KR101782311B1 - 티오아미드 화합물, 이의 제조 방법 및 사용 방법 - Google Patents
티오아미드 화합물, 이의 제조 방법 및 사용 방법 Download PDFInfo
- Publication number
- KR101782311B1 KR101782311B1 KR1020117011425A KR20117011425A KR101782311B1 KR 101782311 B1 KR101782311 B1 KR 101782311B1 KR 1020117011425 A KR1020117011425 A KR 1020117011425A KR 20117011425 A KR20117011425 A KR 20117011425A KR 101782311 B1 KR101782311 B1 KR 101782311B1
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- South Korea
- Prior art keywords
- halo
- alkyl
- alkoxy
- alkylthio
- spp
- Prior art date
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- 238000000034 method Methods 0.000 title claims abstract description 39
- 238000004519 manufacturing process Methods 0.000 title description 13
- 150000003556 thioamides Chemical class 0.000 title description 9
- 150000001875 compounds Chemical class 0.000 claims abstract description 173
- 239000000203 mixture Substances 0.000 claims abstract description 125
- 238000002360 preparation method Methods 0.000 claims abstract description 9
- 229910052720 vanadium Inorganic materials 0.000 claims abstract description 6
- 230000008569 process Effects 0.000 claims abstract description 5
- -1 thioamide compound Chemical class 0.000 claims description 199
- 125000005843 halogen group Chemical group 0.000 claims description 135
- 125000001424 substituent group Chemical group 0.000 claims description 55
- 229910052736 halogen Inorganic materials 0.000 claims description 53
- 150000002367 halogens Chemical class 0.000 claims description 52
- 125000004093 cyano group Chemical group *C#N 0.000 claims description 49
- 239000001257 hydrogen Substances 0.000 claims description 44
- 229910052739 hydrogen Inorganic materials 0.000 claims description 44
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 40
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 claims description 39
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims description 36
- XEEYBQQBJWHFJM-UHFFFAOYSA-N Iron Chemical compound [Fe] XEEYBQQBJWHFJM-UHFFFAOYSA-N 0.000 claims description 34
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 claims description 34
- 125000005110 aryl thio group Chemical group 0.000 claims description 32
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims description 31
- 125000004738 (C1-C6) alkyl sulfinyl group Chemical group 0.000 claims description 29
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 claims description 29
- 125000004916 (C1-C6) alkylcarbonyl group Chemical group 0.000 claims description 27
- 239000002904 solvent Substances 0.000 claims description 27
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 claims description 22
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- UYJXRRSPUVSSMN-UHFFFAOYSA-P ammonium sulfide Chemical compound [NH4+].[NH4+].[S-2] UYJXRRSPUVSSMN-UHFFFAOYSA-P 0.000 claims description 5
- 230000003071 parasitic effect Effects 0.000 claims description 5
- 125000002816 methylsulfanyl group Chemical group [H]C([H])([H])S[*] 0.000 claims description 4
