OA16501A - Pesticidal compositions and processes related thereto. - Google Patents

Pesticidal compositions and processes related thereto. Download PDF

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OA16501A
OA16501A OA1201300316 OA16501A OA 16501 A OA16501 A OA 16501A OA 1201300316 OA1201300316 OA 1201300316 OA 16501 A OA16501 A OA 16501A
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alkyl
haloalkyl
cycloalkyl
alkenyl
phenyl
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OA1201300316
Inventor
Gary D. Crouse
William Thomas LAMBERT
Thomas C. Sparks
Vidyadhar B. Hegde
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Dow Agrosciences Llc
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Publication of OA16501A publication Critical patent/OA16501A/en

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Abstract

This document discloses pesticidal compostions comprising molecules having the following formulas :

Description

The invention disclosed in this document is related to the field of processes to produce molécules that are useful as pesticides (e.g., acaricides, insecticides, molluscicides, and nematicides), such molécules, and processes of using such molécules to control pests.
BACKGROUND OF THE INVENTION
Pests cause millions of human deaths around the world each year. Furthermore, there are more than ten thousand species of pests that cause losses in agriculture. The worldwide agricultural losses amount to billions of U.S. dollars each year.
Termites cause damage to ali kinds of private and public structures. The world-wide termite damage losses amount to billions of U.S. dollars each year.
Stored food pests eat and adulterate stored food. The world-wide stored food losses amount to billions of U.S. dollars each year, but more importantly, deprive people of needed food.
There is an acute need for new pesticides. Certain pests are developing résistance to pesticides in current use. Hundreds of pest species are résistant to one or more pesticides. The development of résistance to some of the older pesticides, such as DDT, the carbamates, and the organophosphates, is well known. But résistance has even developed to some of the newer pesticides.
Therefore, for many reasons, including the above reasons, a need exists for new pesticides.
Page I of77
DEFINITIONS
The examples given in the définitions are generally non-exhaustive and must not be construed as limiting the invention disclosed in this document. It is understood that a substituent should comply with chemical bonding rules and steric compatibility constraints in relation to the particular molécule to which it is attached.
“Acaricide Group” is defined under the heading “ACARICIDES”.
“AI Group” is defined after the place in this document where the “Herbicide Group” is defined.
“Alkenyl” means an acyclic, unsaturated (at least one carbon-carbon double bond), branched or unbranched, substituent consisting of carbon and hydrogen, for example, vinyl, allyl, butenyl, pentenyl, and hexenyl.
“Alkenyloxy” means an alkenyl further consisting of a carbon-oxygen single bond, for example, allyloxy, butenyloxy, pentenyloxy, hexenyloxy.
“Alkoxy” means an alkyl further consisting of a carbon-oxygen single bond, for example, methoxy, ethoxy, propoxy, isopropoxy, butoxy, isobutoxy, and tert-butoxy.
“Alkyl” means an acyclic, saturated, branched or unbranched, substituent consisting of carbon and hydrogen, for example, methyl, ethyl, propyl, isopropyl, butyl, and ieri-butyl.
“Alkynyl” means an acyclic, unsaturated (at least one carbon-carbon triple bond), branched or unbranched, substituent consisting of carbon and hydrogen, for example, ethynyl, propargyl, butynyl, and pentynyl.
“Alkynyloxy” means an alkynyl further consisting of a carbon-oxygen single bond, for example, pentynyloxy, hexynyloxy, heptynyloxy, and octynyloxy.
“Aryl” means a cyclic, aromatic substituent consisting of hydrogen and carbon, for example, phenyl, naphthyl, and biphenyl.
“Cycloalkenyl” means a monocyclic or polycyclic, unsaturated (at least one carboncarbon double bond) substituent consisting of carbon and hydrogen, for example, cyclobutenyl, cyclopentenyl, cyclohexenyl, norbomenyl, bicyclo[2.2.2]octenyl, tetrahydronaphthyl, hexahydronaphthyl, and octahydronaphthyl.
“Cycloalkenyloxy” means a cycloalkenyl further consisting of a carbon-oxygen single bond, for example, cyclobutenyloxy, cyclopentenyloxy, norbomenyloxy, and bicyclo[2.2.2]octenyloxy.
“Cycloalkyl” means a monocyclic or polycyclic, saturated substituent consisting of carbon and hydrogen, for example, cyclopropyl, cyclobutyl, cyclopentyl, norbornyl, bicyclo[2.2.2]octyl, and decahydfonaphthyl.
“Cycloalkoxy” means a cycloalkyl further consisting of a carbon-oxygen single bond, for example, cyclopropyloxy, cyclobutyloxy, cyclopentyloxy, norbomyloxy, and bicyclo[2.2.2]octyloxy.
“Fungicide Group” is defined under the heading “FUNGICIDES.” “Halo” means fluoro, chloro, bromo, and iodo.
“Haloalkoxy” means an alkoxy further consisting of, from one to the maximum possible number of identical or different, halos, for example, fluoromethoxy, trifluoromethoxy, 2,2difluoropropoxy, chloromethoxy, trichloromethoxy, 1,1,2,2-tetrafluoroethoxy, and pentafluoro eth oxy.
“Haloalkyl” means an alkyl further consisting of, from one to the maximum possible number of, identical or different, halos, for example, fluoromethyl, trifluoromethyl, 2,2difluoropropyl, chloromethyl, trichloromethyl, and 1,1,2,2-tetrafluoroethyl.
“Herbicide Group” is defined under the heading “HERBICIDES.” “Heterocyclyl” means a cyclic substituent that may be fully saturated, partially unsaturated, or fully unsaturated, where the cyclic structure contains at least one carbon and at least one heteroatom, where said heteroatom is nitrogen, sulfur, or oxygen. Examples of aromatic heterocyclyls include, but are not limited to, benzofuranyl, benzoisothiazolyl, benzoisoxazolyl, benzoxazolyl, benzothienyl, benzothiazolyl cinnolinyl, furanyl, indazolyl, indolyl, imidazolyl, isoindolyl, isoquinolinyl, isothiazolyl, isoxazolyl, oxadiazolyl, oxazolinyl, oxazolyl, phthalazinyl, pyrazinyl, pyrazolinyl, pyrazolyl, pyridazinyl, pyridyl, pyrimidinyl, pyrrolyl, quinazolinyl, quinolinyl, quinoxalinyl, tetrazolyl, thiazolinyl, thiazolyl, thienyl, triazinyl, and triazolyl. Examples of fully saturated heterocyclyls include, but are not limited to, piperazinyl, piperidinyl, morpholinyl, pyrrolidinyl, tetrahydrofuranyl, and tetrahydropyranyl. Examples of partially unsaturated heterocyclyls include, but are not limited to, 1,2,3,4-tetrahydro-quînolinyl, 4,5-dihydro-oxazolyl, 4,5-dihydro-lH-pyrazolyl, 4,5-dihydro-isoxazolyl, and 2,3-dihydro[l,3,4]-oxadiazolyl.
“Insecticide Group” is defined under the heading “INSECTICIDES.” “Ncniaticide Group” is defined under the heading “NEMATICIDES” “Synergist Group” is defined under the heading “SYNERGISTIC MIXTURES AND SYNERG1STS”
DETA1LED DESCRIPTION OF THE INVENTION
This document discloses molécules having the following formulas:
Page 3of77
“Formula Two”
R1 R3 R4
R2 X1 “Formula Three” or
wherein:
Page 4 of77 “Formula Four” (a) Ari is (each independently) (1) furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, thienyl, or (2) substituted furanyl, substituted phenyl, substituted pyridazinyl, substituted pyridyl, substituted pyrimidinyl, or substituted thienyl, wherein said substituted furanyl, substituted phenyl, substituted pyridazinyl, substituted pyridyl, substituted pyrimidinyl, and substituted thienyl, hâve one or more substituents independently selected from H, F, Cl, Br, I, CN, NO2, Ci-Cô alkyl, Cj-Cè haloalkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C3-C6 cycloalkoxy, C3-C6 halocycloalkoxy, Ci-Cè alkoxy, C|-C6 haloalkoxy, C2-C6 alkenyl, C2-C6 alkynyl, S(=O)n(Ci-Cû alkyl), S(=O)n(C|-C6 haloalkyl), OSC^CcQ; alkyl), OSO2(Ci-C6 haloalkyl), C(=O)NRxRy, (C]-C6 alkyl)NRxRy, C(=O)(CrC6 alkyl), C(=O)O(C|-C6 alkyl), C(=O)(CrC6 haloalkyl), C(=O)O(Ci-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-Cû cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C& alkenyl), (C,-C6 aIkyl)O(CrC6 alkyl), (C,-C6 alkyl)S(C)-C6 alkyl), C(=O)(C,-C6 alkyl)C(=O)O(Ci-C6 alkyl), phenyl, phenoxy, substituted phenyl, and substituted phenoxy, wherein such substituted phenyl and substituted phenoxy hâve one or more substituents independently selected from H, F, Cl, Br, 1, CN, NO2, Cj-C6 alkyl, CpCfi haloalkyl, Ci-Cé hydroxyalkyl, C3-Cô cycloalkyl, C3-C6 halocycloalkyl, C3-C6 hydroxycycloalkyl, C3-C6 cycloalkoxy, C3-C6 halocycloalkoxy, C3-C6 hydroxycycloalkoxy, C(C6 alkoxy, C[-C6 haloalkoxy, C2-C6 alkenyl, C2-C6 alkynyl, S(=O)n(C]-C6 alkyl), S(=O)n(C|-C& haloalkyl), OSO2(C,-C6 alkyl), OSO2(CrC6 haloalkyl), C(=O)NRxRy, (CrC6 alkyl)NRxRy, C(=O)(C|-C6 alkyl), C(=O)O(Ci-C6 alkyl), C(=O)(C,-C6 haloalkyl), C(=O)O(C,-C6 haloalkyl), C(=O)(CrC6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (Ci-C6 alkyl)O(C,-C6 alkyl), (CrC6 alkyl)S(C,-C6 alkyl), C(=O)(CrC6 alkyl)C(=O)O(Ci-C& alkyl) phenyl, and phenoxy;
(b) Het is (each independently) a 5 or 6 membered, saturated or unsaturated, heterocyclic ring, containing one or more heteroatoms independently selected from nitrogen, sulfur, or oxygen, and where Αη and Ar2 are not ortho to each other (but may be meta or para, such as, for a five membered ring they are 1,3 and for a 6 membered ring they are either 1,3 or 1,4), and where said heterocyclic ring may also be substituted with one or more substituents independently selected from H, OH, F, Cl, Br, 1, CN, NO2, oxo, C|-Ce alkyl, C[-C6 haloalkyl, C|Cô hydroxyalkyl, C3-C6 cycloalkyl, C3-Câ halocycloalkyl, C3-C6 hydroxycycloalkyl, C3-C6 cycloalkoxy, C3-C6 halocycloalkoxy, C3-C6 hydroxycycloalkoxy, Cj-Ce alkoxy, Cj-C6 haloalkoxy, C2-Cft alkenyl, C2-Cù alkynyl, S(-O)n(C|-C6 alkyl), S(=O)„(C|-C& haloalkyl),
Page 5 of77 r
OSO2(Ci-C6 alkyl), OSO2(CrC6 haloalkyl), C(=O)NRxRy, (Ci-C6 aIkyl)NRxRy, C(=O)(C|-C6 alkyl), C(=O)O(CrC6 alkyl), C(=O)(C]-C6 haloalkyl), C(=O)O(C|-Cg haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C,-C6 alkyl)O(C|-C6 alkyl), (C(-C6 alkyl)S(C,-C6 alkyl), C(=O)(CrC6 3^1)0(=0)0(0,-06 alkyl), phenyl, phenoxy, substituted phenyl and substituted phenoxy wherein such substituted phenyl and substituted phenoxy hâve one or more substituents independently selected from H, OH, F, Cl, Br, 1, CN, N02, Cj-Cg alkyl, C|-Cû haloalkyl, C,-C6 hydroxyalkyl, C3-C6 cycloalkyl, C3-Cg halocycloalkyl, C3-Cô hydroxycycloalkyl, C3-Cû cycloalkoxy, C3-Cg halocycloalkoxy, C3-C6 hydroxycycloalkoxy, C,C6 alkoxy, C,-C6 haloalkoxy, C2-Cg alkenyl, C2-Cg alkynyl, S(=O)n(Ci-C6 alkyl), S(=O)n(Ci-C6 haloalkyl), OSO2(C,-C6 alkyl), OSO2(C,-C6 haloalkyl), C(=O)H, C(=O)OH, C(=O)NRxRy, (Cr C6 alkyl)NRxRy, C(=O)(CrC6 alkyl), C(=O)O(C|-C6 alkyl), C(=O)(C,-C6 haloalkyl), C(=0)0(CrC6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C]-C6 alkyl)O(Ci-C6 alkyl), (C,-C6 alkyl)S(Ci-C6 alkyl), C(=0)(C|-C6 alkyl)C(=O)O(Ci-Cû alkyl), phenyl, and phenoxy;
(c) Ar2 is (each independently) (1) furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, thienyl, or (2) substituted furanyl, substituted phenyl, substituted pyridazinyl, substituted pyridyl, substituted pyrimidinyl, or substituted thienyl, wherein said substituted furanyl, substituted phenyl, substituted pyridazinyl, substituted pyridyl, substituted pyrimidinyl, and substituted thienyl, hâve one or more substituents independently selected from H, OH, F, Cl, Br, I, CN, NO2, C|-Cg alkyl, C|-Cg haloalkyl, Cj-Cg hydroxyalkyl, Cj-Ce cycloalkyl, C3-C6 halocycloalkyl, C3-C6 hydroxycycloalkyl, C3-Cg cycloalkoxy, C3-Cg halocycloalkoxy, C3-Ce hydroxycycloalkoxy, C[Cg alkoxy, C|-Cg haloalkoxy, C2-C6 alkenyl, C2-Cg alkynyl, S(=0)n(C|-C6 alkyl), S(=0)n(C|-C6 haloalkyl), OSO2(C|-C6 alkyl), OSO2(Ci-C6 haloalkyl), C(=0)NRxRy, (Ci-C6 alkyl)NRxRy, C(=O)(Ct-C6 alkyl), C(=O)O(C]-C6 alkyl), C(=O)(C|-C6 haloalkyl), C(=O)O(C|-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-Cg alkenyl), C(=O)O(C2-C6 alkenyl), (Cj-Cg alkyl)O(C|-C6 alkyl), (C,-Cg alkyl)S(C|-C6 alkyl), C(=O)(Ci-C6 alkyl)C(=0)0(C|-C6 alkyl), phenyl, phenoxy, substituted phenyl and substituted phenoxy wherein such substituted phenyl and substituted phenoxy hâve one or more substituents independently selected from H, OH, F, Cl, Br, 1, CN, NO2, C|-Cû alkyl, Cj-Cû haloalkyl, C|-Cg hydroxyalkyl, C3-Cg cycloalkyl, C3-Cû halocycloalkyl, C3-C& hydroxycycloalkyl, C3-C6 cycloalkoxy, C3-C& halocycloalkoxy, C3-C6 hydroxycycloalkoxy, CiPage 6 of 77
C6 alkoxy, CrC6 haloaikoxy, C2-C6 alkenyl, C2-C6 alkynyl, S(=O)n(CrC6 alkyl), S(=O)n(Ci-Cû haloalkyl), OSChiQ-Cf, alkyl), OSO2(CrC6 haloalkyl), C(=O)H, C(=O)OH, C(=O)NRxRy, (CjC6 alkyl)NRxRy, C(=O)(CrC6 alkyl), C(=O)O(C,-C6 alkyl), C(=O)(C|-C6 haloalkyl), C(=O)0(Cj-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C|-Ce haloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (Ci-C6 aikyl)O(C|-C6 alkyl), (CrC6 alkyl)S(C|-C6 alkyl), C(=O)(C|-C& alkyl)C(=O)O(C|-C6 alkyl), phenyl, and phenoxy);
(d) RI and R2 are independently selected from H, Ci-Cô alkyl, C3-Cû cycloalkyl, C3Cfi hydroxycycloalkoxy, C2-C6 alkenyl, C2-C(, alkynyl, S(=0)n(Cj-C6 alkyl), OSO2(CrC6 alkyl), C(=O)H, C(=O)(CrC6 alkyl), C(=O)O(CrC6 alkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C,-C6 alkylJOtCrCô alkyl), (CrC6 alkyl)S(C|-C6 alkyl), C(=O)(Ci-C6 alkyl)C(=O)O(CrC6 alkyl), and phenyl, wherein each alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, and phenyl are optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, I, CN, NO2, oxo, Ci-Cô alkyl, C[-Cfi haloalkyl, Ci-Cé hydroxyalkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C3-C6 hydroxycycloalkyl, C3-Cô cycloalkoxy, C3-C6 halocycloalkoxy, C3-C6 hydroxycycloalkoxy, Ci-Cè alkoxy, Cj-Cô haloaikoxy, C2-Cô alkenyl, C2-Ce alkynyl, S(=O)n(C|C6 alkyl), S(=O)n(CrC6 haloalkyl), OSO2(CrC6 alkyl), OSO2(CrC6 haloalkyl), C(=O)NRxRy, (Ci-Cô alkyl)NRxRy, C(=O)(CrC6 alkyl), C(=O)O(C,-C6 alkyl), C(=O)(CrC6 haloalkyl), C(=O)O(CrC6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C,-C6 haloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C|-Cô alkyl)O(C|-C(j alkyl), (Cj-Cè alkyl)S(Ci-C6 alkyl), C(=O)(Ci-C6 aIkyI)C(=O)O(C|-C6 alkyl), phenyl, and phenoxy) optionally RI and R2 together with the carbons to which they are attached, form a 3-, 4-, 5-, or 6-membered carbocyclic or heterocyclic ring that is optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, I, CN, NO2, oxo, Cj-Ce alkyl, Ci-Cô haloalkyl, Ci-C& hydroxyalkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C3-C6 hydroxycycloalkyl, C3-Cfi cycloalkoxy, C3-C6 halocycloalkoxy, C3-Cû hydroxycycloalkoxy, CiCe alkoxy, Cj-Ce haloaikoxy, C2-C6 alkenyl, C2-Cé alkynyl, S(=O)n(C|-C6 alkyl), S(=O)n(Ci-Cû haloalkyl), OSO2(Ct-C6 alkyl), OSO2(C,-C6 haloalkyl), C(=O)NRxRy, (C,-C6 alkyl)NRxRy, C(=O)(CrC6 alkyl), C(O)0(C,-C6 alkyl), C(=O)(CrC6 haloalkyl), C(=O)O(C,-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (CrC6 alkyl)O(Ci-C6 alkyl), (CrC6 alkyl)S(C,-C6 alkyl), C(=O)(CrC6 alkyl)C(=O)O(C|-C6 alkyl), phenyl, and phenoxy;
Page 7 of 77 (e) R3 is H, CN, F, Cl, Br, I, C|-Cô alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkoxy, Cj-Cg alkoxy, C2-Cû alkenyl, C2-C& alkynyl, S(=O)n(Ci-C6 alkyl), OSO2(C|-Cg alkyl), OSO2(C|-Cg haloalkyl), C(=0)NRxRy, (Cj-C6 alkyl)NRxRy, C(=O)(C,-C6 alkyl), C(=O)O(Cj-C6 alkyl), C(=O)(CrC6 haloalkyl), C(=O)O(Cj-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (Cj-Cg alkyl)O(CrC6 alkyl), (Cj-C6 alkyl)S(Cj-Cô alkyl), C(=O)(C|-C6 alkyl)C(=O)O(Cj-C6 alkyl), phenyl, and phenoxy, wherein each alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, phenyl, and phenoxy are optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, I, CN, N02, oxo, Cj-Cû alkyl, Cj-Cû haloalkyl, C|-Cg hydroxyalkyl, C3-C6 IO cycloalkyl, C3-C6 halocycloalkyi, C3-C6 hydroxycycloalkyl, C3-C6 cycloalkoxy, C3-C6 halocycloalkoxy, C2-Cg hydroxycycloalkoxy, Cj-Cg alkoxy, Cj-Cg haloalkoxy, C2-Cg alkenyl, C2-Cg alkynyl, S(=0)n(Cj-C6 alkyl), S(=O)n(Ci-C6 haloalkyl), OSO2(C|-Cg alkyl), OSO2(Cj-Cg haloalkyl), C(=O)NRxRy, (C,-C6 alkyl)NRxRy, C(=O)(Cj-C6 alkyl), C(=O)O(C|-C6 alkyl), C(=O)(Cj-C6 haloalkyl), C(=O)O(C]-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-Cg 15 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (Cj-C6 alkyl)O(Cj-C6 alkyl), (Cj-C6 alkyl)S(Cj-C6 alkyl), C(=O)(C|-Cg alkyl)C(=O)O(C|-Cfi alkyl), phenyl, and phenoxy;
(f) R4 is H, CN, F, Cl, Br, 1, Ci-Cû alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkoxy, C|-C& alkoxy, C2-Cg alkenyl, C2-C6 alkynyl, S(=O)h(C|-Cg alkyl), OSO2(C|-C6 alkyl), OSO2(Cj-C6 haloalkyl), C(=O)NRxRy, (Ct-Cfi alkyl)NRxRy, C(=O)(C,-C6 alkyl), C(=O)O(Cj-C6 alkyl), C(=O)(Cj-C6 haloalkyl), C(=O)O(Cj-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-Cg alkenyl), C(=O)O(C2-Cg alkenyl), (Cj-Cg alkyl)0(Cj-C6 alkyl), (Cj-Cû alkyl)S(C|-C6 alkyl), C(=0)(Cj-C6 alkyl)C(=0)0(Cj-C6 alkyl), phenyl, and phenoxy, wherein each alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, phenyl, and 25 phenoxy are optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, I, CN, NO2, oxo, Cj-Cg alkyl, Cj-Cg haloalkyl, C|-Cg hydroxyalkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyi, C3-C6 hydroxycycloalkyl, C3-C6 cycloalkoxy, C3-C6 halocycloalkoxy, C3-CG hydroxycycloalkoxy, Cj-Cg alkoxy, Cj-Cg haloalkoxy, C2-Cg alkenyl, C2-C6 alkynyl, S(=O)n(Cj-C6 alkyl), S(O)n(Cj-C6 haloalkyl), OSO2(Cj-C6 alkyl), OSO2(C,-C6 30 haloalkyl), C(=O)NRxRy, (Cj-C6 alkyl)NRxRy, C(=O)(Ct-C6 alkyl), C(=O)O(Cj-C6 alkyl), C(=O)(C|-C6 haloalkyl), C(=O)O(C1-C6 haloalkyl), C(=O)(C3-Cfi cycloalkyl), C(=O)O(C3-Cg cycloalkyl), C(O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (Cj-C6 alkyl)O(Cj-C6 alkyl), (Cj-C6 alkyl)S(Cj-C6 alkyl), C(=O)(Cj-Cg alkyl)C(=O)O(C|-C6 alkyl), phenyl, and phenoxy;
Page 8 of 77 (g) R5 is H, CN, F, Cl, Br, I, C|-Cô alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkoxy, Ci-Ce alkoxy, C2-C6 alkenyl, C2-C6 alkynyl, S(=O)n(CrC6 alkyl), OSO2(Cl-C6 alkyl), OSO2(C,-C6 haloalkyl), C(=O)NRxRy, (Ci-C6 alkyl)NRxRy, C(=O)(CrC6 alkyl), C(=O)O(C|-C6 alkyl), C(=O)(CrC6 haloalkyl), C(=O)O(C!-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C0 alkenyl), C(=O)O(C2-C6 alkenyl), (C,-C6 alkyl)O(C!-Cû alkyl), (C,-C6 alkyl)S(C|-Cfi alkyl), C(=O)(C|-Cû alkyl)C(=O)O(C[-C6 alkyl), Het, phenyl, and phenoxy, wherein each alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, Het, phenyl, and phenoxy are optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, 1, CN, NO2, oxo, Ci-Ce alkyl, Cj-Cè haloalkyl, Ci-Ce hydroxyalkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C3-C6 hydroxycycloalkyl, C3-C6 cycloalkoxy, C3-C6 halocycloalkoxy, C3-Cê hydroxycycloalkoxy, Ci-C^ alkoxy, Cj-C^ haloalkoxy, C2-Ce alkenyl, C2-C6 alkynyl, S(=O)n(C|-C6 alkyl), S(=O)n(C,-C6 haloalkyl), OSO2(Ci-C6 alkyl), OSO2(C|-C6 haloalkyl), C(=O)NRxRy, (C,-C6 alkyl)NRxRy, C(=O)(C,-C6 alkyl), C(=O)O(C,-C6 alkyl), C(=O)(CrC6 haloalkyl), C(=O)O(Ct-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (Cj-C6 alkyl)O(C,-C6 alkyl), (C,-C6 alkyl)S(C|-Cù alkyl), C(=O)(C]-Cû alkyl)C(=O)O(C|-Cû alkyl), NRxRy, phenyl, and phenoxy;
(h) R6 is H, CN, F, Cl, Br, I, Cj-Cû alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkoxy, Ci-Cô alkoxy, C2-C6 alkenyl, C2-C6 alkynyl, S(=O)n(C|-C6 alkyl), OSO2(C|-C6 alkyl), OSO2(C|-C6 haloalkyl), C(=O)NRxRy, (C|-C6 alkyl)NRxRy, C(=O)(C,-C6 alkyl), C(=O)O(C]-C6 alkyl), C(=O)(C,-C6 haloalkyl), C(=O)O(CrC6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (CrC6 alkyl)O(C,-C6 alkyl), (Ci-C6 alkyl)S(C|-Cô alkyl), C(=O)(C|-C6 alkyl)C(=O)O(C|-C6 alkyl), phenyl, and phenoxy, wherein each alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, phenyl, and phenoxy are optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, I, CN, NO2, oxo, Ci-Ce alkyl, C|-Cû haloalkyl, Ci-Cû hydroxyalkyl, C3-Cû cycloalkyl, C3-Q halocycloalkyl, C3-C6 hydroxycycloalkyl, Cj-C^ cycloalkoxy, C3-C6 halocycloalkoxy, C3-Cè hydroxycycloalkoxy, Ci-Cê alkoxy, Ci-Cô haloalkoxy, C2-C<j alkenyl, C2-C6 alkynyl, S(=O)n(C]-C6 alkyl), S(=O)n(C|-C6 haloalkyl), OSO2(C,-C6 alkyl), OSO2(C|-C6 haloalkyl), C(=O)NRxRy, (CrC6 alkyl)NRxRy, C(=O)(Ct-C6 alkyl), C(=O)O(C!-C6 alkyl), C(=O)(CrC6 haloalkyl), C(=O)O(C,-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(Cj-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C,-C6 alkyl)O(Ci-C6 alkyl), (C,-C6 alkyl)S(C]-Cû alkyl), C(=O)(C|-Cô alkyl)C(=0)0(C|-C6 alkyl), Het, phenyl, and phenoxy;
Page 9 of 77 (i) R7 is H, CN, F, Cl, Br, I, Ci-Cg alkyl, Cj-Cô cycloalkyl, Cj-Cg cycloalkoxy, C|-C6 alkoxy, C2-C6 alkenyl, C2-C6 alkynyl, S(=O)n(Ci-C& alkyl), OSO2(C]-C6 alkyl), 0SO2(CrC6 haloalkyl), C(=O)NRxRy, (C|-C6 alkyl)NRxRy, C(=O)(Ci-C6 alkyl), C(=O)O(CrC6 alkyl), C(=O)(Ci-C6 haloalkyl), C(=O)O(CrC6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (Ci-C6 alkyl)O(Ci-C6 alkyl), (CrC6 alkyl)OC(=O)(Ci-Cfj alkyl), (CrC6 alkyl)S(CrC6 alkyl), C(=O)(CrC6 alkyl)C(=O)O(CrC6 alkyl), phenyl, and phenoxy, wherein each alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, phenyl, and phenoxy are optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, I, CN, NO2, oxo, Ci-Cé alkyl, C|-Cg haloalkyl, Ci-Cs hydroxyalkyl, C3-C& cycloalkyl, C3-Cg halocycloalkyl, C3-C6 hydroxycycloalkyl, C3-Cô cycloalkoxy, C3-Cg halocycloalkoxy, C3-Cô hydroxycycloalkoxy, Ci-C6 alkoxy, C|-C6 haloalkoxy, C2-C6 alkenyl, C2-C6 alkynyl, S(=O)n(CrC6 alkyl), S(=O)n(C!-C6 haloalkyl), OSO2(C(-C6 alkyl), OSO2(CrC6 haloalkyl), C(=O)NRxRy, (Ci-C6 alkyl)NRxRy, C(=O)(C|-C6 alkyl), C(=O)O(CrC6 alkyl), C(=O)(CrC6 haloalkyl), C(=O)O(CrC6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C,-C6 alkyl)O(CrC6 alkyl), (CrC6 alkyl)S(Ci-C<; alkyl), C(=O)(C|-C6 alkyl)C(=O)O(C|-Cô alkyl), phenyl, and phenoxy;
(j) XI îs S or O;
(k) n= 0, l, or 2 (each independently); and (l) Rx and Ry are independently selected from H, Cj-Cô alkyl, Ci-Cê haloalkyl, C[-Cg hydroxyalkyl, C3-Cô cycloalkyl, C3-Cg halocycloalkyl, C3-C6 hydroxycycloalkyl, C2-Cg alkenyl, C2-C6 alkynyl, S(=O)n(C|-C6 alkyl), S(=O)n(CrC6 haloalkyl), OSO^Cj-Cô alkyl), OSO2(Ci-C6 haloalkyl), C(=O)H, C(=O)(Ci-C6 alkyl), C(=O)O(C,-C6 alkyl), C(=O)(C,-C6 haloalkyl), C(=O)O(Ci-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C|-C6 alkyl)O(CrC6 alkyl), (Ct-C6 alkyl)S(C|-C6 alkyl), C(=O)(Ci-C6 alkyl)C(=O)O(Ci-C6 alkyl), and phenyl.
