RU2017104513A - Производные бис(арил)катехина в качестве гербицидов - Google Patents

Производные бис(арил)катехина в качестве гербицидов Download PDF

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RU2017104513A
RU2017104513A RU2017104513A RU2017104513A RU2017104513A RU 2017104513 A RU2017104513 A RU 2017104513A RU 2017104513 A RU2017104513 A RU 2017104513A RU 2017104513 A RU2017104513 A RU 2017104513A RU 2017104513 A RU2017104513 A RU 2017104513A
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compound according
methyl
represents halogen
chloropyridin
yloxy
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Рависекхара Почимиредди РЕДДИ
Лакшми БАЛАГОПАЛ
Паула Луиз Шарп
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Е.И.Дюпон Де Немур Энд Компани
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Claims (41)

1. Соединение формулы 1, его N-оксиды и соли,
Figure 00000001
,
где
A представляет собой фенильное кольцо, необязательно замещенное не более 4 R2; или 5- или 6-членное гетероароматическое кольцо, причем кольцо связано с остальной частью формулы 1 посредством атома углерода и необязательно замещено не более 4 R2;
R1 представляет собой галоген, C1-C4алкил, C1-C4галогеналкил, C2-C6алкенил, C2-C6алкинил, C1-C4алкокси или S(O)mR3;
каждый R2 независимо представляет собой галоген, циано, нитро, SF5, CHO, C(=O)NH2, C(=S)NH2, SO2NH2, C1-C4алкил, C2-C4алкенил, C2-C4алкинил, C1-C4галогеналкил, C2-C4галогеналкенил, C2-C4галогеналкинил, C3-C6циклоалкил, C3-C6галогенциклоалкил, C4-C8алкилциклоалкил, C4-C8циклоалкилалкил, C2-C6алкилкарбонил, C2-C6галогеналкилкарбонил, C2-C6алкоксикарбонил, C3-C7циклоалкилкарбонил, C2-C8алкиламинокарбонил, C3-C10диалкиламинокарбонил, C1-C4алкокси, C3-C4алкенилокси, C3-C4алкинилокси, C1-C4галогеналкокси, C3-C4галогеналкенилокси, C3-C4галогеналкинилокси, C3-C6циклоалкокси, C3-C6галогенциклоалкокси, C4-C8циклоалкилалкокси, C2-C6алкоксиалкил, C2-C6галогеналкоксиалкил, C2-C6алкоксигалогеналкил, C2-C6алкоксиалкокси, C2-C4алкилкарбонилокси, C2-C6цианоалкил, C2-C6цианоалкокси, C1-C4гидроксиалкил, C2-C4алкилтиоалкил, C1-C6алкиламино, C2-C6диалкиламино, S(O)nR4, CH(=NOH), фенил или пиридинил;
каждый из R3 и R4 независимо представляет собой C1-C4алкил, C1-C4галогеналкил, C1-C4алкиламино или C2-C6диалкиламино;
R5 представляет собой галоген, циано или C1-C2галогеналкил;
R6 представляет собой H или F;
m равен 0, 1 или 2; и
каждый n независимо равен 0, 1 или 2;
при условии, что соединение формулы 1 является отличным от 5-бром-2-[3-бром-[2-(5-хлорпиридин-2-илокси]фенокси]пиримидина, 5-бром-2-[6-бром-[2-(5-хлорпиридин-2-илокси]фенокси]пиримидина, 5-хлор-2-[3-фтор-[2-(5-хлорпиридин-2-илокси]фенокси]пиримидина, 5-хлор-2-[6-фтор-[2-(5-хлорпиридин-2-илокси]фенокси]пиримидина, 5-хлор-2-[3-метил-[2-(5-хлорпиридин-2-илокси]фенокси]пиримидина или 5-хлор-2-[6-метил-[2-(5-хлорпиридин-2-илокси]фенокси]пиримидина.
2. Соединение по п. 1, где
A выбран из
Figure 00000002
Figure 00000003
где r равно 0, 1, 2 или 3; а s равняется 0 или 1, и
каждый R2 независимо представляет собой галоген, циано, SF5, C1-C4алкил, C2-C4алкенил, C2-C4алкинил, C1-C4галогеналкил, C2-C4галогеналкенил или C2-C4галогеналкинил.
3. Соединение по п. 2, где
A выбран из A-1, A-2, A-4, A-6, A-9, A-10, A-11, A-12 и A-23;