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- 125000004106 butoxy group Chemical group [*]OC([H])([H])C([H])([H])C(C([H])([H])[H])([H])[H] 0.000 claims description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 claims description 2
- 125000005344 pyridylmethyl group Chemical group [H]C1=C([H])C([H])=C([H])C(=N1)C([H])([H])* 0.000 claims description 2
- HYHCSLBZRBJJCH-UHFFFAOYSA-M sodium hydrosulfide Chemical compound [Na+].[SH-] HYHCSLBZRBJJCH-UHFFFAOYSA-M 0.000 claims description 2
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- 125000005034 trifluormethylthio group Chemical group FC(S*)(F)F 0.000 claims 2
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- 230000036281 parasite infection Effects 0.000 claims 1
- 125000006678 phenoxycarbonyl group Chemical group 0.000 claims 1
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- 125000001072 heteroaryl group Chemical group 0.000 description 14
- 239000003112 inhibitor Substances 0.000 description 14
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- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 11
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- 238000004293 19F NMR spectroscopy Methods 0.000 description 9
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- PMRYVIKBURPHAH-UHFFFAOYSA-N methimazole Chemical compound CN1C=CNC1=S PMRYVIKBURPHAH-UHFFFAOYSA-N 0.000 description 1
- YFBPRJGDJKVWAH-UHFFFAOYSA-N methiocarb Chemical compound CNC(=O)OC1=CC(C)=C(SC)C(C)=C1 YFBPRJGDJKVWAH-UHFFFAOYSA-N 0.000 description 1
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- KDXZREBVGAGZHS-UHFFFAOYSA-M methohexital sodium Chemical compound [Na+].CCC#CC(C)C1(CC=C)C(=O)N=C([O-])N(C)C1=O KDXZREBVGAGZHS-UHFFFAOYSA-M 0.000 description 1
- UHXUZOCRWCRNSJ-QPJJXVBHSA-N methomyl Chemical compound CNC(=O)O\N=C(/C)SC UHXUZOCRWCRNSJ-QPJJXVBHSA-N 0.000 description 1
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- 229960002455 methoxyflurane Drugs 0.000 description 1
- RFKMCNOHBTXSMU-UHFFFAOYSA-N methoxyflurane Chemical compound COC(F)(F)C(Cl)Cl RFKMCNOHBTXSMU-UHFFFAOYSA-N 0.000 description 1
- APEPSMUHNUYMRZ-NTEUORMPSA-N methyl (e)-2-[2-(3,5-dichlorophenoxy)pyridin-3-yl]-3-methoxyprop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CN=C1OC1=CC(Cl)=CC(Cl)=C1 APEPSMUHNUYMRZ-NTEUORMPSA-N 0.000 description 1
- QIHOFSAVNYTADJ-LFIBNONCSA-N methyl (e)-2-[2-(3,5-dimethylbenzoyl)pyrrol-1-yl]-3-methoxyprop-2-enoate Chemical compound CO\C=C(/C(=O)OC)N1C=CC=C1C(=O)C1=CC(C)=CC(C)=C1 QIHOFSAVNYTADJ-LFIBNONCSA-N 0.000 description 1
- DMWUVRNYTWAXBB-GHRIWEEISA-N methyl (e)-2-[2-(3-ethoxyphenoxy)phenyl]-3-methoxyprop-2-enoate Chemical compound CCOC1=CC=CC(OC=2C(=CC=CC=2)\C(=C/OC)C(=O)OC)=C1 DMWUVRNYTWAXBB-GHRIWEEISA-N 0.000 description 1
- BHKNFTHHZWWKIF-DTQAZKPQSA-N methyl (e)-2-[2-(4-tert-butylpyridin-2-yl)oxyphenyl]-3-methoxyprop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(C(C)(C)C)=CC=N1 BHKNFTHHZWWKIF-DTQAZKPQSA-N 0.000 description 1
