NZ757027B2 - Heterocycle-substituted bicyclic azole pesticides - Google Patents

Heterocycle-substituted bicyclic azole pesticides Download PDF

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Publication number
NZ757027B2
NZ757027B2 NZ757027A NZ75702714A NZ757027B2 NZ 757027 B2 NZ757027 B2 NZ 757027B2 NZ 757027 A NZ757027 A NZ 757027A NZ 75702714 A NZ75702714 A NZ 75702714A NZ 757027 B2 NZ757027 B2 NZ 757027B2
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New Zealand
Prior art keywords
pyridinyl
trifluoromethyl
pyrimidinyl
nome
methoxypyridinyl
Prior art date
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NZ757027A
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NZ757027A (en
Inventor
David Alan Clark
Breena Gloriana Fraga
Wenming Zhang
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Fmc Corporation
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Application filed by Fmc Corporation filed Critical Fmc Corporation
Publication of NZ757027A publication Critical patent/NZ757027A/en
Publication of NZ757027B2 publication Critical patent/NZ757027B2/en

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    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N2300/00—Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/08—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing solids as carriers or diluents
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/30—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests characterised by the surfactants
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/50—1,3-Diazoles; Hydrogenated 1,3-diazoles
    • A01N43/52—1,3-Diazoles; Hydrogenated 1,3-diazoles condensed with carbocyclic rings, e.g. benzimidazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
    • A01N43/58—1,2-Diazines; Hydrogenated 1,2-diazines
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
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    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
    • A01N43/647—Triazoles; Hydrogenated triazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/76—1,3-Oxazoles; Hydrogenated 1,3-oxazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/74—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,3
    • A01N43/78—1,3-Thiazoles; Hydrogenated 1,3-thiazoles
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/82—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with three ring hetero atoms
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
    • A01N43/84—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,4
    • A—HUMAN NECESSITIES
    • A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
    • C07D401/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
    • C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings
    • C07D403/04—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D403/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00
    • C07D403/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, not provided for by group C07D401/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D405/00—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/14—Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D407/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D409/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms
    • C07D409/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having sulfur atoms as the only ring hetero atoms containing three or more hetero rings
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
    • C07D413/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings directly linked by a ring-member-to-ring-member bond
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
    • C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
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    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
    • C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
    • C07D417/04—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings directly linked by a ring-member-to-ring-member bond
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    • C07D—HETEROCYCLIC COMPOUNDS
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    • C07D417/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing three or more hetero rings
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    • C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
    • C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
    • C07D471/04—Ortho-condensed systems
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    • C07D513/02—Heterocyclic compounds containing in the condensed system at least one hetero ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for in groups C07D463/00, C07D477/00 or C07D499/00 - C07D507/00 in which the condensed system contains two hetero rings
    • C07D513/04—Ortho-condensed systems

Abstract

Disclosed are compounds of Formula 1, including all geometric and stereoisomers, N oxides, and salts thereof, wherein Q, A, R1, m, X1, X2, X3, X4, Y1, Y2 and Y3 are as defined in the disclosure. Also disclosed are compositions containing the compounds of Formula 1 and methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound or a composition of the invention. ertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound or a composition of the invention.

Description

(12) Granted patent specificaon (19) NZ (11) 757027 (13) B2 (47) Publicaon date: 2021.12.24 (54) HETEROCYCLE-SUBSTITUTED BICYCLIC AZOLE PESTICIDES (51) Internaonal Patent Classificaon(s): C07D 401/14 C07D 405/14 C07D 413/14 A01N 43/56 A01N 43/78 C07D 401/04 C07D 403/04 C07D 407/14 C07D 409/14 C07D 413/04 C07D 417/04 C07D 417/14 C07D 471/04 C07D 513/04 A01P 7/00 A01P 7/04 A01P 5/00 (22) Filing date: (73) Owner(s): 2014.09.09 FMC CORPORATION (23) Complete specificaon filing date: (74) Contact: 2014.09.09 HOULIHAN2 PTY LTD (62) Divided out of 717749 (72) Inventor(s): CLARK, David, Alan (30) Internaonal Priority Data: FRAGA, Breena, Gloriana US 61/877,329 2013.09.13 ZHANG, Wenming (57) Abstract: Disclosed are compounds of Formula 1, including all geometric and stereoisomers, N oxides, and salts thereof, wherein Q, A, R1, m, X1, X2, X3, X4, Y1, Y2 and Y3 are as defined in the disclosure.
Also disclosed are composions containing the compounds of Formula 1 and methods for controlling an invertebrate pest comprising contacng the invertebrate pest or its environment with a biologically effecve amount of a compound or a composion of the invenon.
NZ 757027 B2 TITLE HETEROCYCLE-SUBSTITUTED BICYCLIC AZOLE PESTICIDES The present Application is a Divisional Application from New Zealand Patent Application No. 717749. The entire disclosures of New Zealand Patent Application No. 717749 and its corresponding International Patent Application No. , are incorporated herein by reference. This Application claims priority to US 61/877,329 filed on 13 September 2013, which is herein incorporated by reference in its entirety.
FIELD OF THE INVENTION This invention relates to certain substituted bicyclic azoles, their N-oxides, salts and compositions suitable for agronomic and nonagronomic uses, and methods of their use for controlling invertebrate pests such as arthropods in both agronomic and nonagronomic environments.
BACKGROUND OF THE INVENTION The control of invertebrate pests is extremely important in achieving high crop efficiency. Damage by invertebrate pests to growing and stored agronomic crops can cause significant reduction in productivity and thereby result in increased costs to the consumer.
The control of invertebrate pests in forestry, greenhouse crops, ornamentals, nursery crops, stored food and fiber products, livestock, household, turf, wood products, and public and animal health is also important. Many products are commercially available for these purposes, but the need continues for new compounds that are more effective, less costly, less toxic, environmentally safer or have different sites of action.
SUMMARY OF THE INVENTION This invention is directed to compounds of Formula 1 (including all geometric and stereoisomers), N-oxides, and salts thereof, and compositions containing them and their use for controlling invertebrate pests: wherein Q is A is CH, CR or N; each R is independently halogen, cyano, nitro, C –C alkyl, C –C haloalkyl, C –C 1 4 1 4 1 4 alkoxy, C –C haloalkoxy, C –C alkylthio or C –C haloalkylthio; 1 4 1 4 1 4 m is 0, 1, 2 or 3; 1 2 3 4 2 3 1 X , X , X and X are each independently CR , CR or N, provided that (i) one of X , 2 3 4 2 1 2 3 4 X , X and X is CR , and (ii) no more than one of X , X , X and X is N; 2 6 7 8 9 10 11 a R is C(=Z)NR R , N(R )C(=Z)R , C(=NR )R or Q ; each Z is independently O or S; each R is independently H, halogen, cyano, nitro, C –C alkyl, C –C haloalkyl, C – 1 4 1 4 1 C alkoxy or C –C haloalkoxy; 4 1 4 Y is O, S or NR ; 2 5a Y is N or CR ; 3 5b Y is N or CR ; R is H or C –C alkyl; R is H, halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C haloalkyl, C – 1 4 3 6 1 4 1 C alkoxy or C –C haloalkoxy; 4 1 4 R is H, halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C haloalkyl, C – 1 4 3 6 1 4 1 C alkoxy or C –C haloalkoxy; 4 1 4 6 15 16 17 21 15 16 22 23 11 R is H, NR R , OR , C(=NR )R , C(O)OR , C(O)NR R , C(O)R , S(O) R or Q ; or C –C alkyl, C –C cycloalkyl, C –C alkenyl or C –C alkynyl, each 1 6 3 6 2 6 2 6 unsubstituted or substituted with at least one R ; R is H or Q ; or C –C alkyl, C –C cycloalkyl, C –C alkenyl or C –C alkynyl, 1 6 3 6 2 6 2 6 each unsubstituted or substituted with at least one R ; or R and R are taken together with the nitrogen atom to which they are attached to form a 3- to 10-membered ring containing ring members selected from carbon atoms and up to 2 heteroatoms independently selected from one oxygen atom, one sulfur atom, and up to 2 nitrogen atoms, wherein up to 2 carbon atom ring members are independently selected from C(=O) and C(=S) and the sulfur atom ring member is selected from S, S(O) or S(O) , said ring being unsubstituted or substituted with up to 4 R ; or 6 7 18 19 20 18 19 R and R are taken together as =S(O) R R or =S(=NR )R R ; each R is independently halogen, cyano, nitro, hydroxy, C –C alkyl, C –C 1 6 1 6 haloalkyl, C –C cycloalkyl, C –C alkoxy, C –C haloalkoxy, C –C 3 6 1 6 1 6 3 6 21 15 16 22 25 26 11 cycloalkoxy, C(=NR )R , C(O)OR , C(O)NR R , OC(O)R , NR R , 24 22 22 23 28 28 b NR C(O)R , C(O)R , S(O) R , Si(R ) , OSi(R ) or Q ; n 3 3 8 21 15 16 22 23 b R is H, C(O)OR , C(O)NR R , C(O)R , S(O) R or Q ; or C –C alkyl, C –C n 1 6 3 6 cycloalkyl, C –C alkenyl or C –C alkynyl, each unsubstituted or substituted 2 6 2 6 with at least one R ; 9 10 11 21 15 16 R is H, C(=NR )R , OR or NR R ; or C –C alkyl, C –C cycloalkyl, C –C 1 6 3 6 2 6 alkenyl or C –C alkynyl, each unsubstituted or substituted with at least one R ; or phenyl, phenoxy or a 5- or 6-membered heterocyclic aromatic ring, each unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C 1 4 3 6 cycloalkyl, C –C haloalkyl, C –C alkoxy and C –C haloalkoxy; or a 3- to 6- 1 4 1 4 1 4 membered heterocyclic non-aromatic ring, each ring containing ring members selected from carbon atoms and up to 3 heteroatoms independently selected from one oxygen atom, one sulfur atom, and up to 2 nitrogen atoms, wherein up to 1 carbon atom ring member is independently selected from C(=O) and C(=S) and the sulfur atom ring member is selected from S, S(O) or S(O) , each ring being unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C 1 4 3 6 cycloalkyl, C –C haloalkyl, C –C alkoxy and C –C haloalkoxy; 1 4 1 4 1 4 12 13 14 each R is independently OR , S(O) R or NHR ; each R is independently H; or C –C alkyl, C –C cycloalkyl, C –C alkenyl or C – 1 6 3 6 2 6 2 C alkynyl, each unsubstituted or substituted with at least one R ; or C –C 6 1 6 21 15 16 alkoxy, C –C haloalkoxy, C –C cycloalkoxy, C(O)OR , C(O)NR R , 1 6 3 6 26 24 22 22 b NR R , NR C(O)R , C(O)R or Q ; each R is independently C –C alkyl, C –C cycloalkyl, C –C haloalkyl, C(O)R , 1 4 3 6 1 4 S(O) R or Q ; each R is independently C –C alkyl or C –C haloalkyl; 1 4 1 4 14 22 21 R is C –C alkyl, C –C cycloalkyl, C –C haloalkyl, C(O)R or C(O)OR ; or 1 4 3 6 1 4 phenyl, unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C 1 4 3 6 cycloalkyl, C –C haloalkyl, C –C alkoxy and C –C haloalkoxy; 1 4 1 4 1 4 27 each R is independently H, C –C alkyl, C –C haloalkyl, C(O)R or S(O) R ; or 1 6 1 4 phenyl or a 5- or 6-membered heterocyclic aromatic ring, each unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C 1 4 3 6 1 4 haloalkyl, C –C alkoxy and C –C haloalkoxy; 1 4 1 4 each R is independently H, C –C alkyl or C –C haloalkyl; or 1 6 1 4 16 R and R are taken together with the nitrogen atom to which they are attached to form a 3- to 7-membered ring containing ring members selected from carbon atoms and up to 2 heteroatoms independently selected from one oxygen atom, one sulfur atom, and up to 2 nitrogen atoms, wherein up to 2 carbon atom ring members are independently selected from C(=O) and C(=S) and the sulfur atom ring member is selected from S, S(O) or S(O) , said ring being unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C 1 4 3 6 1 4 haloalkyl, C –C alkoxy and C –C haloalkoxy; 1 4 1 4 R is C –C alkyl, C –C cycloalkyl or C –C haloalkyl; or phenyl, unsubstituted or 1 4 3 6 1 4 substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C 1 4 3 6 1 4 haloalkyl, C –C alkoxy and C –C haloalkoxy; 1 4 1 4 each R is independently C –C alkyl or C –C haloalkyl; or phenyl, unsubstituted or 1 4 1 4 substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C 1 4 3 6 1 4 haloalkyl, C –C alkoxy and C –C haloalkoxy; 1 4 1 4 each R is independently C –C alkyl or C –C haloalkyl; or phenyl, unsubstituted or 1 4 1 4 substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C 1 4 3 6 1 4 haloalkyl, C –C alkoxy and C –C haloalkoxy; or 1 4 1 4 18 19 R and R are taken together with the sulfur atom to which they are attached to form a ring; 22 R is H, cyano, C –C alkyl, C –C haloalkyl or C(O)R ; or phenyl, unsubstituted or 1 4 1 4 substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C 1 4 3 6 1 4 haloalkyl, C –C alkoxy and C –C haloalkoxy; 1 4 1 4 each R is independently C –C alkyl, C –C haloalkyl, C –C cycloalkyl or C –C 1 4 1 4 3 6 3 6 halocycloalkyl; or phenyl, unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C haloalkyl, C –C alkoxy and C –C 1 4 3 6 1 4 1 4 1 4 haloalkoxy; each R is independently C –C alkyl, C –C haloalkyl, C –C cycloalkyl or C –C 1 4 1 4 3 6 3 6 halocycloalkyl; or phenyl, unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C haloalkyl, C –C alkoxy and C –C 1 4 3 6 1 4 1 4 1 4 haloalkoxy; each R is independently C –C alkyl, C –C haloalkyl, C –C cycloalkyl, C –C 1 4 1 4 3 6 3 6 halocycloalkyl, C –C cycloalkylalkyl or C –C halocycloalkylalkyl; or phenyl, 3 6 3 6 unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C 1 4 3 6 cycloalkyl, C –C haloalkyl, C –C alkoxy and C –C haloalkoxy; 1 4 1 4 1 4 each R is independently C –C alkyl; each R is independently H, C –C alkyl or C –C haloalkyl; or phenyl, unsubstituted 1 4 1 4 or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C 1 4 3 6 1 4 haloalkyl, C –C alkoxy and C –C haloalkoxy; 1 4 1 4 each R is independently C –C alkyl or C –C haloalkyl; or phenyl, unsubstituted or 1 4 1 4 substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C 1 4 3 6 1 4 haloalkyl, C –C alkoxy and C –C haloalkoxy; or 1 4 1 4 26 R and R are independently taken together with the nitrogen atom to which they are attached to form a 3- to 7-membered ring containing ring members selected from carbon atoms and up to 2 heteroatoms independently selected from one oxygen atom, one sulfur atom, and up to 2 nitrogen atoms, wherein up to 2 carbon atom ring members are independently selected from C(=O) and C(=S) and the sulfur atom ring member is selected from S, S(O) or S(O) , said ring being unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C 1 4 3 6 cycloalkyl, C –C haloalkyl, C –C alkoxy and C –C haloalkoxy; 1 4 1 4 1 4 each R is independently C –C alkyl, C –C haloalkyl, C –C alkoxy, C –C 1 6 1 6 1 6 1 6 29 30 haloalkoxy or NR R ; or phenyl or a 5- or 6-membered heterocyclic aromatic ring, each unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C 1 4 3 6 cycloalkyl, C –C haloalkyl, C –C alkoxy and C –C haloalkoxy; 1 4 1 4 1 4 each R is independently C –C alkyl, C –C cycloalkyl or phenyl; 1 6 3 6 29 b each R is independently H or Q ; or C –C alkyl, C –C cycloalkyl, C –C alkenyl 1 6 3 6 2 6 or C –C alkynyl, each unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C haloalkyl, C –C alkoxy and C –C haloalkoxy; 3 6 1 4 1 4 1 4 b each R is independently H or Q ; or C –C alkyl, C –C cycloalkyl, C –C alkenyl 1 6 3 6 2 6 or C –C alkynyl, each unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C haloalkyl, C –C alkoxy and C –C haloalkoxy; 3 6 1 4 1 4 1 4 or 29 30 R and R are taken together with the nitrogen atom to which they are attached to form a 3- to 10-membered ring containing ring members selected from carbon atoms and up to 2 heteroatoms independently selected from one oxygen atom, one sulfur atom, and up to 2 nitrogen atoms, wherein up to 2 carbon atom ring members are independently selected from C(=O) and C(=S) and the sulfur atom ring member is selected from S, S(O) or S(O) , said ring being unsubstituted or substituted with up to 4 substituents independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C 1 4 3 6 1 4 haloalkyl, C –C alkoxy and C –C haloalkoxy; 1 4 1 4 Q is a 5- to 10-membered aromatic ring or ring system, each ring or ring system containing ring members selected from carbon atoms and up to 3 heteroatoms independently selected from one oxygen atom, one sulfur atom, and up to 3 nitrogen atoms, wherein up to 2 carbon atom ring members are independently selected from C(=O) and C(=S) and the sulfur atom ring member is selected from S, S(O) or S(O) , each ring or ring system being unsubstituted or substituted with at least one R ; or a 3- to 6-membered partially saturated ring, each ring containing ring members selected from carbon atoms and up to 2 heteroatoms independently selected from one oxygen atom, one sulfur atom, and up to 2 nitrogen atoms, wherein up to 2 carbon atom ring members are independently selected from C(=O) and C(=S) and the sulfur atom ring member is selected from S, S(O) or S(O) , each ring unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C haloalkyl, C –C 1 4 3 6 1 4 1 4 alkoxy and C –C haloalkoxy; each Q is independently phenyl, a 5- or 6-membered heterocyclic aromatic ring or a 3- to 6-membered heterocyclic non-aromatic ring, each ring containing ring members selected from carbon atoms and up to 2 heteroatoms independently selected from one oxygen atom, one sulfur atom, and up to 2 nitrogen atoms, wherein up to 2 carbon atom ring members are independently selected from C(=O) and C(=S) and the sulfur atom ring member is selected from S, S(O) or S(O) , each ring unsubstituted or substituted with at least one substituent independently selected from the group consisting of halogen, cyano, nitro, C –C alkyl, C –C cycloalkyl, C –C haloalkyl, C –C alkoxy and C –C haloalkoxy; 3 6 1 4 1 4 1 4 each n is independently 0, 1 or 2; and p is 1 or 2.
This invention also provides a composition comprising a compound of Formula 1, an N-oxide or a salt thereof, and at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents. In one embodiment, this invention also provides a composition for controlling an invertebrate pest comprising a compound of Formula 1, an N-oxide or a salt thereof, and at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents, said composition optionally further comprising at least one additional biologically active compound or agent.
This invention further provides a spray composition for controlling an invertebrate pest comprising a compound of Formula 1, an N-oxide or a salt thereof, or the compositions described above, and a propellant. This invention also provides a bait composition for controlling an invertebrate pest comprising a compound of Formula 1, an N-oxide or a salt thereof, or the compositions described in the embodiments above, one or more food materials, optionally an attractant, and optionally a humectant.
This invention further provides a trap device for controlling an invertebrate pest comprising said bait composition and a housing adapted to receive said bait composition, wherein the housing has at least one opening sized to permit the invertebrate pest to pass through the opening so the invertebrate pest can gain access to said bait composition from a location outside the housing, and wherein the housing is further adapted to be placed in or near a locus of potential or known activity for the invertebrate pest.
This invention provides a method for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound of Formula 1, an N-oxide or a salt thereof, (e.g., as a composition described herein). This invention also relates to such method wherein the invertebrate pest or its environment is contacted with a composition comprising a biologically effective amount of a compound of Formula 1, an N-oxide or a salt thereof, and at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents, said composition optionally further comprising a biologically effective amount of at least one additional biologically active compound or agent.
This invention also provides a method for protecting a seed from an invertebrate pest comprising contacting the seed with a biologically effective amount of a compound of Formula 1, an N-oxide or a salt thereof, (e.g., as a composition described herein). This invention also relates to the treated seed. This invention further provides a method for protecting an animal from an invertebrate parasitic pest comprising administering to the animal a parasiticidally effective amount of a compound of Formula 1, an N-oxide or a salt thereof, (e.g., as a composition described herein). This invention also provides for the use of a compound of Formula 1, an N-oxide or a salt thereof, (e.g., as a composition described herein) in protecting an animal from an invertebrate pest.
This invention also provides a method for increasing vigor of a crop plant comprising contacting the crop plant, the seed from which the crop plant is grown or the locus (e.g., growth medium) of the crop plant with a biologically effective amount of a compound of Formula 1 (e.g., as a composition described herein).
DETAILS OF THE INVENTION As used herein, the terms “comprises,” “comprising,” “includes,” “including,” “has,” “having,” “contains”, “containing,” “characterized by” or any other variation thereof, are intended to cover a non-exclusive inclusion, subject to any limitation explicitly indicated.
For example, a composition, mixture, process or method that comprises a list of elements is not necessarily limited to only those elements but may include other elements not expressly listed or inherent to such composition, mixture, process or method.
The transitional phrase “consisting of” excludes any element, step, or ingredient not specified. If in the claim, such would close the claim to the inclusion of materials other than those recited except for impurities ordinarily associated therewith. When the phrase “consisting of” appears in a clause of the body of a claim, rather than immediately following the preamble, it limits only the element set forth in that clause; other elements are not excluded from the claim as a whole.
The transitional phrase “consisting essentially of” is used to define a composition or method that includes materials, steps, features, components, or elements, in addition to those literally disclosed, provided that these additional materials, steps, features, components, or elements do not materially affect the basic and novel characteristic(s) of the claimed invention. The term “consisting essentially of” occupies a middle ground between “comprising” and “consisting of”.
Where applicants have defined an invention or a portion thereof with an open-ended term such as “comprising,” it should be readily understood that (unless otherwise stated) the description should be interpreted to also describe such an invention using the terms “consisting essentially of” or “consisting of.” Further, unless expressly stated to the contrary, “or” refers to an inclusive or and not to an exclusive or. For example, a condition A or B is satisfied by any one of the following: A is true (or present) and B is false (or not present), A is false (or not present) and B is true (or present), and both A and B are true (or present).
Also, the indefinite articles “a” and “an” preceding an element or component of the invention are intended to be nonrestrictive regarding the number of instances (i.e. occurrences) of the element or component. Therefore “a” or “an” should be read to include one or at least one, and the singular word form of the element or component also includes the plural unless the number is obviously meant to be singular.
As referred to in this disclosure, the term “invertebrate pest” includes arthropods, gastropods, nematodes and helminths of economic importance as pests. The term “arthropod” includes insects, mites, spiders, scorpions, centipedes, millipedes, pill bugs and symphylans. The term “gastropod” includes snails, slugs and other Stylommatophora. The term “nematode” includes members of the phylum Nematoda, such as phytophagous nematodes and helminth nematodes parasitizing animals. The term “helminth” includes all of the parasitic worms, such as roundworms (phylum Nematoda), heartworms (phylum Nematoda, class Secernentea), flukes (phylum Platyhelminthes, class Tematoda), acanthocephalans (phylum Acanthocephala), and tapeworms (phylum Platyhelminthes, class Cestoda).
In the context of this disclosure “invertebrate pest control” means inhibition of invertebrate pest development (including mortality, feeding reduction, and/or mating disruption), and related expressions are defined analogously.
The term “agronomic” refers to the production of field crops such as for food and fiber and includes the growth of maize or corn, soybeans and other legumes, rice, cereal (e.g., wheat, oats, barley, rye and rice), leafy vegetables (e.g., lettuce, cabbage, and other cole crops), fruiting vegetables (e.g., tomatoes, pepper, eggplant, crucifers and cucurbits), potatoes, sweet potatoes, grapes, cotton, tree fruits (e.g., pome, stone and citrus), small fruit (e.g., berries and cherries) and other specialty crops (e.g., canola, sunflower and olives).
The term “nonagronomic” refers to other than field crops, such as horticultural crops (e.g., greenhouse, nursery or ornamental plants not grown in a field), residential, agricultural, commercial and industrial structures, turf (e.g., sod farm, pasture, golf course, lawn, sports field, etc.), wood products, stored product, agro-forestry and vegetation management, public health (i.e. human) and animal health (e.g., domesticated animals such as pets, livestock and poultry, undomesticated animals such as wildlife) applications.
The term “crop vigor” refers to rate of growth or biomass accumulation of a crop plant.
An “increase in vigor” refers to an increase in growth or biomass accumulation in a crop plant relative to an untreated control crop plant. The term “crop yield” refers to the return on crop material, in terms of both quantity and quality, obtained after harvesting a crop plant.
An “increase in crop yield” refers to an increase in crop yield relative to an untreated control crop plant.
The term “biologically effective amount” refers to the amount of a biologically active compound (e.g., a compound of Formula 1) sufficient to produce the desired biological effect when applied to (i.e. contacted with) an invertebrate pest to be controlled or its environment, or to a plant, the seed from which the plant is grown, or the locus of the plant (e.g., growth medium) to protect the plant from injury by the invertebrate pest or for other desired effect (e.g., increasing plant vigor).
The position of the variable R in the structure of Formula 1 is described by the numbering system shown below.
A wavy line in a structure fragment denotes the attachment point of the fragment to the remainder of the molecule. For example, when the variable Q in Formula 1 is defined as Q-1, the wavy line bisecting the bond in Q-1 means that Q-1 is attached to the remainder of the structure of Formula 1 at said position, as shown below. 1 2 3 4 In structures Q-1, Q-2, Q-3 and Q-4, the variables X , X , X and X are defined as 2 3 1 2 3 4 2 each being independently CR , CR or N, provided that (i) one of X , X , X and X is CR , 1 2 3 4 1 2 3 4 and (ii) no more than one of X , X , X and X is N. This definition of X , X , X and X 1 2 3 4 describes sixteen possible combinations of X , X , X and X , shown in the table below. 1 2 3 4 Combination X X X X 2 3 3 3 1 CR CR CR CR 2 3 3 2 CR N CR CR 2 3 3 3 CR CR N CR 2 3 3 4 CR CR CR N 3 2 3 3 CR CR CR CR 2 3 3 6 N CR CR CR 3 2 3 7 CR CR N CR 3 2 3 8 CR CR CR N 3 3 2 3 9 CR CR CR CR 3 2 3 N CR CR CR 3 2 3 11 CR N CR CR 3 3 2 12 CR CR CR N 3 3 3 2 13 CR CR CR CR 3 3 2 14 N CR CR CR 3 3 2 CR N CR CR 3 3 2 16 CR CR N CR In the above recitations, the term “alkyl”, used either alone or in compound words such as “alkylthio” or “haloalkyl” includes straight-chain or branched alkyl, such as, methyl, ethyl, n-propyl, i-propyl, or the different butyl, pentyl or hexyl isomers. “Alkenyl” includes straight-chain or branched alkenes such as ethenyl, 1-propenyl, 2-propenyl, and the different butenyl, pentenyl and hexenyl isomers. “Alkenyl” also includes polyenes such as 1,2-propadienyl and 2,4-hexadienyl. “Alkynyl” includes straight-chain or branched alkynes such as ethynyl, 1-propynyl, 2-propynyl and the different butynyl, pentynyl and hexynyl isomers. “Alkynyl” can also include moieties comprised of multiple triple bonds such as 2,5-hexadiynyl.
“Alkoxy” includes, for example, methoxy, ethoxy, n-propyloxy, isopropyloxy and the different butoxy, pentoxy and hexyloxy isomers. “Alkylthio” includes branched or straight-chain alkylthio moieties such as methylthio, ethylthio, and the different propylthio, butylthio, pentylthio and hexylthio isomers.
“Cycloalkyl” includes, for example, cyclopropyl, cyclobutyl, cyclopentyl and cyclohexyl.
The term “halogen”, either alone or in compound words such as “haloalkyl”, or when used in descriptions such as “alkyl substituted with halogen” includes fluorine, chlorine, bromine or iodine. Further, when used in compound words such as “haloalkyl”, or when used in descriptions such as “alkyl substituted with halogen” said alkyl may be partially or fully substituted with halogen atoms which may be the same or different. Examples of “haloalkyl” or “alkyl substituted with halogen” include F C-, ClCH -, CF CH - and 3 2 3 2 CF CCl -. The terms “halocycloalkyl”, “haloalkoxy”, “haloalkylthio”, “haloalkenyl”, “haloalkynyl”, and the like, are defined analogously to the term “haloalkyl”. Examples of “haloalkoxy” include CF O-, CCl CH O-, HCF CH CH O- and CF CH O-. Examples of 3 3 2 2 2 2 3 2 “haloalkylthio” include CCl S-, CF S-, CCl CH S- and ClCH CH CH S-. 3 3 3 2 2 2 2 The chemical abbreviations S(O) and S(=O) as used herein represent a sulfinyl moiety.
The chemical abbreviations SO , S(O) and S(=O) as used herein represent a sulfonyl 2 2 2 moiety. The chemical abbreviations C(O) and C(=O) as used herein represent a carbonyl moiety. The chemical abbreviations CO , C(O)O and C(=O)O as used herein represent an oxycarbonyl moiety. “CHO” means formyl.
The total number of carbon atoms in a substituent group is indicated by the “C –C ” prefix where i and j are numbers from 1 to 6. For example, C –C alkylsulfonyl designates methylsulfonyl through butylsulfonyl; C alkoxyalkyl designates CH OCH -; C 2 3 2 3 alkoxyalkyl designates, for example, CH CH(OCH )-, CH OCH CH - or CH CH OCH -; 3 3 3 2 2 3 2 2 and C alkoxyalkyl designates the various isomers of an alkyl group substituted with an alkoxy group containing a total of four carbon atoms, examples including CH CH CH OCH - and CH CH OCH CH -. 3 2 2 2 3 2 2 2 When a compound is substituted with a substituent bearing a subscript that indicates the number of said substituents can exceed 1, said substituents (when they exceed 1) are independently selected from the group of defined substituents, e.g., (R ) , m is 0, 1, 2 or 3.
Further, when the subscript indicates a range, e.g. (R) , then the number of substituents may be selected from the integers between i and j inclusive. When a group contains a substituent which can be hydrogen, for example R or R , then when this substituent is taken as hydrogen, it is recognized that this is equivalent to said group being unsubstituted. When a variable group is shown to be optionally attached to a position, for example (R ) wherein m may be 0, then hydrogen may be at the position even if not recited in the variable group definition. When one or more positions on a group are said to be “not substituted” or “unsubstituted”, then hydrogen atoms are attached to take up any free valency.
Unless otherwise indicated, a “ring” or “ring system” as a component of Formula 1 (e.g., substituent Q ) is carbocyclic or heterocyclic. The term “ring system” denotes two or more fused rings. The terms “bicyclic ring system” and “fused bicyclic ring system” denote a ring system consisting of two fused rings, which can be “ortho-fused”, “bridged bicyclic” or “spirobicyclic”. An “ortho-fused bicyclic ring system” denotes a ring system wherein the two constituent rings have two adjacent atoms in common. A “bridged bicyclic ring system” is formed by bonding a segment of one or more atoms to nonadjacent ring members of a ring. A “spirobicyclic ring system” is formed by bonding a segment of two or more atoms to the same ring member of a ring. The term “fused heterobicyclic ring system” denotes a fused bicyclic ring system in which at least one ring atom is not carbon. The term “ring member” refers to an atom or other moiety (e.g., C(=O), C(=S), S(O) or S(O) ) forming the backbone of a ring or ring system.
The terms “carbocyclic ring”, “carbocycle” or “carbocyclic ring system” denote a ring or ring system wherein the atoms forming the ring backbone are selected only from carbon.
The terms “heterocyclic ring”, “heterocycle” or “heterocyclic ring system” denote a ring or ring system in which at least one atom forming the ring backbone is not carbon, e.g., nitrogen, oxygen or sulfur. Typically a heterocyclic ring contains no more than 4 nitrogens, no more than 2 oxygens and no more than 2 sulfurs. Unless otherwise indicated, a carbocyclic ring or heterocyclic ring can be a saturated or unsaturated ring. “Saturated” refers to a ring having a backbone consisting of atoms linked to one another by single bonds; unless otherwise specified, the remaining atom valences are occupied by hydrogen atoms.
Unless otherwise stated, an “unsaturated ring” may be partially unsaturated or fully unsaturated. The expression “fully unsaturated ring” means a ring of atoms in which the bonds between atoms in the ring are single or double bonds according to valence bond theory and furthermore the bonds between atoms in the ring include as many double bonds as possible without double bonds being cumulative (i.e. no C=C=C or C=C=N). The term “partially unsaturated ring” denotes a ring comprising at least one ring member bonded to an adjacent ring member through a double bond and which conceptually potentially accommodates a number of non-cumulated double bonds between adjacent ring members (i.e. in its fully unsaturated counterpart form) greater than the number of double bonds present (i.e. in its partially unsaturated form).
Unless otherwise indicated, heterocyclic rings and ring systems can be attached through any available carbon or nitrogen by replacement of a hydrogen on said carbon or nitrogen.
“Aromatic” indicates that each of the ring atoms is essentially in the same plane and has a p-orbital perpendicular to the ring plane, and in which (4n + 2) π electrons, where n is a positive integer, are associated with the ring to comply with Hückel’s rule. The term “aromatic ring system” denotes a carbocyclic or heterocyclic ring system in which at least one ring of the ring system is aromatic. When a fully unsaturated carbocyclic ring satisfies Hückel’s rule, then said ring is also called an “aromatic ring” or “aromatic carbocyclic ring”.
The term “aromatic carbocyclic ring system” denotes a carbocyclic ring system in which at least one ring of the ring system is aromatic. When a fully unsaturated heterocyclic ring satisfies Hückel’s rule, then said ring is also called a “heteroaromatic ring”, “aromatic heterocyclic ring” or “heterocyclic aromatic ring”. The term “aromatic heterocyclic ring system” denotes a heterocyclic ring system in which at least one ring of the ring system is aromatic. The term “nonaromatic ring system” denotes a carbocyclic or heterocyclic ring system that may be fully saturated, as well as partially or fully unsaturated, provided that none of the rings in the ring system are aromatic. The term “nonaromatic carbocyclic ring system” denotes a carbocyclic ring in which no ring in the ring system is aromatic. The term “nonaromatic heterocyclic ring system” denotes a heterocyclic ring system in which no ring in the ring system is aromatic.
The term “optionally substituted” in connection with the heterocyclic rings refers to groups which are unsubstituted or have at least one non-hydrogen substituent that does not extinguish the biological activity possessed by the unsubstituted analog. As used herein, the following definitions shall apply unless otherwise indicated. The term "optionally substituted" is used interchangeably with the phrase “substituted or unsubstituted” or with the term “(un)substituted.” Unless otherwise indicated, an optionally substituted group may have a substituent at each substitutable position of the group, and each substitution is independent of the other.
When a substituent is a 5- or 6-membered nitrogen-containing heterocyclic ring, it may be attached to the remainder of Formula 1 though any available carbon or nitrogen ring atom, unless otherwise described. As noted above, Q can be (among others) phenyl optionally substituted with one or more substituents selected from a group of substituents as defined in the Summary of Invention. An example of phenyl optionally substituted with one to five substituents is the ring illustrated as U-1 in Exhibit 1, wherein R is R as defined in the Summary of the Invention for Q and r is an integer from 0 to 5.
As noted above, Q can be (among others) a 5- or 6-membered heterocyclic aromatic ring, optionally substituted with one or more substituents selected from a group of substituents as defined in the Summary of Invention. Examples of a 5- or 6-membered unsaturated aromatic heterocyclic ring optionally substituted with from one or more substituents include the rings U-2 through U-61 illustrated in Exhibit 1 wherein R is any substituent as defined in the Summary of the Invention for Q and r is an integer from 0 to 4, limited by the number of available positions on each U group. As U-29, U-30, U-36, U-37, U-38, U-39, U-40, U-41, U-42 and U-43 have only one available position, for these U groups r is limited to the integers 0 or 1, and r being 0 means that the U group is unsubstituted and a hydrogen is present at the position indicated by (R ) .
