CN110831929A - *二唑啉化合物和有害生物防除剂 - Google Patents
*二唑啉化合物和有害生物防除剂 Download PDFInfo
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- CN110831929A CN110831929A CN201880035351.2A CN201880035351A CN110831929A CN 110831929 A CN110831929 A CN 110831929A CN 201880035351 A CN201880035351 A CN 201880035351A CN 110831929 A CN110831929 A CN 110831929A
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- 238000004382 potting Methods 0.000 description 1
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- 125000006410 propenylene group Chemical group 0.000 description 1
- 102000004169 proteins and genes Human genes 0.000 description 1
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- APTZNLHMIGJTEW-UHFFFAOYSA-N pyraflufen-ethyl Chemical group C1=C(Cl)C(OCC(=O)OCC)=CC(C=2C(=C(OC(F)F)N(C)N=2)Cl)=C1F APTZNLHMIGJTEW-UHFFFAOYSA-N 0.000 description 1
- DDIQWGKUSJOETH-UHFFFAOYSA-N pyrafluprole Chemical compound ClC=1C=C(C(F)(F)F)C=C(Cl)C=1N1N=C(C#N)C(SCF)=C1NCC1=CN=CC=N1 DDIQWGKUSJOETH-UHFFFAOYSA-N 0.000 description 1
- URXNNPCNKVAQRA-XMHGGMMESA-N pyraoxystrobin Chemical compound CO\C=C(\C(=O)OC)C1=CC=CC=C1COC1=CC(C=2C=CC(Cl)=CC=2)=NN1C URXNNPCNKVAQRA-XMHGGMMESA-N 0.000 description 1
- 125000003373 pyrazinyl group Chemical group 0.000 description 1
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- ILMRJRBKQSSXGY-UHFFFAOYSA-N tert-butyl(dimethyl)silicon Chemical group C[Si](C)C(C)(C)C ILMRJRBKQSSXGY-UHFFFAOYSA-N 0.000 description 1
- 125000001973 tert-pentyl group Chemical group [H]C([H])([H])C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- TUNFSRHWOTWDNC-UHFFFAOYSA-N tetradecanoic acid Chemical compound CCCCCCCCCCCCCC(O)=O TUNFSRHWOTWDNC-UHFFFAOYSA-N 0.000 description 1
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- DNVLJEWNNDHELH-UHFFFAOYSA-N thiocyclam Chemical compound CN(C)C1CSSSC1 DNVLJEWNNDHELH-UHFFFAOYSA-N 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- QGHREAKMXXNCOA-UHFFFAOYSA-N thiophanate-methyl Chemical compound COC(=O)NC(=S)NC1=CC=CC=C1NC(=S)NC(=O)OC QGHREAKMXXNCOA-UHFFFAOYSA-N 0.000 description 1
- VJQYLJSMBWXGDV-UHFFFAOYSA-N tiadinil Chemical compound N1=NSC(C(=O)NC=2C=C(Cl)C(C)=CC=2)=C1C VJQYLJSMBWXGDV-UHFFFAOYSA-N 0.000 description 1
- XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
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- HYVWIQDYBVKITD-UHFFFAOYSA-N tolylfluanid Chemical compound CN(C)S(=O)(=O)N(SC(F)(Cl)Cl)C1=CC=C(C)C=C1 HYVWIQDYBVKITD-UHFFFAOYSA-N 0.000 description 1
- 230000000699 topical effect Effects 0.000 description 1
- OEJNXTAZZBRGDN-UHFFFAOYSA-N toxaphene Chemical compound ClC1C(Cl)C2(Cl)C(CCl)(CCl)C(=C)C1(Cl)C2(Cl)Cl OEJNXTAZZBRGDN-UHFFFAOYSA-N 0.000 description 1
- 230000009261 transgenic effect Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 229940055764 triaz Drugs 0.000 description 1
- NKNFWVNSBIXGLL-UHFFFAOYSA-N triazamate Chemical compound CCOC(=O)CSC1=NC(C(C)(C)C)=NN1C(=O)N(C)C NKNFWVNSBIXGLL-UHFFFAOYSA-N 0.000 description 1
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- IMFACGCPASFAPR-UHFFFAOYSA-N tributylamine Chemical compound CCCCN(CCCC)CCCC IMFACGCPASFAPR-UHFFFAOYSA-N 0.000 description 1
- 125000004044 trifluoroacetyl group Chemical group FC(C(=O)*)(F)F 0.000 description 1
- 125000001889 triflyl group Chemical group FC(F)(F)S(*)(=O)=O 0.000 description 1
- RROQIUMZODEXOR-UHFFFAOYSA-N triforine Chemical compound O=CNC(C(Cl)(Cl)Cl)N1CCN(C(NC=O)C(Cl)(Cl)Cl)CC1 RROQIUMZODEXOR-UHFFFAOYSA-N 0.000 description 1
- 125000000026 trimethylsilyl group Chemical group [H]C([H])([H])[Si]([*])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- DFFWZNDCNBOKDI-UHFFFAOYSA-N trinexapac Chemical compound O=C1CC(C(=O)O)CC(=O)C1=C(O)C1CC1 DFFWZNDCNBOKDI-UHFFFAOYSA-N 0.000 description 1
- VLPFTAMPNXLGLX-UHFFFAOYSA-N trioctanoin Chemical compound CCCCCCCC(=O)OCC(OC(=O)CCCCCCC)COC(=O)CCCCCCC VLPFTAMPNXLGLX-UHFFFAOYSA-N 0.000 description 1
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- 210000000689 upper leg Anatomy 0.000 description 1
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- LESVOLZBIFDZGS-UHFFFAOYSA-N vamidothion Chemical compound CNC(=O)C(C)SCCSP(=O)(OC)OC LESVOLZBIFDZGS-UHFFFAOYSA-N 0.000 description 1
- 239000002435 venom Substances 0.000 description 1
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- 229940048462 zinc phosphide Drugs 0.000 description 1
Classifications
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains two hetero rings
- C07D498/10—Spiro-condensed systems
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/02—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
- A01N43/04—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom
- A01N43/22—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with one hetero atom rings with more than six members
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01P—BIOCIDAL, PEST REPELLANT, PEST ATTRACTANT OR PLANT GROWTH REGULATORY ACTIVITY OF CHEMICAL COMPOUNDS OR PREPARATIONS
- A01P7/00—Arthropodicides
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- 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
- A61K31/42—Oxazoles
- A61K31/424—Oxazoles condensed with heterocyclic ring systems, e.g. clavulanic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D271/00—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms
- C07D271/12—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms condensed with carbocyclic rings or ring systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D313/00—Heterocyclic compounds containing rings of more than six members having one oxygen atom as the only ring hetero atom
- C07D313/02—Seven-membered rings
- C07D313/06—Seven-membered rings condensed with carbocyclic rings or ring systems
- C07D313/10—Seven-membered rings condensed with carbocyclic rings or ring systems condensed with two six-membered rings
- C07D313/12—[b,e]-condensed
-
- 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
- C07D471/10—Spiro-condensed systems
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D498/00—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D498/22—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and oxygen atoms as the only ring hetero atoms in which the condensed system contains four or more hetero rings
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Pest Control & Pesticides (AREA)
- Engineering & Computer Science (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Dentistry (AREA)
- Veterinary Medicine (AREA)
- Agronomy & Crop Science (AREA)
- Animal Behavior & Ethology (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Public Health (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Chemical & Material Sciences (AREA)
- Tropical Medicine & Parasitology (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Epidemiology (AREA)
- Insects & Arthropods (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Abstract
本发明提供式(I)(式(I)中,R1表示取代或无取代的C1~6烷基,R2表示取代或无取代的C1~8烷基,R3表示氢原子或者取代或无取代的C1~6烷基,A表示取代或无取代的邻亚苯基、取代或无取代的亚苄基等,B表示氧基、取代或无取代的氧亚甲基等,且Q表示取代或无取代的邻亚苯基)表示的化合物或其盐。
Description
技术领域
本发明涉及二唑啉化合物和有害生物防除剂。更详细而言,本发明涉及具有优异的杀虫活性和/或杀螨活性、安全性优异、且工业上能够有利地合成的二唑啉化合物以及含有其作为有效成分的有害生物防除剂、杀虫或杀螨剂、体外寄生虫防除剂或者缨翅目害虫防除剂。
背景技术
提出了各种具有杀虫、杀螨活性的化合物。为了将这样的化合物作为农药进行实用,要求不仅效力足够高,而且不易产生耐药性,不产生对植物的药害或土壤污染,对家畜、鱼类等的毒性低等。
然而,专利文献1中公开了式(O)表示的化合物等。
现有技术文献
专利文献
专利文献1:WO2017/093409 A
发明内容
本发明的课题在于提供有害生物防除活性、其中尤其是杀虫活性和/或杀螨活性优异、安全性优异、且工业上能够有利地合成的二唑啉化合物。本发明的另一课题在于提供含有二唑啉化合物作为有效成分的有害生物防除剂、杀虫或杀螨剂、体外寄生虫防除剂或者缨翅目害虫防除剂。
为了解决上述课题而进行了研究,结果完成了包含以下形态的本发明。
〔1〕式(I)表示的化合物或其盐。
〔式(I)中,
R1表示氢原子、取代或无取代的C1~6烷基、取代或无取代的C2~6烯基、取代或无取代的C6~10芳基C1~6烷基、或者取代或无取代的C1~6烷基羰基,
R2表示取代或无取代的C1~8烷基、取代或无取代的C3~10环烷基、取代或无取代的C6~10芳基、取代或无取代的C6~10芳基C1~6烷基、或者取代或无取代的C1~6烷氧羰基,
R3表示氢原子、取代或无取代的C1~6烷基、取代或无取代的C2~6烯基、取代或无取代的C2~6炔基、取代或无取代的C6~10芳基C1~6烷基、取代或无取代的C1~6烷基羰基、或者取代或无取代的C1~6烷氧羰基,
R2和R3可以一体地成为取代或无取代的C3~5亚烷基,
A表示取代或无取代的邻亚苯基、取代或无取代的5~6元杂亚芳基、取代或无取代的亚苄基、取代或无取代的二亚甲基、或者1,2-环丙烯基,
B表示单键、氧基、取代或无取代的氧亚甲基、取代或无取代的亚甲氧基、取代或无取代的硫亚甲基、取代或无取代的亚甲硫基、取代或无取代的亚甲基、取代或无取代的二亚甲基、或者取代或无取代的亚乙烯基、硫基、取代或无取代的磺酰基亚甲基、取代或无取代的亚甲基磺酰基、取代或无取代的三亚甲基、取代或无取代的氧亚乙基、取代或无取代的亚乙氧基、取代或无取代的亚丙烯基、取代或无取代的氧亚甲基氧基、式-NRa-表示的基团、式-CH2-NRa-表示的基团、或者式-NRa-CH2-表示的基团,
Ra表示氢原子或者取代或无取代的C1~6烷基,且
Q表示取代或无取代的邻亚苯基。〕
〔2〕根据上述〔1〕所述的化合物,其中,A为取代或无取代的邻亚苯基,
B为取代或无取代的氧亚甲基、取代或无取代的亚甲氧基、取代或无取代的二亚甲基、或者取代或无取代的亚乙烯基。
〔3〕根据上述〔1〕所述的化合物,其中,A为取代或无取代的邻亚苯基,
B为取代或无取代的氧亚甲基、或者取代或无取代的亚甲氧基。
〔4〕一种有害生物防除剂,含有选自上述〔1〕~〔3〕中任一项所述的化合物及其盐中的至少一个作为有效成分。
〔5〕一种杀虫或杀螨剂,含有选自上述〔1〕~〔3〕中任一项所述的化合物及其盐中的至少一个作为有效成分。
〔6〕一种体外寄生虫防除剂,含有选自上述〔1〕~〔3〕中任一项所述的化合物及其盐中的至少一个作为有效成分。
〔7〕一种缨翅目害虫防除剂,含有选自上述〔1〕~〔3〕中任一项所述的化合物及其盐中的至少一个作为有效成分。
本发明的二唑啉化合物能够防除在农作物、卫生方面成为问题的有害生物。本发明的二唑啉化合物能够以更低浓度有效地防除农业害虫和螨类。本发明的二唑啉化合物能够有效地防除危害人畜的体外寄生虫。本发明的二唑啉化合物能够有效地防除缨翅目害虫。
具体实施方式
〔二唑啉化合物〕
本发明中,“无取代(unsubstituted)”的术语表示仅为成为母核的基团。没有记载为“取代”而仅用成为母核的基团的名称记载时,只要没有特别说明,就表示“无取代”。
