JP2014533669A - 置換型１，２，５−オキサジアゾール化合物及びその除草剤としての使用ｉｉ - Google Patents
置換型１，２，５−オキサジアゾール化合物及びその除草剤としての使用ｉｉ Download PDFInfo
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- JP2014533669A JP2014533669A JP2014541656A JP2014541656A JP2014533669A JP 2014533669 A JP2014533669 A JP 2014533669A JP 2014541656 A JP2014541656 A JP 2014541656A JP 2014541656 A JP2014541656 A JP 2014541656A JP 2014533669 A JP2014533669 A JP 2014533669A
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- alkyl
- alkoxy
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- halogen
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- 150000002244 furazanes Chemical class 0.000 title claims abstract description 6
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- 150000001875 compounds Chemical class 0.000 claims abstract description 218
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- 239000001257 hydrogen Substances 0.000 claims abstract description 88
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- 150000002431 hydrogen Chemical class 0.000 claims abstract description 69
- 150000003839 salts Chemical class 0.000 claims abstract description 55
- 125000000171 (C1-C6) haloalkyl group Chemical group 0.000 claims abstract description 45
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 claims abstract description 44
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- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 claims abstract description 19
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- 125000006766 (C2-C6) alkynyloxy group Chemical group 0.000 claims abstract description 5
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- SNOOUWRIMMFWNE-UHFFFAOYSA-M sodium;6-[(3,4,5-trimethoxybenzoyl)amino]hexanoate Chemical compound [Na+].COC1=CC(C(=O)NCCCCCC([O-])=O)=CC(OC)=C1OC SNOOUWRIMMFWNE-UHFFFAOYSA-M 0.000 claims description 74
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- 229910052717 sulfur Inorganic materials 0.000 claims description 49
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- 125000004767 (C1-C4) haloalkoxy group Chemical group 0.000 claims description 46
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 42
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- 125000002619 bicyclic group Chemical group 0.000 claims description 21
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- 125000000217 alkyl group Chemical group 0.000 claims description 20
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- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 claims description 17
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- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims description 16
- 125000003545 alkoxy group Chemical group 0.000 claims description 15
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- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 14
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- JCBJVAJGLKENNC-UHFFFAOYSA-N potassium;ethoxymethanedithioic acid Chemical compound [K+].CCOC(S)=S JCBJVAJGLKENNC-UHFFFAOYSA-N 0.000 claims description 2
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- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 8
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- OISVCGZHLKNMSJ-UHFFFAOYSA-N 2,6-dimethylpyridine Chemical compound CC1=CC=CC(C)=N1 OISVCGZHLKNMSJ-UHFFFAOYSA-N 0.000 description 6
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- FZXISNSWEXTPMF-UHFFFAOYSA-N terbutylazine Chemical compound CCNC1=NC(Cl)=NC(NC(C)(C)C)=N1 FZXISNSWEXTPMF-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
- 150000003512 tertiary amines Chemical class 0.000 description 1