Exhibit 1 v v v (R ) 4 (R ) 4 (R ) (R ) (R ) r r r r r , , , , , 2 5 2 U-2 U-3 U-4 U-5 v v v (R ) (R ) (R ) (R ) (R ) r r r r , , , , , N N O U-6 U-7 U-8 U-9 U-10 v v v v v 4 4 (R ) (R ) (R ) (R ) (R ) r r r r 4 N N , , , , , O S S 2 5 5 2 U-11 U-12 U-13 U-14 U-15 v v v (R ) (R ) (R ) (R ) (R ) r r r r r , , , , , N N N N O U-16 U-17 U-18 U-19 U-20 v v v v v 4 3 4 (R ) 4 (R ) (R ) (R ) (R ) r r r r , , , , , O N N S S S N N U-21 U-22 U-23 U-24 U-25 v v N N (R ) (R ) 4 (R ) r r r , , , , , (R ) (R ) N N N N N r r U-26 U-27 U-28 U-29 U-30 v v v v v (R ) (R ) (R ) (R ) (R ) r r r r r N N N N N N N , , , , , N N N N N N N N U-31 U-32 U-33 U-34 U-35 O N S N N O N S N N N N , , , , , v v v v v (R ) (R ) (R ) (R ) (R ) r r r r r U-36 U-37 U-38 U-39 U-40 N S N (R ) (R ) N N N , , , , , O N S v v v (R ) (R ) (R ) r r r N N N U-41 U-42 U-43 U-44 U-45 v (R ) (R ) v v v (R ) (R ) (R ) r r r 3 , , , , , N N N N N N N N N U-46 U-47 U-48 U-49 U-50 v v v v v 6 (R ) (R ) (R ) 6 (R ) (R ) r r r r r N N N N , , , , , 2 N N N U-51 U-52 U-53 U-54 U-55 (R ) v v v (R ) (R ) (R ) (R ) r r r r N N N N , , , , N N N U-56 U-57 U-58 U-59 U-60 (R ) U-61 As noted above, Q can be (among others) an 8-, 9- or 10-membered ortho-fused bicyclic ring system optionally substituted with one or more substituents selected from a group of substituents as defined in the Summary of Invention. Examples of 8-, 9- or 10- membered ortho-fused bicyclic ring system optionally substituted with from one or more substituents include the rings U-81 through U-123 illustrated in Exhibit 3 wherein R is any substituent as defined in the Summary of the Invention for Q , and r is typically an integer from 0 to 4.
Exhibit 3 S N O S , , , , v v v v (R ) (R ) (R ) (R ) U-81 U-82 U-83 U-84 United States Patent 7008 , , , , v v v (R ) (R ) (R ) r r (R ) U-85 U-86 U-87 U-88 , , , , v (R ) (R ) v (R ) (R ) U-89 U-90 U-91 U-92 N N N , , , , (R ) (R ) (R ) O (R ) U-93 U-94 U-95 U-96 O S N v v v v , , , , (R ) (R ) (R ) (R ) r r r r U-97 U-98 U-99 U-100 , v , , , (R ) (R ) (R ) r O (R ) U-101 U-102 U-103 U-104 (R ) (R ) (R ) r (R ) r , , , , U-105 U-106 U-107 U-108 v (R ) (R ) (R ) r (R ) , , , , U-109 U-110 U-111 U-112 (R ) v (R ) (R ) (R ) , , , , U-113 U-114 U-115 U-116 (R ) (R ) (R ) (R ) , , , , U-117 U-118 U-119 U-120 (R ) (R ) (R ) r and r U-121 U-122 U-123 Although R groups are shown in the structures U-1 through U-123, it is noted that they do not need to be present since they are optional substituents. Note that when R is H when attached to an atom, this is the same as if said atom is unsubstituted. The nitrogen atoms that require substitution to fill their valence are substituted with H or R . Note that when the attachment point between (R ) and the U group is illustrated as floating, (R ) can be attached to any available carbon atom or nitrogen atom of the U group. Note that when the attachment point on the U group is illustrated as floating, the U group can be attached to the remainder of Formula 1 through any available carbon or nitrogen of the U group by replacement of a hydrogen atom. Note that some U groups can only be substituted with less than 4 R groups (e.g., U-2 through U-5, U-7 through U-48, and U-52 through U-61).
A wide variety of synthetic methods are known in the art to enable preparation of aromatic and nonaromatic heterocyclic rings and ring systems; for extensive reviews see the eight volume set of Comprehensive Heterocyclic Chemistry, A. R. Katritzky and C. W. Rees editors-in-chief, Pergamon Press, Oxford, 1984 and the twelve volume set of Comprehensive Heterocyclic Chemistry II, A. R. Katritzky, C. W. Rees and E. F. V. Scriven editors-in-chief, Pergamon Press, Oxford, 1996.
Compounds of this invention can exist as one or more stereoisomers. Stereoisomers are isomers of identical constitution but differing in the arrangement of their atoms in space and include enantiomers, diastereomers, cis-trans isomers (also known as geometric isomers) and atropisomers. Atropisomers result from restricted rotation about single bonds where the rotational barrier is high enough to permit isolation of the isomeric species. One skilled in the art will appreciate that one stereoisomer may be more active and/or may exhibit beneficial effects when enriched relative to the other stereoisomer(s) or when separated from the other stereoisomer(s). Additionally, the skilled artisan knows how to separate, enrich, and/or to selectively prepare said stereoisomers. For a comprehensive discussion of all aspects of stereoisomerism, see Ernest L. Eliel and Samuel H. Wilen, Stereochemistry of Organic Compounds, John Wiley & Sons, 1994.
This invention comprises all stereoisomers, conformational isomers and mixtures thereof in all proportions as well as isotopic forms such as deuterated compounds.
One skilled in the art will appreciate that not all nitrogen-containing heterocycles can form N-oxides since the nitrogen requires an available lone pair for oxidation to the oxide; one skilled in the art will recognize those nitrogen-containing heterocycles which can form N-oxides. One skilled in the art will also recognize that tertiary amines can form N-oxides.
Synthetic methods for the preparation of N-oxides of heterocycles and tertiary amines are very well known by one skilled in the art including the oxidation of heterocycles and tertiary amines with peroxy acids such as peracetic and 3-chloroperbenzoic acid (MCPBA), hydrogen peroxide, alkyl hydroperoxides such as t-butyl hydroperoxide, sodium perborate, and dioxiranes such as dimethyldioxirane. These methods for the preparation of N-oxides have been extensively described and reviewed in the literature, see for example: T. L. Gilchrist in Comprehensive Organic Synthesis, vol. 7, pp 748–750, S. V. Ley, Ed., Pergamon Press; M. Tisler and B. Stanovnik in Comprehensive Heterocyclic Chemistry, vol. 3, pp 18–20, A. J. Boulton and A. McKillop, Eds., Pergamon Press; M. R. Grimmett and B. R. T. Keene in Advances in Heterocyclic Chemistry, vol. 43, pp 149–161, A. R. Katritzky, Ed., Academic Press; M. Tisler and B. Stanovnik in Advances in Heterocyclic Chemistry, vol. 9, pp 285–291, A. R. Katritzky and A. J. Boulton, Eds., Academic Press; and G. W. H. Cheeseman and E. S. G. Werstiuk in Advances in Heterocyclic Chemistry, vol. 22, pp 390–392, A. R. Katritzky and A. J. Boulton, Eds., Academic Press.
One skilled in the art recognizes that because in the environment and under physiological conditions salts of chemical compounds are in equilibrium with their corresponding nonsalt forms, salts share the biological utility of the nonsalt forms. Thus a wide variety of salts of the compounds of Formula 1 are useful for control of invertebrate pests. The salts of the compounds of Formula 1 include acid-addition salts with inorganic or organic acids such as hydrobromic, hydrochloric, nitric, phosphoric, sulfuric, acetic, butyric, fumaric, lactic, maleic, malonic, oxalic, propionic, salicylic, tartaric, 4-toluenesulfonic or valeric acids. When a compound of Formula 1 contains an acidic moiety such as a carboxylic acid or phenol, salts also include those formed with organic or inorganic bases such as pyridine, triethylamine or ammonia, or amides, hydrides, hydroxides or carbonates of sodium, potassium, lithium, calcium, magnesium or barium. Accordingly, the present invention comprises compounds selected from Formula 1, N-oxides and suitable salts thereof.
Compounds selected from Formula 1, stereoisomers, tautomers, N-oxides, and salts thereof, typically exist in more than one form, and Formula 1 thus includes all crystalline and non-crystalline forms of the compounds that Formula 1 represents. Non-crystalline forms include embodiments which are solids such as waxes and gums as well as embodiments which are liquids such as solutions and melts. Crystalline forms include embodiments which represent essentially a single crystal type and embodiments which represent a mixture of polymorphs (i.e. different crystalline types). The term “polymorph” refers to a particular crystalline form of a chemical compound that can crystallize in different crystalline forms, these forms having different arrangements and/or conformations of the molecules in the crystal lattice. Although polymorphs can have the same chemical composition, they can also differ in composition due to the presence or absence of co- crystallized water or other molecules, which can be weakly or strongly bound in the lattice.
Polymorphs can differ in such chemical, physical and biological properties as crystal shape, density, hardness, color, chemical stability, melting point, hygroscopicity, suspensibility, dissolution rate and biological availability. One skilled in the art will appreciate that a polymorph of a compound represented by Formula 1 can exhibit beneficial effects (e.g., suitability for preparation of useful formulations, improved biological performance) relative to another polymorph or a mixture of polymorphs of the same compound represented by Formula 1. Preparation and isolation of a particular polymorph of a compound represented by Formula 1 can be achieved by methods known to those skilled in the art including, for example, crystallization using selected solvents and temperatures. Compounds of this invention may exist as one or more crystalline polymorphs. This invention comprises both individual polymorphs and mixtures of polymorphs, including mixtures enriched in one polymorph relative to others. For a comprehensive discussion of polymorphism see R.
Hilfiker, Ed., Polymorphism In the Pharmaceutical Industry, Wiley-VCH, Weinheim, 2006.
Embodiments of the present invention as described in the Summary of the Invention include those described below. In the following Embodiments, reference to “a compound of Formula 1” includes the definitions of substituents specified in the Summary of the Invention unless further defined in the Embodiments.
Embodiment 1. A compound of Formula 1 wherein Q is Q-1, Q-2 or Q-3.
Embodiment 2. A compound of Formula 1 wherein Q is Q-1, Q-2 or Q-3, and Y is CR .
Embodiment 3. A compound of Formula 1 wherein Q is Q-1 or Q-2.
Embodiment 4. A compound of Formula 1 wherein Q is Q-1.
Embodiment 5. A compound of Formula 1 wherein Q is Q-1, and Y is O or S.
Embodiment 6. A compound of Formula 1 wherein Q is Q-1, and Y is S.
Embodiment 7. A compound of Formula 1 wherein Q is Q-1, and Y is O.
Embodiment 8. A compound of Formula 1 wherein Q is Q-2. 2 5a Embodiment 9. A compound of Formula 1 wherein Q is Q-2, and Y is CR .
Embodiment 10. A compound of Formula 1 or any of Embodiments 1–9 wherein A is CH, CR or N, and R is halogen.
Embodiment 11. A compound of Embodiment 10 wherein A is CH, CF or N.
Embodiment 11a. A compound of Embodiment 10 wherein A is CF or N.
Embodiment 12. A compound of Embodiment 10 wherein A is CH or CF.
Embodiment 13. A compound of Embodiment 10 wherein A is CH.
Embodiment 14. A compound of Embodiment 10 wherein A is N.
Embodiment 15. A compound of Formula 1 or any of Embodiments 1–9 wherein m is 1, and R is C –C alkyl, C –C haloalkyl, C –C alkoxy or halogen. 1 4 1 4 1 4 Embodiment 16. A compound of Embodiment 15 wherein R is CF , OMe, Me, or F.
Embodiment 17. A compound of Embodiment 16 wherein R is CF , OMe, Me, or F, and is in the 4-position.
Embodiment 18. A compound of Embodiment 17 wherein R is CF , and is in the 4- position.
Embodiment 19. A compound of Formula 1 or any of Embodiments 1–9 wherein m is 0.
Embodiment 20. A compound of Formula 1 or any of Embodiments 1–19 wherein X is 2 2 3 4 3 2 2 1 3 CR , and X , X and X are each independently CR ; or X is CR , and X , X and X are each independently CR . 1 2 2 3 Embodiment 21. A compound of Embodiment 20 wherein X is CR , and X , X and X are each independently CR . 2 2 1 3 Embodiment 22. A compound of Embodiment 20 wherein X is CR , and X , X and X are each independently CR .
Embodiment 23. A compound of Formula 1 or any of Embodiments 1–22 wherein each R is independently H or halogen.
Embodiment 24. A compound of Embodiment 23 wherein each R is independently H or F.
Embodiment 25. A compound of Embodiment 24 wherein each R is H.
Embodiment 26. A compound of Formula 1 or any of Embodiments 1–25 wherein R is 6 7 10 11 a C(=Z)NR R , C(=NR )R or Q .
Embodiment 27. A compound of Formula 1 or any of Embodiments 1–25 wherein R is 11 C(=NR )R .
Embodiment 28. A compound of Formula 1 or any of Embodiments 1–25 wherein R is 11 11 C(=NR )R ; R is C –C alkoxy; and R is C –C alkyl substituted with 1 4 1 4 S(O) R .
Embodiment 29. A compound of Formula 1 or any of Embodiments 1–25 wherein R is 6 7 a C(=Z)NR R or Q .
Embodiment 30. A compound of Formula 1 or any of Embodiments 1–25 wherein R is C(=Z)NR R .
Embodiment 31. A compound of Formula 1 or any of Embodiments 1–25 wherein R is C(=O)NR R .
Embodiment 32. A compound of Formula 1 or any of Embodiments 1–25 wherein R is C(=S)NR R .
Embodiment 33. A compound of Formula 1 or any of Embodiments 1–25 wherein R is 6 7 21 22 C(=O)NR R ; and R is H, C(O)OR , C(O)R or C –C alkyl.
Embodiment 35. A compound of Formula 1 or any of Embodiments 1–25 wherein R is C(=O)NR R ; and R is H, C(O)OMe, C(O)Me or methyl.
Embodiment 36. A compound of Formula 1 or any of Embodiments 1–25 wherein R is C(=O)NR R ; and R is H.
Embodiment 36a. A compound of Formula 1 or any of Embodiments 1–25 wherein R is C(=O)NR R ; and R is C(O)OMe.
Embodiment 36b. A compound of Formula 1 or any of Embodiments 1–25 wherein R is C(=O)NR R ; and R is C(O)Me.
Embodiment 36c. A compound of Formula 1 or any of Embodiments 1–25 wherein R is C(=O)NR R ; and R is methyl.
Embodiment 37. A compound of Formula 1 or any of Embodiments 1–25 wherein R is Embodiment 38. A compound of Formula 1 or any of Embodiments 1–25 wherein R is Q ; and Q is a 5- or 6-membered aromatic ring, each ring containing ring members selected from carbon atoms and up to 3 heteroatoms independently selected from one oxygen atom, one sulfur atom, and up to 3 nitrogen atoms, each ring being unsubstituted or substituted with at least one R .
Embodiment 39. A compound of Formula 1 or any of Embodiments 1–25 wherein R is Q ; and Q is a 5- or 6-membered heteroaromatic ring, each ring containing ring members selected from carbon atoms and up to 3 heteroatoms independently selected from one oxygen atom, one sulfur atom, and up to 3 nitrogen atoms, each ring being unsubstituted or substituted with at least one R .
Embodiment 40. A compound of Embodiment 39 wherein the heteroaromatic ring is a -membered heteroaromatic ring.
Embodiment 41. A compound of Embodiment 40 wherein the heteroaromatic ring is a -membered heteroaromatic ring having a nitrogen atom at the 2-position.
Embodiment 42. A compound of Embodiment 39 wherein the heteroaromatic ring is a 6-membered heteroaromatic ring.
Embodiment 43. A compound of Embodiment 42 wherein the heteroaromatic ring is a 6-membered heteroaromatic ring having a nitrogen atom at the 2-position.
Embodiment 44. A compound of Embodiment 43 wherein the heteroaromatic ring is a 6-membered heteroaromatic ring having a nitrogen atom at the 2-position and substituted with C –C haloalkyl.
Embodiment 45. A compound of Embodiment 44 wherein the heteroaromatic ring is a 6-membered heteroaromatic ring having a nitrogen atom at the 2-position and substituted with CF .
Embodiments of this invention, including Embodiments 1–45 above as well as any other embodiments described herein, can be combined in any manner, and the descriptions of variables in the embodiments pertain not only to the compounds of Formula 1 but also to the starting compounds and intermediate compounds useful for preparing the compounds of Formula 1. In addition, embodiments of this invention, including Embodiments 1–45 above as well as any other embodiments described herein, and any combination thereof, pertain to the compositions and methods of the present invention.
Combinations of Embodiments 1–45 are illustrated by: Embodiment A. A compound of Formula 1 wherein 1 2 2 3 4 3 2 2 1 3 X is CR , and X , X and X are each independently CR ; or X is CR , and X , X and X are each independently CR .
Embodiment B. A compound of Embodiment A wherein Q is Q-1 or Q-2.
Embodiment C. A compound of Embodiment B wherein Q is Q-1; and Y is O or S.
Embodiment D. A compound of Embodiment C wherein Q is Q-2; and 2 5a Y is CR .
Embodiment E. A compound of any of Embodiments A–D wherein A is CH or CF; and m is 0.
Embodiment F. A compound of Formula 1 wherein A is CH or CF; m is 0; Q is Q-2; 2 5a Y is CR ; 2 3 4 2 2 1 3 4 X is CR and X , X and X are each CH; or X is CR and X , X and X are CH; 2 6 7 a R is C(=Z)NR R or Q .
Embodiment G. A compound of Formula 1 wherein A is CH or CF; m is 0; Q is Q-2; 2 5a Y is CR ; 2 3 4 X is CR and X , X and X are each CH; 2 6 7 a R is C(=Z)NR R or Q .
Embodiment H. A compound of Formula 1 wherein A is CH or CF; m is 0; Q is Q-2; 2 5a Y is CR ; 2 2 1 3 4 X is CR and X , X and X are CH; 2 6 7 a R is C(=Z)NR R or Q .
Embodiment I. A compound of Formula 1 wherein A is CH; m is 0; Q is Q-2; 2 5a Y is CR ; R is H; 2 3 4 2 2 1 3 4 X is CR and X , X and X are each CH; or X is CR and X , X and X are CH; 2 6 7 R is C(O)NR R ; and R is H.
Embodiment J. A compound of Formula 1 wherein A is CH; m is 0; Q is Q-2; 2 5a Y is CR ; R is H; 2 3 4 X is CR and X , X and X are each CH; 2 6 7 R is C(O)NR R ; and R is H.
Embodiment K. A compound of Formula 1 wherein A is CH; m is 0; Q is Q-2; 2 5a Y is CR ; R is H; 2 2 1 3 4 X is CR and X , X and X are CH; 2 6 7 R is C(O)NR R ; and R is H.
Specific embodiments include compounds of Formula 1 selected from the group consisting of (compound numbers refer to Index Tables A-N): N-(1-methylethyl)(3-pyridinyl)-2H-indazolecarboxamide (compound 8); N-cyclopropyl(3-pyridinyl)-2H-indazolecarboxamide (compound 14); N-cyclohexyl(3-pyridinyl)-2H-indazolecarboxamide (compound 16); 2-(3-pyridinyl)-N-(2,2,2-trifluoroethyl)-2H-indazolecarboxamide (compound 19); 2-(3-pyridinyl)-N-[(tetrahydrofuranyl)methyl]-2H-indazolecarboxamide (compound 41); methyl 2-[[2-(3-pyridinyl)-2H-indazolyl]carbonyl]hydrazinecarboxylate (compound 42); N-[(2,2-difluorocyclopropyl)methyl](3-pyridinyl)-2H-indazolecarboxamide (compound 51); N-(2,2-difluoropropyl)(3-pyridinyl)-2H-indazolecarboxamide (compound 54); 2-(3-pyridinyl)-N-(2-pyrimidinylmethyl)-2H-indazolecarboxamide (compound 55); and N-[(5-methylpyrazinyl)methyl](3-pyridinyl)-2H-indazolecarboxamide (compound 76).
Of note is that compounds of this invention are characterized by favorable metabolic and/or soil residual patterns and exhibit activity controlling a spectrum of agronomic and nonagronomic invertebrate pests.
Of particular note, for reasons of invertebrate pest control spectrum and economic importance, protection of agronomic crops from damage or injury caused by invertebrate pests by controlling invertebrate pests are embodiments of the invention. Compounds of this invention because of their favorable translocation properties or systemicity in plants also protect foliar or other plant parts which are not directly contacted with a compound of Formula 1 or a composition comprising the compound.
Also noteworthy as embodiments of the present invention are compositions comprising a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof, and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent, said compositions optionally further comprising at least one additional biologically active compound or agent.
Further noteworthy as embodiments of the present invention are compositions for controlling an invertebrate pest comprising a compound of any of the preceding Embodiments, as well as any other embodiments described herein, and any combinations thereof, and at least one additional component selected from the group consisting of a surfactant, a solid diluent and a liquid diluent, said compositions optionally further comprising at least one additional biologically active compound or agent. Embodiments of the invention further include methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound of any of the preceding Embodiments (e.g., as a composition described herein).
Embodiments of the invention also include a composition comprising a compound of any of the preceding Embodiments, in the form of a soil drench liquid formulation.
Embodiments of the invention further include methods for controlling an invertebrate pest comprising contacting the soil with a liquid composition as a soil drench comprising a biologically effective amount of a compound of any of the preceding Embodiments.
Embodiments of the invention also include a spray composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of any of the preceding Embodiments and a propellant. Embodiments of the invention further include a bait composition for controlling an invertebrate pest comprising a biologically effective amount of a compound of any of the preceding Embodiments, one or more food materials, optionally an attractant, and optionally a humectant. Embodiments of the invention also include a device for controlling an invertebrate pest comprising said bait composition and a housing adapted to receive said bait composition, wherein the housing has at least one opening sized to permit the invertebrate pest to pass through the opening so the invertebrate pest can gain access to said bait composition from a location outside the housing, and wherein the housing is further adapted to be placed in or near a locus of potential or known activity for the invertebrate pest.
Embodiments of the invention also include methods for protecting a seed from an invertebrate pest comprising contacting the seed with a biologically effective amount of a compound of any of the preceding Embodiments.
Embodiments of the invention also include methods for protecting an animal from an invertebrate parasitic pest comprising administering to the animal a parasiticidally effective amount of a compound of any of the preceding Embodiments.
Embodiments of the invention also include methods for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound of Formula 1, an N-oxide or a salt thereof, (e.g., as a composition described herein), provided that the methods are not methods of medical treatment of a human or animal body by therapy.
This invention also relates to such methods wherein the invertebrate pest or its environment is contacted with a composition comprising a biologically effective amount of a compound of Formula 1, an N-oxide or a salt thereof, and at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents, said composition optionally further comprising a biologically effective amount of at least one additional biologically active compound or agent, provided that the methods are not methods of medical treatment of a human or animal body by therapy.
One or more of the following methods and variations as described in Schemes 1 –13 can be used to prepare the compounds of Formula 1. The definitions of substituents in the compounds of Formulae 1–23 below are as defined above in the Summary of the Invention unless otherwise noted. Compounds of Formulae 1a–1g are various subsets of the compounds of Formula 1, and all substituents for Formulae 1a–1g are as defined above for Formula 1. The following abbreviations are used: THF is tetrahydrofuran, DMF is N,N- dimethylformamide, NMP is N-methylpyrrolidinone, Ac is acetate, MS is mesylate, Tf is triflate, and Nf is nonaflate.
Compounds of Formula 1a (Formula 1 wherein Q is Q-1, Q-3 or Q-4) can be prepared as shown in Scheme 1 by the coupling of a heterocyclic compound of Formula 2 (wherein LG is a suitable leaving group such as Cl, Br, I, Tf or Nf) with a heterocyclic compound of Formula 3 (wherein M is a suitable metal or metalloid such as a Mg, Zn or B species) in the presence of a catalyst and appropriate ligand. Catalysts can be generated from transition metals such as Pd (for example Pd(OAc) or Pd (dba) and mono- or bi-dentate ligands such 2 2 3 as PPh , PCy , Pt-Bu , x-phos, xantphos, s-phos, and dppf. Typical bases used include 3 3 3 carbonates such as sodium carbonate or cesium carbonate, phosphates such as potassium triphosphate, amines such as ethyldiisopropylamine, or alkoxides such as sodium tert- butoxide. Typical solvents include THF, dioxane, toluene, ethanol, DMF, water or mixtures thereof. Typical reaction temperatures range from ambient temperature to the boiling point of the solvent.
Scheme 1 Compounds of Formula 1a (Formula 1 wherein Q is Q-1, Q-3 or Q-4) can also be prepared as shown in Scheme 2 by the coupling of a compound of Formula 4 with a compound of Formula 5 (wherein LG is a suitable leaving group such as Cl, Br, I, Tf or Nf) in the presence of a catalyst and an appropriate ligand. A variety of catalysts can be used in the method of Scheme 2, and these can be generated from a transition metal species such as copper or Pd (for example complexes such as Pd(OAc) or Pd (dba) ) and a ligand. Typical 2 2 3 ligands may be mono- or bi-dentate, and include PPh , PCy , Pt-Bu , x-phos, xantphos, s- 3 3 3 phos, and dppf. Typical bases used include carbonates such as sodium carbonate or cesium carbonate, phosphates such as potassium triphosphate, amines such as ethyldiisopropylamine or alkoxides such as sodium tert-butoxide. Additives such as molecular sieves, Bu N Br or copper or silver salts (e.g., AgOAc) can be beneficial. Typical reaction solvents include THF, dioxane, toluene, ethanol, DMF, water, or mixtures thereof. Typical reaction temperatures range from ambient temperature to the boiling point of the solvent. For examples, see Chemical Communications 2011, 47(17), pages 5043-5045; Journal of the American Chemical Society 2010, 132(11), pages 3674-3675; Heterocycles 2011, 83(6), pages 1371-1376; U.S. Patent Application Publication 20090076266; Bulletin of the Chemical Society of Japan 1998, 71(2), pages 467-473; Tetrahedron Letters 2008, 49(10), pages 1598-1600; and Tetrahedron Letters 2010, 51(42), pages 5624-5627.
Scheme 2 Compounds of Formula 2 wherein LG is halogen can be prepared from the corresponding amines by treatment with a source of ON such as isoamyl nitrite or t-butyl nitrite or nitrous acid in the presence of a halogen source such as CuBr or BnNEt Br .
Preferred reaction conditions include aqueous or organic solvents such as THF or acetonitrile, and reaction temperatures ranging from 0 °C to the boiling point of the solvent.
Compounds of Formula 2 wherein LG is Cl or Br can also be prepared from the corresponding hydroxy compounds by treatment with a halogenating agent such as POCl , PCl , PBr or SOCl . Compounds of Formula 2 wherein LG is OMS or OTf can also be 3 2 prepared from the corresponding hydroxy compounds by treatment with MsCl or Tf O.
Compounds of Formula 4 can be prepared from the corresponding amine compounds by treatment with a source of ON such as isoamyl nitrite or t-butyl nitrite. Preferred reaction conditions include ethereal solvents such as THF at temperatures ranging from ambient temperature to the boiling point of the solvent.
Compounds of Formula 6 can be prepared by electrophilic halogenation of the corresponding compounds of Formula 7 by treatment with a halogenating agent such as N- bromosuccinimide in a suitable solvent such as DMF, NMP or acetic acid at temperatures ranging from ambient temperature up to the boiling point of the solvent (Scheme 3).
Scheme 3 2-Aminobenzothiazoles of Formula 8 can be prepared from ortho-unsubstituted + + + anilines of Formula 9 and a thiocyanate anion (wherein M is K , Na or Bu N ) as shown in Scheme 4. The reaction can be conducted in a single step in acetic acid for example, or through the intermediacy of a thio-urea followed by oxidation. Suitable oxidants include bromine.
Scheme 4 Compounds of Formula 1b can be prepared from compounds of Formula 10 by the method shown in Scheme 5, in which a compound of Formula 10 is treated with an azide reagent (for example, sodium azide or tetrabutylammonium azide). Typical reaction conditions include DMF or NMP as solvent, and reaction temperatures ranging from 80 °C to the boiling point of the solvent.
Scheme 5 Compounds of Formula 1b can also be prepared from compounds of Formula 10a by the method shown in Scheme 5a, in which a compound of Formula 10a is treated with triethyl phosphite.
Scheme 5a Compounds of Formulae 10 and 10a are Schiff bases and can be prepared by methods known in the art (see, for example, March, J., Advanced Organic Chemistry, Wiley, 1992, pages 896-898.
Compounds of Formula 1c can be prepared from compounds of Formula 11 by the method shown in Scheme 6 via oxidation of a compound of Formula 11 with molecular oxygen or a peroxide such as t-butyl hydroperoxide in the presence of a copper (II) catalyst such as Cu(OAc) or CuBr . Typical reaction conditions included alcoholic solvents such as t-amyl alcohol, DMF, NMP or aqueous ammonia, and reaction temperatures from 60 °C to the boiling point of the solvent.
Scheme 6 2-Aminoazo compounds of Formula 11 can be prepared by reaction of an aniline of Formula 9 with a diazonium salt of Formula 12 by methods known in the art (see, for example, March, J., Advanced Organic Chemistry, Wiley, 1992, pages 525-526).
Compounds of Formula 11 can also be prepared by reaction of an aryl nitroso compound of Formula 13 with a diamine of Formula 14 in a solvent such as acetic acid. These two methods are shown in Scheme 7.
Scheme 7 Compounds of Formula 1d can be prepared by condensation of a compound of Formula 14 (wherein Lg is a suitable leaving group such as Cl or Br) with an aminopyridine or aminodiazine of Formula 16 as shown in Scheme 8. Typical reaction conditions include an alcoholic solvent such as ethanol or toluene, and a reaction temperature range from ambient temperature to the boiling point of the solvent. The pyridine nitrogen can optionally be protected as a BH adduct, an N-oxide, or a 2- or 6-halopyridine derivative.
Scheme 8 Compounds of Formula 1e can be prepared as shown in Scheme 9 by the cycloaddition of 2-aminopyridines of Formula 15 with arylnitriles of Formula 16 (see, for example, Journal of the American Chemical Society 2009, 131(42), pages 15080-15081, and WO 2013041472.
Scheme 9 Compounds of Formula 1e can also be prepared by rearrangement of compounds of Formula 17 by treatment with base as shown in Scheme 10 (see, for example, J. Het Chem 1970, 7 page 1019). Compounds of Formula 17 can be prepared by methods described in WO 2008006540 and J. Org. Chem., 1966, page 251.
Scheme 10 Intermediates of Formula 18 can be prepared by the method shown in Scheme 11 by treatment of a 2-aminopyridine of Formula 15 with an isocyanate followed by hydroxylamine and a suitable base such as triethylamine.
Scheme 11 Compounds of Formula 1 wherein Q is Q-4 can also be prepared by the method described in Synthesis Example 6.
Compounds of Formula 1f can be prepared as shown in Scheme 12 by oxidative cyclization of an aryl aldehyde of Formula 20 with an aniline of Formula 19 bearing an ortho-halogen, preferably iodine, in the presence of sulfur which acts as both a source of sulfur and as an oxidizing agent. The reaction is carried out in the presence of a base such as K CO in a suitable solvent such as water or DMF, and is catalyzed by the addition of copper salts (for example, CuI or CuCl ) and preferably a suitable ligand such as 1,10- phenanthroline. Typical reaction temperatures range from 70 °C to the boiling point of the solvent.
Scheme 12 Compounds of Formula 1f can also be prepared by cyclization of 2-halothioamides of Formula 21 as shown in the second reaction of Scheme 12 with a base such as KOtBu, NaH, DBU or Cs CO in a suitable solvent such as toluene or DMF, optionally with the addition of copper salts such as CuI, and preferably a suitable ligand such as 1,10-phenanthroline.
This reaction can also be catalyzed by Pd species such as that prepared from Pd (dba) and (t-Bu) P-o-biphenyl, a base such as Cs CO in a suitable solvent, such as 1,2- 2 2 3 dimethoxyethane or dioxane. Typical reaction temperatures range from 80 °C to the boiling point of the solvent. For copper- and Pd-catalyzed reactions, the halogen substituent on the compound of Formula 21 is preferably Br or I. For example, see Journal of Organic Chemistry 2006, 71(5), pages 1802-1808; Tetrahedron Letters 2003, 44(32), pages 6073- 6077; Synthetic Communications 1991, 21(5), pages 625-33; and Eur. Pat. Appl. No. 450420.
Compounds of Formula 1f can also be prepared by the oxidative cyclization of thioamides of Formula 22 as shown in the third reaction of Scheme 12. Oxidants typically used in this method include bromine or iodine, DDQ and K Fe(CN) . For example, see Tetrahedron 2007, 63(41), pages 10276-10281; Synthesis 2007, (6), 819-823; and U.S. Pat.
Appl. Publ., 20120215154.
The three methods described in Scheme 12 can be used to prepare compounds wherein 1 4 1 4 X -X are carbon atoms, or wherein one of X -X is a nitrogen (for example, see J.
Heterocyclic Chem. 2009, 46, page 1125 and references cited therein).
Compounds of Formula 1, and intermediates used in the preparation of compounds of Formula 1, wherein Z is S can be prepared by thionation of the corresponding compounds wherein Z is O with, for example, Lawesson’s reagent (CAS No. 191725), Belleau’s reagent (CAS No. 888168) or P S . The thionation reactions are typically conducted in solvents such as toluene, xylenes or dioxane, and at elevated temperature from 80 C to the boiling point of the solvent. 2 6 7 Compounds of Formula 1 wherein R is C(O)NR R can be prepared by carbonylation of the corresponding compounds wherein R is halogen (preferably Br or I), or wherein R is a sulfonate (for example, triflate or nonaflate). The reaction is performed in the presence of a source of carbon monoxide such as carbon monoxide gas or Mo(CO) at pressures between atmospheric pressure and 25 bar, optionally with microwave heating, and generally at elevated temperatures in the range of 80 to 160 C. Typical reaction solvents include DMF, NMP, toluene or ethereal solvents such as THF or dioxane.
Compounds of Formula 1 wherein R is Q can be prepared as shown in Scheme 13.
The method of Scheme 13 is similar to the method described in Scheme 1; M is a suitable metal or metalloid such as a Mg, Zn or B species, and R corresponds to LG in Scheme 1 and is a suitable leaving group such as Cl, Br, I, Tf or Nf.
Scheme 13 2 a a Compounds of Formula 1 wherein R is Q and Q is bonded to Q via a nitrogen atom in Q can be prepared by a method similar to that of Scheme 13. In this method, M in the compound of Formula 23 is hydrogen. Coupling reagents include copper(I) salts such as CuI, and a suitable ligand such as trans-bis(N,N-dimethyl-1,2-cyclohexanediamine. Typical reaction conditions include a solvent such as toluene or dioxane, and an elevated reaction temperature ranging from 80 C to the boiling point of the solvent.
Examples of intermediates useful in the preparation of compounds of this invention are shown in Tables I-1 through I-16. The following abbreviations are used in the Tables which follow: Me means methyl, Et means ethyl, Ph means phenyl, C(O) means carbonyl and CHO means formyl.
TABLE I-1 A is CH -COOH -C(O)OMe -C(O)OEt cyano -C(O)Cl -C(O)OPh -C(O)O(4-nitrophenyl) -C(O)Me -CHO Cl Br I -OS(O) CF NH 2 3 2 nitro A is CF -COOH -C(O)OMe -C(O)OEt cyano -C(O)Cl -C(O)OPh -C(O)O(4-nitrophenyl) -C(O)Me -CHO Cl Br I -OS(O) CF NH 2 3 2 nitro A is N -COOH -C(O)OMe -C(O)OEt cyano -C(O)Cl -C(O)OPh -C(O)O(4-nitrophenyl) -C(O)Me -CHO Cl Br I -OS(O) CF NH 2 3 2 nitro TABLE I-2 A is CH -COOH -C(O)OMe -C(O)OEt cyano -C(O)Cl -C(O)OPh -C(O)O(4-nitrophenyl) -C(O)Me -CHO Cl Br I -OS(O) CF NH 2 3 2 nitro A is CF -COOH -C(O)OMe -C(O)OEt cyano -C(O)Cl -C(O)OPh -C(O)O(4-nitrophenyl) -C(O)Me -CHO Cl Br I -OS(O) CF NH 2 3 2 nitro A is N -COOH -C(O)OMe -C(O)OEt cyano -C(O)Cl -C(O)OPh -C(O)O(4-nitrophenyl) -C(O)Me -CHO Cl Br I -OS(O) CF NH 2 3 2 nitro TABLE I-3 A is CH -COOH -C(O)OMe -C(O)OEt cyano -C(O)Cl -C(O)OPh -C(O)O(4-nitrophenyl) -C(O)Me -CHO Cl Br I -OS(O) CF NH 2 3 2 nitro A is CF -COOH -C(O)OMe -C(O)OEt cyano -C(O)Cl -C(O)OPh -C(O)O(4-nitrophenyl) -C(O)Me -CHO Cl Br I -OS(O) CF NH 2 3 2 nitro A is N -COOH -C(O)OMe -C(O)OEt cyano -C(O)Cl -C(O)OPh -C(O)O(4-nitrophenyl) -C(O)Me -CHO Cl Br I -OS(O) CF NH 2 3 2 nitro TABLE I-4 A is CH -COOH -C(O)OMe -C(O)OEt cyano -C(O)Cl -C(O)OPh -C(O)O(4-nitrophenyl) -C(O)Me -CHO Cl Br I -OS(O) CF NH 2 3 2 nitro A is CF -COOH -C(O)OMe -C(O)OEt cyano -C(O)Cl -C(O)OPh -C(O)O(4-nitrophenyl) -C(O)Me -CHO Cl Br I -OS(O) CF NH 2 3 2 nitro A is N -COOH -C(O)OMe -C(O)OEt cyano -C(O)Cl -C(O)OPh -C(O)O(4-nitrophenyl) -C(O)Me -CHO Cl Br I -OS(O) CF NH 2 3 2 nitro TABLE I-5 Table I-5 is identical to Table I-1, except that the structure shown under the heading "Table 1-1" is replaced by the structure shown above.