另一方面,“取代(substituted)”的术语表示成为母核的基团中的任一氢原子被与母核相同或不同结构的基团(取代基)所取代。因此,“取代基”是指与成为母核的基团键合的其它基团。取代基可以为1个,也可以为2个以上。2个以上的取代基可以相同,也可以不同。
“C1~6”等术语表示成为母核的基团的碳原子数为1~6个等。该碳原子数中不包括存在于取代基中的碳原子的个数。例如,具有乙氧基作为取代基的丁基分类为C2烷氧基C4烷基。
“取代基”只要是化学上允许且具有本发明的效果,就没有特别限制。以下,例示可以作为“取代基”的基团。
甲基、乙基、正丙基、异丙基、正丁基、仲丁基、异丁基、叔丁基、正戊基、正己基等C1~6烷基;
乙烯基、1-丙烯基、2-丙烯基(烯丙基)、1-丁烯基、2-丁烯基、3-丁烯基、1-甲基-2-丙烯基、2-甲基-2-丙烯基等C2~6烯基;
乙炔基、1-丙炔基、2-丙炔基、1-丁炔基、2-丁炔基、3-丁炔基、1-甲基-2-丙炔基等C2~6炔基;
环丙基、环丁基、环戊基、环己基、立方烷基(cubanyl)等C3~8环烷基;
苯基、萘基等C6~10芳基;
苄基、苯乙基等C6~10芳基C1~6烷基;
3~6元杂环基;
3~6元杂环基C1~6烷基;
羟基;
甲氧基、乙氧基、正丙氧基、异丙氧基、正丁氧基、仲丁氧基、异丁氧基、叔丁氧基等C1~6烷氧基;
乙烯氧基、烯丙氧基、丙烯氧基、丁烯氧基等C2~6烯氧基;
乙炔氧基、丙炔氧基等C2~6炔氧基;
苯氧基、萘氧基等C6~10芳氧基;
苄氧基、苯乙氧基等C6~10芳基C1~6烷氧基;
噻唑氧基、吡啶氧基等5~6元杂芳氧基;
噻唑基甲氧基、吡啶基甲氧基等5~6元杂芳基C1~6烷氧基;
甲酰基;
乙酰基、丙酰基等C1~6烷基羰基;
甲酰氧基;
乙酰氧基、丙酰氧基等C1~6烷基羰基氧基;
苯甲酰基等C6~10芳基羰基;
甲氧基羰基、乙氧基羰基、正丙氧基羰基、异丙氧基羰基、正丁氧基羰基、叔丁氧基羰基等C1~6烷氧羰基;
甲氧基羰基氧基、乙氧基羰基氧基、正丙氧基羰基氧基、异丙氧基羰基氧基、正丁氧基羰基氧基、叔丁氧基羰基氧基等C1~6烷氧基羰基氧基;
羧基;
氟基、氯基、溴基、碘基等卤素基团;
氯甲基、氯乙基、三氟甲基、1、2-二氯正丙基、1-氟正丁基、全氟正戊基等C1~6卤代烷基;
2-氯-1-丙烯基、2-氟-1-丁烯基等C2~6卤代烯基;
4,4-二氯-1-丁炔基、4-氟-1-戊炔基、5-溴-2-戊炔基等C2~6卤代炔基;
三氟甲氧基、2-氯-正丙氧基、2,3-二氯丁氧基等C1~6卤代烷氧基;
2-氯丙烯氧基、3-溴丁烯氧基等C2~6卤代烯氧基;
氯乙酰基、三氟乙酰基、三氯乙酰基等C1~6卤代烷基羰基;
氨基;
甲基氨基、二甲基氨基、二乙基氨基等C1~6烷基取代氨基;
苯胺基、萘基氨基等C6~10芳基氨基;
苄基氨基、苯乙基氨基等C6~10芳基C1~6烷基氨基;
甲酰基氨基;
乙酰基氨基、丙酰基氨基、丁酰基氨基、异丙基羰基氨基等C1~6烷基羰基氨基;
甲氧基羰基氨基、乙氧基羰基氨基、正丙氧基羰基氨基、异丙氧基羰基氨基等C1~6烷氧基羰基氨基;
氨基羰基、二甲基氨基羰基、苯基氨基羰基、N-苯基-N-甲基氨基羰基等无取代或具有取代基的氨基羰基;
亚氨基甲基、(1-亚氨基)乙基、(1-亚氨基)-正丙基等亚氨基C1~6烷基;
N-羟基-亚氨基甲基、(1-(N-羟基)-亚氨基)乙基、(1-(N-羟基)-亚氨基)丙基、N-甲氧基-亚氨基甲基、(1-(N-甲氧基)-亚氨基)乙基等取代或无取代的N-羟基亚氨基C1~6烷基;
氨基羰基氧基;
乙基氨基羰基氧基、二甲基氨基羰基氧基等C1~6烷基取代氨基羰基氧基;
巯基;
甲基硫基、乙基硫基、正丙基硫基、异丙基硫基、正丁基硫基、异丁基硫基、仲丁基硫基、叔丁基硫基等C1~6烷基硫基;
三氟甲基硫基、2,2,2-三氟乙基硫基等C1~6卤代烷基硫基;
苯基硫基、萘基硫基等C6~10芳基硫基;
噻唑基硫基、吡啶基硫基等5~6元杂芳基硫基;
甲基亚磺酰基、乙基亚磺酰基、叔丁基亚磺酰基等C1~6烷基亚磺酰基;
三氟甲基亚磺酰基、2,2,2-三氟乙基亚磺酰基等C1~6卤代烷基亚磺酰基;
苯基亚磺酰基等C6~10芳基亚磺酰基;
噻唑基亚磺酰基、吡啶基亚磺酰基等5~6元杂芳基亚磺酰基;
甲基磺酰基、乙基磺酰基、叔丁基磺酰基等C1~6烷基磺酰基;
三氟甲基磺酰基、2,2,2-三氟乙基磺酰基等C1~6卤代烷基磺酰基;
苯基磺酰基等C6~10芳基磺酰基;
噻唑基磺酰基、吡啶基磺酰基等5~6元杂芳基磺酰基;
甲基磺酰基氧基、乙基磺酰基氧基、叔丁基磺酰基氧基等C1~6烷基磺酰基氧基;
三氟甲基磺酰基氧基、2,2,2-三氟乙基磺酰基氧基等C1~6卤代烷基磺酰基氧基;
三甲基甲硅烷基、三乙基甲硅烷基、叔丁基二甲基甲硅烷基等三C1~6烷基取代甲硅烷基;
三苯基甲硅烷基等三C6~10芳基取代甲硅烷基;
氰基;硝基;
另外,这些“取代基”中的任一氢原子可以被不同结构的基团所取代。作为该情况下的“取代基”,可以举出C1~6烷基、C1~6卤代烷基、C1~6烷氧基、C1~6卤代烷氧基、卤素基团、氰基、硝基等。
另外,上述的“3~6元杂环基”是指包含选自氮原子、氧原子和硫原子中的1~4个杂原子作为环的构成原子的基团。杂环基可以为单环和多环中的任一种。多环杂环基只要至少一个环为杂环,则其余的环可以为饱和脂环、不饱和脂环或芳香环中的任一种。作为“3~6元杂环基”,可举出3~6元饱和杂环基、5~6元杂芳基、5~6元部分不饱和杂环基等。
作为3~6元饱和杂环基,可举出吖丙啶基、环氧基、吡咯烷基、四氢呋喃基、噻唑烷基、哌啶基、哌嗪基、吗啉基、二氧戊环基、二烷基等。
作为6元杂芳基,可举出吡啶基、吡嗪基、嘧啶基、哒嗪基、三嗪基等。
〔R1〕
式(I)中的R1表示氢原子、取代或无取代的C1~6烷基、取代或无取代的C2~6烯基、取代或无取代的C6~10芳基C1~6烷基、或者取代或无取代的C1~6烷基羰基。
作为R1中的“C1~6烷基”,可以为直链,只要碳原子数为3以上也可以为支链。作为烷基,可以举出甲基、乙基、正丙基、正丁基、正戊基、正己基、异丙基、异丁基、仲丁基、叔丁基、异戊基、新戊基、2-甲基丁基、2,2-二甲基丙基、异己基等。
作为“具有取代基的C1~6烷基”的具体例,可以举出:
氟甲基、氯甲基、溴甲基、二氟甲基、二氯甲基、二溴甲基、三氟甲基、三氯甲基、三溴甲基、1-氯乙基、2,2,2-三氟乙基、2,2,2-三氯乙基、五氟乙基、4-氟丁基、4-氯丁基、3,3,3-三氟丙基、2,2,2-三氟-1-三氟甲基乙基、1,1,1,3,3,3-六氟丙烷-2-基、全氟丙烷-2-基、全氟己基、全氯己基、2,4,6-三氯己基等C1~6卤代烷基;
羟基甲基、羟基乙基等羟基C1~6烷基;
甲氧基甲基、乙氧基甲基、甲氧基乙基、乙氧基乙基、甲氧基-正丙基、正丙氧基甲基、异丙氧基乙基、仲丁氧基甲基、叔丁氧基乙基等C1~6烷氧基C1~6烷基;
环丙基甲基、2-环丙基乙基、环戊基甲基、2-环己基乙基、2-环辛基乙基等C3~8环烷基C1~6烷基;甲硫基甲基、乙硫基乙基等C1~6烷硫基C1~6烷基;甲氧基羰基甲基、乙氧基羰基甲基等C1~6烷氧基羰基C1~6烷基;三甲基甲硅烷氧基甲基、叔丁基二甲基甲硅烷氧基甲基、叔丁基二苯基甲硅烷氧基甲基等取代甲硅烷氧基C1~6烷基;等。
作为R1中的“C1~6烷基”上的取代基,可以优选举出氟基、氯基、溴基、碘基等卤素基团;甲氧基、乙氧基、正丙氧基、异丙氧基、正丁氧基、仲丁氧基、异丁氧基、叔丁氧基等C1~6烷氧基;2-氯-正丙氧基、2,3-二氯丁氧基、三氟甲氧基等C1~6卤代烷氧基;氰基;甲基硫基、乙基硫基等C1~6烷基硫基。
作为R1中的“C2~6烯基”,可以举出乙烯基、1-丙烯基、2-丙烯基、1-丁烯基、2-丁烯基、3-丁烯基、1-甲基-2-丙烯基、2-甲基-2-丙烯基、1-戊烯基、2-戊烯基、3-戊烯基、4-戊烯基、1-甲基-2-丁烯基、2-甲基-2-丁烯基、1-己烯基、2-己烯基、3-己烯基、4-己烯基、5-己烯基等。
作为R1中的“C2~6烯基”上的取代基,可以优选举出氟基、氯基、溴基、碘基等卤素基团;甲氧基、乙氧基、正丙氧基、异丙氧基、正丁氧基、仲丁氧基、异丁氧基、叔丁氧基等C1~6烷氧基;2-氯-正丙氧基、2,3-二氯丁氧基、三氟甲氧基等C1~6卤代烷氧基;氰基。
作为R1中的“C6~10芳基C1~6烷基”,可以举出苄基、苯乙基等。
作为R1中的“C6~10芳基C1~6烷基”上的取代基,可以优选举出氟基、氯基、溴基、碘基等卤素基团;甲基、乙基、正丙基、异丙基、正丁基、仲丁基、异丁基、叔丁基等C1~6烷基;2-氯-正丙基、2,3-二氯丁基、三氟甲基等C1~6卤代烷基;甲氧基、乙氧基、正丙氧基、异丙氧基、正丁氧基、仲丁氧基、异丁氧基、叔丁氧基等C1~6烷氧基;2-氯-正丙氧基、2,3-二氯丁氧基、三氟甲氧基等C1~6卤代烷氧基;氰基;硝基。
作为R1中的“C1~6烷基羰基”,可以举出乙酰基、丙酰基等。
作为R1中的“C1~6烷基羰基”上的取代基,可以优选举出氟基、氯基、溴基、碘基等卤素基团;甲氧基、乙氧基、正丙氧基、异丙氧基、正丁氧基、仲丁氧基、异丁氧基、叔丁氧基等C1~6烷氧基;2-氯-正丙氧基、2,3-二氯丁氧基、三氟甲氧基等C1~6卤代烷氧基;氰基。
〔R2〕
式(I)中的R2表示取代或无取代的C1~8烷基、取代或无取代的C3~10环烷基、取代或无取代的C6~10芳基、取代或无取代的C6~10芳基C1~6烷基、或者取代或无取代的C1~6烷氧羰基。
作为R2中的“取代或无取代的C6~10芳基C1~6烷基”,可以举出与在R1中具体例示的基团相同的基团。
作为R2中的“取代或无取代的C1~8烷基”,可以为直链,只要碳原子数为3以上也可以为支链。作为烷基,可以举出甲基、乙基、正丙基、正丁基、正戊基、正己基、异丙基、异丁基、仲丁基、叔丁基、异戊基、新戊基、叔戊基、2-甲基丁基、2,2-二甲基丙基、异己基、2-甲基戊烷-2-基、正庚基、正辛基、2,4,4-三甲基戊烷-2-基等。
作为“具有取代基的C1~8烷基”的具体例,可以举出:
氟甲基、氯甲基、溴甲基、二氟甲基、二氯甲基、二溴甲基、三氟甲基、三氯甲基、三溴甲基、1-氯乙基、2,2,2-三氟乙基、2,2,2-三氯乙基、五氟乙基、4-氟丁基、4-氯丁基、3,3,3-三氟丙基、2、2、2-三氟-1-三氟甲基乙基、1,1,1,3,3,3-六氟丙烷-2-基、全氟丙烷-2-基、全氟己基、全氯己基、2,4,6-三氯己基等C1~8卤代烷基;
羟基甲基、羟基乙基等羟基C1~8烷基;
甲氧基甲基、乙氧基甲基、甲氧基乙基、乙氧基乙基、甲氧基-正丙基、正丙氧基甲基、异丙氧基乙基、仲丁氧基甲基、叔丁氧基乙基等C1~6烷氧基C1~8烷基;
环丙基甲基、2-环丙基乙基、环戊基甲基、2-环己基乙基、2-环辛基乙基等C3~8环烷基C1~8烷基;甲硫基甲基、乙硫基乙基等C1~6烷硫基C1~8烷基;甲氧基羰基甲基、乙氧基羰基甲基等C1~6烷氧基羰基C1~8烷基;三甲基甲硅烷氧基甲基、叔丁基二甲基甲硅烷氧基甲基、叔丁基二苯基甲硅烷氧基甲基等取代甲硅烷氧基C1~8烷基;等。
作为R2中的“C1~8烷基”上的取代基,可以优选举出氟基、氯基、溴基、碘基等卤素基团;甲氧基、乙氧基、正丙氧基、异丙氧基、正丁氧基、仲丁氧基、异丁氧基、叔丁氧基等C1~6烷氧基;2-氯-正丙氧基、2,3-二氯丁氧基、三氟甲氧基等C1~6卤代烷氧基;氰基;甲基硫基、乙基硫基等C1~6烷基硫基。
作为R2中的“C3~10环烷基”,可以举出环丙基、环丁基、环戊基、环己基、立方烷基等单环的环烷基;双环辛基等双环烷基;金刚烷-1-基等三环烷基;等。
作为R2中的“C6~10芳基”,可以举出苯基、萘基等。
作为R2中的“C3~10环烷基”或者“C6~10芳基”上的取代基,可以优选举出氟基、氯基、溴基、碘基等卤素基团;甲基、乙基、正丙基、异丙基、正丁基、仲丁基、异丁基、叔丁基等C1~6烷基;2-氯-正丙基、2,3-二氯丁基、三氟甲基等C1~6卤代烷基;甲氧基、乙氧基、正丙氧基、异丙氧基、正丁氧基、仲丁氧基、异丁氧基、叔丁氧基等C1~6烷氧基;2-氯-正丙氧基、2,3-二氯丁氧基、三氟甲氧基等C1~6卤代烷氧基;氰基;硝基。
作为R2中的“C1~6烷氧羰基”,可以举出甲氧基羰基、乙氧基羰基、正丙氧基羰基、异丙氧基羰基、叔丁氧基羰基等。
作为R2中的“C1~6烷氧羰基”上的取代基,可以优选举出氟基、氯基、溴基、碘基等卤素基团;甲氧基、乙氧基、正丙氧基、异丙氧基、正丁氧基、仲丁氧基、异丁氧基、叔丁氧基等C1~6烷氧基;2-氯-正丙氧基、2,3-二氯丁氧基、三氟甲氧基等C1~6卤代烷氧基;氰基。
〔R3〕
式(I)中的R3表示氢原子、取代或无取代的C1~6烷基、取代或无取代的C2~6烯基、取代或无取代的C2~6炔基、取代或无取代的C6~10芳基C1~6烷基、取代或无取代的C1~6烷基羰基、或者取代或无取代的C1~6烷氧羰基。
作为R3中的“取代或无取代的C1~6烷基”、“取代或无取代的C2~6烯基”、“取代或无取代的C6~10芳基C1~6烷基”、或者“取代或无取代的C1~6烷基羰基”,可以举出与在R1中具体例示的基团相同的基团。
作为R3中的“取代或无取代的C1~6烷氧羰基”,可以举出与在R2中具体例示的基团相同的基团。
作为R3中的“C2~6炔基”,可以举出乙炔基、1-丙炔基、2-丙炔基、1-丁炔基、2-丁炔基、3-丁炔基、1-甲基-2-丙炔基等。
作为R3中的“C2~6炔基”上的取代基,可以优选举出氟基、氯基、溴基、碘基等卤素基团;甲氧基、乙氧基、正丙氧基、异丙氧基、正丁氧基、仲丁氧基、异丁氧基、叔丁氧基等C1~6烷氧基;2-氯-正丙氧基、2,3-二氯丁氧基、三氟甲氧基等C1~6卤代烷氧基;氰基。
R2和R3可以一体地成为取代或无取代的C3~5亚烷基。
作为成为一体的R3和R2中的“C3~5亚烷基”,可以举出三亚甲基、四亚甲基、五亚甲基。
作为“C3~5亚烷基”上的取代基,可以优选举出氟基、氯基、溴基、碘基等卤素基团;甲基、乙基、正丙基、异丙基、正丁基、仲丁基、异丁基、叔丁基等C1~6烷基;2-氯-正丙基、2,3-二氯丁基、三氟甲基等C1~6卤代烷基。
〔Q〕
式(I)中的Q表示取代或无取代的邻亚苯基。
作为“取代邻亚苯基”中的邻亚苯基上的取代基,可以优选举出氟基、氯基、溴基、碘基等卤素基团;甲基、乙基、正丙基、异丙基、正丁基、仲丁基、异丁基、叔丁基等C1~6烷基;乙烯基、1-丙烯基、2-丙烯基(烯丙基)、1-丁烯基、2-丁烯基、3-丁烯基、1-甲基-2-丙烯基、2-甲基-2-丙烯基等C2~6烯基;2-氯-正丙基、2,3-二氯丁基、三氟甲基等C1~6卤代烷基;甲氧基、乙氧基、正丙氧基、异丙氧基、正丁氧基、仲丁氧基、异丁氧基、叔丁氧基等C1~6烷氧基;2-氯-正丙氧基、2,3-二氯丁氧基、三氟甲氧基、2,2,2-三氟乙氧基、4,4,4-三氟丁氧基等C1~6卤代烷氧基;苄基氧基;氰基;硝基;苯基等C6~10芳基;环丙基、环丁基、环戊基、环己基、环庚基等C3~6环烷基;甲基硫基、乙基硫基、正丙基硫基、正丁基硫基、正戊基硫基、正己基硫基、异丙基硫基等C1~6烷基硫基;甲基亚磺酰基、乙基亚磺酰基、叔丁基亚磺酰基等C1~6烷基亚磺酰基;甲氧基羰基、乙氧基羰基等C1~6烷氧羰基;甲氧基羰基甲基、乙氧基羰基甲基等C1~6烷氧基羰基C1~6烷基;等。
〔A〕
式(I)中的A表示取代或无取代的邻亚苯基、取代或无取代的5~6元杂亚芳基、取代或无取代的亚苄基、取代或无取代的二亚甲基、或者1,2-环丙烯基。
作为A中的“取代邻亚苯基”中的邻亚苯基上的取代基,可以举出与在上述的“Q”中作为邻亚苯基上的取代基而具体例示的基团相同的基团。
“5~6元杂亚芳基”为杂芳基化合物中的2个氢原子脱离而成的2价基团。杂芳基化合物是含有选自氮原子、氧原子和硫原子中的1~4个的杂原子作为环的构成原子的芳香族化合物。
作为5~6元杂亚芳基,可以举出噻吩二基(具体而言,可以举出2,3-噻吩二基、3,4-噻吩二基)、呋喃二基、吡咯二基等5元杂亚芳基;亚吡啶基、亚吡嗪基、亚嘧啶基、亚哒嗪基等6元杂亚芳基。
作为“取代5~6元杂亚芳基”中的5~6元杂亚芳基上的取代基,可以举出与在上述的邻亚苯基中具体例示的基团相同的基团。
“亚苄基”为式(II)表示的基团。
作为“取代亚苄基”中的亚苄基上的取代基,可以举出与在上述的邻亚苯基中具体例示的基团相同的基团。
作为“取代二亚甲基”中的二亚甲基上的取代基,可以举出与在上述的邻亚苯基中具体例示的基团相同的基团。
取代基在同一个碳上有多个时,它们可以一起形成2价的取代基。作为形成的2价的取代基,可以举出二亚甲基、三亚甲基、四亚甲基等C2~5亚烷基。
〔B〕
式(I)中的B表示单键、氧基、取代或无取代的氧亚甲基、取代或无取代的亚甲氧基、取代或无取代的硫亚甲基、取代或无取代的亚甲硫基、取代或无取代的亚甲基、取代或无取代的二亚甲基、或者取代或无取代的亚乙烯基、硫基、取代或无取代的磺酰基亚甲基、取代或无取代的亚甲基磺酰基、取代或无取代的三亚甲基、取代或无取代的氧亚乙基、取代或无取代的亚乙氧基、取代或无取代的亚丙烯基、取代或无取代的氧亚甲基氧基、式-NRa-表示的基团、式-CH2-NRa-表示的基团、或者式-NRa-CH2-表示的基团。
“无取代的氧亚甲基”具体而言为式:*O-CH2 **表示的基团。
“无取代的亚甲氧基”为式:*CH2-O**表示的基团。
“无取代的硫亚甲基”具体而言为式:*S-CH2 **表示的基团。
“无取代的亚甲硫基”为式:*CH2-S**表示的基团。
“无取代的磺酰基亚甲基”具体而言为式:*SO2-CH2 **表示的基团。
“无取代的亚甲基磺酰基”为式:*CH2-SO2 **表示的基团。
“无取代的氧亚乙基”具体而言为式:*O-CH2CH2 **表示的基团。
“无取代的亚乙氧基”为式:*CH2CH2-O**表示的基团。
“无取代的氧亚甲基氧基”为式:*O-CH2-O**表示的基团。
任一式中的标有*的原子都表示键合于式(I)中的“A”的原子。标有**的原子表示键合于式(I)中的“Q”的原子。
Ra表示氢原子、或者取代或无取代的C1~6烷基。
作为Ra中的“C1~6烷基”,可以举出与在上述的R1中具体例示的基团相同的基团。
作为“取代氧亚甲基”、“取代亚甲氧基”、“取代硫亚甲基”、“取代亚甲硫基”、“取代亚甲基”、“取代二亚甲基”、“取代亚乙烯基”、“取代三亚甲基”、“取代氧亚乙基”、“取代亚乙氧基”、“取代亚丙烯基”、或者“取代氧亚甲基氧基”中的各基团上的取代基,可以举出与在上述的邻亚苯基中具体例示的基团相同的基团。取代基在同一个碳上有多个时,它们可以一起形成2价的取代基。作为形成的2价的取代基,可以举出二亚甲基、三亚甲基、四亚甲基等C2~5亚烷基。
作为各基团上的优选的取代基的具体例,可以举出氟基、氯基、溴基、碘基等卤素基团;甲基、乙基、正丙基、异丙基、正丁基、仲丁基、异丁基、叔丁基等C1~6烷基;氰基;等。
应予说明,式(I-2)中,R1~R3表示与式(I)中的R1~R3相同的含义,
Xq表示邻亚苯基上的取代基,
m表示取代基的个数,表示0~4中的任一整数,
Xa表示邻亚苯基上的取代基,
n表示取代基的个数,表示0~4中的任一整数,且
Ba表示取代或无取代的氧亚甲基、取代或无取代的亚甲氧基、取代或无取代的二亚甲基、或者取代或无取代的亚乙烯基。
作为取代基Xq、Xa的具体例,可以举出与在上述的〔Q〕中作为邻亚苯基上的取代基而具体例示的基团相同的基团。
应予说明,式(I-1)中,R1~R3表示与式(I)中的R1~R3相同的含义,
Xq表示邻亚苯基上的取代基,
m表示取代基的个数,表示0~4中的任一整数,
Xa表示邻亚苯基上的取代基,且
n表示取代基的个数,表示0~4中任一整数。
作为取代基Xq、Xa的具体例,可以举出与在上述的〔Q〕作为邻亚苯基上的取代基而具体例示的基团相同的基团。
化合物(I)的盐只要是农业园艺学允许的盐,就没有特别限制。作为化合物(I)的盐,例如可举出盐酸、硫酸等无机酸的盐;乙酸、乳酸等有机酸的盐;锂、钠、钾等碱金属的盐;钙、镁等碱土金属的盐;铁、铜等过渡金属的盐;氨、三乙胺、三丁胺、吡啶、肼等有机碱的盐等。
化合物(I)或化合物(I)的盐不受其制造方法的特别限定。例如,本发明的化合物(I)或化合物(I)的盐可以按照实施例等中记载的公知的制造方法而得到。另外,化合物(I)的盐可以由化合物(I)按照公知的方法而得到。
此外,近年来,在小菜蛾、稻飞虱、叶蝉、蚜虫等许多害虫中发展出对各种现有农药的抗性,产生这些药剂的效力不足的问题,期待抗性品系的害虫也有效的药剂。本发明的二唑啉化合物不仅对敏感品系表现出优异的防除效果,而且对各种抗性品系的害虫以及杀螨剂抗性品系的螨类也表现出优异的防除效果。本发明的二唑啉化合物对缨翅目害虫表现出优异的防除效果。