- NVGXTWUVIMLKSY-RVDMUPIBSA-N methyl (e)-2-[2-[(5-bromopyridin-2-yl)oxymethyl]phenyl]-3-methoxyprop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC=C(Br)C=N1 NVGXTWUVIMLKSY-RVDMUPIBSA-N 0.000 description 1
- IOCDUXBRZHUYRM-XDJHFCHBSA-N methyl (e)-2-[2-[3-(2-fluorophenoxy)phenoxy]phenyl]-3-methoxyprop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC=CC(OC=2C(=CC=CC=2)F)=C1 IOCDUXBRZHUYRM-XDJHFCHBSA-N 0.000 description 1
- AGBLWOJBWFKJJQ-CJLVFECKSA-N methyl (e)-2-[2-[3-(3-cyanophenoxy)phenoxy]phenyl]-3-methoxyprop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC=CC(OC=2C=C(C=CC=2)C#N)=C1 AGBLWOJBWFKJJQ-CJLVFECKSA-N 0.000 description 1
- MNJUGZBQACUZSL-NBVRZTHBSA-N methyl (e)-2-[2-[3-(3-iodopyridin-2-yl)oxyphenoxy]phenyl]-3-methoxyprop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC=CC(OC=2C(=CC=CN=2)I)=C1 MNJUGZBQACUZSL-NBVRZTHBSA-N 0.000 description 1
- NDQFUGYXILJPEE-SDNWHVSQSA-N methyl (e)-2-[2-[6-(2-chloropyridin-3-yl)oxypyrimidin-4-yl]oxyphenyl]-3-methoxyprop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=NC=CC=2)Cl)=NC=N1 NDQFUGYXILJPEE-SDNWHVSQSA-N 0.000 description 1
- VQVKXPVWVSCFDO-NTCAYCPXSA-N methyl (e)-2-[2-[6-(2-fluorophenoxy)pyrimidin-4-yl]oxyphenyl]-3-methoxyprop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)F)=NC=N1 VQVKXPVWVSCFDO-NTCAYCPXSA-N 0.000 description 1
- GEPDYQSQVLXLEU-AATRIKPKSA-N methyl (e)-3-dimethoxyphosphoryloxybut-2-enoate Chemical compound COC(=O)\C=C(/C)OP(=O)(OC)OC GEPDYQSQVLXLEU-AATRIKPKSA-N 0.000 description 1
- QPBXDUQTQNAHRX-NTCAYCPXSA-N methyl (e)-3-methoxy-2-(2-phenoxyphenyl)prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC=CC=C1 QPBXDUQTQNAHRX-NTCAYCPXSA-N 0.000 description 1
- VEJCBCPEURAYAS-JUEGYJDASA-N methyl (e)-3-methoxy-2-[2-(2-phenylethenyl)phenyl]prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1C=CC1=CC=CC=C1 VEJCBCPEURAYAS-JUEGYJDASA-N 0.000 description 1
- KXACSLSEUQVTDK-FOWTUZBSSA-N methyl (e)-3-methoxy-2-[2-(3-methoxyphenoxy)phenyl]prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC=CC(OC)=C1 KXACSLSEUQVTDK-FOWTUZBSSA-N 0.000 description 1
- DKPOURYMDPQGLX-QGOAFFKASA-N methyl (e)-3-methoxy-2-[2-(3-propan-2-yloxyphenoxy)phenyl]prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC=CC(OC(C)C)=C1 DKPOURYMDPQGLX-QGOAFFKASA-N 0.000 description 1
- MZYYKQOKDIRBEP-NBVRZTHBSA-N methyl (e)-3-methoxy-2-[2-(3-pyrimidin-2-yloxyphenoxy)phenyl]prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC=CC(OC=2N=CC=CN=2)=C1 MZYYKQOKDIRBEP-NBVRZTHBSA-N 0.000 description 1
- KIJNRHWBPXCXEC-XDJHFCHBSA-N methyl (e)-3-methoxy-2-[2-(4-phenoxypyridin-2-yl)oxyphenyl]prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C=CC=CC=2)=CC=N1 KIJNRHWBPXCXEC-XDJHFCHBSA-N 0.000 description 1
- CAVNGXBDJHRHOZ-RCCKNPSSSA-N methyl (e)-3-methoxy-2-[2-[3-(4-nitrophenoxy)phenoxy]phenyl]prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC=CC(OC=2C=CC(=CC=2)[N+]([O-])=O)=C1 CAVNGXBDJHRHOZ-RCCKNPSSSA-N 0.000 description 1
- LSUAEGKHOVSUKQ-XMHGGMMESA-N methyl (e)-3-methoxy-2-[2-[3-(5-methylpyrimidin-2-yl)oxyphenoxy]phenyl]prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC=CC(OC=2N=CC(C)=CN=2)=C1 LSUAEGKHOVSUKQ-XMHGGMMESA-N 0.000 description 1