TABLE I-6 Table I-6 is identical to Table I-1, except that the structure shown under the heading "Table 1-1" is replaced by the structure shown above.
TABLE I-7 Table I-7 is identical to Table I-1, except that the structure shown under the heading "Table 1-1" is replaced by the structure shown above.
TABLE I-8 Table I-8 is identical to Table I-1, except that the structure shown under the heading "Table 1-1" is replaced by the structure shown above.
TABLE I-9 Table I-9 is identical to Table I-1, except that the structure shown under the heading "Table 1-1" is replaced by the structure shown above.
TABLE I-10 Table I-10 is identical to Table I-1, except that the structure shown under the heading "Table 1-1" is replaced by the structure shown above.
TABLE I-11 Table I-4 is identical to Table I-1, except that the structure shown under the heading "Table 1-1" is replaced by the structure shown above.
TABLE I-12 Table I-4 is identical to Table I-1, except that the structure shown under the heading "Table 1-1" is replaced by the structure shown above.
TABLE I-13 Table I-13 is identical to Table I-1, except that the structure shown under the heading "Table 1-1" is replaced by the structure shown above.
TABLE I-14 Table I-14 is identical to Table I-1, except that the structure shown under the heading "Table 1-1" is replaced by the structure shown above.
TABLE I-15 Table I-15 is identical to Table I-1, except that the structure shown under the heading "Table 1-1" is replaced by the structure shown above.
TABLE I-16 Table I-16 is identical to Table I-1, except that the structure shown under the heading "Table 1-1" is replaced by the structure shown above.
It is recognized that some reagents and reaction conditions described above for preparing compounds of Formula 1 may not be compatible with certain functionalities present in the intermediates. In these instances, the incorporation of protection/deprotection sequences or functional group interconversions into the synthesis will aid in obtaining the desired products. The use and choice of the protecting groups will be apparent to one skilled in chemical synthesis (see, for example, Greene, T. W.; Wuts, P. G. M. Protective Groups in Organic Synthesis, 2nd ed.; Wiley: New York, 1991). One skilled in the art will recognize that, in some cases, after introduction of the reagents depicted in the individual schemes, additional routine synthetic steps not described in detail may be needed to complete the synthesis of compounds of Formula 1. One skilled in the art will also recognize that it may be necessary to perform a combination of the steps illustrated in the above schemes in an order other than that implied by the particular sequence presented to prepare the compounds of Formula 1.
One skilled in the art will also recognize that compounds of Formula 1 and the intermediates described herein can be subjected to various electrophilic, nucleophilic, radical, organometallic, oxidation, and reduction reactions to add substituents or modify existing substituents.
Without further elaboration, it is believed that one skilled in the art using the preceding description can utilize the present invention to its fullest extent. The following Synthesis Examples are, therefore, to be construed as merely illustrative, and not limiting of the disclosure in any way whatsoever. Steps in the following Synthesis Examples illustrate a procedure for each step in an overall synthetic transformation, and the starting material for each step may not have necessarily been prepared by a particular preparative run whose procedure is described in other Examples or Steps. Percentages are by weight except for chromatographic solvent mixtures or where otherwise indicated. Parts and percentages for chromatographic solvent mixtures are by volume unless otherwise indicated. H NMR spectra are reported in ppm downfield from tetramethylsilane; “s” means singlet, “d” means doublet, “t” means triplet, “q” means quartet, “m” means multiplet, “dd” means doublet of doublets, “dt” means doublet of triplets, “br s” means broad singlet. DMF means N,N- dimethylformamide. Compound numbers refer to Index Tables A-N.
SYNTHESIS EXAMPLE 1 Preparation of N-[2-(methylthio)ethyl](3-pyridinyl)benzothiazolecarboxamide (compound 84) Step A: Preparation of 3-[(aminothioxomethyl)amino]benzoic acid ethyl ester Ethyl 3-aminobenzoate (35.25 g, 213.6 mmol) was dissolved in chlorobenzene (250 mL) and cooled to -10 °C. Concentrated sulfuric acid (5.93 mL) was added followed by KSCN (21.76 g) and 18-crown-6 (600 mg), and the reaction mixture was heated at 100 °C for 14 hours. Hexanes was added to the cooled mixture, and the precipitated solid was isolated by filtration. The solid was slurried in a mixture of water and hexanes, and the slurry was stirred for 1 hour. The solid was isolated by filtration and dried in vacuo overnight to give the title compound as a gray solid (40.7 g). H NMR (DMSO-d ) : 10.10 + 9.87 (two s, 1H), 8.08 + 8.05 (two s, 1H), 7.66-7.80 (m, 2H), 7.43-7.51 (m, 1H), 8.0-7.0 (br s, 2H), 4.28-4.35 (m, 2H), 1.29-1.35 (m, 3H).
Step B: Preparation of 2-aminobenzothiazolecarboxylic acid ethyl ester The product of Step A was taken up in chloroform (300 mL) and acetic acid (200 mL) and bromine (21 mL) in chloroform (100 mL) was added dropwise over 1.5 hours. The reaction mixture was then heated at 70 °C for 4 hours, cooled, filtered, and the isolated solid was washed with 50 mL of 1:1 acetone/chloroform. The solid was added to a solution of Na CO (25 g) in water (400 mL) and stirred for 20 minutes. The suspension was filtered, and the isolated solid was washed with water, and dried in vacuo overnight to give the title compound (6.73 g) as a white solid. The organic filtrate was concentrated and re-slurried in 100 mL of 1:1 chloroform/acetone, and processed as described above to give an additional 8.1 g of white solid (90% purity, the remaining 10% being the regioisomeric benzothiazole).
H NMR (DMSO-d ) : 7.66 (dd, J=7.7, 0.9 Hz, 1H), 7.60 (s, 1H), 7.57 (dd, 1H), 7.35 (t, J=7.8 Hz, 1H), 4.37 (q, J=7.1 Hz, 2H), 1.36 (t, J=7.1 Hz, 3H).
Step C: Preparation of 2-chlorobenzothiazolecarboxylic acid ethyl ester The product of Step B (7.97 g, 9:1 mixture of regioisomers, 35.9 mmol) was added portionwise over 45 minutes to a mixture of tert-butylnitrite (7.1 mL) and CuCl (5.31 g) in acetonitrile (360 mL) at 65 °C. After stirring for an additional 15 minutes, the cooled mixture was extracted 6 times with hexanes. The combined extracts were concentrated to give the title compound (5.85 g) as a yellow solid. The acetonitrile layer was diluted with water (200 mL), extracted with hexanes, and the hexane fraction was filtered through a pad of silica gel eluting with butyl chloride to yield an additional 0.55 g of product upon concentration. H NMR (CDCl ) : 8.14 (d, 2H), 7.58 (t, 1H), 4.49 (q, J=7.1 Hz, 2H), 1.47 (t, J=7.2 Hz, 3H).
Step D: Preparation of 2-(3-pyridinyl)benzothiazolecarboxylic acid The product of Step C (6.2 g, 9:1 mixture of regioisomers) was combined with 3- pyridinylboronic acid (3.79 g), PPh (1.35 g) and Na CO (5.44 g) in toluene (100 mL), water (25 mL) and ethanol (15 mL), and the reaction mixture was sparged with nitrogen for minutes. Pd dba (588 mg) was added, and the reaction mixture was heated at reflux for 4 hours. The cooled reaction mixture was diluted with water, extracted twice with dichloromethane, and the combined organic extracts were dried over MgSO and concentrated. The residue was purified by column chromatography (silica gel eluted with 10% to 50% ethyl acetate in hexanes) to give an orange solid (6.7 g) Recrystallization from ethanol (25 mL) yielded the ethyl ester of the title compound (5.65 g) as the single desired regioisomer. H NMR (CDCl ) : 9.38 (br s, 1H), 8.75 (br s, 1H), 8.44 (dt, J=8.0, 1.9 Hz, 1H), 8.30 (dd, J=8.2, 1.1 Hz, 1H), 8.19 (dd, J=7.6, 1.1 Hz, 1H), 7.62 (t, 1H), 7.47 (dd, J=8.4, 4.4 Hz, 1H), 4.53 (q, J=7.2 Hz, 2H), 1.50 (t, J=7.2 Hz, 3H).
The product obtained above was dissolved in ethanol (100 mL) and treated with a 1N solution of NaOH (24.8 mL). The reaction mixture was heated at reflux for 1.5 hours before being cooled, neutralized with concentrated HCl (2.0 mL), and concentrated. The residue was dried in vacuo to give a mixture of the title compound and NaCl, which was used without further purification in the next step.
Step E: Preparation of N-[2-(methylthio)ethyl](3-pyridinyl) benzothiazolecarboxamide Thionyl chloride (40 mL) was added to the product of Step D (0.55 g), and the reaction mixture was heated at reflux for 3 hour. The reaction mixture was then cooled and concentrated. The resulting residue was suspended in toluene and concentrated to yield the crude acid chloride, which was used without further purification.
The crude acid chloride (containing 120 mol% NaCl, 114 mg, 0.3 mmol) was treated with dichloromethane (5 mL), MeSCH CH NH (33 L) and triethylamine (125 L), and 2 2 2 the reaction mixture was then stirred at ambient temperature for 14 hours. The reaction mixture was diluted with a saturated aqueous solution of NaHCO , extracted twice with dichloromethane, and dried over MgSO . The combined organic layers were concentrated, and the residue was purified by column chromatography (silica gel eluted with 30% ethyl acetate in hexanes to 100% ethyl acetate) to give 65 mg of the title compound, a compound of this invention. H NMR (CDCl ) : 9.39 (d, J=1.7 Hz, 1H), 8.74 (d, J=3.3 Hz, 1H), 8.40- 8.47 (dt, 1H), 8.26 (dd, J=8.0, 0.9 Hz, 1H), 7.71 (dd, J=7.6, 0.9 Hz, 1H), 7.58-7.64 (t, 1H), 7.47 (dd, J=7.2, 5.0 Hz, 1H), 6.94 (br t, 1H), 3.75-3.82 (q, 2H), 2.80-2.88 (t, 2H), 2.18 (s, 3H).
SYNTHESIS EXAMPLE 2 Preparation of 2-(5-fluoropyridinyl)-N-(2,2,2-trifluoroethyl)benzothiazolecarboxamide (compound 127) Step A: Preparation of 2-(5-fluoropyridinyl)benzothiazolecarboxylic acid Methyl 4-aminoiodobenzoate (1.93 g, 6.96 mmol) was combined with K CO (1.92 g), S (668 mg), CuCl -2H O (119 mg), 1,10-phenanthroline (125 mg) and 5-fluoro 8 2 2 pyridinecarboxaldehyde (957 mg) in H O (30 mL), and the reaction mixture was heated at reflux 16 hours. The cooled reaction mixture was filtered, and the filtrate was treated with NH Cl (1.49 g). The reaction mixture was stirred at ambient temperature for 10 minutes, filtered, and the solid was dried in vacuo to yield a gray solid. The solid was suspended in dioxane, the suspension was heated to reflux, cooled, and filtered to isolate a solid. The solid was rinsed with ethyl ether to give the title compound (0.66 g). H NMR (DMSO-d ) : 9.15 (s, 1H), 8.80 (d, J=2.7 Hz, 1H), 8.65 (s, 1H), 8.39 (dt, J=9.5, 2.2 Hz, 1H), 8.10 (d, 1H), 8.05 (d, 1H), 8.0-6.5 (br s).
Step B: Preparation of 2-(5-fluoropyridinyl)-N-(2,2,2-trifluoroethyl) benzothiazolecarboxamide Thionyl chloride (5 mL) was added to the product of Step A (0.66 g), and the mixture was heated at reflux for 16 hours. The reaction mixture was then cooled and concentrated.
The resulting residue was suspended in toluene and concentrated to provide the crude acid chloride, which was used without further purification.
The crude acid chloride (103 mg, 0.31 mmol) was treated with dichloromethane (5 mL), triethylamine (131 L) and CF CH NH (29 L), and the reaction mixture was stirred 3 2 2 at ambient temperature for 3 days. The reaction mixture was diluted with a saturated aqueous solution of NaHCO , extracted twice with dichloromethane, and dried over MgSO .
The combined organic layers were concentrated, and the residue was purified by column chromatography (silica gel eluted with 20% to 40% ethyl acetate in hexanes) to give the title compound, a compound of this invention, as a white solid (52 mg). H NMR (CDCl ) : 9.32 (br s, 1H), 8.77 (d, J=4.3 Hz, 1H), 8.48 (d, J=1.4 Hz, 1H), 8.40 (dt, J=7.9, 2.0 Hz, 1H), 8.16 (d, J=8.5 Hz, 1H), 7.90 (dd, J=8.5, 1.7 Hz, 1H), 7.48 (dd, J=7.8, 4.7 Hz, 1H), 6.48 (br t, 1H), 4.20 (qd, J=9.0 Hz, 1H).
SYNTHESIS EXAMPLE 3 Preparation of N-(1-methylethyl)(3-pyridinyl)-2H-indazolecarboxamide (compound 8) Step A: Preparation of N-[(2-bromofluorophenyl)methylene]pyridinamine A solution of 2-bromofluorobenzaldehyde (5 g, 24.6 mmol) and 3-aminopyridine (2.7 g, 29.5 mmol) in EtOH (4 mL) was heated to reflux overnight. The reaction mixture was concentrated and the resulting solid was purified by column chromatography (silica gel eluted with 0-40% ethyl acetate in hexanes) to afford the title compound (4.5 g) as an orange solid. H NMR (CDCl ) : 8.66-8.70 (s, 1H), 8.48-8.53 (m, 2H), 7.52-7.58 (m, 1H), 7.41- 7.48 (m, 1H), 7.31-7.37 (m, 1H), 6.95-7.06 (m, 2H).
Step B: Preparation of 4-bromo(3-pyridinyl)-2H-indazole A solution of the product of Step A (4.5 g, 16.1. mmol) and NaN (1.2 g, 19.3 mmol) in DMF (20 mL) was heated to 90 °C for 24 hours. The cooled mixture was diluted with water and extracted 3 times with dichloromethane. The combined organic layers were dried (MgSO ), filtered, concentrated, and the residue was purified by column chromatography (silica gel eluted with 0-30% ethyl acetate in hexanes) to give the title compound (4.0 g) as a yellow solid. H NMR (CDCl ) : 9.21 (d, J=2.4 Hz, 1H), 8.69 (dd, J=4.8, 1.3 Hz, 1H), 8.46-8.49 (d, 1H), 8.28 (ddd, J=8.3, 2.7, 1.5 Hz, 1H), 7.73 (d, J=8.7 Hz, 1H), 7.50 (ddd, J=8.2, 4.8, 0.7 Hz, 1H), 7.31 (d, 1H), 7.21 (dd, J=8.7, 7.3 Hz, 1H).
Step C: Preparation of N-(1-methylethyl)(3-pyridinyl)-2H-indazolecarboxamide The product of Step B (200 mg, 0.727 mmol), isopropylamine (183 µL, 2.18 mmol), trans-bis(acetato)bis[o-(di-o-tolylphosphino)benzyl]dipalladium(II) (17 mg, 0.018 mmol), tri-tert-butylphosphonium tetrafluoroborate (10.5 mg, 0.036 mmol), molybdenum hexacarbonyl (192 mg, 0.727 mmol, 1,8-diazabicycloundecene (473 µL, 2.18 mmol) and DMF (5 mL) were placed in a microwave vial and irradiated at 160 °C for 40 minutes. The reaction mixture was then cooled to room temperature and filtered through a pad of Celite®.
The filtrate was diluted with a saturated solution of NaHCO and extracted with dichloromethane. The organic layer was dried (MgSO ), filtered, concnentrated, and the residue was purified by column chromatography (silica gel eluted with 0-10% acetone in chloroform). Trituration of the resulting solid with ethyl ether provided the title compound, a compound of this invention, as a white solid (45 mg). H NMR (CDCl ) : 9.26 (d, J=2.2 Hz, 1H), 9.09 (d, J=0.9 Hz, 1H), 8.67 (dd, J=4.7, 1.4 Hz, 1H), 8.29 (ddd, J=8.3, 2.6, 1.4 Hz, 1H), 7.92 (dt, J=8.5, 0.9 Hz, 1H), 7.48 (m, 1H), 7.31-7.41 (m, 2H), 6.15 (s, 1H), 4.31-4.41 (m, 1H), 1.33 (d, J=6.6 Hz, 6H).
SYNTHESIS EXAMPLE 4 Preparation of 2-(3-pyridinyl)-N-[1-(2,2,2-trifluoroethyl)]imidazo[1,2-a]pyridine carboxamide (compound 457) Step A: Preparation of 2-(3-pyridinyl)imidazo[1,2-a]pyridinecarboxylic acid methyl ester Following the procedure described in US Patent Application Publication No. 20110189794, to a mixture of methyl 6-aminonicotinate (5.0 g, 33 mmol) in ethanol (140 mL) at 60 °C was added solid sodium bicarbonate (5.52 g, 65.7 mmol), followed by 3- (bromoacetyl)pyridine hydrogen bromide salt (10.16 g, 36.2 mmol). The resulting mixture was heated to reflux for 9 hours. The reaction mixture was then cooled, concentrated, and saturated aqueous sodium bicarbonate solution (50 mL) and dichloromethane (50 mL) were added to the resulting residue. The aqueous phase was extracted with dichloromethane (5 X mL). The combined organic phases were concentrated and purified by column chromatography (silica gel eluted with ethyl acetate) to give the title compound.
Step B: Preparation of 2-(3-pyridinyl)-N-[1-(2,2,2-trifluoroethyl)]imidazo[1,2-a] pyridinecarboxamide A mixture of the ester prepared in Step A (0.4 g, 2.4 mmol) and aqueous NaOH (1 N, 7.1 mL, 7.1 mmol) was stirred in methanol (10 mL) for 2 hours. The reaction mixture was then concentrated under reduced pressure to remove methanol, and the resulting aqueous solution was neutralized with 1N HCl to pH 5 to precipitate the carboxylic acid. The solid carboxylic acid was isolated by filtration, dried, and used directly in the next step without further purification.
A mixture of the carboxylic acid prepared above (0.31 g, 1.30 mmol), EDC-HCl (0.27 g, 1.43 mmol), HOBt-H O (0.22 g, 1.43 mmol), and triethylamine (0.72 mL, 5.2 mmol) in DMF (10 mL) was stirred at 40 °C for 30 minutes. A quarter of the reaction mixture volume was then removed, treated with CF CH NH (0.13 g, 1.3 mmol), and stirred at 40 °C 3 2 2 overnight. The reaction mixture was then concentrated under vacuum to remove DMF, and the residue was purified by column chromatography (silica gel eluted with ethyl acetate:methanol:triethylamine, 8:1:1) to obtain 43.8 mg of the title compound, a compound of this invention.
SYNTHESIS EXAMPLE 5 Preparation of methyl 2-[[2-(3-pyridinyl)-2H-indazolyl]carbonyl]hydrazinecarboxylate (compound 42) Step A: Preparation of 4-nitro-[(3-pyridinylimino)methyl]benzoic acid methyl ester A solution of methyl 3-formylnitrobenzoate (5 g, 25 mmol) and 3-aminopyridine (2.7 g, 30 mmol) in ethanol (4 mL) was heated to reflux overnight. The reaction mixture was then cooled, concentrated under reduced pressure, and the resulting crude solid was purified by silica gel chromatography (eluting with 0-40% ethyl acetate/hexanes) to afford 4.5 g of the title product as an orange solid.
Step B: Preparation of 2-(3-pyridinyl)-2H-indazolecarboxylic acid methyl ester A solution of the product of Step A (4.5 g, 16 mmol) and sodium azide (1.2 g, 19 mmol) in DMF (20 mL) was heated to 90 °C for 16 hours. The reaction mixture was then cooled to room temperature and diluted with water. The resulting two layers were separated, and the aqueous layer was extracted three times with dichloromethane. The combined organic layers were dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The resulting crude solid was purified by silica gel chromatography (0-30% ethyl acetate/hexantes ) to afford 4.0 g of the title product as a yellow solid.
Step C: Preparation of 2-(3-pyridinyl)-2H-indazolecarbonyl chloride The methyl ester prepared in Step B (4.1 g, 16 mmol) was dissolved in methanol (150 mL), 50% sodium hydroxide in water (7.1 mL) was added, and the reaction mixture was heated to reflux for 4 hours. The reaction mixture was then cooled to room temperature, and the solvent was removed under reduced pressure. The crude product was acidified with aqueous 1N HCl, and the resulting precipitate was isolated by filtration, washed with diethyl ether, and dried under reduced pressure at 60 °C overnight. The crude carboxylic acid was then redissolved in thionyl chloride (60 mL), and the reaction mixture was heated to 75 °C.
The reaction mixture was then cooled to room temperature and the solvent was removed under reduced pressure. The crude carbonyl chloride was used in the next step without further purification.
Step D: Preparation of methyl 2-[[2-(3-pyridinyl)-2H-indazol yl]carbonyl]hydrazinecarboxylate The acyl chloride prepared in Step C (200 mg, 0.836 mmol) was combined with hydrazinocarboxylate (82 mg, 0.91 mmol) in dichloromethane (5 mL). The reaction mixture was cooled to 0 °C, and triethylamine (360 µl, 2.51 mmol) was added dropwise. The reaction was warmed to room temperature and allowed stirred overnight. The reaction mixture was then cooled and quenched with saturated aqueous sodium bicarbonate solution.
The two layers were separated, and the aqueous layer was extracted three times with dichloromethane. The combined organic layers were dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The resulting crude solid was purified by silica gel chromatography (20-80% ethyl acetate/hexanes) to yield the title compound, a compound of this invention, as a white solid.
SYNTHESIS EXAMPLE 6 Preparation of 2-(3-pyridinyl)-N-[(tetrahydrofuranyl)methyl]pyrazolo[1,5-a]pyridine carboxamide (compound 467) Step A: Preparation of 3-(dimethoxymethyl)(3-pyridinyl)-1H-pyrazole Lithium hexamethyldisilane (55 mL of a 1.0M solution in tetrahydrofuran, 55 mmoles) was added to a solution of 3-acetylpyridine (5.5 mL, 50 mmoles), methyl dimethoxy acetate (6.7 mL, 55 mmoles) and anhydrous tetrahydrofuran (100 mL) with cooling at -45 °C. The resulting reaction mixture was allowed to warm to 25 °C over 1 hour, and stirred at this temperature for 3 hours. The reaction mixture was then concentrated under reduced pressure, and the residue was suspended in methanol (50 mL) and concentrated under reduced pressure. The resulting residue was suspended in methanol (150 mL) and treated with hydrazine monohydrate (2.62 mL, 55 mmoles) and glacial acetic acid (6.29 mL, 110 mmoles), and the reaction mixture was heated at reflux for 14 hours. The resulting reaction mixture was cooled to 25 °C and concentrated under reduced pressure.
The residue was partitioned between ethyl acetate (200 mL) and 1N aqueous sodium hydroxide solution (100 mL). The layers were separated, and the organic layer was washed successively with 1N aqueous sodium hydroxide solution (50 mL) and brine (50 mL), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to yield 8.83 g of the title compound as a beige solid.
H NMR (CDCl ): δ 10.5 (br s, 1H) 9.03 (d, 1H), 8.57 (dd, 1H), 8.09 (dt, 1H), 7.34 (dd, 1H), 6.65 (s, 1H), 5.63 (s, 1H), 3.39 (s, 6H).
Step B: Preparation of 5-(3-pyridinyl)-1H-pyrazolecarboxaldehyde To a solution of the product from Step A (715 mg, 3.3 mmoles) and chloroform (5 mL) was added a solution of trifluoroacetic acid (2.5 mL) and water (2.5 mL); the reaction mixture temperature was maintained below 5 °C with an ice-water bath. The reaction mixture was then stirred at 0-5 °C for 2 hours, treated with triethylamine (5 mL) at 0 °C, stirred for 15 minutes, treated with water (10 mL), and filtered to isolate a brown solid. This solid was washed with chloroform (20 mL) and water (20 mL), and air dried to yield 605 mg of the title compound as a light beige solid that was used in the next step without further purification.
Step C: Preparation of 2-(3-pyridinyl)pyrazolo[1,5-a]pyridinecarboxylic acid ethyl ester A mixture of the product from Step B (596 mg, 3.4 mmoles), ethylbromocrotonate (75%, 0.95 mL, 5.2 mmoles), anhydrous potassium carbonate (1.42 g, 10.3 mmoles) and anhydrous N,N-dimethylformamide (17 mL) was stirred at 25 °C for 14 hours. The reaction mixture was then partitioned between ethyl acetate and saturated aqueous ammonium chloride solution, and the organic layer was separated, washed with water (3X), brine, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to give a crude product. This resulting product was purified by MPLC on a 24 g silica column eluting with 0 to 100% ethyl acetate in hexanes to give the title compound as a light beige solid (105 mg).
H NMR (CDCl ): δ 9.20 (d, 1H), 8.63 (dd, 1H), 8.50 (d, 1H), 8.33 (d, 1H), 8.27 (dt, 1H), 7.43-7.35 (m, 2H), 7.05 (s, 1H), 4.43 (q, 2H), 1.44 (t, 3H).
Step D: Preparation of 2-(3-pyridinyl)-N-[(tetrahydrofuranyl)methyl]pyrazolo[1,5- a]pyridinecarboxamide To a solution of the product from Step C (31 mg, 0.11 mmoles), tetrahydrofurfurylamine (0.12 mL, 1.2 mmoles), and anhydrous toluene (2.3 mL) was added trimethylaluminum (0.6 mL of a 2.0M solution in toluene, 1.2 mmoles). The resulting solution was stirred for 2 hours at 25 °C, for 2 hours at 80 °C, and then cooled to 0 °C and treated carefully with water (3 mL). The resulting reaction mixture was stirred at 25 °C for minutes, treated with a saturated aqueous solution of sodium-potassium tartrate (2 mL), stirred for 30 minutes, and then partitioned between dichloromethane and water. The organic layer was separated, dried over anhydrous magnesium sulfate, and concentrated under reduced pressure to isolate a brown residue that was triturated with diethyl ether to yield the title compound, a compound of this invention, as a beige solid (15 mg).
H NMR (CDCl ): δ 9.19 (d, 1H), 8.63 (dd, 1H), 8.51 (d, 1H), 8.26 (dt, 1H), 8.03 (s, 1H), 7.39 (dd, 1H), 7.16 (dd, 1H), 7.00 (s, 1H), 6.60 (br s, 1H), 4.10 (qd, 1H), 3.93 (dt, 1H), 3.89-3.76 (m, 2H), 3.38-3.29 (m, 1H), 2.11-2.02 (m, 1H), 2.00-1.83 (m, 3H).
By the procedures described herein together with methods known in the art, the following compounds of Tables 1 to 24d can be prepared. The following abbreviations are used in the Tables which follow: t means tertiary, s means secondary, i means iso, c means cyclo, Me means methyl, Et means ethyl, Pr means propyl, Bu means butyl, Ph means phenyl, OMe means methoxy, OEt means ethoxy, SMe means methylthio, SEt means ethylthio, -CN means cyano, Ph means phenyl, Py means pyridinyl, -NO means nitro, S(O)Me means methylsulfinyl, and S(O) Me means methylsulfonyl.
A "-" at the beginning of a fragment definition denotes the attachment point of said fragment to the remainder of the molecule; for example, "-CH CH OMe" denotes the fragment 2-methoxyethyl. Cyclic fragments are represented by the use of two "-" within parentheses; for example, the fragment 1-pyrrolidinyl is represented by "N(- CH CH CH CH -)", wherein a nitrogen atom is bonded to both terminal carbon atoms of 2 2 2 2 the four-carbon chain, as illustrated below.