另外,本发明的二唑啉化合物在作为防除对象的生物的整个生长阶段显示效力,例如,对螨、昆虫等的卵、若虫、幼虫、蛹、成虫显示优异的防除效果。
〔有害生物防除剂、杀虫剂、杀螨剂、缨翅目害虫防除剂〕
本发明的有害生物防除剂、或者杀虫剂、杀螨剂或缨翅目害虫防除剂含有选自本发明的二唑啉化合物中的至少1种作为有效成分。本发明的有害生物防除剂、或者杀虫或杀螨剂中含有的二唑啉化合物的量只要表现出有害生物、农业害虫或螨类的防除效果就没有特别限制。
本发明的有害生物防除剂、或者杀虫剂、杀螨剂或缨翅目害虫防除剂优选用于谷物类;蔬菜类;根菜类;球茎类;花卉类;果树类;观叶植物、茶、咖啡、可可树等树木类;牧草类;禾本类;棉花等植物。
在对植物施用时,本发明的有害生物防除剂、或者杀虫剂、杀螨剂或缨翅目害虫防除剂可以用于叶、茎、柄、花、蕾、果实、种子、芽、根、块茎、块根、幼苗、插条等任意部位。
另外,本发明的有害生物防除剂、或者杀虫剂、杀螨剂或缨翅目害虫防除剂不受所施用的植物的种的特别限制。作为植物的种,例如可举出原种、变种、改良品种、栽培品种、突变体、杂交体、转基因体(GMO)等。
本发明的有害生物防除剂可以用于种子处理、茎叶散布、土壤施用、水面施用等以防除各种农业害虫和螨类。
以下示出可以由本发明的有害生物防除剂来防除的各种农业害虫和螨类的具体例。
(1)鳞翅目(Lepidoptera)的蝶或蛾
(a)灯蛾科(Arctiidae)的蛾:例如,美国白蛾(Hyphantria cunea)、奇特望灯蛾(Lemyra imparilis);
(b)稜巢蛾科(Bucculatricidae)的蛾:例如,梨角折蛾(Bucculatrixpyrivorella);
(c)蛀果蛾科(Carposinidae):例如,桃蛀果蛾(Carposina sasakii);
(d)草螟科(Crambidae)的蛾:例如,绢野螟属(Diaphania spp.)的瓜绢野螟(Diaphania indica)、黄瓜绢野螟(Diaphania nitidalis);例如,秆野螟属(Ostriniaspp.)的亚洲玉米螟(Ostrinia furnacalis)、欧洲玉米螟(Ostrinia nubilalis)、麻田豆秆野螟(Ostrinia scapulalis);以及二化螟(Chilo suppressalis)、稻纵卷叶螟(Cnaphalocrocis medinalis)、桃蛀螟(Conogethes punctiferalis)、西南玉米螟(Diatraea grandiosella)、桑绢野螟(Glyphodes pyloalis)、菜螟(Hellula undalis)、早熟禾拟茎草螟(Parapediasia teterrella);
(e)麦蛾科(Gelechiidae)的蛾:例如,甘薯麦蛾(Helcystogrammatriannulella)、棉红铃虫(Pectinophora gossypiella)、马铃薯块茎蛾(Phthorimaeaoperculella)、麦蛾(Sitotroga cerealella);
(f)尺蛾科(Geometridae)的蛾:例如,大造桥虫(Ascotis selenaria);
(g)细蛾科(Gracillariidae)的蛾:例如,茶细蛾(Caloptilia theivora)、柑桔潜叶蛾(Phyllocnistis citrella)、金纹细蛾(Phyllonorycter ringoniella);
(h)弄蝶科(Hesperiidae)的蝶:例如,直纹稻弄蝶(Parnara guttata);
(i)枯叶蛾科(Lasiocampidae)的蛾:例如,天幕毛虫(Malacosoma neustria);
(j)毒蛾科(Lymantriidae)的蛾:例如,毒蛾属(Lymantria spp.)的舞毒蛾(Lymantria dispar)、模毒蛾(Lymantria monacha);其它的茶毛虫(Euproctispseudoconspersa)、旋古毒蛾(Orgyia thyellina);
(k)潜蛾科(Lyonetiidae)的蛾:例如,潜蛾属(Lyonetia spp.)的桃潜叶蛾(Lyonetia clerkella)、银纹潜叶蛾(Lyonetia prunifoliella malinella);
(l)夜蛾科(Noctuidae)的蛾:例如,灰翅夜蛾属(Spodoptera spp.)的淡剑袭夜蛾(Spodoptera depravata)、南部灰翅夜蛾(Spodoptera eridania)、甜菜夜蛾(Spodopteraexigua)、草地夜蛾(Spodoptera frugiperda)、非洲棉叶虫蛾(Spodoptera littoralis)、斜纹夜蛾(Spodoptera litura);例如,丫纹夜蛾属(Autographa spp.)的银纹夜蛾(Autographa gamma)、黑点银纹夜蛾(Autographa nigrisigna);例如,地夜蛾属(Agrotisspp.)的小地老虎(Agrotis ipsilon)、黄地老虎(Agrotis segetum);例如,铃夜蛾属(Helicoverpa spp.)的棉铃虫(Helicoverpa armigera)、烟夜蛾(Helicoverpa assulta)、谷实夜蛾(Helicoverpa zea);例如,实夜蛾属(Heliothis spp.)的棉铃虫(Heliothisarmigera)、烟芽夜蛾(Heliothis virescens);其它的白斑烦夜蛾(Aedia leucomelas)、银纹夜蛾(Ctenoplusia agnata)、枯叶夜蛾(Eudocima tyrannus)、甘蓝夜蛾(Mamestrabrassicae)、粘虫(Mythimna separata)、稻螟蛉(Naranga aenescens)、松切蛾(Panolisjaponica)、疆夜蛾(Peridroma saucia)、大豆夜蛾(Pseudoplusia includens)、粉纹夜蛾(Trichoplusia ni);
(m)瘤蛾科(Nolidae)的蛾:例如,棉斑实蛾(Earias insulana);
(n)粉蝶科(Pieridae)的蝶:例如,粉蝶属(Pieris spp.)的欧洲粉蝶(Pierisbrassicae)、纹白蝶(Pieris rapae crucivora);
(o)菜蛾科(Plutellidae)的蛾:例如,葱菜蛾属(Acrolepiopsis spp.)的葱菜蛾(Acrolepiopsis sapporensis)、铃木伪菜蛾(Acrolepiopsis suzukiella);以及小菜蛾(Plutella xylostella);
(p)螟蛾科(Pyralidae)的蛾:例如,粉斑螟蛾(Cadra cautella)、小玉米茎蛀虫(Elasmopalpus lignosellus)、豆荚斑螟(Etiella zinckenella)、大蜡螟(Galleriamellonella);
(q)天蛾科(Sphingidae)的蛾:例如,天蛾属(Manduca spp.)的番茄天蛾(Manducaquinquemaculata)、烟草天蛾(Manduca sexta);
(r)举肢蛾科(Stathmopodidae)的蛾:例如,柿举肢蛾(Stathmopoda masinissa);
(s)谷蛾科(Tineidae)的蛾:例如,衣蛾(Tinea translucens);
(t)卷蛾科(Tortricidae)的蛾:例如,褐带卷蛾属(Adoxophyes spp.)的茶小卷叶蛾(Adoxophyes honmai)、苹小卷叶蛾(Adoxophyes orana);例如,黄卷蛾属(Archipsspp.)的梨黄卷蛾(Archips breviplicanus)、苹果黄卷蛾(Archips fuscocupreanus);其它的云杉芽卷蛾(Choristoneura fumiferana)、苹果蠹蛾(Cydia pomonella)、女贞细卷蛾(Eupoecilia ambiguella)、梨小食心虫(Grapholitha molesta)、后黄卷叶蛾(Homonamagnanima)、大豆食心虫(Leguminivora glycinivorella)、葡萄花翅小卷蛾(Lobesiabotrana)、豆小卷叶蛾(Matsumuraeses phaseoli)、苹褐卷蛾(Pandemis heparana)、葡萄长须卷叶蛾(Sparganothis pilleriana);
(u)巢蛾科(Yponomeutidae)的蛾:例如,苹果银蛾(Argyresthia conjugella)。
(2)缨翅目(Thysanoptera)害虫
(a)管蓟马科(Phlaeothripidae)的:例如,柿管蓟马(Ponticulothripsdiospyrosi);
(b)蓟马科(Thripidae)的:例如,花蓟马属(Frankliniella spp.)的水稻花蓟马(Frankliniella intonsa)、西花蓟马(Frankliniella occidentalis);例如,蓟马属(Thrips spp.)的棕榈蓟马(Thrips palmi)、烟蓟马(Thripstabaci);其它的温室蓟马(Heliothrips haemorrhoidalis)、茶黄蓟马(Scirtothrips dorsalis)。
(3)半翅目(Hemiptera)的害虫
(A)古喙亚目(Archaeorrhyncha)
(a)飞虱科(Delphacidae)的:例如,灰飞虱(Laodelphax striatella)、褐飞虱(Nilaparvata lugens)、甘蔗扁角飞虱(Perkinsiella saccharicida)、白背飞虱(Sogatella furcifera)。
(B)盾喙亚目(Clypeorrhyncha)
(a)叶蝉科(Cicadellidae)的:例如,小绿叶蝉属(Empoasca spp.)的马铃薯小绿叶蝉(Empoasca fabae)、日本小绿叶蝉(Empoasca nipponica)、小贯小绿叶蝉(Empoascaonukii)、板井小绿叶蝉(Empoasca sakaii);其它的葡萄斑叶蝉(Arboridia apicalis)、黑胸二室叶蝉(Balclutha saltuella)、二点大叶蝉(Epiacanthus stramineus)、黑额二叉叶蝉(Macrosteles striifrons)、黑尾叶蝉(Nephotettix cinctinceps)。
(C)异翅亚目(Heteroptera)
(a)蛛缘蝽科(Alydidae)的:例如,点蜂缘椿象(Riptortus clavatus);
(b)缘蝽科(Coreidae)的:例如,稻棘缘蝽(Cletus punctiger)、中稻缘蝽(Leptocorisa chinensis);
(c)长蝽科(Lygaeidae)的:例如,美洲谷长蝽(Blissus leucopterus)、甘蔗异背长蝽(Cavelerius saccharivorus)、葫芦长蝽(Togo hemipterus);
(d)盲蝽科(Miridae)的:例如,日本跳盲蝽(Halticus insularis)、美国牧草盲蝽(Lygus lineolaris)、棉盲蝽(Psuedatomoscelis seriatus)、西伯利亚狭盲蝽(Stenodemasibiricum)、赤条纤盲蝽(Stenotus rubrovittatus)、赤须盲蝽(Trigonotyluscaelestialium);
(e)蝽科(Pentatomidae)的:例如,绿蝽属(Nezara spp.)的黑须稻绿蝽(Nezaraantennata)、稻绿蝽(Nezara viridula);例如,二星蝽属(Eysarcoris spp.)的北二星蝽(Eysarcoris aeneus)、日本二星蝽(Eysarcoris lewisi)、广二星蝽(Eysarcorisventralis);其它的细毛蝽(Dolycoris baccarum)、皱纹菜蝽(Eurydema rugosum)、青蝽(Glaucias subpunctatus)、茶翅蝽(Halyomorpha halys)、璧蝽(Piezodorus hybneri)、珀蝽(Plautia crossota)、稻黑蝽(Scotinophora lurida);
(f)红蝽科(Pyrrhocoridae)的:例如,离斑棉红蝽(Dysdercus cingulatus);
(g)姬缘蝽科(Rhopalidae)的:例如,黄伊缘蝽(Rhopalus msculatus);
(h)盾蝽科(Scutelleridae)的:例如,麦扁盾蝽(Eurygaster integriceps);
(i)网蝽科(Tingidae)的:例如,梨冠网蝽(Stephanitis nashi)。
(D)腹吻亚目(Sternorrhyncha)
(a)球蚜科(Adelgidae)的:例如,落叶松球蚜(Adelges laricis);
(b)粉虱科(Aleyrodidae)的:例如,小粉虱属(Bemisia spp.)的银叶粉虱(Bemisia argentifolii)、烟粉虱(Bemisia tabaci);其它的黑刺粉虱(Aleurocanthusspiniferus)、柑橘粉虱(Dialeurodes citri)、温室白粉虱(Trialeurodesvaporariorum);
(c)蚜科(Aphididae)的:例如,蚜属(Aphis spp.)的豆蚜(Aphis craccivora)、黑豆蚜(Aphis fabae)、草莓根蚜(Aphis forbesi)、棉蚜(Aphis gossypii)、苹蚜(Aphispomi)、接骨木蚜(Aphis sambuci)、绣线菊蚜(Aphis spiraecola);例如,缢管蚜属(Rhopalosiphum spp.)的玉米蚜(Rhopalosiphum maidis)、禾谷缢管蚜(Rhopalosiphumpadi);例如,西圆尾蚜属(Dysaphis spp.)的玫瑰苹果蚜(Dysaphis plantaginea)、居根西圆尾蚜(Dysaphis radicola);例如,长管蚜属(Macrosiphum spp.)的麦长管蚜(Macrosiphum avenae)、大戟长管蚜(Macrosiphum euphorbiae);例如,瘤蚜属(Myzusspp.)的李瘤蚜(Myzus cerasi)、桃蚜(Myzus persicae)、黄药子瘤蚜(Myzus varians);其它的豌豆蚜(Acyrthosiphon pisum)、茄沟无网蚜(Aulacorthum solani)、金盏菊李短尾蚜(Brachycaudus helichrysi)、甘蓝蚜(Brevicoryne brassicae)、草莓钉蚜(Chaetosiphonfragaefolii)、桃粉大尾蚜(Hyalopterus pruni)、茶藨苦菜超瘤蚜(Hyperomyzuslactucae)、萝卜蚜(Lipaphis erysimi)、巢菜修尾蚜(Megoura viciae)、麦无网长管蚜(Metopolophium dirhodum)、莴苣衲长管蚜(Nasonovia ribis-nigri)、指头蚜(Phorodonhumuli)、麦二叉蚜(Schizaphis graminum)、麦长管蚜(Sitobion avenae)、橘二叉蚜(Toxoptera aurantii);
(d)蜡蚧科(Coccidae)的:例如,蜡蚧属(Ceroplastes spp.)的,角蜡蚧(Ceroplastes ceriferus)、红蜡蚧(Ceroplastes rubens);
(e)盾蚧科(Diaspididae)的:白盾蚧属(Pseudaulacaspis spp.)的桑白蚧(Pseudaulacaspis pentagona)、李白盾蚧(Pseudaulacaspis prunicola);例如,矢尖蚧属(Unaspis spp.)的卫矛矢尖蚧(Unaspis euonymi)、柑桔矢尖蚧(Unaspis yanonensis);其它的红圆蚧(Aonidiella aurantii)、圣琼斯康盾蚧(Comstockaspis perniciosa)、茶围盾蚧(Fiorinia theae)、牡丹网盾蚧(Pseudaonidia paeoniae);
(f)硕蚧科(Margarodidae)的:例如,草履蚧(Drosicha corpulenta)、吹绵蚧(Icerya purchasi);
(g)根瘤蚜科(Phylloxeridae)的:例如,葡萄根瘤蚜(Viteus vitifolii);
(h)粉蚧科(Pseudococcidae)的:例如,臀纹粉蚧属(Planococcus spp.)的柑桔粉蚧(Planococcus citri)、日本臀纹粉蚧(Planococcus kuraunhiae);其它的石蒜绵粉蚧(Phenacoccus solani)、康氏粉蚧(Pseudococcus comstocki);
(i)木虱科(Psyllidae)的:例如,木虱属(Psylla spp.)的苹木虱(Psylla mali)、梨木虱(Psylla pyrisuga);其它的柑橘木虱(Diaphorina citri)。
(4)多食亚目(Polyphaga)的害虫
(a)番死虫科(Anobiidae)的:例如,烟草甲(Lasioderma serricorne);
(b)卷象科(Attelabidae)的:例如,梨卷叶象甲(Byctiscus betulae)、日本苹虎(Rhynchites heros);
(c)长蠢科(Bostrichidae)的:例如,褐粉蠹(Lyctus brunneus);
(d)三锥象甲科(Brentidae)的:例如,甘薯蚁象(Cylas formicarius);
(e)吉丁科(Buprestidae)的:例如,梨窄吉丁(Agrilus sinuatus);
(f)天牛科(Cerambycidae)的:例如,白斑星天牛(Anoplophora malasiaca)、松墨天牛(Monochamus alternatus)、黄星天牛(Psacothea hilaris)、葡萄脊虎天牛(Xylotrechus pyrrhoderus);
(g)叶甲科(Chrysomelidae)的:例如,豆象属(Bruchus spp.)的豌豆象(Bruchuspisorum)、蚕豆象(Bruchus rufimanus);例如,叶甲属(Diabrotica spp.)的北方玉米根虫甲(Diabrotica barberi)、十一星黄瓜甲虫(Diabrotica undecimpunctata)、玉米根萤叶甲(Diabrotica virgifera);例如,黄条跳甲属(Phyllotreta spp.)的大豆淡足跳甲(Phyllotreta nemorum)、黄曲条跳甲(Phyllotreta striolata);其它的黄守瓜(Aulacophora femoralis)、绿豆象(Callosobruchus chinensis)、甜菜大龟甲(Cassidanebulosa)、甜菜跳甲(Chaetocnema concinna)、马铃薯甲虫(Leptinotarsadecemlineata)、水稻负泥虫(Oulema oryzae)、狭胸蚤跳甲(Psylliodes angusticollis);
(h)瓢虫科(Coccinellidae)的:例如,食植瓢虫属(Epilachna spp.)的墨西哥豆瓢虫(Epilachna varivestis)、二十八星瓢虫(Epilachna vigintioctopunctata);