- DZLFLBLQUQXARW-UHFFFAOYSA-N tetrabutylammonium Chemical compound CCCC[N+](CCCC)(CCCC)CCCC DZLFLBLQUQXARW-UHFFFAOYSA-N 0.000 description 1
- CBXCPBUEXACCNR-UHFFFAOYSA-N tetraethylammonium Chemical compound CC[N+](CC)(CC)CC CBXCPBUEXACCNR-UHFFFAOYSA-N 0.000 description 1
- 125000004853 tetrahydropyridinyl group Chemical group N1(CCCC=C1)* 0.000 description 1
- RAOIDOHSFRTOEL-UHFFFAOYSA-N tetrahydrothiophene Chemical compound C1CCSC1 RAOIDOHSFRTOEL-UHFFFAOYSA-N 0.000 description 1
- CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 1
- QEMXHQIAXOOASZ-UHFFFAOYSA-N tetramethylammonium Chemical compound C[N+](C)(C)C QEMXHQIAXOOASZ-UHFFFAOYSA-N 0.000 description 1
- 125000000437 thiazol-2-yl group Chemical group [H]C1=C([H])N=C(*)S1 0.000 description 1
- 125000004495 thiazol-4-yl group Chemical group S1C=NC(=C1)* 0.000 description 1
- 125000004496 thiazol-5-yl group Chemical group S1C=NC=C1* 0.000 description 1
- GLDAZAQRGCSFNP-UHFFFAOYSA-N thiencarbazone Chemical compound O=C1N(C)C(OC)=NN1C(=O)NS(=O)(=O)C1=C(C)SC=C1C(O)=O GLDAZAQRGCSFNP-UHFFFAOYSA-N 0.000 description 1
- XSKZXGDFSCCXQX-UHFFFAOYSA-N thiencarbazone-methyl Chemical compound COC(=O)C1=CSC(C)=C1S(=O)(=O)NC(=O)N1C(=O)N(C)C(OC)=N1 XSKZXGDFSCCXQX-UHFFFAOYSA-N 0.000 description 1
- JWCVYQRPINPYQJ-UHFFFAOYSA-N thiepane Chemical compound C1CCCSCC1 JWCVYQRPINPYQJ-UHFFFAOYSA-N 0.000 description 1
- BISQTCXKVNCDDA-UHFFFAOYSA-N thiepine Chemical compound S1C=CC=CC=C1 BISQTCXKVNCDDA-UHFFFAOYSA-N 0.000 description 1
- 125000004275 thietan-2-yl group Chemical group [H]C1([H])SC([H])(*)C1([H])[H] 0.000 description 1
- 125000006300 thietan-3-yl group Chemical group [H]C1([H])SC([H])([H])C1([H])* 0.000 description 1
- LOQQVLXUKHKNIA-UHFFFAOYSA-N thifensulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C2=C(SC=C2)C(O)=O)=N1 LOQQVLXUKHKNIA-UHFFFAOYSA-N 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 125000004569 thiomorpholin-2-yl group Chemical group N1CC(SCC1)* 0.000 description 1
- 125000004570 thiomorpholin-3-yl group Chemical group N1C(CSCC1)* 0.000 description 1
- 125000004571 thiomorpholin-4-yl group Chemical group N1(CCSCC1)* 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 235000010215 titanium dioxide Nutrition 0.000 description 1
- IYMLUHWAJFXAQP-UHFFFAOYSA-N topramezone Chemical compound CC1=C(C(=O)C2=C(N(C)N=C2)O)C=CC(S(C)(=O)=O)=C1C1=NOCC1 IYMLUHWAJFXAQP-UHFFFAOYSA-N 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 229910052723 transition metal Inorganic materials 0.000 description 1
- 150000003624 transition metals Chemical class 0.000 description 1
- 238000013519 translation Methods 0.000 description 1
- XOPFESVZMSQIKC-UHFFFAOYSA-N triasulfuron Chemical compound COC1=NC(C)=NC(NC(=O)NS(=O)(=O)C=2C(=CC=CC=2)OCCCl)=N1 XOPFESVZMSQIKC-UHFFFAOYSA-N 0.000 description 1
- BQZXUHDXIARLEO-UHFFFAOYSA-N tribenuron Chemical compound COC1=NC(C)=NC(N(C)C(=O)NS(=O)(=O)C=2C(=CC=CC=2)C(O)=O)=N1 BQZXUHDXIARLEO-UHFFFAOYSA-N 0.000 description 1
- YMXOXAPKZDWXLY-QWRGUYRKSA-N tribenuron methyl Chemical group COC(=O)[C@H]1CCCC[C@@H]1S(=O)(=O)NC(=O)N(C)C1=NC(C)=NC(OC)=N1 YMXOXAPKZDWXLY-QWRGUYRKSA-N 0.000 description 1
- REEQLXCGVXDJSQ-UHFFFAOYSA-N trichlopyr Chemical compound OC(=O)COC1=NC(Cl)=C(Cl)C=C1Cl REEQLXCGVXDJSQ-UHFFFAOYSA-N 0.000 description 1
- AZHZOGYUMMIAOF-UHFFFAOYSA-N trifludimoxazin Chemical compound O=C1N(C)C(=S)N(C)C(=O)N1C(C(=C1)F)=CC2=C1OC(F)(F)C(=O)N2CC#C AZHZOGYUMMIAOF-UHFFFAOYSA-N 0.000 description 1
- 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
- 239000002753 trypsin inhibitor Substances 0.000 description 1
- JABYJIQOLGWMQW-UHFFFAOYSA-N undec-4-ene Chemical compound CCCCCCC=CCCC JABYJIQOLGWMQW-UHFFFAOYSA-N 0.000 description 1
