AR100192A1 - 3-PHENYL-4-FLUOROBENZOIL PIRAZOLES SUBSTITUTED HERBICIDE COMPOUNDS - Google Patents
3-PHENYL-4-FLUOROBENZOIL PIRAZOLES SUBSTITUTED HERBICIDE COMPOUNDSInfo
- Publication number
- AR100192A1 AR100192A1 ARP150101257A ARP150101257A AR100192A1 AR 100192 A1 AR100192 A1 AR 100192A1 AR P150101257 A ARP150101257 A AR P150101257A AR P150101257 A ARP150101257 A AR P150101257A AR 100192 A1 AR100192 A1 AR 100192A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- alkyl
- haloalkyl
- haloalkenyl
- cycloalkylalkyl
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 5
- 230000002363 herbicidal effect Effects 0.000 title 1
- 239000004009 herbicide Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 6
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 abstract 5
- 125000003342 alkenyl group Chemical group 0.000 abstract 5
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 5
- 125000000304 alkynyl group Chemical group 0.000 abstract 5
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 5
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 5
- 125000001188 haloalkyl group Chemical group 0.000 abstract 5
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 4
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 125000004076 pyridyl group Chemical group 0.000 abstract 4
- 125000005843 halogen group Chemical group 0.000 abstract 3
- 125000004786 difluoromethoxy group Chemical group [H]C(F)(F)O* 0.000 abstract 2
- 125000001028 difluoromethyl group Chemical group [H]C(F)(F)* 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 2
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 2
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 1
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 1
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 150000001204 N-oxides Chemical class 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000005081 alkoxyalkoxyalkyl group Chemical group 0.000 abstract 1
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 abstract 1
- 125000000278 alkyl amino alkyl group Chemical group 0.000 abstract 1
- 125000005093 alkyl carbonyl alkyl group Chemical group 0.000 abstract 1
- 125000004687 alkyl sulfinyl alkyl group Chemical group 0.000 abstract 1
- 125000004688 alkyl sulfonyl alkyl group Chemical group 0.000 abstract 1
- 125000006350 alkyl thio alkyl group Chemical group 0.000 abstract 1
- -1 amino, hydroxyl Chemical group 0.000 abstract 1
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 1
- 125000004966 cyanoalkyl group Chemical group 0.000 abstract 1
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 abstract 1
- 125000004994 halo alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 1
- 125000004461 halocycloalkylalkyl group Chemical group 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- CBOIHMRHGLHBPB-UHFFFAOYSA-N hydroxymethyl Chemical compound O[CH2] CBOIHMRHGLHBPB-UHFFFAOYSA-N 0.000 abstract 1
- 125000004971 nitroalkyl group Chemical group 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