- WNAIXDFONSCLHB-GHRIWEEISA-N methyl (e)-3-methoxy-2-[2-[6-(2-methylphenoxy)pyrimidin-4-yl]oxyphenyl]prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2C(=CC=CC=2)C)=NC=N1 WNAIXDFONSCLHB-GHRIWEEISA-N 0.000 description 1
- BKLNXWIVUBHFKG-FOWTUZBSSA-N methyl (e)-3-methoxy-2-[2-[6-(6-methylpyridin-2-yl)oxypyrimidin-4-yl]oxyphenyl]prop-2-enoate Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1OC1=CC(OC=2N=C(C)C=CC=2)=NC=N1 BKLNXWIVUBHFKG-FOWTUZBSSA-N 0.000 description 1
- GTPBCDCTUUHTDD-NBVRZTHBSA-N methyl (e)-3-methoxy-2-[2-[[4-(2-propylphenoxy)-1,3,5-triazin-2-yl]oxy]phenyl]prop-2-enoate Chemical compound CCCC1=CC=CC=C1OC1=NC=NC(OC=2C(=CC=CC=2)\C(=C/OC)C(=O)OC)=N1 GTPBCDCTUUHTDD-NBVRZTHBSA-N 0.000 description 1
- BXBHZLHTTHMUTG-UHFFFAOYSA-N methyl 1h-pyrrolo[3,2-b]pyridine-2-carboxylate Chemical compound C1=CC=C2NC(C(=O)OC)=CC2=N1 BXBHZLHTTHMUTG-UHFFFAOYSA-N 0.000 description 1
- USSIUIGPBLPCDF-JMIUGGIZSA-N methyl 2-(4,6-dimethoxypyrimidin-2-yl)oxy-6-[(z)-n-methoxy-c-methylcarbonimidoyl]benzoate Chemical compound CO\N=C(\C)C1=CC=CC(OC=2N=C(OC)C=C(OC)N=2)=C1C(=O)OC USSIUIGPBLPCDF-JMIUGGIZSA-N 0.000 description 1
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- 229960003223 tripelennamine Drugs 0.000 description 1
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- KVEQCVKVIFQSGC-UHFFFAOYSA-N tritosulfuron Chemical compound FC(F)(F)C1=NC(OC)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(F)(F)F)=N1 KVEQCVKVIFQSGC-UHFFFAOYSA-N 0.000 description 1
- WFKWXMTUELFFGS-UHFFFAOYSA-N tungsten Chemical compound [W] WFKWXMTUELFFGS-UHFFFAOYSA-N 0.000 description 1
- 229910052721 tungsten Inorganic materials 0.000 description 1
- 239000010937 tungsten Substances 0.000 description 1
- 229960004059 tylosin Drugs 0.000 description 1
- WBPYTXDJUQJLPQ-VMXQISHHSA-N tylosin Chemical compound O([C@@H]1[C@@H](C)O[C@H]([C@@H]([C@H]1N(C)C)O)O[C@@H]1[C@@H](C)[C@H](O)CC(=O)O[C@@H]([C@H](/C=C(\C)/C=C/C(=O)[C@H](C)C[C@@H]1CC=O)CO[C@H]1[C@@H]([C@H](OC)[C@H](O)[C@@H](C)O1)OC)CC)[C@H]1C[C@@](C)(O)[C@@H](O)[C@H](C)O1 WBPYTXDJUQJLPQ-VMXQISHHSA-N 0.000 description 1
- 235000019375 tylosin Nutrition 0.000 description 1
- QTFFGPOXNNGTGZ-RCSCTSIBSA-N u3c8e5bwkr Chemical compound O.CS(O)(=O)=O.C1=CC=C2C(C(OC3C[C@@H]4CC5C[C@@H](N4CC5=O)C3)=O)=CNC2=C1 QTFFGPOXNNGTGZ-RCSCTSIBSA-N 0.000 description 1
- MSRILKIQRXUYCT-UHFFFAOYSA-M valproate semisodium Chemical compound [Na+].CCCC(C(O)=O)CCC.CCCC(C([O-])=O)CCC MSRILKIQRXUYCT-UHFFFAOYSA-M 0.000 description 1
- 229960000604 valproic acid Drugs 0.000 description 1
- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 229940045605 vanadium Drugs 0.000 description 1
- GPPXJZIENCGNKB-UHFFFAOYSA-N vanadium Chemical compound [V]#[V] GPPXJZIENCGNKB-UHFFFAOYSA-N 0.000 description 1
- 229960003165 vancomycin Drugs 0.000 description 1