(i)象甲科(Curculionidae)的:例如,花象属(Anthonomus spp.)的棉铃象甲虫(Anthonomus grandis)、梨花象(Anthonomus pomorum);例如,谷象属(Sitophilus spp.)的谷象(Sitophilus granarius)、玉米象(Sitophilus zeamais);其它的稻象甲(Echinocnemus squameus)、西印度甘薯象甲(Euscepes postfasciatus)、欧洲松树皮象(Hylobius abietis)、苜蓿叶象(Hypera postica)、稻水象甲(Lissohoptrusoryzophilus)、葡萄黑象甲(Otiorhynchus sulcatus)、豌豆根瘤象(Sitona lineatus)、猎食谷象(Sphenophorus venatus);
(j)叩甲科(Elateridae)的:例如,梳爪叩甲属(Melanotus spp.)的褐纹金针虫(Melanotus fortnumi)、栉叩头虫(Melanotus tamsuyensis);
(k)露尾甲科(Nitidulidae)的:例如,姬扁出尾虫(Epuraea domina);
(l)金龟子科(Scarabaeidae)的:例如,异丽金龟属(Anomala spp.)的赤铜丽金龟(Anomala cuprea)、红铜丽金龟(Anomala rufocuprea);其它的金花金龟(Cetoniaaurata)、小青花金龟(Gametis jucunda)、豆黄鳃金龟(Heptophylla picea)、大栗鳃角金龟(Melolontha melolontha)、日本金龟子(Popillia japonica);
(m)小蠹科(Scolytidae)的:例如,云杉八齿小蠹(Ips typographus);
(n)隐翅虫科(Staphylinidae)的:例如,红胸隐翅虫(Paederus fuscipes);
(o)拟步甲科(Tenebrionidae)的:例如,黄粉虫(Tenebrio molitor)、赤拟谷盗(Tribolium castaneum);
(p)谷盗科(Trogossitidae)的:例如,大谷盗(Tenebroides mauritanicus)。
(5)双翅目(Diptera)的害虫
(A)短角亚目(Brachycera)
(a)潜蝇科(Agromyzidae)的:例如,斑潜蝇属(Liriomyza spp.)的番茄斑潜蝇(Liriomyza bryoniae)、葱潜叶蝇(Liriomyza chinensis)、美洲斑潜蝇(Liriomyzasativae)、三叶斑潜蝇(Liriomyza trifolii);其它的豌豆潜叶蝇(Chromatomyiahorticola)、日本稻潜蝇(Agromyza oryzae);
(b)花蝇科(Anthomyiidae)的:例如,地种蝇属(Delia spp.)的种蝇(Deliaplatura)、甘蓝根蝇(Delia radicum);其它的油菜肖藜泉蝇(Pegomya cunicularia);
(c)果蝇科(Drosophilidae)的:例如,果蝇属(Drosophila spp.)的黑腹果蝇(Drosophila melanogaster)、斑翅果蝇(Drosophila suzukii);
(d)水蝇科(Ephydridae)的:例如,水稻潜叶蝇(Hydrellia griseola);
(e)茎蝇科(Psilidae)的:例如,胡萝卜茎蝇(Psila rosae);
(f)实蝇科(Tephritidae)的:例如,果实蝇属(Bactrocera spp.)的瓜实蝇(Bactrocera cucurbitae)、橘小实蝇(Bactrocera dorsalis);例如,绕实蝇属(Rhagoletis spp.)的樱桃绕实蝇(Rhagoletis cerasi)、苹果绕实蝇(Rhagoletispomonella);其它的地中海果蝇(Ceratitis capitata)、橄榄果蝇(Dacus oleae)。
(B)长角亚目(Nematocera)
(a)瘿蚊科(Cecidomyiidae)的:例如,大豆荚瘿蚊(Asphondylia yushimai)、高粱瘿蚊(Contarinia sorghicola)、黑森瘿蚊(Mayetiola destructor)、麦红吸浆虫(Sitodiplosis mosellana)。
(6)直翅目(Orthoptera)的害虫
(a)蝗科(Acrididae)的:例如,沙漠蝗属(Schistocerca spp.)的南美沙漠蝗(Schistocerca americana)、沙漠蝗(Schistocerca gregaria);其它的澳大利亚灾蝗(Chortoicetes terminifera)、摩洛哥戟纹蝗(Dociostaurus maroccanus)、东亚飞蝗(Locusta migratoria)、褐飞蝗(Locustana pardalina)、红翅蝗(Nomadacrisseptemfasciata)、小翅稻蝗(Oxya yezoensis);
(b)蟋蟀科(Gryllidae)的:例如,家蟋蟀(Acheta domestica)、黄脸油葫芦(Teleogryllus emma);
(c)蝼蛄科(Gryllotalpidae)的:例如,东方蝼蛄(Gryllotalpa orientalis);
(d)螽斯科(Tettigoniidae)的:例如,温室灶马(Tachycines asynamorus)。
(7)蜱螨亚纲类(Acari)
(A)无气门目(Astigmata)的粉螨亚目类(Acaridida)
(a)粉螨科(Acaridae)的螨:例如,根螨属(Rhizoglyphus spp.)的刺足根螨(Rhizoglyphus echinopus)、罗宾根螨(Rhizoglyphus robini);例如,食酪螨属(Tyrophagus spp.)的瓜食酪螨(Tyrophagus neiswanderi)、尘食酪螨(Tyrophagusperniciosus)、腐食酪螨(Tyrophagus putrescentiae)、似食酪螨(Tyrophagus similis);其它的粗脚粉螨(Acarus siro)、椭圆食粉螨(Aleuroglyphus ovatus)、菌食嗜菌螨(Mycetoglyphus fungivorus);
(B)前气门目(Prostigmata)的辐螨亚目类(Actinedida)
(a)叶螨科(Tetranychidae)的螨:例如,苔螨属(Bryobia spp.)的苜蓿苔螨(Bryobia praetiosa)、果苔螨(Bryobia rubrioculus);例如,始叶螨属(Eotetranychusspp.)的六点始叶螨(Eotetranychus asiaticus)、北始叶螨(Eotetranychus boreus)、朴始叶螨(Eotetranychus celtis)、膝状始叶螨(Eotetranychus geniculatus)、柑橘始叶螨(Eotetranychus kankitus)、李始叶螨(Eotetranychus pruni)、栲始叶螨(Eotetranychusshii)、史氏始叶螨(Eotetranychus smithi)、桑始叶螨(Eotetranychus suginamensis)、弯钩始叶螨(Eotetranychus uncatus);例如,小爪螨属(Oligonychus spp.)的柳杉小爪螨(Oligonychus hondoensis)、冬青小爪螨(Oligonychus ilicis)、落叶松小爪螨(Oligonychus karamatus)、芒果小爪螨(Oligonychus mangiferus)、甘蔗小爪螨(Oligonychus orthius)、鳄梨小爪螨(Oligonychus perseae)、虾夷云杉叶螨(Oligonychus pustulosus)、真梶小爪螨(Oligonychus shinkajii)、针叶小爪螨(Oligonychus ununguis);例如,全爪螨属(Panonychus spp.)的桔全爪螨(Panonychuscitri)、桑全爪螨(Panonychus mori)、苹果全爪螨(Panonychus ulmi);例如,叶螨属(Tetranychus spp.)的朱砂叶螨(Tetranychus cinnabarinus)、伊氏叶螨(Tetranychusevansi)、神泽氏叶螨(Tetranychus kanzawai)、卢氏叶螨(Tetranychus ludeni)、柞木叶螨(Tetranychus quercivorus)、豆叶螨(Tetranychus phaselus)、二斑叶螨(Tetranychusurticae)、山楂叶螨(Tetranychus viennensis);例如,缺爪螨属(Aponychus spp.)的竹缺爪螨(Aponychus corpuzae)、梧桐缺爪螨(Aponychus firmianae);例如,绿叶螨属(Sasanychus spp.)的绿叶螨(Sasanychus akitanus)、姬绿叶螨(Sasanychus pusillus);例如,裂爪螨属(Shizotetranychus spp.)的嗜竹裂爪螨(Shizotetranychus celarius)、长肌裂爪螨(Shizotetranychus longus)、芒草裂爪螨(Shizotetranychusmiscanthi)、勒氏裂爪螨(Shizotetranychus recki)、柳裂爪螨(Shizotetranychus schizopus);另外,酢浆草如叶螨(Tetranychina harti)、孔雀杜克叶螨(Tuckerella pavoniformis)、札幌叶螨(Yezonychussapporensis);
(b)细须螨科(Tenuipalpidae)的螨:例如,短须螨属(Brevipalpus spp.)的刘氏短须螨(Brevipalpus lewisi)、卵形短须螨(Brevipalpus obovatus)、紫红短须螨(Brevipalpus phoenicis)、仙人掌短须螨(Brevipalpus russulus)、加州短须螨(brevipalpus californicus);例如,细须螨属(Tenuipalpus spp.)的太平洋细须螨(Tenuipalpus pacificus)、柿细须螨(Tenuipalpus zhizhilashviliae);以及菠萝长叶螨(Dolichotetranychus floridanus);
(c)瘿螨科(Eriophyidae)的螨:例如,瘤瘿螨属(Aceria spp.)的柿子芽螨(Aceria diospyri)、无花果瘤瘿螨(Aceria ficus)、日本瘤瘿螨(Aceria japonica)、枸杞瘤瘿螨(Aceria kuko)、石竹瘤瘿螨(Aceria paradianthi)、枸杞叶潜瘤瘿螨(Aceriatiyingi)、郁金香瘤瘿螨(Aceria tulipae)、结缕草瘤瘿螨(Aceria zoysiea);例如,瘿螨属(Eriophyes spp.)的伪梨锈蜱(Eriophyes chibaensis)、梅瘿螨(Eriophyesemarginatae);例如,刺皮瘿螨属(Aculops spp.)的番茄刺皮瘿螨(Aculopslycopersici)、皮氏刺皮瘿螨(Aculops pelekassi);例如,刺瘿螨属(Aculus spp.)的佛氏刺瘿螨(Aculus fockeui)、苹果刺锈螨(Aculus schlechtendali);以及茶尖叶节蜱(Acaphylla theavagrans)、茶叶瘿螨(Calacarus carinatus)、葡萄缺节瘿螨(Colomerusvitis)、葡萄叶锈螨(Calepitrimerus vitis)、梨上瘿螨(Epitrimerus pyri)、菊花叶锈螨(Paraphytoptus kikus)、罗汉松副丽瘿螨(Paracalacarus podocarpi)、柑橘锈螨(Phyllocotruta citri);
(d)跗线螨科(Transonemidae)的螨,例如,跗线螨属(Tarsonemus spp.)的双叶跗线螨(Tarsonemus bilobatus)、韦氏跗线螨(Tarsonemus waitei);另外,樱草植食螨(Phytonemus pallidus)、侧多食跗线螨(Polyphagotarsonemus latus);
(e)叶爪螨科(Penthaleidae)的螨:例如,叶爪螨属(Penthaleus spp.)的、白菜螨(Penthaleus erythrocephalus)、麦叶爪螨(Penthaleus major)。
本发明的有害生物防除剂可以将杀菌剂、杀虫·杀螨剂、杀线虫剂、杀土壤害虫剂其它有效成分与植物调节剂、除草剂、增效剂、肥料、土壤改良剂、动物用饲料等混用或并用。
本发明的二唑啉化合物与其它有效成分的组合可以对杀虫·杀螨·杀线虫活性期待协同效果。协同效果可以根据常规方法利用Colby公式(Colby.S.R.;CalculatingSynergistic and Antagonistic Responses of Herbicide Combinations;Weeds15,20-22页,1967)来确认。
以下示出可以与本发明的有害生物防除剂混用或并用的杀虫·杀螨剂、杀线虫剂、杀土壤害虫剂、驱虫剂等的具体例。
(1)乙酰胆碱酯酶抑制剂:
(a)氨基甲酸酯系:棉铃威(alanycarb)、涕灭威(aldicarb)、虫威(bendiocarb)、丙硫克百威(benfuracarb)、丁叉威(butocarboxim)、氧丁叉威(butoxycarboxim)、甲萘威(carbaryl)、克百威(carbofuran)、丁硫克百威(carbosulfan)、乙硫苯威(ethiofencarb)、仲丁威(fenobucarb)、伐虫脒(formetanate)、呋线威(furathiocarb)、异丙威(isoprocarb)、甲硫威(methiocarb)、灭多威(methomyl)、杀线威(oxamyl)、抗蚜威(pirimicarb)、残杀威(propoxur)、硫双威(thiodicarb)、久效威(thiofanox)、唑蚜威(triazamate)、混杀威(trimetacarb)、灭除威(XMC)、灭杀威(xylylcarb);苯硫威(fenothiocarb)、异丙威(MIPC)、二甲杀威(MPMC)、速灭威(MTMC)、砜灭威(aldoxycarb)、除害威(allyxycarb)、灭害威(aminocarb)、合杀威(bufencarb)、除线威(cloethocarb)、威百亩钠(metam sodium)、猛杀威(promecarb);
(b)有机磷系:乙酰甲胺磷(acephate),、甲基吡磷(azamethiphos)、乙基谷硫磷(azinphos-ethyl)、甲基谷硫磷(azinphos-methyl)、硫线磷(cadusafos)、氯氧磷(chlorethoxyphos)、毒虫畏(chlorfenvinphos)、氯甲磷(chlormephos)、氯吡硫磷(chlorpyrifos)、甲基毒死蜱(chlorpyrifos-methyl)、蝇毒磷(coumaphos)、杀螟腈(cyanophos)、甲基内吸磷(demeton-S-methyl)、二嗪磷(diazinon)、敌敌畏/DDVP(dichlorvos/DDVP)、百治磷(dicrotophos)、乐果(dimethoate)、甲基毒虫畏(dimethylvinphos)、乙拌磷(disulfoton)、苯硫磷(EPN)、乙硫磷(ethion)、丙线磷(ethoprophos)、氨磺磷(famphur)、苯线磷(fenamphos)、杀螟硫磷(fenitrothion)、倍硫磷(fenthion)、噻唑硫磷(fosthiazate)、庚烯磷(heptenophos)、新烟磷(imicyafos)、异柳磷(isofenphos)、水胺硫磷(isocarbophos)、异唑磷(isoxathio)、马拉硫磷(malathion)、灭蚜磷(mecarbam)、甲胺磷(methamidophos)、杀扑磷(methidathion)、速灭磷(mevinphos)、久效磷(monocrotophos)、二溴磷(naled)、氧化乐果(omethoate)、砜吸磷(oxydemeton-methyl)、对硫磷(parathion)、甲基对硫磷(parathion-methyl)、稻丰散(phentoate)、甲拌磷(phorate)、伏杀硫磷(phosalone)、亚胺硫磷(phosmet)、磷胺(phosphamidone)、辛硫磷(phoxim)、甲基嘧啶磷(pirimiphos-methyl)、丙溴磷(profenofos)、胺丙畏(propetamphos)、丙硫磷(prothiofos)、吡唑硫磷(pyraclofos)、哒嗪硫磷(pyridaphenthion)、喹硫磷(quinalphos)、治螟磷(sulfotep)、丁基嘧啶磷(tebupirimfos)、双硫磷(temephos)、特丁硫磷(terbufos)、杀虫威(tetrachlorvinphos)、甲基乙拌磷(thiometon)、三唑磷(triazophos)、敌百虫(trichlorfon)、蚜灭多(vamidothion);乙基溴硫磷(bromophos ethyl)、BRP、三硫磷(carbophenothion)、苯腈膦(cyanophenphos)、甲基内吸磷砜(demethon-S-methylsulfone)、氯亚胺硫磷(dialifos)、除线磷(diclofenthion)、蔬果磷(dioxabenzofos)、乙嘧硫磷(etrimfos)、丰索磷(fensulfothion)、吡氟硫磷(flupyrazofos)、地虫硫磷(fonofos)、安果(formothion)、甲基异柳磷(phosmethylan)、氯唑磷(isazofos)、碘硫磷(iodofenphos)、虫螨畏(methacrifos)、乙基嘧啶磷(pyrimiphos-ethyl)、磷虫威(phosphocarb)、丙虫磷(propaphos)、发果(prothoate)、甲丙硫磷(sulprofos)。
(2)GABA-激动性氯离子通道拮抗剂:乙酰虫腈(acetoprole)、氯丹(chlordane)、硫丹(endosulfan)、乙虫腈(ethiprole)、氟虫腈(fipronil)、吡嗪氟虫腈(pyrafluprole)、吡啶氟虫腈(pyriprole)、毒杀芬(camfechlor)、七氯(heptachlor)、除螨灵(dienochlor)。
(3)钠通道调节剂:氟丙菊酯(acrinathrin)、d-顺式-反式丙烯菊酯(d-cis-transallethrin)、d-反式丙烯菊酯(d-transarethrin)、联苯菊酯(bifenthrin)、生物丙烯菊酯(bioallethrin)、生物丙烯菊酯S-环戊基异构体(bioaresulin S-cyclopentyl isomer)、生物苄呋菊酯(bioresmethrin)、乙氰菊酯(cycloprothrin)、氟氯氰菊酯(cyfluthrin)、β-氟氯氰菊酯(beta-cyfluthrin)、氯氟氰菊酯(cyhalothrin)、λ-氯氟氰菊酯(lambda-cyhalothrin)、γ-氯氟氰菊酯(gamma-cyhalothrin permethrin)、氯氰菊酯(cypermethrin)、α-氯氰菊酯(alpha-cypermethrin)、β-氯氰菊酯(beta-cypermethrin)、θ-氯氰菊酯(theta-cypermethrin)、ζ-氯氰菊酯(zeta-cypermethrin)、苯氰菊酯[(1R)-反式异构体](cyphenothrin[(1R)-trans isomer])、溴氰菊酯(deltamethrin)、烯炔菊酯[(EZ)-(1R)-异构体](empenthrin[(EZ)-(1R)-isomer])、顺式氰戊菊酯(esfenvalerate)、醚菊酯(ethofenprox)、甲氰菊酯(fenpropathrine)、氰戊菊酯(fenvalerate)、氟氰戊菊酯(flucythrinate)、氟氯苯菊酯(flumethrin)、τ-氟胺氰菊酯(taufulvalinate)、苄螨醚(halfenprox)、炔咪菊酯(imiprothrin)、噻嗯菊酯(kadethrin)、氯菊酯(permethrin)、苯醚菊酯[(1R)-反式异构体](phenothrin[(1R)-trans isomer]、炔丙菊酯(prallethrin)、除虫菊(pyrethram)、苄呋菊酯(resmethrin)、氟硅菊酯(silafluofen)、七氟菊酯(tefluthrin)、胺菊酯[(1R)-异构体](tetramethrin[(1R)-isomer])、四溴菊酯(tralomethrin)、四氟苯菊酯(transfluthrin);丙烯菊酯(allethrin)、除虫菊酯(pyrethrin)、除虫菊酯I(pyrethrin I)、除虫菊酯II(pyrethrin II)、丙氟菊酯(profluthrin)、四氟甲醚菊酯(dimefluthrin)、生物苄呋烯菊酯(bioethanomethrin)、生物氯菊酯(biopermethrin)、反式氯菊酯(trans-biopermethrin)、芬氟司林(fenfluthrin)、氯氰吡菊酯(fenpirithrin)、溴氟菊酯(flubrocythrinate)、三氟醚菊酯(flufenprox)、甲氧苄氟菊酯(metofluthrin)、丙苯烃菊酯(protrifenbute)、反灭虫菊(pyresmethrin)、环戊烯丙菊酯(terallethrin)。