TABLE 1a A is CH R R R Me Et Pr i-Pr -CH (c-Pr) -CH(Me)(c-Pr) Bu s-Bu i-Bu t-Bu -CH Ph -CH CH=CH 2 2 2 -CH C≡CH -C(Me) C≡CH -CH CH F 2 2 2 2 -CH CHF -CH CF -CH(Me)CF 2 2 2 3 3 -CH CH CF -CH CF CF -CH CF CH 2 2 3 2 2 3 2 2 3 -CH CH CF CF -CH(i-Pr)CF -CH CH OMe 2 2 2 3 3 2 2 -CH OEt -CH CH O(i-Pr) -CH CH OEt 2 2 2 2 2 -CH CH CH OMe -CH CH(Me)OMe -CH(Et)CH OMe 2 2 2 2 2 -CH(Me)CH OMe -CH CH S(O)Me -CH CH SMe 2 2 2 2 2 -CH CH SEt -CH CH SO Me -CH CH SO Et 2 2 2 2 2 2 2 2 -CH CH S(O)Et -CH CH S(O)(t-Bu) -CH CH S(t-Bu) 2 2 2 2 2 2 -CH(Me)CH SMe -CH CH SO (t-Bu) -CH(Me)CH SO Me 2 2 2 2 2 2 -CH(Me)CH S(O)Me -CH CH S(O)CH CF -CH CH SCH CF 2 2 2 2 3 2 2 2 3 -CH CH SO CH CF -CH CH SO CH CH CF -CH CH SCH CH CF 2 2 2 2 3 2 2 2 2 2 3 2 2 2 2 3 -CH CH S(O)CH CH CF -CH CN -CH CH CN 2 2 2 2 3 2 2 2 -C(Me) CN -CH CH N(i-Pr) -CH CH N(Me) 2 2 2 2 2 2 2 -CH2CH(OMe) c-Pr c-Bu 1-methylcyclopropyl 3-methoxycyclobutyl -CH(Ph)(c-Pr) -CH(Me)(c-Pr) 3-thietanyl 3,3-difluorocyclobutyl 3-oxetanyl -CH (oxiranyl) 3-thietanyl-1,1-dioxide 3-thietanyloxide -CH (CH(-OC(Me) OCH -)) -CH (tetrahydrofuranyl) 2 2 2 2 -CH (2-furanyl) tetrahydrofuranyl -CH (2-thienyl) -CH (CH(-OCH CH O-) -CH CO Me -CH (2,2-difluorocyclopropyl) 2 2 2 2 2 2 -C(-CH CH -)CO Me -CH(Me)CO Et -CH(i-Pr)CO Me 2 2 2 2 2 -CH C(O)NHMe -CH C(O)NMe -CH(Me)C(O)NHMe 2 2 2 -CH(Me)C(O)NH(t-Bu) -OCH (c-Pr) -CH(Me)C(O)NMe -OCH CH=CH -NHC(O)(i-Pr) -NHC(O)Me -NHCO Me -NHC(O)(3-pyridinyl) -NHC(O)(t-Bu) -NHC(O)Ph -NH(c-hexyl) -NHC(O)NH(i-Pr) -NH(c-Pr) -NHC(O)(2-thienyl) -NH(CH CF ) -NHC(O)CF -NHCO Et -NHC(O)(2-furanyl) -C(O)C(O)Me -NHCO CH CF -C(O)CO Me 2 2 3 2 -C(O)(2-pyridinyl) -NHC(O)NMe -NHC(O)NHMe -NHC(O)NHCH CF -NHC(O)CH CH CF -NHC(O)Et 2 3 2 2 3 -NHC(O)CH CF -NHSO CF -NHSO CH CF 2 3 2 3 2 2 3 -NHSO CH CH CF -NH(2-pyridinyl) -NH(3-pyridinyl) 2 2 2 3 -NH(4-pyridinyl) -NH(2-pyrimidinyl) -NH(4-pyrimidinyl) -NH(5-pyrimidinyl) -NH(6-CF pyridinyl) -NH(4-CF pyridinyl) -NH(3-CF pyridinyl) -NH(5-CF pyrimidinyl) -NH(5-CF pyridinyl) 3 3 3 -NH(4-CF pyrimidinyl) -NH(6-methylpyridinyl) -NH(4-methylpyridinyl) -NH(3-methylpyridinyl) -NH(5-methylpyrimidinyl) -NH(5-methylpyridinyl) -NH(4-methylpyrimidinyl) -NH(6-methoxypyridinyl) -NH(4-methoxypyridinyl) -NH(3-methoxypyridinyl) -NH(5-methoxypyrimidinyl) -NH(5-methoxypyridinyl) -NH(4-methoxypyrimidinyl) -CH (6-CF pyridinyl) -CH (4-CF pyridinyl) 2 3 2 3 -CH (3-CF pyridinyl) -CH (5-CF pyrimidinyl) -CH (5-CF pyridinyl) 2 3 2 3 2 3 -CH (4-CF pyrimidinyl) -CH (6-methylpyridinyl) -CH (4-methylpyridinyl) 2 3 2 2 -CH (3-methylpyridinyl) -CH (5-methylpyrimidinyl) -CH (5-methylpyridinyl) 2 2 2 -CH (4-methylpyrimidinyl) -CH (6-methoxypyridinyl) -CH (4-methoxypyridinyl) 2 2 2 -CH (3-methoxypyridinyl) -CH (5-methoxypyrimidinyl) -CH (5-methoxypyridinyl) 2 2 2 -CH (4-methoxypyrimidinyl) -CH (5-pyrimidinyl) -CH (6-bromopyridinyl) 2 2 2 -CH (2-pyrimidinyl) -CH (3-(OCF )phenyl) -CH (2-thiazolyl) 2 2 3 2 -CH (5-methylpyrazinyl) -CH (4-pyridinyl) -CH (2-pyridinyl) 2 2 2 Ph 3-pyridinyl -CH (3-pyridinyl) 2-pyridinyl 2-pyrazinyl -CH CH (2-pyridinyl) 4-pyridinyl 4-CF pyridinyl -CH CH CH (2-pyridinyl) 3 2 2 2 3-CF pyridinyl 4-CF pyrimidinyl 6-CF pyridinyl 3 3 3 -CF pyridinyl 5-CF pyrazinyl 5-CF pyrimidinyl 3 3 3 -CH CH N(-C(O)CH CH C(O)-) -CH CH CH (1-imidazolyl) -CH(-C(O)OCH CH -) 2 2 2 2 2 2 2 2 2 -CH (4-pyrimidinyl) pyridazinyl 6-CF pyrazinyl A is CF R R R Me Et Pr i-Pr -CH (c-Pr) -CH(Me)(c-Pr) Bu s-Bu i-Bu t-Bu -CH Ph -CH CH=CH 2 2 2 -CH C≡CH -C(Me) C≡CH -CH CH F 2 2 2 2 -CH CHF -CH CF -CH(Me)CF 2 2 2 3 3 -CH CH CF -CH CF CF -CH CF CH 2 2 3 2 2 3 2 2 3 -CH CH CF CF -CH(i-Pr)CF -CH CH OMe 2 2 2 3 3 2 2 -CH OEt -CH CH O(i-Pr) -CH CH OEt 2 2 2 2 2 -CH CH CH OMe -CH CH(Me)OMe -CH(Et)CH OMe 2 2 2 2 2 -CH(Me)CH OMe -CH CH S(O)Me -CH CH SMe 2 2 2 2 2 -CH CH SEt -CH CH SO Me -CH CH SO Et 2 2 2 2 2 2 2 2 -CH CH S(O)Et -CH CH S(O)(t-Bu) -CH CH S(t-Bu) 2 2 2 2 2 2 -CH(Me)CH SMe -CH CH SO (t-Bu) -CH(Me)CH SO Me 2 2 2 2 2 2 -CH(Me)CH S(O)Me -CH CH S(O)CH CF -CH CH SCH CF 2 2 2 2 3 2 2 2 3 -CH CH SO CH CF -CH CH SO CH CH CF -CH CH SCH CH CF 2 2 2 2 3 2 2 2 2 2 3 2 2 2 2 3 -CH CH S(O)CH CH CF -CH CN -CH CH CN 2 2 2 2 3 2 2 2 -C(Me) CN -CH CH N(i-Pr) -CH CH N(Me) 2 2 2 2 2 2 2 -CH2CH(OMe) c-Pr c-Bu 1-methylcyclopropyl 3-methoxycyclobutyl -CH(Ph)(c-Pr) -CH(Me)(c-Pr) 3-thietanyl 3,3-difluorocyclobutyl 3-oxetanyl -CH (oxiranyl) 3-thietanyl-1,1-dioxide 3-thietanyloxide -CH (CH(-OC(Me) OCH -)) -CH (tetrahydrofuranyl) 2 2 2 2 -CH (2-furanyl) tetrahydrofuranyl -CH (2-thienyl) -CH (CH(-OCH CH O-) -CH CO Me -CH (2,2-difluorocyclopropyl) 2 2 2 2 2 2 -C(-CH CH -)CO Me -CH(Me)CO Et -CH(i-Pr)CO Me 2 2 2 2 2 -CH C(O)NHMe -CH C(O)NMe -CH(Me)C(O)NHMe 2 2 2 -CH(Me)C(O)NH(t-Bu) -OCH (c-Pr) -CH(Me)C(O)NMe -OCH CH=CH -NHC(O)(i-Pr) -NHC(O)Me -NHCO Me -NHC(O)(3-pyridinyl) -NHC(O)(t-Bu) -NHC(O)Ph -NH(c-hexyl) -NHC(O)NH(i-Pr) -NH(c-Pr) -NHC(O)(2-thienyl) -NH(CH CF ) -NHC(O)CF -NHCO Et -NHC(O)(2-furanyl) -C(O)C(O)Me -NHCO CH CF -C(O)CO Me 2 2 3 2 -C(O)(2-pyridinyl) -NHC(O)NMe -NHC(O)NHMe -NHC(O)NHCH CF -NHC(O)CH CH CF -NHC(O)Et 2 3 2 2 3 -NHC(O)CH CF -NHSO CF -NHSO CH CF 2 3 2 3 2 2 3 -NHSO CH CH CF -NH(2-pyridinyl) -NH(3-pyridinyl) 2 2 2 3 -NH(4-pyridinyl) -NH(2-pyrimidinyl) -NH(4-pyrimidinyl) -NH(5-pyrimidinyl) -NH(6-CF pyridinyl) -NH(4-CF pyridinyl) -NH(3-CF pyridinyl) -NH(5-CF pyrimidinyl) -NH(5-CF pyridinyl) 3 3 3 -NH(4-CF pyrimidinyl) -NH(6-methylpyridinyl) -NH(4-methylpyridinyl) -NH(3-methylpyridinyl) -NH(5-methylpyrimidinyl) -NH(5-methylpyridinyl) -NH(4-methylpyrimidinyl) -NH(6-methoxypyridinyl) -NH(4-methoxypyridinyl) -NH(3-methoxypyridinyl) -NH(5-methoxypyrimidinyl) -NH(5-methoxypyridinyl) -NH(4-methoxypyrimidinyl) -CH (6-CF pyridinyl) -CH (4-CF pyridinyl) 2 3 2 3 -CH (3-CF pyridinyl) -CH (5-CF pyrimidinyl) -CH (5-CF pyridinyl) 2 3 2 3 2 3 -CH (4-CF pyrimidinyl) -CH (6-methylpyridinyl) -CH (4-methylpyridinyl) 2 3 2 2 -CH (3-methylpyridinyl) -CH (5-methylpyrimidinyl) -CH (5-methylpyridinyl) 2 2 2 -CH (4-methylpyrimidinyl) -CH (6-methoxypyridinyl) -CH (4-methoxypyridinyl) 2 2 2 -CH (3-methoxypyridinyl) -CH (5-methoxypyrimidinyl) -CH (5-methoxypyridinyl) 2 2 2 -CH (4-methoxypyrimidinyl) -CH (5-pyrimidinyl) -CH (6-bromopyridinyl) 2 2 2 -CH (2-pyrimidinyl) -CH (3-(OCF )phenyl) -CH (2-thiazolyl) 2 2 3 2 -CH (5-methylpyrazinyl) -CH (4-pyridinyl) -CH (2-pyridinyl) 2 2 2 Ph 3-pyridinyl -CH (3-pyridinyl) 2-pyridinyl 2-pyrazinyl -CH CH (2-pyridinyl) 4-pyridinyl 4-CF pyridinyl -CH CH CH (2-pyridinyl) 3 2 2 2 3-CF pyridinyl 4-CF pyrimidinyl 6-CF pyridinyl 3 3 3 -CF pyridinyl 5-CF pyrazinyl 5-CF pyrimidinyl 3 3 3 -CH CH N(-C(O)CH CH C(O)-) -CH CH CH (1-imidazolyl) -CH(-C(O)OCH CH -) 2 2 2 2 2 2 2 2 2 -CH (4-pyrimidinyl) pyridazinyl 6-CF pyrazinyl A is N R R R Me Et Pr i-Pr -CH (c-Pr) -CH(Me)(c-Pr) Bu s-Bu i-Bu t-Bu -CH Ph -CH CH=CH 2 2 2 -CH C≡CH -C(Me) C≡CH -CH CH F 2 2 2 2 -CH CHF -CH CF -CH(Me)CF 2 2 2 3 3 -CH CH CF -CH CF CF -CH CF CH 2 2 3 2 2 3 2 2 3 -CH CH CF CF -CH(i-Pr)CF -CH CH OMe 2 2 2 3 3 2 2 -CH OEt -CH CH O(i-Pr) -CH CH OEt 2 2 2 2 2 -CH CH CH OMe -CH CH(Me)OMe -CH(Et)CH OMe 2 2 2 2 2 -CH(Me)CH OMe -CH CH S(O)Me -CH CH SMe 2 2 2 2 2 -CH CH SEt -CH CH SO Me -CH CH SO Et 2 2 2 2 2 2 2 2 -CH CH S(O)Et -CH CH S(O)(t-Bu) -CH CH S(t-Bu) 2 2 2 2 2 2 -CH(Me)CH SMe -CH CH SO (t-Bu) -CH(Me)CH SO Me 2 2 2 2 2 2 -CH(Me)CH S(O)Me -CH CH S(O)CH CF -CH CH SCH CF 2 2 2 2 3 2 2 2 3 -CH CH SO CH CF -CH CH SO CH CH CF -CH CH SCH CH CF 2 2 2 2 3 2 2 2 2 2 3 2 2 2 2 3 -CH CH S(O)CH CH CF -CH CN -CH CH CN 2 2 2 2 3 2 2 2 -C(Me) CN -CH CH N(i-Pr) -CH CH N(Me) 2 2 2 2 2 2 2 -CH2CH(OMe) c-Pr c-Bu 1-methylcyclopropyl 3-methoxycyclobutyl -CH(Ph)(c-Pr) -CH(Me)(c-Pr) 3-thietanyl 3,3-difluorocyclobutyl 3-oxetanyl -CH (oxiranyl) 3-thietanyl-1,1-dioxide 3-thietanyloxide -CH (CH(-OC(Me) OCH -)) -CH (tetrahydrofuranyl) 2 2 2 2 -CH (2-furanyl) tetrahydrofuranyl -CH (2-thienyl) -CH (CH(-OCH CH O-) -CH CO Me -CH (2,2-difluorocyclopropyl) 2 2 2 2 2 2 -C(-CH CH -)CO Me -CH(Me)CO Et -CH(i-Pr)CO Me 2 2 2 2 2 -CH C(O)NHMe -CH C(O)NMe -CH(Me)C(O)NHMe 2 2 2 -CH(Me)C(O)NH(t-Bu) -OCH (c-Pr) -CH(Me)C(O)NMe -OCH CH=CH -NHC(O)(i-Pr) -NHC(O)Me -NHCO Me -NHC(O)(3-pyridinyl) -NHC(O)(t-Bu) -NHC(O)Ph -NH(c-hexyl) -NHC(O)NH(i-Pr) -NH(c-Pr) -NHC(O)(2-thienyl) -NH(CH CF ) -NHC(O)CF -NHCO Et -NHC(O)(2-furanyl) -C(O)C(O)Me -NHCO CH CF -C(O)CO Me 2 2 3 2 -C(O)(2-pyridinyl) -NHC(O)NMe -NHC(O)NHMe -NHC(O)NHCH CF -NHC(O)CH CH CF -NHC(O)Et 2 3 2 2 3 -NHC(O)CH CF -NHSO CF -NHSO CH CF 2 3 2 3 2 2 3 -NHSO CH CH CF -NH(2-pyridinyl) -NH(3-pyridinyl) 2 2 2 3 -NH(4-pyridinyl) -NH(2-pyrimidinyl) -NH(4-pyrimidinyl) -NH(5-pyrimidinyl) -NH(6-CF pyridinyl) -NH(4-CF pyridinyl) -NH(3-CF pyridinyl) -NH(5-CF pyrimidinyl) -NH(5-CF pyridinyl) 3 3 3 -NH(4-CF pyrimidinyl) -NH(6-methylpyridinyl) -NH(4-methylpyridinyl) -NH(3-methylpyridinyl) -NH(5-methylpyrimidinyl) -NH(5-methylpyridinyl) -NH(4-methylpyrimidinyl) -NH(6-methoxypyridinyl) -NH(4-methoxypyridinyl) -NH(3-methoxypyridinyl) -NH(5-methoxypyrimidinyl) -NH(5-methoxypyridinyl) -NH(4-methoxypyrimidinyl) -CH (6-CF pyridinyl) -CH (4-CF pyridinyl) 2 3 2 3 -CH (3-CF pyridinyl) -CH (5-CF pyrimidinyl) -CH (5-CF pyridinyl) 2 3 2 3 2 3 -CH (4-CF pyrimidinyl) -CH (6-methylpyridinyl) -CH (4-methylpyridinyl) 2 3 2 2 -CH (3-methylpyridinyl) -CH (5-methylpyrimidinyl) -CH (5-methylpyridinyl) 2 2 2 -CH (4-methylpyrimidinyl) -CH (6-methoxypyridinyl) -CH (4-methoxypyridinyl) 2 2 2 -CH (3-methoxypyridinyl) -CH (5-methoxypyrimidinyl) -CH (5-methoxypyridinyl) 2 2 2 -CH (4-methoxypyrimidinyl) -CH (5-pyrimidinyl) -CH (6-bromopyridinyl) 2 2 2 -CH (2-pyrimidinyl) -CH (3-(OCF )phenyl) -CH (2-thiazolyl) 2 2 3 2 -CH (5-methylpyrazinyl) -CH (4-pyridinyl) -CH (2-pyridinyl) 2 2 2 Ph 3-pyridinyl -CH (3-pyridinyl) 2-pyridinyl 2-pyrazinyl -CH CH (2-pyridinyl) 4-pyridinyl 4-CF pyridinyl -CH CH CH (2-pyridinyl) 3 2 2 2 3-CF pyridinyl 4-CF pyrimidinyl 6-CF pyridinyl 3 3 3 -CF pyridinyl 5-CF pyrazinyl 5-CF pyrimidinyl 3 3 3 -CH CH N(-C(O)CH CH C(O)-) -CH CH CH (1-imidazolyl) -CH(-C(O)OCH CH -) 2 2 2 2 2 2 2 2 2 -CH (4-pyrimidinyl) pyridazinyl 6-CF pyrazinyl TABLE 1b A is CH R R R Me Et Pr i-Pr -CH (c-Pr) -CH(Me)(c-Pr) Bu s-Bu i-Bu t-Bu -CH Ph -CH CH=CH 2 2 2 -CH C≡CH -C(Me) C≡CH -CH CH F 2 2 2 2 -CH CHF -CH CF -CH(Me)CF 2 2 2 3 3 -CH CH CF -CH CF CF -CH CF CH 2 2 3 2 2 3 2 2 3 -CH CH CF CF -CH(i-Pr)CF -CH CH OMe 2 2 2 3 3 2 2 -CH OEt -CH CH O(i-Pr) -CH CH OEt 2 2 2 2 2 -CH CH CH OMe -CH CH(Me)OMe -CH(Et)CH OMe 2 2 2 2 2 -CH(Me)CH OMe -CH CH S(O)Me -CH CH SMe 2 2 2 2 2 -CH CH SEt -CH CH SO Me -CH CH SO Et 2 2 2 2 2 2 2 2 -CH CH S(O)Et -CH CH S(O)(t-Bu) -CH CH S(t-Bu) 2 2 2 2 2 2 -CH(Me)CH SMe -CH CH SO (t-Bu) -CH(Me)CH SO Me 2 2 2 2 2 2 -CH(Me)CH S(O)Me -CH CH S(O)CH CF -CH CH SCH CF 2 2 2 2 3 2 2 2 3 -CH CH SO CH CF -CH CH SO CH CH CF -CH CH SCH CH CF 2 2 2 2 3 2 2 2 2 2 3 2 2 2 2 3 -CH CH S(O)CH CH CF -CH CN -CH CH CN 2 2 2 2 3 2 2 2 -C(Me) CN -CH CH N(i-Pr) -CH CH N(Me) 2 2 2 2 2 2 2 -CH2CH(OMe) c-Pr c-Bu 1-methylcyclopropyl 3-methoxycyclobutyl -CH(Ph)(c-Pr) -CH(Me)(c-Pr) 3-thietanyl 3,3-difluorocyclobutyl 3-oxetanyl -CH (oxiranyl) 3-thietanyl-1,1-dioxide 3-thietanyloxide -CH (CH(-OC(Me) OCH -)) -CH (tetrahydrofuranyl) 2 2 2 2 -CH (2-furanyl) tetrahydrofuranyl -CH (2-thienyl) -CH (CH(-OCH CH O-) -CH CO Me -CH (2,2-difluorocyclopropyl) 2 2 2 2 2 2 -C(-CH CH -)CO Me -CH(Me)CO Et -CH(i-Pr)CO Me 2 2 2 2 2 -CH C(O)NHMe -CH C(O)NMe -CH(Me)C(O)NHMe 2 2 2 -CH(Me)C(O)NH(t-Bu) -OCH (c-Pr) -CH(Me)C(O)NMe -OCH CH=CH -NHC(O)(i-Pr) -NHC(O)Me -NHCO Me -NHC(O)(3-pyridinyl) -NHC(O)(t-Bu) -NHC(O)Ph -NH(c-hexyl) -NHC(O)NH(i-Pr) -NH(c-Pr) -NHC(O)(2-thienyl) -NH(CH CF ) -NHC(O)CF -NHCO Et -NHC(O)(2-furanyl) -C(O)C(O)Me -NHCO CH CF -C(O)CO Me 2 2 3 2 -C(O)(2-pyridinyl) -NHC(O)NMe -NHC(O)NHMe -NHC(O)NHCH CF -NHC(O)CH CH CF -NHC(O)Et 2 3 2 2 3 -NHC(O)CH CF -NHSO CF -NHSO CH CF 2 3 2 3 2 2 3 -NHSO CH CH CF -NH(2-pyridinyl) -NH(3-pyridinyl) 2 2 2 3 -NH(4-pyridinyl) -NH(2-pyrimidinyl) -NH(4-pyrimidinyl) -NH(5-pyrimidinyl) -NH(6-CF pyridinyl) -NH(4-CF pyridinyl) -NH(3-CF pyridinyl) -NH(5-CF pyrimidinyl) -NH(5-CF pyridinyl) 3 3 3 -NH(4-CF pyrimidinyl) -NH(6-methylpyridinyl) -NH(4-methylpyridinyl) -NH(3-methylpyridinyl) -NH(5-methylpyrimidinyl) -NH(5-methylpyridinyl) -NH(4-methylpyrimidinyl) -NH(6-methoxypyridinyl) -NH(4-methoxypyridinyl) -NH(3-methoxypyridinyl) -NH(5-methoxypyrimidinyl) -NH(5-methoxypyridinyl) -NH(4-methoxypyrimidinyl) -CH (6-CF pyridinyl) -CH (4-CF pyridinyl) 2 3 2 3 -CH (3-CF pyridinyl) -CH (5-CF pyrimidinyl) -CH (5-CF pyridinyl) 2 3 2 3 2 3 -CH (4-CF pyrimidinyl) -CH (6-methylpyridinyl) -CH (4-methylpyridinyl) 2 3 2 2 -CH (3-methylpyridinyl) -CH (5-methylpyrimidinyl) -CH (5-methylpyridinyl) 2 2 2 -CH (4-methylpyrimidinyl) -CH (6-methoxypyridinyl) -CH (4-methoxypyridinyl) 2 2 2 -CH (3-methoxypyridinyl) -CH (5-methoxypyrimidinyl) -CH (5-methoxypyridinyl) 2 2 2 -CH (4-methoxypyrimidinyl) -CH (5-pyrimidinyl) -CH (6-bromopyridinyl) 2 2 2 -CH (2-pyrimidinyl) -CH (3-(OCF )phenyl) -CH (2-thiazolyl) 2 2 3 2 -CH (5-methylpyrazinyl) -CH (4-pyridinyl) -CH (2-pyridinyl) 2 2 2 Ph 3-pyridinyl -CH (3-pyridinyl) 2-pyridinyl 2-pyrazinyl -CH CH (2-pyridinyl) 4-pyridinyl 4-CF pyridinyl -CH CH CH (2-pyridinyl) 3 2 2 2 3-CF pyridinyl 4-CF pyrimidinyl 6-CF pyridinyl 3 3 3 -CF pyridinyl 5-CF pyrazinyl 5-CF pyrimidinyl 3 3 3 -CH CH N(-C(O)CH CH C(O)-) -CH CH CH (1-imidazolyl) -CH(-C(O)OCH CH -) 2 2 2 2 2 2 2 2 2 -CH (4-pyrimidinyl) pyridazinyl 6-CF pyrazinyl A is CF R R R Me Et Pr i-Pr -CH (c-Pr) -CH(Me)(c-Pr) Bu s-Bu i-Bu t-Bu -CH Ph -CH CH=CH 2 2 2 -CH C≡CH -C(Me) C≡CH -CH CH F 2 2 2 2 -CH CHF -CH CF -CH(Me)CF 2 2 2 3 3 -CH CH CF -CH CF CF -CH CF CH 2 2 3 2 2 3 2 2 3 -CH CH CF CF -CH(i-Pr)CF -CH CH OMe 2 2 2 3 3 2 2 -CH OEt -CH CH O(i-Pr) -CH CH OEt 2 2 2 2 2 -CH CH CH OMe -CH CH(Me)OMe -CH(Et)CH OMe 2 2 2 2 2 -CH(Me)CH OMe -CH CH S(O)Me -CH CH SMe 2 2 2 2 2 -CH CH SEt -CH CH SO Me -CH CH SO Et 2 2 2 2 2 2 2 2 -CH CH S(O)Et -CH CH S(O)(t-Bu) -CH CH S(t-Bu) 2 2 2 2 2 2 -CH(Me)CH SMe -CH CH SO (t-Bu) -CH(Me)CH SO Me 2 2 2 2 2 2 -CH(Me)CH S(O)Me -CH CH S(O)CH CF -CH CH SCH CF 2 2 2 2 3 2 2 2 3 -CH CH SO CH CF -CH CH SO CH CH CF -CH CH SCH CH CF 2 2 2 2 3 2 2 2 2 2 3 2 2 2 2 3 -CH CH S(O)CH CH CF -CH CN -CH CH CN 2 2 2 2 3 2 2 2 -C(Me) CN -CH CH N(i-Pr) -CH CH N(Me) 2 2 2 2 2 2 2 -CH2CH(OMe) c-Pr c-Bu 1-methylcyclopropyl 3-methoxycyclobutyl -CH(Ph)(c-Pr) -CH(Me)(c-Pr) 3-thietanyl 3,3-difluorocyclobutyl 3-oxetanyl -CH (oxiranyl) 3-thietanyl-1,1-dioxide 3-thietanyloxide -CH (CH(-OC(Me) OCH -)) -CH (tetrahydrofuranyl) 2 2 2 2 -CH (2-furanyl) tetrahydrofuranyl -CH (2-thienyl) -CH (CH(-OCH CH O-) -CH CO Me -CH (2,2-difluorocyclopropyl) 2 2 2 2 2 2 -C(-CH CH -)CO Me -CH(Me)CO Et -CH(i-Pr)CO Me 2 2 2 2 2 -CH C(O)NHMe -CH C(O)NMe -CH(Me)C(O)NHMe 2 2 2 -CH(Me)C(O)NH(t-Bu) -OCH (c-Pr) -CH(Me)C(O)NMe -OCH CH=CH -NHC(O)(i-Pr) -NHC(O)Me -NHCO Me -NHC(O)(3-pyridinyl) -NHC(O)(t-Bu) -NHC(O)Ph -NH(c-hexyl) -NHC(O)NH(i-Pr) -NH(c-Pr) -NHC(O)(2-thienyl) -NH(CH CF ) -NHC(O)CF -NHCO Et -NHC(O)(2-furanyl) -C(O)C(O)Me -NHCO CH CF -C(O)CO Me 2 2 3 2 -C(O)(2-pyridinyl) -NHC(O)NMe -NHC(O)NHMe -NHC(O)NHCH CF -NHC(O)CH CH CF -NHC(O)Et 2 3 2 2 3 -NHC(O)CH CF -NHSO CF -NHSO CH CF 2 3 2 3 2 2 3 -NHSO CH CH CF -NH(2-pyridinyl) -NH(3-pyridinyl) 2 2 2 3 -NH(4-pyridinyl) -NH(2-pyrimidinyl) -NH(4-pyrimidinyl) -NH(5-pyrimidinyl) -NH(6-CF pyridinyl) -NH(4-CF pyridinyl) -NH(3-CF pyridinyl) -NH(5-CF pyrimidinyl) -NH(5-CF pyridinyl) 3 3 3 -NH(4-CF pyrimidinyl) -NH(6-methylpyridinyl) -NH(4-methylpyridinyl) -NH(3-methylpyridinyl) -NH(5-methylpyrimidinyl) -NH(5-methylpyridinyl) -NH(4-methylpyrimidinyl) -NH(6-methoxypyridinyl) -NH(4-methoxypyridinyl) -NH(3-methoxypyridinyl) -NH(5-methoxypyrimidinyl) -NH(5-methoxypyridinyl) -NH(4-methoxypyrimidinyl) -CH (6-CF pyridinyl) -CH (4-CF pyridinyl) 2 3 2 3 -CH (3-CF pyridinyl) -CH (5-CF pyrimidinyl) -CH (5-CF pyridinyl) 2 3 2 3 2 3 -CH (4-CF pyrimidinyl) -CH (6-methylpyridinyl) -CH (4-methylpyridinyl) 2 3 2 2 -CH (3-methylpyridinyl) -CH (5-methylpyrimidinyl) -CH (5-methylpyridinyl) 2 2 2 -CH (4-methylpyrimidinyl) -CH (6-methoxypyridinyl) -CH (4-methoxypyridinyl) 2 2 2 -CH (3-methoxypyridinyl) -CH (5-methoxypyrimidinyl) -CH (5-methoxypyridinyl) 2 2 2 -CH (4-methoxypyrimidinyl) -CH (5-pyrimidinyl) -CH (6-bromopyridinyl) 2 2 2 -CH (2-pyrimidinyl) -CH (3-(OCF )phenyl) -CH (2-thiazolyl) 2 2 3 2 -CH (5-methylpyrazinyl) -CH (4-pyridinyl) -CH (2-pyridinyl) 2 2 2 Ph 3-pyridinyl -CH (3-pyridinyl) 2-pyridinyl 2-pyrazinyl -CH CH (2-pyridinyl) 4-pyridinyl 4-CF pyridinyl -CH CH CH (2-pyridinyl) 3 2 2 2 3-CF pyridinyl 4-CF pyrimidinyl 6-CF pyridinyl 3 3 3 -CF pyridinyl 5-CF pyrazinyl 5-CF pyrimidinyl 3 3 3 -CH CH N(-C(O)CH CH C(O)-) -CH CH CH (1-imidazolyl) -CH(-C(O)OCH CH -) 2 2 2 2 2 2 2 2 2 -CH (4-pyrimidinyl) pyridazinyl 6-CF pyrazinyl A is N R R R Me Et Pr i-Pr -CH (c-Pr) -CH(Me)(c-Pr) Bu s-Bu i-Bu t-Bu -CH Ph -CH CH=CH 2 2 2 -CH C≡CH -C(Me) C≡CH -CH CH F 2 2 2 2 -CH CHF -CH CF -CH(Me)CF 2 2 2 3 3 -CH CH CF -CH CF CF -CH CF CH 2 2 3 2 2 3 2 2 3 -CH CH CF CF -CH(i-Pr)CF -CH CH OMe 2 2 2 3 3 2 2 -CH OEt -CH CH O(i-Pr) -CH CH OEt 2 2 2 2 2 -CH CH CH OMe -CH CH(Me)OMe -CH(Et)CH OMe 2 2 2 2 2 -CH(Me)CH OMe -CH CH S(O)Me -CH CH SMe 2 2 2 2 2 -CH CH SEt -CH CH SO Me -CH CH SO Et 2 2 2 2 2 2 2 2 -CH CH S(O)Et -CH CH S(O)(t-Bu) -CH CH S(t-Bu) 2 2 2 2 2 2 -CH(Me)CH SMe -CH CH SO (t-Bu) -CH(Me)CH SO Me 2 2 2 2 2 2 -CH(Me)CH S(O)Me -CH CH S(O)CH CF -CH CH SCH CF 2 2 2 2 3 2 2 2 3 -CH CH SO CH CF -CH CH SO CH CH CF -CH CH SCH CH CF 2 2 2 2 3 2 2 2 2 2 3 2 2 2 2 3 -CH CH S(O)CH CH CF -CH CN -CH CH CN 2 2 2 2 3 2 2 2 -C(Me) CN -CH CH N(i-Pr) -CH CH N(Me) 2 2 2 2 2 2 2 -CH2CH(OMe) c-Pr c-Bu 1-methylcyclopropyl 3-methoxycyclobutyl -CH(Ph)(c-Pr) -CH(Me)(c-Pr) 3-thietanyl 3,3-difluorocyclobutyl 3-oxetanyl -CH (oxiranyl) 3-thietanyl-1,1-dioxide 3-thietanyloxide -CH (CH(-OC(Me) OCH -)) -CH (tetrahydrofuranyl) 2 2 2 2 -CH (2-furanyl) tetrahydrofuranyl -CH (2-thienyl) -CH (CH(-OCH CH O-) -CH CO Me -CH (2,2-difluorocyclopropyl) 2 2 2 2 2 2 -C(-CH CH -)CO Me -CH(Me)CO Et -CH(i-Pr)CO Me 2 2 2 2 2 -CH C(O)NHMe -CH C(O)NMe -CH(Me)C(O)NHMe 2 2 2 -CH(Me)C(O)NH(t-Bu) -OCH (c-Pr) -CH(Me)C(O)NMe -OCH CH=CH -NHC(O)(i-Pr) -NHC(O)Me -NHCO Me -NHC(O)(3-pyridinyl) -NHC(O)(t-Bu) -NHC(O)Ph -NH(c-hexyl) -NHC(O)NH(i-Pr) -NH(c-Pr) -NHC(O)(2-thienyl) -NH(CH CF ) -NHC(O)CF -NHCO Et -NHC(O)(2-furanyl) -C(O)C(O)Me -NHCO CH CF -C(O)CO Me 2 2 3 2 -C(O)(2-pyridinyl) -NHC(O)NMe -NHC(O)NHMe -NHC(O)NHCH CF -NHC(O)CH CH CF -NHC(O)Et 2 3 2 2 3 -NHC(O)CH CF -NHSO CF -NHSO CH CF 2 3 2 3 2 2 3 -NHSO CH CH CF -NH(2-pyridinyl) -NH(3-pyridinyl) 2 2 2 3 -NH(4-pyridinyl) -NH(2-pyrimidinyl) -NH(4-pyrimidinyl) -NH(5-pyrimidinyl) -NH(6-CF pyridinyl) -NH(4-CF pyridinyl) -NH(3-CF pyridinyl) -NH(5-CF pyrimidinyl) -NH(5-CF pyridinyl) 3 3 3 -NH(4-CF pyrimidinyl) -NH(6-methylpyridinyl) -NH(4-methylpyridinyl) -NH(3-methylpyridinyl) -NH(5-methylpyrimidinyl) -NH(5-methylpyridinyl) -NH(4-methylpyrimidinyl) -NH(6-methoxypyridinyl) -NH(4-methoxypyridinyl) -NH(3-methoxypyridinyl) -NH(5-methoxypyrimidinyl) -NH(5-methoxypyridinyl) -NH(4-methoxypyrimidinyl) -CH (6-CF pyridinyl) -CH (4-CF pyridinyl) 2 3 2 3 -CH (3-CF pyridinyl) -CH (5-CF pyrimidinyl) -CH (5-CF pyridinyl) 2 3 2 3 2 3 -CH (4-CF pyrimidinyl) -CH (6-methylpyridinyl) -CH (4-methylpyridinyl) 2 3 2 2 -CH (3-methylpyridinyl) -CH (5-methylpyrimidinyl) -CH (5-methylpyridinyl) 2 2 2 -CH (4-methylpyrimidinyl) -CH (6-methoxypyridinyl) -CH (4-methoxypyridinyl) 2 2 2 -CH (3-methoxypyridinyl) -CH (5-methoxypyrimidinyl) -CH (5-methoxypyridinyl) 2 2 2 -CH (4-methoxypyrimidinyl) -CH (5-pyrimidinyl) -CH (6-bromopyridinyl) 2 2 2 -CH (2-pyrimidinyl) -CH (3-(OCF )phenyl) -CH (2-thiazolyl) 2 2 3 2 -CH (5-methylpyrazinyl) -CH (4-pyridinyl) -CH (2-pyridinyl) 2 2 2 Ph 3-pyridinyl -CH (3-pyridinyl) 2-pyridinyl 2-pyrazinyl -CH CH (2-pyridinyl) 4-pyridinyl 4-CF pyridinyl -CH CH CH (2-pyridinyl) 3 2 2 2 3-CF pyridinyl 4-CF pyrimidinyl 6-CF pyridinyl 3 3 3 -CF pyridinyl 5-CF pyrazinyl 5-CF pyrimidinyl 3 3 3 -CH CH N(-C(O)CH CH C(O)-) -CH CH CH (1-imidazolyl) -CH(-C(O)OCH CH -) 2 2 2 2 2 2 2 2 2 -CH (4-pyrimidinyl) pyridazinyl 6-CF pyrazinyl TABLE 1c A is CH N(-CH CH CH -) N(-CH CH(OMe)CH -) 2 2 2 2 2 N(-CH CH CF CH CH -) N(-CH CH CH CF CH -) 2 2 2 2 2 2 2 2 2 2 N(-CH CH CH CH -) N(-CH CH SCH CH -) 2 2 2 2 2 2 2 2 N(-CH CH CH CH CH -) N(-CH CH OCH CH -) 2 2 2 2 2 2 2 2 2 N(-CH CH N(C(O)(c-Pr))CH CH -) N(-CH CH N(Me)CH CH -) 2 2 2 2 2 2 2 2 N(-CH C(Me) N=CH-) N(-CH CH CH CH(CF )CH -) 2 2 2 2 2 3 2 N(CH C≡CH) N(Et) 2 2 2 N(Pr)CH (c-Pr) N(Et)(c-hexyl) N(-CHC(O)SCH CH -) A is CF N(-CH CH CH -) N(-CH CH(OMe)CH -) 2 2 2 2 2 N(-CH CH CF CH CH -) N(-CH CH CH CF CH -) 2 2 2 2 2 2 2 2 2 2 N(-CH CH CH CH -) N(-CH CH SCH CH -) 2 2 2 2 2 2 2 2 N(-CH CH CH CH CH -) N(-CH CH OCH CH -) 2 2 2 2 2 2 2 2 2 N(-CH CH N(C(O)(c-Pr))CH CH -) N(-CH CH N(Me)CH CH -) 2 2 2 2 2 2 2 2 N(-CH C(Me) N=CH-) N(-CH CH CH CH(CF )CH -) 2 2 2 2 2 3 2 N(CH C≡CH) N(Et) 2 2 2 N(Pr)CH (c-Pr) N(Et)(c-hexyl) N(-CHC(O)SCH CH -) A is N N(-CH CH CH -) N(-CH CH(OMe)CH -) 2 2 2 2 2 N(-CH CH CF CH CH -) N(-CH CH CH CF CH -) 2 2 2 2 2 2 2 2 2 2 N(-CH CH CH CH -) N(-CH CH SCH CH -) 2 2 2 2 2 2 2 2 N(-CH CH CH CH CH -) N(-CH CH OCH CH -) 2 2 2 2 2 2 2 2 2 N(-CH CH N(C(O)(c-Pr))CH CH -) N(-CH CH N(Me)CH CH -) 2 2 2 2 2 2 2 2 N(-CH C(Me) N=CH-) N(-CH CH CH CH(CF )CH -) 2 2 2 2 2 3 2 N(CH C≡CH) N(Et) 2 2 2 N(Pr)CH (c-Pr) N(Et)(c-hexyl) N(-CHC(O)SCH CH -) TABLE 1d A is CH N(-CH CH CH -) N(-CH CH(OMe)CH -) 2 2 2 2 2 N(-CH CH CF CH CH -) N(-CH CH CH CF CH -) 2 2 2 2 2 2 2 2 2 2 N(-CH CH CH CH -) N(-CH CH SCH CH -) 2 2 2 2 2 2 2 2 N(-CH CH CH CH CH -) N(-CH CH OCH CH -) 2 2 2 2 2 2 2 2 2 N(-CH CH N(C(O)(c-Pr))CH CH -) N(-CH CH N(Me)CH CH -) 2 2 2 2 2 2 2 2 N(-CH C(Me) N=CH-) N(-CH CH CH CH(CF )CH -) 2 2 2 2 2 3 2 N(CH C≡CH) N(Et) 2 2 2 N(Pr)CH (c-Pr) N(Et)(c-hexyl) N(-CHC(O)SCH CH -) A is CF N(-CH CH CH -) N(-CH CH(OMe)CH -) 2 2 2 2 2 N(-CH CH CF CH CH -) N(-CH CH CH CF CH -) 2 2 2 2 2 2 2 2 2 2 N(-CH CH CH CH -) N(-CH CH SCH CH -) 2 2 2 2 2 2 2 2 N(-CH CH CH CH CH -) N(-CH CH OCH CH -) 2 2 2 2 2 2 2 2 2 N(-CH CH N(C(O)(c-Pr))CH CH -) N(-CH CH N(Me)CH CH -) 2 2 2 2 2 2 2 2 N(-CH C(Me) N=CH-) N(-CH CH CH CH(CF )CH -) 2 2 2 2 2 3 2 N(CH C≡CH) N(Et) 2 2 2 N(Pr)CH (c-Pr) N(Et)(c-hexyl) N(-CHC(O)SCH CH -) A is N N(-CH CH CH -) N(-CH CH(OMe)CH -) 2 2 2 2 2 N(-CH CH CF CH CH -) N(-CH CH CH CF CH -) 2 2 2 2 2 2 2 2 2 2 N(-CH CH CH CH -) N(-CH CH SCH CH -) 2 2 2 2 2 2 2 2 N(-CH CH CH CH CH -) N(-CH CH OCH CH -) 2 2 2 2 2 2 2 2 2 N(-CH CH N(C(O)(c-Pr))CH CH -) N(-CH CH N(Me)CH CH -) 2 2 2 2 2 2 2 2 N(-CH C(Me) N=CH-) N(-CH CH CH CH(CF )CH -) 2 2 2 2 2 3 2 N(CH C≡CH) N(Et) 2 2 2 N(Pr)CH (c-Pr) N(Et)(c-hexyl) N(-CHC(O)SCH CH -) TABLE 1e A is CH 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 3-methylpyrazinyl 3-methoxypyrazinyl 3-(trifluoromethyl)pyrazinyl 3-(CH(=NOMe))pyrazinyl -methylpyrazinyl 5-methoxypyrazinyl -(trifluoromethyl)pyrazinyl 5-(CH(=NOMe))pyrazinyl 6-methylpyrazinyl 6-methoxypyrazinyl 6-(trifluoromethyl)pyrazinyl 6-(CH(=NOMe))pyrazinyl 4-methylpyrimidinyl 4-methoxypyrimidinyl 4-(trifluoromethyl)pyrimidinyl 4-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 2-methylpyrimidinyl 2-methoxypyrimidinyl 2-(trifluoromethyl)pyrimidinyl 2-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 6-methylpyrimidinyl 6-methoxypyrimidinyl 6-(trifluoromethyl)pyrimidinyl 6-(CH(=NOMe))pyrimidinyl 3-methylpyrazolyl 3-methoxypyrazolyl 3-(trifluoromethyl)pyrazolyl 3-(CH(=NOMe))pyrazolyl 4-methylpyrazolyl 4-methoxypyrazolyl 4-(trifluoromethyl)pyrazolyl 4-(CH(=NOMe))pyrazolyl -methylpyrazolyl 5-methoxypyrazolyl -(trifluoromethyl)pyrazolyl 5-(CH(=NOMe))pyrazolyl 4-methyl-1,2,3-triazinyl 4-methoxy-1,2,3-triazinyl 4-(trifluoromethyl)-1,2,3-triazinyl 4-(CH(=NOMe))-1,2,3-triazinyl 6-(2-pyrimidinyl)pyridinyl 2-(2-pyridinyl)thiazolyl 2-(2-thiazolyl)thiazolyl 2-(2-pyrimidinyl)ethynyl 1,3,4-oxadiazolyl tetrahydrofuranyl tetrahydrofuranyl 4,5-dihydroisoxazolyl 3-isoxazolyl phenyl 2-(trifluoromethyl)phenyl 3-(trifluoromethyl)phenyl 4-(trifluoromethyl)phenyl 6-(trifluoromethyl)pyrazinyl A is CF 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 3-methylpyrazinyl 3-methoxypyrazinyl 3-(trifluoromethyl)pyrazinyl 3-(CH(=NOMe))pyrazinyl -methylpyrazinyl 5-methoxypyrazinyl -(trifluoromethyl)pyrazinyl 