- C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
- C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
- C07D231/28—Two oxygen or sulfur atoms
- C07D231/30—Two oxygen or sulfur atoms attached in positions 3 and 5
- C07D231/32—Oxygen atoms
- C07D231/36—Oxygen atoms with hydrocarbon radicals, substituted by hetero atoms, attached in position 4
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
La presente solicitud describe compuestos, las composiciones que contienen los compuestos y los métodos para controlar vegetación indeseada o su medio ambiente; el método comprende la etapa de poner la vegetación indeseada o su medio ambiente en contacto con una cantidad eficaz de un compuesto o una composición de la presente. Reivindicación 1: Un compuesto seleccionado de la fórmula (1), N-óxidos y sales de estos, caracterizado porque X¹ es halógeno, -CF₃, -CF₂H, -OCF₃, -OCF₂H, -SCHF₂ o -CºCH; X² es halógeno, -CF₃, -CF₂H, -OCF₃, -OCF₂H, -SCHF₂ o -CºCH; X³ es H o halógeno; n es 1, 2, 3, 4 ó 5; P es H, alquilo C₁₋₇, alquenilo C₃₋₇, alquinilo C₃₋₇, cicloalquilo C₃₋₇, haloalquilo C₁₋₇, haloalquenilo C₂₋₇, haloalquinilo C₃₋₇, alcoxialquilo C₂₋₇, cicloalquilalquilo C₄₋₇, alcoxi C₁₋₇, alcoxialcoxialquilo C₃₋₇, alquilcarbonilalquilo C₃₋₇, alcoxicarbonilalquilo C₃₋₇, halocicloalquilalquilo C₄₋₇, haloalcoxialquilo C₂₋₇, alquiltioalquilo C₂₋₇, alquilsulfonilalquilo C₂₋₇, alquilsulfinilalquilo C₂₋₇, haloalquiltioalquilo C₂₋₇, haloalquilsulfonilalquilo C₂₋₇, haloalquilsulfinilalquilo C₂₋₇, haloalcoxicarbonilalquilo C₃₋₇, haloalquilcarbonilalquilo C₃₋₇, alquilaminoalquilo C₂₋₇, dialquilaminoalquilo C₃₋₇, cianoalquilo C₂₋₇, nitroalquilo C₁₋₇, amino, hidroxilo, CH₂OH, C(=O)R¹, SO₂R², C(=O)NR³R⁴, SO₂NR³R⁴, CO₂R⁵, CH(OR⁶)₂, CH(CO₂CH₃)₂ o CH(CO₂C₂H₅)₂; R¹ es H, alquilo C₁₋₇, alquenilo C₂₋₇, alquinilo C₂₋₇, cicloalquilo C₃₋₇, haloalquilo C₁₋₇, haloalquenilo C₃₋₇, alcoxialquilo C₂₋₇ o cicloalquilalquilo C₄₋₇; o fenilo opcionalmente sustituido con R⁷; o bencilo opcionalmente sustituido en miembros del anillo con R⁷; o piridilo opcionalmente sustituido con R⁷; R² es H, alquilo C₁₋₇, alquenilo C₂₋₇, alquinilo C₂₋₇, cicloalquilo C₃₋₇, haloalquilo C₁₋₇, haloalquenilo C₃₋₇, alcoxialquilo C₂₋₇ o cicloalquilalquilo C₄₋₇; o fenilo opcionalmente sustituido con R⁷; o bencilo opcionalmente sustituido en miembros del anillo con R⁷; o piridilo opcionalmente sustituido con R⁷; R³ es H, alquilo C₁₋₇, alquenilo C₂₋₇, alquinilo C₂₋₇, cicloalquilo C₃₋₇, haloalquilo C₁₋₇, haloalquenilo C₃₋₇, alcoxialquilo C₂₋₇ o cicloalquilalquilo C₄₋₇; o fenilo opcionalmente sustituido con R⁷; o bencilo opcionalmente sustituido en miembros del anillo con R⁷; o piridilo opcionalmente sustituido con R⁷; R⁴ es H o alquilo C₁₋₄; R⁵ es alquilo C₁₋₇, alquenilo C₃₋₇, alquinilo C₃₋₇, cicloalquilo C₃₋₇, haloalquilo C₂₋₇, haloalquenilo C₃₋₇, alcoxialquilo C₂₋₇ o cicloalquilalquilo C₄₋₇; o fenilo opcionalmente sustituido con R⁷; o bencilo opcionalmente sustituido