In another embodiment Αη is a substituted phenyl wherein said substituted phenyl, has one or more substituents independently selected from Ci-Cô haloalkoxy.
Page 10 of 77
In another embodiment Het is a triazoiyl. In another embodiment Het is a l ,2,4-triazolyl.
In another embodiment Het is a l ,2,4-triazolyl with one ring nitrogen atom bonded to Αη and one ring carbon bonded to Ar2.
In another embodiment Ar2 is a phenyl.
In another embodiment RI is H.
In another embodiment R2 is H.
In another embodiment RI, R2, and the carbons they are attached to form a cyclopropyl structure, in which case, RI & R2 are the linking carbon atom.
In another embodiment R3 is H.
In another embodiment R4 is H, In another embodiment R4 is a phenyl optionally substituted with one or more substituents independently selected from Cj-Cû alkyl.
In another embodiment R5 is Het or phenyl wherein each are optionally substituted with one or more substituents independently selected from F, Cl, Ci-Cg alkyl, Cj-Cù haloalkyl, C|-Cfi alkoxy, or NRxRy.
In another embodiment R.6 is Ci-Cô alkyl or phenyl wherein each are optionally substituted with one or more substituents independently selected from F, Cl, Ci-Cô alkyl, C|-Cû haloalkyl, Cj-Cé cycloalkyl, C|-C& alkoxy, Het, or phenyl.
In another embodiment R7 is (Cj-Ce alkyl)OC(=O)(C|-C6 alkyl).
While these embodiments hâve been expressed, other embodiments and combinations of these expressed embodiments and other embodiments are possible.
The molécules of Formula One, Two, Tliree, and Four will generally hâve a molecular mass of about 100 Daltons to about 1200 Daltons. However, it is generally preferred if the molecular mass is from about I20 Daltons to about 900 Daltons, and it is even more generally preferred if the molecular mass is from about I40 Daltons to about 600 Daltons.
Page 11 of77
EXAMPLES
The examples are for illustration purposes and are not to be construed as limiting the invention disclosed in this document to only the embodiments disclosed in these examples.
Starting materials, reagents, and solvents that were obtained from commercial sources were used without further purification unless otherwise stated. Anhydrous solvents were purchased as Sure/Seal™ from Aldrich and were used as received. Melting points were obtained on a Thomas Hoover Unimelt capillary melting point apparatus or an OptiMelt Automated Melting Point System from Stanford Research Systems and are uncorrected. Molécules are given their known names, named according to naming programs within ISIS Draw, ChemDraw or ACD Name Pro. If such programs are unable to name a molécule, the molécule is named using conventional naming rules. ’H NMR spectral data are in ppm (δ) and were recorded at 300, 400 or 600 MHz, and l3C NMR spectral data are in ppm (δ) and were recorded at 75, 100 or 150 MHz, unless otherwise stated.
Compounds of this invention can be prepared by making a triaryl intermediate, Ari-HetAr>, and then linking it to the desired intermediate to form the desired compound. A wide variety of triaryl intermediates can be used to préparé compounds of this invention, provided that such triaryl intermediates contain a suitable functional group on Ar2 to which the rest of the desired intennediate can be attached. Suitable functional groups include an oxoalkyl or a formyl group. These triaryl intermediates can be prepared by methods previously described in the chemical literature, including Crouse et al. PCT Int. Appl. Publ. W02009/102736 AL
PREPARATION OF CYCLOPROPYL-LINKED COMPOUNDS
Cyclopropyl-linked compounds of Formula One can be prepared from the correspondîng aryl aldéhydes via reaction with r-butyl diethylphosphonoacetate and a base, such as sodium hydride (NaH), in tetrahydrofuran (THF), al 0 °C. The unsaturated ester is converted to the cyclopropyl ester with trimethylsulfoxonium iodide in dimethyl sulfoxide (DMSO) at ambient température. The cyclopropyl acyl azide A can be prepared from the precursor ester in two steps by reaction first with trifluoroacetic acid (TFA) in dichloromethane (CH2Cl2) at températures from 0 to 25 °C and then with diphenylphosphorylazide (DPPA) and a base, such as triethylamine, in toluene at ambient température. The acyl azide A is converted via Curtius rearrangement with tert-butyl alcohol (r-BuOH) in toluene at 90 °C to the tert-butyl carbamate. The r-butyl carbamate is removed using TFA in dichloromethane at températures from 0 to 25 °C to provide the tri fl uoro acetate sait of the amine B. The thioureas can be prepared from the sait B with an appropriately substituted isothiocyanate (R5-NCX1, wherein XI = S) in the presence of
Page 12 of77 a base, such as triethylamine, in THF at 80 °C, or in a two-step process, by first reacting the sait
B with thiophosgene to generate an isothiocyanate, which is allowed to react with an appropriately substituted amine (R4R5NH) Likewise, ureas can be generated with an appropriately substituted isocyanate (R5-NCX1, wherein XI = O) in the presence of a base, such as triethylamine, in THF at 80 °C.
O o
OEt O-t-Bu
Me3S+0 r
--------------------->NaH, THF, 0 to 25 C
NaH, DMSO, 25 °C
1, TFA, CH2CI2, 0 to 25 °C
Het
A<
A f-BuOH, PhCH3, 90 °C
2, DPPA, Et3N, PhCH3, 25 °C
R5-N-C=X1, Et3N, THF, 80 °C
----------------------------------------------------------------------------------------------------------------s or
1. thiophosgene, CH2CI2l NaHCO3, 25 °C
2. R4R5-NH, dioxane, 25 “C
TFA, CH2CI2, 0 to 25 “C
ArfHekArr<LNH2 «TFA
B
X1 Rs
Formula One
Compounds of Formula Two may be synthesized by Curtius rearrangement of acyl azide A and other alcohols ((R6)OH) with or without a base, such as triethylamine, at 100 °C.
Altematively, the trifluoroacetate sait of the amine B can be allowed to react with substituted (R6) chloroformâtes in the presence of a base to give the compounds of Formulas Two.
Het
A<
A (R6)OH, PhCH3, 100 °C
Formula Two
-TFA (R6)OC(O)CI, CH2CI2i Et3N, 4-DMAP, 25 °C
Page 13 of77
B
Compounds of Formula Three can be produced via alkylation of compounds of Formula
One with an alkyl halide (R7) in a non-reactive solvent such as chloroform (CHCI3) at 100 °C.
alkyl halide (R7), CHCI3, 100 °C
Formula One
Formula Three
Compounds of Formula Four can be generated by reaction of the cyclopropyl carboxylic acid DPPA and a base, such as triethylamine, in ί-BuOH at 90 °C.
. 9 DPPA, Et3hl, t-BuOH, 90 “C
Het .<Aoh -------------Αη Ar2
Formula Four
Example 1: Préparation of (£)-3-{4-[ 1 -(4-trifluoromethoxyphenyl)-1 H-[ 1,2,4|triazoI-3yl]phenyl}acrylic acid fôri-butyl ester
Sodium hydride (NaH, 60% suspension in minerai oil; 440 milligrams (mg), 11.0 millimoles (mmol)) was suspended in THF (20 milliliters (mL)), and the mixture was cooled to 0 °C. r-Butyl diethylphophonoacetate (2.57 mL; 11.0 mmol) was added over 2 minutes (min). The mixture was stirred at 0 °C for another 15 min, during which time the grey slurry tumed clear within 5 min. 4-[l-(4-Trifluoromethoxyphenyl)-l//-[l,2,4]triazol-3-yl]-benzaldehyde (3.04 grams (g); 9.13 mmol) was suspended in THF (20 mL) and then added dropwise via cannula to the solution above. The mixture was then warmed to 25 °C, poured into saturated (satd) aqueous (aq) ammonium chloride (NH4CI; 200 mL), and extracted with 50% ethyl acetate (EtOAc)/hexanes (3 xlOO mL). The combined organic extracts were then dried over sodium sulfate (NaîSCM and concentrated in vacuo. The yellow solid residue was dissolved in dichloromethane (CH2CI2; 10 mL) and rapidly stirred as hexanes (100 mL) was added dropwise over 30 min. The light yellow crystals were collected on a Büchner funnel and dried in vacuo to afford the title compound ((2.93 g, 74%). The filtrate was concentrated in vacuo and purified by chromatography on silica gel (gradient elution with 15% to 40% to 80% EtOAc in hexanes) to afford additional product (0.215 g, 5%); mp 167-169 °C; ‘H NMR (400 MHz, CDClj) δ 8.58 (s, 1 H), 8.20 (d, J = 8.3 Hz, 2H), 7.80 (d, J = 8.9 Hz, 2H), 7.63 (d, J = 15.8 Hz, 1 H), 7.62 (d, J = 8.5
Page 14 of 77
Hz, 2H), 7.39 (d, J= 8.6 Hz, 2H), 6.44 (d, J = 16.0 Hz, 1H), 1.54 (s, 9H); HRMS-ES1 (m/z) [M]+ calcd for CiîI-HoFîNjCX 431.146; found, 431.1457.
Exaniple 2: Préparation of 2-{4-|l-(4-trifliioroniethoxyphenyl)-l//-l 1,2,4 jtri;izol-3yl]phenyi)cyclopropanecarboxylic acid tert-butyl ester
NaH (60% suspension in minerai oil; 400 mg, 10.1 mmol) and trimethylsulfoxonium iodide (2.22 g, 10 mmol) were charged into a round bottom flask with a stir bar and placed in an ice bath. DMSO (20 mL) was added over a period of 10 min with vigorous stirring, and then the resulting grey slurry was warmed to 25 °C and stirred for 1 h, during which time the slurry became clear. The enoate from Example 1 was dissolved in DMSO (20 mL) and added to the above solution via cannula over a period of 30 min. DMSO (5 mL) was used to transfer any remaining material from the flask. The resulting yellow-orange solution was stirred at 25 °C for 2 h, then warmed to 50 °C and stirred for 3 h. The solution was then cooled back down to 25 °C, stirred for another 12 h, and poured into ice water (300 mL). The mixture was extracted with 50% EtOAc/hexanes (3 xl50 mL), and the combined organic extracts were washed with brine, dried over Na2SO4, and concentrated in vacuo to give a pale orange solid. Purification by silica gel chromatography (gradient elution with 15% to 40% to 80% EtOAc in hexanes) afforded the product (2.19 g, 73%) as a light pink solid: mp 100-101 °C; 1H NMR (300 MHz, CDClj) δ 8.55 (s, 1 H), 8.10 (d, J = 8.4 Hz, 2H), 7.79 (d, J = 9.1 Hz, 2H), 7.38 (dd, J = 9.0, 0.8 Hz, 2H), 7.19 (d, J= 8.3 Hz, 2H), 2.49 (ddd, J = 9.2, 6.4, 4.2 Hz, 1H), 1.90 (ddd, J= 8.4, 5.4, 4.2 Hz, 1H), 1.57 (ddd, J = 9.9, 9.2, 4.6 Hz, 1H), 1.48 (s, 9H), 1.29 (ddd, J = 8.4, 6.4, 4.5 Hz, 1H); ESIMS m/z 446 (M+H).
Exaniple 3: Préparation of 2-{4-[l-(4-trifluoroniethoxyphcnyl)-l/7-[l,2,4|triazoI-3yl|phenyl}cyclopropanecarbonyl azide
Page 15 of77
Step l. To a solution of the Ze/7-butyl ester from Example 2 (0,562 g; 1.26 mmol) in
CH2CI2 (8.0 mL) at 25 °C was added trifluoroacetic acid (TFA; 4,0 mL). The solution was stirred at 25 °C for 18 h and was then concentrated in vacuo to afford the carboxylic acid TFA sait (665 mg) as a light pink solid.
Step 2. Without further purification, a portion of this solid (558 mg, 1.11 mmol) was slurried in toluene (PI1CH3; 3.2 mL). Triethylamine (EtîN; 0.368 mL, 2.66 mmol) was added, and the slurry clarified to give a yellow solution. Diphenylphosphoryl azide (DPPA; 0,287 mL,
1.33 mmol) was then added in one portion. The mixture was stirred for 2 h at 25 °C , at which point analysis of an aliquot by liquid chromatography-mass spectrometry (LC-MS) showed complété conversion to the product. The crude reaction mixture was directly applied to a silica gel column and purified (gradient elution with 15% to 30% EtOAc in hexanes) to afford the product (0.356 g, 78%) as a white solid: 'H NMR (300 MHz, CDCI3) δ 8.54 (s, 1H), 8.10 (d, J =
8.3 Hz, 2H), 7.78 (d, J= 9.0 Hz, 2H), 7.37 (d, J = 8.6 Hz, 2H), 7.18 (d, J = 8.2 Hz, 2H), 2.68 (ddd, J = 9.4, 6.8,4.1 Hz, 1H), 2.03-1.90 (m, 1H), 1.83-1.70 (m, 1H), 1.52 (ddd, J =8.3, 6.8,4.7 Hz, 1H); ESIMS m/z 387 (M+H).
Example 4: Préparation of (2-{4-fl-(4-trifluoromethoxyplienyl)-lZ/-{l,2,4]triazol-3 yl]phenyl}cyclopropyl)carbamic acid terr-butyl ester
2-{4-[l-(4-trifluoromethoxyphenyl)-lH-[l,2,4]triazol-3-yl]phenyl}cyclopropanecarbonyl azide (0.301 g, 0.727 mmol) was slurried in PhCH3 (2.0 mL). toï-Butyl alcohol (r-BuOH; 0.250 mL, 2.64 mmol) was added, and the resulting mixture was heated at 90 °C for 24 h. During this time the slurry became homogenous to give a yellow solution. The mixture was cooled to 25 °C , and an off-white precipitate was observed to form. The slurry was diluted with hexanes (3 mL) and filtered on a Buchner funnel to afford the product (0.252 g, 75%) as an off-white solid. The filtrate was concentrated in vacuo and purified by silica gel chromatography (gradient elution with 15% to 40% to 80% EtOAc in hexanes) to afford additional product (0.0154 g, 5%): mp 169-172 °C; *H NMR (300 MHz, CDCI3) δ 8.54 (s, 1H), 8.07 (d, J= 8.1 Hz, 2H), 7.78 (d, J =
8.9 Hz, 2H), 7.37 (d, J= 8.6 Hz, 2H), 7.21 (d, J= 8.1 Hz, 2H), 4.91 (s, J = 0.9 Hz, 1H), 2.86-
2.72 (m, 1H), 2.15-2.03 (m, 1H), 1.46 (s, 9H), 1.29-1.15 (m, 2H); ESIMS m/z 461 (M+H).
Examplc 5: Préparation of 2-{4-|l-(4-trifluoromethoxyphenyl)-lH-[l,2,4|triazol-3yl|phenyl}cyclopropylamine
The carbamate from Example 4 (0.249 g, 0.541 mmol) was slurried in CH2CI2 (3.5 mL) at 25 °C, and TFA (1.5 mL) was added. The solids dissolved to give an orange solution. The mixture was stirred at 25 °C for 2 h and was then concentrated in vacuo to afford an orange oil. This material was carried forward without further purification. An analytical sample was prepared by dîssolving ca. 20 mg of the oil in CH2CI2 (0.4 mL) and adding Et3N (0.007 mL, 0.05 mmol). After l h, a white precipitate was observed to form. The solid was collected on a Büchner funnel and dried in vacuo to afford the pure amine in freebase form (10.5 mg) as a white solid: mp 149-152 °C; 'H NMR (300 MHz, methanol-i/4) δ 9.15 (s, IH), 8.09 (d, J= 8.4 Hz, 2H), 8.02 (d, J= 9.2 Hz, 2H), 7.50 (dd, J= 9.1, 0.8 Hz, 2H), 7.30 (d, J= 8.3 Hz, 2H), 2.93 (ddd, J =7.9, 4.5,3.6 Hz, IH), 2.43 (ddd, J= 10.1,6.7, 3.6 Hz, IH), 1.54-1.34 (m, 2H); ESIMS m/z 361 (M+H).
Examplc 6: Préparation of l-phenyI-3-(2-[4-[l-(4-trifluoromethoxyphenyl)-lZ/[l,2,4]triazol-3-yljphenyl}cyclopropyl)thiourea (Compound 1)
The amine trifluoroacetate sait from Example 5 (0.064 g, 0.135 mmol) was dissolved in THF (0.5 mL). Et3N (0.037 mL, 0.27 mmol) was added, followed by phenyl isothiocyanate (0.020 mL, 0.15 mmol). The resulting dark yellow solution was heated to 80 °C and stirred for 4 h. The solution was cooled to 25 °C , loaded directly onto a silica gel column and purified (gradient elution with 15% to 40% to 80% EtOAc in hexanes) to afford the product (0.0222 g, 33%) as a yellow oil: IR vniax 3380, 3218 (br), 1617, 1598, 1518, 1497, 1448, 1356, 1326, 1264, 1221, 1168, 1111, 1065, 986,910, 851,756, 732, 694 cm'1; 'H NMR (300 MHz, CDCi3) δ 8.56 (s, IH), 8.11 (d, J = 8.3 Hz, 2H), 7.90 (br s, 1 H), 7.78 (d, J = 9.0 Hz, 2H), 7.46 - 7.32 (m, 5H), Page 17 of77
7.31 - 7.21 (m, 5H), 3.10 (brs, l H), 2.25 (brs, IH), l.5l - l.30(m,2H); HRMS-ESI (m/z) [M]+ calcd for C25H20F3N5OS, 495.134; found, 495.1341.