(4)烟碱型乙酰胆碱受体激动剂:啶虫脒(acetamiprid)、噻虫胺(clothianidin)、呋虫胺(dinotefuran)、吡虫啉(imidacloprid)、烯啶虫胺(nitenpyram)、硝虫噻嗪(nithiazine)、噻虫啉(thiacloprid)、噻虫嗪(thiamethoxam)、氟啶虫胺腈(sulfoxaflor)、尼古丁(nicotine)、氟吡呋喃酮(flupyradifurone)。
(5)烟碱型乙酰胆碱受体变构调节剂:乙基多杀菌素(spinetoram)、多杀菌素(spinosad)。
(6)氯离子通道活化剂:阿维菌素(abamectin)、甲氨基阿维菌素苯甲酸盐(emamectin benzoate)、雷皮菌素(lepimectin)、密灭汀(milbemectin);伊维菌素(ivermectin)、塞拉菌素(selamectin)、多拉菌素(doramectin)、依普菌素(eprinomectin)、莫西菌素(moxidectin)、米尔倍霉素(milbemycin)、米尔贝霉素肟(milbemycin oxime)、奈马菌素(nemadectin)。
(7)保幼激素类似物:烯虫乙酯(hydroprene)、烯虫炔酯(kinoprene)、甲氧普烯(methoprene)、苯氧威(fenoxycarb)、吡丙醚(pyriproxyfen);苯虫醚(diofenolan)、保幼醚(epofenonane)、烯虫硫酯(triprene)。
(8)其它非特异性抑制剂:甲基溴、氯化苦(chloropicrin)、硫酰氟(sulfurylfluoride)、硼砂、吐酒石。
(9)同翅目选择性摄食抑制剂:氟啶虫酰胺(flonicamid)、吡蚜酮(pymetrozine)、新喹唑啉(pyrifluquinazon)。
(10)螨类繁殖抑制剂:四螨嗪(clofentezine)、氟螨嗪(diflovidazin)、噻螨酮(hexythiazox)、乙螨唑(etoxazole)。
(11)源自微生物的昆虫中肠内膜破坏剂:苏云金芽孢杆菌以色列亚种(Bacillusthuringiensis subsp.Israelensis)、球形芽孢杆菌(Bacillus sphaericus)、苏云金芽孢杆菌鲇泽亚种(Bacillus thuringiensis subsp.Aizawai)、苏云金芽孢杆菌库尔斯塔克亚种(Bacillus thuringiensis subsp.Kurstaki)、苏云金芽孢杆菌拟步行甲亚种(Bacillusthuringiensis subsp.)、Bt作物蛋白质:Cry1Ab、Cry1Ac、Cry1Fa、Cry1A.105、Cry2Ab、Vip3A、mCry3A、Cry3Ab、Cry3Bb、Cry34Ab1/Cry35Ab1。
(12)线粒体ATP生物合成酶抑制剂:丁醚脲(diafenthiuron)、三唑锡(azocyclotin)、三环锡(cyhexatin)、苯丁锡(fenbutatin oxide)、克螨特(propargite)、三氯杀螨砜(tetradiphon)。
(13)氧化磷酸化解偶联剂:溴虫腈(chlorfenapyr)、氟虫胺(sulfluramid)、DNOC、乐杀螨(binapacryl)、消螨通(dinobuton)、消螨普(dinocap)。
(14)烟碱型乙酰胆碱受体通道阻断剂:杀虫磺(bensultap)、杀螟丹盐酸盐(cartap hydrochloride);沙蚕毒素(nereistoxin);杀虫单(thiosultap-monosodium)、杀虫环(thiocyclam)。
(15)壳多糖合成抑制剂:双三氟虫脲(bistrifluron)、氟啶脲(chlorfluazuron)、除虫脲(diflubenzuron)、氟环脲(flucycloxuron)、氟虫脲(flufenoxuron)、氟铃脲(hexaflumuron)、虱螨脲(lufenuron)、双苯氟脲(novaluron)、多氟脲(noviflumuron)、伏虫隆(teflubenzuron)、杀铃脲(triflumuron)、噻螨酮(buprofezin)、吡虫隆(fluazuron)。
(16)双翅目蜕皮干扰剂:灭蝇胺(cyromazine)。
(17)蜕皮激素受体激动剂:环虫酰肼(chromafenozide)、氯虫酰肼(halofenozide)、甲氧虫酰肼(methoxyphenozide)、虫酰肼(tebufenozide)。
(18)章鱼胺受体激动剂:双甲脒(amitraz)、得米地曲(demiditraz)、杀虫脒(chlordimeform)。
(19)线粒体电子传递系统复合体III抑制剂:灭螨醌(acequinosyl)、嘧螨酯(fluacrylpyrim)、伏蚁腙(hydramethylnon)、联苯肼酯(bifenazate)。
(20)线粒体电子传递系统复合体I抑制剂:喹螨醚(fenazaquin)、唑螨酯(fenpyroximate)、嘧螨醚(pyrimidifen)、哒螨灵(pyridaben)、吡螨胺(tebufenpyrad)、唑虫酰胺(tolfenpyrad)、鱼藤酮(rotenone)。
(21)电压依赖性钠通道阻滞剂:茚虫威(indoxacarb)、氰氟虫腙(metaflumizone)。
(22)乙酰基CoA羧化酶抑制剂:螺螨酯(spirodiclofen)、螺甲螨酯(spiromesifen)、螺虫乙酯(spirotetramat)、spiropidion。
(23)线粒体电子传递系统复合体IV抑制剂:磷化铝、磷化钙、膦、磷化锌、氰化物。
(24)线粒体电子传递系统复合体II抑制剂:腈吡螨酯(cyenopyrafen)、丁氟螨酯(cyflumetofen)、皮福鲁不米多(pyflubumide)。
(25)兰尼碱受体调节剂:氯虫酰胺(chlorantraniliprole)、溴氰虫酰胺(cyantraniliprole)、氟虫酰胺(fulbendiamide)、环溴虫酰胺(cyclaniliprole)、氟氰虫酰胺(tetraniliprole)。
(26)混合功能氧化酶抑制剂化合物:增效醚(piperonyl butoxide)。
(27)蛛毒素受体激动剂:缩酚酸肽(depsipeptide)、环状缩酚酸肽、24元环状缩酚酸肽、艾莫德赛(emodepside)。
(28)其它药剂(作用机理未知):印楝素(azadirachtin)、苯螨特(benzoximate)、溴螨酯(bromopropylate)、冰晶石(cryolite)、三氯杀螨醇(dicofol)、啶虫丙醚(pyridalyl);异噻虫唑(bencrothiaz)、硫、磺胺螨酯(amidoflumet)、1,3-二氯丙烯、二氯异丙醚(DCIP)、溴螨酯(phenisobromolate)、苯螨特(benzomate)、四聚乙醛(metaldehyde)、乙酯杀螨醇(chlorbenzilate)、氯噻苯(clothiazoben)、环虫腈(dicyclanyl)、分萨克林(fenoxacrim)、芳氟胺(fentrifanil)、氟螨噻(fulbenzimine)、氟奋乃静(fluphenazine)、诱虫十六酯(gossyplure)、日本金龟子性引诱剂(Japonilure)、虫酮(methoxadiazone)、石油、油酸钾、杀螨好(tetrasul)、苯螨噻(trialathene);阿非多皮罗奋(afidopyropen)、氟麦托醌(flometoquin)、丁虫腈(flufiprole)、氟噻虫砜(fluenesulfone)、氯氟醚菊酯(meperfluthrin)、四氟醚菊酯(tetramethylfluthrin)、溴代吡咯腈(tralopyril)、四氟甲醚菊酯(dimefluthrin)、甲基新癸酰胺(methylneodecanamide);fluralaner、afoxolaner、fluxametamide、5-[5-(3,5-二氯苯基)-5-三氟甲基-4,5-二氢异唑-3-基]-2-(1H-1,2,4-三唑-1-基)苯甲腈(CAS:943137-49-3)、溴虫氟苯双酰胺(brofuranilide)、三氟苯嘧啶(triflumezopyrim)、dicloromezotiaz、oxazosulfyl、其它的间二酰胺类。
(29)驱虫剂:
(a)苯并咪唑系:芬苯达唑(fenbendazole)、阿苯达唑(albendazole)、三氯苯达唑(triclabendazole)、奥苯达唑(oxibendazole)、甲苯达唑(mebendazole)、奥芬达唑(oxfendazole)、帕苯达唑(perbendazole)、氟苯达唑(flubendazole);非班太尔(febantel)、奈韦拉平(netobimin)、托布津(thiophanate);噻苯咪唑(thiabendazole)、堪苯达唑(canbendazole);
(b)水杨酰苯胺类:氯氰碘柳胺(closantel)、五氯柳胺(oxyclozanide)、碘醚柳胺(rafoxanide)、氯硝柳胺(niclosamide);
(c)取代酚类:硝碘酚腈(nitroxinyl)、硝硫氰酯(nitroscanate);
(d)嘧啶类:噻嘧啶(pyrantel)、莫仑太(morantel);
(e)咪唑并噻唑类:左旋咪唑(levamisole)、四咪唑(tetramisole);
(f)四氢嘧啶类:吡喹酮(praziquantel)、依西太尔(epsiprantel);
(g)其它驱虫药:环二烯、鱼尼丁(ryania)、氯舒隆(clorsulon)、甲硝唑(metronidazole)、得米地曲(demiditraz);哌嗪、乙胺嗪(diethylcarbamazine)、二氯芬(dichlorophene)、糠酸莫米松(monepantel)、三苯双脒(tribenzymidine)、阿米太尔(amidantel);硫乙胂胺(thiacetalsamide)、美拉沙胺(melorsamine)、硫乙胂胺(arsenamide)。
以下示出可以与本发明的有害生物防除剂混用或并用的杀菌剂的具体例。
(1)核酸生物合成抑制剂:;Cloziracone)(
(a)RNA聚合酶I抑制剂:苯霜灵(benalaxyl)、精苯霜灵(benalaxyl-M)、呋霜灵(furarlaxyl)、甲霜灵(metalaxyl)、精甲霜灵(metalaxyl-M);霜灵(oxadixil);柯罗泽尔昆(clozylacon)、呋酰胺(ofurace);
(b)腺苷脱氨酶抑制剂:乙嘧酚磺酸酯(bupirimate)、甲菌定(dimethirimol)、乙嘧酚(ethirimol);
(2)有丝核分裂抑制剂及细胞分裂抑制剂:
(a)β-微管蛋白聚合抑制剂:苯菌灵(benomyl)、多菌灵(carbendazim)、苯咪唑菌(chlorfenazole)、麦穗宁(fuberidazole)、噻苯咪唑(thiabendazole)、托布津(thiophanate)、甲基硫菌灵(thiophanate-methyl)、乙霉威(dietofencarb)、苯酰菌胺(zoxamide)、噻唑菌胺(ethaboxam);
(b)细胞分裂抑制剂:戊菌隆(pencycuron);
(c)类血影蛋白(spectrin-like protein)的离域抑制剂:氟吡菌胺(fluopicolide)。
(3)呼吸抑制剂:
(a)复合体I NADH氧化还原酶抑制剂:氟嘧菌胺(diflumetrim)、、唑虫酰胺(tolfenpyrad);
(b)复合体II琥珀酸脱氢酶抑制剂:麦锈灵(benodanil)、氟酰胺(flutolanil)、灭锈胺(mepronil)、异丙噻菌胺(isofetamide)、氟吡菌酰胺(fluopyram)、甲呋酰胺(fenfuram)、拌种胺(frumecyclox)、萎锈灵(carboxin)、氧化萎锈灵(oxycarboxin)、噻呋酰胺(tifluzamide)、苯并烯氟菌唑(benzovindiflupyr)、联苯吡菌胺(bixafen)、氟唑菌酰胺(fluxapyroxad)、呋吡菌胺(furametpyr)、吡唑萘菌胺(isopyrazam)、戊苯吡菌胺(penflufen)、吡噻菌胺(penthiopyrad)、环苯吡菌胺(sedaxane)、啶酰菌胺(boscalid)、pyraziflumid;
(c)复合体III泛醌氧化酶Qo抑制剂:嘧菌脂(azoxystrobin)、丁香菌酯(cumoxystrobin)、甲香菌酯(cumethoxystrobin)、烯肟菌酯(enoxastrobin)、氟菌螨酯(flufenoxystrobin)、啶氧菌酯(picoxystrobin)、吡唑醚菌酯(pyraoxystrobin)、吡唑醚菌酯(pyraclostrobin)、唑胺菌酯(pyrametostrobin)、氯啶菌酯(triclopyricarb)、醚菌酯(kresoxim-methyl)、肟菌酯(trifloxystrobin)、醚菌胺(dimoxystrobin)、烯肟菌胺(fenaminestrobin)、苯氧菌胺(metominostrobin)、肟醚菌胺(orysastrobin)、唑菌酮(famoxadone)、氟嘧菌酯(fluoxastrobin)、咪唑菌酮(fenamidon)、吡菌苯威(pyribencarb)、mandestrobin;
(d)复合体III泛醌还原酶Qi抑制剂:氰霜唑(cyazofamid);吲唑磺菌胺(amisulbrom);
(e)氧化磷酸化的解偶联剂:乐杀螨(binapacryl)、敌螨普(meptyldinocap)、消螨普(dinocap);氟啶胺(fluazinam);嘧菌腙;(ferimzone)
(f)氧化磷酸化抑制剂(ATP合成酶的抑制剂):薯瘟锡(fentin acetate)、氯化三苯基锡(fentin chloride)、三苯基氢氧化锡(fentin hydroxide);
(g)ATP生成抑制剂:硅噻菌胺(silthiofam);
(h)复合体III:细胞色素bc1(泛醌还原酶)的Qx(未知)抑制剂:唑嘧菌胺(ametoctrazine)。
(4)氨基酸及蛋白质合成抑制剂
(a)蛋氨酸生物合成抑制剂:安朵普灵(andoprim)、嘧菌环胺(cyprodinil)、嘧菌胺(mepanipyrim)、嘧霉胺(pyrimethanil);
(b)蛋白质合成抑制剂:灭瘟素(blasticidin-S)、春雷霉素(kasugamycin)、春雷霉素盐酸盐(kasugamycin hydrochloride)、链霉素(streptomycin)、土霉素(oxytetracycline)。
(5)信号传导抑制剂:
(a)信号传导抑制剂:喹氧灵(quinoxyfen)、丙氧喹啉(proquinazid);
(b)渗透压信号传导中的MAP·组氨酸激酶抑制剂:拌种咯(fenpiclonil)、咯菌腈(fludioxonil);乙菌利(clozolinate)、异菌脲(iprodione)、腐霉利(procymidone)、乙烯菌核利(vinclozolin)。
(6)脂质和细胞膜合成抑制剂:
(a)磷脂生物合成、甲基转移酶抑制剂:克瘟散(edifenphos)、异稻瘟净(iprobenfos)、吡菌磷(pyrazophos)、稻瘟灵(isoprothiolane);
(b)脂质的过氧化剂:联苯、地茂散(chloroneb)、氯硝胺(dicloran)、五氯硝基苯(quintozene)、四氯硝基苯(tecnazene)、甲基立枯磷(tolclofos-methyl)、土菌灵(etridiazole);
(c)作用于细胞膜的药剂:碘代丙炔基正丁氨基甲酸酯(iodocarb)、霜霉威(propamocarb)、霜霉威盐酸盐(propamocarb hydrochloride)、霜霉威乙膦酸盐(propamocarb focetylate)、硫菌威(prothiocarb);
(d)扰乱病原菌细胞膜的微生物:枯草芽孢杆菌、枯草芽孢杆菌QST713菌株、枯草芽孢杆菌FZB24菌株、枯草芽孢杆菌MBI600菌株、枯草芽孢杆菌D747菌株;
(e)扰乱细胞膜的药剂:互生叶白千层(茶树)的提取物。
(7)细胞膜的甾醇生物合成抑制剂:
(a)甾醇生物合成中的C14位的脱甲基化抑制剂:嗪氨灵(triforine);啶斑肟(pyrifenox)、啶菌唑(pyrisoxazole);氯苯嘧啶醇(fenarimol)、呋嘧醇(flurprimidol)、氟苯嘧啶醇(nuarimol);抑霉唑(imazalil)、抑霉唑硫酸盐(imazalilsulfate)、咪唑(oxpoconazole)、稻瘟酯(pefurzoate)、咪鲜胺(prochloraz)、氟菌唑(triflumizole)、烯效唑(viniconazole);
戊环唑(azaconazole)、双苯三唑醇(bitertanol)、糠菌唑(bromuconazole)、环唑醇(cyproconazole)、苄氯三唑醇(diclobutrazole)、苯醚甲环唑(difenoconazole)、烯唑醇(diniconazole)、烯唑醇-M(diniconazole-M)、氟环唑(epoxiconazole)、乙环唑(etaconazole)、腈苯唑(fenbuconazole)、氟喹唑(fluquinconazole)、氟硅唑(flusilazole)、粉唑醇(flutriafol)、氟康唑(fluconazole)、顺式氟康唑(fluconazole-cis)、己唑醇(hexaconazole)、亚胺唑(imibenconazole)、种菌唑(ipconazole)、叶菌唑(metconazole)、腈菌唑(mycrobutanil)、戊菌唑(penconazole)、丙环唑(propiconazole)、喹康唑(fluquinconazole)、硅氟唑(simeconazole)、戊唑醇(tebuconazole)、氟醚唑(tetraconazole)、三唑酮(triadimethone)、三唑醇(triadimenol)、灭菌唑(triticonazole);丙硫菌唑(prothioconazole)、伏立康唑(voriconazole)、mefentrifluconazole;
(b)甾醇生物合成中的Δ14还原酶及Δ8→Δ7-异构酶的抑制剂:
十二吗啉(aldimorph)、十二环吗啉(dodemorph)、十二环吗啉乙酸盐(dodemorphacetate)、丁苯吗啉(fenpropimorph)、十三吗啉(tridemorph)、苯锈啶(fenpropidin)、粉病灵(piperalin)、螺环菌胺(spiroxamine);
(c)甾醇生物合成体系的C4位脱甲基化中的3-酮还原酶抑制剂:环酰菌胺(fenhexamid)、胺苯吡菌酮(fenpyrazamine);