en miembros del anillo con R⁷; o piridilo opcionalmente sustituido con R⁷; R⁶ es alquilo C₁₋₃; o dos R⁶ se toman conjuntamente como -(CH₂)₂-, -(CH₂)₃- o -CH₂CH(CH₃)- para formar un anillo; y R⁷ es halógeno, ciano, alquilo C₁₋₂, haloalquilo C₁₋₃, haloalcoxi C₁₋₃ o alcoxi C₁₋₃.The present application describes compounds, the compositions containing the compounds and the methods for controlling unwanted vegetation or its environment; The method comprises the step of putting the unwanted vegetation or its environment in contact with an effective amount of a compound or a composition of the present. Claim 1: A compound selected from the formula (1), N-oxides and salts thereof, characterized in that X¹ is halogen, -CF₃, -CF₂H, -OCF₃, -OCF₂H, -SCHF₂ or -CºCH; X² is halogen, -CF₃, -CF₂H, -OCF₃, -OCF₂H, -SCHF₂ or -CºCH; X³ is H or halogen; n is 1, 2, 3, 4 or 5; P is H, C₁₋₇ alkyl, C₃₋₇ alkenyl, C₃₋₇ alkynyl, C₃₋₇ cycloalkyl, C₁₋₇ haloalkyl, C₃₋₇ haloalkenyl, C₂₋₇ alkoxyalkyl, C₄₋₇ cycloalkylalkyl, alkoxy C₁₋₇, alkoxyalkoxyalkyl C₃₋₇, alkylcarbonylalkyl C₃₋₇, alkoxycarbonylalkyl C₃₋₇, halocycloalkylalkyl C₄₋₇, haloalkoxyalkyl C₂₋₇, alkylthioalkyl C₂₋₇, alkylsulfonylalkyl C₂₋₇, alkylsulfinylalkyl C₂₋₇, haloalkyl alkyl alkylalkyl C₂₋₇, haloalkylsulfinylalkyl C₂₋₇, haloalkoxycarbonylalkyl C₃₋₇, haloalkylcarbonylalkyl C₃₋₇, alkylaminoalkyl C₂₋₇, dialkylaminoalkyl C₃₋₇, cyanoalkyl C₂₋₇, nitroalkyl C₁₋₇, amino, hydroxyl, CH₂OH, C (= O) R¹, SO₂R², C (= O) NR³R⁴, SO₂NR³R⁴, CO₂R⁵, CH (OR⁶) ₂, CH (CO₂CH₃) ₂ or CH (CO₂C₂H₅) ₂; R¹ is H, C₁₋₇ alkyl, C₂₋₇ alkenyl, C₂₋₇ alkynyl, C₃₋₇ cycloalkyl, C₁₋₇ haloalkyl, C₃₋₇ haloalkenyl, C₂₋₇ alkoxyalkyl or C₄₋₇ cycloalkylalkyl; or phenyl optionally substituted with R⁷; or optionally substituted benzyl in ring members with R⁷; or pyridyl optionally substituted with R⁷; R² is H, C₁₋₇ alkyl, C₂₋₇ alkenyl, C₂₋₇ alkynyl, C₃₋₇ cycloalkyl, C₁₋₇ haloalkyl, C₃₋₇ haloalkenyl, C₂₋₇ alkoxyalkyl or C₄₋₇ cycloalkylalkyl; or phenyl optionally substituted with R⁷; or optionally substituted benzyl in ring members with R⁷; or pyridyl optionally substituted with R⁷; R³ is H, C₁₋₇ alkyl, C₂₋₇ alkenyl, C₂₋₇ alkynyl, C₃₋₇ cycloalkyl, C₁₋₇ haloalkyl, C₃₋₇ haloalkenyl, C₂₋₇ alkoxyalkyl or C₄₋₇ cycloalkylalkyl; or phenyl optionally substituted with R⁷; or optionally substituted benzyl in ring members with R⁷; or pyridyl optionally substituted with R⁷; R⁴ is H or C₁₋₄ alkyl; R⁵ is C₁₋₇ alkyl, C₃₋₇ alkenyl, C₃₋₇ alkynyl, C₃₋₇ cycloalkyl, C₂₋₇ haloalkyl, C₃₋₇ haloalkenyl, C₂₋₇ alkoxyalkyl or C₄₋₇ cycloalkylalkyl; or phenyl optionally substituted with R⁷; or optionally substituted benzyl in ring members with R⁷; or pyridyl optionally substituted with R⁷; R⁶ is C₁₋₃ alkyl; or two R⁶ are taken together as - (CH₂) ₂-, - (CH₂) ₃- or -CH₂CH (CH₃) - to form a ring; and R⁷ is halogen, cyano, C₁₋₂ alkyl, C₁₋₃ haloalkyl, C₁₋₃ haloalkoxy or C₁₋₃ alkoxy.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201461985430P | 2014-04-28 | 2014-04-28 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR100192A1 true AR100192A1 (en) | 2016-09-14 |