The following compounds were synthesized in accordance with Example 6 above.
l-(2,6-Dichloropiienyl)-3-(2-{4-| l-(4-triiluoroniethoxyphenyl)-U/-| l,2,4]triazol-3yl|phenyl}cyclopropyl)thiourca (Compound 2)
The product was isolated as a yellow solid (0.021 g, 28%); mp 118-123 °C; 'H NMR (300 MHz, CDCI3) 6 8.56 (s, IH), 8.10 (d, J = 8.3 Hz, 2H), 7.78 (d, J= 9.1 Hz, 2H), 7.47 - 7.33 (m, 5H), 7.29 - 7.16 (m, 4H), 3.00 (br s, IH), 2.42 (br s, IH), 1.57 - 1.42 (m, 2H); HRMS-ESI (m/z) [M]+ calcd for C25H|8Ci2F3NsOS, 563.056; found, 563.0562.
l-(4-Methoxy-2-methylphenyl)-3-(2-{4-| l-(4-trifluoromethoxyphenyl)-l#-[ 1,2,4] triazol-3yl]phenyl}cyclopropyl)thiourea (Compound 3)
The product was isolated as a yellow solid (0.013 g, 18%): IR vmax 3377, 3220 (br), 2928, 2854, 1612, 1517, 1446, 1247, 1162, 1113, 1047, 986, 909, 850, 731 cm'1; 'H NMR (300 MHz, CDCI3) δ 8.55 (s, IH), 8.09 (d, J= 8.3 Hz, 2H), 7.79 (d, J = 9.1 Hz, 2H), 7.44 (br s, IH), 7.38 (m, 2H), 7.28 (br s, 2H), 7.17 (br s, 1 H), 6.81 (br s, 1 H), 6.78 (d, J = 8.6, 2.7 Hz, I H), 5.80 (br s, IH), 3.81 (s, 3H), 3.20 (br s, 1 H), 2.25 (s, 3H), 2.17 (br s, IH), 1.29- 1.22 (m, 2H); HRMS-ESI (m/z) [M]+ calcd for C27H24F3N5O2S, 539.160; found, 539.1602.
l-(4-ChloiO-2-mcthylphenyl)-3-(2-{4-[l-(4-trifluoiOmethoxyphenyl)-l/7-[l,2,4|trÎazol-3yl]pheny!}cyclopropyl)thiourca (Compound 4)
Page 18 of77
The product was isolated as an off-white oily foam (53.4 mg, 82%): IR νπι:ιχ 3210 (br), 3029, 2978, 1728, 1518, 1492, 1446, 1354, 1327, 1264 cm'1; *H NMR (300 MHz, CDClj) 5 8.55 (s, 1 H), 8.11 (d, J = 8.3 Hz, 2H), 7.78 (d, J = 9.0 Hz, 2H), 7.51 (br s, 1 H), 7.42 - 7.35 (m, 2H),
7.30 - 7.08 (m, 6H), 3.10 (br s, IH), 2.38 - 2.09 (app s, 4H), 1.55 - 1.29 (m, 2H); HRMS-ESI (m/z) [M]+ calcd for C26H21CIF3N5OS, 543.1107; found, 543.1109.
l-(2-Chlorophenyl)-3-(2-{4-[l-(4-trifIiioromethoxyphenyl)-l//-[li2,4]triazol-3yljphenyl]cyclopropyl)thiourea (Compound 5)
The product was isolated as a white solid (49.0 mg, 78%): mp 176-179 °C; ’H NMR (300 MHz, CDCh) δ 8.56 (s, 1H), 8.12 (d, J = 8.3 Hz, 2H), 8.02 (br s, 1H), 7.79 (d, J= 9.0 Hz, 2H),
7.43 -7.35 (m, 3H), 7.31 (td,J=7.9, 1.4 Hz, 1 H), 7.25 - 7.10 (m, 4H),6.81 (brs, 1H), 3.04 (br s, 1H), 2.49 - 2.28 (m, 1H), 1.62 - 1.39 (m, 2H); HRMS-ESI (m/z) [M]+ calcd for C25H19C1F3N5OS, 529.0951; found, 529.0950.
l-(2,6-Dicthylphenyi)-3-(2-{4-| l-(4-trifluoromethoxyphcnyl)-lH-[ 1,2,4] triazol-3yl]phenyl}cyclopropyl)thiourea (Compound 6)
Page 19 of77
The product was isolated as a light yellow oil (24.5 mg, 36%): IR vmax 3375, 3180 (br),
2971, 2937, 2876, 1518, 1326, 1264, 1168,1111,1064, 986, 910, 851, 731 cm'1 ; 1H NMR (400
MHz, CDCI3) 8 8.55 (s, 1 H), 8.09 (d, J = 8.2 Hz, 2H), 7.79 (d, J= 9.0 Hz, 2H), 7.41 - 7.36 (m,
2I-I), 7.35-7.28 (m, 3H), 7.24 - 7.12 (m, 3H), 5.55 (s, IH), 3.29 - 3.22 (m, IH), 2.73 - 2.52 (m,
4H), 2.13 - 2.05 (m, IH), l.4l - l.09 (m, 8H); HRMS-ESI (m/z) [M]+ calcd for C29H28F3N5OS,
551.197; found, 551.1967.
l-(4-Diniethylaminophenyl)-3-(2-{4-[l-(4-tnfIuoromethoxyphcnyl)-l//-|l,2,4|triazol-3yl]phenyl}cyclopropyl)thiourea (Compound 7)
The product was isolated as a yellow-orange solid (47.8 mg, 75%): mp 190.5-192.5 °C; lH NMR (300 MHz, CDC13) δ 8.54 (s, IH), 8.09 (d, J = 8.3 Hz, 2H), 7.79 (d, J= 9.0 Hz, 2H),
7.58 (s, 1 H), 7.37 (d, J = 9.0 Hz, 2H), 7.27 (d, J = 9.4 Hz, 2H), 7.10 (br d, J = 7.5 Hz, 2H), 6.70 (d, 7=9.0 Hz, 2H), 6.10 (brs, 1 H), 3.30 - 3.10 (m, 111),2.98 (s, 6H), 2.25-2.12 (m, IH), 1.47 - 1.18 (m, 2H); HRMS-ESI (m/z) [M]+ calcd for C27H25F3N6OS, 538.1763; found, 538.1754.
l-(2-{4-[l-(4-TrifluoiOmethoxyphenyl)-lJ/-|l,2,4]triazol-3-yI]phenyl}-cyclopropyl)-3-(4- trifluoromethylphenyl)thiourea (Compound 8)
The product was isolated as a white foam (50.5 mg, 73%): IR vmiW 3377, 3217 (br), 3027, 1617, 1518, 1446, 1417, 1327, 1267, 1223, 1167, 1126, 1067, 1018, 987, 909, 841, 732 cm'1; ’H NMR (300 MHz, CDC13) δ 8.57 (s, IH), 8.15 (d, J= 8.3 Hz, 2H), 7.94 (brs, IH), 7.79 (d, J= 9.0 Hz, 2H), 7.67 - 7.56 (m, 4H), 7.39 (d, J = 8.5 Hz, 2H), 7.24 (d, J = 9.5 Hz, 2H), 6.82 (br s, IH), 2.98 (br s, IH), 2.41 - 2.25 (m, IH), 1.70 - 1.39 (m, 2H); HRMS-ESI (m/z) [M]+ calcd for C26H|9F6N5OS, 563.122; found, 563.1217.
l-(2-{4-(l-(4-Trifluoi,omethoxyphenyl)-l/7-|l,2,4|triazol-3-yl|phenyI}-cyclopropyl)-3-(2,4,6trimetliylphcnyl)thiourca (Compound 9)
Page 20 of 77
The product was isolated as a white foain (55.0 mg, 78%): IR vmM 3373, 3205 (br), 3025, 2922, 1616, 1517, 1492, 1262, 1221, I166, 986, 910, 852, 731 cm’1; 'H NMR (300 MHz, CDClj) δ 8.54 (s, 1 H), 8.09 (d, J = 7.8 Hz, 2H), 7.78 (d, J = 9.0 Hz, 2H), 7.37 (d, J = 8.5 Hz, 2H), 7.33 - 7.27 (m, 2H), 7.24 - 7.13 (m, 1H), 6.96 (app s, 2H), 5.59 (s, IH), 3.26 (br s, IH),
2.30 (s, 3H), 2.22 (s, 6H), 2.17 - 2.06 (m, IH), 1.42 - 1.04 (m, 2H); HRMS-ESI (m/z) [M]+ calcd for C28H26F3N5OS, 537.181; found, 537.1812.
l-(2,4-Diniethoxyphenyl)-3-(2-{4-[l-(4-trifluoromethoxyphenyl)-l/7-ll,2,4]triazol-3yl]phenyl}cyclopropyl)thiourea (Compound 10)
The product was isolated as a light yellow foam (58.2 mg, 69%): IR vmax 3357, 3204 (br), 2976, 2838, 1619, 1549, 1517, 1495, 1460, 1262, 1208, 1182, 1159, 1047, 1031,985 cm'1; 'H NMR (400 MHz, CDCI3) Ô 8.56 (s, 1 H), 8.50-7.60 (br, 2H), 8.11 (d, J = 8.3 Hz, 2H), 7.79 (d, J =
9.1 Hz, 2H), 7.38 (d, J= 8.9 Hz, 2H), 7.24 (d, 7.8 Hz, IH), 6.40 - 6.90 (br m, 2H), 6.50 (dd,
J= 8.8, 2.6 Hz, IH), 6.44 (s, IH), 3.79 (s, 3H), 3.62 (br s, 3H), 3.05 (br s, IH), 2.29 (br s, IH),
1.50 - 1.35 (m, 2H); HRMS-ESI (m/z) [M]+ calcd for C^HmFîNsOjS, 555.1552; found, 555.156.
Example 7: Préparation of 3-(4-(2-isothiocyanatocyclopropyl)phenyl)-l-(4(trifluoromethoxy)phcnyl)-17/-1,2,4-triazole
Page 21 of77
1650*1
Thiophosgene (0.173 mL, 2.256 mmol) was added to a rapidly stirred mixture of CH2Cl2 (11 mL) and satd aq NaHCOj (11 mL) at 25 °C. The amine trifluoroacetate sait from Example 5 (1.07 g, 2.256 mmol) was then added, and stirring was continued for 10 min, during which time the solids completely dissolved. The layers were separated, the aqueous phase was extracted with CH2C12, and the combined organic extracts were concentrated to afford the isothiocyanate as a yellow solid (0.86 g, 95%); mp 99-104 °C; 'H NMR (400 MHz, CDC13) δ 8.55 (s, IH), 8.12 (d, J = 8.4 Hz, 2H), 7.79 (d, J = 9.1 Hz, 2H), 7.38 (dd, J = 9.0, 0.7 Hz, 2H), 7.16 (d, J - 8.2 Hz, 2H), 3.05 (ddd, J = 7.5, 4.3, 3.3 Hz, IH), 2.49 (ddd, J = 10.1,7.0, 3.2 Hz, IH), 1.56 (ddd, J = 10.0,
6.3, 4.3 Hz, IH), 1.47 - 1.37 (m, IH); ESIMS m/z 403 (M+H).
Exaniple 8: Préparation of l-(2,4-Dimethylphenyl)-3-(2-(4-(l-(4-(trifluoroniethoxy)phcnyl)127-1,2,4-triazol-3-yl)phenyl)cycIopropyl)thiourca (Compound 11)
The isothiocyanate from Example 7 (50 mg, 0.124 mmol) was dissolved in dioxane (0.35 mL) at 25 °C, and 2,4-dimethylaniline (16.6 mg, 0.137 mmol) was added in one portion. The mixture was stirred at 25 °C for 20 h and was then concentrated in vacuo. Silica gel chromatography (gradient elution with 10% to 50% to 100% EtOAc in hexanes) provided the title compound (43.3 mg, 67%) as a Iight yellow oil: IR vllKW 3379, 3215, 3025, 1616, 1446, 1517, 1326, 1262, 1165, 1111, 1064, 986, 909, 850, 731 cm'1; 'H NMR (400 MHz, CDCh) δ
8.55 (s, IH), 8.10 (d, J = 8.3 Hz, 2H), 7.79 (d, J = 9.0 Hz, 2H), 7.46 (s, IH), 7.38 (dd, J = 9.0, 0.7 Hz, 2H), 7.33 - 7.22 (m, 2H), 7.21 - 7.01 (m, 3H), 3.19 (br s, IH), 2.34 (s, 3H), 2.24 (s, 3H), 2.20 (br s, IH), 1.40 (br s, IH), 1.34 - 1.21 (m, 2H); HRMS-ESI (m/z) [M]+ calcd for C27H24F3N5OS, 523.1654; found, 523.1653.
The following compounds were synthesized in accordance with Example 8.
l-(2,6-Diniethylphenyl)-3-(2-(4-(l-(4~(trifluoromethoxy)phenyl)-lH-l,2,4-triazol-3yl)phenyl)cyclopropyi)thiourea (Compound 12)
Page 22 of 77
The réaction mixture was heated at 100 °C for 12 h, and the product was isolated as a tan foam (26.9 mg, 4l%): IR vmax 3372, 3208, 3032, 2976, 2916, 2143, 1617, 1517, 1493, 1445, 1326, 1262, 1167, 1111, 1064 cm*1; lH NMR (400 MHz, CDC13, data for major rotamer) δ 8.55 (s, 1H), 8.08 (d, J = 7.4 Hz, 2H), 7.78 (d, J = 9.0 Hz, 2H), 7.58 (br s, 1H), 7.37 (d, J = 8.3 Hz, 2H), 7.34 - 7.08 (m, 5H), 5.58 (br s, 1H), 3.26 (br, 1H), 2.28 (s, 6H), 2.11 (br s, 1H), 1.34 (s, 1H), 1.18 (s, 1H); HRMS-ESI (m/z) [M]+ calcd for C27H24F3N5OS, 523.1654; found, 523.1653.
l-(2-Isopropyl-4-methoxyphenyl)-3-(2-(4-(l-(4-(trîfluoroniethoxy)phenyI)-l/Z-l,2,4-triazol-
3-yI)phenyl)cycIopropyl)thiourea (Compound 13)
The reaction mixture was stirred at 25 °C for 4 h, and the product was isolated as a lavender solid via filtration of the reaction mixture (43 mg, 51%): mp 130-134 °C; 'H NMR (400 MHz, CDC13) δ 8.54 (s, 1 H), 8.10 (d, J = 8.3 Hz, 2H), 7.79 (d, J = 9.0 Hz, 2H), 7.44 - 7.34 (m, 3H), 7.28 (d, J = 7.9 Hz, 2H), 7.21-7.10 (m, 1H), 6.89 (d, J = 2.6 Hz, 1H), 6.78 (dd, J =
8.6,2.9 Hz, 1H), 5.78 (br, 1H), 3.83 (s,3H),3.21 (brs, 1H), 3.14 - 3.03 (m, 1H), 2.16 (br s, 1H), 1.42 - 1.32 (m, 1 H), 1.30 - 1.17 (m, 1 H), 1.20 (d, J = 6.9 Hz, 3H), 1.19 (d, J = 6.9 Hz, 3H); HRMS-ESI (m/z) [M]+ calcd for C29H28F3N5O2S, 567.1916; found, 567.1928.
l-(6-Methoxy-2,4-diniethylpyridin-3-yl)-3-(2-(4-(l-(4-(trifluoi'omethoxy)-phcnyI)-177-1,2,4triazol-3“yl)phenyl)cyclopropyl)tluourea (Compound 14)
Page 23 of77
The réaction mixture was stirred for 20 h at 25 °C, and the product was isolated as an offwhite solid (59.6 mg, 72%): mp 182-188 °C; ’H NMR (400 MHz, CDCI3, mixture of rotamers) δ 8.54 (s, 1H), 8.10 (br d, 7= 6.1 Hz, 2H), 7.78 (d, J = 9.0 Hz, 2H), 7.38 (d, J= 8.3 Hz, 2H), 7.35 -7.05(m, 4H), 6.51 (brs, ÎH), 5.57 (br s, 0.5H), 3.91 (s, 3H), 3.48-3.21 (m, 0.5H), 2.93 (dd,J = 8.6,5.1 Hz, 0.5H), 2.39 (br s, 3H), 2.21 (brs, 3H), 2.12 (br, 0.5H), 1.64 - 1.46 (br, 1H), 1.431.32 (br, 0.5H), 1.25 - 1.10 (br, 0.5H); HRMS-ES1 (m/z) [M]+ calcd for CavHisFsNeOaS, 554.1712; found, 554.1727.
Example 9: Préparation of (Z)-(/V-(2,6-dimethylphenyI)-A-(2-(4-(l-(4(trifluoromethoxy)phenyl)-17/-1,2,4-triazol-3-yl)phcnyl)cyclopropyl)carbaniinndoylthiojmethyl isobutyrate (Compound 15)
To a solution of l-(2,6-dimethylphenyl)-3-(2-(4-(l-(4-(trifluoromethoxy)-phenyl)-l//l,2,4-triazol-3-yl)phenyl)cyclopropyl)thiourea (75 mg, 0.143 mmol) in chloroform (CHCI3; 0.72 mL) was added chloromethyl isobutyrate (3.1.1 mg, 0.172 mmol). The mixture was heated at 100 °C for 1 h. The mixture was cooled to 25 °C, and the residue was purified by siiica gel chromatography (EtOAc-hexanes gradient) to afford the title compound (17.3 mg, 19%) as a yellow oil: IR vmax 3332 (br), 3124, 2976, 2939, 1739, 1631, 1590, 1518, 1264, 1171, 986 cm'1; ’H NMR (400 MHz, CDCI3) δ 8.54 (s, 1H), 8.09 (d, J = 8.3 Hz, 2H), 7.79 (d, J = 9.0 Hz, 2H), 7.37 (d, J = 8.3 Hz, 2H), 7.20 (d, J = 7.2 Hz, 2H), 7.02 (d, J = 7.5 Hz, 2H), 6.88 (t, J = 7.5 Hz, l H), 5.65 (br s, 2H), 2.88 (br s, 1 H), 2.68 - 2.52 (m, 1 H), 2.10 (s, 6H), 1.82 - 1.46 (m, 2H), 1.46 - 1.22 (m, 2H), 1.22- 1.18 (m, 6H); ESIMS m/z 624 (M+H).
The following compound was synthesized in accordance with Example 9.
(Z)-(7V1-lVIesityl-/V-(2-(4-(l-(4-(trifiiioromethoxy)phenyl)-lZ/-l,2,4-tnazol-3yl)phcnyl)cyclopropyl)carbaminüdoyltiuo)inethyl isobutyrate (Compound 16)
Page 24 of 77
The product was isolated as a reddish-brown foam (48.3 mg, 20%): IR vmax 2974, 2921, 1739, 1612, 1515, 1298, 1205, 1163, 1053, 1025, 1006, 985, 852, 818, 755 cm'1; 'H NMR (600 MHz, DMSO-rfô, 100 °C) δ 9.22 (s, 1H), 8.03 (d, J = 9.0 Hz, 2H), 7.99 (d, J = 8.2 Hz, 2H), 7.55 (d, J = 8.9 Hz, 2H), 7.24 (d, J = 8.0 Hz, 2H), 6.78 (s, 2H), 5.55 (s, 2H), 2.60 - 2.52 (m, 1H), 2.26 - 2.12 (m, 1 H), 2.18 (s, 3H), 2.04 (s, 6H), 1.55 - 1.34 (m, 1 H), 1.32 - 1.22 (m, 1 H), 1.13 (d, J = 7.0 Hz, 3H), 1.12 (d, J = 7.0 Hz, 3H); ESIMS m/z 638 (M+H).
Exaniple 10: fert-Butyl 2-(4-(l-(4-(trifluoromethoxy)plienyl)-l//~l,2,4-triazol-3-yl)phenyl)cyclopropylcarbamate (Compound 17)
2-{4-[ l-(4-trifluoromethoxyphenyl)-1 H-[ 1,2,4]triazol-3-yl]phenyl}cyclopropanecarbonyl azide (0.301 g, 0.727 mmol) was slurried in PhCH3 (2.0 mL). ferf-Butyl alcohol (Z-BuOH; 0.250 mL, 2.64 mmol) was added, and the resulting mixture was heated at 90 °C for 24 h. During this time the slurry became homogenous to give a yellow solution. The mixture was cooled to 25 °C , and an off-white precipitate was observed to form. The slurry was diluted with hexanes (3 mL) and filtered on a Buchner funnel to afford the title compound (0.252 g, 75%) as an off-white solid. The filtrate was concentrated in vacuo and purified by silica gel chromatography (gradient elution with 15% to 40% to 80% EtOAc in hexanes) to afford additional product (0.0154 g, 5%): mp 169-172 °C; 'H NMR (300 MHz, CDC13) δ 8.54 (s, 1H), 8.07 (d, J= 8.1 Hz, 2H), 7.78 (d, J = 8.9 Hz, 2H), 7.37 (d, J =8.6 Hz, 2H), 7.21 (d, J =8.1 Hz, 2H), 4.91 (s, J =0.9 Hz, 1H), 2.86-
2.72 (m, 1 H), 2.15-2.03 (m, 1 H), 1.46 (s, 9H), 1.29-1.15 (m, 2H); ESIMS m/z 461 (M+H).
The following compounds were synthesized in accordance with Example 10.
Methyl 2-(4-(1-(4-(trifluoromethoxy)phenyI)-l//-1,2,4-triazol-3-yl)phenyl)cyclopropylcarbaniate (Compound 18)
Page 25 of 77
The product was isolated as an off-white solid (43.6 mg, 74%): mp 227-228.5 °C; ’h
NMR (400 MHz, DMSO-i/fi) δ 9.38 (s, IH), 8.06 (d, J = 9.0 Hz, 2H), 7.99 (d, J = 8.2 Hz, 2H),
7.61 (d, J = 8.6 Hz, 2H), 7.24 (d, J = 8.3 Hz, 2H), 3.54 (s, 3H), 2.82 - 2.38 (m, IH), 2.00 (td, J = 7.7, 2.5 Hz, IH), 1.26 - 1.13 (m, 2H); HRMS-ESI (m/z) [M]+ calcd for C30H|7F3N4O3,
418.125; found, 418.1252.
l-Phenylethyl 2-(4-(l-(4-(trifluoromethoxy)phenyl)-lJ/-l,2,4-triazol-3-yl)phenyl)- cyclopropylcarbaniate (Compound 19)
The product was purified by silica gel chromatography (EtOAc-hexanes gradient) and isolated as a light yellow solid (73.7 mg, 66%): mp 125-137 °C; ‘H NMR (400 MHz, CDC13, 1:1 dr) δ 8.55 (s, IH), 8.08 (d, J = 8.3 Hz, 2H), 7.79 (d, J = 9.0 Hz, 2H), 7.44 - 7.12 (m, 9H), 5.85 (q, J = 6.6 Hz, IH), 5.08 (s, IH), 2.87 - 2.77 (m, IH), 2.20 - 2.05 (m, IH), 1.56 (diastereomer A, d, J = 4.7 Hz, 1.5 H), 1.54 (diastereomer B, d, J = 4.7 Hz, 1.5 H), 1.41 - 1.15 (m, 2H); ESIMS m/z 510 (M+H).
l-(Pyridin-2-yl)ethyl 2-(4-(l-(4-(trifluoromethoxy)phenyl)-l/f-l,2,4-triazol-3-yI)phenyl)cyclopropylcarbaniate (Compound 20)
The product was purified by silica gel chromatography (EtOAc-hexanes gradient) and isolated as a light yellow solid (83.6 mg, 73%). mp 122-130 °C. 'H NMR (400 MHz, CDC13, 3:2 dr, data for major diastereomer) δ 8.59 (d, J = 3.4 Hz, IH), 8.55 (s, 1 H), 8.08 (d, J = 8.3 Hz, Page 26 of 77
2H), 7.79 (d, J = 8.9 Hz, 2H), 7.67 (s, l H), 7.43 - 7.35 (m, 2H), 7.35 -7.29 (m, l H), 7.25 - 7.13 (m, 3H), 5.88 (q, J = 6.6 Hz, lH), 5.22 (br s, IH), 2.84 (br s, lH), 2.28 -2.06 (m, IH), l.6l (d,J = 6.2 Hz, 3H), 1.40 - l .15 (m, 2H); ESIMS m/z 5 U (M+H).
Examplc 11: Phenyl 2-(4-(l-(4-(trifluoromethoxy)phenyI)-l/Z-l,2,4-triazol-3-
2- (4-[ 1 -(4-trifluoromethoxyphenyl)-l H-[ 1,2,4]triazol-3-yl]phenyl} cyclopropanecarbonyl azide (75 mg, 0.18 mmol, 1.0 equiv) was slurried in PI1CH3 (0.52 mL, 0.35 M). Phénol (18.7 mg, 0.199 mmol, l.l equiv) was added, and the resulting mixture was heated at 100 °C for 2 h. During this time the slurry homogenized to give a yellow solution. The mixture was then cooled to 25 °C and Et3N (32.8 pL, 0.235 mmol, 1.3 equiv) was added. An off-white precipitate was observed to form. The mixture was diluted with 20% EtOAc in hexanes, and the product was collected by vacuum filtration to afford the title compound (62.9 mg, 72%) as an off-white solid: mp 171-173 °C; *H NMR (400 MHz, CDC13) δ 8.54 (s, IH), 8.09 (d, J = 8.3 Hz, 2H), 7.79 (d, J = 9.0 Hz, 2H), 7.44 - 7.31 (m, 4H), 7.28 (d, J = 7.7 Hz, 2H), 7.21 (t, J = 7.4 Hz, 1 H), 7.15 (d, J = 7.9 Hz, 2H), 5.42 (s, IH), 2.90 (s, IH), 2.27 (ddd, J = 9.6, 6.6, 3.2 Hz, IH), 1.27 - 1.04 (m, 2H); ESIMS m/z 480 (M+H).
The following compounds were synthesized in accordance with Example 11.
4-Fluoro-2-methylphenyi 2-(4-(l-(4-(trifluoromethoxy)phcnyl)-lZZ-l,2,4-triazol-3-yl)phenyl)cyclopropylcarbamate (Compound 22)
The product was isolated as an off-white solid (58.7 mg, 63%): mp 172-175 C; 'H NMR (400 MHz, CDCI3) Ô 8.55 (s, 1 H), 8.09 (d, J = 8.3 Hz, 2H), 7.78 (d, J = 9.0 Hz, 2H), 7.44 - 7.35 (m, 2H), 7.35 - 7.21 (m, 2H), 7.04 (dd, J = 8.1, 5.0 Hz, IH), 6.95 - 6.81 (m, 2H), 5.46 (s, IH),
Page 27 of 77
3.16 - 2.67 (m, IH), 2.28 (dd, J = 6.4, 3.2 Hz, l H), 2.21 (s, 3H), 1.46 - 1.23 (m, 2H); ESIMS m/z5l3 (M+H).
2-Cyclopcntylphenyl 2-(4-(l-(4-(trifluoromethoxy)phenyl)-7//-l,2,4-triazol-3-yl)phenyl)cyciopropylcarbamate (Compound 23)
The product was purified by silica gel chromatography (EtOAc-hexanes gradient) and isolated as a white solid (64.9 mg, 63%): mp 187-189 °C; *H NMR (400 MHz, CDClj, data for major rotamer) δ 8.54 (s, IH), 8.09 (d, J = 8.3 Hz, 2H), 7.79 (d, J = 9.0 Hz, 2H), 7.41 - 7.34 (m, 2H), 7.33 - 7.27 (m, 3H), 7.22 - 7.14 (m, 2H), 7.11 - 7.04 (m, IH), 5.44 (br s, IH), 3.26 - 3.10 (m, IH), 2.91 (br s, IH), 2.26 (ddd, J = 9.5, 6.6, 3.2 Hz, IH), 2.01 (br s, 2H), 1.79 (br s, 2H), l .72 - l .53 (m, 4H), 1.41 - 1.28 (m, 2H); ESIMS m/z 550 (M+H).