- MYPYJXKWCTUITO-LYRMYLQWSA-O vancomycin(1+) Chemical compound O([C@@H]1[C@@H](O)[C@H](O)[C@@H](CO)O[C@H]1OC1=C2C=C3C=C1OC1=CC=C(C=C1Cl)[C@@H](O)[C@H](C(N[C@@H](CC(N)=O)C(=O)N[C@H]3C(=O)N[C@H]1C(=O)N[C@H](C(N[C@@H](C3=CC(O)=CC(O)=C3C=3C(O)=CC=C1C=3)C([O-])=O)=O)[C@H](O)C1=CC=C(C(=C1)Cl)O2)=O)NC(=O)[C@@H](CC(C)C)[NH2+]C)[C@H]1C[C@](C)([NH3+])[C@H](O)[C@H](C)O1 MYPYJXKWCTUITO-LYRMYLQWSA-O 0.000 description 1
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- VEPSYABRBFXYIB-PWXDFCLTSA-M vecuronium bromide Chemical compound [Br-].N1([C@@H]2[C@@H](OC(C)=O)C[C@@H]3CC[C@H]4[C@@H]5C[C@@H]([C@@H]([C@]5(CC[C@@H]4[C@@]3(C)C2)C)OC(=O)C)[N+]2(C)CCCCC2)CCCCC1 VEPSYABRBFXYIB-PWXDFCLTSA-M 0.000 description 1
- 229960004298 vecuronium bromide Drugs 0.000 description 1
- 229960001722 verapamil Drugs 0.000 description 1
- 239000000273 veterinary drug Substances 0.000 description 1
- KDQAABAKXDWYSZ-PNYVAJAMSA-N vinblastine sulfate Chemical compound OS(O)(=O)=O.C([C@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 KDQAABAKXDWYSZ-PNYVAJAMSA-N 0.000 description 1
- 229960004982 vinblastine sulfate Drugs 0.000 description 1
- AQTQHPDCURKLKT-JKDPCDLQSA-N vincristine sulfate Chemical compound OS(O)(=O)=O.C([C@@H](C[C@]1(C(=O)OC)C=2C(=CC3=C([C@]45[C@H]([C@@]([C@H](OC(C)=O)[C@]6(CC)C=CCN([C@H]56)CC4)(O)C(=O)OC)N3C=O)C=2)OC)C[C@@](C2)(O)CC)N2CCC2=C1NC1=CC=CC=C21 AQTQHPDCURKLKT-JKDPCDLQSA-N 0.000 description 1
- 229960002110 vincristine sulfate Drugs 0.000 description 1
- 229920002554 vinyl polymer Polymers 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 235000013343 vitamin Nutrition 0.000 description 1
- 239000011782 vitamin Substances 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 229940046009 vitamin E Drugs 0.000 description 1
- 235000019165 vitamin E Nutrition 0.000 description 1
- 239000011709 vitamin E Substances 0.000 description 1
- 150000003722 vitamin derivatives Chemical class 0.000 description 1
- 239000007762 w/o emulsion Substances 0.000 description 1
- 229960002647 warfarin sodium Drugs 0.000 description 1
- 239000001993 wax Substances 0.000 description 1
- 238000001238 wet grinding Methods 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- QYEFBJRXKKSABU-UHFFFAOYSA-N xylazine hydrochloride Chemical compound Cl.CC1=CC=CC(C)=C1NC1=NCCCS1 QYEFBJRXKKSABU-UHFFFAOYSA-N 0.000 description 1
- 239000008096 xylene Substances 0.000 description 1
- 150000003738 xylenes Chemical class 0.000 description 1
- WCJYTPVNMWIZCG-UHFFFAOYSA-N xylylcarb Chemical compound CNC(=O)OC1=CC=C(C)C(C)=C1 WCJYTPVNMWIZCG-UHFFFAOYSA-N 0.000 description 1
- BLGXFZZNTVWLAY-SCYLSFHTSA-N yohimbine Chemical compound C1=CC=C2C(CCN3C[C@@H]4CC[C@H](O)[C@@H]([C@H]4C[C@H]33)C(=O)OC)=C3NC2=C1 BLGXFZZNTVWLAY-SCYLSFHTSA-N 0.000 description 1
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- LRXTYHSAJDENHV-UHFFFAOYSA-H zinc phosphate Chemical compound [Zn+2].[Zn+2].[Zn+2].[O-]P([O-])([O-])=O.[O-]P([O-])([O-])=O LRXTYHSAJDENHV-UHFFFAOYSA-H 0.000 description 1
- 229910000165 zinc phosphate Inorganic materials 0.000 description 1
- NWONKYPBYAMBJT-UHFFFAOYSA-L zinc sulfate Chemical compound [Zn+2].[O-]S([O-])(=O)=O NWONKYPBYAMBJT-UHFFFAOYSA-L 0.000 description 1