R1 представляет собой галоген, C1-C4алкил или C1-C4 галогеналкил; и
каждый R2 независимо представляет собой галоген, C1-C4алкил или C1-C4галогеналкил.
4. Соединение по п. 3, где
A выбран из A-1, A-2 и A-6;
каждый R2 независимо представляет собой галоген, CH3 или CF3;
R5 представляет собой галоген, циано, CHF2 или CF3; и
R6 представляет собой H.
5. Соединение по п. 4, где
A представляет собой A-6;
R1 представляет собой галоген; и
R5 представляет собой F, Cl, Br или циано.
6. Соединение по п. 5, где
A представляет собой A-6a.
7. Соединение по п. 1, выбранное из группы, состоящей из:
8. Гербицидная композиция, содержащая соединение по п. 1 и по меньшей мере один компонент, выбранный из группы, состоящей из поверхностно-активных веществ, твердых разбавителей и жидких разбавителей.
9. Гербицидная композиция, содержащая соединение по п. 1, по меньшей мере один дополнительный активный ингредиент, выбранный из группы, состоящей из других гербицидов и антидотов гербицидов, и по меньшей мере один компонент, выбранный из группы, состоящей из поверхностно-активных веществ, твердых разбавителей и жидких разбавителей.
10. Гербицидная смесь, содержащая (a) соединение по п. 1 и (b) по меньшей мере один дополнительный активный ингредиент, выбранный из (b1) - (b16) и солей соединений (b1) - (b16).
11. Гербицидная смесь, содержащая (a) соединение по п. 1 и (b) по меньшей мере один дополнительный активный ингредиент, выбранный из (b1) ингибиторов фотосистемы II, (b2) ингибиторов синтазы ацетогидроксикислот (AHAS), (b4) миметиков ауксина, (b5) ингибиторов 5-енол-пирувилшикимат-3-фосфатсинтазы (EPSP), (b7) ингибиторов протопорфириногеноксидазы (PPO), (b9) ингибиторов элонгазы жирных кислот с очень длинной цепью (VLCFA) и (b12) ингибиторов 4-гидроксифенилпируватдиоксигеназы (HPPD).
12. Гербицидная смесь, содержащая (a) соединение по п. 1 и (b) по меньшей мере один дополнительный активный ингредиент, выбранный из группы, состоящей из 2,4-D, ацетохлора, алахлора, атразина, бромоксинила, бентазона, бициклопирона, карфентразон-этила, клорансулам-метила, дикамбы, диметенамида-p, флорасулама, флуфенацета, флумиоксазина, флупирсульфурон-метила, флуроксипир-мептила, глифосата, галауксифен-метила, изоксафлутола, MCPA, мезотриона, метолахлора, метсульфурон-метила, никосульфурона, пирасульфотола, пироксасульфона, пироксулама, римсульфурона, сафлуфенацила, темботриона, тифенсульфурон-метила, топрамазона и трибенурона.
13. Способ подавления роста нежелательной растительности, включающий приведение в контакт растительности или окружающей ее среды с гербицидно эффективным количеством соединения по п. 1.
14. Способ подавления роста нежелательной растительности на местах произрастания генетически модифицированных растений, характеризующихся устойчивостью к глифосату, глюфосинату, гербициду, ингибирующего ALS, дикамбы, имидазолиноновым гербицидам, к 2,4-D, HPPD и мезотриону, включающий приведение в контакт растительности или окружающей ее среды с гербицидно эффективным количеством соединения по п. 1.
RU2017104513A 2014-07-14 2015-07-01 Производные бис(арил)катехина в качестве гербицидов RU2017104513A (ru)

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TWI713530B (zh) 2015-06-05 2020-12-21 美商艾佛艾姆希公司 作為除草劑之嘧啶氧基苯衍生物
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