- 229940035893 uracil Drugs 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 150000004669 very long chain fatty acids Chemical class 0.000 description 1
- 230000003612 virological effect Effects 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- 239000003021 water soluble solvent Substances 0.000 description 1
- 239000004563 wettable powder Substances 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- 239000000230 xanthan gum Substances 0.000 description 1
- 229920001285 xanthan gum Polymers 0.000 description 1
- 235000010493 xanthan gum Nutrition 0.000 description 1
- 229940082509 xanthan gum Drugs 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
- C07D409/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings
- C07D409/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- 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
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
Landscapes
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Health & Medical Sciences (AREA)
- Plant Pathology (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Agronomy & Crop Science (AREA)
- Plural Heterocyclic Compounds (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161560333P | 2011-11-16 | 2011-11-16 | |
| US61/560,333 | 2011-11-16 | ||
| PCT/EP2012/072692 WO2013072402A1 (en) | 2011-11-16 | 2012-11-15 | Substituted 1,2,5-oxadiazole compounds and their use as herbicides ii |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| JP2014533669A true JP2014533669A (ja) | 2014-12-15 |
Family
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|---|---|---|---|
| JP2014541656A Pending JP2014533669A (ja) | 2011-11-16 | 2012-11-15 | 置換型１，２，５−オキサジアゾール化合物及びその除草剤としての使用ｉｉ |
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|---|---|
| US (1) | US9096583B2 (enExample) |
| EP (1) | EP2780339A1 (enExample) |
| JP (1) | JP2014533669A (enExample) |
| KR (1) | KR20140098140A (enExample) |
| CN (1) | CN104053656A (enExample) |
| AR (1) | AR088886A1 (enExample) |
| AU (1) | AU2012338879A1 (enExample) |
| BR (1) | BR112014011622A2 (enExample) |
| CA (1) | CA2853340A1 (enExample) |
| CO (1) | CO6950507A2 (enExample) |
| CR (1) | CR20140217A (enExample) |
| IL (1) | IL232279A0 (enExample) |
| IN (1) | IN2014MN00832A (enExample) |
| MX (1) | MX2014005607A (enExample) |
| WO (1) | WO2013072402A1 (enExample) |
| ZA (1) | ZA201404296B (enExample) |
Families Citing this family (15)
| Publication number | Priority date | Publication date | Assignee | Title |
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| BR112015004648A2 (pt) * | 2012-09-05 | 2017-07-04 | Bayer Cropscience Ag | amidas de ácidos bicicloaril carboxílicos com atividade herbicida |
| WO2014184074A1 (en) * | 2013-05-15 | 2014-11-20 | Basf Se | Substituted n-(tetrazol-5-yl)- and n-(triazol-5-yl)hetarylcarboxamide compounds and their use as herbicides |
| WO2014184019A1 (en) * | 2013-05-15 | 2014-11-20 | Basf Se | N-(1,2,5-oxadiazol-3-yl)carboxamide compounds and their use as herbicides |
| BR112015029899B1 (pt) * | 2013-05-31 | 2020-07-21 | Nissan Chemical Corporation | composto de amida heterocíclica e sal do mesmo da formula (1), produto quimico agrícola e herbicida obtido |
| CN106459986B (zh) | 2014-03-11 | 2020-06-30 | 拜耳作物科学有限合伙公司 | Hppd变体和使用方法 |
| AR101230A1 (es) * | 2014-07-28 | 2016-11-30 | Bayer Cropscience Ag | Amidas del ácido arilcarboxílico bicíclicas y su uso como herbicidas |
| WO2016128470A1 (en) | 2015-02-11 | 2016-08-18 | Basf Se | Herbicide-resistant hydroxyphenylpyruvate dioxygenases |
| AU2016292678B2 (en) * | 2015-07-10 | 2020-12-24 | BASF Agro B.V. | Method for controlling herbicide resistant or tolerant weeds |