- 229960001763 zinc sulfate Drugs 0.000 description 1
- 229910000368 zinc sulfate Inorganic materials 0.000 description 1
- LPEBYPDZMWMCLZ-CVBJKYQLSA-L zinc;(z)-octadec-9-enoate Chemical compound [Zn+2].CCCCCCCC\C=C/CCCCCCCC([O-])=O.CCCCCCCC\C=C/CCCCCCCC([O-])=O LPEBYPDZMWMCLZ-CVBJKYQLSA-L 0.000 description 1
- IFNXAMCERSVZCV-UHFFFAOYSA-L zinc;2-ethylhexanoate Chemical compound [Zn+2].CCCCC(CC)C([O-])=O.CCCCC(CC)C([O-])=O IFNXAMCERSVZCV-UHFFFAOYSA-L 0.000 description 1
- JDLYKQWJXAQNNS-UHFFFAOYSA-L zinc;dibenzoate Chemical compound [Zn+2].[O-]C(=O)C1=CC=CC=C1.[O-]C(=O)C1=CC=CC=C1 JDLYKQWJXAQNNS-UHFFFAOYSA-L 0.000 description 1
- CHJMFFKHPHCQIJ-UHFFFAOYSA-L zinc;octanoate Chemical compound [Zn+2].CCCCCCCC([O-])=O.CCCCCCCC([O-])=O CHJMFFKHPHCQIJ-UHFFFAOYSA-L 0.000 description 1
- DUBNHZYBDBBJHD-UHFFFAOYSA-L ziram Chemical compound [Zn+2].CN(C)C([S-])=S.CN(C)C([S-])=S DUBNHZYBDBBJHD-UHFFFAOYSA-L 0.000 description 1
- UBQNRHZMVUUOMG-UHFFFAOYSA-N zonisamide Chemical compound C1=CC=C2C(CS(=O)(=O)N)=NOC2=C1 UBQNRHZMVUUOMG-UHFFFAOYSA-N 0.000 description 1
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Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/16—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms condensed with carbocyclic rings or ring systems
- C07D249/18—Benzotriazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/41—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with two or more ring hetero atoms, at least one of which being nitrogen, e.g. tetrazole
- A61K31/4192—1,2,3-Triazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0019—Injectable compositions; Intramuscular, intravenous, arterial, subcutaneous administration; Compositions to be administered through the skin in an invasive manner
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/10—Anthelmintics
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Organic Chemistry (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Tropical Medicine & Parasitology (AREA)
- Dermatology (AREA)
- Nutrition Science (AREA)
- Physiology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Plural Heterocyclic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Thiazole And Isothizaole Compounds (AREA)
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| PCT/US2009/061337 WO2010048191A1 (en) | 2008-10-21 | 2009-10-20 | Thioamide compounds, method of making and method of using thereof |
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| ES (1) | ES2393965T3 (enExample) |
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| WO2012020568A1 (ja) * | 2010-08-10 | 2012-02-16 | 川崎重工業株式会社 | 原動機システム及び船舶 |
| PH12014500537A1 (en) | 2011-09-12 | 2014-04-21 | Merial Inc | Parasiticidal compositions comprising an isoxazoline active agent, methods and uses thereof |
| SG11201404595TA (en) | 2012-02-06 | 2014-09-26 | Merial Ltd | Parasiticidal oral veterinary compositions comprising systemically-acting active agents, methods and uses thereof |