2-teri-ButyIphenyl 2-(4-( l-(4-(trifIuoromethoxy)phenyl)-1/7-1,2,4-triazol-3-yl)phenyl)- cyclopropylcarbamate (Compound 24)
The product was purified by silica gel chromatography (EtOAc-hexanes gradient) and isolated as a white solid (70.5 mg, 67%): mp 143.5-145.0 °C; ’H NMR (400 MHz, CDC13, data for major rotamer) δ 8.54 (s, 1 H), 8.09 (d, J = 8.2 Hz, 2H), 7.79 (d, J = 9.0 Hz, 2H), 7.42 - 7.36 (m, 3H), 7.29 (d, J = 7.7 Hz, 2H), 7.23 (td, J = 7.6, 1.6 Hz, IH), 7.15 (td, J = 7.6, 1.5 Hz, IH), 7,09 (d, J = 7.6 Hz, IH), 5.46 (s, IH), 2.93 (s, IH), 2.32 - 2.21 (m, IH), 1.42 - 1.28 (m, 2H), l .39 (s, 9H); ESIMS m/z 538 (M+H).
2-(Trifluoromethyl)phenyl 2-(4-(l-(4-(trifluorometlioxy)phenyl)-l//-l,2,4-triazoI-3-yl)phcnyl)cyclopropylcarbaniatc (Compound 25)
Page 28 of 77
The product was isolated as an off-white solid (66.9 mg, 46%). The filtrate was concentrated in vacuo and purified by silica gel chromatography (EtOAc-hexanes gradient) to afford additional product (26.2 mg, 20%): mp 183—187 °C; 'H NMR (400 MHz, CDClj, data for major rotamer) 5 8.54 (s, III), 8.09 (d, J = 8.3 Hz, 2H), 7.79 (d, J = 9.0 Hz, 2H), 7.65 (d, J = 7.7 Hz, ÎH), 7.61 - 7.53 (m, ÎH), 7.45 - 7.06 (m, 6H), 5.59 (s, ÎH), 3.03 -2.80 (m, ÎH), 2.37 -2.2l (m, 1H), l .43 - l .29 (m, 2H); ESIMS m/z 549 (M+H).
Exaniple 12: Mesityl 2-(4-(1-(4-(trifluoroniethoxy)phenyl)-l/7-1,2,4-triazol-3yl)phenyl)cyclopropyl-carbamate (Compound 26)
Step 1. 2,4,6-trimethylphenol (272 mg, 2.00 mmol, 1.0 equiv) was dissolved in CH2CI2 (3.33 mL, 0.3 M) under nitrogen (N2) and cooled to 0 °C. Triphosgene (208 mg, 0.700 mmol, 0.35 equiv) was dissolved in CH2CI2 (3.33 mL) and added dropwise, followed by pyridine (0,162 mL, 2.00 mmol, 1.0 equiv). The mixture was allowed to warm to 25 °C over 18 h, at which point the reaction was quenched with 10 mL 1 normal (N) hydrochloric acid (HCl; aq) and extracted with EtOAc. The organic layer was washed with 1 N HCl (aq), dried over Na2SO4, and concentrated to give mesityl chlorofonnate as an oil (88% purity by *H NMR spectroscopy). The chloroformate so prepared was used directly in the next step without further purification.
Step 2. 2- (4-[ 1 -(4-trifluoiOinethoxyphenyl)-1 H-[ 1,2,4]triazol-3yl]phenyl)cyclopropylamine (46.0 mg, 0.13 mmol, 1.0 equiv) was dissolved in CH2CI2 (0.55 mL) under N2. 4-Dimethylamînopyridine (DMAP; 0.8 mg, 0.006 mmol, 0.05 equiv) and EtjN (27 pL, 0.19 mmol, 1.5 equiv) were added, followed by mesityl chloroformais prepared above (33 mg, 0.17 mmol, 1.2 equiv). The reaction was stirred for 5 min and was then quenched with
NaHCO3 (aq). The layers were separated, and the aqueous layer was extracted twice more with
CH2CI2. The combined organic extracts were concentrated, and the crude product was purified
Page 29 of 77 by silica gel chromatography (EtOAc-hexanes gradient) to afford the title compound as a white solid (53.0 mg, 79%): mp 199-202 °C; *H NMR (400 MHz, CDCI3, data for major rotamer) δ
8.54 (s, 1 H), 8.08 (d, J = 8.3 Hz, 2H), 7.78 (d, J = 9.0 Hz, 2H), 7.39 (d, J = 0.7 Hz, 2H), 7.32 7.21 (m, 2H), 6.86 (s, 2H), 5.71 - 5.36 (m, 0.7H), 5.22 -4.82 (m, 0.3H), 3.09 - 2.81 (m, IH),
2.26 (s, 4H), 2.17 (s, 6H), 1.43 - 1.26 (m, 2H); ESIMS m/z 523 (M+H).
The following compounds were synthesized in accordance with Example 12.
4-Methoxy phenyl 2-(4-(1 -(4-(trifluoromethoxy)phenyI)~l//-l, 2,4-triazol-3-yl)phenyl)- cyclopropylcarbamatc (Compound 27)
The product was isolated as a white solid (60.0 mg, 66%): mp 163-164 °C; ‘H NMR (400 MHz, CDCh) δ 8.54 (s, 1 H), 8.09 (d, J = 8.3 Hz, 2H), 7.79 (d, J = 9.0 Hz, 2H), 7.38 (dd, J = 9.0, 0.7 Hz, 2H), 7.29 (d, J = 7.9 Hz, 2H), 7.06 (d, J = 8.9 Hz, 2H), 6.88 (d, J - 9.1 Hz, 2H),
5.35 (s, IH), 3.80 (s, 3H), 2.89 (s, IH), 2.27 (ddd, J = 9.6, 6.6, 3.2 Hz, IH), 1.40 - 1.26 (m, 2H); ESIMS m/z 511 (M+H), 509 (M-H).
2,6-DichIorophcnyl 2-(4-(l-(4-(tnfluoromethoxy)phenyl)-lZ/-l,2,4-triazol-3-yl)phenyl)cyclopropylcarbamate (Compound 28)
Page 30 of 77
The product was isolated as a white solid (26.1 mg, 33%); mp 160-162 °C; *H NMR (400
MHz, CDClj, data for major rotamer) δ 8.54 (s, III), 8.09 (d, J = 8.3 Hz, 2H), 7.79 (d, J = 9.0
Hz, 2H), 7.38 (d, J = 8.1 Hz, 2H), 7.35 (d, J = 8.2 Hz, 2H), 7.28 (d, J = 8.0 Hz, 2H), 7.13 (t, J =
8.1 Hz, IH), 5.62 (s, IH), 2.94 (s, IH), 2.31 (s, IH), 1.46 - 1.28 (m, 2H); ESIMS m/z 550 (M+H).
2-Isopropylphcnyl 2-(4-(l-(4-(trÎfluoromethoxy)phenyl)-l//-l,2,4-triazol-3-yl)phenyl)cyclopropylcarbamatc (Compound 29)
The product was isolated as a white solid (52.8 mg, 63%): mp 186—188 °C; 'H NMR (400 MHz, CDCl3, data for major rotamer) δ 8.54 (s, IH), 8.09 (d, J = 8.3 Hz, 2H), 7.79 (d, J = 9.0 Hz, 2H), 7.44 - 7.34 (m, 2H), 7.33 - 7.26 (m, 2H), 7.23 - 7.16 (m, 2H), 7.13 - 7.05 (m, IH),
5.43 (brs, IH), 3.19 - 3.07 (m, IH), 2.91 (brs, l H), 2.27 (ddd, J = 9.5, 6.7,3.1 Hz, IH), 1.42-
1.33 (m, 2H), 1.22 (br d, J = 6.1 Hz, 3H); ESIMS m/z 523 (M+H).
Example 13:
l-Mesityl-3-(2-(4-( l-(4-(triiluüromethoxy)phcnyl)-l/7-1,2,4-triazol-3-yl)phenyl)cyclopropyl)urea (Compound 30)
2- {4-[ 1 -(4-trifluoromethoxyphenyl)-1 H-[ 1,2,4]triazol-3-yl]phenyl} cyclopropylamine trifluoroacetate sait (58 mg, 0.12 mmol, 1.0 equiv) was dissolved in THF (0.60 mL, 0.20 M) at 25 °C under N2. The isocyanate (22 mg, 0.13 mmol, 1.1 equiv) was added in one portion, followed by EtîN (19 pL, 0.13 mmol, 1.1 equiv). The mixture was stirred at 25 °C for 1 h, and then methyl alcohol-water (1:1) was added. The precipitate was collected by vacuum filtration and rinsed with methyl alcohol to afford the title compound as a white solid (41.3 mg, 65%): mp 254-256 °C; 'H NMR (300 MHz, DMSO-dfi) δ 9.35 (s, IH), 8.04 (d, J = 9.0 Hz, 2H), 7.97 (d, J = 8.3 Hz, 2H), 7.59 (d, J = 8.5 Hz, 2H), 7.32 (s, 1 H), 7.22 (d, J = 8.3 Hz, 2H), 6.82 (s, 2H), 6.48 (s, IH), 2.87-2.73 (m, 1 H), 2.19 (s, 3H), 2.10(s,6H), 2.06-1.95 (m, IH), 1.28 - 1.11 (m, 2H); ESIMS m/z 522 (M+H).
The following compound was synthesized in accordance with Example 13.
Page 31 of77 l“(2,6~Dichlorophenyl)-3-(2-(4-(l-(4-(trifluoroniethoxy)phenyl)-l£M,2,4-triazol-3yl)phenyl)cyclopropyl)urca (Compound 31)
The product was isolated as a white solid (44.6 mg, 80%): mp 215.5-217.5 °C; 'H NMR (300 MHz, DMSO-rfô) δ 9.35 (s, 1H), 8.05 (d, 9.1 Hz, 2H), 7.98 (app d, J= 8.1 Hz, 3H), 7.61 (s, 2H), 7.47 (d, J = 8.0 Hz, 2H), 7.32 - 7.22 (m, 3H), 6.87 (d, J= 3.2 Hz, 1H), 2.88 - 2.66 (m, 1H), 2.13 - 1.96 (m, 1 H), 1.31 - 1.14 (m, 2H); ESIMS m/z 549 (M+H), 547 (M-H).
Example 14: Préparation of l,3-bis(2-(4-(l-(4-(trifluoromethoxy)phenyl)-lH-I,2,4-triazol-
3-yl)phcnyl)cyclopropyl)urea (Compound 32)
Step 2 in Example 3 was carried out using t-butyl alcohol as solvent instead of PhCH3. The mixture was heated at 90 °C for 3 h, cooled to 25 °C, and diluted with 1:1 r-butyl alcoholwater. The mixture was then filtered to afford the title compound (202.2 mg, 93%) as an offwhite solid. The intended product (the Z-butyl carbamate) was not isolated: mp 232-234 °C dec; 'H NMR (300 MHz, DMSO-î/6) δ 9.37 (s, 2H), 8.06 (d, J= 9.0 Hz, 4H), 7.99 (d, J= 8.2 Hz, 4H), 7.61 (d, J =8.8 Hz, 4H), 7.23 (d, J =8.3 Hz, 4H), 6.39 (d,J=3.0 Hz, 2H), 2.89-2.66 (m, 2H), 2.12-1.89 (m, 2H), 1.25 - 1.07 (m, 4H); ESIMS m/z 747 (M+H).
Example 15: Bioassays on Beet Armyworm (“BAW”) and Corn Earworm (“CEW”)
BAW has few effective parasites, diseases, or predators to lower its population. BAW infests many weeds, trees, grasses, legumes, and field crops. In various places, it is of économie concem upon asparagus, cotton, corn, soybeans, tobacco, alfalfa, sugar beets, peppers, tomatoes, potatoes, onions, peas, sunflowers, and citrus, among other plants. CEW is known to attack com and tomatoes, but it also attacks artichoke, asparagus, cabbage, cantaloupe, collards, cowpeas, cucumbers, eggplant, lettuce, lima beans, melon, okra, peas, peppers, potatoes, pumpkin, snap
Page 32 of 77 beans, spinach, squash, sweet potatoes, and watermelon, among other plants. CEW is also known to be résistant to certain insecticides. Consequently, because of the above factors control of these pests is important. Furthermore, molécules that control these pests are useful in controliing other pests.
Certain molécules disclosed in this document were tested against BAW and CEW using procedures described in the following examples. In the reporting of the results, the “BAW & CEW Rating Table” was used (See Table Section).
BIOASSAYS ON BAW (Spodoptera exigua)
Bioassays on BAW were conducted using a 128-well diet tray assay. one to five second instar BAW larvae were placed in each well (3 mL) of the diet tray that had been previously filled with l mL of artificial diet to which 50 pg/cm2 of the test compound (dissolved in 50 pL of 90:10 acetone-water mixture) had been applied (to each of eight wells) and then allowed to dry. Trays were covered with a clear self-adhesive cover, and held at 25 °C, 14:10 light-dark for five to seven days. Percent mortality was recorded for the larvae in each well; activity in the eight wells was then averaged. The results are indicated in the table entitled “Table: Bio Results” (See Table Section).
Bioassays on CEW (Helicoverpa zea)
Bioassays on CEW were conducted using a 128-well diet tray assay. one to five second instar CEW larvae were placed in each well (3 mL) of the diet tray that had been previously filled with 1 mL of artificial diet to which 50 pg /cm2 of the test compound (dissolved in 50 pL of 90:10 acetone-water mixture) had been applied (to each of eight wells) and then allowed to dry. Trays were covered with a clear self-adhesive cover, and held at 25 °C, 14:10 light-dark for five to seven days. Percent mortality was recorded for the larvae in each well; activity in the eight wells was then averaged. The results are indicated in the table entitled “Table: Bio Results” (See Table Section).
Examplelô: BIOASSAYS ON Green PeacII APHID (“GPA”) (Myzus persicae).
GPA is the most significant aphid pest of peach trees, causing decreased growth, shriveling of the leaves, and the death of various tissues. It is aiso hazardous because it acts as a vector for the transport of plant viruses, such as potato virus Y and potato leafroll virus to members of the nightshade/potato family Solanaceae, and various mosaic viruses to many other food crops. GPA attacks such plants as broccoli, burdock, cabbage, carrot, cauliflower, daikon, eggplant, green beans, lettuce, macadamia, papaya, peppers, sweet potatoes, tomatoes,
Page 33 of77 watercress, and zucchini, among other plants. GPA also attacks many omamental crops such as carnation, chrysanthemum, flowering white cabbage, poinsettia, and roses. GPA has developed résistance to many pesticides.
Certain molécules disclosed in this document were tested against GPA using procedures described in the following example. In the reporting of the results, the “GPA Rating Table” was used (See Table Section).
Cabbage seedlings grown in 3-inch pots, with 2-3 small (3-5 cm) true leaves, were used as test substrate. The seedlings were infested with 20-50 GPA (wingless adult and nymph stages) one day prior to chemical application. Four pots with individual seedlings were used for each treatment. Test compounds (2 mg) were dissolved in 2 mL of acetone/methanol (l:l) solvent, forming stock solutions of 1000 ppm test compound. The stock solutions were diluted 5X with 0.025% Tween 20 in H2O to obtain the solution at 200 ppm test compound. A hand-held aspirator-type sprayer was used for spraying a solution to both sides of cabbage leaves until runoff. Reference plants (solvent check) were sprayed with the diluent only containing 20% by volume of acetone/methanol (1:1) solvent. Treated plants were held in a holding room for three days at approximately 25 °C and ambient relative humidity (RH) prior to grading. Evaluation was conducted by counting the number of live aphids per plant under a microscope. Percent Control was measured by using Abbott’s correction formula (W.S. Abbott, “A Method of Computing the Effectiveness of an Insecticide” J. Econ. Entomol. 18 (1925), pp.265-267) as follows.
Corrected % Control = 100 * (X - Y) / X where
X = No. of live aphids on solvent check plants and
Y = No. of live aphids on treated plants
The results are indicated in the table entîtled “Table: Bio Results” (See Table Section).
PESTICIDALLY ACCEPTABLE ACID ADDITION SALTS, SALT DERIVATIVES, SOLVATES, ESTER DERIVATIVES, POLYMORPHS, ISOTOPES AND RADIONUCLIDES
Molécules of Formula One, Two, Three, and Four may be formulated into pesticidally acceptable acid addition salts. By way of a non-limiting example, an amine function can form salts with hydrochloric, hydrobromic, sulfuric, phosphoric, acetic, benzoic, citric, malonic, salicylic, malic, fumaric, oxalic, succinic, tartaric, lactic, gluconic, ascorbic, maleic, aspartic, benzenesulfonic, methanesulfonic, ethanesulfonic, hydroxymethanesulfonic, and hydroxyethanesulfonic acids. Additionally, by way of a non-limiting example, an acid function
Page 34 of 77 can form salts including those derived from alkali or alkaline earth metals and those derived from ammonia and amines. Examples of preferred cations include sodium, potassium, and magnésium.
Molécules of Formula One, Two, Three, and Four may be formulated into sait dérivatives. By way of a non-limiting example, a sait dérivative can be prepared by contacting a free base with a sufficient amount of the desired acid to produce a sait. A free base may be regenerated by treating the sait with a suitable dilute aqueous base solution such as dilute aqueous sodium hydroxide (NaOH), potassium carbonate, ammonia, and sodium bicarbonate. As an example, in many cases, a pesticide, such as 2,4-D, is made more water-soluble by converting 10 it to its dimethylamine sait..
Molécules of Formula One, Two, Three, and Four may be formulated into stable complexes with a solvent, such that the complex remains intact after the non-complexed solvent is removed. These complexes are often referred to as solvatés.” However, it is partîcularly désirable to form stable hydrates with water as the solvent.
Molécules of Formula One, Two, Three, and Four may be made into ester dérivatives.
These ester dérivatives can then be applied in the same manner as the invention disclosed in this document is applied.
Molécules of Formula One, Two, Three, and Four may be made as various crystal polymorphs. Polymorphism is important in the development of agrochemicals since different 20 crystal polymorphs or structures of the same molécule can hâve vastly different physical properties and biological performances.
Molécules of Formula One, Two, Three, and Four may be made with different isotopes. Of particular importance are molécules having 2H (also known as deuterium) in place of ’H.
Molécules of Formula One, Two, Three, and Four may be made with different 25 radionuclides. Of particular importance are molécules having l4C.
STEREOISOMERS
Molécules of Formula One, Two, Three, and Four may exist as one or more stereoisomers. Thus, certain molécules can be produced as racemic mixtures. It will be 30 appreciated by those skilled in the art that one stereoisomer may be more active than the other stereoisomers. Individual stereoisomers may be obtained by known sélective synthetic procedures, by conventional synthetic procedures using resolved starting materials, or by conventional resolution procedures.
INSECTICIDES
Page 35 of77
Moiecules of Formula One, Two, Three, and Four may also be used in combination (such as, in a compositional mixture, or a simultaneous or sequential application) with one or more of the following insecticides - l ,2-dichloropropane, abamectin, acephate, acetamiprid, acethion, acetoprole, acrinathrin, acrylonitrile, alanycarb, aldicarb, aldoxycarb, aldrin, allethrin, allosamidin, allyxycarb, n/p/m-cypermetlirin, α/ρ/m-ecdysone, «/p/m-endosulfan, amidithion, aminocarb, amiton, amiton oxalate, amitraz, anabasine, athidathion, azadirachtin, azamethiphos, azinphos-ethyl, azinphos-methyl, azothoate, barium hexafluorosilicate, barthrin, bendiocarb, benfuracarb, bensultap, ôeta-cyfluthrin, ôeta-cypermethrin, bifenthrin, bioallethrin, bioethanometlirin, biopermethrin, bistrifluron, borax, boric acid, bromfenvinfos, bromocyclen, bromo-DDT, bromophos, bromophos-ethyl, bufencarb, buprofezin, butacarb, butathiofos, butocarboxim, butonate, butoxycarboxim, BYl-02960, cadusafos, calcium arsenate, calcium polysulfide, camphechlor, carbanolate, carbaryl, carbofuran, carbon disulfide, carbon tetrachloride, carbophenothion, carbosulfan, cartap, cartap hydrochloride, chlorantraniliprole, chlorbicyclen, chlordane, chlordecone, chlordimeform, chlordimeform hydrochloride, chlorethoxyfos, chlorfenapyr, chlorfenvinphos, chlorfluazuron, chlormephos, chloroform, chloropicrin, chlorphoxim, chlorprazophos, chlorpyrifos, chlorpyrifos-methyl, chlorthiophos, chromafenozide, cinerin I, cinerin II, cinerins, cismethrin, cloethocarb, closantel, clothianidin, copper acetoarsenite, copper arsenate, copper naphthenate, copper oleate, coumaphos, coumithoate, crotamiton, crotoxyphos, crufomate, cryolite, cyanofenphos, cyanophos, cyanthoate, cyantraniliprole, cyclethrin, cycloprothrin, cyfluthrin, cyhalothrin, cypermethrin, cyphenothrin, cyromazine, cythioate, DDT, decarbofuran, deltamethrin, demephion, demephionO, demephion-S, demeton, demeton-methyl, demeton-O, demeton-O-methyl, demeton-S, demeton-S-methyl, demeton-S-methylsulphon, diafenthiuron, dialifos, diatomaceous earth, diazinon, dicapthon, dichlofenthion, dichlorvos, dicresyl, dicrotophos, dicyclanil, dieldrin, diflubenzuron, dilor, dimefluthrin, dimefox, dimetan, dimethoate, dimethrin, dimethylvinphos, dimetilan, dinex, dinex-diclexine, dinoprop, dinosam, dinotefuran, diofenolan, dioxabenzofos, dioxacarb, dioxathion, dîsulfoton, dithîcrofos, d-limonene, DNOC, DNOC-ammonium, DNOCpotassium, DNOC-sodium, doramectin, ecdysterone, emamectin, emamectin benzoate, EMPC, empenthrin, endosulfan, endothion, endrin, EPN, epofenonane, eprinomectin, esdepalléthrine, esfenvalerate, etaphos, ethiofencarb, ethion, ethiprole, ethoate-methyl, ethoprophos, ethyl formate, ethyl-DDD, ethylene dibromide, ethylene dichloride, ethylene oxide, etofenprox, etrimfos, EXD, famphur, fenamiphos, fenazaflor, fenchlorphos, fenethacarb, fenfluthrin, fenitrothion, fenobucarb, fenoxacrim, fenoxycarb, fenpirithrin, fenpropathrin, fensulfothion, fenthion, fenthion-ethyl, fenvalerate, fipronil, flonicamid, flubendiamide (additionally resolved isomers thereof). flucofuron, flucycloxuron, flucythrinate, flufenerim, flufenoxuron, flufenprox,
Page 36 of 77 fluvalinate, fonofos, formetanate, formetanate hydrochlorîde, formothion, formparanate, formparanate hydrochlorîde, fosmethilan, fospirate, fosthietan, fufenozîde, furathiocarb, furethrin, gom/Ho-cyhalothrin, ga/nma-HCH, halfenprox, halofenozide, HCH, HEOD, heptachlor, heptenophos, heterophos, hexaflumuron, HHDN, hydramethylnon, hydrogen 5 cyanide, hydroprene, hyquincarb, imidacloprid, imiprothrin, indoxacarb, iodomethane, IPSP, isazofos, isobenzan, îsocarbophos, isodrin, isofenphos, isofenphos-methyl, isoprocarb, isoprothiolane, isothioate, isoxathion, ivermectin, jasmolin I, jasmolin II, jodfenphos, juvénile hormone I, juvénile hormone II, juvénile hormone III, kelevan, kinoprene, lambda-cyhalothrin, lead arsenate, lepimectin, leptophos, lindane, lirimfos, lufenuron, lythidathion, malathion, 10 malonoben, mazidox, mecarbam, mecarphon, menazon, meperfluthrin, mephosfolan, mercurous chloride, mesulfenfos, metaflumizone, methacrifos, methamidophos, methidathion, methiocarb, methocrotophos, methomyl, methoprene, methothrin, methoxychlor, methoxyfenozide, methyl bromide, methyl isothiocyanate, methylchloroform, methylene chloride, metofluthrin, metolcarb, metoxadiazone, mevinphos, mexacarbate, milbemectin, milbemycin oxime, mipafox, mirex, 15 molosultap, monocrotophos, monomehypo, monosultap, morphothion, moxidectin, naftalofos, naled, naphthalene, nicotine, nifluridide, nitenpyram, nithiazine, nitrilacarb, novaluron, noviflumuron, omethoate, oxamyl, oxydemeton-methyl, oxydeprofos, oxydisulfoton, paradichlorobenzene, parathion, parathion-methyl, penfluron, pentachlorophenol, permethrin, phenkapton, phenothrin, phenthoate, phorate, phosalone, phosfolan, phosmet, phosnichlor, 20 phosphamidon, phosphine, phoxim, phoxim-methyl, pirimetaphos, pirimicarb, pirimiphos-ethyl, pirimiphos-methyl, potassium arsenite, potassium thiocyanate, pp'-DDT, prallethrin, precocene I, precocene II, precocene III, primidophos, profenofos, profluralin, profluthrin, promacyl, promecarb, propaphos, propetamphos, propoxur, prothidathion, prothiofos, prothoate, protrifenbute, pymetrozine, pyraclofos, pyrafluprole, pyrazophos, pyresmethrin, pyrethrin I, 25 pyrethrin II, pyrethrins, pyridaben, pyridalyl, pyridaphenthion, pyrifluquinazon, pyrimidifen, pyrimitate, pyriprole, pyriproxyfen, quassia, quinalphos, quinalphos-methyl, quinothion, rafoxanîde, resmethrin, rotenone, ryania, sabadilla, schradan, selamectin, silafluofen, silica gel, sodium arsenite, sodium fluoride, sodium hexafluorosilicate, sodium thiocyanate, sophamide, spinetoram, spinosad, spiromesifen, spirotetramat, sulcofuron, sulcofuron-sodium, sulfluramid, 30 sulfotep, sulfoxaflor, sulfuryl fluoride, sulprofos, tau-fluvalinate, tazimcarb, TDE, tebufenozide, tebufenpyrad, tebupirimfos, teflubenzuron, tefluthrin, temephos, TEPP, terallethrin, terbufos, tetrachloroethane, tetrachlorvinphos, tetramethrin, tetramethylfluthrin, /Aeta-cypermethrin, thiacloprid, thiamethoxam, thicrofos, thiocarboxime, thiocyclam, thiocyclam oxalate, thiodicarb, thiofanox, thiometon, thiosultap, thiosultap-disodium, thiosultap-monosodium, thuringiensin, 35 tolfenpyrad, tralomethrin, transflutlirin, transpermethrin, triarathene, triazamate, triazophos,
Page 37 of 77 trichlorfon, trichlormetaphos-3, trichloronat, trifenofos, triflumuron, trimethacarb, triprene, vamidothion, vaniliprole, XMC, xylylcarb, zeta-cypennethrin, and zolaprofos (collectively these commonly named insecticides are defined as the “Insecticide Group”).