(d)甾醇生物合成体系的角鲨烯环氧酶抑制剂:稗草丹(pyribaticarb)、萘替芬(naftifen)、特比萘芬(terbinafine)。
(8)细胞壁合成抑制
(a)海藻糖酶抑制剂:井冈霉素(validamycin);
(b)壳多糖合成酶抑制剂:多抗霉素(polyoxin)、多氧霉素(polyoxorim);
(c)纤维素合成酶抑制剂:烯酰吗啉(dimethomorph)、氟吗啉(flumorph)、丁吡吗啉(pyrimorph);苯噻菌胺(benthiavaricarb)、丙森锌(iprovaricarb)、托普罗卡布(tolprocarb)、霜霉灭(varifenate)、双炔酰菌胺(mandipropamide)。
(9)黑色素生物合成抑制剂
(a)黑色素生物合成的还原酶抑制剂:四氯苯酞(fthalide);咯喹酮(pyroquilone);三环唑(tricyclazole);
(b)黑色素生物合成的脱水酶抑制剂:环丙酰菌胺(carpropamide);双氯氰菌胺(diclocimet);氰菌胺(fenoxanyl);
(10)宿主植物的抗性诱导剂:
(a)作用于水杨酸合成路线的药剂:阿拉酸式苯-S-甲基;
(b)其它:烯丙苯噻唑(probenazole);噻酰菌胺(tiazinyl);异噻菌胺(isotianil);昆布多糖(laminarin);大虎杖提取液。
(11)作用性不明的药剂:霜脲氰(cymoxanil)、三乙膦酸铝(fosetyl-aluminum)、磷酸(磷酸盐)、叶枯酞(teclofthalam)、咪唑嗪(triazoxide)、磺菌胺(flusulfamide)、哒菌清(diclomezine)、磺菌威(methasulfocarb)、环氟菌胺(cyflufenamid)、苯菌酮(metrafenone)、甲氧苯唳菌(pyriofenone)、多果定(dozine)、多果定游离碱(dozine freebase)、氟噻菌净(flutianil)。
(12)具有多作用点的药剂:铜(铜盐)、波尔多液、氢氧化铜、萘二甲酸铜、氧化铜、氧氯化铜、硫酸铜、硫、硫产品、多硫化钙、福美铁(ferbam)、代森锰锌(mancozeb)、代森锰(maneb)、代森锰铜(mancopper)、代森联(metiram)、代森福美锌(polycarbamate)、丙森锌(propineb)、福美双(thiram)、代森锌(zinebu)、福美锌(ziram)、克菌丹(captan)、敌菌丹(captahol)、灭菌丹(folpet)、百菌清(chlorotalonil)、抑菌灵(dichlofluanid)、对甲抑菌灵(tolylfluanid)、双胍辛胺(guazatine)、双胍辛胺乙酸盐(iminoctadinetriacetate)、双胍三辛烷基苯磺酸盐(iminoctadine trialbesilate)、敌菌灵(anilazine)、二噻农(dithianon)、灭螨猛(chinomethionate)、唑呋草(fluorimide)。
(13)其它药剂:DBEDC、氟灭菌丹(fluorfolpet)、双胍辛乙酸盐(guazatineacetate)、双(8-羟基喹啉)铜(II)、丙烷脒(propamidine)、氯化苦(chloropicrin)、酯菌胺(cyprofuram)、农杆菌(agrobacterium)、贝斯氧杂嗪(bethoxazine)、二苯胺、异硫氰酸甲酯(MITC)、米多霉素(mildiomycin)、辣椒素(capsaicin)、硫杂灵(cufraneb)、环丙磺酰胺(cyprosulfamide)、棉隆(dazomet)、咪菌威(debacarb)、双氯酚(dichlorophen)、野燕枯(difenzoquat)、野燕枯甲基磺酸酯(difenzoquat methylsulfonate)、氟联苯菌(flumetover)、乙膦钙(fosetyl calcium)、乙膦钠(fosetyl sodium)、人间霉素(irumamycin)、纳他霉素(natamycin)、酞菌酯(nitrothal-isopropyl)、奥克斯莫卡宾(oxamocarb)、普罗帕诺欣钠(propanosine sodium)、硝吡咯菌素(pyrrolnitrin)、异丁乙氧喹啉(tebufloquin)、甲磺菌胺(tolnifanide)、氰菌胺(zaliramide)、Algophase、拌种灵(Amicarthiazol)、氟噻唑吡乙酮(Oxathiapiprolin)、代森联锌(metiram zinc)、苯噻硫氰(benthiazol)、水杨菌胺(trichlamide)、优康唑(uniconazole)、米多霉素(mildiomycin)、氧代奋欣(Oxyfenthiin)、picarbutrazox、fenpicoxamid、dichlobentiazox、quinofumelin。
以下示出可以与本发明的有害生物防除剂混用或并用的植物调节剂的具体例。
1-甲基环丙烯、2,3,5-三碘苯甲酸、IAA、IBA、MCPA、MCPB、4-CPA、5-氨基乙酰丙酸盐酸盐、6-苄基氨基嘌呤、脱落酸(abscisic acid)、四烯雌酮盐酸盐(aviglycinehydrochloride)、嘧啶醇、地乐胺(butotralin)、碳酸钙、氯化钙、甲酸钙、过氧化钙、石灰硫、硫酸钙、矮壮素(Chlormequat chloride)、氯苯胺灵(chloropropham)、氯化胆碱、调果酸(cloprop)、氨基氰(cyanamide)、环丙酰草胺(cyclanilide)、丁酰肼(daminozide)、癸醇、2,4-滴丙酸(dichloroprop)、调呋酸(dikegulac)、噻节因(dimethipin)、敌草快(diquat)、乙烯利(ethephon)、吲熟酯(ethyclozate)、氟节胺(flumetralin)、调嘧醇(flurprimidol)、氯吡脲(forchlorfenuron)、赤霉素A(gibberellin A)、赤霉素A3(gibberellin A3)、霉灵(hymexazol)、抗倒胺(inabenfide)、稻瘟灵(isoprothiolane)、激动素(kinetin)、马来酰肼、氟磺酰草胺(mefluidide)、甲哌(mepiquat chloride)、氧化型谷胱甘肽、多效唑(paclobutrazol)、二甲戊灵(pendimethalin)、调环酸钙(prohexadione calcium)、茉莉酸丙酯(prohydrojasmon)、吡草醚(pyraflufen ethyl)、杀雄啉(cintofen)、1-萘乙酸钠、氰酸钠、链霉素(streptomycin)、噻苯隆(thidiazuron)、抑芽唑(triapenthenol)、脱叶磷(tribufos)、抗倒酯(trinexapac ethyl)、烯效唑P(uniconazole P)、1-萘乙酰胺。
为了容易与上述的杀虫剂等混用或并用,优选制备将本发明的有害生物防除剂和杀虫剂等混合而得的组合物。
这样的组合物为包含含有选自式(I)表示的化合物或其盐中的至少一个作为有效成分的有害生物防除剂以及选自杀虫·杀螨剂、杀线虫剂、杀土壤害虫剂、杀菌剂中的至少一种有效成分的组合物。
更详细而言,所述组合物包含含有选自式(I)表示的化合物或其盐中的至少一个作为有效成分的有害生物防除剂、以及选自(1)乙酰胆碱酯酶抑制剂、(2)GABA-激动性氯离子通道拮抗剂、(3)钠通道调节剂、(4)烟碱型乙酰胆碱受体激动剂、(5)烟碱型乙酰胆碱受体变构调节剂、(6)氯离子通道活化剂、(7)保幼激素类似物、(8)其它非特异性抑制剂、(9)同翅目选择性摄食抑制剂、(10)螨类繁殖抑制剂、(11)源自微生物的昆虫中肠内膜破坏剂、(12)线粒体ATP生物合成酶抑制剂、(13)氧化磷酸化解偶联剂、(14)烟碱型乙酰胆碱受体通道阻断剂、(15)壳多糖合成抑制剂、(16)双翅目蜕皮干扰剂、(17)蜕皮激素受体激动剂、(18)章鱼胺受体激动剂、(19)线粒体电子传递系统复合体III抑制剂、(20)线粒体电子传递系统复合体I抑制剂、(21)电压依赖性钠通道阻滞剂、(22)乙酰基CoA羧化酶抑制剂、(23)线粒体电子传递系统复合体IV抑制剂、(24)线粒体电子传递系统复合体II抑制剂、(25)兰尼碱受体调节剂、(26)混合功能氧化酶抑制剂化合物、(27)蛛毒素受体激动剂、(28)其它药剂(作用机理未知)中的至少一个有效成分。
〔体外寄生虫防除剂〕
作为本发明的外部寄生虫防除剂的处理对象的宿主动物,可举出狗、猫等宠物动物;宠物鸟;牛、马、猪、绵羊等家畜;家禽等温血动物。除此以外,可以举出鲑鱼、鳟鱼、河豚、鲤鱼、金鱼等鱼类;蜜蜂、锹形虫、独角仙等昆虫类。
本发明的外部寄生虫防除剂可以通过公知的兽医学方法(局部、口服、非口服或皮下给药)进行施用。作为该方法,可举出通过片剂、胶囊、混入饲料等向动物口服给药的方法;通过浸渍液、栓剂、注射(肌内、皮下、静脉内、腹腔内等)等向动物给药的方法;通过喷雾、浇泼(pour on)、点涂(spot on)等将油性或水性液体制剂局部给药的方法;在树脂中混入外部寄生虫防除剂,将上述混炼物成型为项圈、耳标等合适的形状,将其佩戴在动物身上,从而局部给药的方法等。
体外寄生虫寄生于宿主动物、特别是温血动物、鱼类的体内和皮肤。详细而言,寄生在宿主动物的后背、腋下、下腹部、大腿的内侧部等而从动物获得血液或皮屑等营养源从而得以生息。作为外部寄生虫,可举出螨类、虱类、蚤类、蚊子、角蝇、麻蝇、鲸虱等。以下示出可由本发明的体外寄生虫防除剂来防除的体外寄生虫的具体例。
(1)螨类(Acari)
皮刺螨科(Dermanyssidae)的螨、巨刺螨科(Macronyssidae)的螨、厉螨科(Laelapidae)的螨、瓦螨科(Varroidae)的螨、软蜱科(Argasidae)的螨、硬蜱科(Ixodidae)的螨、痒螨科(Psoroptidae)的螨、疥螨科(Sarcoptidae)的螨、膝螨科(Knemidokoptidae)的螨、蠕形螨科(Demodixidae)的螨、恙螨科(Trombiculidae)的螨、锹形虫类等昆虫寄生性螨。
(2)虱目(Phthiraptera)
盲虱科(Haematopinidae)的虱、颚虱科(Linognathidae)的虱、短角鸟虱科(Menoponidae)的鸟虱、长角鸟虱科(Philopteridae)的鸟虱、兽鸟虱科(Trichodectidae)的鸟虱。
(3)将蚤目(Siphonaptera)
蚤科(Pulicidae)的蚤,例如,犬蚤属(Ctenocephalides spp.)的犬蚤(Ctenocephalides canis)、猫蚤(Ctenocephalides felis);
潜蚤科(Tungidae)的蚤、角叶蚤科(Ceratophyllidae)的蚤、细蚤科(Leptopsyllidae)的蚤。
(4)半翅目(Hemiptera)。
(5)双翅目(Diptera)的害虫
蚊科(Culicidae)的蚊、蚋科(Simuliidae)的蚋、蠓科(Ceratopogonidae)的蠓、虻科(Tabanidae)的虻、蝇科(Muscidae)的蝇、舌蝇科(Glossinidae)的舌蝇、麻蝇科的麻蝇、虱蝇科(Hippoboscidae)的蝇、丽蝇科(Calliphoridae)的蝇、狂蝇科(Oestridae)的蝇。
〔其他有害生物的防除剂〕
以下示出其具体例。
(1)膜翅目(Hymenoptera)的害虫
三节叶蜂科(Argidae)的蜂、瘿蜂科(Cynipidae)的蜂、松叶蜂科(Diprionidae)的蜂、蚁科(Formicidae)的蚂蚁、蚁蜂科(Mutillidae)的蜂、胡蜂科(Vespidae)的蜂。
(2)其他害虫
蟑螂类(Blattodea)、白蚁类(termite)、蜘蛛类(Araneae)、蜈蚣类(cetipede)、马陆类(millipede)、甲壳类(crustacea)、臭虫(Cimex lectularius)。
〔制剂处方〕
虽然示出若干本发明的有害生物防除剂、杀虫或杀螨剂、或者缨翅目害虫防除剂的制剂处方,但添加物和添加比例不应限定于这些制剂实施例,可以在大范围内变化。制剂处方中的份表示重量份。
以下示出农业园艺用和水稻用的制剂处方。
(制剂例1:水合剂)
(制剂例2:乳剂)
(制剂例3:粒剂)
(制剂例4:粒剂)
(制剂例5:悬浮剂)
以下示出体外寄生虫防除剂的制剂处方。
(制剂例6:颗粒剂)
(制剂例7:注入剂)
(制剂例8:浇泼(pour-on)剂)
(制剂例9:点涂剂)
(制剂例10:喷涂剂)
接下来,示出化合物实施例,对本发明进行更具体的说明。但是,本发明不受以下的化合物实施例的任何限制。
〔参考例1〕
1-(叔丁基)-3-(6,11-二氢二苯并[b,e]氧杂环庚烷-11-基)硫脲〔1-(tert-butyl)-3-(6,11-dihydrodibenzo[b,e]oxepin-11-yl)thiourea〕的合成
按照Chemical and Pharmaceutical Bulletin,1991,39,0,2564.记载的方法来合成6,11-二氢二苯并[b,e]氧杂环庚烷-11-醇。
将6,11-二氢二苯并[b,e]氧杂环庚烷-11-醇(4.2g)溶解于二氯甲烷(100mL)后添加1-(叔丁基)硫脲(2.8g)和三氟甲磺酸铝(0.10g)。搅拌25小时后馏去反应溶剂,然后利用硅胶柱色谱进行精制而得到目标物6.1g。
熔点:167-168℃
〔参考例2〕
N-叔丁基-N-(6,11-二氢二苯并[b,e]氧杂环庚烷-11-基)甲烷二亚胺〔N-tert-butyl-N-(6,11-dihydrodibenzo[b,e]oxepin-11-yl)methanediimine〕的合成
向参考例1中得到的硫脲(6.7g)的乙腈溶液(54ml)中加入三乙胺(6.8ml)和2-氯-1-甲基吡啶碘化物(6.3g),在室温下搅拌4小时。过滤不溶物,将滤液减压浓缩。利用硅胶柱色谱对残渣进行精制,得到目标物4.7g。
1H-NMR(CDCl3)δppm:1.06(s,9H),4.94(d,1H),5.51(s,1H),5.87(d,1H),6.90(m,2H),7.20(m,1H),7.33(m,5H).
〔实施例1〕
N-(叔丁基)-2’-甲基-2’6H-螺[二苯并[b,e]氧杂环庚烷-11,5’1,2,4]二唑]-3’胺〔N-(tert-butyl)-2’-methyl-2’6H-spiro[dibenzo[b,e]oxepine-11,5’1,2,4]oxadiazol]-3’amine〕(化合物编号:a-11)的合成
向参考例2中得到的碳二亚胺(4.7g)的乙腈溶液(53ml)中加入N-甲基羟胺盐酸盐(1.6g)和三乙胺(2.6ml),在室温下搅拌3小时。将反应液减压浓缩后,加入二氯甲烷(80ml)和二氧化锰(1.4g),室温下搅拌4小时。对反应液进行硅藻土过滤,将不溶物用乙酸乙酯清洗,减压浓缩滤液。将粗产物用己烷清洗,得到目标物4.6g。
1H-NMR(CDCl3)δppm:1.58(s,9H),2.82(s,3H),3.78(s,1H),5.05(d,1H),6.02(d,1H),6.83(d,1H),6.90(t,1H),7.18(t,1H),7.28(m,3H),7.77(m,2H).
〔实施例2〕
N-(叔丁基)-N-乙基-2’-甲基-2’H,6H-螺[二苯并[b,e]氧杂环庚烷-11,5’-[1,2,4]二唑]-3’-胺〔N-(tert-butyl)-N-ethyl-2’-methyl-2’H,6H-spiro[dibenzo[b,e]oxepine-11,5’-[1,2,4]oxadiazol]-3’-amine〕(化合物编号:a-10)的合成
在0℃下向实施例1中得到的胺(4.6g)的DMF溶液(45ml)中加入氢化钠(0.8g)搅拌30分钟。加入碘乙烷(2.1ml)在0℃下搅拌3小时。将反应液加入到冰水中,用乙酸乙酯进行萃取,将有机层用饱和食盐水进行清洗,用无水硫酸镁使其干燥,进行过滤,接着进行减压浓缩。将得到的粗产物用硅胶柱色谱进行精制,得到目标物2.5g。
1H-NMR(CDCl3)δppm:1.17(t,3H),1.62(s,9H),2.78(s,3H),3.36(q,2H),5.12(d,1H),6.02(d,1H),6.85(m,2H),7.19(t,1H),7.28(m,3H),7.77(m,2H).
〔参考例3〕
1-(叔丁基)-3-(10,11-二氢二苯并[b,f]氧杂环庚烷-10-基)硫脲〔1-(tert-butyl)-3-(10,11-dihydrodibenzo[b,f]oxepin-10-yl)thiourea〕的合成
按照Angewandte Chemie-International Edition,2015,54,17,5049.中记载的方法来合成10,11-二氢-二苯并[b,f]氧杂环庚烷-10-胺(10,11-dihydro-dibenz[b,f]oxepin-10-ylamine)。
将10,11-二氢-二苯并[b,f]氧杂环庚烷-10-胺(0.59g)溶解于四氢呋喃(10ml)后,加入异硫氰酸叔丁酯(0.55g)。在室温下搅拌17小时后,馏去溶剂。利用硅胶柱色谱进行精制,由此得到目标物0.10g。
〔实施例3〕
N-(叔丁基)-2’-甲基-2’H,11H-螺[二苯并[b,f]氧杂环庚烷-10,5’-[1,2,4]二唑]-3’-胺〔N-(tert-butyl)-2’-methyl-2’H,11H-spiro[dibenzo[b,f]oxepine-10,5’-[1,2,4]oxadiazol]-3’-amine〕(化合物编号:a-22)的合成
将参考例3中得到的硫脲(0.10g)溶解于乙腈(3ml)后,加入三乙胺(88mg)和2-氯-1-甲基吡啶碘化物(0.11g),在室温下搅拌4小时。向反应液中加入N-甲基羟胺盐酸盐(48mg)和三乙胺(58mg),室温下搅拌18小时。将反应液减压浓缩后,利用硅胶柱色谱进行精制,由此得到目标物0.06g。
〔参考例4〕
2’-甲基-2’H,6H-螺[二苯并[b,e]氧杂环庚烷-10,5’-[1,2,4]二唑]-3’-胺〔2’-methyl-2’H,6H-spiro[dibenzo[b,e]oxepine-11,5’-[1,2,4]oxadiazol]-3’-amine〕的合成
将二苯并[b,e]氧杂环庚烷-11(6H)-酮(3.2g)溶解于二氯甲烷(30ml)后加入四氯化钛(5.7g)。滴加N,N-双(三甲基甲硅烷基)碳二亚胺(5.6g)后,在室温下搅拌1小时后加入水而使反应停止。用二氯甲烷对有机层进行萃取后,减压馏去溶剂。将得到的粗产物溶解于四氢呋喃(30ml)后加入N-甲基羟胺盐酸盐(2.5g)和三乙胺(3.0g),在60℃下搅拌1小时。通过过滤除去固体物质后,减压馏去溶剂,利用硅胶柱色谱进行精制,由此得到目标物2.9g。
1H-NMR(CDCl3)δppm:2.98(s,3H),5.22(d,1H),5.82(d,1H),6.87(d,1H),6.94(m,1H),7.24-7.30(m,4H),7.76-7.82(m,2H).
〔实施例4〕
N-(叔丁基)-2’-甲基-2’H,6H-螺[二苯并[b,e]氧杂环庚烷-11,5’-[1,2,4]二唑]-3’-胺〔N-(tert-butyl)-2’-methyl-2’H,6H-spiro[dibenzo[b,e]oxepine-11,5’-[1,2,4]oxadiazol]-3’-amine〕(化合物编号:a-11)的合成
向参考例4中得到的胺(0.1g)的1,2-二氯乙烷溶液(1.8ml)中加入叔丁基2,2,2-三氯乙酰亚胺酯(0.13ml)和三氟化硼乙醚络合物(46μl),在加热回流下搅拌2小时。将反应液加入到饱和碳酸氢钠水溶液中,用乙酸乙酯进行萃取,用无水硫酸镁使其干燥,进行过滤,接着进行减压浓缩。将得到的粗产物利用硅胶柱色谱进行精制,得到目标物2.5mg(收率2%)。
1H-NMR(CDCl3)δppm:1.58(s,9H),2.82(s,3H),3.78(s,1H),5.05(d,1H),6.02(d,1H),6.83(d,1H),6.90(t,1H),7.18(t,1H),7.28(m,3H),7.77(m,2H).