Family
ID=53008891
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP150101257A AR100192A1 (en) | 2014-04-28 | 2015-04-27 | 3-PHENYL-4-FLUOROBENZOIL PIRAZOLES SUBSTITUTED HERBICIDE COMPOUNDS |
Country Status (3)
| Country | Link |
|---|---|
| AR (1) | AR100192A1 (en) |
| TW (1) | TW201620879A (en) |
| WO (1) | WO2015167795A1 (en) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2015179038A2 (en) | 2014-05-23 | 2015-11-26 | E. I. Du Pont De Nemours And Company | Sulfonyl hydrazide compounds and a regio-selective process to prepare 4-aroyl pyrazole derivatives |
| CA3242779A1 (en) | 2022-01-14 | 2023-07-20 | Enko Chem, Inc. | PROTOPORPHYRINOGEN OXIDASE INHIBITORS |
Family Cites Families (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2891855A (en) | 1954-08-16 | 1959-06-23 | Geigy Ag J R | Compositions and methods for influencing the growth of plants |
| US3235361A (en) | 1962-10-29 | 1966-02-15 | Du Pont | Method for the control of undesirable vegetation |
| US3060084A (en) | 1961-06-09 | 1962-10-23 | Du Pont | Improved homogeneous, readily dispersed, pesticidal concentrate |
| US3299566A (en) | 1964-06-01 | 1967-01-24 | Olin Mathieson | Water soluble film containing agricultural chemicals |
| US3309192A (en) | 1964-12-02 | 1967-03-14 | Du Pont | Method of controlling seedling weed grasses |
| US4144050A (en) | 1969-02-05 | 1979-03-13 | Hoechst Aktiengesellschaft | Micro granules for pesticides and process for their manufacture |
| US3920442A (en) | 1972-09-18 | 1975-11-18 | Du Pont | Water-dispersible pesticide aggregates |
| US4172714A (en) | 1976-12-20 | 1979-10-30 | E. I. Du Pont De Nemours And Company | Dry compactible, swellable herbicidal compositions and pellets produced therefrom |
| GB2095558B (en) | 1981-03-30 | 1984-10-24 | Avon Packers Ltd | Formulation of agricultural chemicals |
| DE3246493A1 (en) | 1982-12-16 | 1984-06-20 | Bayer Ag, 5090 Leverkusen | METHOD FOR PRODUCING WATER-DISPERSIBLE GRANULES |
| US5180587A (en) | 1988-06-28 | 1993-01-19 | E. I. Du Pont De Nemours And Company | Tablet formulations of pesticides |
| ES2166919T3 (en) | 1989-08-30 | 2002-05-01 | Kynoch Agrochemicals Proprieta | PREPARATION OF A DOSING DEVICE. |
| JPH05504964A (en) | 1990-03-12 | 1993-07-29 | イー・アイ・デユポン・ドウ・ヌムール・アンド・カンパニー | Water-dispersible or water-soluble pest control granules from heat-activated binders |
| EP0480679B1 (en) | 1990-10-11 | 1996-09-18 | Sumitomo Chemical Company Limited | Pesticidal composition |
| AU4632696A (en) | 1995-02-07 | 1996-08-27 | Nissan Chemical Industries Ltd. | Pyrazole derivatives and herbicides |
| TW200724033A (en) | 2001-09-21 | 2007-07-01 | Du Pont | Anthranilamide arthropodicide treatment |
| TW200738701A (en) | 2005-07-26 | 2007-10-16 | Du Pont | Fungicidal carboxamides |
| US8722660B2 (en) | 2010-02-17 | 2014-05-13 | Takeda Pharmaceutical Company Limited | Heterocyclic compound |