ACARICIDES
Molécules of Formula One, Two, Three, and Four may also be used in combination (such as, in a compositional mixture, or a simultaneous or sequential application) with one or more of the following acaricides - acequinocyl, amidoflumet, arsenous oxide, azobenzene, azocyclotin, benomyl, benoxafos, benzoximate, benzyl benzoate, bifenazate, binapacryl, bromopropylate, chinomethionat, chlorbenside, chlorfenetliol, chlorfenson, chlorfensulphide, chlorobenzilate, chloromebuform, chloromethiuron, chloropropylate, clofentezine, eyenopyrafen, cyflumetofen, cyhexatin, dichlofluanid, dicofol, dienochlor, diflovidazin, dînobuton, dinocap, dinocap-4, dinocap-6, dinocton, dinopenton, dinosulfon, dinoterbon, diphenyl sulfone, disulfiram, dofenapyn, etoxazole, fenazaquin, fenbutatin oxide, fenothiocarb, fenpyroximate, fenson, fentrifanil, fluacrypyrim, fluazuron, flubenzimine, fluenetil, flumethrin, fluorbenside, hexythiazox, mesulfen, MNAF, nikkomycins, proclonol, propargite, quintiofos, spirodiclofen, sulfiram, sulfur, tetradifon, tetranactin, tetrasul, and thioquinox (collectively these commonly named acaricides are defined as the “Acaricide Group”).
NEMATICIDES
Molécules of Formula One, Two, Three, and Four may also be used in combination (such as, in a compositional mixture, or a simultaneous or sequential application) with one or more of the following nematicides - l ,3-dichloropropene, benclothiaz, dazomet, dazomet-sodium, DBCP, DCIP, diamidafos, fluensulfone, fosthiazate, furfural, imicyafos, isamidofos, isazofos, metam, metam-ammonium, metam-potassium, metam-sodium, phosphocarb, and thionazin (collectively these commonly named nematicides are defined as the “Ncmaticide Group”)
FUNGICIDES
Molécules of Formula One, Two, Three, and Four may also be used in combination (such as, in a compositional mixture, or a simultaneous or sequential application) with one or more of the following fungicides - (3-ethoxypropyl)mercury bromide, 2-methoxyethylmercury chloride,
2-phenylphenol, 8-hydroxyquinoline sulfate, 8-phenylmercurioxyquinoline, acibenzolar, acibenzolar-S-methyl, acypetacs, acypetacs-copper, acypetacs-zinc, aldimorph, allyl alcohol, ametoctradin, amisulbrom, ampropylfos, anilazine, aureofungîn, azaconazole, azithiram, azoxystrobin, barium polysulfide, benalaxyl, bcnalaxyl-M, benodanil, benomyl, benquinox, Page 38 of 77 bentaluron, benthiavalicarb, benthiavalicarb-isopropyl, benzalkonium chloride, benzamacril, benzamacril-isobutyl, benzamorf, benzohydroxamic acid, bethoxazin, binapacryl, biphenyl, bitertanol, bithionol, bixafen, blasticidin-S, Bordeaux mixture, boscalid, bromuconazole, bupirimate, Burgundy mixture, buthiobate, butylamine, calcium polysulfide, captafol, captan, carbamorph, carbendazim, carboxin, carpropamid, carvone, Cheshunt mixture, chinomethionat, chlobenthiazone, chloraniformethan, chloranil, chlorfenazole, chlorodinitronaphthalene, chloroneb, chloropicrin, chlorothalonil, chlorquinox, chlozolinate, climbazole, clotrimazole, copper acetate, copper carbonate, basic, copper hydroxide, copper naphthenate, copper oleate, copper oxychloride, copper silicate, copper sulfate, copper zinc chromate, cresol, cufraneb, cuprobam, cuprous oxide, cyazofamid, cyclafuramid, cycloheximide, cyflufenamid, cymoxanîl, cypendazole, cyproconazole, cyprodinil, dazomet, dazomet-sodium, DBCP, debacarb, decafentin, dehydroacetic acid, dichlofluanid, dichlone, dichlorophen, dichlozoline, diclobutrazol, diclocymet, diclomezine, diclomezine-sodium, dicloran, diethofencarb, diethyl pyrocarbonate, difenoconazole, diflumetorim, dimethirimol, dimethomorph, dimoxystrobin, diniconazole, diniconazole-M, dinobuton, dinocap, dinocap-4, dinocap-6, dinocton, dinopenton, dinosulfon, dinoterbon, diphenylamine, dipyrithione, disulfiram, ditalimfos, dithianon, DNOC, DNOC-ammonium, DNOC-potassium, DNOC-sodium, dodemorph, dodemorph acetate, dodemorph benzoate, dodicin, dodicin-sodium, dodine, drazoxolon, edifenphos, epoxiconazole, etaconazole, etem, ethaboxam, ethirimol, ethoxyquin, ethylmercury 2,3-dihydroxypropyl mercaptide, ethylmercury acetate, ethylmercury bromide, ethylmercury chloride, ethylmercury phosphate, etridiazole, famoxadone, fenamidone, fenaminosulf, fenapanil, fenarimol, fenbuconazole, fenfuram, fenhexamid, fenitropan, fenoxanil, fenpiclonil, fenpropidin, fenpropimorph, fentin, fentin chloride, fentin hydroxide, ferbam, feriinzone, fluazinam, fludioxonil, flumetover, flumorph, fluopicolide, fluopyram, fluoroimide, fluotrimazole, fluoxastrobin, fluquinconazole, flusilazole, flusulfamide, flutianil, flutolanil, flutriafol, fluxapyroxad, folpet, formaldéhyde, fosetyl, fosetyl-aluminium, fuberidazole, furalaxyl, furametpyr, fùrcarbanil, fùrconazole, furconazole-cis, furfural, furmecyclox, furophanate, glyodin, griseofulvin, guazatine, halacrinate, hexachlorobenzene, hexachlorobutadiene, hexaconazole, hexylthiofos, hydrargaphen, hymexazol, imazalil, imazalil nitrate, imazalil sulfate, imibenconazole, iminoctadine, iminoctadine triacetate, iminoctadine trialbesilate, iodomethane, ipconazole, iprobenfos, iprodione, iprovalicarb, isoprothiolane, isopyrazam, isotianil, isovaledione, kasugamycin, kresoxim-methyl, mancopper, mancozeb, mandipropamid, maneb, mebenil, mecarbinzid, mepanipyrim, mepronil, meptyldinocap, mercuric chloride, mercuric oxide, mercurous chloride, metalaxyl, metalaxyl-M, metam, metam-arnmoniuni, metampotassium, metam-sodium, metazoxolon, metconazole, methasulfocarb, methfuroxam, methyl
Page 39 of’77 bromide, methyl isothiocyanate, methylmercury benzoate, methyhnercury dicyandiamide, methylmercury pentachlorophenoxide, metiram, metominostrobin, metrafenone, metsulfovax, milneb, myclobutanil, myclozolin, N-(ethylmercury)-p-toluenesulphonanilide, nabam, natamycin, nitrostyrene, nitrothal-isopropyl, nuarimol, OCH, octhilînone, oforace, orysastrobin, oxadixyl, oxine-copper, oxpoconazole, oxpoconazole fumarate, oxycarboxin, peforazoate, penconazole, pencycuron, penflufen, pentachlorophenol, penthiopyrad, phenylmercuriurea, phenylmercury acetate, phenylmercury chloride, phenylmercury dérivative of pyrocatechol, phenylmercury nitrate, phenylmercury salicylate, phosdiphen, phthalide, picoxystrobin, piperalin, polycarbamate, polyoxins, polyoxorim, polyoxorim-zinc, potassium azide, potassium polysulfide, potassium thiocyanate, probenazole, prochloraz, procymidone, propamocarb, propamocarb hydrochloride, propiconazole, propineb, proquinazid, prothiocarb, prothiocarb hydrochloride, prothioconazole, pyracarbolid, pyraclostrobin, pyraclostrobin, pyrametostrobin, pyraoxystrobin, pyrazophos, pyribencarb, pyridinitril, pyrifenox, pyrimethanil, pyriofenone, pyroquilon, pyroxychlor, pyroxyfur, quinacetol, quinacetol sulfate, quinazamid, quinconazole, quinoxyfen, quintozene, rabenzazole, salicylanilide, sedaxane, silthiofam, simeconazole, sodium azide, sodium orthophenylphenoxide, sodium pentachlorophenoxide, sodium polysulfide, spiroxamine, streptomycin, sulfur, sultropen, TCMTB, tebuconazole, tebufloquin, teclofialam, tecnazene, tecoram, tetraconazole, thiabendazoie, thiadifluor, thicyofen, thifluzamide, thiochlorfenphim, thiomersal, thiophanate, thiophanate-methyl, thioquinox, thiram, tiadinil, tioxymid, tolclofos-methyl, tolylfluanid, tolylmercury acetate, triadimefon, triadimenol, triamiphos, triarimol, triazbutil, triazoxide, tributyltin oxide, trichlamide, tricyclazoie, tridemorph, trifloxystrobin, triflumizole, triforine, triticonazole, uniconazole, uniconazole-P, validamycin, valifenalate, vinclozolin, zarilamid, zinc naphthenate, zineb, ziram, zoxamide (collectively these commonly named fongicides are defined as the “Fungicide Group”).
HERBICIDES
Molécules of Formula One, Two, Three, and Four may also be used in combination (such as, in a compositional mixture, or a simultaneous or sequential application) with one or more of the following herbicides - 2,3,6-TBA, 2,3,6-TBA-dimethylamrnonium, 2,3,6-TBA-sodium,
2.4.5- T, 2,4,5-T-2-butoxypropyl, 2,4,5-T-2-ethyIhexyl, 2,4,5-T-3-butoxypropyl, 2,4,5-TB, 2,4,5T-butometyl, 2,4,5-T-butotyl, 2,4,5-T-butyl, 2,4,5-T-isobutyl, 2,4,5-T-isoctyl, 2,4,5-T-isopropyl,
2.4.5- T-methyl, 2,4,5-T-pentyl, 2,4,5-T-sodium, 2,4,5-T-triethylammonium, 2,4,5-T-trolamine,
2.4- D, 2,4-D-2-butoxypropyl, 2,4-D-2-ethylhexyl, 2,4-D-3-butoxypropyl, 2,4-D-aininonium,
2.4- DB, 2,4-DB-butyl, 2,4-DB-dimethylammonium, 2,4-DB-isoctyl, 2,4-DB-potassium, 2,4-DBsodium, 2,4-D-butotyl, 2,4-D-butyl, 2,4-D-diethylammonium, 2,4-D-diniethylammonium, 2,4-D-
Page 40 of 77 diolamine, 2,4-D-dodecylammonium, 2,4-DEB, 2,4-DEP, 2,4-D-ethyl, 2,4-D-heptylammonium,
2,4-D-isobutyl, 2,4-D-isoctyl, 2,4-D-isopropyl, 2,4-D-isopropylammonium, 2,4-D-lithium, 2,4D-meptyl, 2,4-D-methyl, 2,4-D-octyl, 2,4-D-pentyl, 2,4-D-potassium, 2,4-D-propyl, 2,4-Dsodium, 2,4-D-tefuryl, 2,4-D-tetradecylammonium, 2,4-D-triethylammonium, 2,4-D-tris(2hydroxypropyl)ammonium, 2,4-D-trolamine, 3,4-DA, 3,4-DB, 3,4-DP, 4-CPA, 4-CPB, 4-CPP, acetochlor, acifluorfen, acifluorfen-methyl, acifluorfen-sodium, aclonifen, acrolein, alachlor, allidochlor, alloxydim, alloxydim-sodîum, allyl alcohol, alorac, ametridione, ametryn, amibuzin, amîcarbazone, amidosulfuron, aminocyclopyrachlor, aminocyclopyrachlor-methyl, aminocyclopyrachlor-potassium, aminopyralid, aminopyralid-potassium, aminopyralid-tris(2hydroxypropyl)ammonium, amiprofos-methyl, amitrole, ammonium sulfamate, anilofos, anisuron, asulam, asulam-potassium, asulam-sodium, atraton, atrazine, azafenidin, azimsulfuron, aziprotryne, barban, BCPC, beflubutamid, benazolin, benazolin-dimethylammonium, benazolinethyl, benazolin-potassium, bencarbazone, benfluralin, benfuresate, bensulfuron, bensulfuronmethyl, bensulide, bentazone, bentazone-sodium, benzadox, benzadox-ammonium, benzfendizone, benzipram, benzobicyclon, benzofenap, benzofluor, benzoylprop, benzoylpropethyl, benzthiazuron, bicyclopyrone, bifenox, bilanafos, bilanafos-sodium, bispyribac, bispyribac-sodium, borax, bromacil, bromacii-lithium, bromacii-sodium, bromobonil, bromobutide, bromofenoxim, bromoxynil, bromoxynil butyrate, bromoxynil heptanoate, bromoxynil octanoate, bromoxynil-potassium, brompyrazon, butachlor, butafenacil, butamifos, butenachlor, buthidazole, buthiuron, butralin, butroxydim, buturon, butylate, cacodylic acid, cafenstrole, calcium chlorate, calcium cyanamide, cambendichlor, carbasulam, carbetamide, carboxazole, carfentrazone, carfentrazone-ethyl, CDEA, CEPC, chlomethoxyfen, chloramben, chloramben-ammonium, chloramben-diolamine, chloramben-methyl, chlorambenmethylammonium, chloramben-sodium, chloranocryl, chlorazifop, chlorazifop-propargyl, chlorazine, chlorbromuron, chlorbufam, chloreturon, chlorfenac, chlorfenac-sodium, chlorfenprop, chlorfenprop-methyl, chlorflurazole, chlorflurenol, chlorflurenol-methyl, chloridazon, chlorimuron, chlorimuron-ethyl, chlomitrofen, chloropon, chlorotoluron, chloroxuron, chloroxynil, chlorprocarb, chlorpropham, chlorsulfuron, chlorthal, chlorthaldimethyl, chlorthal-monomethyl, chlorthiamid, cinidon-ethyl, cinmethylin, cînosulfuron, cisanilide, clethodim, cliodinate, clodinafop, clodinafop-propargyl, clofop, clofop-isobutyl, clomazone, clomeprop, cloprop, cloproxydim, clopyralid, clopyralid-methyl, clopyralid-olamine, clopyralid-potassium, clopyralid-tris(2-hydroxypropyl)ammonium, cloransulam, cloransulammethyl, CMA, copper sulfate, CPMF, CPPC, credazine, cresol, cumyluron, cyanamide, cyanatryn, cyanazine, cycioate, cyclosulfamuron, cycloxydim, cycluron, cyhalofop, cyhaiofopbutyl, cyperquat, cyperquat chloride, cyprazine, cyprazoie, cypromîd, daimuron, dalapon,
Page 41 of77 dalapon-calcium, dalapon-magnesîum, dalapon-sodium, dazomet, dazomet-sodium, delachlor, desmedipham, desmetryn, di-allate, dicamba, dicamba-dimethylammonium, dicamba-diolamine, dicamba-isopropylammonium, dicamba-methyl, dicamba-olamine, dicamba-potassium, dicamba-sodium, dicamba-trolamine, dichlobenil, dichloralurea, dichlormate, dichlorprop, dichlorprop-2-ethylhexyl, dichlorprop-butotyl, dichlorprop-dîmethylammonium, dichlorpropethylammonium, dichlorprop-isoctyi, dichlorprop-methyl, dichlorprop-P, dichlorprop-Pdimethylammonium, dichlorprop-potassium, dichlorprop-sodium, diclofop, diclofop-methyl, dîclosulam, diethamquat, diethamquat dichloride, diethatyl, diethatyl-ethyl, difenopenten, difenopenten-ethyl, difenoxuron, difenzoquat, difenzoquat metilsulfate, diflufenican, diflufenzopyr, diflufenzopyr-sodium, dimefuron, dimepiperate, dimethachlor, dimethametryn, dimethenamid, dimethenamid-P, dimexano, dimidazon, dinitramine, dinofenate, dinoprop, dinosam, dinoseb, dinoseb acetate, dinoseb-ammonium, dinoseb-diolamine, dinoseb-sodium, dinoseb-trolamine, dinoterb, dînoterb acetate, diphacînone-sodium, diphenamid, dipropetryn, diquat, diquat dibromide, disul, disul-sodium, dithiopyr, diuron, DMPA, DNOC, DNOCammonium, DNOC-potassium, DNOC-sodium, DSMA, EBEP, eglinazine, eglinazine-ethyl, endothal, endothal-diammonium, endothal-dipotassium, endothal-disodium, epronaz, EPTC, erbon, esprocarb, ethalfluralin, ethametsulfüron, ethametsulfuron-methyl, ethidimuron, ethiolate, ethofumesate, ethoxyfen, ethoxyfen-ethyl, ethoxysulfuron, etinofen, etnipromid, etobenzanid, EXD, fenasulam, fenoprop, fenoprop-3-butoxypropyl, fenoprop-butometyl, fenoprop-butotyl, fenoprop-butyl, fenoprop-isoctyl, fenoprop-methyl, fenoprop-potassium, fenoxaprop, fenoxaprop-ethyl, fenoxaprop-P, fenoxaprop-P-ethyl, fenoxasulfone, fenteracol, fenthiaprop, fenthiaprop-ethyl, fentrazamide, fenuron, fenuron TCA, ferrous sulfate, flamprop, flampropisopropyl, flamprop-M, flamprop-methyl, flamprop-M-isopropyl, flamprop-M-methyl, flazasulfuron, florasulam, fluazifop, fluazifop-butyl, fiuazifop-methyl, fluazifop-P, fluazifop-Pbutyl, fluazolate, flucarbazone, flucarbazone-sodium, flucetosulfuron, fluchloralin, flufenacet, flufenican, flufenpyr, flufenpyr-ethyl, flumetsulam, flumezin, flumiclorac, flumîclorac-pentyl, flumioxazin, flumipropyn, fluometuron, fluorodifen, fluoroglycofen, fluoroglycofen-ethyl, fluoromidine, fluoronitrofen, fluothiuron, flupoxam, flupropacil, flupropanate, flupropanatesodium, fiupyrsulfuron, flupyrsulfuron-methyl-sodium, fluridone, flurochloridone, fluroxypyr, fluroxypyr-butometyl, fluroxypyr-meptyl, flurtamone, fluthiacet, fluthiacet-methyl, fomesafen, fomesafen-sodium, foramsulfuron, fosamine, fosamine-ammonium, furyloxyfen, glufosinate, glufosinate-ammonium, glufosinate-P, ghifosinate-P-ammonium, glufosinate-P-sodium, glyphosate, glyphosate-diammonium, glyphosate-dimethylammonium, glyphosateisopropylammonium, glyphosate-monoammonium, glyphosate-potassium, glyphosatesesquisodium, glyphosate-trimesium, halosafen, halosulfuron, halosulfuron-methyl, haloxydine,
Page 42 of 77 haloxyfop, haloxyfop-etotyl, haloxyfop-methyl, haloxyfop-P, haloxyfop-P-etotyl, haloxyfop-Pmethyl, haloxyfop-sodium, hexachloroacetone, hexaflurate, hexazinone, imazamethabenz, imazamethabcnz-methyl, imazamox, imazamox-ammonium, imazapic, imazapic-ammonium, imazapyr, imazapyr-isopropylammonium, imazaquin, imazaquin-ammonium, imazaquin-methyl, imazaquin-sodium, imazethapyr, irnazethapyr-ammonium, imazosulfuron, indanofan, indaziflam, iodobonil, iodomethane, iodosulfuron, iodosulfuron-methyl-sodium, ioxynil, ioxynil octanoate, îoxynil-lithium, ioxynil-sodium, ipazine, ipfencarbazone, iprymidam, isocarbamid, isocil, isomethiozin, isonoruron, isopolinate, isopropalin, isoproturon, isouron, isoxaben, isoxachlortole, isoxaflutole, isoxapyrifop, karbutilate, ketospiradox, lactofen, lenacil, linuron, MAA, ΜΑΜΑ, MCPA, MCPA-2-ethylhexyl, MCPA-butotyl, MCPA-butyl, MCPAdimethylammonium, MCPA-diolamine, MCPA-ethyl, MCPA-isobutyl, MCPA-isoctyl, MCPAisopropyl, MCPA-methyl, MCPA-olamine, MCPA-potassium, MCPA-sodium, MCPA-thioethyl, MCPA-trolamine, MCPB, MCPB-ethyl, MCPB-methyl, MCPB-sodium, mecoprop, mecoprop-
2-ethylhexyl, mecoprop-dimethylammonium, mecoprop-diolamine, mecoprop-ethadyl, mecoprop-isoctyl, mecoprop-methyl, mecoprop-P, mecoprop-P-dimethylammonium, mecopropP-îsobutyl, mecoprop-potassium, mecoprop-P-potassium, niecoprop-sodium, mecoproptrolamine, medinoterb, medinoterb acetate, mefenacet, mefluidide, mefluidide-diolamine, mefluidide-potassium, mesoprazine, mesosulfuron, mesosulfuron-methyl, mesotrione, metam, metam-ammonium, metamifop, metamitron, metam-potassium, metam-sodium, metazachlor, metazosulfuron, metflurazon, methabenzthiazuron, methalpropalin, methazole, methiobencarb, methiozolin, methiuron, methometon, methoprotryne, methyl bromide, methyl isothiocyanate, methyl dymron, metobenzuron, metolachlor, metosulam, metoxuron, metribuzin, metsulfuron, metsulfuron-methyl, molinate, monalide, monisouron, monochloroacetic acid, monolinuron, monuron, monuron TCA, morfamquat, morfamquat dichlorîde, MSMA, naproanilide, napropamide, naptalam, naptalam-sodium, neburon, nicosulfuron, nipyraclofen, nitralin, nitrofen, nitrofluorfen, norflurazon, noruron, OCH, orbencarb, ortho-dichlorobenzene, orthosulfamuron, oryzalin, oxadiargyl, oxadiazon, oxapyrazon, oxapyrazon-dimolamine, oxapyrazon-sodium, oxasulfuron, oxaziclomefone, oxyfluorfen, parafluron, paraquat, paraquat dichlorîde, paraquat dimetilsulfate, pebulate, pelargonic acid, pendimethalin, penoxsulam, pentachlorophenol, pentanochlor, pentoxazone, perfluidone, pethoxamid, phenisopham, phenmedipham, phenmedipham-ethyl, phenobenzuron, phenylmercury acetate, picloram, picloram-2-ethylhexyl, picloram-isoctyl, picloram-methyl, picloram-olamine, piclorampotassium, picloram-triethylammonium, picloram-tris(2-hydroxypropyl)animonium, picolinafen, pinoxaden, piperophos, potassium arsenite, potassium azide, potassium cyanate, pretilachlor, primisulfuron, primisulfuron-methyl, procyazine, prodiamine, profluazol, profluralin,
Page 43 of77 profoxydim, proglinazine, proglinazine-ethyl, prometon, prometryn, propachlor, propanil, propaquizafop, propazine, prophatn, propisochlor, propoxycarbazone, propoxycarbazonesodium, propyrisulfuron, propyzamide, prosulfalin, prosulfocarb, prosuIfuron, proxan, proxansodium, prynachlor, pydanon, pyraclonil, pyraflufen, pyraflufen-ethyl, pyrasulfotole, pyrazolynate, pyrazosulfuron, pyrazosulfuron-ethyl, pyrazoxyfen, pyribenzoxim, pyributicarb, pyriclor, pyridafol, pyridate, pyriftalid, pyriminobac, pyrimînobac-methyl, pyrimisulfan, pyrithiobac, pyrithiobac-sodium, pyroxasulfone, pyroxsulam, quinclorac, quinmerac, quinoclamine, quinonamid, quizalofop, quizalofop-ethyl, quizalofop-P, quizalofop-P-ethyl, quizalofop-P-tefuryl, rhodethanil, rimsulfuron, saflufenacil, sebuthylazine, secbumeton, sethoxydim, siduron, simazine, simeton, simetryn, SMA, S-metolachlor, sodium arsenite, sodium azîde, sodium chlorate, sulcotrione, sulfallate, sulfentrazone, sulfometuron, sulfometuronmethyl, sulfosulfuron, sulfuric acid, sulglycapin, swep, TCA, TCA-ammonium, TCA-calcium, TCA-ethadyl, TCA-magnesÎum, TCA-sodium, tebutam, tebuthiuron, tefuryltrione, tembotrione, tepraloxydim, terbacil, terbucarb, terbuchlor, terbumeton, terbuthylazine, terbutryn, tetrafluron, thenyichlor, thiazafluron, thîazopyr, thidiazimin, thidiazuron, thiencarbazone, thiencarbazonemethyl, thifensulfuron, thifensulfiiron-methyi, thiobencarb, tiocarbazil, tioclorim, topramezone, tralkoxydim, tri-allate, triasulfuron, triaziflam, tribenuron, tribenuron-methyl, tricamba, triclopyr, triclopyr-butotyl, triclopyr-ethyl, triclopyr-triethylammonium, tridiphane, trietazine, trifloxysulfuron, trifloxysulfüron-sodium, trifluralin, triflusulfuron, triflusulfuron-methyl, trifop, trifop-methyl, trifopsime, trihydroxytriazine, trimeturon, tripropindan, tritac, tritosulfuron, vemolate, xylachlor, (collectively these commonly named herbicides are defined as the “Herbicide Group”).