〔参考例5〕
1-(叔丁基)-3-(6-氟-2,2-二甲基苯并二氢吡喃-4-基)硫脲〔1-(tert-butyl)-3-(6-fluoro-2,2-dimethylchroman-4-yl)thiourea〕的合成
向6-氟-2,2-二甲基苯并二氢吡喃-4-胺(3.2g)的二氯甲烷溶液(54ml)中加入异硫氰酸叔丁酯(1.9g),在加热回流下搅拌6小时。将反应液浓缩,将得到的固体用醚进行清洗,得到目标物3.9g。
〔参考例6〕
2-(叔丁基)-3-(6-氟-2,2-二甲基苯并二氢吡喃-4-基)-1-羟基-1-甲基胍〔2-(tert-butyl)-3-(6-fluoro-2,2-dimethylchroman-4-yl)-1-hydroxy-1-methylguanidine〕的合成
向参考例5中得到的硫脲(1.84g)的乙腈溶液(20ml)中加入三乙胺(2.0ml)和2-氯-1-甲基吡啶碘化物(1.8g),在室温下搅拌18小时。向反应液中加入N-甲基羟胺盐酸盐(0.6g)和吡啶(1.2ml),在室温下搅拌14小时。将反应液加入到水中,用乙酸乙酯进行萃取,将有机层用饱和食盐水进行清洗,用无水硫酸镁使其干燥,进行过滤,接着进行减压浓缩。将得到的粗产物利用硅胶柱色谱进行精制,得到目标物0.4g。
〔实施例5〕
N-叔丁基-6-氟-2,2,2’-三甲基-2’H-螺[苯并二氢吡喃-4,5’-[1,2,4]二唑]-3’-胺〔N-(tert-butyl)-6-fluoro-2,2,2’-trimethyl-2’H-spiro[chromane-4,5’-[1,2,4]oxadiazol]-3’-amine〕(化合物编号:a-20)的合成
向参考例6中得到的胍(0.4g)的氯仿溶液(10ml)中加入二氧化锰(0.4g),室温下搅拌3天。对反应液进行硅藻土过滤,将不溶物用乙酸乙酯进行清洗,减压浓缩滤液。将得到的粗产物利用硅胶柱色谱进行精制,得到目标物0.15g。
m.p.95~96℃
m.p.113-114℃
m.p.154-156℃
m.p.130-132℃
1H-NMR(400MHz,CDCl3)δppm:1.67(s,9H),2.80(s,3H),3.24(s,3H),4.69(d,2H),5.15(d,1H),5.99(d,1H),6.82-6.88(m,2H),7.18(m,1H),7.25-7.30(m,3H),7.73(m,1H).
m.p.175~177℃
m.p.:148~150℃
m.p.:163~166℃
m.p.:181~183℃
m.p.:85~86℃
m.p.:196~198℃
1H-NMR(400MHz,CDCl3)δppm:1.13(t,3H),1.52(s,9H),2.75(s,3H),3.10(m,2H),3.32(q,2H),3.69(m,2H),7.09-7.13(m,6H),7.78-7.81(m,2H).
m.p.:130~131℃
m.p.:68~71℃
m.p.:149~151℃
m.p.:168~170℃
m.p.:144~146℃
1H-NMR(400MHz,CDCl3)δppm:1.09(t,3H),1.63(s,9H),2.49(s,3H),3.27(q,2H),7.10(s,2H),7.35(m,6H),7.97(d,2H).
m.p.:156~158℃
m.p.:94~97℃
m.p.:94.8~97.5℃
m.p.:132~135℃
m.p.:122~124℃
m.p.:82~84℃
m.p.:118~120℃
m.p.:85~87℃
m.p.:100~102℃
m.p.:143~145℃
m.p.:151~153℃
m.p.:107~109℃
m.p.:142~143℃
1H-NMR(400MHz,CDCl3)δppm:1.40(s,9H),3.02(s,3H),3.27(d,1H),3.40(s,3H),3.56(d,1H),6.91(t,1H),7.01(m,1H),7.08-7.25(m,5H),7.42(d,1H).
1H-NMR(400MHz,CDCl3)δppm:1.40(s,9H),3.04(s,3H),3.72(d,1H),3.84(d,1H),7.09-7.15(m,3H),7.19(m,1H),7.32(d,1H),7.41(d,1H),7.48-7.53(m,2H).
1H-NMR(400MHz,CDCl3)δppm:1.40(s,9H),2.89(s,3H),3.07(s,3H),3.35(d,1H),3.40(s,3H),3.55(d,1H),6.92(t,1H),7.01-7.25(m,6H),7.42(d,1H).
m.p.:94~96℃
m.p.:153~155℃
m.p.:141~143℃
m.p.:75~77℃
m.p.:149~151℃
m.p.:67~69℃
m.p.:148~150℃
m.p.:159~161℃
m.p.:133~135℃
表1中的Me表示甲基,Et表示乙基,n-Pr表示正丙基,t-Bu表示叔丁基,Bn表示苄基,Ac表示乙酰基,BOC表示叔丁氧基羰基,Ph表示苯基,c-Pr表示环丙基。
[表1]
[表2]
[表3]
[表4]
[表5]
[表6]
[表7]
以下示出上述的化合物中性状为非晶或粘稠油状的化合物的NMR数据。
化合物编号(b-22):1H-NMR(400MHz,CDCl3)δppm:1.59(s,9H),2.41(s,3H),2.82(s,3H),3.83(s,1H),5.05(d,1H),5.99(d,1H),6.79(d,1H),7.15(d,1H),7.31(m,3H),7.77(m,2H).
化合物编号(b-27):1H-NMR(400MHz,CDCl3)δppm:1.02(t,3H),1.31(t,3H),1.60(s,9H),2.87(q,2H),3.15(q,2H),5.01(d,1H),6.15(d,1H),6.81(m,2H),7.15(dd,1H),7.27(m,3H),7.72(m,2H).
化合物编号(b-28):1H-NMR(400MHz,CDCl3)δppm:1.17(t,3H),1.62(s,9H),2.77(s,3H),3.35(q,2H),4.24(q,2H),5.10(d,1H),6.05(d,1H),6.37(d,1H),6.50(d,1H),7.27(m,3H),7.72(m,2H).
化合物编号(b-30):1H-NMR(400MHz,CDCl3)δppm:1.17(t,3H),1.59(s,9H),2.78(s,3H),3.37(q,2H),5.18(d,1H),6.00(d,1H),7.20(m,2H),7.29(m,2H),7.47(d,1H),7.72(m,2H).
化合物编号(b-33):1H-NMR(400MHz,CDCl3)δppm:1.59(s,9H),2.85(s,3H),3.82(s,1H),4.98(d,1H),5.84(d,1H),7.00(t,1H),7.12(m,1H),7.29-7.40(m,8H),7.81(m,2H).
化合物编号(b-35):1H-NMR(400MHz,CDCl3)δppm:1.16(t,3H),1.61(s,9H),2.40(s,3H),2.81(s,3H),3.32(q,2H),5.05(d,1H),6.01(d,1H),6.70(d,1H),6.80(dd,1H),7.28(m,3H),7.68(d,1H),7.75(dd,1H).
化合物编号(b-40):1H-NMR(400MHz,CDCl3)δppm:1.18(t,3H),1.59(s,9H),2.60(s,3H),2.82(s,3H),3.38(q,2H),5.23(dd,1H),6.11(dd,1H),7.04(d,1H),7.18(dd,1H),7.29(m,3H),7.78(d,1H),7.95(dd,1H).
化合物编号(b-50):1H-NMR(400MHz,CDCl3)δppm:1.59(s,9H),2.74(s,3H),2.90(s,3H),5.11(d,1H),6.07(d,1H),6.68(m,2H),7.30(m,3H),7.72(m,1H),7.80(d,1H).
化合物编号(b-51):1H-NMR(400MHz,CDCl3)δppm:1.15(t,3H),1.60(s,9H),2.77(s,3H),3.35(q,2H),5.15(d,1H),6.06(d,1H),6.70(m,2H),7.30(m,3H),7.72(m,1H),7.79(d,1H).
化合物编号(b-56):1H-NMR(400MHz,CDCl3)δppm:1.15(t,3H),1.61(s,9H),2.20(s,3H),2.79(s,3H),3.35(q,2H),5.15(d,1H),5.96(d,1H),6.73(d,1H),6.96(m,1H),7.28(m,3H),7.56(d,1H),7.73(m,1H).
化合物编号(b-58):1H-NMR(400MHz,CDCl3)δppm:1.61(s,9H),2.77(s,3H),3.96(m,2H),5.11(d,2H),5.19(d,1H),5.90(m,1H),6.03(d,1H),6.83(m,2H),7.18(t,1H),7.25-7.30(m,3H),7.73(m,2H).
化合物编号(b-59):1H-NMR(400MHz,CDCl3)δppm:0.81(t,3H),1.58(m,2H),1.61(s,9H),2.77(s,3H),3.21(m,2H),5.13(d,1H),6.03(d,1H),6.83(m,2H),7.18(t,1H),7.25-7.30(m,3H),7.73(m,2H).
化合物编号(b-63):1H-NMR(400MHz,CDCl3)δppm:1.61(s,9H),2.84(s,3H),3.82(s,3H),5.15(d,1H),6.11(d,1H),6.84(d,1H),7.30(m,3H),7.73(m,1H),7.82(dd,1H),8.59(d,1H).
化合物编号(b-67):1H-NMR(400MHz,CDCl3)δppm:1.67(s,9H),1.73(s,3H),2.96(s,3H),4.97(d,1H),6.18(d,1H),6.91(m,2H),7.30(m,4H),7.69(d,1H),7.81(d,1H).
化合物(b-70):1H-NMR(400MHz,CDCl3)δppm:0.94(t,3H),1.17(t,3H),1.56(m,6H),2.05(q,1H),2.21(q,1H),2.78(s,3H),3.31(q,2H),5.05(d,1H),6.08(d,1H),6.83(m,2H),7.15(t,1H),7.25(t,3H),7.75(m,2H).
化合物(b-76):1H-NMR(400MHz,CDCl3)δppm:2.75(s,3H),5.17(d,1H),5.85(d,1H),6.85(m,1H),6.92(m,1H),7.21-7.32(m,8H),7.61(m,1H),7.66(m,1H).
化合物(b-77):1H-NMR(400MHz,CDCl3)δppm:2.74(s,3H),5.15(d,1H),5.86(d,1H),6.83(m,1H),6.91(m,1H),7.15-7.20(m,4H),7.27-7.35(m,4H),7.60(m,1H),7.64(m,1H).
化合物(b-83):1H-NMR(400MHz,CDCl3)δppm:1.16(t,3H),1.54(s,9H),2.81(s,3H),3.32(q,2H),5.25(d,1H),5.60(d,1H),6.37-6.40(m,2H),7.25(m,1H),7.29-7.30(m,2H),7.86(m,1H).
化合物(b-95):1H-NMR(400MHz,CDCl3)δppm:1.15(t,3H),1.60(s,9H),2.79(s,3H),3.33(q,2H),5.33(d,1H),6.05(d,1H),6.75(t,1H),7.25-7.28(m,3H),7.46(m,1H),7.70-7.75(m,2H).
化合物(b-97):1H-NMR(400MHz,CDCl3)δppm:1.16(t,3H),1.61(s,9H),2.19(s,3H),2.78(s,3H),3.33(q,2H),5.16(d,1H),5.97(d,1H),6.79(t,1H),7.07(m,1H),7.20-7.26(m,3H),7.59(m,1H),7.75(m,1H).
化合物(b-107):1H-NMR(400MHz,CDCl3)δppm:1.16(t,3H),1.60(s,9H),2.63(m,2H),2.74(s,3H),2.89(s,3H),5.10(d,1H),5.94(d,1H),6.64(t,1H),7.09(m,1H),7.16-7.26(m,3H),7.59(m,1H),7.76(m,1H).
化合物(b-109):1H-NMR(400MHz,CDCl3)δppm:1.15-1.17(m,6H),1.61(s,9H),2.53(q,2H),2.78(s,3H),3.34(q,2H),5.08(d,1H),6.01(d,1H),6.66(s,1H),6.73(d,1H),7.24-7.26(m,3H),7.65(d,1H),7.74(m,1H).
化合物(b-110):1H-NMR(400MHz,CDCl3)δppm:1.58(s,9H),2.81(s,3H),3.72(s,3H),5.01(d,1H),6.03(d,1H),6.37(d,1H),6.45(m,1H),7.25-7.28(m,3H),7.68-7.70(m,2H).
化合物(b-111):1H-NMR(400MHz,CDCl3)δppm:1.60(s,9H),2.74(s,3H),2.90(s,3H),3.72(s,3H),5.02(d,1H),6.04(d,1H),6.36(d,1H),6.44(m,1H),7.25-7.28(m,3H),7.66(d,1H),7.73(m,1H).
化合物(b-112):1H-NMR(400MHz,CDCl3)δppm:1.16(t,3H),1.61(s,9H),2.77(s,3H),3.34(q,2H),3.72(s,3H),5.04(d,1H),6.04(d,1H),6.36(d,1H),6.46(m,1H),7.25-7.28(m,3H),7.67(d,1H),7.73(m,1H).
化合物(b-138):1H-NMR(400MHz,CDCl3)δppm:1.34(t,3H),1.59(s,9H),2.24(s,3H),2.63(m,2H),2.74(s,3H),5.11(d,1H),5.98(d,1H),6.64(t,1H),6.79(m,1H),7.16-7.26(m,3H),7.57(m,1H),7.76(m,1H).
化合物(b-139):1H-NMR(400MHz,CDCl3)δppm:1.21(t,3H),1.61(s,9H),1.89(m,2H),2.21(s,3H),2.73(m,2H),2.71(s,3H),5.15(d,1H),5.81(d,1H),6.61(d,1H),6.78(m,1H),7.11-7.31(m,3H),7.61(m,1H),7.88(m,1H).
化合物(b-141):1H-NMR(400MHz,CDCl3)δppm:0.91(t,3H),1.16(t,3H),1.53(s,6H),2.03(m,1H),2.16(m,1H),2.79(s,3H),3.31(m,2H),5.24(d,1H),6.03(d,1H),6.77(m,1H),7.01(m,1H),7.25-7.29(m,3H),7.50(m,1H),7.72(m,1H).
化合物(b-143):1H-NMR(400MHz,CDCl3)δppm:0.92(t,3H),1.16(t,3H),1.53(s,6H),2.18(s,3H),2.78(s,3H),3.31(q,2H),5.11(d,1H),6.02(d,1H),6.79(t,1H),7.05(m,1H),7.20-7.26(m,3H),7.58(m,1H),7.72(m,1H).
化合物(b-149):1H-NMR(400MHz,CDCl3)δppm:1.07(s,9H),1.18(t,3H),1.65(s,3H),1.68(s,3H),2.12(d,1H),2.30(d,1H),2.78(s,3H),3.34(q,2H),5.09(d,1H),6.07(d,1H),6.80-6.86(m,2H),7.16(m,1H),7.25-7.28(m,3H),7.76-7.79(m,2H).
化合物(b-161):1H-NMR(400MHz,CDCl3)δppm:1.60(s,9H),2.77(s,3H),2.91(s,3H),5.09(d,1H),6.98(d,1H),6.75(d,1H),7.10(m,1H),7.24-7.28(m,3H),7.72-7.75(m,2H).
化合物(b-163):1H-NMR(400MHz,CDCl3)δppm:0.94(t,3H),1.18(t,3H),1.56(m,6H),2.15(m,2H),2.80(s,3H),3.34(q,2H),5.06(d,1H),6.03(d,1H),6.75(d,1H),7.10(m,1H),7.25-7.30(m,3H),7.69-7.72(m,2H).
化合物(b-165):1H-NMR(400MHz,CDCl3)δppm:84-03101.15-1.18(m,6H),1.61(s,9H),2.61(m,2H),2.77(s,3H),3.33(q,2H),5.14(d,1H),5.95(d,1H),6.84(m,1H),7.08(m,1H),7.21-7.26(m,3H),7.60(m,1H),7.75(m,1H).
化合物(b-167):1H-NMR(400MHz,CDCl3)δppm:84-03120.93(t,3H),1.15-1.18(m,6H),1.53(s,6H),2.08(m,1H),2.10(m,1H),2.62(m,2H),2.77(s,3H),3.32(q,2H),5.09(d,1H),5.98(d,1H),6.83(t,1H),7.08(m,1H),7.21-7.26(m,3H),7.60(m,1H),7.73(m,1H).
化合物(b-174):1H-NMR(400MHz,CDCl3)δppm:0.99(t,3H),1.56(s,6H),2.18(q,2H),2.27(s,3H),2.80(s,3H),2.93(s,3H),5.07(d,1H),6.09(d,1H),6.70(s,1H),6.73(d,1H),7.29(m,3H),7.67(d,1H),7.77(m,1H).
化合物(b-175):1H-NMR(400MHz,CDCl3)δppm:1.00(t,3H),1.41(m,2H),1.55(s,6H),2.09(q,2H),2.24(s,3H),2.77(s,3H),2.90(s,3H),5.06(d,1H),6.05(d,1H),6.67(s,1H),6.71(d,1H),7.27(m,3H),7.64(d,1H),7.73(m,1H).
化合物(b-176):1H-NMR(400MHz,CDCl3)δppm:0.87(t,3H),1.16(t,3H),1.54(s,6H),2.13(m,2H),2.22(s,3H),2.78(s,3H),3.32(m,2H),5.04(d,1H),6.04(d,1H),6.64(s,1H),6.69(d,1H),7.25(m,3H),7.61(d,1H),7.70(m,1H).
化合物(b-178):1H-NMR(400MHz,CDCl3)δppm:0.94(t,3H),1.53(s,6H),2.09-2.14(m,2H),2.76(s,3H),2.89(s,3H),5.06(d,1H),6.05(d,1H),7.81-7.83(m,2H),7.26(m,3H),7.67-7.70(m,2H).
化合物(b-179):1H-NMR(400MHz,CDCl3)δppm:0.97(t,3H),1.52(s,6H),2.03-2.06(m,2H),2.75(s,3H),2.88(s,3H),5.04(d,1H),6.03(d,1H),6.82(m,2H),7.24-7.27(m,3H),7.66-7.71(m,2H).
化合物(b-180):1H-NMR(400MHz,CDCl3)δppm:0.91(t,3H),1.16(t,3H),1.53(s,3H),1.55(s,3H),2.00-2.05(m,1H),2.17-2.21(m,2H),2.78(s,3H),3.32(q,2H),5.09(d,1H),6.05(d,1H),6.82-6.84(m,2H),7.27(m,3H),7.66-7.71(m,2H).
化合物(b-194):1H-NMR(400MHz,CDCl3)δppm:1.15(t,3H),1.60(s,9H),2.53(q,2H),2.75(s,3H),2.89(s,3H),5.04(d,1H),6.02(d,1H),6.66(s,1H),6.73(d,1H),7.25(m,3H),7.65(d,1H),7.73(m,1H).
表2中的Me表示甲基,Et表示乙基,t-Bu表示叔丁基,Bn表示苄基,Ph表示苯基。
[表8]
[表9]
以下示出上述的化合物中的性状为非晶或者粘稠油状的化合物的NMR数据。
化合物编号(c-23):1H-NMR(400MHz,CDCl3)δppm:1.20(t,3H),1.41(m,15H),2.15(d,1H),2.33(d,1H),3.01(s,3H),3.31(q,2H),3.71(s,3H),6.71(d,1H),6.82(m,2H).