5-(CH(=NOMe))pyrazinyl 6-methylpyrazinyl 6-methoxypyrazinyl 6-(trifluoromethyl)pyrazinyl 6-(CH(=NOMe))pyrazinyl 4-methylpyrimidinyl 4-methoxypyrimidinyl 4-(trifluoromethyl)pyrimidinyl 4-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 2-methylpyrimidinyl 2-methoxypyrimidinyl 2-(trifluoromethyl)pyrimidinyl 2-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 6-methylpyrimidinyl 6-methoxypyrimidinyl 6-(trifluoromethyl)pyrimidinyl 6-(CH(=NOMe))pyrimidinyl 3-methylpyrazolyl 3-methoxypyrazolyl 3-(trifluoromethyl)pyrazolyl 3-(CH(=NOMe))pyrazolyl 4-methylpyrazolyl 4-methoxypyrazolyl 4-(trifluoromethyl)pyrazolyl 4-(CH(=NOMe))pyrazolyl -methylpyrazolyl 5-methoxypyrazolyl -(trifluoromethyl)pyrazolyl 5-(CH(=NOMe))pyrazolyl 4-methyl-1,2,3-triazinyl 4-methoxy-1,2,3-triazinyl 4-(trifluoromethyl)-1,2,3-triazinyl 4-(CH(=NOMe))-1,2,3-triazinyl 6-(2-pyrimidinyl)pyridinyl 2-(2-pyridinyl)thiazolyl 2-(2-thiazolyl)thiazolyl 2-(2-pyrimidinyl)ethynyl 1,3,4-oxadiazolyl tetrahydrofuranyl tetrahydrofuranyl 4,5-dihydroisoxazolyl 3-isoxazolyl phenyl 2-(trifluoromethyl)phenyl 3-(trifluoromethyl)phenyl 4-(trifluoromethyl)phenyl 6-(trifluoromethyl)pyrazinyl A is N 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 3-methylpyrazinyl 3-methoxypyrazinyl 3-(trifluoromethyl)pyrazinyl 3-(CH(=NOMe))pyrazinyl -methylpyrazinyl 5-methoxypyrazinyl -(trifluoromethyl)pyrazinyl 5-(CH(=NOMe))pyrazinyl 6-methylpyrazinyl 6-methoxypyrazinyl 6-(trifluoromethyl)pyrazinyl 6-(CH(=NOMe))pyrazinyl 4-methylpyrimidinyl 4-methoxypyrimidinyl 4-(trifluoromethyl)pyrimidinyl 4-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 2-methylpyrimidinyl 2-methoxypyrimidinyl 2-(trifluoromethyl)pyrimidinyl 2-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 6-methylpyrimidinyl 6-methoxypyrimidinyl 6-(trifluoromethyl)pyrimidinyl 6-(CH(=NOMe))pyrimidinyl 3-methylpyrazolyl 3-methoxypyrazolyl 3-(trifluoromethyl)pyrazolyl 3-(CH(=NOMe))pyrazolyl 4-methylpyrazolyl 4-methoxypyrazolyl 4-(trifluoromethyl)pyrazolyl 4-(CH(=NOMe))pyrazolyl -methylpyrazolyl 5-methoxypyrazolyl -(trifluoromethyl)pyrazolyl 5-(CH(=NOMe))pyrazolyl 4-methyl-1,2,3-triazinyl 4-methoxy-1,2,3-triazinyl 4-(trifluoromethyl)-1,2,3-triazinyl 4-(CH(=NOMe))-1,2,3-triazinyl 6-(2-pyrimidinyl)pyridinyl 2-(2-pyridinyl)thiazolyl 2-(2-thiazolyl)thiazolyl 2-(2-pyrimidinyl)ethynyl 1,3,4-oxadiazolyl tetrahydrofuranyl tetrahydrofuranyl 4,5-dihydroisoxazolyl 3-isoxazolyl phenyl 2-(trifluoromethyl)phenyl 3-(trifluoromethyl)phenyl 4-(trifluoromethyl)phenyl 6-(trifluoromethyl)pyrazinyl TABLE 1f A is CH 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 3-methylpyrazinyl 3-methoxypyrazinyl 3-(trifluoromethyl)pyrazinyl 3-(CH(=NOMe))pyrazinyl -methylpyrazinyl 5-methoxypyrazinyl -(trifluoromethyl)pyrazinyl 5-(CH(=NOMe))pyrazinyl 6-methylpyrazinyl 6-methoxypyrazinyl 6-(trifluoromethyl)pyrazinyl 6-(CH(=NOMe))pyrazinyl 4-methylpyrimidinyl 4-methoxypyrimidinyl 4-(trifluoromethyl)pyrimidinyl 4-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 2-methylpyrimidinyl 2-methoxypyrimidinyl 2-(trifluoromethyl)pyrimidinyl 2-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 6-methylpyrimidinyl 6-methoxypyrimidinyl 6-(trifluoromethyl)pyrimidinyl 6-(CH(=NOMe))pyrimidinyl 3-methylpyrazolyl 3-methoxypyrazolyl 3-(trifluoromethyl)pyrazolyl 3-(CH(=NOMe))pyrazolyl 4-methylpyrazolyl 4-methoxypyrazolyl 4-(trifluoromethyl)pyrazolyl 4-(CH(=NOMe))pyrazolyl -methylpyrazolyl 5-methoxypyrazolyl -(trifluoromethyl)pyrazolyl 5-(CH(=NOMe))pyrazolyl 4-methyl-1,2,3-triazinyl 4-methoxy-1,2,3-triazinyl 4-(trifluoromethyl)-1,2,3-triazinyl 4-(CH(=NOMe))-1,2,3-triazinyl 6-(2-pyrimidinyl)pyridinyl 2-(2-pyridinyl)thiazolyl 2-(2-thiazolyl)thiazolyl 2-(2-pyrimidinyl)ethynyl 1,3,4-oxadiazolyl tetrahydrofuranyl tetrahydrofuranyl 4,5-dihydroisoxazolyl 3-isoxazolyl phenyl 2-(trifluoromethyl)phenyl 3-(trifluoromethyl)phenyl 4-(trifluoromethyl)phenyl 6-(trifluoromethyl)pyrazinyl A is CF 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 3-methylpyrazinyl 3-methoxypyrazinyl 3-(trifluoromethyl)pyrazinyl 3-(CH(=NOMe))pyrazinyl -methylpyrazinyl 5-methoxypyrazinyl -(trifluoromethyl)pyrazinyl 5-(CH(=NOMe))pyrazinyl 6-methylpyrazinyl 6-methoxypyrazinyl 6-(trifluoromethyl)pyrazinyl 6-(CH(=NOMe))pyrazinyl 4-methylpyrimidinyl 4-methoxypyrimidinyl 4-(trifluoromethyl)pyrimidinyl 4-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 2-methylpyrimidinyl 2-methoxypyrimidinyl 2-(trifluoromethyl)pyrimidinyl 2-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 6-methylpyrimidinyl 6-methoxypyrimidinyl 6-(trifluoromethyl)pyrimidinyl 6-(CH(=NOMe))pyrimidinyl 3-methylpyrazolyl 3-methoxypyrazolyl 3-(trifluoromethyl)pyrazolyl 3-(CH(=NOMe))pyrazolyl 4-methylpyrazolyl 4-methoxypyrazolyl 4-(trifluoromethyl)pyrazolyl 4-(CH(=NOMe))pyrazolyl -methylpyrazolyl 5-methoxypyrazolyl -(trifluoromethyl)pyrazolyl 5-(CH(=NOMe))pyrazolyl 4-methyl-1,2,3-triazinyl 4-methoxy-1,2,3-triazinyl 4-(trifluoromethyl)-1,2,3-triazinyl 4-(CH(=NOMe))-1,2,3-triazinyl 6-(2-pyrimidinyl)pyridinyl 2-(2-pyridinyl)thiazolyl 2-(2-thiazolyl)thiazolyl 2-(2-pyrimidinyl)ethynyl 1,3,4-oxadiazolyl tetrahydrofuranyl tetrahydrofuranyl 4,5-dihydroisoxazolyl 3-isoxazolyl phenyl 2-(trifluoromethyl)phenyl 3-(trifluoromethyl)phenyl 4-(trifluoromethyl)phenyl 6-(trifluoromethyl)pyrazinyl A is N 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 3-methylpyrazinyl 3-methoxypyrazinyl 3-(trifluoromethyl)pyrazinyl 3-(CH(=NOMe))pyrazinyl -methylpyrazinyl 5-methoxypyrazinyl -(trifluoromethyl)pyrazinyl 5-(CH(=NOMe))pyrazinyl 6-methylpyrazinyl 6-methoxypyrazinyl 6-(trifluoromethyl)pyrazinyl 6-(CH(=NOMe))pyrazinyl 4-methylpyrimidinyl 4-methoxypyrimidinyl 4-(trifluoromethyl)pyrimidinyl 4-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 2-methylpyrimidinyl 2-methoxypyrimidinyl 2-(trifluoromethyl)pyrimidinyl 2-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 6-methylpyrimidinyl 6-methoxypyrimidinyl 6-(trifluoromethyl)pyrimidinyl 6-(CH(=NOMe))pyrimidinyl 3-methylpyrazolyl 3-methoxypyrazolyl 3-(trifluoromethyl)pyrazolyl 3-(CH(=NOMe))pyrazolyl 4-methylpyrazolyl 4-methoxypyrazolyl 4-(trifluoromethyl)pyrazolyl 4-(CH(=NOMe))pyrazolyl -methylpyrazolyl 5-methoxypyrazolyl -(trifluoromethyl)pyrazolyl 5-(CH(=NOMe))pyrazolyl 4-methyl-1,2,3-triazinyl 4-methoxy-1,2,3-triazinyl 4-(trifluoromethyl)-1,2,3-triazinyl 4-(CH(=NOMe))-1,2,3-triazinyl 6-(2-pyrimidinyl)pyridinyl 2-(2-pyridinyl)thiazolyl 2-(2-thiazolyl)thiazolyl 2-(2-pyrimidinyl)ethynyl 1,3,4-oxadiazolyl tetrahydrofuranyl tetrahydrofuranyl 4,5-dihydroisoxazolyl 3-isoxazolyl phenyl 2-(trifluoromethyl)phenyl 3-(trifluoromethyl)phenyl 4-(trifluoromethyl)phenyl 6-(trifluoromethyl)pyrazinyl TABLE 2a A is CH R R R Me Et Pr i-Pr -CH (c-Pr) -CH(Me)(c-Pr) Bu s-Bu i-Bu t-Bu -CH Ph -CH CH=CH 2 2 2 -CH C≡CH -C(Me) C≡CH -CH CH F 2 2 2 2 -CH CHF -CH CF -CH(Me)CF 2 2 2 3 3 -CH CH CF -CH CF CF -CH CF CH 2 2 3 2 2 3 2 2 3 -CH CH CF CF -CH(i-Pr)CF -CH CH OMe 2 2 2 3 3 2 2 -CH OEt -CH CH O(i-Pr) -CH CH OEt 2 2 2 2 2 -CH CH CH OMe -CH CH(Me)OMe -CH(Et)CH OMe 2 2 2 2 2 -CH(Me)CH OMe -CH CH S(O)Me -CH CH SMe 2 2 2 2 2 -CH CH SEt -CH CH SO Me -CH CH SO Et 2 2 2 2 2 2 2 2 -CH CH S(O)Et -CH CH S(O)(t-Bu) -CH CH S(t-Bu) 2 2 2 2 2 2 -CH(Me)CH SMe -CH CH SO (t-Bu) -CH(Me)CH SO Me 2 2 2 2 2 2 -CH(Me)CH S(O)Me -CH CH S(O)CH CF -CH CH SCH CF 2 2 2 2 3 2 2 2 3 -CH CH SO CH CF -CH CH SO CH CH CF -CH CH SCH CH CF 2 2 2 2 3 2 2 2 2 2 3 2 2 2 2 3 -CH CH S(O)CH CH CF -CH CN -CH CH CN 2 2 2 2 3 2 2 2 -C(Me) CN -CH CH N(i-Pr) -CH CH N(Me) 2 2 2 2 2 2 2 -CH2CH(OMe) c-Pr c-Bu 1-methylcyclopropyl 3-methoxycyclobutyl -CH(Ph)(c-Pr) -CH(Me)(c-Pr) 3-thietanyl 3,3-difluorocyclobutyl 3-oxetanyl -CH (oxiranyl) 3-thietanyl-1,1-dioxide 3-thietanyloxide -CH (CH(-OC(Me) OCH -)) -CH (tetrahydrofuranyl) 2 2 2 2 -CH (2-furanyl) tetrahydrofuranyl -CH (2-thienyl) -CH (CH(-OCH CH O-) -CH CO Me -CH (2,2-difluorocyclopropyl) 2 2 2 2 2 2 -C(-CH CH -)CO Me -CH(Me)CO Et -CH(i-Pr)CO Me 2 2 2 2 2 -CH C(O)NHMe -CH C(O)NMe -CH(Me)C(O)NHMe 2 2 2 -CH(Me)C(O)NH(t-Bu) -OCH (c-Pr) -CH(Me)C(O)NMe -OCH CH=CH -NHC(O)(i-Pr) -NHC(O)Me -NHCO Me -NHC(O)(3-pyridinyl) -NHC(O)(t-Bu) -NHC(O)Ph -NH(c-hexyl) -NHC(O)NH(i-Pr) -NH(c-Pr) -NHC(O)(2-thienyl) -NH(CH CF ) -NHC(O)CF -NHCO Et -NHC(O)(2-furanyl) -C(O)C(O)Me -NHCO CH CF -C(O)CO Me 2 2 3 2 -C(O)(2-pyridinyl) -NHC(O)NMe -NHC(O)NHMe -NHC(O)NHCH CF -NHC(O)CH CH CF -NHC(O)Et 2 3 2 2 3 -NHC(O)CH CF -NHSO CF -NHSO CH CF 2 3 2 3 2 2 3 -NHSO CH CH CF -NH(2-pyridinyl) -NH(3-pyridinyl) 2 2 2 3 -NH(4-pyridinyl) -NH(2-pyrimidinyl) -NH(4-pyrimidinyl) -NH(5-pyrimidinyl) -NH(6-CF pyridinyl) -NH(4-CF pyridinyl) -NH(3-CF pyridinyl) -NH(5-CF pyrimidinyl) -NH(5-CF pyridinyl) 3 3 3 -NH(4-CF pyrimidinyl) -NH(6-methylpyridinyl) -NH(4-methylpyridinyl) -NH(3-methylpyridinyl) -NH(5-methylpyrimidinyl) -NH(5-methylpyridinyl) -NH(4-methylpyrimidinyl) -NH(6-methoxypyridinyl) -NH(4-methoxypyridinyl) -NH(3-methoxypyridinyl) -NH(5-methoxypyrimidinyl) -NH(5-methoxypyridinyl) -NH(4-methoxypyrimidinyl) -CH (6-CF pyridinyl) -CH (4-CF pyridinyl) 2 3 2 3 -CH (3-CF pyridinyl) -CH (5-CF pyrimidinyl) -CH (5-CF pyridinyl) 2 3 2 3 2 3 -CH (4-CF pyrimidinyl) -CH (6-methylpyridinyl) -CH (4-methylpyridinyl) 2 3 2 2 -CH (3-methylpyridinyl) -CH (5-methylpyrimidinyl) -CH (5-methylpyridinyl) 2 2 2 -CH (4-methylpyrimidinyl) -CH (6-methoxypyridinyl) -CH (4-methoxypyridinyl) 2 2 2 -CH (3-methoxypyridinyl) -CH (5-methoxypyrimidinyl) -CH (5-methoxypyridinyl) 2 2 2 -CH (4-methoxypyrimidinyl) -CH (5-pyrimidinyl) -CH (6-bromopyridinyl) 2 2 2 -CH (2-pyrimidinyl) -CH (3-(OCF )phenyl) -CH (2-thiazolyl) 2 2 3 2 -CH (5-methylpyrazinyl) -CH (4-pyridinyl) -CH (2-pyridinyl) 2 2 2 Ph 3-pyridinyl -CH (3-pyridinyl) 2-pyridinyl 2-pyrazinyl -CH CH (2-pyridinyl) 4-pyridinyl 4-CF pyridinyl -CH CH CH (2-pyridinyl) 3 2 2 2 3-CF pyridinyl 4-CF pyrimidinyl 6-CF pyridinyl 3 3 3 -CF pyridinyl 5-CF pyrazinyl 5-CF pyrimidinyl 3 3 3 -CH CH N(-C(O)CH CH C(O)-) -CH CH CH (1-imidazolyl) -CH(-C(O)OCH CH -) 2 2 2 2 2 2 2 2 2 -CH (4-pyrimidinyl) pyridazinyl 6-CF pyrazinyl A is CF R R R Me Et Pr i-Pr -CH (c-Pr) -CH(Me)(c-Pr) Bu s-Bu i-Bu t-Bu -CH Ph -CH CH=CH 2 2 2 -CH C≡CH -C(Me) C≡CH -CH CH F 2 2 2 2 -CH CHF -CH CF -CH(Me)CF 2 2 2 3 3 -CH CH CF -CH CF CF -CH CF CH 2 2 3 2 2 3 2 2 3 -CH CH CF CF -CH(i-Pr)CF -CH CH OMe 2 2 2 3 3 2 2 -CH OEt -CH CH O(i-Pr) -CH CH OEt 2 2 2 2 2 -CH CH CH OMe -CH CH(Me)OMe -CH(Et)CH OMe 2 2 2 2 2 -CH(Me)CH OMe -CH CH S(O)Me -CH CH SMe 2 2 2 2 2 -CH CH SEt -CH CH SO Me -CH CH SO Et 2 2 2 2 2 2 2 2 -CH CH S(O)Et -CH CH S(O)(t-Bu) -CH CH S(t-Bu) 2 2 2 2 2 2 -CH(Me)CH SMe -CH CH SO (t-Bu) -CH(Me)CH SO Me 2 2 2 2 2 2 -CH(Me)CH S(O)Me -CH CH S(O)CH CF -CH CH SCH CF 2 2 2 2 3 2 2 2 3 -CH CH SO CH CF -CH CH SO CH CH CF -CH CH SCH CH CF 2 2 2 2 3 2 2 2 2 2 3 2 2 2 2 3 -CH CH S(O)CH CH CF -CH CN -CH CH CN 2 2 2 2 3 2 2 2 -C(Me) CN -CH CH N(i-Pr) -CH CH N(Me) 2 2 2 2 2 2 2 -CH2CH(OMe) c-Pr c-Bu 1-methylcyclopropyl 3-methoxycyclobutyl -CH(Ph)(c-Pr) -CH(Me)(c-Pr) 3-thietanyl 3,3-difluorocyclobutyl 3-oxetanyl -CH (oxiranyl) 3-thietanyl-1,1-dioxide 3-thietanyloxide -CH (CH(-OC(Me) OCH -)) -CH (tetrahydrofuranyl) 2 2 2 2 -CH (2-furanyl) tetrahydrofuranyl -CH (2-thienyl) -CH (CH(-OCH CH O-) -CH CO Me -CH (2,2-difluorocyclopropyl) 2 2 2 2 2 2 -C(-CH CH -)CO Me -CH(Me)CO Et -CH(i-Pr)CO Me 2 2 2 2 2 -CH C(O)NHMe -CH C(O)NMe -CH(Me)C(O)NHMe 2 2 2 -CH(Me)C(O)NH(t-Bu) -OCH (c-Pr) -CH(Me)C(O)NMe -OCH CH=CH -NHC(O)(i-Pr) -NHC(O)Me -NHCO Me -NHC(O)(3-pyridinyl) -NHC(O)(t-Bu) -NHC(O)Ph -NH(c-hexyl) -NHC(O)NH(i-Pr) -NH(c-Pr) -NHC(O)(2-thienyl) -NH(CH CF ) -NHC(O)CF -NHCO Et -NHC(O)(2-furanyl) -C(O)C(O)Me -NHCO CH CF -C(O)CO Me 2 2 3 2 -C(O)(2-pyridinyl) -NHC(O)NMe -NHC(O)NHMe -NHC(O)NHCH CF -NHC(O)CH CH CF -NHC(O)Et 2 3 2 2 3 -NHC(O)CH CF -NHSO CF -NHSO CH CF 2 3 2 3 2 2 3 -NHSO CH CH CF -NH(2-pyridinyl) -NH(3-pyridinyl) 2 2 2 3 -NH(4-pyridinyl) -NH(2-pyrimidinyl) -NH(4-pyrimidinyl) -NH(5-pyrimidinyl) -NH(6-CF pyridinyl) -NH(4-CF pyridinyl) -NH(3-CF pyridinyl) -NH(5-CF pyrimidinyl) -NH(5-CF pyridinyl) 3 3 3 -NH(4-CF pyrimidinyl) -NH(6-methylpyridinyl) -NH(4-methylpyridinyl) -NH(3-methylpyridinyl) -NH(5-methylpyrimidinyl) -NH(5-methylpyridinyl) -NH(4-methylpyrimidinyl) -NH(6-methoxypyridinyl) -NH(4-methoxypyridinyl) -NH(3-methoxypyridinyl) -NH(5-methoxypyrimidinyl) -NH(5-methoxypyridinyl) -NH(4-methoxypyrimidinyl) -CH (6-CF pyridinyl) -CH (4-CF pyridinyl) 2 3 2 3 -CH (3-CF pyridinyl) -CH (5-CF pyrimidinyl) -CH (5-CF pyridinyl) 2 3 2 3 2 3 -CH (4-CF pyrimidinyl) -CH (6-methylpyridinyl) -CH (4-methylpyridinyl) 2 3 2 2 -CH (3-methylpyridinyl) -CH (5-methylpyrimidinyl) -CH (5-methylpyridinyl) 2 2 2 -CH (4-methylpyrimidinyl) -CH (6-methoxypyridinyl) -CH (4-methoxypyridinyl) 2 2 2 -CH (3-methoxypyridinyl) -CH (5-methoxypyrimidinyl) -CH (5-methoxypyridinyl) 2 2 2 -CH (4-methoxypyrimidinyl) -CH (5-pyrimidinyl) -CH (6-bromopyridinyl) 2 2 2 -CH (2-pyrimidinyl) -CH (3-(OCF )phenyl) -CH (2-thiazolyl) 2 2 3 2 -CH (5-methylpyrazinyl) -CH (4-pyridinyl) -CH (2-pyridinyl) 2 2 2 Ph 3-pyridinyl -CH (3-pyridinyl) 2-pyridinyl 2-pyrazinyl -CH CH (2-pyridinyl) 4-pyridinyl 4-CF pyridinyl -CH CH CH (2-pyridinyl) 3 2 2 2 3-CF pyridinyl 4-CF pyrimidinyl 6-CF pyridinyl 3 3 3 -CF pyridinyl 5-CF pyrazinyl 5-CF pyrimidinyl 3 3 3 -CH CH N(-C(O)CH CH C(O)-) -CH CH CH (1-imidazolyl) -CH(-C(O)OCH CH -) 2 2 2 2 2 2 2 2 2 -CH (4-pyrimidinyl) pyridazinyl 6-CF pyrazinyl A is N R R R Me Et Pr i-Pr -CH (c-Pr) -CH(Me)(c-Pr) Bu s-Bu i-Bu t-Bu -CH Ph -CH CH=CH 2 2 2 -CH C≡CH -C(Me) C≡CH -CH CH F 2 2 2 2 -CH CHF -CH CF -CH(Me)CF 2 2 2 3 3 -CH CH CF -CH CF CF -CH CF CH 2 2 3 2 2 3 2 2 3 -CH CH CF CF -CH(i-Pr)CF -CH CH OMe 2 2 2 3 3 2 2 -CH OEt -CH CH O(i-Pr) -CH CH OEt 2 2 2 2 2 -CH CH CH OMe -CH CH(Me)OMe -CH(Et)CH OMe 2 2 2 2 2 -CH(Me)CH OMe -CH CH S(O)Me -CH CH SMe 2 2 2 2 2 -CH CH SEt -CH CH SO Me -CH CH SO Et 2 2 2 2 2 2 2 2 -CH CH S(O)Et -CH CH S(O)(t-Bu) -CH CH S(t-Bu) 2 2 2 2 2 2 -CH(Me)CH SMe -CH CH SO (t-Bu) -CH(Me)CH SO Me 2 2 2 2 2 2 -CH(Me)CH S(O)Me -CH CH S(O)CH CF -CH CH SCH CF 2 2 2 2 3 2 2 2 3 -CH CH SO CH CF -CH CH SO CH CH CF -CH CH SCH CH CF 2 2 2 2 3 2 2 2 2 2 3 2 2 2 2 3 -CH CH S(O)CH CH CF -CH CN -CH CH CN 2 2 2 2 3 2 2 2 -C(Me) CN -CH CH N(i-Pr) -CH CH N(Me) 2 2 2 2 2 2 2 -CH2CH(OMe) c-Pr c-Bu 1-methylcyclopropyl 3-methoxycyclobutyl -CH(Ph)(c-Pr) -CH(Me)(c-Pr) 3-thietanyl 3,3-difluorocyclobutyl 3-oxetanyl -CH (oxiranyl) 3-thietanyl-1,1-dioxide 3-thietanyloxide -CH (CH(-OC(Me) OCH -)) -CH (tetrahydrofuranyl) 2 2 2 2 -CH (2-furanyl) tetrahydrofuranyl -CH (2-thienyl) -CH (CH(-OCH CH O-) -CH CO Me -CH (2,2-difluorocyclopropyl) 2 2 2 2 2 2 -C(-CH CH -)CO Me -CH(Me)CO Et -CH(i-Pr)CO Me 2 2 2 2 2 -CH C(O)NHMe -CH C(O)NMe -CH(Me)C(O)NHMe 2 2 2 -CH(Me)C(O)NH(t-Bu) -OCH (c-Pr) -CH(Me)C(O)NMe -OCH CH=CH -NHC(O)(i-Pr) -NHC(O)Me -NHCO Me -NHC(O)(3-pyridinyl) -NHC(O)(t-Bu) -NHC(O)Ph -NH(c-hexyl) -NHC(O)NH(i-Pr) -NH(c-Pr) -NHC(O)(2-thienyl) -NH(CH CF ) -NHC(O)CF -NHCO Et -NHC(O)(2-furanyl) -C(O)C(O)Me -NHCO CH CF -C(O)CO Me 2 2 3 2 -C(O)(2-pyridinyl) -NHC(O)NMe -NHC(O)NHMe -NHC(O)NHCH CF -NHC(O)CH CH CF -NHC(O)Et 2 3 2 2 3 -NHC(O)CH CF -NHSO CF -NHSO CH CF 2 3 2 3 2 2 3 -NHSO CH CH CF -NH(2-pyridinyl) -NH(3-pyridinyl) 2 2 2 3 -NH(4-pyridinyl) -NH(2-pyrimidinyl) -NH(4-pyrimidinyl) -NH(5-pyrimidinyl) -NH(6-CF pyridinyl) -NH(4-CF pyridinyl) -NH(3-CF pyridinyl) -NH(5-CF pyrimidinyl) -NH(5-CF pyridinyl) 3 3 3 -NH(4-CF pyrimidinyl) -NH(6-methylpyridinyl) -NH(4-methylpyridinyl) -NH(3-methylpyridinyl) -NH(5-methylpyrimidinyl) -NH(5-methylpyridinyl) -NH(4-methylpyrimidinyl) -NH(6-methoxypyridinyl) -NH(4-methoxypyridinyl) -NH(3-methoxypyridinyl) -NH(5-methoxypyrimidinyl) -NH(5-methoxypyridinyl) -NH(4-methoxypyrimidinyl) -CH (6-CF pyridinyl) -CH (4-CF pyridinyl) 2 3 2 3 -CH (3-CF pyridinyl) -CH (5-CF pyrimidinyl) -CH (5-CF pyridinyl) 2 3 2 3 2 3 -CH (4-CF pyrimidinyl) -CH (6-methylpyridinyl) -CH (4-methylpyridinyl) 2 3 2 2 -CH (3-methylpyridinyl) -CH (5-methylpyrimidinyl) -CH (5-methylpyridinyl) 2 2 2 -CH (4-methylpyrimidinyl) -CH (6-methoxypyridinyl) -CH (4-methoxypyridinyl) 2 2 2 -CH (3-methoxypyridinyl) -CH (5-methoxypyrimidinyl) -CH (5-methoxypyridinyl) 2 2 2 -CH (4-methoxypyrimidinyl) -CH (5-pyrimidinyl) -CH (6-bromopyridinyl) 2 2 2 -CH (2-pyrimidinyl) -CH (3-(OCF )phenyl) -CH (2-thiazolyl) 2 2 3 2 -CH (5-methylpyrazinyl) -CH (4-pyridinyl) -CH (2-pyridinyl) 2 2 2 Ph 3-pyridinyl -CH (3-pyridinyl) 2-pyridinyl 2-pyrazinyl -CH CH (2-pyridinyl) 4-pyridinyl 4-CF pyridinyl -CH CH CH (2-pyridinyl) 3 2 2 2 3-CF pyridinyl 4-CF pyrimidinyl 6-CF pyridinyl 3 3 3 -CF pyridinyl 5-CF pyrazinyl 5-CF pyrimidinyl 3 3 3 -CH CH N(-C(O)CH CH C(O)-) -CH CH CH (1-imidazolyl) -CH(-C(O)OCH CH -) 2 2 2 2 2 2 2 2 2 -CH (4-pyrimidinyl) pyridazinyl 6-CF pyrazinyl TABLE 2b A is CH R R R Me Et Pr i-Pr -CH (c-Pr) -CH(Me)(c-Pr) Bu s-Bu i-Bu t-Bu -CH Ph -CH CH=CH 2 2 2 -CH C≡CH -C(Me) C≡CH -CH CH F 2 2 2 2 -CH CHF -CH CF -CH(Me)CF 2 2 2 3 3 -CH CH CF -CH CF CF -CH CF CH 2 2 3 2 2 3 2 2 3 -CH CH CF CF -CH(i-Pr)CF -CH CH OMe 2 2 2 3 3 2 2 -CH OEt -CH CH O(i-Pr) -CH CH OEt 2 2 2 2 2 -CH CH CH OMe -CH CH(Me)OMe -CH(Et)CH OMe 2 2 2 2 2 -CH(Me)CH OMe -CH CH S(O)Me -CH CH SMe 2 2 2 2 2 -CH CH SEt -CH CH SO Me -CH CH SO Et 2 2 2 2 2 2 2 2 -CH CH S(O)Et -CH CH S(O)(t-Bu) -CH CH S(t-Bu) 2 2 2 2 2 2 -CH(Me)CH SMe -CH CH SO (t-Bu) -CH(Me)CH SO Me 2 2 2 2 2 2 -CH(Me)CH S(O)Me -CH CH S(O)CH CF -CH CH SCH CF 2 2 2 2 3 2 2 2 3 -CH CH SO CH CF -CH CH SO CH CH CF -CH CH SCH CH CF 2 2 2 2 3 2 2 2 2 2 3 2 2 2 2 3 -CH CH S(O)CH CH CF -CH CN -CH CH CN 2 2 2 2 3 2 2 2 -C(Me) CN -CH CH N(i-Pr) -CH CH N(Me) 2 2 2 2 2 2 2 -CH2CH(OMe) c-Pr c-Bu 1-methylcyclopropyl 3-methoxycyclobutyl -CH(Ph)(c-Pr) -CH(Me)(c-Pr) 3-thietanyl 3,3-difluorocyclobutyl 3-oxetanyl -CH (oxiranyl) 3-thietanyl-1,1-dioxide 3-thietanyloxide -CH (CH(-OC(Me) OCH -)) -CH (tetrahydrofuranyl) 2 2 2 2 -CH (2-furanyl) tetrahydrofuranyl -CH (2-thienyl) -CH (CH(-OCH CH O-) -CH CO Me -CH (2,2-difluorocyclopropyl) 2 2 2 2 2 2 -C(-CH CH -)CO Me -CH(Me)CO Et -CH(i-Pr)CO Me 2 2 2 2 2 -CH C(O)NHMe -CH C(O)NMe -CH(Me)C(O)NHMe 2 2 2 -CH(Me)C(O)NH(t-Bu) -OCH (c-Pr) -CH(Me)C(O)NMe -OCH CH=CH -NHC(O)(i-Pr) -NHC(O)Me -NHCO Me -NHC(O)(3-pyridinyl) -NHC(O)(t-Bu) -NHC(O)Ph -NH(c-hexyl) -NHC(O)NH(i-Pr) -NH(c-Pr) -NHC(O)(2-thienyl) -NH(CH CF ) -NHC(O)CF -NHCO Et -NHC(O)(2-furanyl) -C(O)C(O)Me -NHCO CH CF -C(O)CO Me 2 2 3 2 -C(O)(2-pyridinyl) -NHC(O)NMe -NHC(O)NHMe -NHC(O)NHCH CF -NHC(O)CH CH CF -NHC(O)Et 2 3 2 2 3 -NHC(O)CH CF -NHSO CF -NHSO CH CF 2 3 2 3 2 2 3 -NHSO CH CH CF -NH(2-pyridinyl) -NH(3-pyridinyl) 2 2 2 3 -NH(4-pyridinyl) -NH(2-pyrimidinyl) -NH(4-pyrimidinyl) -NH(5-pyrimidinyl) -NH(6-CF pyridinyl) -NH(4-CF pyridinyl) -NH(3-CF pyridinyl) -NH(5-CF pyrimidinyl) -NH(5-CF pyridinyl) 3 3 3 -NH(4-CF pyrimidinyl) -NH(6-methylpyridinyl) -NH(4-methylpyridinyl) -NH(3-methylpyridinyl) -NH(5-methylpyrimidinyl) -NH(5-methylpyridinyl) -NH(4-methylpyrimidinyl) -NH(6-methoxypyridinyl) -NH(4-methoxypyridinyl) -NH(3-methoxypyridinyl) -NH(5-methoxypyrimidinyl) -NH(5-methoxypyridinyl) -NH(4-methoxypyrimidinyl) -CH (6-CF pyridinyl) -CH (4-CF pyridinyl) 2 3 2 3 -CH (3-CF pyridinyl) -CH (5-CF pyrimidinyl) -CH (5-CF pyridinyl) 2 3 2 3 2 3 -CH (4-CF pyrimidinyl) -CH (6-methylpyridinyl) -CH (4-methylpyridinyl) 2 3 2 2 -CH (3-methylpyridinyl) -CH (5-methylpyrimidinyl) -CH (5-methylpyridinyl) 2 2 2 -CH (4-methylpyrimidinyl) -CH (6-methoxypyridinyl) -CH (4-methoxypyridinyl) 2 2 2 -CH (3-methoxypyridinyl) -CH (5-methoxypyrimidinyl) -CH (5-methoxypyridinyl) 2 2 2 -CH (4-methoxypyrimidinyl) -CH (5-pyrimidinyl) -CH (6-bromopyridinyl) 2 2 2 -CH (2-pyrimidinyl) -CH (3-(OCF )phenyl) -CH (2-thiazolyl) 2 2 3 2 -CH (5-methylpyrazinyl) -CH (4-pyridinyl) -CH (2-pyridinyl) 2 2 2 Ph 3-pyridinyl -CH (3-pyridinyl) 2-pyridinyl 2-pyrazinyl -CH CH (2-pyridinyl) 4-pyridinyl 4-CF pyridinyl -CH CH CH (2-pyridinyl) 3 2 2 2 3-CF pyridinyl 4-CF pyrimidinyl 6-CF pyridinyl 3 3 3 -CF pyridinyl 5-CF pyrazinyl 5-CF pyrimidinyl 3 3 3 -CH CH N(-C(O)CH CH C(O)-) -CH CH CH (1-imidazolyl) -CH(-C(O)OCH CH -) 2 2 2 2 2 2 2 2 2 -CH (4-pyrimidinyl) pyridazinyl 6-CF pyrazinyl A is CF R R R Me Et Pr i-Pr -CH (c-Pr) -CH(Me)(c-Pr) Bu s-Bu i-Bu t-Bu -CH Ph -CH CH=CH 2 2 2 -CH C≡CH -C(Me) C≡CH -CH CH F 2 2 2 2 -CH CHF -CH CF -CH(Me)CF 2 2 2 3 3 -CH CH CF -CH CF CF -CH CF CH 2 2 3 2 2 3 2 2 3 -CH CH CF CF -CH(i-Pr)CF -CH CH OMe 2 2 2 3 3 2 2 -CH OEt -CH CH O(i-Pr) -CH CH OEt 2 2 2 2 2 -CH CH CH OMe -CH CH(Me)OMe -CH(Et)CH OMe 2 2 2 2 2 -CH(Me)CH OMe -CH CH S(O)Me -CH CH SMe 2 2 2 2 2 -CH CH SEt -CH CH SO Me -CH CH SO Et 2 2 2 2 2 2 2 2 -CH CH S(O)Et -CH CH S(O)(t-Bu) -CH CH S(t-Bu) 2 2 2 2 2 2 -CH(Me)CH SMe -CH CH SO (t-Bu) -CH(Me)CH SO Me 2 2 2 2 2 2 -CH(Me)CH S(O)Me -CH CH S(O)CH CF -CH CH SCH CF 2 2 2 2 3 2 2 2 3 -CH CH SO CH CF -CH CH SO CH CH CF -CH CH SCH CH CF 2 2 2 2 3 2 2 2 2 2 3 2 2 2 2 3 -CH CH S(O)CH CH CF -CH CN -CH CH CN 2 2 2 2 3 2 2 2 -C(Me) CN -CH CH N(i-Pr) -CH CH N(Me) 2 2 2 2 2 2 2 -CH2CH(OMe) c-Pr c-Bu 1-methylcyclopropyl 3-methoxycyclobutyl -CH(Ph)(c-Pr) -CH(Me)(c-Pr) 3-thietanyl 3,3-difluorocyclobutyl 3-oxetanyl -CH (oxiranyl) 3-thietanyl-1,1-dioxide 3-thietanyloxide -CH (CH(-OC(Me) OCH -)) -CH (tetrahydrofuranyl) 2 2 2 2 -CH (2-furanyl) tetrahydrofuranyl -CH (2-thienyl) -CH (CH(-OCH CH O-) -CH CO Me -CH (2,2-difluorocyclopropyl) 2 2 2 2 2 2 -C(-CH CH -)CO Me -CH(Me)CO Et -CH(i-Pr)CO Me 2 2 2 2 2 -CH C(O)NHMe -CH C(O)NMe -CH(Me)C(O)NHMe 2 2 2 -CH(Me)C(O)NH(t-Bu) -OCH (c-Pr) -CH(Me)C(O)NMe -OCH CH=CH -NHC(O)(i-Pr) -NHC(O)Me -NHCO Me -NHC(O)(3-pyridinyl) -NHC(O)(t-Bu) -NHC(O)Ph -NH(c-hexyl) -NHC(O)NH(i-Pr) -NH(c-Pr) -NHC(O)(2-thienyl) -NH(CH CF ) -NHC(O)CF -NHCO Et -NHC(O)(2-furanyl) -C(O)C(O)Me -NHCO CH CF -C(O)CO Me 2 2 3 2 -C(O)(2-pyridinyl) -NHC(O)NMe -NHC(O)NHMe -NHC(O)NHCH CF -NHC(O)CH CH CF -NHC(O)Et 2 3 2 2 3 -NHC(O)CH CF -NHSO CF -NHSO CH CF 2 3 2 3 2 2 3 -NHSO CH CH CF -NH(2-pyridinyl) -NH(3-pyridinyl) 2 2 2 3 -NH(4-pyridinyl) -NH(2-pyrimidinyl) -NH(4-pyrimidinyl) -NH(5-pyrimidinyl) -NH(6-CF pyridinyl) -NH(4-CF pyridinyl) -NH(3-CF pyridinyl) -NH(5-CF pyrimidinyl) -NH(5-CF pyridinyl) 3 3 3 -NH(4-CF pyrimidinyl) -NH(6-methylpyridinyl) -NH(4-methylpyridinyl) -NH(3-methylpyridinyl) -NH(5-methylpyrimidinyl) -NH(5-methylpyridinyl) -NH(4-methylpyrimidinyl) -NH(6-methoxypyridinyl) -NH(4-methoxypyridinyl) -NH(3-methoxypyridinyl) -NH(5-methoxypyrimidinyl) -NH(5-methoxypyridinyl) -NH(4-methoxypyrimidinyl) -CH (6-CF pyridinyl) -CH (4-CF pyridinyl) 2 3 2 3 -CH (3-CF pyridinyl) -CH (5-CF pyrimidinyl) -CH (5-CF pyridinyl) 2 3 2 3 2 3 -CH (4-CF pyrimidinyl) -CH (6-methylpyridinyl) -CH (4-methylpyridinyl) 2 3 2 2 -CH (3-methylpyridinyl) -CH (5-methylpyrimidinyl) -CH (5-methylpyridinyl) 2 2 2 -CH (4-methylpyrimidinyl) -CH (6-methoxypyridinyl) -CH (4-methoxypyridinyl) 2 2 2 -CH (3-methoxypyridinyl) -CH (5-methoxypyrimidinyl) -CH (5-methoxypyridinyl) 2 2 2 -CH (4-methoxypyrimidinyl) -CH (5-pyrimidinyl) -CH (6-bromopyridinyl) 2 2 2 -CH (2-pyrimidinyl) -CH (3-(OCF )phenyl) -CH (2-thiazolyl) 2 2 3 2 -CH (5-methylpyrazinyl) -CH (4-pyridinyl) -CH (2-pyridinyl) 2 2 2 Ph 3-pyridinyl -CH (3-pyridinyl) 2-pyridinyl 2-pyrazinyl -CH CH (2-pyridinyl) 4-pyridinyl 4-CF pyridinyl -CH CH CH (2-pyridinyl) 3 2 2 2 3-CF pyridinyl 4-CF pyrimidinyl 6-CF pyridinyl 3 3 3 -CF pyridinyl 5-CF pyrazinyl 5-CF pyrimidinyl 3 3 3 -CH CH N(-C(O)CH CH C(O)-) -CH CH CH (1-imidazolyl) -CH(-C(O)OCH CH -) 2 2 2 2 2 2 2 2 2 -CH (4-pyrimidinyl) pyridazinyl 6-CF pyrazinyl A is N R R R Me Et Pr i-Pr -CH (c-Pr) -CH(Me)(c-Pr) Bu s-Bu i-Bu t-Bu -CH Ph -CH CH=CH 2 2 2 -CH C≡CH -C(Me) C≡CH -CH CH F 2 2 2 2 -CH CHF -CH CF -CH(Me)CF 2 2 2 3 3 -CH CH CF -CH CF CF -CH CF CH 2 2 3 2 2 3 2 2 3 -CH CH CF CF -CH(i-Pr)CF -CH CH OMe 2 2 2 3 3 2 2 -CH OEt -CH CH O(i-Pr) -CH CH OEt 2 2 2 2 2 -CH CH CH OMe -CH CH(Me)OMe -CH(Et)CH OMe 2 2 2 2 2 -CH(Me)CH OMe -CH CH S(O)Me -CH CH SMe 2 2 2 2 2 -CH CH SEt -CH CH SO Me -CH CH SO Et 2 2 2 2 2 2 2 2 -CH CH S(O)Et -CH CH S(O)(t-Bu) -CH CH S(t-Bu) 2 2 2 2 2 2 -CH(Me)CH SMe -CH CH SO (t-Bu) -CH(Me)CH SO Me 2 2 2 2 2 2 -CH(Me)CH S(O)Me -CH CH S(O)CH CF -CH CH SCH CF 2 2 2 2 3 2 2 2 3 -CH CH SO CH CF -CH CH SO CH CH CF -CH CH SCH CH CF 2 2 2 2 3 2 2 2 2 2 3 2 2 2 2 3 -CH CH S(O)CH CH CF -CH CN -CH CH CN 2 2 2 2 3 2 2 2 -C(Me) CN -CH CH N(i-Pr) -CH CH N(Me) 2 2 2 2 2 2 2 -CH2CH(OMe) c-Pr