic halogenated 3-(acetyl)-1-((1,3-thiazol-5-yl)methyl)-1h-imidazo(1,2-a)pyridin-4-ium-2-olate derivatives and related compounds as insecticides |
| WO2017109795A1 (en) * | 2015-12-21 | 2017-06-29 | Council Of Scientific & Industrial Research | Novel compounds useful as potential insect antifeedant and a process for the preparation thereof |
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