BIOPESTICIDES
Molécules of Formula One, Two, Three, and Four may also be used in combination (such as în a compositional mixture, or a simultaneous or sequential application) with one or more biopesticides. The term “biopesticide” is used for mîcrobial biological pest control agents that are applied in a similar manner to chemical pesticides. Commonly these are bacterial, but there are also examples of fungal control agents, including Trichoderma spp. and Ampeloinyces quisqualis (a control agent for grape powdery mildew). Bacillus subtilis are used to control plant pathogens. Weeds and rodents hâve also been controlled with mîcrobial agents. One well-known insecticide example is Bacillus thuiïiigiensis, a bacterial disease of Lepidoptera, Coleoptera, and Diptera. Because it has little effect on other organisme, it is considered more environmentally friendly than synthetic pesticides. Biological insecticides include products based on:
l. entomopathogenic fungi (e.g. Metarhizium anisopliae)\
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2. entomopathogenic nematodes (e.g. Steinernema feltiae)', and
3. entomopathogenic viruses (e.g. Cydia pomonella granulovirus).
Other examples of entomopathogenic organisms include, but are not limited to, baculoviruses, bacteria and other prokaryotic organisms, fungi, protozoa and Microsproridia. Biologically derived insecticides include, but not limited to, rotenone, veratridine, as well as microbial toxins; insect tolérant or résistant plant varieties; and organisms modified by recombinant DNA technology to either produce insecticides or to convey an insect résistant property to the genetically modified organism. In one embodiment, the molécules of Formula One, Two, Three, and Four may be used with one or more biopesticides in the area of seed treatments and soil amendments. The Manual of Biocontrol Agents gives a review of the available biological insecticide (and other biology-based control) products. Copping L.G. (ed.) (2004). The Manual of Biocontrol Agents (formerly the Biopesticide Manual) 3rd Edition. British Crop Production Council (BCPC), Famham, Surrey UK.
OTHER ACTIVE COMPOUNDS
Molécules of Formula One, Two, Three, and Four may also be used in combination (such as in a compositional mixture, or a simultaneous or sequential application) with one or more of the following:
1. 3-(4-chloro-2,6-dimethylphenyl)-4-hydroxy-8-oxa-l-azaspiro[4,5]dec-3-en-2-one;
2. 3 -(4’-chloro-2,4-dimethyl[ 1,1 ’-biphenyl]-3-yl)-4-hydroxy-8-oxa-1 -azaspiro[4,5]dec-3en-2-one;
3. 4-[[(6-chloro-3-pyridinyl)methyl]methylamino]-2(5//)-furanone;
4. 4-[[(6-chloro-3-pyridinyl)methyl]cyclopropylamino]-2(5/7)-furanone;
5. 3-chloro-Afè-[(lS)-l-methyl-2-(methylsulfonyl)ethyl]-Afl-[2-methyl-4-[l,2,2,2tetrafluoro-1 -(trifluoromethyl)ethyl]phenyl]-1,2-benzenedicarboxamide;
6. 2-cyano-/V-ethyl-4-fluoro-3-methoxy-benenesulfonamide;
7. 2-cyano-N-ethyl-3-methoxy-benzenesulfonamide;
8. 2-cyano-3-difluoromethoxy-A-ethyl-4-fluoro-benzenesulfonamide;
9. 2-cyano-3-fluoiOrnethoxy-jV-ethyl-benzenesulfonamide;
10. 2-cyano-6-fluoro-3-methoxy-AUV-dimethyl-benzenesulfonamide;
11. 2-cyano-ALethyl-6-fluoro-3-methoxy-/V-methyl-benzenesulfonamide;
12. 2-cyano-3-difluoromethoxy-MA,-dimethylbenzenesuifon-amide;
13. 3-(difluoromethyl)-N-[2-(3,3-dimethylbutyl)phenyl]-l-methyl-l/T-pyrazole-4carboxamide;
14. Ar-ethyl-2,2-dimethylpropionamide-2-(2,6-dichloro-a,a,a-trifluoro-p-tolyl) hydrazone;
Page 45 of 77 /----16501
15. 7V-ethyl-2,2-d ich loro-1 -methylcyclopropane-carboxamide-2-(2,6-dichloro-a,a,a-trifluorojc-tolyl) hydrazone nicotine;
16. O- {(E-)-[2-(4-chloro-phenyl)-2-cyano-1 -(2-trifluoromethyiphenyl)-vinyl)} S-methyl thiocarbonate;
17. (E)-N l -[(2-chloro-1,3-thiazol-5-ylmethyl)]-N2-cyano-N l -methylacetamidine;
18. l-(6-chloropyridin-3-ylmethyl)-7-methyl-8-nitro-1,2,3,5,6,7-hexahydro-imidazo[ 1,2a]pyridin-5-ol;
19. 4-[4-chlorophenyl-(2-butylidîne-hydrazono)methyl)]phenyl mesylate; and
20. N-Ethyl-2,2-dichloro-1 -methylcyclopropanecarboxamide-2-(2,6-dichloro- iï//?/iiz,a/^/ia,a/p/îa-trifluoro-p-tolyl)hydrazone.
Molécules of Formula One, Two, Three, and Four may also be used in combination (such as in a compositional mixture, or a simultaneous or sequential application) with one or more compounds in the following groups: algicides, antifeedants, avicides, bactéricides, bird repellents, chemosterilants, herbicide safeners, insect attractants, insect repellents, mammal 15 repellents, mating disrupters, molluscicides, plant activators, plant growth regulators, rodenticides, and/or virucides (collectively these commonly named groups are defined as the “AI Group”). It should be noted that compounds falling within the AI Group, Insecticide Group, Fungicide Group, Herbicide Group, Acaricide Group, or Nematicide Group rnight be in more than one group, because of multiple activities the compound has. For more information consul! 20 the “Compendium of Pesticide Common Names” located at http://www.alanwood.net/pesticides/index.html. Also consult “The Pesticide Manual” 14th Edition, edited by C D S Tomlin, copyright 2006 by British Crop Production Council, or its prior. or more recent éditions,
SYNERGISTIC MIXTURES AND SYNERGISTS
Molécules of Formula One, Two, Three, and Four may be used with the compounds in the Insecticide Group to form synergistic mixtures where the mode of action of such compounds compared to the mode of action of the molécules of Formula One, Two, Three, and Four are the same, similar, or different. Examples of modes of action include, but are not limited to: 30 acetylcholinesterase inhibitor; sodium channel modulator; chitin biosynthesis inhibitor; GABAgated chloride channel antagonist; GABA and glutamate-gated chloride channel agonist; acétylcholine receptor agonist; MET I inhibitor; Mg-stimulated ATPase inhibitor; nicotinic acétylcholine receptor; Midgut membrane disrupter; oxidativc phosphorylation disrupter, and ryanodine receptor (RyRs). Additionally, molécules of Formula One, Two, Three, and Four may 35 be used with compounds in the Fungicide Group, Acaricide Group, Herbicide Group, or
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Nematicide Group to form synergistic mixtures. Furthermore, molécules of Formula One, Two, Three, and Four may be used with other active compounds, such as the compounds under the heading “OTHER ACTIVE COMPOUNDS”, algicîdes, avicides, bactéricides, molluscicides, rodenticides, virucides, herbicide safeners, adjuvants, and/or surfactants to form synergistic mixtures. Generally, weight ratios of the molécules of Formula One, Two, Three, and Four in a synergistic mixture with another compound are from about 10:1 to about 1:10, preferably from about 5:l to about 1:5, and more preferably from about 3:1, and even more preferably about 1:1. Additionally, the following compounds are known as synergists and may be used with the molécules disclosed in Formula One: piperonyl butoxide, piprotal, propyl isome, sesamex, sesamolin, sulfoxide, and tribufos (collectively these synergists are defined as the “Synergists Group”).
FORMULATIONS
A pesticide is rarely suitable for application in its pure form. It is usually necessary to add other substances so that the pesticide can be used at the required concentration and in an appropriate form, permitting ease of application, handling, transportation, storage, and maximum pesticide activity. Thus, pesticides are formulated into, for example, baits, concentrated émulsions, dusts, emulsifiable concentrâtes, fumigants, gels, granules, microencapsulations, seed treatments, suspension concentrâtes, suspoemulsions, tablets, water soluble liquids, water dispersible granules or dry flowables, wettable powders, and ultra low volume solutions. For further information on formulation types see “Catalogue of Pesticide Formulation Types and International Coding System” Technical Monograph n°2, 5th Edition by CropLife International (2002).
Pesticides are applied most often as aqueous suspensions or émulsions prepared from concentrated formulations of such pesticides. Such water-soluble, water-suspendable, or emulsifiable formulations are either solids, usually known as wettable powders, or water dispersible granules, or liquids usually known as emulsifiable concentrâtes, or aqueous suspensions. Wettable powders, which may be compacted to form water dispersible granules, comprise an intimate mixture of the pesticide, a carrier, and surfactants. The concentration of the pesticide is usually from about 10% to about 90% by weight. The carrier is usually chosen fforn among the attapulgite clays, the montmorillonite clays, the diatomaceous earths, or the purified silicates. Effective surfactants, comprising from about 0.5% to about 10% of the wettable powder, are found among sulfonated lignins, condensed naphthalenesulfonates, naphthalenesulfonates, alkylbenzenesulfonates, alkyl sulfates, and non-ionic surfactants such as ethylene oxide adducts of alkyl phénols.
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Emulsîfiable concentrâtes of pesticides comprise a convenient concentration of a pesticide, such as from about 50 to about 500 grams per liter of liquid dissolved in a carrier that is either a water miscible solvent or a mixture of water-immiscible organic solvent and emulsifiers· Useful organic solvents include aromatics, especially xylenes and petroleum fractions, especially the high-boiling naphthalenic and olefinic portions of petroleum such as heavy aromatic naphtha. Other organic solvents may also be used, such as the terpenîc solvents including rosin dérivatives, aliphatic ketones such as cyclohexanone, and complex alcohols such as 2-ethoxyethanol. Suitable emulsifiers for emulsîfiable concentrâtes are chosen from conventional anionic and non-ionic surfactants.
Aqueous suspensions comprise suspensions of water-insoluble pesticides dispersed in an aqueous carrier at a concentration in the range from about 5% to about 50% by weight. Suspensions are prepared by finely grinding the pesticide and vigorously mixing it into a carrier comprised of water and surfactants. Ingrédients, such as inorganic salts and synthetic or natural gums may also be added, to increase the density and viscosity of the aqueous carrier. It is often most effective to grind and mix the pesticide at the same time by preparing the aqueous mixture and homogenizing it in an implement such as a sand mill, bail mill, or piston-type homogenizer.
Pesticides may also be applied as granular compositions that are particularly useful for applications to the soil. Granular compositions usually contain from about 0.5% to about 10% by weight of the pesticide, dispersed in a carrier that comprises clay or a similar substance. Such compositions are usually prepared by dissolving the pesticide in a suitable solvent and applying it to a granular carrier which has been pre-formed to the appropriate particle size, in the range of from about 0.5 to about 3 mm. Such compositions may also be formulated by making a dough or paste of the carrier and compound and crushing and drying to obtain the desired granular particle size.
Dusts containing a pesticide are prepared by intimately mixing the pesticide in powdered form with a suitable dusty agricultural carrier, such as kaolin clay, ground volcanic rock, and the like. Dusts can suitably contain from about I% to about 10% of the pesticide. They can be applied as a seed dressing or as a foliage application with a dust blower machine.
It is equally practical to apply a pesticide in the form of a solution in an appropriate organic solvent, usually petroleum oil, such as the spray oils, which are widely used in agricultural chemistry.
Pesticides can also be applied in the form of an aérosol composition. In such compositions the pesticide is dissolved or dispersed in a carrier, which is a pressure-generating propellant mixture. The aérosol composition is packaged in a container from which the mixture is dispensed through an atomizing valve.
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Pesticide baits are formed when the pesticide is mixed with food or an attractant or both.
When the pests eat the bait they also consume the pesticide. Baits may take the form of granules, gels, flowable powders, liquids, or solids. They can be used in pest harborages.
Fumigants are pesticides that have a relatively high vapor pressure and hence can exist as a gas in sufficient concentrations to kill pests in soil or enclosed spaces. The toxicity of the fumigant is proportional to its concentration and the exposure time. They are characterized by a good capacity for diffusion and act by penetrating the pest’s respiratory system or being absorbed through the pest’s cutîcle, Fumigants are applied to control stored product pests under gas proof sheets, in gas sealed rooms or buildings or in spécial chambers.
Pesticides can be microencapsulated by suspending the pesticide particles or droplets in plastic polymers of various types. By altering the chemistry of the polymer or by changing factors in the processing, microcapsules can be formed of various sizes, solubility, wall thicknesses, and degrees of penetrability. These factors govem the speed with which the active ingrédient within is released, which in tum, affects the residual performance, speed of action, and odor of the product.
Oil solution concentrâtes are made by dissolving pesticide in a solvent that will hoid the pesticide in solution. Oil solutions of a pesticide usually provide faster knockdown and kill of pests than other formulations due to the solvents themselves having pesticidal action and the dissolution of the waxy covering of the integument increasing the speed of uptake of the pesticide. Other advantages of oil solutions include better storage stability, better pénétration of crevices, and better adhesion to greasy surfaces.
Another embodiment is an oil-in-water émulsion, wherein the émulsion comprises oily globules which are each provided with a lamellar liquid crystal coating and are dispersed in an aqueous phase, wherein each oily globule comprises at least one compound which is agriculturally active, and is individually coated with a monolamellar or oligolamellar layer comprising: (l) at least one non-ionic lipophilie surface-active agent, (2) at least one non-ionic hydrophilic surface-active agent and (3) at least one ionic surface-active agent, wherein the globules having a mean particle diameter of less than 800 nanometers. Further information on the embodiment is disclosed in U.S. patent publication 20070027034 published February l, 2007, having Patent Application serial number 11/495,228. For ease of use, this embodiment will be referred to as “OIWE”.
For further information consult “Insect Pest Management” 2nd Edition by D. Dent, copyright CAB International (2000). Additionally, for more detailed information consult “Handbook of Pest Control - The Behavior, Life History, and Control of Household Pests” by
Arnold Mallis, 9th Edition, copyright 2004 by GIE Media Inc.
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OTHER FORMULATION COMPONENTS
Generally, when the molécules disclosed in Formula One are used in a formulation, such formulation can also contain other components. These components include, but are not limited to, (this is a non-exhaustive and non-mutually exclusive list) wetters, spreaders, stickers, pénétrants, buffers, sequestering agents, drift réduction agents, compatibility agents, anti-foam agents, cleaning agents, and emulsifiers. A few components are described forthwith.
A wetting agent is a substance that when added to a liquid increases the spreading or pénétration power of the liquid by reducing the interfacial tension between the liquid and the surface on which it is spreading. Wetting agents are used for two main fonctions in agrochemical formulations: during processing and manufacture to increase the rate of wetting of powders in water to make concentrâtes for soluble liquids or suspension concentrâtes; and during mixing of a product with water in a spray tank to reduce the wetting time of wettable powders and to improve the pénétration of water into water-dispersible granules. Examples of wetting agents used în wettable powder, suspension concentrate, and water-dispersible granule formulations are: sodium lauryl sulfate; sodium dioctyl sulfosuccinate; alkyl phénol ethoxylates; and aliphatic alcohol ethoxylates.
A dispersing agent is a substance which adsorbs onto the surface of particles and helps to preserve the state of dispersion of the particles and prevents them from reaggregatîng. Dispersing agents are added to agrochemical formulations to facilitate dispersion and suspension during manufacture, and to ensure the particles redisperse into water in a spray tank. They are widely used in wettable powders, suspension concentrâtes and water-dispersible granules. Surfactants that are used as dispersing agents hâve the ability to adsorb strongly onto a particle surface and provide a charged or steric barrier to reaggregation of particles. The most commonly used surfactants are anionic, non-ionic, or mixtures of the two types. For wettable powder formulations, the most common dispersing agents are sodium lignosulfonates. For suspension concentrâtes, very good adsorption and stabilization are obtained using polyelectrolytes, such as sodium naphthalene sulfonate formaldéhyde condensâtes. Tristyrylphenol ethoxylate phosphate esters are also used. Non-ionics such as alkylarylethylene oxide condensâtes and EO-PO block copolymers are sometimes combined with anionics as dispersing agents for suspension concentrâtes. In recent years, new types of very high molecular weight polymeric surfactants hâve been developed as dispersing agents. These hâve very long hydrophobie ‘backbones’ and a large number of ethylene oxide chains forming the ‘teeth’ of a ‘comb’ surfactant. These high molecular weight polymers can give very good long-tenn stability to suspension concentrâtes because the hydrophobie backbones hâve many anchoring points onto the particle surfaces.
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Examples of dispersing agents used in agrochemical formulations are: sodium lignosulfonates;
sodium naphthalene sulfonate formaldéhyde condensâtes; tristyrylphenol ethoxylate phosphate esters; aliphatic alcohol ethoxylates; alkyl ethoxylates; EO-PO block copolymers; and graft copolymers.
An emulsifying agent is a substance which stabilizes a suspension of droplets of one liquid phase in another liquid phase. Without the emulsifying agent the two liquids would separate into two immiscible liquid phases. The most commonly used emulsifier blends contain alkylphenol or aliphatic alcohol with twelve or more ethylene oxide units and the oîl-soluble calcium sait of dodecyibenzenesulfonic acid. A range of hydrophile-lipophile balance (“HLB”) values from 8 to 18 will normally provide good stable émulsions. Emulsion stability can sometimes be improved by the addition of a small amount of an EO-PO block copolymer surfactant.
A solubilizing agent is a surfactant which will form micelles in water at concentrations above the critical micelle concentration. The micelles are then able to dissolve or solubilize water-insoluble materials inside the hydrophobie part of the micelle. The types of surfactants usually used for solubilization are non-ionics, sorbitan monooleates, sorbitan monooleate ethoxylates, and methyl oleate esters.
Surfactants are sometimes used, either alone or with other additives such as minerai or vegetable oils as adjuvants to spray-tank mixes to improve the biological performance of the pesticide on the target. The types of surfactants used for bioenhancement dépend generally on the nature and mode of action of the pesticide. However, they are often non-ionics such as: alkyl ethoxylates; linear aliphatic alcohol ethoxylates; aliphatic amine ethoxylates.
A carrier or diluent in an agricultural formulation is a material added to the pesticide to give a product of the required strength. Carriers are usually materials with high absorptive capacities, while diluents are usually materials with low absorptive capacities. Carriers and diluents are used in the formulation of dusts, wettable powders, granules and water-dispersible granules.
Organic solvents are used mainly in the formulation of emulsifiable concentrâtes, oil-inwater émulsions, suspoemulsions, and ultra low volume formulations, and to a lesser extent, granular formulations. Sometimes mixtures of solvents are used. The first main groups of solvents are aliphatic paraffinic oils such as kerosene or refined paraffins. The second main group (and the most common) comprises the aromatic solvents such as xylene and higher molecular weight fractions of C9 and CIO aromatic solvents. Chlorinated hydrocarbons are useful as cosolvents to prevent crystallization of pesticides when the formulation is emulsified
Page 51 of77 into water. Aicohols are sometimes used as cosolvents to increase solvent power. Other solvents may include vegetable oils, seed oils, and esters of vegetable and seed oils.
Thickeners or gelling agents are used mainly in the formulation of suspension concentrâtes, émulsions and suspoemulsions to modify the rheology or flow properties of the liquid and to prevent séparation and settling of the dispersed particles or droplets. Thickening, gelling, and anti-settling agents generally fall into two categories, namely water-insoluble particulates and water-soluble polymers. It is possible to produce suspension concentrate formulations using clays and silicas. Examples of these types of materials, include, but are not limited to, montmorillonite, bentonite, magnésium aluminum silicate, and attapulgite. Watersoluble polysaccharides have been used as thickening-gelling agents for many years. The types of polysaccharides most commonly used are natural extracts of seeds and seaweeds or are synthetic dérivatives of cellulose. Exemples of these types of materials include, but are not limited to, guar gum; locust bean gum; carrageenam; alginates; methyl cellulose; sodium carboxymethyl cellulose (SCMC); hydroxyethyl cellulose (HEC). Other types of anti-settling agents are based on modified starches, polyacrylates, polyvinyl alcohol and polyethylene oxide. Another good anti-settling agent is xanthan gum.
Microorganisms can cause spoilage of formulated products. Therefore préservation agents are used to eliminate or reduce their effect. Examples of such agents include, but are not limited to: propionic acid and its sodium sait; sorbic acid and its sodium or potassium salts; benzoic acid and its sodium sait; p-hydroxybenzoic acid sodium sait; methyl p-hydroxybenzoate; and l ,2-benzisothiazolin-3-one (BIT).
The presence of surfactants often causes water-based formulations to foam during mixing operations in production and in application through a spray tank, ln order to reduce the tendency to foam, anti-foam agents are often added either during the production stage or before filiing into bottles. Generally, there are two types of anti-foam agents, namely silicones and non-silicones. Silicones are usually aqueous émulsions of diméthyl polysiloxane, while the non-silicone antifoam agents are water-insoluble oils, such as octanol and nonanol, or silica. ln both cases, the function of the anti-foam agent is to displace the surfactant from the air-water interface.
“Green” agents (e.g., adjuvants, surfactants, solvents) can reduce the overall environmental footprint of crop protection formulations. Green agents are biodégradable and generally derived from natural and/or sustainable sources, e.g. plant and animal sources. Spécifie examples are: vegetable oils, seed oils, and esters thereof, also alkoxylated alkyl polyglucosides.
For lùrther information, see “Chemistry and Technology of Agrochemical Formulations” edited by D.A. Knowles, copyright 1998 by Kluwer Academie Publishers. Also see “Insecticides
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in Agriculture and Environment - Retrospects and Prospects” by A.S. Perry, I. Yamamoto, I.
Ishaaya, and R. Perry, copyright 1998 by Springer-Verlag.
PESTS
In general, the molécules of Formula One, Two, Three, and Four may be used to control pests e.g. beetles, earwigs, cockroaches, flies, aphids, scales, whiteflies, leafhoppers, ants, wasps, termites, moths, butterflies, lice, grasshoppers, locusts, crickets, fleas, thrips, bristletails, mites, ticks, nematodes, and symphylans.