c-Bu 1-methylcyclopropyl 3-methoxycyclobutyl -CH(Ph)(c-Pr) -CH(Me)(c-Pr) 3-thietanyl 3,3-difluorocyclobutyl 3-oxetanyl -CH (oxiranyl) 3-thietanyl-1,1-dioxide 3-thietanyloxide -CH (CH(-OC(Me) OCH -)) -CH (tetrahydrofuranyl) 2 2 2 2 -CH (2-furanyl) tetrahydrofuranyl -CH (2-thienyl) -CH (CH(-OCH CH O-) -CH CO Me -CH (2,2-difluorocyclopropyl) 2 2 2 2 2 2 -C(-CH CH -)CO Me -CH(Me)CO Et -CH(i-Pr)CO Me 2 2 2 2 2 -CH C(O)NHMe -CH C(O)NMe -CH(Me)C(O)NHMe 2 2 2 -CH(Me)C(O)NH(t-Bu) -OCH (c-Pr) -CH(Me)C(O)NMe -OCH CH=CH -NHC(O)(i-Pr) -NHC(O)Me -NHCO Me -NHC(O)(3-pyridinyl) -NHC(O)(t-Bu) -NHC(O)Ph -NH(c-hexyl) -NHC(O)NH(i-Pr) -NH(c-Pr) -NHC(O)(2-thienyl) -NH(CH CF ) -NHC(O)CF -NHCO Et -NHC(O)(2-furanyl) -C(O)C(O)Me -NHCO CH CF -C(O)CO Me 2 2 3 2 -C(O)(2-pyridinyl) -NHC(O)NMe -NHC(O)NHMe -NHC(O)NHCH CF -NHC(O)CH CH CF -NHC(O)Et 2 3 2 2 3 -NHC(O)CH CF -NHSO CF -NHSO CH CF 2 3 2 3 2 2 3 -NHSO CH CH CF -NH(2-pyridinyl) -NH(3-pyridinyl) 2 2 2 3 -NH(4-pyridinyl) -NH(2-pyrimidinyl) -NH(4-pyrimidinyl) -NH(5-pyrimidinyl) -NH(6-CF pyridinyl) -NH(4-CF pyridinyl) -NH(3-CF pyridinyl) -NH(5-CF pyrimidinyl) -NH(5-CF pyridinyl) 3 3 3 -NH(4-CF pyrimidinyl) -NH(6-methylpyridinyl) -NH(4-methylpyridinyl) -NH(3-methylpyridinyl) -NH(5-methylpyrimidinyl) -NH(5-methylpyridinyl) -NH(4-methylpyrimidinyl) -NH(6-methoxypyridinyl) -NH(4-methoxypyridinyl) -NH(3-methoxypyridinyl) -NH(5-methoxypyrimidinyl) -NH(5-methoxypyridinyl) -NH(4-methoxypyrimidinyl) -CH (6-CF pyridinyl) -CH (4-CF pyridinyl) 2 3 2 3 -CH (3-CF pyridinyl) -CH (5-CF pyrimidinyl) -CH (5-CF pyridinyl) 2 3 2 3 2 3 -CH (4-CF pyrimidinyl) -CH (6-methylpyridinyl) -CH (4-methylpyridinyl) 2 3 2 2 -CH (3-methylpyridinyl) -CH (5-methylpyrimidinyl) -CH (5-methylpyridinyl) 2 2 2 -CH (4-methylpyrimidinyl) -CH (6-methoxypyridinyl) -CH (4-methoxypyridinyl) 2 2 2 -CH (3-methoxypyridinyl) -CH (5-methoxypyrimidinyl) -CH (5-methoxypyridinyl) 2 2 2 -CH (4-methoxypyrimidinyl) -CH (5-pyrimidinyl) -CH (6-bromopyridinyl) 2 2 2 -CH (2-pyrimidinyl) -CH (3-(OCF )phenyl) -CH (2-thiazolyl) 2 2 3 2 -CH (5-methylpyrazinyl) -CH (4-pyridinyl) -CH (2-pyridinyl) 2 2 2 Ph 3-pyridinyl -CH (3-pyridinyl) 2-pyridinyl 2-pyrazinyl -CH CH (2-pyridinyl) 4-pyridinyl 4-CF pyridinyl -CH CH CH (2-pyridinyl) 3 2 2 2 3-CF pyridinyl 4-CF pyrimidinyl 6-CF pyridinyl 3 3 3 -CF pyridinyl 5-CF pyrazinyl 5-CF pyrimidinyl 3 3 3 -CH CH N(-C(O)CH CH C(O)-) -CH CH CH (1-imidazolyl) -CH(-C(O)OCH CH -) 2 2 2 2 2 2 2 2 2 -CH (4-pyrimidinyl) pyridazinyl 6-CF pyrazinyl TABLE 2c A is CH N(-CH CH CH -) N(-CH CH(OMe)CH -) 2 2 2 2 2 N(-CH CH CF CH CH -) N(-CH CH CH CF CH -) 2 2 2 2 2 2 2 2 2 2 N(-CH CH CH CH -) N(-CH CH SCH CH -) 2 2 2 2 2 2 2 2 N(-CH CH CH CH CH -) N(-CH CH OCH CH -) 2 2 2 2 2 2 2 2 2 N(-CH CH N(C(O)(c-Pr))CH CH -) N(-CH CH N(Me)CH CH -) 2 2 2 2 2 2 2 2 N(-CH C(Me) N=CH-) N(-CH CH CH CH(CF )CH -) 2 2 2 2 2 3 2 N(CH C≡CH) N(Et) 2 2 2 N(Pr)CH (c-Pr) N(Et)(c-hexyl) N(-CHC(O)SCH CH -) A is CF N(-CH CH CH -) N(-CH CH(OMe)CH -) 2 2 2 2 2 N(-CH CH CF CH CH -) N(-CH CH CH CF CH -) 2 2 2 2 2 2 2 2 2 2 N(-CH CH CH CH -) N(-CH CH SCH CH -) 2 2 2 2 2 2 2 2 N(-CH CH CH CH CH -) N(-CH CH OCH CH -) 2 2 2 2 2 2 2 2 2 N(-CH CH N(C(O)(c-Pr))CH CH -) N(-CH CH N(Me)CH CH -) 2 2 2 2 2 2 2 2 N(-CH C(Me) N=CH-) N(-CH CH CH CH(CF )CH -) 2 2 2 2 2 3 2 N(CH C≡CH) N(Et) 2 2 2 N(Pr)CH (c-Pr) N(Et)(c-hexyl) N(-CHC(O)SCH CH -) A is N N(-CH CH CH -) N(-CH CH(OMe)CH -) 2 2 2 2 2 N(-CH CH CF CH CH -) N(-CH CH CH CF CH -) 2 2 2 2 2 2 2 2 2 2 N(-CH CH CH CH -) N(-CH CH SCH CH -) 2 2 2 2 2 2 2 2 N(-CH CH CH CH CH -) N(-CH CH OCH CH -) 2 2 2 2 2 2 2 2 2 N(-CH CH N(C(O)(c-Pr))CH CH -) N(-CH CH N(Me)CH CH -) 2 2 2 2 2 2 2 2 N(-CH C(Me) N=CH-) N(-CH CH CH CH(CF )CH -) 2 2 2 2 2 3 2 N(CH C≡CH) N(Et) 2 2 2 N(Pr)CH (c-Pr) N(Et)(c-hexyl) N(-CHC(O)SCH CH -) TABLE 2d A is CH N(-CH CH CH -) N(-CH CH(OMe)CH -) 2 2 2 2 2 N(-CH CH CF CH CH -) N(-CH CH CH CF CH -) 2 2 2 2 2 2 2 2 2 2 N(-CH CH CH CH -) N(-CH CH SCH CH -) 2 2 2 2 2 2 2 2 N(-CH CH CH CH CH -) N(-CH CH OCH CH -) 2 2 2 2 2 2 2 2 2 N(-CH CH N(C(O)(c-Pr))CH CH -) N(-CH CH N(Me)CH CH -) 2 2 2 2 2 2 2 2 N(-CH C(Me) N=CH-) N(-CH CH CH CH(CF )CH -) 2 2 2 2 2 3 2 N(CH C≡CH) N(Et) 2 2 2 N(Pr)CH (c-Pr) N(Et)(c-hexyl) N(-CHC(O)SCH CH -) A is CF N(-CH CH CH -) N(-CH CH(OMe)CH -) 2 2 2 2 2 N(-CH CH CF CH CH -) N(-CH CH CH CF CH -) 2 2 2 2 2 2 2 2 2 2 N(-CH CH CH CH -) N(-CH CH SCH CH -) 2 2 2 2 2 2 2 2 N(-CH CH CH CH CH -) N(-CH CH OCH CH -) 2 2 2 2 2 2 2 2 2 N(-CH CH N(C(O)(c-Pr))CH CH -) N(-CH CH N(Me)CH CH -) 2 2 2 2 2 2 2 2 N(-CH C(Me) N=CH-) N(-CH CH CH CH(CF )CH -) 2 2 2 2 2 3 2 N(CH C≡CH) N(Et) 2 2 2 N(Pr)CH (c-Pr) N(Et)(c-hexyl) N(-CHC(O)SCH CH -) A is N N(-CH CH CH -) N(-CH CH(OMe)CH -) 2 2 2 2 2 N(-CH CH CF CH CH -) N(-CH CH CH CF CH -) 2 2 2 2 2 2 2 2 2 2 N(-CH CH CH CH -) N(-CH CH SCH CH -) 2 2 2 2 2 2 2 2 N(-CH CH CH CH CH -) N(-CH CH OCH CH -) 2 2 2 2 2 2 2 2 2 N(-CH CH N(C(O)(c-Pr))CH CH -) N(-CH CH N(Me)CH CH -) 2 2 2 2 2 2 2 2 N(-CH C(Me) N=CH-) N(-CH CH CH CH(CF )CH -) 2 2 2 2 2 3 2 N(CH C≡CH) N(Et) 2 2 2 N(Pr)CH (c-Pr) N(Et)(c-hexyl) N(-CHC(O)SCH CH -) TABLE 2e A is CH 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 3-methylpyrazinyl 3-methoxypyrazinyl 3-(trifluoromethyl)pyrazinyl 3-(CH(=NOMe))pyrazinyl -methylpyrazinyl 5-methoxypyrazinyl -(trifluoromethyl)pyrazinyl 5-(CH(=NOMe))pyrazinyl 6-methylpyrazinyl 6-methoxypyrazinyl 6-(trifluoromethyl)pyrazinyl 6-(CH(=NOMe))pyrazinyl 4-methylpyrimidinyl 4-methoxypyrimidinyl 4-(trifluoromethyl)pyrimidinyl 4-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 2-methylpyrimidinyl 2-methoxypyrimidinyl 2-(trifluoromethyl)pyrimidinyl 2-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 6-methylpyrimidinyl 6-methoxypyrimidinyl 6-(trifluoromethyl)pyrimidinyl 6-(CH(=NOMe))pyrimidinyl 3-methylpyrazolyl 3-methoxypyrazolyl 3-(trifluoromethyl)pyrazolyl 3-(CH(=NOMe))pyrazolyl 4-methylpyrazolyl 4-methoxypyrazolyl 4-(trifluoromethyl)pyrazolyl 4-(CH(=NOMe))pyrazolyl -methylpyrazolyl 5-methoxypyrazolyl -(trifluoromethyl)pyrazolyl 5-(CH(=NOMe))pyrazolyl 4-methyl-1,2,3-triazinyl 4-methoxy-1,2,3-triazinyl 4-(trifluoromethyl)-1,2,3-triazinyl 4-(CH(=NOMe))-1,2,3-triazinyl 6-(2-pyrimidinyl)pyridinyl 2-(2-pyridinyl)thiazolyl 2-(2-thiazolyl)thiazolyl 2-(2-pyrimidinyl)ethynyl 1,3,4-oxadiazolyl tetrahydrofuranyl tetrahydrofuranyl 4,5-dihydroisoxazolyl 3-isoxazolyl 6-(trifluoromethyl)pyrazinyl A is CF 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 3-methylpyrazinyl 3-methoxypyrazinyl 3-(trifluoromethyl)pyrazinyl 3-(CH(=NOMe))pyrazinyl -methylpyrazinyl 5-methoxypyrazinyl -(trifluoromethyl)pyrazinyl 5-(CH(=NOMe))pyrazinyl 6-methylpyrazinyl 6-methoxypyrazinyl 6-(trifluoromethyl)pyrazinyl 6-(CH(=NOMe))pyrazinyl 4-methylpyrimidinyl 4-methoxypyrimidinyl 4-(trifluoromethyl)pyrimidinyl 4-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 2-methylpyrimidinyl 2-methoxypyrimidinyl 2-(trifluoromethyl)pyrimidinyl 2-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 6-methylpyrimidinyl 6-methoxypyrimidinyl 6-(trifluoromethyl)pyrimidinyl 6-(CH(=NOMe))pyrimidinyl 3-methylpyrazolyl 3-methoxypyrazolyl 3-(trifluoromethyl)pyrazolyl 3-(CH(=NOMe))pyrazolyl 4-methylpyrazolyl 4-methoxypyrazolyl 4-(trifluoromethyl)pyrazolyl 4-(CH(=NOMe))pyrazolyl -methylpyrazolyl 5-methoxypyrazolyl -(trifluoromethyl)pyrazolyl 5-(CH(=NOMe))pyrazolyl 4-methyl-1,2,3-triazinyl 4-methoxy-1,2,3-triazinyl 4-(trifluoromethyl)-1,2,3-triazinyl 4-(CH(=NOMe))-1,2,3-triazinyl 6-(2-pyrimidinyl)pyridinyl 2-(2-pyridinyl)thiazolyl 2-(2-thiazolyl)thiazolyl 2-(2-pyrimidinyl)ethynyl 1,3,4-oxadiazolyl tetrahydrofuranyl tetrahydrofuranyl 4,5-dihydroisoxazolyl 3-isoxazolyl 6-(trifluoromethyl)pyrazinyl A is N 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 3-methylpyrazinyl 3-methoxypyrazinyl 3-(trifluoromethyl)pyrazinyl 3-(CH(=NOMe))pyrazinyl -methylpyrazinyl 5-methoxypyrazinyl -(trifluoromethyl)pyrazinyl 5-(CH(=NOMe))pyrazinyl 6-methylpyrazinyl 6-methoxypyrazinyl 6-(trifluoromethyl)pyrazinyl 6-(CH(=NOMe))pyrazinyl 4-methylpyrimidinyl 4-methoxypyrimidinyl 4-(trifluoromethyl)pyrimidinyl 4-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 2-methylpyrimidinyl 2-methoxypyrimidinyl 2-(trifluoromethyl)pyrimidinyl 2-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 6-methylpyrimidinyl 6-methoxypyrimidinyl 6-(trifluoromethyl)pyrimidinyl 6-(CH(=NOMe))pyrimidinyl 3-methylpyrazolyl 3-methoxypyrazolyl 3-(trifluoromethyl)pyrazolyl 3-(CH(=NOMe))pyrazolyl 4-methylpyrazolyl 4-methoxypyrazolyl 4-(trifluoromethyl)pyrazolyl 4-(CH(=NOMe))pyrazolyl -methylpyrazolyl 5-methoxypyrazolyl -(trifluoromethyl)pyrazolyl 5-(CH(=NOMe))pyrazolyl 4-methyl-1,2,3-triazinyl 4-methoxy-1,2,3-triazinyl 4-(trifluoromethyl)-1,2,3-triazinyl 4-(CH(=NOMe))-1,2,3-triazinyl 6-(2-pyrimidinyl)pyridinyl 2-(2-pyridinyl)thiazolyl 2-(2-thiazolyl)thiazolyl 2-(2-pyrimidinyl)ethynyl 1,3,4-oxadiazolyl tetrahydrofuranyl tetrahydrofuranyl 4,5-dihydroisoxazolyl 3-isoxazolyl 6-(trifluoromethyl)pyrazinyl TABLE 2f A is CH 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 3-methylpyrazinyl 3-methoxypyrazinyl 3-(trifluoromethyl)pyrazinyl 3-(CH(=NOMe))pyrazinyl -methylpyrazinyl 5-methoxypyrazinyl -(trifluoromethyl)pyrazinyl 5-(CH(=NOMe))pyrazinyl 6-methylpyrazinyl 6-methoxypyrazinyl 6-(trifluoromethyl)pyrazinyl 6-(CH(=NOMe))pyrazinyl 4-methylpyrimidinyl 4-methoxypyrimidinyl 4-(trifluoromethyl)pyrimidinyl 4-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 2-methylpyrimidinyl 2-methoxypyrimidinyl 2-(trifluoromethyl)pyrimidinyl 2-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 6-methylpyrimidinyl 6-methoxypyrimidinyl 6-(trifluoromethyl)pyrimidinyl 6-(CH(=NOMe))pyrimidinyl 3-methylpyrazolyl 3-methoxypyrazolyl 3-(trifluoromethyl)pyrazolyl 3-(CH(=NOMe))pyrazolyl 4-methylpyrazolyl 4-methoxypyrazolyl 4-(trifluoromethyl)pyrazolyl 4-(CH(=NOMe))pyrazolyl -methylpyrazolyl 5-methoxypyrazolyl -(trifluoromethyl)pyrazolyl 5-(CH(=NOMe))pyrazolyl 4-methyl-1,2,3-triazinyl 4-methoxy-1,2,3-triazinyl 4-(trifluoromethyl)-1,2,3-triazinyl 4-(CH(=NOMe))-1,2,3-triazinyl 6-(2-pyrimidinyl)pyridinyl 2-(2-pyridinyl)thiazolyl 2-(2-thiazolyl)thiazolyl 2-(2-pyrimidinyl)ethynyl 1,3,4-oxadiazolyl tetrahydrofuranyl tetrahydrofuranyl 4,5-dihydroisoxazolyl 3-isoxazolyl 6-(trifluoromethyl)pyrazinyl A is CF 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 3-methylpyrazinyl 3-methoxypyrazinyl 3-(trifluoromethyl)pyrazinyl 3-(CH(=NOMe))pyrazinyl -methylpyrazinyl 5-methoxypyrazinyl -(trifluoromethyl)pyrazinyl 5-(CH(=NOMe))pyrazinyl 6-methylpyrazinyl 6-methoxypyrazinyl 6-(trifluoromethyl)pyrazinyl 6-(CH(=NOMe))pyrazinyl 4-methylpyrimidinyl 4-methoxypyrimidinyl 4-(trifluoromethyl)pyrimidinyl 4-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 2-methylpyrimidinyl 2-methoxypyrimidinyl 2-(trifluoromethyl)pyrimidinyl 2-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 6-methylpyrimidinyl 6-methoxypyrimidinyl 6-(trifluoromethyl)pyrimidinyl 6-(CH(=NOMe))pyrimidinyl 3-methylpyrazolyl 3-methoxypyrazolyl 3-(trifluoromethyl)pyrazolyl 3-(CH(=NOMe))pyrazolyl 4-methylpyrazolyl 4-methoxypyrazolyl 4-(trifluoromethyl)pyrazolyl 4-(CH(=NOMe))pyrazolyl -methylpyrazolyl 5-methoxypyrazolyl -(trifluoromethyl)pyrazolyl 5-(CH(=NOMe))pyrazolyl 4-methyl-1,2,3-triazinyl 4-methoxy-1,2,3-triazinyl 4-(trifluoromethyl)-1,2,3-triazinyl 4-(CH(=NOMe))-1,2,3-triazinyl 6-(2-pyrimidinyl)pyridinyl 2-(2-pyridinyl)thiazolyl 2-(2-thiazolyl)thiazolyl 2-(2-pyrimidinyl)ethynyl 1,3,4-oxadiazolyl tetrahydrofuranyl tetrahydrofuranyl 4,5-dihydroisoxazolyl 3-isoxazolyl 6-(trifluoromethyl)pyrazinyl A is N 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 4-methylpyridinyl 4-methoxypyridinyl 4-(trifluoromethyl)pyridinyl 4-(CH(=NOMe))pyridinyl -methylpyridinyl 5-methoxypyridinyl -(trifluoromethyl)pyridinyl 5-(CH(=NOMe))pyridinyl 6-methylpyridinyl 6-methoxypyridinyl 6-(trifluoromethyl)pyridinyl 6-(CH(=NOMe))pyridinyl 2-methylpyridinyl 2-methoxypyridinyl 2-(trifluoromethyl)pyridinyl 2-(CH(=NOMe))pyridinyl 3-methylpyridinyl 3-methoxypyridinyl 3-(trifluoromethyl)pyridinyl 3-(CH(=NOMe))pyridinyl 3-methylpyrazinyl 3-methoxypyrazinyl 3-(trifluoromethyl)pyrazinyl 3-(CH(=NOMe))pyrazinyl -methylpyrazinyl 5-methoxypyrazinyl -(trifluoromethyl)pyrazinyl 5-(CH(=NOMe))pyrazinyl 6-methylpyrazinyl 6-methoxypyrazinyl 6-(trifluoromethyl)pyrazinyl 6-(CH(=NOMe))pyrazinyl 4-methylpyrimidinyl 4-methoxypyrimidinyl 4-(trifluoromethyl)pyrimidinyl 4-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 2-methylpyrimidinyl 2-methoxypyrimidinyl 2-(trifluoromethyl)pyrimidinyl 2-(CH(=NOMe))pyrimidinyl -methylpyrimidinyl 5-methoxypyrimidinyl -(trifluoromethyl)pyrimidinyl 5-(CH(=NOMe))pyrimidinyl 6-methylpyrimidinyl 6-methoxypyrimidinyl 6-(trifluoromethyl)pyrimidinyl 6-(CH(=NOMe))pyrimidinyl 3-methylpyrazolyl 3-methoxypyrazolyl 3-(trifluoromethyl)pyrazolyl 3-(CH(=NOMe))pyrazolyl 4-methylpyrazolyl 4-methoxypyrazolyl 4-(trifluoromethyl)pyrazolyl 4-(CH(=NOMe))pyrazolyl -methylpyrazolyl 5-methoxypyrazolyl -(trifluoromethyl)pyrazolyl 5-(CH(=NOMe))pyrazolyl 4-methyl-1,2,3-triazinyl 4-methoxy-1,2,3-triazinyl 4-(trifluoromethyl)-1,2,3-triazinyl 4-(CH(=NOMe))-1,2,3-triazinyl 6-(2-pyrimidinyl)pyridinyl 2-(2-pyridinyl)thiazolyl 2-(2-thiazolyl)thiazolyl 2-(2-pyrimidinyl)ethynyl 1,3,4-oxadiazolyl tetrahydrofuranyl tetrahydrofuranyl 4,5-dihydroisoxazolyl 3-isoxazolyl 6-(trifluoromethyl)pyrazinyl TABLE 3a Table 3a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 3c Table 3c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 3e Table 3e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 4a Table 4a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 4c Table 4c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 4e Table 4e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 5a Table 5a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 5b Table 5b is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 5c Table 5c is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 5d Table 5d is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 5e Table 5e is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 5f Table 5f is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 6a Table 6a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 6c Table 6c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 6e Table 6e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 7a Table 7a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 7c Table 7c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 7e Table 7e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 8a Table 8a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 8c Table 8c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 8e Table 8e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 9a Table 9a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 9c Table 9c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 9e Table 9e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 10a Table 10a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 10b Table 10b is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 10c Table 10c is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 10d Table 10d is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 11a Table 11a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 11b Table 11b is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 11c Table 11c is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 11d Table 11d is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 12a Table 12a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 12c Table 12c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 12e Table 12e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 13a Table 13a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 13c Table 13c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 13e Table 13e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 14a Table 14a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 14c Table 14c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 14e Table 14e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 15a Table 15a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 15c Table 15c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 15e Table 15e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 16a Table 16a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 16c Table 16c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 16e Table 16e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 17a Table 17a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 17c Table 17c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 17e Table 17e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 18a Table 18a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 18c Table 18c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 18e Table 18e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 19a Table 19a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 19c Table 19c is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 19e Table 19e is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 20a Table 20a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 20b Table 20b is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 21a Table 21a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 21b Table 21b is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 22a Table 22a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 22b Table 22b is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 23a Table 23a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 23b Table 23b is identical to Table 1e, except that the structure shown under the heading "Table 1e" is replaced by the structure shown above.
TABLE 24a Table 24a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 24b Table 24b is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
TABLE 25a Table 25a is identical to Table 1a, except that the structure shown under the heading "Table 1a" is replaced by the structure shown above.
TABLE 25b Table 25b is identical to Table 1c, except that the structure shown under the heading "Table 1c" is replaced by the structure shown above.
A compound of this invention will generally be used as an invertebrate pest control active ingredient in a composition, i.e. formulation, with at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents, which serves as a carrier. The formulation or composition ingredients are selected to be consistent with the physical properties of the active ingredient, mode of application and environmental factors such as soil type, moisture and temperature.
Useful formulations include both liquid and solid compositions. Liquid compositions include solutions (including emulsifiable concentrates), suspensions, emulsions (including microemulsions, oil in water emulsions, flowable concentrates and/or suspoemulsions) and the like, which optionally can be thickened into gels. The general types of aqueous liquid compositions are soluble concentrate, suspension concentrate, capsule suspension, concentrated emulsion, microemulsion, oil in water emulsion, flowable concentrate and suspoemulsion. The general types of nonaqueous liquid compositions are emulsifiable concentrate, microemulsifiable concentrate, dispersible concentrate and oil dispersion.
The general types of solid compositions are dusts, powders, granules, pellets, prills, pastilles, tablets, filled films (including seed coatings) and the like, which can be water-dispersible (“wettable”) or water-soluble. Films and coatings formed from film- forming solutions or flowable suspensions are particularly useful for seed treatment. Active ingredient can be (micro)encapsulated and further formed into a suspension or solid formulation; alternatively the entire formulation of active ingredient can be encapsulated (or “overcoated”). Encapsulation can control or delay release of the active ingredient. An emulsifiable granule combines the advantages of both an emulsifiable concentrate formulation and a dry granular formulation. High-strength compositions are primarily used as intermediates for further formulation.
Sprayable formulations are typically extended in a suitable medium before spraying.
Such liquid and solid formulations are formulated to be readily diluted in the spray medium, usually water, but occasionally another suitable medium like an aromatic or paraffinic hydrocarbon or vegetable oil. Spray volumes can range from about one to several thousand liters per hectare, but more typically are in the range from about ten to several hundred liters per hectare. Sprayable formulations can be tank mixed with water or another suitable medium for foliar treatment by aerial or ground application, or for application to the growing medium of the plant. Liquid and dry formulations can be metered directly into drip irrigation systems or metered into the furrow during planting. Liquid and solid formulations can be applied onto seeds of crops and other desirable vegetation as seed treatments before planting to protect developing roots and other subterranean plant parts and/or foliage through systemic uptake.
The formulations will typically contain effective amounts of active ingredient, diluent and surfactant within the following approximate ranges which add up to 100 percent by weight.
Weight Percent Active Ingredient Diluent Surfactant Water-Dispersible and Water- 0.001–90 0–99.999 0–15 soluble Granules, Tablets and Powders Oil Dispersions, Suspensions, 1–50 40–99 0–50 Emulsions, Solutions (including Emulsifiable Concentrates) Dusts 1–25 70–99 0–5 Granules and Pellets 0.001–99 5–99.999 0–15 High Strength Compositions 90–99 0–10 0–2 Solid diluents include, for example, clays such as bentonite, montmorillonite, attapulgite and kaolin, gypsum, cellulose, titanium dioxide, zinc oxide, starch, dextrin, sugars (e.g., lactose, sucrose), silica, talc, mica, diatomaceous earth, urea, calcium carbonate, sodium carbonate and bicarbonate, and sodium sulfate. Typical solid diluents are described in Watkins et al., Handbook of Insecticide Dust Diluents and Carriers, 2nd Ed., Dorland Books, Caldwell, New Jersey.
Liquid diluents include, for example, water, N,N-dimethylalkanamides (e.g., N,N-dimethylformamide), limonene, dimethyl sulfoxide, N-alkylpyrrolidones (e.g., N-methylpyrrolidinone), alkyl phosphates (e.g., triethylphosphate), ethylene glycol, triethylene glycol, propylene glycol, dipropylene glycol, polypropylene glycol, propylene carbonate, butylene carbonate, paraffins (e.g., white mineral oils, normal paraffins, isoparaffins), alkylbenzenes, alkylnaphthalenes, glycerine, glycerol triacetate, sorbitol, aromatic hydrocarbons, dearomatized aliphatics, alkylbenzenes, alkylnaphthalenes, ketones such as cyclohexanone, 2-heptanone, isophorone and 4-hydroxymethylpentanone, acetates such as isoamyl acetate, hexyl acetate, heptyl acetate, octyl acetate, nonyl acetate, tridecyl acetate and isobornyl acetate, other esters such as alkylated lactate esters, dibasic esters alkyl and aryl benzoates, γ-butyrolactone, and alcohols, which can be linear, branched, saturated or unsaturated, such as methanol, ethanol, n-propanol, isopropyl alcohol, n-butanol, isobutyl alcohol, n-hexanol, 2-ethylhexanol, n-octanol, decanol, isodecyl alcohol, isooctadecanol, cetyl alcohol, lauryl alcohol, tridecyl alcohol, oleyl alcohol, cyclohexanol, tetrahydrofurfuryl alcohol, diacetone alcohol, cresol and benzyl alcohol. Liquid diluents also include glycerol esters of saturated and unsaturated fatty acids (typically C –C ), such as plant seed and fruit oils (e.g., oils of olive, castor, linseed, sesame, corn 6 22 (maize), peanut, sunflower, grapeseed, safflower, cottonseed, soybean, rapeseed, coconut and palm kernel), animal-sourced fats (e.g., beef tallow, pork tallow, lard, cod liver oil, fish oil), and mixtures thereof. Liquid diluents also include alkylated fatty acids (e.g., methylated, ethylated, butylated) wherein the fatty acids may be obtained by hydrolysis of glycerol esters from plant and animal sources, and can be purified by distillation. Typical liquid diluents are described in Marsden, Solvents Guide, 2nd Ed., Interscience, New York, 1950.