化合物编号(c-26):1H-NMR(400MHz,CDCl3)δppm:1.39(m,15H),2.11(d,1H),2.23(d,1H),2.91(s,3H),4.45(q,2H),6.76(d,1H),6.81(d,1H),7.06(d,1H),7.36(m,5H).
化合物(c-34):1H-NMR(400MHz,CDCl3)δppm:1.45(s,9H),2.26(m,1H),2.73(m,1H),2.86(s,3H),2.96(s,3H),4.81(m,1H),7.07-7.15(m,3H),7.25-7.50(m,5H).
表3中的Me表示甲基,Et表示乙基,t-Bu表示叔丁基。
[表10]
以下示出上述的化合物中的性状为非晶的化合物的NMR数据。
化合物编号(d-3):1H-NMR(400MHz,CDCl3)δppm:0.87(t,3H),1.69(s,9H),2.74(s,2H),3.38(q,2H),7.24-7.27(m,4H),7.46-7.49(m,2H),7.79-7.81(m,2H).
化合物编号(d-6):1H-NMR(400MHz,CDCl3)δppm:1.23(t,3H),1.30(t,3H),1.67(s,9H),2.65(q,2H),2.76(s,3H),2.83(q,2H),3.90(s,1H),7.04(s,1H),7.26-7.28(m,2H),7.52(m,1H),7.57(,1H),7.79(m,1H).
化合物(d-9):1H-NMR(400MHz,CDCl3)δppm:1.18-1.25(m,6H),1.29(t,3H),1.70(s,9H),2.63(q,2H),2.72(s,3H),2.83(q,2H),3.38(q,2H),7.01(s,1H),7.23-7.25(m,2H),7.49(m,1H),7.57(s,1H),7.77(m,1H).
表4中的Me表示甲基,Et表示乙基,n-Pr表示正丙基,t-Bu表示叔丁基。
[表11]
[表12]
以下示出上述的化合物中的性状为非晶的化合物的NMR数据。
化合物编号(e-6):1H-NMR(400MHz,CDCl3)δppm:1.13(t,3H),1.57(s,9H),2.76(s,3H),3.13(m,2H),3.32(q,2H),3.40(m,1H),3.86(m,1H),6.90(m,1H),7.10-7.17(m,4H),7.64(d,1H),7.76(d,1H).
化合物编号(e-16):1H-NMR(400MHz,CDCl3)δppm:0.87(t,3H),1.14(t,3H),1.52(s,6H),2.12(q,2H),2.74(s,3H),3.05(m,2H),3.29(q,2H),3.75(m,2H),7.08-7.16(m,6H),7.76-7.78(d,2H).
化合物编号(e-32):1H-NMR(400MHz,CDCl3)δppm:1.05(s,9H),1.62(s,6H),2.20(s,2H),2.71(s,3H),2.89(s,3H),3.08(m,2H),3.72(m,2H),7.08-7.12(m,6H),7.82(m,2H).
化合物编号(e-33):1H-NMR(400MHz,CDCl3)δppm:1.04(s,9H),1.14(t,3H),1.63(s,6H),2.19(s,2H),2.74(s,3H),3.05(m,2H),3.31(q,2H),3.74(m,2H),7.07-7.14(m,6H),7.83(m,2H).
此外,对其它的化合物实施例进行说明。
〔参考例7〕
1-(叔丁基)-3-(5,6,7,12-四氢二苯并[a,d][8]轮烯-12-基)硫脲〔1-(tert-butyl)-3-(5,6,7,12-tetrahydrodibenzo[a,d][8]annulen-12-yl)thiourea〕的合成
按照J.Med.Chem.1992,35,2481.中记载的方法来合成5,6,7,12-tetrahydrodibenzo[a,d][8]annulen-12-ol。
将5,6,7,12-四氢二苯并[a,d][8]轮烯-12-醇(0.48g)溶解于二氯乙烷(7ml)后,添加1-(叔丁基)硫脲(0.32g)和三氟甲磺酸铝(0.10g)。搅拌2小时后馏去反应溶剂,利用硅胶柱色谱进行精制,由此得到目标物0.47g。
1H-NMR(400MHz,CDCl3)δppm:1.39(s,9H),2.38(m,2H),2.97(m,2H),3.35(m,2H),5.74(m,1H),6.42(m,1H),6.68(m,1H),7.05(m,4H),7.33(t,2H),7.42(d,2H).
〔参考例8〕
N-叔丁基-N-(5,6,7,12-四氢二苯并[a,d][8]轮烯-12-基)甲烷二亚胺〔N-tert-butyl-N-(5,6,7,12-tetrahydrodibenzo[a,d][8]annulen-12-yl)methanediimine〕的合成
向参考例7中得到的硫脲(0.55g)的乙腈溶液(5ml)中加入三乙胺(0.58ml)和2-氯-1-甲基吡啶碘化物(0.54g),室温下搅拌4小时。将不溶物过滤,对滤液进行减压浓缩。将残渣利用硅胶柱色谱进行精制,得到目标物0.45g。
1H-NMR(400MHz,CDCl3)δppm:1.29(s,9H),2.32(m,2H),2.97(m,2H),3.25(m,2H),6.38(m,1H),7.05(m,4H),7.13(t,2H),7.63(d,2H).
〔实施例6〕
N-(叔丁基)-2’-甲基-6,7-二氢-2’H,5H-螺[二苯并[a,d][8]轮烯-12,5’-[1,2,4]二唑]-3’-胺〔N-(tert-butyl)-2’-methyl-6,7-dihydro-2’H,5H-spiro[dibenzo[a,d][8]annulene-12,5’-[1,2,4]oxadiazol]-3’-amine〕(化合物编号A-1)的合成
向参考例8中得到的碳二亚胺(0.45g)的乙腈溶液(8ml)中加入N-甲基羟胺盐酸盐(0.15g)和三乙胺(0.25ml),室温下搅拌2小时。将反应液减压浓缩后,加入二氯甲烷(8ml)和二氧化锰(0.13g),室温下搅拌2小时。对反应液进行硅藻土过滤,将不溶物用乙酸乙酯进行清洗,对滤液进行减压浓缩。将粗产物用己烷进行清洗,得到目标物0.5g。以下示出物性(熔点和NMR)。
熔点:153-155℃
1H-NMR(400MHz,CDCl3)δppm:1.42(s,9H),2.58(m,4H),2.76(s,3H),2.95(m,2H),3.64(m,1H),7.05(m,4H),7.23(m,2H),7.62(m,2H).
〔实施例7〕
N-(叔丁基)-N,2’-二甲基-6,7-二氢-2’H,5H-螺[二苯并[a,d][8]轮烯-12,5’-[1,2,4]二唑]-3’-胺〔N-(tert-butyl)-N,2’-dimethyl-6,7-dihydro-2’H,5H-spiro[dibenzo[a,d][8]annulene-12,5’-[1,2,4]oxadiazol]-3’-amine〕(化合物编号A-2)的合成
在0℃下向实施例6中得到的胺(0.1g)的DMF溶液(1ml)中加入氢化钠(0.018g)搅拌30分钟。加入碘甲烷(0.04mL)在0℃下搅拌1小时。将反应液加入到冰水中,用乙酸乙酯进行萃取,将有机层用饱和食盐水进行清洗,用无水硫酸镁使其干燥,进行过滤,接着进行减压浓缩。将得到的粗产物利用硅胶柱色谱进行精制,得到目标物0.075g。以下示出物性(熔点和NMR)。
熔点:111-113℃
1H-NMR(400MHz,CDCl3)δppm:1.49(s,9H),2.51-2.98(m,12H),6.91-7.23(m,5H),7.61-7.88(m,3H).
nD 21.2℃=1.6214
nD 21.2℃=1.6311
m.p.165~167℃
m.p.162~164℃
m.p.76~78℃
nD 21.7℃=1.6398
m.p.113~115℃
m.p.129~131℃
m.p.138~140℃
m.p.134~136℃
nD 21.9℃1.6097
nD 21.9℃1.613
m.p.98-100℃
nD 22℃1.6097
〔生物试验〕
(试验用乳剂的制备)
将本发明化合物5份、二甲基甲酰胺93.6份和聚氧乙烯烷基芳基醚1.4份混合溶解,制备有效成分5%的乳剂(I)。
杀虫率通过下述公式进行计算。
杀虫率(%)=(死亡虫数/受试虫数)×100
(试验例1)对粘虫(Mythimna separata)的效力试验
将乳剂(I)用水稀释成本发明化合物的浓度为125ppm。将玉米叶浸渍于上述稀释液30秒。将该玉米叶放入培养皿中,投放5只粘虫2龄幼虫。将培养皿放置于温度25℃、湿度60%的恒温室内。从投放粘虫开始经过6天时进行生死判定,算出杀虫率。
对表13中示出的化合物进行对粘虫的效力试验。表13中示出的化合物均对粘虫表现出80%以上的杀虫率。
[表13]
(试验例2)对棉蚜(Aphisgossypii)的效力试验
将棉蚜若虫接种到黄瓜苗上。将乳剂(I)用水稀释成本发明化合物为125ppm,将上述稀释液散布到棉蚜若虫所寄生的黄瓜上。将该黄瓜放置于温度25℃、湿度60%的恒温室内。从散布开始经过6天时进行棉蚜的生死判定,算出杀虫率。
对表14中示出的化合物进行对棉蚜的效力试验。表14中示出的化合物均对棉蚜表现出80%以上的杀虫率。
[表14]
(试验例3)对西花蓟马(Frankliniella occidentalis)的效力试验
将8只西花蓟马成虫接种到黄瓜苗上。将乳剂(I)用水稀释到本发明化合物的浓度为125ppm。将该稀释液散布到黄瓜苗上,进行风干。从散布起经过7天时数出寄生幼虫数。化合物的效力通过下述所示的防除率进行评价。
防除率(%)={1-(Nt)/(Nc)}×100
Nt:散布处理区的寄生虫数
Nc:未处理区的寄生虫数
对表15-1、表15-2中示出的化合物进行对西花蓟马的效力试验。表15-1、表15-2中示出的化合物均对西花蓟马表现出80%以上的防除率。
[表15-1]
[表15-2]
另外,对专利文献1(WO2017/093409A)中记载的化合物P1.4也进行同样的试验。该化合物在125ppm时表现出80%以上的防除率。
与此相对,化合物编号b-198和b-184的化合物在7.8ppm时也表现出80%以上的防除率。此外,化合物编号b-160的化合物在1.9ppm时也表现出80%以上的防除率。
(式中,R1和R2为Ph,R3为t-Bu,R4为Me)
(试验例4)对烟蓟马(Thrips tabaci)的效力试验
将8只烟蓟马若虫接种到扁豆叶盘上。将乳剂(I)用水稀释到本发明化合物的浓度为125ppm。将该稀释液散布到扁豆叶盘上,进行风干。从散布起经过7天时数出寄生幼虫数。化合物的效力通过下述示出的防除率进行评价。
防除率(%)={1-(Nt)/(Nc)}×100
Nt:散布处理区的寄生虫数
Nc:未处理区的寄生虫数
对表16-1、16-2所示的化合物进行对烟蓟马的效力试验。表16-1、16-2中示出的化合物均对烟蓟马表现出80%以上的防除率。
[表16-1]
[表16-2]
(试验例5)对西花蓟马(Frankliniella occidentalis)的黄瓜盆栽灌溉试验
将8只西花蓟马成虫接种到黄瓜苗上。将乳剂(I)用水稀释到本发明化合物的浓度为500ppm。将10mL该稀释液灌溉于黄瓜苗。从散布起经过7天时数出寄生虫数。化合物的效力通过下述示出的防除率进行评价。
防除率(%)={1-(Nt)/(Nc)}×100
Nt:散布处理区的寄生虫数
Nc:未处理区的寄生虫数
对化合物编号a-10的化合物进行对西花蓟马的效力试验。该化合物对西花蓟马表现出80%以上的防除率。
(试验例6)对茶黄蓟马(Scirtothrips dorsalis)的效力试验
将8只茶黄蓟马幼虫接种到茶的叶盘上。将乳剂(I)用水稀释到本发明化合物的浓度为125ppm。将该稀释液散布到茶的叶盘上,进行风干。从散布起经过3天时数出寄生虫数。化合物的效力通过下述示出的防除率进行评价。
防除率(%)={1-(Nt)/(Nc)}×100
Nt:散布处理区的寄生虫数
Nc:未处理区的寄生虫数
对化合物编号a-1和a-10的化合物进行对茶黄蓟马的效力试验。任一化合物都对茶黄蓟马表现出80%以上的防除率。
(试验例7)对水稻花蓟马(Frankliniella intonsa)的效力试验
将8只水稻花蓟马幼虫接种到豇豆叶盘上。将乳剂(I)用水稀释到本发明化合物的浓度为125ppm。将该稀释液散布到水稻叶盘上,进行风干。从散布起经过3天时数出寄生虫数。化合物的效力通过下述示出的防除率进行评价。
防除率(%)={1-(Nt)/(Nc)}×100
Nt:散布处理区的寄生虫数
Nc:未处理区的寄生虫数
对化合物编号a-10的化合物进行对水稻花蓟马的效力试验。该化合物对水稻花蓟马表现出80%以上的防除率。
(试验例8)对西花蓟马(Frankliniella occidentalis)的浸达试验
将乳剂(I)用水稀释到本发明化合物的浓度为125ppm,仅将其散布到黄瓜的叶子表面并进行风干。然后,作成叶盘,将8只西花蓟马成虫接种到背面。从接种起经过2天时数出寄生虫数。化合物的效力通过下述示出的防除率进行评价。
防除率(%)={1-(Nt)/(Nc)}×100
Nt:散布处理区的寄生虫数
Nc:未处理区的寄生虫数
对化合物编号a-10和a-12的化合物进行对西花蓟马的浸达试验。各化合物都对西花蓟马表现出80%以上的防除率。
(试验例9)对西花蓟马(Frankliniella occidentalis)的使用盆栽棉苗的效力试验
将8只西花蓟马成虫接种到种植于育苗盆中的棉苗上。将乳剂(I)用水稀释到本发明化合物的浓度为125ppm。将该稀释液散布到上述棉苗上。从散布起经过3天时数出寄生虫数。化合物的效力通过下述示出的防除率进行评价。
防除率(%)={1-(Nt)/(Nc)}×100
Nt:散布处理区的寄生虫数
Nc:未处理区的寄生虫数
对化合物编号a-10的化合物进行对西花蓟马的使用盆栽棉苗的效力试验。该化合物对西花蓟马表现出80%以上的防除率。
(试验例10)对西花蓟马(Frankliniella occidentalis)的棉花灌溉试验
将10只西花蓟马成虫接种到种植于托盘的棉苗上。将乳剂(I)用水稀释成本发明化合物的浓度为500ppm。将7mL该稀释液灌溉于上述棉苗。处理经过7天时数出寄生虫数。化合物的效力通过下述示出的防除率进行评价。
防除率(%)={1-(Nt)/(Nc)}×100
Nt:散布处理区的寄生虫数
Nc:未处理区的寄生虫数
对化合物编号a-10的化合物进行对西花蓟马的棉花灌溉试验。该化合物对西花蓟马表现出80%以上的防除率。
Claims (7)
1.式(I)表示的化合物或其盐,
式(I)中,
R1表示氢原子、取代或无取代的C1~6烷基、取代或无取代的C2~6烯基、取代或无取代的C6~10芳基C1~6烷基、或者取代或无取代的C1~6烷基羰基,
R2表示取代或无取代的C1~8烷基、取代或无取代的C3~10环烷基、取代或无取代的C6~10芳基、取代或无取代的C6~10芳基C1~6烷基、或者取代或无取代的C1~6烷氧羰基,
R3表示氢原子、取代或无取代的C1~6烷基、取代或无取代的C2~6烯基、取代或无取代的C2~6炔基、取代或无取代的C6~10芳基C1~6烷基、取代或无取代的C1~6烷基羰基、或者取代或无取代的C1~6烷氧羰基,
R2和R3可以一体地成为取代或无取代的C3~5亚烷基,
A表示取代或无取代的邻亚苯基、取代或无取代的5~6元杂亚芳基、取代或无取代的亚苄基、取代或无取代的二亚甲基、或者1,2-环丙烯基,
B表示单键、氧基、取代或无取代的氧亚甲基、取代或无取代的亚甲氧基、取代或无取代的硫亚甲基、取代或无取代的亚甲硫基、取代或无取代的亚甲基、取代或无取代的二亚甲基、取代或无取代的亚乙烯基、硫基、取代或无取代的磺酰基亚甲基、取代或无取代的亚甲基磺酰基、取代或无取代的三亚甲基、取代或无取代的氧亚乙基、取代或无取代的亚乙氧基、取代或无取代的亚丙烯基、取代或无取代的氧亚甲基氧基、式-NRa-表示的基团、式-CH2-NRa-表示的基团、或者式-NRa-CH2-表示的基团,
Ra表示氢原子、或者取代或无取代的C1~6烷基,且
Q表示取代或无取代的邻亚苯基。
2.根据权利要求1所述的化合物,其中,A为取代或无取代的邻亚苯基,
B为取代或无取代的氧亚甲基、取代或无取代的亚甲氧基、取代或无取代的二亚甲基、或者取代或无取代的亚乙烯基。
3.根据权利要求1所述的化合物,其中,A为取代或无取代的邻亚苯基,
B为取代或无取代的氧亚甲基、或者取代或无取代的亚甲氧基。
4.一种有害生物防除剂,含有选自权利要求1~3中任一项所述的化合物及其盐中的至少一个作为有效成分。
5.一种杀虫剂或杀螨剂,含有选自权利要求1~3中任一项所述的化合物及其盐中的至少一个作为有效成分。
6.一种体外寄生虫防除剂,含有选自权利要求1~3中任一项所述的化合物及其盐中的至少一个作为有效成分。
7.一种缨翅目害虫防除剂,含有选自权利要求1~3中任一项所述的化合物及其盐中的至少一个作为有效成分。
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| CN102348698A (zh) * | 2009-03-13 | 2012-02-08 | 生命医药公司 | β-分泌酶的抑制剂 |
| US20130079271A1 (en) * | 2009-10-01 | 2013-03-28 | Kevin D. McCormick | Reversed biaryl spiroaminooxazoline analogues as alpha2c adrenergic receptor modulators |
| CN104364258A (zh) * | 2012-05-31 | 2015-02-18 | 阿瑞斯贸易股份有限公司 | 用于治疗神经变性疾病的螺四氢-苯并噻吩衍生物 |
Also Published As
| Publication number | Publication date |
|---|---|
| WO2018230555A1 (ja) | 2018-12-20 |
| JPWO2018230555A1 (ja) | 2020-02-06 |
| BR112019025212A2 (pt) | 2020-06-16 |
| AU2018282859B2 (en) | 2020-06-18 |
| EP3640244A4 (en) | 2020-11-25 |
| KR20190141753A (ko) | 2019-12-24 |
| TWI717057B (zh) | 2021-01-21 |
| AU2018282859A1 (en) | 2019-12-12 |
| TWI677493B (zh) | 2019-11-21 |
| JP6785965B2 (ja) | 2020-11-18 |
| CA3065915A1 (en) | 2018-12-20 |
| TW201946911A (zh) | 2019-12-16 |
| EP3640244A1 (en) | 2020-04-22 |
| MX2019014352A (es) | 2020-01-23 |
| TW201906824A (zh) | 2019-02-16 |
| US20200170254A1 (en) | 2020-06-04 |
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