In another embodiment, the Molécules of Formula One, Two, Three, and Four may be used to control pests in the Phyla Nematoda and/or Arthropoda.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests in the Subphyla Chelîcerata, Myriapoda, and/or Hexapoda.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests in the Classes of Arachnida, Symphyla, and/or Insecta.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Anoplura. A non-exhaustive list of particular généra includes, but is not limited to, Haematopinus spp., Hoplopleura spp., Linognathus spp., Pediculus spp., and Polyplax spp. A non-exhaustive list of particular species includes, but is not limited to, Haematopinus asini, Haematopinus suis, Linognathus setosus, Linognathus ovillus, Pediculus humanus capitis, Pediculus humanus humanus, and Pthiruspubis.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests in the Order Coleoptera. A non-exhaustive list of particular généra includes, but is not limited to, Acanthoscelides spp., Agriotes spp., Anthonomus spp., Apion spp., Apogonia spp., Aulacophora spp., Bruchus spp., Cerosterna spp., Ceroloma spp,, Ceutorhynchus spp., Chaetocnema spp., Colaspis spp., Ctenicera spp., Curculio spp., Cyclocephala spp., Diabrotica spp., Hypera spp., Ips spp., Lyctus spp., Megascelis spp., Meligethes spp., Otiorhynchus spp., Pantomorus spp., Phyllophaga spp., Phyllotreta spp., Rhizotrogus spp., Rhynchites spp., Rhynchophorus spp., Scolytus spp., Sphenophorus spp., Sitophilus spp., and Tribolium spp. A non-exhaustive list of particular species includes, but is not limited to, Acanthoscelides obtectus, Agrilus planipennis, Anoplophora glabripennis, Anthonomus grandis, Ataenius spretulus, Atomaria linearis, Bothynoderes punctiventris, Bruchus pisorum, Callosobruchus maculatus, Carpophilus hemipterus, Cassida vittata, Ceroloma trifurcata, Ceutorhynchus assimilis, Ceutorhynchus napi, Conoderus scalaris, Conoderus stigmosus, Conotrachelus nénuphar, Cotinis nitida, Crioceris asparagi. Cryptolestes ferrugineus. Cryptolestes pusillus, Cryplolestes turcicus, Cylindrocopturus adspersus, Deporaus marginatus.
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Dermestes lardarius, Dermestes maculalus, Epilachna varivestis, Faustinus cubae, Hylobius pales, Hypera postica, Hypothenemus hampei, Lasioderma serricome, Leptinotarsa decemlineata, Liogenys fuscus, Liogenys suturalïs, Lissorhoptrus oryzophilus, Maecolaspis joliveti, Melanotus commuais, Meligethes aeneus, Melolontha melolontha, Oberea brevis, Oberea linearis, Oryctes rhinocéros, Oryzaephilus mercator, Oryzaephilus surinamensis, Ouléma melanopus, Ouléma oryzae, Phyllophaga cuyabana, Popillia japonica, Prostephanus truncatus, Rhyzopertha dominica,, Sitona lineatus, Sitophilus granarius, Sitophilus oryzae, Sitophilus zeamais, Stegobium paniceum, Tribolium castaneum, Tribolium confusion, Trogoderma variabile, and Zabrus tenebrioides.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Dermaptera.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Blattaria, A non-exhaustive list of particular species includes, but is not limited to, Blattella germanica, Blatta orientalis, Parcoblatta pennsylvanica, Periplaneta americana, Periplaneta australasiae, Periplaneta brunnea, Periplaneta fuliginosa, Pycnoscelus surinamensis, and Supella longipalpa.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Diptera. A non-exhaustive list of particular généra includes, but is not limited to, Aedes spp., Agromyza spp., Anastrepha spp., Anopheles spp., Bactrocera spp., Ceratitis spp., Chrysops spp., Cochliomyia spp., Contarinia spp., Culex spp., Dasineura spp., Délia spp., Drosophila spp., Fannia spp., Hylemyia spp., Liriomyza spp., Musca spp., Phorbia spp., Tabanus spp., and Tipula spp. A non-exhaustive list of particular species includes, but is not limited to, Agromyza frontella, Anastrepha suspensa, Anastrepha ludens, Anastrepha obliqa, Bactrocera cucurbitae, Bactrocera dorsalis, Bactrocera invadens, Bactrocera zonata, Ceratitis capitata, Dasineura brassicae, Délia platura, Fannia canicularis, Fannia scalaris, Gasterophilus intestinalis, Gracillia perseae, Haematobia irritons, Hypoderma lineatum, Liriomyza brassicae, Melophagus ovinus, Musca autumnalis, Musca domestica, Oestrus ovis, Oscinella frit, Pegomya betae, Psila rosae, Rhagoletis cerasi, Rhagoletis pomonella, Rhagoletis mendax, Sitodiplosis mosellana, and Stomoxys calcitrans.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Heniiptera. A non-exhaustive list of particular généra includes, but is not limited to, Adelges spp., Aulacaspis spp., Aphrophora spp., Aphis spp.,
Bemisia spp., Ceroplastes spp., Chionaspis spp., Chrysomphalus spp., Coccus spp., Empoasca spp., Lepidosaphes spp., Lagynotomus spp., Lygus spp., Macrosiphum spp., Nephotettix spp.,
Nezara spp., Philaenus spp., Phytocoris spp., Piezodorus spp., Planococcus spp., Pseudococcus
Page 54 of 77 spp., Rhopalosiphum spp., Saissetia spp., Therioaphis spp., Toumeyella spp., Toxoptera spp., Trialeurodes spp., Triatoma spp. and Unaspis spp. A non-exhaustive list of particular species includes, but is not limited to, Acrosternum hilare, Acyrthosiphon pisttm, Aleyrodes proletella, Aleurodicus dispersus, Aleurothrixus floccosus, Amrasca biguttula biguttula, Aonidiella aurantii, Aphis gossypii, Aphis glycines, Aphis pomi, Aulacorthum solani, Bemisia argenlifolii, Bemisia tabaci, Blissus leucopterus, Brachycorynella asparagi, Brevennia rehî, Brevicoryne brassicae, Calocoris norvégiens, Ceroplastes rubens, Cimex hemipterus, Cimex lectularius, Dagbertus fasciatus, Dichelops furcatus, Diuraphis noxia, Diaphorina citri, Dysaphis plantaginea, Dysdercus suturellus, Edessa meditabunda, Eriosoma lanigerum, Eurygaster maura, Euschistus héros, Euschistus servus, Helopeltis antonii, Helopeltis theivora, Icerya pitrchasi, Idioscopus nitidulus, Laodelphax striatellus, Leptocorisa oratorius, Leptocorisa varicornis, Lygus hesperus, Maconellicoccus hirsutus, Macrosiphum euphorbiae, Macrosiphum granarium, Macrosiphum rosae, Macrosteles quadrilineatus, Mahanarva frimbiolata, Metopolophium dirhodum, Midis longicornis, Myzus persicae, Nephotettix cinctipes, Neurocolpus longirostris, Nezara viridula, Nilaparvata lugens, Parlatoria pergandii, Parlatoria ziziphi, Peregrinus maidis, Phylloxéra vitifoliae, Physokermes piceae,, Phytocoris californiens, Phytocoris relativus, Piezodorus guildmii, Poecilocapsus lineatus, Psallus vaccinicola, Pseudacysta perseae, Pseudococcus brevipes, Quadraspidiotus perniciosus, Rhopalosiphum maidis, Rhopalosiphum padi, Saissetia oleae, Scaptocoris castanea, Schizaphis graminum, Sitobion avenue, Sogatella furcifera, Trialeurodes vaporariorum, Trialeurodes abutiloneus, Unaspis yanonensis, and Zulia entrerriana.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Hymenoptera. A non-exhaustive list of particular généra includes, but is not limited to, Acromyrmex spp., Atta spp., Camponotus spp., Diprion spp., Formica spp., Monomorium spp., Neodiprion spp., Pogonomyrmex spp., Polistes spp., Solenopsis spp., Vespula spp., and Xylocopa spp. A non-exhaustive list of particular species includes, but is not limited to, Athalia rosae, Atta texana, Iridomyrmex humilis, Monomorium minimum, Monomorium pharaonis, Solenopsis invicta, Solenopsis geminata, Solenopsis molesta, Solenopsis richtery, Solenopsis xyloni, and Tapinoma sessile.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Isoptera. A non-exhaustive list of particular généra includes, but is not limited to, Coptotermes spp., Cornitermes spp., Cryptotermes spp., Heterotermes spp.,
Kalotermes spp., Incisitermes spp., Macrotermes spp., Marginitermes spp., Microcerotermes spp., Procornitermes spp., Reticulitermes spp., Schedorhinotermes spp., and Zootermopsis spp.
A non-exhaustive list of particular species includes, but is not limited to, Coptotermes
Page 55 of 77 curvignathus, Coptotermes frenchi, Coptotermes formosanus, Heterotermes aureus, Microtermes obesi, Reticulitermes banyulensis, Reticulitermes grassei, Reticulitermes flavipes, Reticulitermes hageni, Reticulitermes hesperus, Reticulitermes santonensis, Reticulitermes speratus,
Reticulitermes tibialis, and Reticulitermes virginicus.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Lepidoptera. A non-exhaustive list of particular généra includes, but is not limited to, Adoxophyes spp., Agrotis spp., Argyrotaenia spp., Cacoecia spp., Caloptilia spp., Chilo spp., Chrysodeixis spp., Colias spp., Crambus spp., Diaphania spp., Diatraea spp., Earias spp., Ephestia spp., Epimecis spp., Feltia spp., Gortyna spp., Helicoverpa spp., Heliothis spp., Indarbela spp., Lithocolletis spp., Loxagrotis spp., Malacosoma spp., Peridroma spp., Phyllonorycter spp., Pseudaletia spp., Sesamia spp., Spodoptera spp., Synanthedon spp., and Yponomeuta spp. A non-exhaustive list of particular species includes, but is not limited to, Achaea janata, Adoxophyes orana, Agrotis ipsilon, Alabama argillacea, Amorbia cuneana, Amyelois transitella, Anacamptodes defectaria, Anarsia lineatella, Anomis sabulifera, Anticarsia gemmatalis, Archips argyrospila, Archips rosana, Argyrotaenia citrana, Autographe gamma, Bonagota cranaodes, Borbo cinnara, Bucculatrix thurberiella, Capua reticulana, Carposina niponensis, Chlumetia transversa, Choristoneura rosaceana, Cnaphalocrocis medinalis, Conopomorpha cramerella, Cossus cossus, Cydia caryana, Cydia funebrana, Cydia molesta, Cydia nigricana, Cydia pomonella, Dama diducta, Diatraea saccharalis, Diatraea grandiosella, Earias insulana, Earias vittella, Ecdytolopha aurantianum, Elasmopalpus lignosellus, Ephestia cautella, Ephestia elutella, Ephestia kuehniella, Epinotia aporema, Epiphyas postvittana, Erionota thrax, Eupoecilia ambiguella, Euxoa auxiliaris, Grapholita molesta, Hedylepta indicata, Helicoverpa armigera, Helicoverpa zea, Heliothis virescens, Hellula undalis, Keiferia lycopersicella, Leucinodes orbonalis, Leucoptera coffeella, Leucoptera malifoliella, Lobesia botrana, Loxagrotis albicosta, Lymantria dispar, Lyonetia clerkella, Mahasena corbetti, Mamestra brassicae, Maruca testulalis, Metisa plana, Mythimna unipuncta, Neoleucinodes elegantalis, Nymphula depunctalis, Operophtera brumata, Oslrinia nubilalis, Oxydia vesulia, Pandemis cerasana, Pandemis heparana, Papilio demodocus, Pectinophora gossypiella, Peridroma saucia, Perileucoptera coffeella, Phthorimaea operculella, Phyllocnistis citrella, Pieris rapae, Plathypena scabra, Plodia interpunctella, Plutella xylostella, Polychrosis viteana, Prays endocarpa, Prays oleae, Pseudaletia unipuncta, Pseitdoplusia includens, Rachiplusia nu, Scirpophaga incertulas, Sesamia inférons, Sesamia nonagrioides, Setora nitens, Sitotroga cerealella, Sparganothis pilleriana, Spodoptera exigua, Spodoptera frugiperda, Spodoptera eridania, Thecla basilides, Tineola bisselliella, Trichoplusia ni, Tuta absoluta, Zeuzera coffeae, and Zeuzera pyrina.
Page 56 of 77
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Mallophaga. A non-exhaustive list of particular généra includes, but is not limited to, Anaticola spp., Bovicola spp., Chelopistes spp., Goniodes spp., Menacanthus spp., and Trichodectes spp. A non-exhaustive list of particular species includes, but is not limited to, Bovicola bovis, Bovicola caprae, Bovicola ovis, Chelopistes meleagridis, Goniodes dissimilis, Goniodes gigas, Menacanthus stramineus, Menopon gallinae, and Trichodectes canis.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Ortlioptera. A non-exhaustive list of particular généra includes, but is not limited to, Melanoplus spp., and Pterophylla spp. A non-exhaustive list of particular species includes, but is not limited to, Anabrus simplex, Gryllotalpa africana, Gryllotalpa australis, Gryllotalpa brachyptera, Gryllotalpa hexadactyla, Locusta migratoria, Microcentrum retinerve, Schistocerca gregaria, and Scudderia furcata.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Siphonaptera. A non-exhaustive list of particular species includes, but is not limited to, Ceratophyllus gallinae, Ceratophyllus niger, Ctenocephalides canis, Ctenocephalides felis, and Pulex irritons.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Thysanoptera. A non-exhaustive list of particular généra includes, but is not limited to, Caliothrips spp., Frankliniella spp., Scirtothrips spp., and Thrips spp. A non-exhaustive list of particular sp. includes, but is not limited to, Frankliniella fusca, Frankliniella occidentalis, Frankliniella schultzei, Frankliniella williamsi, Heliothrips haemorrhoidalis, Rhipiphorothrips cruentatus, Scirtothrips citri, Scirtothrips dorsalis, and Taeniothrips rhopalantennalis, Thrips hawaiiensis, Thrips nigropilosus, Thrips orientalis, Thrips tabaci.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Thysanura. A non-exhaustive list of particular généra includes, but is not limited to, Lepisma spp. and Thermobia spp.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Order Acarina. A non-exhaustive list of particular généra includes, but is not limited to, Acarus spp., Aculops spp., Boophihts spp., Demodex spp., Dermacentor spp., Epitrimerus spp., Eriophyes spp., Ixodes spp., Oligonychiis spp., Panonychus spp., Rhizoglyphus spp., and Tetranychus spp. A non-exhaustive list of particular species includes, but is not limited to, Acarapis woodi, Acarus siro, Aceria mangiferae, Aculops lycopersici, Acttlus pelekassi, Acttlus schlechtendali, Amblyonuna americanum, Brevipalpus obovatus, Brevipalpus
Page 57 of 77 phoenicis, Dermacentor variabilis, Dermatophagoides pteronyssinus, Eotetranychus carpini,
Notoedres cati, Oligonychus cojfeae, Oligonychus ilicis, Panonychus citri, Panonychus ulmi,
Phyllocoptruta oleivora, Polyphagotarsonemus lattis, Rhipicephalus sanguineus, Sarcoptes scabiei, Tegolophus perseaflorae, Tetranychus urticae, and Varroa destructor.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pest of the Order Syniphyla. A non-exhaustive list of particular sp. includes, but is not limited to, Scutigerella immaculata.
In another embodiment, the molécules of Formula One, Two, Three, and Four may be used to control pests of the Phylum Nématode. A non-exhaustive list of particular généra includes, but is not limited to, Aphelenchoides spp., Belonolaimus spp., Criconemella spp., Ditylenchus spp,, Heterodera spp., Hirschmanniella spp., Hoplolaimus spp., Meloidogyne spp., Pratylenchus spp., and Radopholus spp. A non-exhaustive list of particular sp. includes, but is not limited to, Diroftlaria immitis, Heterodera zeae, Meloidogyne incognito, Meloidogyne Javanica, Oncltocerca volvulus, Radopholus similis, and Rotylenchulus reniformis.
For additional information consult “Handbook OF PEST Control - The Behavior, Life History, and Control of Household Pests” by Arnold Mallis, 9th Edition, copyright 2004 by GIE Media Inc.
APPLICATIONS
Molécules of Formula One, Two, Three, and Four are generally used in amounts from about 0.01 grams per hectare to about 5000 grams per hectare to provide control. Amounts from about 0.1 grams per hectare to about 500 grams per hectare are generally preferred, and amounts from about l gram per hectare to about 50 grams per hectare are generally more preferred.
The area to which a molécule of Formula One is applied can be any area inhabited (or maybe inhabited, or traversed by) a pest, for example: where crops, trees, fruits, cereals, fodder species, vines, turf and ornamental plants, are growing; where domesticated animais are residing; the interior or exterior surfaces of buildings (such as places where grains are stored), the materials of construction used in building (such as impregnated wood), and the soil around buildings. Particular crop areas to use a molécule of Formula One include areas where apples, corn, sunflowers, cotton, soybeans, canola, wheat, rice, sorghum, barley, oats, potatoes, oranges, alfalfa, lettuce, strawberries, tomatoes, peppers, crucifers, pears, tobacco, almonds, sugar beets, beans and other valuable crops are growing or the seeds thereof are going to be planted. It is also advantageous to use aluminum sulfate with a molécule of Formula One when growing various plants.
Page 58 of 77
Controlling pests generally means that pest populations, pest activity, or both, are reduced in an area. This can corne about when: pest populations are repulsed from an area; when pests are incapacitated in or around an area; or pests are extenninated, in whole, or in part, in or around an area. Of course, a combination of these results can occur. Generally, pest populations, activity, or both are desirably reduced more than fifty percent, preferably more than 90 percent. Generally, the area is not in or on a human; consequently, the locus is generally a non-human area.
The molécules of Formula One, Two, Three, and Four may be used in mixtures, applied simultaneously or sequentially, alone or with other compounds to enhance plant vigor (e.g. to grow a better root systern, to better withstand stressful growing conditions). Such other compounds are, for example, compounds that modulate plant ethylene receptors, most notably lmethylcyclopropene (also known as l-MCP).
The molécules of Formula One, Two, Three, and Four can be applied to the foliar and fruiting portions of plants to control pests. The molécules will either corne in direct contact with the pest, or the pest will consume the pesticide when eating leaf, fruit mass, or extracting sap, that contains the pesticide. The molécules of Formula One, Two, Three, and Four can also be applied to the soil, and when applied in this manner, root and stem feeding pests can be controlled. The roots can absorb a molécule taking it up into the foliar portions of the plant to control above ground chewing and sap feeding pests.
Generally, with baits, the baits are placed in the ground where, for example, termites can corne into contact with, and/or be attracted to, the bait. Baits can also be applied to a surface of a building, (horizontal, vertical, or slant surface) where, for example, ants, termites, cockroaches, and flies, can corne into contact with, and/or be attracted to, the bait. Baits can comprise a molécule of Formula One.
The molécules of Formula One, Two, Three, and Four can be encapsulated inside, or placed on the surface of a capsule, The size of the capsules can range from nanometer size (about 100-900 nanometers in diameter) to micrometer size (about 10-900 microns in diameter).
Because of the unique ability of the eggs of some pests to resist certain pesticides, repeated applications of the molécules of Formula One, Two, Three, and Four may be désirable to control newly emerged larvae.
Systemic movement of pesticides in plants may be utilized to control pests on one portion of the plant by applying (for example by spraying an area) the molécules of Formula One, Two, Three, and Four to a different portion of the plant. For example, control of foliar-feeding insects can be achieved by drip irrigation or furrow application, by treating the soil with for example pre- or post-planting soil drench, or by treating the seeds of a plant before planting.
Page 59 of 77 —
Seed treatment can be applied to ail types of seeds, including those from which plants genetically modified to express specialized traits will germinate. Représentative examples include those expressing proteins toxic to invertebrate pests, such as Bacillus thuringiensis or other insecticidal toxins, those expressing herbicide résistance, such as “Roundup Ready” seed, or those with “stacked” foreign genes expressing insecticidal toxins, herbicide résistance, nutrition-enhancement, drought résistance, or any other bénéficiai traits. Furthermore, such seed treatments with the molécules of Formula One, Two, Three, and Four may further enhance the ability of a plant to better withstand stressful growing conditions. This results in a healthier, more vigorous plant, which can lead to higher yields at harvest time. Generally, about l gram of the molécules of Formula One, Two, Three, and Four to about 500 grams per 100,000 seeds is expected to provide good benefits, amounts from about 10 grams to about 100 grams per 100,000 seeds is expected to provide better benefits, and amounts from about 25 grams to about 75 grams per 100,000 seeds is expected to provide even better benefits.
It should be readily apparent that the molécules of Formula One, Two, Three, and Four may be used on, in, or around plants genetically modified to express specialized traits, such as Bacillus thuringiensis or other insecticidal toxins, or those expressing herbicide résistance, or those with “stacked” foreign genes expressing insecticidal toxins, herbicide résistance, nutritionenhancement, or any other bénéficiai traits.
The molécules of Formula One, Two, Three, and Four may be used for controlling endoparasites and ectoparasites in the veterinary medicine sector or in the field of non-human animal keeping. The molécules of Formula One, Two, Three, and Four are applied, such as by oral administration in the form of, for example, tablets, capsules, drinks, granules, by dermal application in the form of, for example, dipping, spraying, pouring on, spotting on, and dusting, and by parentéral administration in the form of, for example, an injection.
The molécules of Formula One, Two, Three, and Four may also be employed advantageously in livestock keeping, for example, cattle, sheep, pigs, chickens, and geese, They may also be employed advantageously in pets such as, horses, dogs, and cats. Particular pests to control would be fleas and ticks that are bothersome to such animais. Suitable formulations are administered orally to the animais with the drinking water or feed. The dosages and formulations that are suitable dépend on the species.
The molécules of Formula One, Two, Three, and Four may also be used for controlling parasitic worms, especially of the intestine, in the animais listed above.
The molécules of Formula One, Two, Three, and Four may also be employed in therapeutic methods for human health care. Such methods include, but are limited to, oral
Page 60 of 77 administration in the form of, for example, tablets, capsules, drinks, granules, and by dermal application.
Pests around the world bave been migrating to new environments (for such pest) and thereafter becoming a new invasive species in such new environment. The molécules of Formula One, Two, Three, and Four may also be used on such new invasive species to control them in such new environment.
The molécules of Formula One, Two, Three, and Four may also be used in an area where plants, such as crops, are growing (e.g. pre-planting, planting, pre-harvesting) and where there are low levels (even no actual presence) of pests that can commercially damage such plants. The use of such molécules in such area is to benefit the plants being grown in the area. Such benefits, may include, but are not limited to, improving the health of a plant, improving the yield of a plant (e.g. increased biomass and/or increased content of valuable ingrédients), improving the vigor of a plant (e.g. improved plant growth and/or greener leaves), improving the quality of a plant (e.g. improved content or composition of certain ingrédients), and improving the tolérance to abiotic and/or biotic stress of the plant.
Before a pesticide can be used or sold commercially, such pesticide undergoes lengthy évaluation processes by various governmental authorities (local, régional, state, national, and international). Voluminous data requirements are specified by regulatory authorities and must be addressed through data génération and submission by the product regîstrant or by a third party on the product registrant's behalf, often using a computer with a connection to the World Wide Web. These governmental authorities then review such data and if a détermination of safety is concluded, provide the potential user or seller with product registration approval. Thereafter, in that locality where the product registration is granted and supported, such user or seller may use or sell such pesticide.
A molécules according to Formula One, Two, Three, and Four can be tested to détermine its efficacy against pests. Furthermore, mode of action studies can be conducted to détermine if said molécule has a different mode of action than other pesticides. Thereafter, such acquired data can be disseminated, such as by the internet, to third parties.
The headings in this document are for convcnicnce only and must not be used to interpret any portion hereof.