| WO2013062887A1 (en) | 2011-10-26 | 2013-05-02 | Merck Sharp & Dohme Corp. | Substituted pyridine derivatives useful as gpr131 agonists |
| US8822464B2 (en) | 2011-11-28 | 2014-09-02 | Boehringer Ingelheim International Gmbh | N-aryl-piperazine derivatives and their use as positive allosteric modulators of mGluR5 receptors |
| CN104540808A (en) * | 2012-06-22 | 2015-04-22 | 杜邦公司 | Fungicidal 4-methylanilinopyrazole |
-
2015
- 2015-03-23 TW TW104109155A patent/TW201620879A/en unknown
- 2015-04-14 WO PCT/US2015/025731 patent/WO2015167795A1/en not_active Ceased
- 2015-04-27 AR ARP150101257A patent/AR100192A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| WO2015167795A1 (en) | 2015-11-05 |
| TW201620879A (en) | 2016-06-16 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| EA201691439A1 (en) | Pyrimidiniloxibenzene derivatives as herbicides | |
| AR090862A1 (en) | TETRAZOLINONE COMPOUNDS AND ITS USE TO COMBAT PESTS | |
| EA201692186A1 (en) | PYRIDAZINO NEW HERBICIDES | |
| AR099415A1 (en) | BENZOILFENIL-FORMAMIDINAS WITH FUNGICIDE ACTIVITY, ITS AGRONOMIC COMPOSITIONS AND ITS USE FOR THE CONTROL OF PHYTO-PATHOGENIC FUNGIANS OF AGRICULTURAL CROPS | |
| MX389921B (en) | PIPERIDINONE HERBICIDES. | |
| MX387367B (en) | ARYLOXYPYRIMIDINYL ETHERS AS HERBICIDES. | |
| AR093579A1 (en) | BMI-1 INHIBITORS OF REPLACED PYRIMIDINE REPLACED | |
| EA201691134A1 (en) | NEW GLUTAMINASE INHIBITORS | |
| AR106301A1 (en) | PIRROLPIRIMIDINE COMPOSITIONS AS KINASE INHIBITORS | |
| MX395250B (en) | SUBSTITUTED PYRIMIDINYLOXYPYRIDINE DERIVATIVES AS HERBICIDES. | |
| TR201900050T4 (en) | Fused heterocyclic compound and its pest control application. | |
| AR101600A1 (en) | SPIRO COMPOUNDS [3H-INDOL-3,2-PIRROLIDIN] -2 (1H) -ONA AND DERIVATIVES AS INHIBITORS OF MDM2-p53 | |
| EA201390880A1 (en) | IMIDAZOPIRIDIN AS ANTI-VIRUS AGAINST THE RESPIRATORY-SYNCIAL VIRUS | |
| EA201692249A1 (en) | PHOSPHATIDYLINOSITOL-3-KINASE INHIBITORS | |
| UY36712A (en) | PIRIMIDINYLOXI BENZENE DERIVATIVES AS HERBICIDES | |
| MX381140B (en) | METHODS FOR TREATING EPITHELIOID CELL TUMORS. | |
| EA201692266A1 (en) | PHOSPHATIDYLINOSITOL-3-KINASE INHIBITORS | |
| AR097866A1 (en) | 4-AZAINDOL DERIVATIVES | |
| PE20170439A1 (en) | DERIVED FROM BIS (ARIL) CATECOL AS HERBICIDES | |
| MX388175B (en) | THERAPEUTIC COMPOUNDS AND METHODS OF USING THEM | |
| AR095303A1 (en) | 4-AMINO-6- (PIRIDIL AND PHENYL 2-REPLACED) -PICOLINATES AND 6-AMINO-2- (PIRIDIL AND PHENYL 2-REPLACED) -PIRIMIDIN-4 CARBOXYLATES AND THEIR USE AS HERBICIDES | |
| EA201690523A1 (en) | TRIAZOLOPIRIDIN, COMPOSITIONS AND METHODS OF THEIR APPLICATION | |
| AR101906A1 (en) | 1,3,4-TIADIAZOLES THAT HAVE HERBICIDE ACTIVITY, ITS AGRONOMIC COMPOSITIONS AND RELATED USE | |
| EA201791671A1 (en) | 4-SUBSTITUTED BENZOXOBOROL COMPOUNDS AND THEIR APPLICATION | |
| AR095728A1 (en) | METHODS TO CONTROL NEONICOTINOID RESISTANT PESTS |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| FB | Suspension of granting procedure |