| ES2933673T3 (es) | 2015-09-11 | 2023-02-13 | BASF Agricultural Solutions Seed US LLC | Variantes de HPPD y métodos de uso |
| US11624076B2 (en) | 2016-04-21 | 2023-04-11 | BASF Agricultural Solutions Seed US LLC | TAL-effector mediated herbicide tolerance |
| CA3055389A1 (en) | 2017-03-07 | 2018-09-13 | BASF Agricultural Solutions Seed US LLC | Hppd variants and methods of use |
| BR112020008092A2 (pt) | 2017-10-24 | 2020-09-15 | BASF Agricultural Solutions Seed US LLC | método para conferir tolerância a um herbicida e planta de soja transgênica |
| US20210032651A1 (en) | 2017-10-24 | 2021-02-04 | Basf Se | Improvement of herbicide tolerance to hppd inhibitors by down-regulation of putative 4-hydroxyphenylpyruvate reductases in soybean |
| CN113582970B (zh) * | 2021-07-02 | 2023-07-14 | 凯里学院 | 含酰胺及肟或肟醚结构的硫色满-4-酮衍生物的制备方法及应用 |
| CN113956247B (zh) * | 2021-10-27 | 2023-07-11 | 凯里学院 | 含1,3,4-噁二唑硫醚及肟醚结构的硫色满-4-酮衍生物的制备方法及应用 |
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| ES2018274T5 (es) | 1986-03-11 | 1996-12-16 | Plant Genetic Systems Nv | Celulas vegetales resistentes a los inhibidores de glutamina sintetasa, preparadas por ingenieria genetica. |
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| AU2012228366B2 (en) * | 2011-03-15 | 2017-01-05 | Bayer Cropscience Aktiengesellschaft | Herbicide safener compositions |
| JP5847920B2 (ja) | 2011-03-25 | 2016-01-27 | バイエル・インテレクチュアル・プロパティ・ゲゼルシャフト・ミット・ベシュレンクテル・ハフツングＢａｙｅｒ Ｉｎｔｅｌｌｅｃｔｕａｌ Ｐｒｏｐｅｒｔｙ ＧｍｂＨ | Ｈｐｐｄインヒビター除草剤に対して耐性であるトランスジェニック作物植物の領域において望まぬ植物を制御するためのｎ−（１，２，５−オキサジアゾール−３−イル）ベンズアミドの使用 |
| MX2014005175A (es) | 2011-11-14 | 2014-05-28 | Basf Se | Compuestos de 1,2,5-oxadiazol sustituido y su uso como herbicidas. |
| KR20140107280A (ko) | 2011-11-18 | 2014-09-04 | 바스프 에스이 | 치환된 1,2,5-옥사디아졸 화합물 및 이의 제초제 ｉｉｉ 로서의 용도 |
-
2012
- 2012-11-15 CA CA2853340A patent/CA2853340A1/en not_active Abandoned
- 2012-11-15 JP JP2014541656A patent/JP2014533669A/ja active Pending
- 2012-11-15 MX MX2014005607A patent/MX2014005607A/es not_active Application Discontinuation
- 2012-11-15 AU AU2012338879A patent/AU2012338879A1/en not_active Abandoned
- 2012-11-15 KR KR1020147016432A patent/KR20140098140A/ko not_active Withdrawn
- 2012-11-15 AR ARP120104312A patent/AR088886A1/es not_active Application Discontinuation
- 2012-11-15 US US14/357,877 patent/US9096583B2/en not_active Expired - Fee Related
- 2012-11-15 IN IN832MUN2014 patent/IN2014MN00832A/en unknown
- 2012-11-15 EP EP12787713.2A patent/EP2780339A1/en not_active Withdrawn
- 2012-11-15 CN CN201280066981.9A patent/CN104053656A/zh active Pending
- 2012-11-15 BR BR112014011622A patent/BR112014011622A2/pt not_active IP Right Cessation
- 2012-11-15 WO PCT/EP2012/072692 patent/WO2013072402A1/en not_active Ceased
-
2014
- 2014-04-28 IL IL232279A patent/IL232279A0/en unknown
- 2014-05-12 CR CR20140217A patent/CR20140217A/es unknown
- 2014-05-13 CO CO14102718A patent/CO6950507A2/es not_active Application Discontinuation
- 2014-06-11 ZA ZA2014/04296A patent/ZA201404296B/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CN104053656A (zh) | 2014-09-17 |
| CO6950507A2 (es) | 2014-05-20 |
| EP2780339A1 (en) | 2014-09-24 |
| ZA201404296B (en) | 2015-12-23 |
| IN2014MN00832A (enExample) | 2015-05-22 |
| AR088886A1 (es) | 2014-07-16 |
| US9096583B2 (en) | 2015-08-04 |
| WO2013072402A1 (en) | 2013-05-23 |
| MX2014005607A (es) | 2014-07-30 |
| CR20140217A (es) | 2014-06-19 |
| AU2012338879A1 (en) | 2014-06-05 |
| BR112014011622A2 (pt) | 2017-05-09 |
| CA2853340A1 (en) | 2013-05-23 |
| IL232279A0 (en) | 2014-06-30 |
| KR20140098140A (ko) | 2014-08-07 |
| US20140309116A1 (en) | 2014-10-16 |
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