Page 61 of77
TABLE SECTION
BAW & CEW Rating Table
% Control (or Mortality) Rating
50-100 A
More than 0 - Less than 50 B
Not Tested C
No activity noticed in this bioassay D
GPA Rating Table
% Control (or Mortality) Rating
80-100 A
More than 0 - Less than 80 B
Not Tested C
No activity noticed in this bioassay D
Page 62of77
Table:Bio Results
Compound Number % Mortality BAW 50 gg/cn? % Mortality CEW 50 pg/cm2 % Mortality GPA 200 ppm
1 A A D
2 A A B
3 A A B
4 A A D
5 A A D
6 A A B
7 A A D
8 A A B
9 A A D
10 A A B
11 A A B
12 A A B
13 A A D
14 A A B
15 C C B
16 C C D
17 A A D
18 D B D
19 D A B
20 A A B
21 A A D
22 A A D
23 D A B
24 A D B
25 D D B
26 A B D
27 B A D
28 D D B
29 A A D
30 D D B
3> D D D
Page 63 of77
Compound Number % Mortality BAW 50 pg/cn? % Mortality CEW 50 pg/cm2 % Mortality GPA 200 ppm
32 D A B

Claims (16)

  1. l. A pesticidal composition comprising a molécule according to Formula One, Two, Three, or Four
    Formula Ί hrce ’ “Formula Four” wherein:
    Page 65 of 77 (a) Ari is (each independently)
    15 (l) furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, thienyl, or (2) substituted furanyl, substituted phenyl, substituted pyridazinyl, substituted pyridyl, substituted pyrimidinyl, or substituted thienyl, wherein said substituted furanyl, substituted phenyl, substituted pyridazinyl, substituted pyridyl, substituted pyrimidinyl, and substituted thienyl, hâve one or more substituents independently selected from H, F, Cl, Br, l, CN, NO2, Cj-Cg alkyl, Ci-Cg haloalkyl, C3-Cg cycloalkyl, C3-Cû halocycloalkyl, C3-Cg cycloalkoxy, C3-Cg halocycloalkoxy, Cj-Cg alkoxy, C|-C6 haloalkoxy, C2-Cg alkenyl, C2-Cg alkynyl, S(=O)n(Ci-C6 alkyl), S(=0)n(Cj-C6 haloalkyl), OSO2(C]-C6 alkyl), OSO2(Ci-C6 haloalkyl), C(=0)NRxRy, (Cj-C6 alkyl)NRxRy, C(=O)(Ci-C6 alkyl), C(=O)O(Cj-C6 alkyl), C(=O)(CrC6 haloalkyl), C(O)0(Cj-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (Ci-C6 alkyl)O(Cj-C6 alkyl), (Ci-C6 aIkyl)S(CrC6 alkyl), C(=O)(Ci-C6 alkyl)C(=O)O(C]-C6 alkyl), phenyl, phenoxy, substituted phenyl, and substituted phenoxy, wherein such substituted phenyl and substituted phenoxy hâve one or more substituents independently selected from H, F, Cl, Br, I, CN, NO2, C|-Cg alkyl, Cî-Cg haloalkyl, Ci-Cg hydroxyalkyl, C3-Cg cycloalkyl, C3-Cg halocycloalkyl, C3-Cg hydroxycycloalkyl, C3-Cg cycloalkoxy, C3-Cû halocycloalkoxy, C3-Cg hydroxycycloalkoxy, C|-Cg alkoxy, Ci-Cû haloalkoxy, C2-C6 alkenyl, C2-Cg alkynyl, S(=O)n(C|-C6 alkyl), S(=0)n(Cj-C6 haloalkyl), OSO2(CrC6 alkyl), OSO2(Ci-C6 haloalkyl), C(=O)NRxRy, (C|-C6 alkyl)NRxRy, C(=O)(Cj-C6 alkyl), C(=O)O(Cj-C6 alkyl), C(=O)(Cj-C6 haloalkyl), C(=O)O(Ci-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-Cg cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-Cg alkenyl), (C|-C6 aIkyl)O(C]-C6 alkyl), (C|-C6 alkyl)S(CrC6 alkyl), C(=O)(Cj-C6 alkyl)C(=O)O(C,-C6 alkyl) phenyl, and phenoxy;
    (b) Het is (each independently) a 5 or 6 membered, saturated or unsaturated, heterocyclic ring, containing one or more heteroatoms independently selected from nitrogen, sulfur, or oxygen, and where Αη and Ar2 are not ortho to each other (but may be meta or para, such as, for a five membered ring they are 1,3 and for a 6 membered ring they are either 1,3 or 1,4), and where said heterocyclic ring may also be substituted with one or more substituents independently selected from H, OH, F, Cl, Br, I, CN, NO2, oxo, C]-Cg alkyl, Cj-Cg haloalkyl, C|-Cg hydroxyalkyl, C3-C6 cycloalkyl, C3-Cg halocycloalkyl, C3-Cg hydroxycycloalkyl, C3-Cg cycloalkoxy, C3-C0 halocycloalkoxy, C3-C6 hydroxycycloalkoxy, Cj-Cg alkoxy, Ci-Cg haloalkoxy, C2-Cg alkenyl, C2-Cg alkynyl, S(=0)n(Cj-C6 alkyl), S(=O)n(Cj-C6 haloalkyl), OSO2(Cj-C6 alkyl), OSO2(Cj-Cà haloalkyl), C(=O)NRxRy, (Cj-C6 alkyl)NRxRy, C(=O)(C|-C6 alkyl), C(=O)O(Cj-C6 alkyl), C(=O)(C,-C6 haloalkyl), C(=O)O(Cj-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-Cô cycloalkyl), C(=O)(C2-Cg alkenyl), C(=O)O(C2-Cg alkenyl), (Cj-Cg alkyl)O(Cj-C6 alkyl), (Cj-Cg alkyl)S(C,-C6 alkyl), C(=O)(Cj-C6 alkyl)C(=O)O(Cj-C6 alkyl), phenyl, phenoxy, substituted phenyl and substituted phenoxy
    Page 66 of 77 wherein such substituted phenyl and substituted phenoxy hâve one or more substituents independently selected from H, OH, F, Cl, Br, I, CN, NO2, Ci-C* alkyl, Ci-Cù haloalkyl, C|-Cù hydroxyalkyl, C3-Cû cycloalkyl, C3-C6 halocycloalkyl, C3-Cô hydroxycycloalkyl, C3-Cg cycloalkoxy, C3-Cû halocycloalkoxy, C3-Cé hydroxycycloalkoxy, Cj-Cû alkoxy, Ci-C& haloalkoxy, C2-Cû alkenyl, C2-Ce alkynyl, S(=O)n(C(-C6 alkyl), S(=O)n(C]-C6 haloalkyl), OSO2(CrC6 alkyl), OSO2(C[-C6 haloalkyl), C(=O)H, C(=O)OH, C(=O)NRxRy, (Ci-C6 alkyl)NRxRy, C(=O)(C,-C6 alkyl), C(=O)O(C,-C6 alkyl), C(=O)(C)-C6 haloalkyl), C(=O)O(C,C6 haloalkyl), C(=O)(CrCû cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (Ci-C6 alkyl)O(Ci-C6 alkyl), (C,-C6 alkyl)S(CrC6 alkyl), 0(=0)(0^ alkyl)C(=O)O(C]-C6 alkyl), phenyl, and phenoxy;
    (c) Ar2 is (each independently) (1) furanyl, phenyl, pyridazinyl, pyridyl, pyrimidinyl, thienyl, or (2) substituted furanyl, substituted phenyl, substituted pyridazinyl, substituted pyridyl, substituted pyrimidinyl, or substituted thienyl, wherein said substituted furanyl, substituted phenyl, substituted pyridazinyl, substituted pyridyl, substituted pyrimidinyl, and substituted thienyl, hâve one or more substituents independently selected from H, OH, F, Cl, Br, I, CN, N02, C|-Cô alkyl, Ci-Cé haloalkyl, C|-Cô hydroxyalkyl, C3-Cû cycloalkyl, Cj-Cc halocycloalkyl, C3-Cô hydroxycycloalkyl, C3’C6 cycloalkoxy, C3-Cû halocycloalkoxy, C3-Cû hydroxycycloalkoxy, CiCe alkoxy, C|-Cô haloalkoxy, C2-Cû alkenyl, C2-Ce alkynyl, S(=0)n(Ci-C6 alkyl), S(=O)n(Ci-Câ haloalkyl), 0SO2(C]-C6 alkyl), OSO2(C|-C6 haloalkyl), C(=O)NRxRy, (C^Cc alkyi)NRxRy, C(=O)(Ci-C6 alkyl), C(=O)O(C,-C6 alkyl), C(=O)(Ci-C6 haloalkyl), C(=O)O(Ct-C6 haloalkyl), C(=O)(C3-C0 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C,-C6 alkyl)O(CrC6 alkyl), (CrC6 alkyl)S(CrC6 alkyl), C(=O)(C,-C6 alkyl)C(=O)O(C|-Cfi alkyl), phenyl, phenoxy, substituted phenyl and substituted phenoxy wherein such substituted phenyl and substituted phenoxy hâve one or more substituents independently selected from H, OH, F, Cl, Br, I, CN, NO2, Ci-Cô alkyl, C]-Cù haloalkyl, Cj-Cô hydroxyalkyl, C3-C& cycloalkyl, C3-Cô halocycloalkyl, C3-Cû hydroxycycloalkyl, C3-Cô cycloalkoxy, Cj-Cô halocycloalkoxy, C3-Ce hydroxycycloalkoxy, C[C& alkoxy, Ci-Cè haloalkoxy, C2-C& alkenyl, C2-Cô alkynyl, S(=O)h(C|-C6 alkyl), S(=O)n(Ci-Ce haloalkyl), OSO2(CrC6 alkyl), OSO2(CrC6 haloalkyl), C(=O)H, C(=O)OH, C(=O)NRxRy, (Cr C6 alkyl)NRxRy, C(=O)(CrC6 alkyl), C(=O)O(CrC6 alkyl), C(=0)(C,-C6 haloalkyl), C(=O)O(C,-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(CrC6
    Page 67 of 77 haloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C,-C6 alkyl)O(CpC6 alkyl), (CpC6 alkyl)S(Ci-C6 alkyl), C(=O)(C,-C6 alkyl)C(=O)O(CpC6 alkyl), phenyl, and phenoxy);
    (d) RI and R2 are independently selected from H, CpC& alkyl, C3-Cé cycloalkyl, C3-Cô hydroxycycloalkoxy, C2-C6 alkenyl, C2-C6 alkynyl, S(=O)n(C]-C6 alkyl), OSO2(CpCô alkyl), C(=O)H, C(=O)(Ct-C6 alkyl), C(=O)O(CrC6 alkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (CpC6 alkyl)O(C|-C6 alkyl), (CrC6 alkyl)S(Ci-C6 alkyl), C(=O)(C,-C6 alkyl)C(=O)O(CpC6 alkyl), and phenyl, wherein each alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, and phenyl are optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, I, CN, NO2, oxo, Cj-Ce alkyl, CpQ haloalkyl, CpCô hydroxyalkyl, C3-Cô cycloalkyl, C3-Cô halocycloalkyl, C3-C6 hydroxycycloalkyl, C3-C6 cycloalkoxy, C3-C6 halocycloalkoxy, C3-C6 hydroxycycloalkoxy, CpC6 alkoxy, CpC6 haloalkoxy, C2-C6 alkenyl, C2-C6 alkynyl, S(=O)n(Cp C6 alkyl), S(=O)n(CpC6 haloalkyl), OSO2(CpC6 alkyl), OSO2(CpCû haloalkyl), C(=O)NRxRy, (C|-C6 alkyl)NRxRy, C(=O)(CrC6 alkyl), C(=O)O(C,-C6 alkyl), C(=O)(CpC6 haloalkyl), C(=O)O(Ci-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(CrC6 haloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (CrC6 alkyl)O(C,-C6 alkyl), (CpC6 alkyl)S(C|-Cô alkyl), C(=O)(Cj-C6 alkyl)C(=O)O(CpC6 alkyl), phenyl, and phenoxy) optionally RI and R2 together with the carbons to which they are attached, form a 3-, 4-,
    5-, or 6-membered carbocyclic or heterocyclic ring that is optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, 1, CN, NO2, oxo, CpCe alkyl, Cp Cé haloalkyl, CpC6 hydroxyalkyl, C3-Cô cycloalkyl, C3-Ce halocycloalkyl, C3-Ce hydroxycycloalkyl, C3-C6 cycloalkoxy, C3-C& halocycloalkoxy, C3-Cô hydroxycycloalkoxy, Cp Cô alkoxy, CpCô haloalkoxy, C2-Ce alkenyl, C2-C& alkynyl, S(=O)n(CpC6 alkyl), S(=O)n(CpC6 haloalkyl), OSO2(CpC6 alkyl), OSO2(CpC6 haloalkyl), C(=O)NRxRy, (CrC6 alkyl)NRxRy, C(=O)(CpC6 alkyl), C(=O)O(CpC6 alkyl), C(=O)(CpC6 haloalkyl), C(=O)O(CpC6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (CpC6 alkyl)O(CpC6 alkyl), (CrC6 alkyl)S(CpC6 alkyl), C(=O)(CrC6 alkyl)C(=O)O(CpCô alkyl), phenyl, and phenoxy;
    (e) R3 is H, CN, F, Cl, Br, I, CpCÊ alkyl, C3-C6 cycloalkyl, C3-Ce cycloalkoxy, CpC6 alkoxy, C2-C6 alkenyl, C2-C6 alkynyl, S(=O)„(CpC(, alkyl), OSO2(CpC6 alkyl), OSO2(CpC6 haloalkyl), C(=O)NRxRy, (CpC6 alkyl)NRxRy, C(=O)(CrC6 alkyl), C(=O)O(CrC6 alkyl), C(=O)(CpC6 haloalkyl), C(=O)O(CpCô haloalkyl), C(=O)(C3-Cè cycloalkyl), C(=O)O(C3-Cé
    Page 68 of 77 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (Ct-C6 alkyl)O(CrC6 alkyl), (CrC6 alkyl)S(C|-C6 alkyl), C(=O)(C[-C6 alkyl)C(=O)O(C|-Cû alkyl), phenyl, and phenoxy, wherein each alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, phenyl, and phenoxy are optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, I, CN, NO2, oxo, Ci-Cê alkyl, C)-Cô haloalkyl, Ci-Q hydroxyalkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, Cs-C* hydroxycycloalkyl, C3-C6 cycloalkoxy, C3-C6 halocycloalkoxy, C3-C6 hydroxycycloalkoxy, C|-Câ alkoxy, Cj-Cô haloalkoxy, C2-Cfi alkenyl, C2-C6 alkynyl, S(=O)n(CrC6 alkyl), S(=O)n(C,-C6 haloalkyl), OSO2(C|-C6 alkyl), OSO2(Ci-C6 haloalkyl), C(=O)NRxRy, (Ct-C6 alkyl)NRxRy, C(=O)(C,-C6 alkyl), C(=O)O(C)-C6 alkyl), C(=O)(C|-C6 haloalkyl), C(=O)O(CrC6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (Ci-C6 alkyl)O(Ci-C6 alkyl), (C,-C6 alkyl)S(Ci-C6 alkyl), C(=O)(Ci-Cô alkyl)C(=0)0(Ci-Q alkyl), phenyl, and phenoxy;
    (f) R4 is H, CN, F, Cl, Br, I, Ci-C6 alkyl, C3-C6 cycloalkyl, C3-Cé cycloalkoxy, Ci-C6 alkoxy, C2-Cô alkenyl, C2-C6 alkynyl, S(=O)n(Ci-C6 alkyl), OSO2(Ci-Cs alkyl), OSO2(C]-C6 haloalkyl), C(=O)NRxRy, (C,-C6 alkyl)NRxRy, C(=O)(CrC6 alkyl), C(=O)O(Ci-C6 alkyl), C(=0)(Ci-C6 haloalkyl), C(=O)O(C,-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (CrC6 alkyl)O(CrC6 alkyl), (Ci-C6 alkyl)S(C|-C6 alkyl), C(=O)(C|-Cô alkyl)C(=O)O(C|-Cû alkyl), phenyl, and phenoxy, wherein each alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, phenyl, and phenoxy are optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, I, CN, NO2, oxo, C|-Câ alkyl, Cj-Ct haloalkyl, C|-Cô hydroxyalkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C3-C6 hydroxycycloalkyl, C3-C6 cycloalkoxy, C3-C6 halocycloalkoxy, C3-C6 hydroxycycloalkoxy, Ci-Cô alkoxy, CpCe haloalkoxy, C2-Cg alkenyl, C2-C6 alkynyl, S(=O)n(CrC6 alkyl), S(=O)n(CrC6 haloalkyl), OSO2(C]-C6 alkyl), OSOîtC^Ce haloalkyl), C(=O)NRxRy, (CrC6 alkyl)NRxRy, C(=O)(CrC6 alkyl), C(=O)O(CrC6 alkyl), C(=O)(CrC6 haloalkyl), C(=O)O(Ci-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C)-C6 alkyl)O(C|-C6 alkyl), (C]-C6 alkyl)S(Ci-Cô alkyl), C(=O)(Cj-Cû alkyl)C(=O)O(CpC6 alkyl), phenyl, and phenoxy;
    (g) R.5 is H, CN, F, Cl, Br, I, C|-Cg alkyl, C3-CÛ cycloalkyl, C3-C6 cycloalkoxy, C|-Cô alkoxy, C2-Cô alkenyl, C2-C6 alkynyl, S(=O)n(C|-C& alkyl), OSO2(CrCû alkyl), OSO2(CrCé haloalkyl), C(=O)NRxRy, (CrC6 alkyl)NRxRy, C(=O)(C]-C6 alkyl), C(=O)O(C|-C6 alkyl), C(=O)(CrC6 haloalkyl), C(=O)O(C,-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6
    Page 69 of 77 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (Ci-C6 alkyl)O(Ci-C6 alkyl), (CrC6 alkyl)S(Ci-Cé alkyl), C(=O)(CrCû alkyl)C(=O)O(Ci-Cû alkyl), Het, phenyl, and phenoxy, wherein each alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, Het, phenyl, and phenoxy are optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, I, CN, NO2, oxo, C]-C6 alkyl, C1-C& haloalkyl, C]-Ce hydroxyalkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C3-C6 hydroxycycloalkyl, C3-C6 cycloalkoxy, C3-C6 halocycloalkoxy, C3-C6 hydroxycycloalkoxy, Ci-C^ alkoxy, Ci-C& haloaikoxy, C2-Cû alkenyl, C2-C6 alkynyl, S(=O)n(C|-C6 alkyl), S(=O)n(C,-C6 haloalkyl), OSO2(C|-C6 alkyl), OSO2(CrC6 haloalkyl), C(=O)NRxRy, (Ci-C6 alkyl)NRxRy, C(=O)(C,-C6 alkyl), C(=O)O(C,-C6 alkyl), C(=O)(Ci-C6 haloalkyl), C(=O)O(CrC6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (CrC6 alkyl)O(C)-C6 alkyl), (CrC6 alkyl)S(Ci-Cé alkyl), C(=O)(C]-Cû alkyl^3(=0)0(^-^ alkyl), NRxRy, phenyl, and phenoxy;
    (h) R6 is H, CN, F, Cl, Br, I, C|-C6 alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkoxy, C|-C6 alkoxy, C2-Cô alkenyl, C2-C6 alkynyl, S(=O)n(C|-C6 alkyl), OSO2(Cj-Cô alkyl), OSO2(C|-Cô haloalkyl), C(=O)NRxRy, (Ci-C6 alkyl)NRxRy, C(=O)(Ct-C6 alkyl), C(=O)O(Ci-C6 alkyl), C(=O)(C1-C6 haloalkyl), C(=O)O(C|-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C|-C6 alkyl)O(C|-C6 alkyl), (CrCô alkyl)S(C]-C6 alkyl), C(=O)(Ci-Cè alkyl)C(=O)O(C|-Cû alkyl), phenyl, and phenoxy, wherein each alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, phenyl, and phenoxy are optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, 1, CN, NO2, oxo, C|-C6 alkyl, Cj-Cè haloalkyl, C|-Cô hydroxyalkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C3-C6 hydroxycycloalkyl, C3-C6 cycloalkoxy, C3-C6 halocycloalkoxy, C3-C6 hydroxycycloalkoxy, C|-Cô alkoxy, Cj-Cè haloaikoxy, C2-Ce alkenyl, C2-C6 alkynyl, S(=O)n(Ci-C6 alkyl), S(=O)n(CrC6 haloalkyl), OSO2(C1-C6 alkyl), OSO2(C!-C6 haloalkyl), C(=O)NRxRy, (CrC6 alkyl)NRxRy, C(=O)(C,-C6 alkyl), C(=O)O(CrC6 alkyl), C(=O)(Ci-C6 haloalkyl), C(=O)O(Ci-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C,-C6 alkyl)O(CrC6 alkyl), (CrC6 alkyl)S(Ci-C6 alkyl), C(=O)(Ci-C6 alkyl)C(=O)O(C|-C6 alkyl), Het, phenyl, and phenoxy;
    (i) R7 is H, CN, F, Cl, Br, I, Ci-Cé alkyl, C3-C6 cycloalkyl, C3-C6 cycloalkoxy, CpCô alkoxy, C2-Cù alkenyl, C2-C6 alkynyl, S(=O)n(Ci-C6 alkyl), OS02(C|-Cû alkyl), OSO2(C|-Cô haloalkyl), C(=O)NRxRy, (C,-C6 alkyl)NRxRy, C(=O)(C|-C6 alkyl), C(=O)O(CrC6 alkyl), C(=O)(CrC6 haloalkyl), C(=O)O(Ci-C6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (Ci-C6 alkyl)O(Cj-C6 alkyl), (C|-C6
    Page 70of77 alkyl)OC(=O)(Ct-C6 alkyl), (CrC6 alkyl)S(CrC6 alkyl), C(=O)(C]-C6 alkyl)C(=O)O(CrC6 alkyl), phenyl, and phenoxy, wherein each alkyl, cycloalkyl, cycloalkoxy, alkoxy, alkenyl, alkynyl, phenyl, and phenoxy are optionally substituted with one or more substituents independently selected from OH, F, Cl, Br, L, CN, NO2, oxo, Cj-Cô alkyl, C|-C& haloalkyl, Cj-Cô hydroxyalkyl, Cj-Cô cycloalkyl, C3-C& halocycloalkyl, C3-Q, hydroxycycloalkyl, C3-C6 cycloalkoxy, C3-C6 halocycloalkoxy, C3-C6 hydroxycycloalkoxy, Cj-Cô alkoxy, Ci-Cé haloalkoxy, C2-C& alkenyl, C2-Cfi alkynyl, S(=O)n(C|-Cù alkyl), S(=O)n(C|-C6 haloalkyl), OSO2(Ci-Cô alkyl), OSO2(C|-Cè haloalkyl), C(=O)NRxRy, (C,-C6 alkyl)NRxRy, C(=O)(CrC6 alkyl), C(=O)O(C]-C6 alkyl), C(=O)(Ci-C6 haloalkyl), C(=O)O(C|-C6 haloalkyl), C(=O)(C3-Câ cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C,-C6 alkyl)O(C)-C6 alkyl), (C,-C6 aIkyl)S(C|-C6 alkyl), C(=O)(C|-C& alkyl)C(=O)O(Ci-C6 alkyl), phenyl, and phenoxy;
    (j) XI is S or O;
    (k) n= 0, l, or 2 (each independently); and (l) Rx and Ry are independently selected from H, Ci-Cû alkyl, Ct-Cfi haloalkyl, Cj-Cs hydroxyalkyl, C3-C6 cycloalkyl, C3-C6 halocycloalkyl, C3-C6 hydroxycycloalkyl, C2-C0 alkenyl, C2-C6 alkynyl, S(=O)n(C,-C6 alkyl), S(=O)n(Ci-C6 haloalkyl), OSO2(C,-C6 alkyl), OSO2(CrC6 haloalkyl), C(=O)H, C(=O)(C!-C6 alkyl), C(=O)O(C|-C6 alkyl), C(=O)(C|-C6 haloalkyl), C(=O)O(CrC6 haloalkyl), C(=O)(C3-C6 cycloalkyl), C(=O)O(C3-C6 cycloalkyl), C(=O)(C2-C6 alkenyl), C(=O)O(C2-C6 alkenyl), (C,-C6 alkyl)O(Ct-C6 alkyl), (Ci-C6 alkyl)S(C)-C6 alkyl), C(=O)(Cl-C6 alkyl)C(=O)O(CrC6 alkyl), and phenyl.
  2. 2. A pesticidal composition according to claim l wherein said molécule said Αη is a substituted phenyl wherein said substituted phenyl has one or more substituents independently selected from Ci-Q haloalkoxy.
  3. 3. A pesticidal composition according to claim l wherein said molécule said Het is a triazolyl.
  4. 4. A pesticidal composition according to claim l wherein said molécule said Het is a l ,2,4triazolyl.
    Page 71 of77
  5. 5. A pesticidal composition according to claim l wherein said molécule said Het is a 1,2,4triazolyl with one ring nitrogen atom bonded to Αη and one ring carbon bonded to Ar2.
  6. 6. A pesticidal composition according to claim 1 wherein said molécule said Ar2 is a phenyl.
  7. 7. A pesticidal composition according to claim 1 wherein said molécule said RI is H.
  8. 8. A pesticidal composition according to claim I wherein said molécule said R2 is H.
  9. 9. A pesticidal composition according to claim 1 wherein said molécule said RI, R2, and the carbons they are attached to form a cyclopropyl structure, in which case, RI & R2 are the linkîng carbon atom.
  10. 10. A pesticidal composition according to claim 1 wherein said molécule said R3 is H.
  11. 11. A pesticidal composition according to claim 1 wherein said molécule said R4 is H.
  12. 12. A pesticidal composition according to claim 1 wherein said molécule said R4 is a phenyl optionally substituted with one or more substituents independently selected from Ci-C& alkyl.
  13. 13. A pesticidal composition according to claim 1 wherein said molécule said R5 is Het or phenyl wherein each are optionally substituted with one or more substituents independently selected from F, Cl, Ci-Cû alkyl, Ci-C6 haloalkyl, C(-C6 alkoxy, or NRxRy.
  14. 14. A pesticidal composition according to claim 1 wherein said molécule said R6 is Cj-Cg alkyl or phenyl wherein each are optionally substituted with one or more substituents independently selected from F, Cl, CpCô alkyl, Ci-Ce haloalkyl, Cj-Cô cycloalkyl, Ci-Ce alkoxy, Het, or phenyl.
  15. 15. A pesticidal composition according to claim 1 wherein said molécule said R7 is (Ci-Cû alkyl)OC(=O)(C|-C6 alkyl).
  16. 16. A pesticidal composition according to claim 1 wherein said inolecule has one of the foliowing structures
OA1201300316 2011-02-09 2012-02-08 Pesticidal compositions and processes related thereto. OA16501A (en)

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