| JO3626B1 (ar) | 2012-02-23 | 2020-08-27 | Merial Inc | تركيبات موضعية تحتوي على فيبرونيل و بيرميثرين و طرق استخدامها |
| HRP20181448T1 (hr) | 2012-11-20 | 2018-11-02 | Merial, Inc. | Antihelmintski spojevi i sastavi te postupak za njihovu uporabu |
| CN103073487B (zh) * | 2013-01-15 | 2014-11-19 | 西华大学 | N-双取代硫代乙酰胺类化合物的合成方法 |
| AR094961A1 (es) | 2013-03-15 | 2015-09-09 | Lilly Co Eli | 1-hidroxi-benzooxaboroles como agentes antiparasitarios |
| AP2016009184A0 (en) | 2013-11-01 | 2016-04-30 | Merial Ltd | Antiparisitic and pesticidal isoxazoline compounds |
| CN104610110A (zh) * | 2014-03-12 | 2015-05-13 | 广东东阳光药业有限公司 | 一种制备4-取代硫代苯甲酰胺衍生物的方法 |
| AU2015247463B2 (en) | 2014-04-17 | 2018-03-29 | Basf, Se | Use of malononitrile compounds for protecting animals from parasites |
| WO2015179414A1 (en) | 2014-05-19 | 2015-11-26 | Merial, Inc. | Anthelmintic compounds |
| EP3211998B1 (en) | 2014-10-31 | 2021-04-07 | Boehringer Ingelheim Animal Health USA Inc. | Parasiticidal composition comprising fipronil |
| UY36570A (es) | 2015-02-26 | 2016-10-31 | Merial Inc | Formulaciones inyectables de acción prolongada que comprenden un agente activo isoxazolina, métodos y usos de las mismas |
| HRP20211041T1 (hr) | 2015-05-20 | 2021-10-01 | Boehringer Ingelheim Animal Health USA Inc. | Anthelmintski depsipeptidni spojevi |
| UY37137A (es) | 2016-02-24 | 2017-09-29 | Merial Inc | Compuestos antiparasitarios de isoxazolina, formulaciones inyectables de acción prolongada que los comprenden, métodos y usos de los mismos |
| WO2018039508A1 (en) | 2016-08-25 | 2018-03-01 | Merial, Inc. | Method for reducing unwanted effects in parasiticidal treatments |
| CA3040278A1 (en) | 2016-10-14 | 2018-04-19 | Boehringer Ingelheim Animal Health USA Inc. | Pesticidal and parasiticidal vinyl isoxazoline compounds |
| JP2020504710A (ja) | 2016-11-16 | 2020-02-13 | ベーリンガー インゲルハイム アニマル ヘルス ユーエスエイ インコーポレイテッド | 駆虫性デプシペプチド化合物 |
| ES2944616T3 (es) | 2017-08-14 | 2023-06-22 | Boehringer Ingelheim Animal Health Usa Inc | Compuestos de pirazol-isoxazolina plaguicidas y parasiticidas |
| WO2020014068A1 (en) | 2018-07-09 | 2020-01-16 | Boehringer Ingelheim Animal Health USA Inc. | Anthelminthic heterocyclic compounds |
| US11773066B2 (en) | 2018-11-20 | 2023-10-03 | Boehringer Ingelheim Animal Health USA Inc. | Indazolylcyanoethylamino compound, compositions of same, method of making, and methods of using thereof |
| KR102281492B1 (ko) * | 2018-12-24 | 2021-07-26 | 동인당제약 주식회사 | 세벨라머 함유 경구투여용 현탁제 조성물 및 그 제조방법 |
| CA3133100A1 (en) | 2019-03-19 | 2020-09-24 | Boehringer Ingelheim Animal Health USA Inc. | Anthelmintic aza-benzothiophene and aza-benzofuran compounds |
| AU2021278889A1 (en) | 2020-05-29 | 2023-02-02 | Boehringer Ingelheim Pharma Gmbh & Co. Kg | Anthelmintic heterocyclic compounds |
| CN111781291A (zh) * | 2020-06-23 | 2020-10-16 | 广西壮族自治区水产科学研究院 | 一种水中13种大环内酯类抗生素的高分辨质谱检测方法 |
| WO2022140728A1 (en) | 2020-12-21 | 2022-06-30 | Boehringer Ingelheim Animam Health Usa Inc. | Parasiticidal collar comprising isoxazoline compounds |