The solid and liquid compositions of the present invention often include one or more surfactants. When added to a liquid, surfactants (also known as “surface-active agents”) generally modify, most often reduce, the surface tension of the liquid. Depending on the nature of the hydrophilic and lipophilic groups in a surfactant molecule, surfactants can be useful as wetting agents, dispersants, emulsifiers or defoaming agents.
Surfactants can be classified as nonionic, anionic or cationic. Nonionic surfactants useful for the present compositions include, but are not limited to: alcohol alkoxylates such as alcohol alkoxylates based on natural and synthetic alcohols (which may be branched or linear) and prepared from the alcohols and ethylene oxide, propylene oxide, butylene oxide or mixtures thereof; amine ethoxylates, alkanolamides and ethoxylated alkanolamides; alkoxylated triglycerides such as ethoxylated soybean, castor and rapeseed oils; alkylphenol alkoxylates such as octylphenol ethoxylates, nonylphenol ethoxylates, dinonyl phenol ethoxylates and dodecyl phenol ethoxylates (prepared from the phenols and ethylene oxide, propylene oxide, butylene oxide or mixtures thereof); block polymers prepared from ethylene oxide or propylene oxide and reverse block polymers where the terminal blocks are prepared from propylene oxide; ethoxylated fatty acids; ethoxylated fatty esters and oils; ethoxylated methyl esters; ethoxylated tristyrylphenol (including those prepared from ethylene oxide, propylene oxide, butylene oxide or mixtures thereof); fatty acid esters, glycerol esters, lanolin-based derivatives, polyethoxylate esters such as polyethoxylated sorbitan fatty acid esters, polyethoxylated sorbitol fatty acid esters and polyethoxylated glycerol fatty acid esters; other sorbitan derivatives such as sorbitan esters; polymeric surfactants such as random copolymers, block copolymers, alkyd peg (polyethylene glycol) resins, graft or comb polymers and star polymers; polyethylene glycols (pegs); polyethylene glycol fatty acid esters; silicone-based surfactants; and sugar-derivatives such as sucrose esters, alkyl polyglycosides and alkyl polysaccharides.
Useful anionic surfactants include, but are not limited to: alkylaryl sulfonic acids and their salts; carboxylated alcohol or alkylphenol ethoxylates; diphenyl sulfonate derivatives; lignin and lignin derivatives such as lignosulfonates; maleic or succinic acids or their anhydrides; olefin sulfonates; phosphate esters such as phosphate esters of alcohol alkoxylates, phosphate esters of alkylphenol alkoxylates and phosphate esters of styryl phenol ethoxylates; protein-based surfactants; sarcosine derivatives; styryl phenol ether sulfate; sulfates and sulfonates of oils and fatty acids; sulfates and sulfonates of ethoxylated alkylphenols; sulfates of alcohols; sulfates of ethoxylated alcohols; sulfonates of amines and amides such as N,N-alkyltaurates; sulfonates of benzene, cumene, toluene, xylene, and dodecyl and tridecylbenzenes; sulfonates of condensed naphthalenes; sulfonates of naphthalene and alkyl naphthalene; sulfonates of fractionated petroleum; sulfosuccinamates; and sulfosuccinates and their derivatives such as dialkyl sulfosuccinate salts.
Useful cationic surfactants include, but are not limited to: amides and ethoxylated amides; amines such as N-alkyl propanediamines, tripropylenetriamines and dipropylenetetramines, and ethoxylated amines, ethoxylated diamines and propoxylated amines (prepared from the amines and ethylene oxide, propylene oxide, butylene oxide or mixtures thereof); amine salts such as amine acetates and diamine salts; quaternary ammonium salts such as quaternary salts, ethoxylated quaternary salts and diquaternary salts; and amine oxides such as alkyldimethylamine oxides and bis-(2-hydroxyethyl)-alkylamine oxides.
Also useful for the present compositions are mixtures of nonionic and anionic surfactants or mixtures of nonionic and cationic surfactants. Nonionic, anionic and cationic surfactants and their recommended uses are disclosed in a variety of published references including McCutcheon’s Emulsifiers and Detergents, annual American and International Editions published by McCutcheon’s Division, The Manufacturing Confectioner Publishing Co.; Sisely and Wood, Encyclopedia of Surface Active Agents, Chemical Publ. Co., Inc., New York, 1964; and A. S. Davidson and B. Milwidsky, Synthetic Detergents, Seventh Edition, John Wiley and Sons, New York, 1987.
Compositions of this invention may also contain formulation auxiliaries and additives, known to those skilled in the art as formulation aids (some of which may be considered to also function as solid diluents, liquid diluents or surfactants). Such formulation auxiliaries and additives may control: pH (buffers), foaming during processing (antifoams such polyorganosiloxanes), sedimentation of active ingredients (suspending agents), viscosity (thixotropic thickeners), in-container microbial growth (antimicrobials), product freezing (antifreezes), color (dyes/pigment dispersions), wash-off (film formers or stickers), evaporation (evaporation retardants), and other formulation attributes. Film formers include, for example, polyvinyl acetates, polyvinyl acetate copolymers, polyvinylpyrrolidone-vinyl acetate copolymer, polyvinyl alcohols, polyvinyl alcohol copolymers and waxes. Examples of formulation auxiliaries and additives include those listed in McCutcheon’s Volume 2: Functional Materials, annual International and North American editions published by McCutcheon’s Division, The Manufacturing Confectioner Publishing Co.; and PCT Publication WO 03/024222.
The compound of Formula 1 and any other active ingredients are typically incorporated into the present compositions by dissolving the active ingredient in a solvent or by grinding in a liquid or dry diluent. Solutions, including emulsifiable concentrates, can be prepared by simply mixing the ingredients. If the solvent of a liquid composition intended for use as an emulsifiable concentrate is water-immiscible, an emulsifier is typically added to emulsify the active-containing solvent upon dilution with water. Active ingredient slurries, with particle diameters of up to 2,000 μm can be wet milled using media mills to obtain particles with average diameters below 3 μm. Aqueous slurries can be made into finished suspension concentrates (see, for example, U.S. 3,060,084) or further processed by spray drying to form water-dispersible granules. Dry formulations usually require dry milling processes, which produce average particle diameters in the 2 to 10 μm range. Dusts and powders can be prepared by blending and usually grinding (such as with a hammer mill or fluid-energy mill). Granules and pellets can be prepared by spraying the active material upon preformed granular carriers or by agglomeration techniques. See Browning, “Agglomeration”, Chemical Engineering, December 4, 1967, pp 147–48, Perry’s Chemical Engineer’s Handbook, 4th Ed., McGraw-Hill, New York, 1963, pages 8–57 and following, and WO 91/13546. Pellets can be prepared as described in U.S. 4,172,714.
Water-dispersible and water-soluble granules can be prepared as taught in U.S. 4,144,050, U.S. 3,920,442 and DE 3,246,493. Tablets can be prepared as taught in U.S. 5,180,587, U.S. 5,232,701 and U.S. 5,208,030. Films can be prepared as taught in GB 2,095,558 and U.S. 3,299,566.
For further information regarding the art of formulation, see T. S. Woods, “The Formulator’s Toolbox – Product Forms for Modern Agriculture” in Pesticide Chemistry and Bioscience, The Food–Environment Challenge, T. Brooks and T. R. Roberts, Eds., Proceedings of the 9th International Congress on Pesticide Chemistry, The Royal Society of Chemistry, Cambridge, 1999, pp. 120–133. See also U.S. 3,235,361, Col. 6, line 16 through Col. 7, line 19 and Examples 10–41; U.S. 3,309,192, Col. 5, line 43 through Col. 7, line 62 and Examples 8, 12, 15, 39, 41, 52, 53, 58, 132, 138–140, 162–164, 166, 167 and 169–182; U.S. 2,891,855, Col. 3, line 66 through Col. 5, line 17 and Examples 1–4; Klingman, Weed Control as a Science, John Wiley and Sons, Inc., New York, 1961, pp 81–96; Hance et al., Weed Control Handbook, 8th Ed., Blackwell Scientific Publications, Oxford, 1989; and Developments in formulation technology, PJB Publications, Richmond, UK, 2000.
In the following Examples, all formulations are prepared in conventional ways.
Compound numbers refer to compounds in Index Tables A–N. Without further elaboration, it is believed that one skilled in the art using the preceding description can utilize the present invention to its fullest extent. The following Examples are, therefore, to be construed as merely illustrative, and not limiting of the disclosure in any way whatsoever. Percentages are by weight except where otherwise indicated.
Example A High Strength Concentrate Compound 8 98.5% silica aerogel 0.5% synthetic amorphous fine silica 1.0% Example B Wettable Powder Compound 14 65.0% dodecylphenol polyethylene glycol ether 2.0% sodium ligninsulfonate 4.0% sodium silicoaluminate 6.0% montmorillonite (calcined) 23.0% Example C Granule Compound 16 10.0% 90.0% attapulgite granules (low volatile matter, 0.71/0.30 mm; U.S.S. No. 25–50 sieves) Example D Extruded Pellet Compound 19 25.0% anhydrous sodium sulfate 10.0% crude calcium ligninsulfonate 5.0% sodium alkylnaphthalenesulfonate 1.0% calcium/magnesium bentonite 59.0% Example E Emulsifiable Concentrate Compound 41 10.0% polyoxyethylene sorbitol hexoleate 20.0% C –C fatty acid methyl ester 70.0% 6 10 Example F Microemulsion Compound 42 5.0% polyvinylpyrrolidone-vinyl acetate copolymer 30.0% alkylpolyglycoside 30.0% glyceryl monooleate 15.0% water 20.0% Example G Seed Treatment Compound 51 20.00% polyvinylpyrrolidone-vinyl acetate copolymer 5.00% montan acid wax 5.00% calcium ligninsulfonate 1.00% polyoxyethylene/polyoxypropylene block copolymers 1.00% stearyl alcohol (POE 20) 2.00% polyorganosilane 0.20% colorant red dye 0.05% water 65.75% Example H Fertilizer Stick Compound 54 2.5% pyrrolidone-styrene copolymer 4.8% tristyrylphenyl 16-ethoxylate 2.3% talc 0.8% corn starch 5.0% slow-release fertilizer 36.0% kaolin 38.0% water 10.6% Example I Suspension Concentrate compound 55 35% butyl polyoxyethylene/polypropylene block copolymer 4.0% stearic acid/polyethylene glycol copolymer 1.0% styrene acrylic polymer 1.0% xanthan gum 0.1% propylene glycol 5.0% silicone based defoamer 0.1% 1,2-benzisothiazolinone 0.1% water 53.7% Example J Emulsion in Water compound 76 10.0% butyl polyoxyethylene/polypropylene block copolymer 4.0% stearic acid/polyethylene glycol copolymer 1.0% styrene acrylic polymer 1.0% xanthan gum 0.1% propylene glycol 5.0% silicone based defoamer 0.1% 1,2-benzisothiazolinone 0.1% aromatic petroleum based hydrocarbon 20.0 water 58.7% Example K Oil Dispersion compound 19 25% polyoxyethylene sorbitol hexaoleate 15% organically modified bentonite clay 2.5% fatty acid methyl ester 57.5% Example L Suspoemulsion compound 42 10.0% imidacloprid 5.0% butyl polyoxyethylene/polypropylene block copolymer 4.0% stearic acid/polyethylene glycol copolymer 1.0% styrene acrylic polymer 1.0% xanthan gum 0.1% propylene glycol 5.0% silicone based defoamer 0.1% 1,2-benzisothiazolinone 0.1% aromatic petroleum based hydrocarbon 20.0% water 53.7% Compounds of this invention exhibit activity against a wide spectrum of invertebrate pests. These pests include invertebrates inhabiting a variety of environments such as, for example, plant foliage, roots, soil, harvested crops or other foodstuffs, building structures or animal integuments. These pests include, for example, invertebrates feeding on foliage (including leaves, stems, flowers and fruits), seeds, wood, textile fibers or animal blood or tissues, and thereby causing injury or damage to, for example, growing or stored agronomic crops, forests, greenhouse crops, ornamentals, nursery crops, stored foodstuffs or fiber products, or houses or other structures or their contents, or being harmful to animal health or public health. Those skilled in the art will appreciate that not all compounds are equally effective against all growth stages of all pests.
These present compounds and compositions are thus useful agronomically for protecting field crops from phytophagous invertebrate pests, and also nonagronomically for protecting other horticultural crops and plants from phytophagous invertebrate pests. This utility includes protecting crops and other plants (i.e. both agronomic and nonagronomic) that contain genetic material introduced by genetic engineering (i.e. transgenic) or modified by mutagenesis to provide advantageous traits. Examples of such traits include tolerance to herbicides, resistance to phytophagous pests (e.g., insects, mites, aphids, spiders, nematodes, snails, plant-pathogenic fungi, bacteria and viruses), improved plant growth, increased tolerance of adverse growing conditions such as high or low temperatures, low or high soil moisture, and high salinity, increased flowering or fruiting, greater harvest yields, more rapid maturation, higher quality and/or nutritional value of the harvested product, or improved storage or process properties of the harvested products. Transgenic plants can be modified to express multiple traits. Examples of plants containing traits provided by genetic engineering or mutagenesis include varieties of corn, cotton, soybean and potato expressing an insecticidal Bacillus thuringiensis toxin such as YIELD GARD , KNOCKOUT , ® ® ® ® STARLINK , BOLLGARD , NuCOTN and NEWLEAF , INVICTA RR2 PRO , and herbicide-tolerant varieties of corn, cotton, soybean and rapeseed such as ROUNDUP ® ® ® ® ® READY , LIBERTY LINK , IMI , STS and CLEARFIELD , as well as crops expressing N-acetyltransferase (GAT) to provide resistance to glyphosate herbicide, or crops containing the HRA gene providing resistance to herbicides inhibiting acetolactate synthase (ALS).
The present compounds and compositions may interact synergistically with traits introduced by genetic engineering or modified by mutagenesis, thus enhancing phenotypic expression or effectiveness of the traits or increasing the invertebrate pest control effectiveness of the present compounds and compositions. In particular, the present compounds and compositions may interact synergistically with the phenotypic expression of proteins or other natural products toxic to invertebrate pests to provide greater-than-additive control of these pests.
Compositions of this invention can also optionally comprise plant nutrients, e.g., a fertilizer composition comprising at least one plant nutrient selected from nitrogen, phosphorus, potassium, sulfur, calcium, magnesium, iron, copper, boron, manganese, zinc, and molybdenum. Of note are compositions comprising at least one fertilizer composition comprising at least one plant nutrient selected from nitrogen, phosphorus, potassium, sulfur, calcium and magnesium. Compositions of the present invention which further comprise at least one plant nutrient can be in the form of liquids or solids. Of note are solid formulations in the form of granules, small sticks or tablets. Solid formulations comprising a fertilizer composition can be prepared by mixing the compound or composition of the present invention with the fertilizer composition together with formulating ingredients and then preparing the formulation by methods such as granulation or extrusion. Alternatively solid formulations can be prepared by spraying a solution or suspension of a compound or composition of the present invention in a volatile solvent onto a previous prepared fertilizer composition in the form of dimensionally stable mixtures, e.g., granules, small sticks or tablets, and then evaporating the solvent.
Nonagronomic uses refer to invertebrate pest control in the areas other than fields of crop plants. Nonagronomic uses of the present compounds and compositions include control of invertebrate pests in stored grains, beans and other foodstuffs, and in textiles such as clothing and carpets. Nonagronomic uses of the present compounds and compositions also include invertebrate pest control in ornamental plants, forests, in yards, along roadsides and railroad rights of way, and on turf such as lawns, golf courses and pastures. Nonagronomic uses of the present compounds and compositions also include invertebrate pest control in houses and other buildings which may be occupied by humans and/or companion, farm, ranch, zoo or other animals. Nonagronomic uses of the present compounds and compositions also include the control of pests such as termites that can damage wood or other structural materials used in buildings.
Nonagronomic uses of the present compounds and compositions also include protecting human and animal health by controlling invertebrate pests that are parasitic or transmit infectious diseases. The controlling of animal parasites includes controlling external parasites that are parasitic to the surface of the body of the host animal (e.g., shoulders, armpits, abdomen, inner part of the thighs) and internal parasites that are parasitic to the inside of the body of the host animal (e.g., stomach, intestine, lung, veins, under the skin, lymphatic tissue). External parasitic or disease transmitting pests include, for example, chiggers, ticks, lice, mosquitoes, flies, mites and fleas. Internal parasites include heartworms, hookworms and helminths. Compounds and compositions of the present invention are suitable for systemic and/or non-systemic control of infestation or infection by parasites on animals. Compounds and compositions of the present invention are particularly suitable for combating external parasitic or disease transmitting pests. Compounds and compositions of the present invention are suitable for combating parasites that infest agricultural working animals, such as cattle, sheep, goats, horses, pigs, donkeys, camels, buffalos, rabbits, hens, turkeys, ducks, geese and bees; pet animals and domestic animals such as dogs, cats, pet birds and aquarium fish; as well as so-called experimental animals, such as hamsters, guinea pigs, rats and mice. By combating these parasites, fatalities and performance reduction (in terms of meat, milk, wool, skins, eggs, honey, etc.) are reduced, so that applying a composition comprising a compound of the present invention allows more economic and simple husbandry of animals.
Examples of agronomic or nonagronomic invertebrate pests include eggs, larvae and adults of the order Lepidoptera, such as armyworms, cutworms, loopers, and heliothines in the family Noctuidae (e.g., pink stem borer (Sesamia inferens Walker), corn stalk borer (Sesamia nonagrioides Lefebvre), southern armyworm (Spodoptera eridania Cramer), fall armyworm (Spodoptera frugiperda J. E. Smith), beet armyworm (Spodoptera exigua Hübner), cotton leafworm (Spodoptera littoralis Boisduval), yellowstriped armyworm (Spodoptera ornithogalli Guenée), black cutworm (Agrotis ipsilon Hufnagel), velvetbean caterpillar (Anticarsia gemmatalis Hübner), green fruitworm (Lithophane antennata Walker), cabbage armyworm (Barathra brassicae Linnaeus), soybean looper (Pseudoplusia includens Walker), cabbage looper (Trichoplusia ni Hübner), tobacco budworm (Heliothis virescens Fabricius)); borers, casebearers, webworms, coneworms, cabbageworms and skeletonizers from the family Pyralidae (e.g., European corn borer (Ostrinia nubilalis Hübner), navel orangeworm (Amyelois transitella Walker), corn root webworm (Crambus caliginosellus Clemens), sod webworms (Pyralidae: Crambinae) such as sod worm (Herpetogramma licarsisalis Walker), sugarcane stem borer (Chilo infuscatellus Snellen), tomato small borer (Neoleucinodes elegantalis Guenée), green leafroller (Cnaphalocrocis medinalis), grape leaffolder (Desmia funeralis Hübner), melon worm (Diaphania nitidalis Stoll), cabbage center grub (Helluala hydralis Guenée), yellow stem borer (Scirpophaga incertulas Walker), early shoot borer (Scirpophaga infuscatellus Snellen), white stem borer (Scirpophaga innotata Walker), top shoot borer (Scirpophaga nivella Fabricius), dark- headed rice borer (Chilo polychrysus Meyrick), striped riceborer (Chilo suppressalis Walker), cabbage cluster caterpillar (Crocidolomia binotalis English)); leafrollers, budworms, seed worms, and fruit worms in the family Tortricidae (e.g., codling moth (Cydia pomonella Linnaeus), grape berry moth (Endopiza viteana Clemens), oriental fruit moth (Grapholita molesta Busck), citrus false codling moth (Cryptophlebia leucotreta Meyrick), citrus borer (Ecdytolopha aurantiana Lima), redbanded leafroller (Argyrotaenia velutinana Walker), obliquebanded leafroller (Choristoneura rosaceana Harris), light brown apple moth (Epiphyas postvittana Walker), European grape berry moth (Eupoecilia ambiguella Hübner), apple bud moth (Pandemis pyrusana Kearfott), omnivorous leafroller (Platynota stultana Walsingham), barred fruit-tree tortrix (Pandemis cerasana Hübner), apple brown tortrix (Pandemis heparana Denis & Schiffermüller)); and many other economically important lepidoptera (e.g., diamondback moth (Plutella xylostella Linnaeus), pink bollworm (Pectinophora gossypiella Saunders), gypsy moth (Lymantria dispar Linnaeus), peach fruit borer (Carposina niponensis Walsingham), peach twig borer (Anarsia lineatella Zeller), potato tuberworm (Phthorimaea operculella Zeller), spotted teniform leafminer (Lithocolletis blancardella Fabricius), Asiatic apple leafminer (Lithocolletis ringoniella Matsumura), rice leaffolder (Lerodea eufala Edwards), apple leafminer (Leucoptera scitella Zeller)); eggs, nymphs and adults of the order Blattodea including cockroaches from the families Blattellidae and Blattidae (e.g., oriental cockroach (Blatta orientalis Linnaeus), Asian cockroach (Blatella asahinai Mizukubo), German cockroach (Blattella germanica Linnaeus), brownbanded cockroach (Supella longipalpa Fabricius), American cockroach (Periplaneta americana Linnaeus), brown cockroach (Periplaneta brunnea Burmeister), Madeira cockroach (Leucophaea maderae Fabricius)), smoky brown cockroach (Periplaneta fuliginosa Service), Australian Cockroach (Periplaneta australasiae Fabr.), lobster cockroach (Nauphoeta cinerea Olivier) and smooth cockroach (Symploce pallens Stephens)); eggs, foliar feeding, fruit feeding, root feeding, seed feeding and vesicular tissue feeding larvae and adults of the order Coleoptera including weevils from the families Anthribidae, Bruchidae, and Curculionidae (e.g., boll weevil (Anthonomus grandis Boheman), rice water weevil (Lissorhoptrus oryzophilus Kuschel), granary weevil (Sitophilus granarius Linnaeus), rice weevil (Sitophilus oryzae Linnaeus)), annual bluegrass weevil (Listronotus maculicollis Dietz), bluegrass billbug (Sphenophorus parvulus Gyllenhal), hunting billbug (Sphenophorus venatus vestitus), Denver billbug (Sphenophorus cicatristriatus Fahraeus)); flea beetles, cucumber beetles, rootworms, leaf beetles, potato beetles, and leafminers in the family Chrysomelidae (e.g., Colorado potato beetle (Leptinotarsa decemlineata Say), western corn rootworm (Diabrotica virgifera virgifera LeConte)); chafers and other beetles from the family Scarabaeidae (e.g., Japanese beetle (Popillia japonica Newman), oriental beetle (Anomala orientalis Waterhouse, Exomala orientalis (Waterhouse) Baraud), northern masked chafer (Cyclocephala borealis Arrow), southern masked chafer (Cyclocephala immaculata Olivier or C. lurida Bland), dung beetle and white grub (Aphodius spp.), black turfgrass ataenius (Ataenius spretulus Haldeman), green June beetle (Cotinis nitida Linnaeus), Asiatic garden beetle (Maladera castanea Arrow), May/June beetles (Phyllophaga spp.) and European chafer (Rhizotrogus majalis Razoumowsky)); carpet beetles from the family Dermestidae; wireworms from the family Elateridae; bark beetles from the family Scolytidae and flour beetles from the family Tenebrionidae.
In addition, agronomic and nonagronomic pests include: eggs, adults and larvae of the order Dermaptera including earwigs from the family Forficulidae (e.g., European earwig (Forficula auricularia Linnaeus), black earwig (Chelisoches morio Fabricius)); eggs, immatures, adults and nymphs of the orders Hemiptera and Homoptera such as, plant bugs from the family Miridae, cicadas from the family Cicadidae, leafhoppers (e.g. Empoasca spp.) from the family Cicadellidae, bed bugs (e.g., Cimex lectularius Linnaeus) from the family Cimicidae, planthoppers from the families Fulgoroidae and Delphacidae, treehoppers from the family Membracidae, psyllids from the family Psyllidae, whiteflies from the family Aleyrodidae, aphids from the family Aphididae, phylloxera from the family Phylloxeridae, mealybugs from the family Pseudococcidae, scales from the families Coccidae, Diaspididae and Margarodidae, lace bugs from the family Tingidae, stink bugs from the family Pentatomidae, chinch bugs (e.g., hairy chinch bug (Blissus leucopterus hirtus Montandon) and southern chinch bug (Blissus insularis Barber)) and other seed bugs from the family Lygaeidae, spittlebugs from the family Cercopidae squash bugs from the family Coreidae, and red bugs and cotton stainers from the family Pyrrhocoridae.
Agronomic and nonagronomic pests also include : eggs, larvae, nymphs and adults of the order Acari (mites) such as spider mites and red mites in the family Tetranychidae (e.g., European red mite (Panonychus ulmi Koch), two spotted spider mite (Tetranychus urticae Koch), McDaniel mite (Tetranychus mcdanieli McGregor)); flat mites in the family Tenuipalpidae (e.g., citrus flat mite (Brevipalpus lewisi McGregor)); rust and bud mites in the family Eriophyidae and other foliar feeding mites and mites important in human and animal health, i.e. dust mites in the family Epidermoptidae, follicle mites in the family Demodicidae, grain mites in the family Glycyphagidae; ticks in the family Ixodidae, commonly known as hard ticks (e.g., deer tick (Ixodes scapularis Say), Australian paralysis tick (Ixodes holocyclus Neumann), American dog tick (Dermacentor variabilis Say), lone star tick (Amblyomma americanum Linnaeus)) and ticks in the family Argasidae, commonly known as soft ticks (e.g., relapsing fever tick (Ornithodoros turicata), common fowl tick (Argas radiatus)); scab and itch mites in the families Psoroptidae, Pyemotidae, and Sarcoptidae; eggs, adults and immatures of the order Orthoptera including grasshoppers, locusts and crickets (e.g., migratory grasshoppers (e.g., Melanoplus sanguinipes Fabricius, M. differentialis Thomas), American grasshoppers (e.g., Schistocerca americana Drury), desert locust (Schistocerca gregaria Forskal), migratory locust (Locusta migratoria Linnaeus), bush locust (Zonocerus spp.), house cricket (Acheta domesticus Linnaeus), mole crickets (e.g., tawny mole cricket (Scapteriscus vicinus Scudder) and southern mole cricket (Scapteriscus borellii Giglio-Tos)); eggs, adults and immatures of the order Diptera including leafminers (e.g., Liriomyza spp. such as serpentine vegetable leafminer (Liriomyza sativae Blanchard)), midges, fruit flies (Tephritidae), frit flies (e.g., Oscinella frit Linnaeus), soil maggots, house flies (e.g., Musca domestica Linnaeus), lesser house flies (e.g., Fannia canicularis Linnaeus, F. femoralis Stein), stable flies (e.g., Stomoxys calcitrans Linnaeus), face flies, horn flies, blow flies (e.g., Chrysomya spp., Phormia spp.), and other muscoid fly pests, horse flies (e.g., Tabanus spp.), bot flies (e.g., Gastrophilus spp., Oestrus spp.), cattle grubs (e.g., Hypoderma spp.), deer flies (e.g., Chrysops spp.), keds (e.g., Melophagus ovinus Linnaeus) and other Brachycera, mosquitoes (e.g., Aedes spp., Anopheles spp., Culex spp.), black flies (e.g., Prosimulium spp., Simulium spp.), biting midges, sand flies, sciarids, and other Nematocera; eggs, adults and immatures of the order Thysanoptera including onion thrips (Thrips tabaci Lindeman), flower thrips (Frankliniella spp.), and other foliar feeding thrips; insect pests of the order Hymenoptera including ants of the Family Formicidae including the Florida carpenter ant (Camponotus floridanus Buckley), red carpenter ant (Camponotus ferrugineus Fabricius), black carpenter ant (Camponotus pennsylvanicus De Geer), white-footed ant (Technomyrmex albipes fr. Smith), big headed ants (Pheidole sp.), ghost ant (Tapinoma melanocephalum Fabricius); Pharaoh ant (Monomorium pharaonis Linnaeus), little fire ant (Wasmannia auropunctata Roger), fire ant (Solenopsis geminata Fabricius), red imported fire ant (Solenopsis invicta Buren), Argentine ant (Iridomyrmex humilis Mayr), crazy ant (Paratrechina longicornis Latreille), pavement ant (Tetramorium caespitum Linnaeus), cornfield ant (Lasius alienus Förster) and odorous house ant (Tapinoma sessile Say). Other Hymenoptera including bees (including carpenter bees), hornets, yellow jackets, wasps, and sawflies (Neodiprion spp.; Cephus spp.); insect pests of the order Isoptera including termites in the Termitidae (e.g., Macrotermes sp., Odontotermes obesus Rambur), Kalotermitidae (e.g., Cryptotermes sp.), and Rhinotermitidae (e.g., Reticulitermes sp., Coptotermes sp., Heterotermes tenuis Hagen) families, the eastern subterranean termite (Reticulitermes flavipes Kollar), western subterranean termite (Reticulitermes hesperus Banks), Formosan subterranean termite (Coptotermes formosanus Shiraki), West Indian drywood termite (Incisitermes immigrans Snyder), powder post termite (Cryptotermes brevis Walker), drywood termite (Incisitermes snyderi Light), southeastern subterranean termite (Reticulitermes virginicus Banks), western drywood termite (Incisitermes minor Hagen), arboreal termites such as Nasutitermes sp. and other termites of economic importance; insect pests of the order Thysanura such as silverfish (Lepisma saccharina Linnaeus) and firebrat (Thermobia domestica Packard); insect pests of the order Mallophaga and including the head louse (Pediculus humanus capitis De Geer), body louse (Pediculus humanus Linnaeus), chicken body louse (Menacanthus stramineus Nitszch), dog biting louse (Trichodectes canis De Geer), fluff louse (Goniocotes gallinae De Geer), sheep body louse (Bovicola ovis Schrank), short-nosed cattle louse (Haematopinus eurysternus Nitzsch), long-nosed cattle louse (Linognathus vituli Linnaeus) and other sucking and chewing parasitic lice that attack man and animals; insect pests of the order Siphonoptera including the oriental rat flea (Xenopsylla cheopis Rothschild), cat flea (Ctenocephalides felis Bouche), dog flea (Ctenocephalides canis Curtis), hen flea (Ceratophyllus gallinae Schrank), sticktight flea (Echidnophaga gallinacea Westwood), human flea (Pulex irritans Linnaeus) and other fleas afflicting mammals and birds.
Additional arthropod pests covered include: spiders in the order Araneae such as the brown recluse spider (Loxosceles reclusa Gertsch & Mulaik) and the black widow spider (Latrodectus mactans Fabricius), and centipedes in the order Scutigeromorpha such as the house centipede (Scutigera coleoptrata Linnaeus).
Examples of invertebrate pests of stored grain include larger grain borer (Prostephanus truncatus), lesser grain borer (Rhyzopertha dominica), rice weevil (Stiophilus oryzae), maize weevil (Stiophilus zeamais), cowpea weevil (Callosobruchus maculatus), red flour beetle (Tribolium castaneum), granary weevil (Stiophilus granarius), Indian meal moth (Plodia interpunctella), Mediterranean flour beetle (Ephestia kuhniella) and flat or rusty grain beetle (Cryptolestis ferrugineus).
Compounds of the present invention may have activity on members of the Classes Nematoda, Cestoda, Trematoda, and Acanthocephala including economically important members of the orders Strongylida, Ascaridida, Oxyurida, Rhabditida, Spirurida, and Enoplida such as but not limited to economically important agricultural pests (i.e. root knot nematodes in the genus Meloidogyne, lesion nematodes in the genus Pratylenchus, stubby root nematodes in the genus Trichodorus, etc.) and animal and human health pests (i.e. all economically important flukes, tapeworms, and roundworms, such as Strongylus vulgaris in horses, Toxocara canis in dogs, Haemonchus contortus in sheep, Dirofilaria immitis Leidy in dogs, Anoplocephala perfoliata in horses, Fasciola hepatica Linnaeus in ruminants, etc.).
Compounds of the invention may have activity against pests in the order Lepidoptera (e.g., Alabama argillacea Hübner (cotton leaf worm), Archips argyrospila Walker (fruit tree leaf roller), A. rosana Linnaeus (European leaf roller) and other Archips species, Chilo suppressalis Walker (rice stem borer), Cnaphalocrosis medinalis Guenée (rice leaf roller), Crambus caliginosellus Clemens (corn root webworm), Crambus teterrellus Zincken (bluegrass webworm), Cydia pomonella Linnaeus (codling moth), Earias insulana Boisduval (spiny bollworm), Earias vittella Fabricius (spotted bollworm), Helicoverpa armigera Hübner (American bollworm), Helicoverpa zea Boddie (corn earworm), Heliothis virescens Fabricius (tobacco budworm), Herpetogramma licarsisalis Walker (sod webworm), Lobesia botrana Denis & Schiffermüller (grape berry moth), Pectinophora gossypiella Saunders (pink bollworm), Phyllocnistis citrella Stainton (citrus leafminer), Pieris brassicae Linnaeus (large white butterfly), Pieris rapae Linnaeus (small white butterfly), Plutella xylostella Linnaeus (diamondback moth), Spodoptera exigua Hübner (beet armyworm), Spodoptera litura Fabricius (tobacco cutworm, cluster caterpillar), Spodoptera frugiperda J. E. Smith (fall armyworm), Trichoplusia ni Hübner (cabbage looper) and Tuta absoluta Meyrick (tomato leafminer)).
Compounds of the invention have significant activity on members from the order Homoptera including: Acyrthosiphon pisum Harris (pea aphid), Aphis craccivora Koch (cowpea aphid), Aphis fabae Scopoli (black bean aphid), Aphis gossypii Glover (cotton aphid, melon aphid), Aphis pomi De Geer (apple aphid), Aphis spiraecola Patch (spirea aphid), Aulacorthum solani Kaltenbach (foxglove aphid), Chaetosiphon fragaefolii Cockerell (strawberry aphid), Diuraphis noxia Kurdjumov/Mordvilko (Russian wheat aphid), Dysaphis plantaginea Paaserini (rosy apple aphid), Eriosoma lanigerum Hausmann (woolly apple aphid), Hyalopterus pruni Geoffroy (mealy plum aphid), Lipaphis erysimi Kaltenbach (turnip aphid), Metopolophium dirrhodum Walker (cereal aphid), Macrosiphum euphorbiae Thomas (potato aphid), Myzus persicae Sulzer (peach-potato aphid, green peach aphid), Nasonovia ribisnigri Mosley (lettuce aphid), Pemphigus spp. (root aphids and gall aphids), Rhopalosiphum maidis Fitch (corn leaf aphid), Rhopalosiphum padi Linnaeus (bird cherry-oat aphid), Schizaphis graminum Rondani (greenbug), Sitobion avenae Fabricius (English grain aphid), Therioaphis maculata Buckton (spotted alfalfa aphid), Toxoptera aurantii Boyer de Fonscolombe (black citrus aphid), and Toxoptera citricida Kirkaldy (brown citrus aphid); Adelges spp. (adelgids); Phylloxera devastatrix Pergande (pecan phylloxera); Bemisia tabaci Gennadius (tobacco whitefly, sweetpotato whitefly), Bemisia argentifolii Bellows & Perring (silverleaf whitefly), Dialeurodes citri Ashmead (citrus whitefly) and Trialeurodes vaporariorum Westwood (greenhouse whitefly); Empoasca fabae Harris (potato leafhopper), Laodelphax striatellus Fallen (smaller brown planthopper), Macrolestes quadrilineatus Forbes (aster leafhopper), Nephotettix cinticeps Uhler (green leafhopper), Nephotettix nigropictus Stål (rice leafhopper), Nilaparvata lugens Stål (brown planthopper), Peregrinus maidis Ashmead (corn planthopper), Sogatella furcifera Horvath (white-backed planthopper), Sogatodes orizicola Muir (rice delphacid), Typhlocyba pomaria McAtee white apple leafhopper, Erythroneoura spp. (grape leafhoppers); Magicidada septendecim Linnaeus (periodical cicada); Icerya purchasi Maskell (cottony cushion scale), Quadraspidiotus perniciosus Comstock (San Jose scale); Planococcus citri Risso (citrus mealybug); Pseudococcus spp. (other mealybug complex); Cacopsylla pyricola Foerster (pear psylla), Trioza diospyri Ashmead (persimmon psylla).