| CN118715163A (zh) | 2022-02-17 | 2024-09-27 | 勃林格殷格翰动物保健有限公司 | 用于提供流体制品邮寄封的方法和系统 |
| CN117837424A (zh) * | 2024-02-04 | 2024-04-09 | 黄淮学院 | 一种控制农作物灰飞虱的方法 |
| WO2025257633A1 (en) | 2024-06-12 | 2025-12-18 | Boehringer Ingelheim Vetmedica Gmbh | Long-acting castor oil-containing injectable formulations and methods of use thereof |
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| WO2003097036A1 (en) | 2002-05-22 | 2003-11-27 | Novartis Ag | N-acylaminoacetonitrile derivatives and their use for controlling parasites |
| WO2004024704A1 (en) | 2002-09-11 | 2004-03-25 | Novartis Ag | Organic compounds |
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| US6289076B1 (en) | 1997-05-06 | 2001-09-11 | Sumitomo Heavy Industries, Ltd. | Transmission system for synchrotron radiation light |
| US6239077B1 (en) | 1998-05-01 | 2001-05-29 | Nihon Nohyaku Co., Ltd. | Aminoacetonitrile derivative agricultural and horticultural insecticide containing the same and use thereof |
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| AU2002224942A1 (en) | 2000-12-20 | 2002-07-01 | Syngenta Participations Ag | N-acyl aminoacetonitriles having pesticidal properties |
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2009
- 2009-10-20 JP JP2011533272A patent/JP5614853B2/ja active Active
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- 2009-10-20 AU AU2009307736A patent/AU2009307736B2/en active Active
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- 2009-10-20 WO PCT/US2009/061337 patent/WO2010048191A1/en not_active Ceased
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| WO2003097036A1 (en) | 2002-05-22 | 2003-11-27 | Novartis Ag | N-acylaminoacetonitrile derivatives and their use for controlling parasites |
| WO2004024704A1 (en) | 2002-09-11 | 2004-03-25 | Novartis Ag | Organic compounds |
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|---|---|
| US8314146B2 (en) | 2012-11-20 |
| ES2393965T3 (es) | 2013-01-03 |
| ES2393965T9 (es) | 2013-07-19 |
| WO2010048191A1 (en) | 2010-04-29 |
| EA026649B1 (ru) | 2017-05-31 |
| CA2741186C (en) | 2016-07-19 |
| JP5614853B2 (ja) | 2014-10-29 |
| CN102239151B (zh) | 2014-07-02 |
| CN102239151A (zh) | 2011-11-09 |
| EP2358687A1 (en) | 2011-08-24 |
| KR20110071140A (ko) | 2011-06-28 |
| BRPI0920145B8 (pt) | 2021-05-25 |
| NZ592382A (en) | 2013-03-28 |
| BRPI0920145B1 (pt) | 2021-03-30 |
| US7964621B2 (en) | 2011-06-21 |
| EP2358687B9 (en) | 2013-04-17 |
| AU2009307736B2 (en) | 2015-02-05 |
| KR101782308B1 (ko) | 2017-09-27 |
| US20110190231A1 (en) | 2011-08-04 |
| ZA201103033B (en) | 2012-02-29 |
| CL2011000917A1 (es) | 2011-09-16 |
| BRPI0920145A2 (pt) | 2017-06-06 |
| AU2009307736A1 (en) | 2010-04-29 |
| KR20170003704A (ko) | 2017-01-09 |
| EP2358687B1 (en) | 2012-09-19 |
| CA2741186A1 (en) | 2010-04-29 |
| US20100130565A1 (en) | 2010-05-27 |
| MX2011004217A (es) | 2011-06-20 |
| EA201100666A1 (ru) | 2011-12-30 |
| JP2012506441A (ja) | 2012-03-15 |
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