Compounds of this invention also have activity on members from the order Hemiptera including: Acrosternum hilare Say (green stink bug), Anasa tristis De Geer (squash bug), Blissus leucopterus leucopterus Say (chinch bug), Cimex lectularius Linnaeus (bed bug) Corythuca gossypii Fabricius (cotton lace bug), Cyrtopeltis modesta Distant (tomato bug), Dysdercus suturellus Herrich-Schäffer (cotton stainer), Euchistus servus Say (brown stink bug), Euchistus variolarius Palisot de Beauvois (one-spotted stink bug), Graptosthetus spp. (complex of seed bugs), Halymorpha halys Stål (brown marmorated stink bug), Leptoglossus corculus Say (leaf-footed pine seed bug), Lygus lineolaris Palisot de Beauvois (tarnished plant bug), Nezara viridula Linnaeus (southern green stink bug), Oebalus pugnax Fabricius (rice stink bug), Oncopeltus fasciatus Dallas (large milkweed bug), Pseudatomoscelis seriatus Reuter (cotton fleahopper). Other insect orders controlled by compounds of the invention include Thysanoptera (e.g., Frankliniella occidentalis Pergande (western flower thrips), Scirthothrips citri Moulton (citrus thrips), Sericothrips variabilis Beach (soybean thrips), and Thrips tabaci Lindeman (onion thrips); and the order Coleoptera (e.g., Leptinotarsa decemlineata Say (Colorado potato beetle), Epilachna varivestis Mulsant (Mexican bean beetle) and wireworms of the genera Agriotes, Athous or Limonius).
Note that some contemporary classification systems place Homoptera as a suborder within the order Hemiptera.
Of note is use of compounds of this invention for controlling western flower thrips (Frankliniella occidentalis). Of note is use of compounds of this invention for controlling potato leafhopper (Empoasca fabae). Of note is use of compounds of this invention for controlling cotton melon aphid (Aphis gossypii). Of note is use of compounds of this invention for controlling green peach aphid (Myzus persicae). Of note is use of compounds of this invention for controlling sweetpotato whitefly (Bemisia tabaci).
Compounds of the present invention may also be useful for increasing vigor of a crop plant. This method comprises contacting the crop plant (e.g., foliage, flowers, fruit or roots) or the seed from which the crop plant is grown with a compound of Formula 1 in amount sufficient to achieve the desired plant vigor effect (i.e. biologically effective amount).
Typically the compound of Formula 1 is applied in a formulated composition. Although the compound of Formula 1 is often applied directly to the crop plant or its seed, it can also be applied to the locus of the crop plant, i.e. the environment of the crop plant, particularly the portion of the environment in close enough proximity to allow the compound of Formula 1 to migrate to the crop plant. The locus relevant to this method most commonly comprises the growth medium (i.e. medium providing nutrients to the plant), typically soil in which the plant is grown. Treatment of a crop plant to increase vigor of the crop plant thus comprises contacting the crop plant, the seed from which the crop plant is grown or the locus of the crop plant with a biologically effective amount of a compound of Formula 1.
Increased crop vigor can result in one or more of the following observed effects: (a) optimal crop establishment as demonstrated by excellent seed germination, crop emergence and crop stand; (b) enhanced crop growth as demonstrated by rapid and robust leaf growth (e.g., measured by leaf area index), plant height, number of tillers (e.g., for rice), root mass and overall dry weight of vegetative mass of the crop; (c) improved crop yields, as demonstrated by time to flowering, duration of flowering, number of flowers, total biomass accumulation (i.e. yield quantity) and/or fruit or grain grade marketability of produce (i.e. yield quality); (d) enhanced ability of the crop to withstand or prevent plant disease infections and arthropod, nematode or mollusk pest infestations; and (e) increased ability of the crop to withstand environmental stresses such as exposure to thermal extremes, suboptimal moisture or phytotoxic chemicals.
The compounds of the present invention may increase the vigor of treated plants compared to untreated plants by killing or otherwise preventing feeding of phytophagous invertebrate pests in the environment of the plants. In the absence of such control of phytophagous invertebrate pests, the pests reduce plant vigor by consuming plant tissues or sap, or transmiting plant pathogens such as viruses. Even in the absence of phytophagous invertebrate pests, the compounds of the invention may increase plant vigor by modifying metabolism of plants. Generally, the vigor of a crop plant will be most significantly increased by treating the plant with a compound of the invention if the plant is grown in a nonideal environment, i.e. an environment comprising one or more aspects adverse to the plant achieving the full genetic potential it would exhibit in an ideal environment.
Of note is a method for increasing vigor of a crop plant wherein the crop plant is grown in an environment comprising phytophagous invertebrate pests. Also of note is a method for increasing vigor of a crop plant wherein the crop plant is grown in an environment not comprising phytophagous invertebrate pests. Also of note is a method for increasing vigor of a crop plant wherein the crop plant is grown in an environment comprising an amount of moisture less than ideal for supporting growth of the crop plant.
Of note is a method for increasing vigor of a crop plant wherein the crop is rice. Also of note is a method for increasing vigor of a crop plant wherein the crop is maize (corn). Also of note is a method for increasing vigor of a crop plant wherein the crop is soybean.
Compounds of this invention can also be mixed with one or more other biologically active compounds or agents including insecticides, fungicides, nematocides, bactericides, acaricides, herbicides, herbicide safeners, growth regulators such as insect molting inhibitors and rooting stimulants, chemosterilants, semiochemicals, repellents, attractants, pheromones, feeding stimulants, other biologically active compounds or entomopathogenic bacteria, virus or fungi to form a multi-component pesticide giving an even broader spectrum of agronomic and nonagronomic utility. Thus the present invention also pertains to a composition comprising a biologically effective amount of a compound of Formula 1, at least one additional component selected from the group consisting of surfactants, solid diluents and liquid diluents, and at least one additional biologically active compound or agent. For mixtures of the present invention, the other biologically active compounds or agents can be formulated together with the present compounds, including the compounds of Formula 1, to form a premix, or the other biologically active compounds or agents can be formulated separately from the present compounds, including the compounds of Formula 1, and the two formulations combined together before application (e.g., in a spray tank) or, alternatively, applied in succession.
Examples of such biologically active compounds or agents with which compounds of this invention can be formulated are insecticides such as abamectin, acephate, acequinocyl, acetamiprid, acrinathrin, afidopyropen ([(3S,4R,4aR,6S,6aS,12R,12aS,12bS) [(cyclopropylcarbonyl)oxy]-1,3,4,4a,5,6,6a,12,12a,12b-decahydro-6,12-dihydroxy-4,6a,12b- trimethyloxo(3-pyridinyl)-2H,11H-naphtho[2,1-b]pyrano[3,4-e]pyranyl]methyl cyclopropanecarboxylate), amidoflumet, amitraz, avermectin, azadirachtin, azinphos-methyl, benfuracarb, bensultap, bifenthrin, bifenazate, bistrifluron, borate, , buprofezin, cadusafos, carbaryl, carbofuran, cartap, carzol, chlorantraniliprole, chlorfenapyr, chlorfluazuron, chlorpyrifos, chlorpyrifos-methyl, chromafenozide, clofentezin, clothianidin, cyantraniliprole (3-bromo(3-chloropyridinyl)-N-[4-cyanomethyl [(methylamino)carbonyl]phenyl]-1H-pyrazolecarboxamide), cyclaniliprole (3-bromo-N- [2-bromochloro[[(1-cyclopropylethyl)amino]carbonyl]phenyl](3-chloro pyridinyl)-1H-pyrazolecarboxamide), cycloprothrin, cycloxaprid ((5S,8R)[(6-chloro pyridinyl)methyl]-2,3,5,6,7,8-hexahydronitro-5,8-Epoxy-1H-imidazo[1,2-a]azepine) cyflumetofen, cyfluthrin, beta-cyfluthrin, cyhalothrin, gamma-cyhalothrin, lambda- cyhalothrin, cypermethrin, alpha-cypermethrin, zeta-cypermethrin, cyromazine, deltamethrin, diafenthiuron, diazinon, dieldrin, diflubenzuron, dimefluthrin, dimehypo, dimethoate, dinotefuran, diofenolan, emamectin, endosulfan, esfenvalerate, ethiprole, etofenprox, etoxazole, fenbutatin oxide, fenitrothion, fenothiocarb, fenoxycarb, fenpropathrin, fenvalerate, fipronil, flometoquin (2-ethyl-3,7-dimethyl[4- (trifluoromethoxy)phenoxy]quinolinyl methyl carbonate), flonicamid, flubendiamide, flucythrinate, flufenerim, flufenoxuron, flufenoxystrobin (methyl (αE)[[2-chloro (trifluoromethyl)phenoxy]methyl]-α-(methoxymethylene)benzeneacetate), fluensulfone (5- chloro[(3,4,4-trifluorobutenyl)sulfonyl]thiazole), fluhexafon, fluopyram, flupiprole (1-[2,6-dichloro(trifluoromethyl)phenyl][(2-methylpropenyl)amino] [(trifluoromethyl)sulfinyl]-1H-pyrazolecarbonitrile), flupyradifurone (4-[[(6-chloro pyridinyl)methyl](2,2-difluoroethyl)amino]-2(5H)-furanone), fluvalinate, tau-fluvalinate, fonophos, formetanate, fosthiazate, halofenozide, heptafluthrin ([2,3,5,6-tetrafluoro (methoxymethyl)phenyl]methyl 2,2-dimethyl[(1Z)-3,3,3-trifluoropropen yl]cyclopropanecarboxylate), hexaflumuron, hexythiazox, hydramethylnon, imidacloprid, indoxacarb, insecticidal soaps, isofenphos, lufenuron, malathion, meperfluthrin ([2,3,5,6- tetrafluoro(methoxymethyl)phenyl]methyl (1R,3S)(2,2-dichloroethenyl)-2,2- dimethylcyclopropanecarboxylate), metaflumizone, metaldehyde, methamidophos, methidathion, methiodicarb, methomyl, methoprene, methoxychlor, metofluthrin, methoxyfenozide, metofluthrin, monocrotophos, monofluorothrin ([2,3,5,6-tetrafluoro (methoxymethyl)phenyl]methyl 3-(2-cyanopropenyl)-2,2- dimethylcyclopropanecarboxylate), nicotine, nitenpyram, nithiazine, novaluron, noviflumuron, oxamyl, parathion, parathion-methyl, permethrin, phorate, phosalone, phosmet, phosphamidon, pirimicarb, profenofos, profluthrin, propargite, protrifenbute, pyflubumide (1,3,5-trimethyl-N-(2-methyloxopropyl)-N-[3-(2-methylpropyl)[2,2,2- trifluoromethoxy(trifluoromethyl)ethyl]phenyl]-1H-pyrazolecarboxamide), pymetrozine, pyrafluprole, pyrethrin, pyridaben, pyridalyl, pyrifluquinazon, pyriminostrobin (methyl (αE)[[[2-[(2,4-dichlorophenyl)amino](trifluoromethyl) pyrimidinyl]oxy]methyl]-α-(methoxymethylene)benzeneacetate), pyriprole, pyriproxyfen, rotenone, ryanodine, silafluofen, spinetoram, spinosad, spirodiclofen, spiromesifen, spirotetramat, sulprofos, sulfoxaflor (N-[methyloxido[1-[6-(trifluoromethyl) pyridinyl]ethyl]-λ -sulfanylidene]cyanamide), tebufenozide, tebufenpyrad, teflubenzuron, tefluthrin, terbufos, tetrachlorvinphos, tetramethrin, tetramethylfluthrin ([2,3,5,6-tetrafluoro- 4-(methoxymethyl)phenyl]methyl 2,2,3,3-tetramethylcyclopropanecarboxylate), tetraniliprole, thiacloprid, thiamethoxam, thiodicarb, thiosultap-sodium, tioxazafen (3- phenyl(2-thienyl)-1,2,4-oxadiazole), tolfenpyrad, tralomethrin, triazamate, trichlorfon, triflumezopyrim (2,4-dioxo(5-pyrimidinylmethyl)[3-(trifluoromethyl)phenyl]-2H- pyrido[1,2-a]pyrimidinium inner salt), triflumuron, Bacillus thuringiensis delta-endotoxins, entomopathogenic bacteria, entomopathogenic viruses and entomopathogenic fungi.
Of note are insecticides such as abamectin, acetamiprid, acrinathrin, afidopyropen, amitraz, avermectin, azadirachtin, benfuracarb, bensultap, bifenthrin, buprofezin, cadusafos, carbaryl, cartap, chlorantraniliprole, chlorfenapyr, chlorpyrifos, clothianidin, cyantraniliprole, cyclaniliprole, cycloprothrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, gamma-cyhalothrin, lambda-cyhalothrin, cypermethrin, alpha-cypermethrin, zeta- cypermethrin, cyromazine, deltamethrin, dieldrin, dinotefuran, diofenolan, emamectin, endosulfan, esfenvalerate, ethiprole, etofenprox, etoxazole, fenitrothion, fenothiocarb, fenoxycarb, fenvalerate, fipronil, flometoquin, flonicamid, flubendiamide, flufenoxuron, flufenoxystrobin, fluensulfone, flupiprole, flupyradifurone, fluvalinate, formetanate, fosthiazate, heptafluthrin, hexaflumuron, hydramethylnon, imidacloprid, indoxacarb, lufenuron, meperfluthrin, metaflumizone, methiodicarb, methomyl, methoprene, methoxyfenozide, metofluthrin, monofluorothrin, nitenpyram, nithiazine, novaluron, oxamyl, pyflubumide, pymetrozine, pyrethrin, pyridaben, pyridalyl, pyriminostrobin, pyriproxyfen, ryanodine, spinetoram, spinosad, spirodiclofen, spiromesifen, spirotetramat, sulfoxaflor, tebufenozide, tetramethrin, tetramethylfluthrin, thiacloprid, thiamethoxam, thiodicarb, thiosultap-sodium, tralomethrin, triazamate, triflumezopyrim, triflumuron, Bacillus thuringiensis delta-endotoxins, all strains of Bacillus thuringiensis and all strains of nucleo polyhedrosis viruses.
One embodiment of biological agents for mixing with compounds of this invention include entomopathogenic bacteria such as Bacillus thuringiensis, and the encapsulated delta-endotoxins of Bacillus thuringiensis such as MVP and MVPII bioinsecticides ® ® ® ® prepared by the CellCap process (CellCap , MVP and MVPII are trademarks of Mycogen Corporation, Indianapolis, Indiana, USA); entomopathogenic fungi such as green muscardine fungus; and entomopathogenic (both naturally occurring and genetically modified) viruses including baculovirus, nucleopolyhedro virus (NPV) such as Helicoverpa zea nucleopolyhedrovirus (HzNPV), Anagrapha falcifera nucleopolyhedrovirus (AfNPV); and granulosis virus (GV) such as Cydia pomonella granulosis virus (CpGV).
Of particular note is such a combination where the other invertebrate pest control active ingredient belongs to a different chemical class or has a different site of action than the compound of Formula 1. In certain instances, a combination with at least one other invertebrate pest control active ingredient having a similar spectrum of control but a different site of action will be particularly advantageous for resistance management. Thus, a composition of the present invention can further comprise a biologically effective amount of at least one additional invertebrate pest control active ingredient having a similar spectrum of control but belonging to a different chemical class or having a different site of action.
These additional biologically active compounds or agents include, but are not limited to, acetylcholinesterase (AChE) inhibitors such as the carbamates methomyl, oxamyl, thiodicarb, triazamate, and the organophosphates chlorpyrifos; GABA-gated chloride channel antagonists such as the cyclodienes dieldrin and endosulfan, and the phenylpyrazoles ethiprole and fipronil; sodium channel modulators such as the pyrethroids bifenthrin, cyfluthrin, beta-cyfluthrin, cyhalothrin, lambda-cyhalothrin, cypermethrin, deltamethrin, dimefluthrin, esfenvalerate, metofluthrin and profluthrin; nicotinic acetylcholinereceptor (nAChR) agonists such as the neonicotinoids acetamiprid, clothianidin, dinotefuran, imidacloprid, nitenpyram, nithiazine, thiacloprid, and thiamethoxam, and sulfoxaflor; nicotinic acetylcholine receptor (nAChR) allosteric activators such as the spinosyns spinetoram and spinosad; chloride channel activators such as the avermectins abamectin and emamectin; juvenile hormone mimics such as diofenolan, methoprene, fenoxycarb and pyriproxyfen; selective homopteran feeding blockers such as pymetrozine and flonicamid; mite growth inhibitors such as etoxazole; inhibitors of mitochondrial ATP synthase such as propargite; ucouplers of oxidative phosphorylation via disruption of the proton gradient such as chlorfenapyr; nicotinic acetylcholine receptor (nAChR) channel blockers such as the nereistoxin analogs cartap; inhibitors of chitin biosynthesis such as the benzoylureas flufenoxuron, hexaflumuron, lufenuron, novaluron, noviflumuron and triflumuron, and buprofezin; dipteran moulting disrupters such as cyromazine; ecdysone receptor agonists such as the diacylhydrazines methoxyfenozide and tebufenozide; octopamine receptor agonists such as amitraz; mitochondrial complex III electron transport inhibitors such as hydramethylnon; mitochondrial complex I electron transport inhibitors such as pyridaben; voltage-dependent sodium channel blockers such as indoxacarb; inhibitors of acetyl CoA carboxylase such as the tetronic and tetramic acids spirodiclofen, spiromesifen and spirotetramat; mitochondrial complex II electron transport inhibitors such as the ß-ketonitriles cyenopyrafen and cyflumetofen; ryanidine receptor modulators such as the anthranilic diamides chlorantraniliprole, cyantraniliprole and cyantraniliprole, diamides such as flubendiamide, and ryanodine receptor ligands such as ryanodine; compounds wherein the target site responsible for biological activity is unknown or uncharacterized such as azadirachtin, bifenazate, pyridalyl, pyrifluquinazon and triflumezopyrim; microbial disrupters of insect midgut membranes such as Bacillus thuringensis and the delta-endotoxins they produce and Bacillus sphaericus; and biological agents including nucleo polyhedro viruses (NPV) and other naturally occurring or genetically modified insecticidal viruses.
Further examples of biologically active compounds or agents with which compounds of this invention can be formulated are: fungicides such as acibenzolar-S-methyl, aldimorph, ametoctradin, amisulbrom, anilazine, azaconazole, azoxystrobin, benalaxyl (including benalaxyl-M), benodanil, benomyl, benthiavalicarb (including benthiavalicarb-isopropyl), benzovindiflupyr, bethoxazin, binapacryl, biphenyl, bitertanol, bixafen, blasticidin-S, boscalid, bromuconazole, bupirimate, buthiobate, carboxin, carpropamid, captafol, captan, carbendazim, chloroneb, chlorothalonil, chlozolinate, copper hydroxide, copper oxychloride, copper sulfate, coumoxystrobin, cyazofamid, cyflufenamid, cymoxanil, cyproconazole, cyprodinil, dichlofluanid, diclocymet, diclomezine, dicloran, diethofencarb, difenoconazole, diflumetorim, dimethirimol, dimethomorph, dimoxystrobin, diniconazole (including diniconazole-M), dinocap, dithianon, dithiolanes, dodemorph, dodine, econazole, etaconazole, edifenphos, enoxastrobin (also known as enestroburin), epoxiconazole, ethaboxam, ethirimol, etridiazole, famoxadone, fenamidone, fenaminstrobin, fenarimol, fenbuconazole, fenfuram, fenhexamide, fenoxanil, fenpiclonil, fenpropidin, fenpropimorph, fenpyrazamine, fentin acetate, fentin hydroxide, ferbam, ferimzone, flometoquin, fluazinam, fludioxonil, flufenoxystrobin, flumorph, fluopicolide, fluopyram, fluoxastrobin, fluquinconazole, flusilazole, flusulfamide, flutianil, flutolanil, flutriafol, fluxapyroxad, folpet, fthalide (also known as phthalide), fuberidazole, furalaxyl, furametpyr, hexaconazole, hymexazole, guazatine, imazalil, imibenconazole, iminoctadine albesilate, iminoctadine triacetate, iodicarb, ipconazole, isofetamid, iprobenfos, iprodione, iprovalicarb, isoprothiolane, isopyrazam, isotianil, kasugamycin, kresoxim-methyl, mancozeb, mandipropamid, mandestrobin, maneb, mapanipyrin, mepronil, meptyldinocap, metalaxyl (including metalaxyl-M/mefenoxam), metconazole, methasulfocarb, metiram, metominostrobin, metrafenone, myclobutanil, naftitine, neo-asozin (ferric methanearsonate), nuarimol, octhilinone, ofurace, orysastrobin, oxadixyl, oxathiapiprolin, oxolinic acid, oxpoconazole, oxycarboxin, oxytetracycline, penconazole, pencycuron, penflufen, penthiopyrad, perfurazoate, phosphorous acid (including salts thereof, e.g., fosetyl- aluminm), picoxystrobin, piperalin, polyoxin, probenazole, prochloraz, procymidone, propamocarb, propiconazole, propineb, proquinazid, prothiocarb, prothioconazole, pyraclostrobin, pyrametostrobin, pyraoxystrobin, pyrazophos, pyribencarb, pyributacarb, pyrifenox, pyriofenone, perisoxazole, pyrimethanil, pyrifenox, pyrrolnitrin, pyroquilon, quinconazole, quinmethionate, quinoxyfen, quintozene, silthiofam, sedaxane, simeconazole, spiroxamine, streptomycin, sulfur, tebuconazole, tebufloquin, teclofthalam, tecloftalam, tecnazene, terbinafine, tetraconazole, thiabendazole, thifluzamide, thiophanate, thiophanate- methyl, thiram, tiadinil, tolclofos-methyl, tolprocarb, tolyfluanid, triadimefon, triadimenol, triarimol, triazoxide, tribasic copper sulfate, triclopyricarb, tridemorph, trifloxystrobin, triflumizole, trimoprhamide tricyclazole, trifloxystrobin, triforine, triticonazole, uniconazole, validamycin, valifenalate (also known as valifenal), vinclozolin, zineb, ziram, zoxamide and 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydroisoxazolyl]thiazolyl]piperidinyl][5- methyl(trifluoromethyl)-1H-pyrazolyl]ethanone; nematocides such as fluopyram, spirotetramat, thiodicarb, fosthiazate, abamectin, iprodione, fluensulfone, dimethyl disulfide, tioxazafen, 1,3-dichloropropene (1,3-D), metam (sodium and potassium), dazomet, chloropicrin, fenamiphos, ethoprophos, cadusaphos, terbufos, imicyafos, oxamyl, carbofuran, tioxazafen, Bacillus firmus and Pasteuria nishizawae; bactericides such as streptomycin; acaricides such as amitraz, chinomethionat, chlorobenzilate, cyhexatin, dicofol, dienochlor, etoxazole, fenazaquin, fenbutatin oxide, fenpropathrin, fenpyroximate, hexythiazox, propargite, pyridaben and tebufenpyrad.
In certain instances, combinations of a compound of this invention with other biologically active (particularly invertebrate pest control) compounds or agents (i.e. active ingredients) can result in a greater-than-additive (i.e. synergistic) effect. Reducing the quantity of active ingredients released in the environment while ensuring effective pest control is always desirable. When synergism of invertebrate pest control active ingredients occurs at application rates giving agronomically satisfactory levels of invertebrate pest control, such combinations can be advantageous for reducing crop production cost and decreasing environmental load.
Compounds of this invention and compositions thereof can be applied to plants genetically transformed to express proteins toxic to invertebrate pests (such as Bacillus thuringiensis delta-endotoxins). Such an application may provide a broader spectrum of plant protection and be advantageous for resistance management. The effect of the exogenously applied invertebrate pest control compounds of this invention may be synergistic with the expressed toxin proteins.
General references for these agricultural protectants (i.e. insecticides, fungicides, nematocides, acaricides, herbicides and biological agents) include The Pesticide Manual, 13th Edition, C. D. S. Tomlin, Ed., British Crop Protection Council, Farnham, Surrey, U.K., 2003 and The BioPesticide Manual, 2 Edition, L. G. Copping, Ed., British Crop Protection Council, Farnham, Surrey, U.K., 2001.
For embodiments where one or more of these various mixing partners are used, the weight ratio of these various mixing partners (in total) to the compound of Formula 1 is typically between about 1:3000 and about 3000:1. Of note are weight ratios between about 1:300 and about 300:1 (for example ratios between about 1:30 and about 30:1). One skilled in the art can easily determine through simple experimentation the biologically effective amounts of active ingredients necessary for the desired spectrum of biological activity. It will be evident that including these additional components can expand the spectrum of invertebrate pests controlled beyond the spectrum controlled by the compound of Formula 1 alone.
Table A lists specific combinations of a compound of Formula 1 with other invertebrate pest control agents illustrative of the mixtures, compositions and methods of the present invention. The first column of Table A lists the specific invertebrate pest control agents (e.g., “Abamectin” in the first line). The second column of Table A lists the mode of action (if known) or chemical class of the invertebrate pest control agents. The third column of Table A lists embodiment(s) of ranges of weight ratios for rates at which the invertebrate pest control agent can be applied relative to a compound of Formula 1 (e.g., “50:1 to 1:50” of abamectin relative to a compound of Formula 1 by weight). Thus, for example, the first line of Table A specifically discloses the combination of a compound of Formula 1 with abamectin can be applied in a weight ratio between 50:1 to 1:50. The remaining lines of Table A are to be construed similarly. Of further note Table A lists specific combinations of a compound of Formula 1 with other invertebrate pest control agents illustrative of the mixtures, compositions and methods of the present invention and includes additional embodiments of weight ratio ranges for application rates.
Table A Invertebrate Pest Mode of Action or Chemical Class Typical Control Agent Weight Ratio Abamectin chloride channel activator 50:1 to 1:50 Acetamiprid nicotinic acetylcholinereceptor (nAChR) 150:1 to 1:200 agonist Amitraz octopamine receptor agonists 200:1 to 1:100 Avermectin macrocyclic lactones 50:1 to 1:50 Azadirachtin unknown site of action 100:1 to 1:120 Beta-cyfluthrin sodium channel modulators 150:1 to 1:200 Bifenthrin sodium channel modulators 100:1 to 1:10 Buprofezin chitin biosynthesis inhibitors 500:1 to 1:50 Cartap nicotinic acetylcholine receptor (nAChR) 100:1 to 1:200 channel blocker Chlorantraniliprole ryanodine receptor modulator 100:1 to 1:120 Chlorfenapyr uncouplers of oxidative phosphorylation 300:1 to 1:200 Chlorpyrifos acetylcholinesterase inhibitor 500:1 to 1:200 Clothianidin nicotinic acetylcholine receptor (nAChR) 100:1 to 1:400 agonist Cyantraniliprole Ryanodine receptor modulator 100:1 to 1:120 Cyfluthrin sodium channel modulator 150:1 to 1:200 Cyhalothrin sodium channel modulator 150:1 to 1:200 Cypermethrin sodium channel modulator 150:1 to 1:200 Cyromazine dipteran moulting disrupter 400:1 to 1:50 Deltamethrin sodium channel modulators 50:1 to 1:400 Dieldrin GABA-gated chloride channel antagonist 200:1 to 1:100 Dinotefuran nicotinic acetylcholine receptor (nAChR) 150:1 to 1:200 agonist Diofenolan juvenile hormone mimic 150:1 to 1:200 Emamectin chloride channel activator 50:1 to 1:10 Endosulfan GABA-gated chloride channel antagonist 200:1 to 1:100 Esfenvalerate sodium channel modulator 100:1 to 1:400 Invertebrate Pest Mode of Action or Chemical Class Typical Control Agent Weight Ratio Ethiprole GABA-regulated chloride channel 200:1 to 1:100 antagonist Fenothiocarb 150:1 to 1:200 Fenoxycarb juvenile hormone mimic 500:1 to 1:100 Fenvalerate sodium channel modulator 150:1 to 1:200 Fipronil GABA-regulated chloride channel 150:1 to 1:100 antagonist Flonicamid selective homopteran feeding blocker 200:1 to 1:100 Flubendiamide ryanodine receptor modulator 100:1 to 1:120 Flufenoxuron chitin biosynthesis inhibitor 200:1 to 1:100 Hexaflumuron chitin biosynthesis inhibitor 300:1 to 1:50 Hydramethylnon mitochondrial Complex III electron 150:1 to 1:250 transport inhibitors Imidacloprid nicotinic acetylcholine receptor (nAChR) 1000:1 to 1:1000 agonist Indoxacarb voltage-dependent sodium channel 200:1 to 1:50 blocker Lambda-cyhalothrin sodium channel modulator 50:1 to 1:250 Lufenuron chitin biosynthesis inhibitor 500:1 to 1:250 Metaflumizone voltage-dependent sodium channel 200:1 to 1:200 blocker Methomyl acetylcholinesterase inhibitor 500:1 to 1:100 Methoprene juvenile hormone mimic 500:1 to 1:100 Methoxyfenozide ecdysone receptor agonist 50:1 to 1:50 Nitenpyram nicotinic acetylcholine receptor (nAChR) 150:1 to 1:200 agonist Nithiazine nicotinic acetylcholine receptor (nAChR) 150:1 to 1:200 agonist Novaluron chitin biosynthesis inhibitor 500:1 to 1:150 Oxamyl acetylcholinesterase inhibitors 200:1 to 1:200 Pymetrozine selective homopteran feeding blocker 200:1 to 1:100 Pyrethrin sodium channel modulator 100:1 to 1:10 Pyridaben mitochondrial Complex I electron 200:1 to 1:100 transport inhibitor Pyridalyl unknown site of action 200:1 to 1:100 Pyriproxyfen juvenile hormone mimic 500:1 to 1:100 Invertebrate Pest Mode of Action or Chemical Class Typical Control Agent Weight Ratio Ryanodine ryanodine receptor ligand 100:1 to 1:120 Spinetoram nicotinic acetylcholine receptor (nAChR) 150:1 to 1:100 allosteric activator Spinosad nicotinic acetylcholine receptor (nAChR) 500:1 to 1:10 allosteric activators Spirodiclofen acetyl CoA carboxylase inhibitor 200:1 to 1:200 Spiromesifen acetyl CoA carboxylase inhibitor 200:1 to 1:200 Tebufenozide ecdysone receptor agonist 500:1 to 1:250 Thiacloprid nicotinic acetylcholine receptor (nAChR) 100:1 to 1:200 agonist Thiamethoxam nicotinic acetylcholine receptor (nAChR) 1250:1 to 1:1000 agonist Thiodicarb acetylcholinesterase inhibitors 500:1 to 1:400 Thiosultap-sodium Nicotinic acetylcholine receptor (nAChR) 150:1 to 1:100 channel blocker Tralomethrin sodium channel modulator 150:1 to 1:200 Triazamate acetyl cholinesterase inhibitors 250:1 to 1:100 Triflumezopyrim Triflumuron chitin synthesis inhibitor 200:1 to 1:100 Bacillus thuringiensis biological agents 50:1 to 1:10 Bacillus thuringiensis biological agents 50:1 to 1:10 delta-endotoxin NPV (e.g., Gemstar) biological agents 50:1 to 1:10 Of note is the composition of the present invention wherein the at least one additional biologically active compound or agent is selected from the Invertebrate Pest Control Agents listed in Table A above.
The weight ratios of a compound, including a compound of Formula 1, an N-oxide or a salt thereof, to the additional invertebrate pest control agent typically are between 1000:1 and 1:1000, with one embodiment being between 500:1 and 1:500, another embodiment being between 250:1 and 1:200 and another embodiment being between 100:1 and 1:50.
Listed below in Tables B1 to B10 are embodiments of specific compositions comprising a compound of Formula 1 (compound numbers refer to compounds in Index Tables A-N) and an additional invertebrate pest control agent.
Table B1 Mixture Cmpd. and Invertebrate Pest Control Mixture Cmpd. and Invertebrate Pest No. No. Agent No. No. Control Agent Mixture Cmpd. and Invertebrate Pest Control Mixture Cmpd. and Invertebrate Pest No. No. Agent No. No. Control Agent B1-1 8 and Abamectin 8 B1-38 and Indoxacarb B1-2 8 and Acetamiprid 8 B1-39 and Lambda-cyhalothrin B1-3 8 and Amitraz 8 B1-40 and Lufenuron B1-4 8 and Avermectin 8 B1-41 and Metaflumizone B1-5 8 and Azadirachtin 8 B1-42 and Methomyl B1-6 8 and Bensultap 8 B1-43 and Methoprene B1-7 8 and Beta-cyfluthrin 8 B1-44 and Methoxyfenozide B1-8 8 and Bifenthrin 8 B1-45 and Nitenpyram B1-9 8 and Buprofezin 8 B1-46 and Nithiazine B1-10 8 and Cartap 8 B1-47 and Novaluron B1-11 8 and Chlorantraniliprole 8 B1-48 and Oxamyl B1-12 8 and Chlorfenapyr 8 B1-49 and Phosmet B1-13 8 and Chlorpyrifos 8 B1-50 and Pymetrozine B1-14 8 and Clothianidin 8 B1-51 and Pyrethrin B1-15 8 and Cyantraniliprole 8 B1-52 and Pyridaben B1-16 8 and Cyfluthrin 8 B1-53 and Pyridalyl B1-17 8 and Cyhalothrin 8 B1-54 and Pyriproxyfen B1-18 8 and Cypermethrin 8 B1-55 and Ryanodine B1-19 8 and Cyromazine 8 B1-56 and Spinetoram B1-20 8 and Deltamethrin 8 B1-57 and Spinosad B1-21 8 and Dieldrin 8 B1-58 and Spirodiclofen B1-22 8 and Dinotefuran 8 B1-59 and Spiromesifen B1-23 8 and Diofenolan 8 B1-60 and Spirotetramat B1-24 8 and Emamectin 8 B1-61 and Sulfoxaflor B1-25 8 and Endosulfan 8 B1-62 and Tebufenozide B1-26 8 and Esfenvalerate 8 B1-63 and Tefluthrin B1-27 8 and Ethiprole 8 B1-64 and Thiacloprid B1-28 8 and Fenothiocarb 8 B1-65 and Thiamethoxam B1-29 8 and Fenoxycarb 8 B1-66 and Thiodicarb B1-30 8 and Fenvalerate 8 B1-67 and Thiosultap-sodium B1-31 8 and Fipronil 8 B1-68 and Tolfenpyrad B1-32 8 and Flonicamid 8 B1-69 and Tralomethrin B1-33 8 and Flubendiamide 8 B1-70 and Triazamate B1-34 8 and Flufenoxuron 8 B1-71 and Triflumezopyrim B1-35 8 and Hexaflumuron B1-72 8 and Triflumuron B1-36 8 and Hydramethylnon 8 and B1-73 Bacillus thuringiensis B1-37 8 and Imidacloprid 8 Bacillus thuringiensis B1-74 and Mixture Cmpd. and Invertebrate Pest Control Mixture Cmpd. and Invertebrate Pest No. No. Agent No. No. Control Agent delta-endotoxin B1-75 and NPV (e.g., Gemstar) Table B2 Table B2 is identical to Table B1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 14. For example, the first mixture in Table B2 is designated B2-1 and is a mixture of compound 14 and the additional invertebrate pest control agent abamectin.
Table B3 Table B3 is identical to Table B1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 16. For example, the first mixture in Table B3 is designated B3-1 and is a mixture of compound 16 and the additional invertebrate pest control agent abamectin.
Table B4 Table B4 is identical to Table B1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 19. For example, the first mixture in Table B4 is designated B4-1 and is a mixture of compound 19 and the additional invertebrate pest control agent abamectin.
Table B5 Table B5 is identical to Table B1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 41. For example, the first mixture in Table B5 is designated B5-1 and is a mixture of compound 41 and the additional invertebrate pest control agent abamectin.
Table B6 Table B6 is identical to Table B1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 42. For example, the first mixture in Table B6 is designated B6-1 and is a mixture of compound 42 and the additional invertebrate pest control agent abamectin.
Table B7 Table B7 is identical to Table B1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 51. For example, the first mixture in Table B7 is designated B7-1 and is a mixture of compound 51 and the additional invertebrate pest control agent abamectin.
Table B8 Table B8 is identical to Table B1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 54. For example, the first mixture in Table B8 is designated B8-1 and is a mixture of compound 54 and the additional invertebrate pest control agent abamectin.
Table B9 Table B9 is identical to Table B1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 55. For example, the first mixture in Table B9 is designated B9-1 and is a mixture of compound 55 and the additional invertebrate pest control agent abamectin.
Table B10 Table B10 is identical to Table B1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 76. For example, the first mixture in Table B10 is designated B10-1 and is a mixture of compound 76 and the additional invertebrate pest control agent abamectin.
The specific mixtures listed in Tables B1 to B10 typically combine a compound of Formula 1 with the other invertebrate pest agent in the ratios specified in Table A.
Listed below in Tables C1 to C10 are specific mixtures comprising a compound of Formula 1 (compound numbers (Cmpd. No.) refer to compounds in Index Tables A-N) and an additional invertebrate pest control agent. Tables C1 to C10 further list specific weight ratios typical of the mixtures of Tables C1 to C10. For example, the first weight ratio entry of the first line of Table C1 specifically discloses the mixture of Compound 8 of Index Table A with abamectin applied in a weight ratio of 100 parts Compound 1 to 1 part abamectin.
Table C1 Mixture Cmpd. Invertebrate Pest and Typical Mixture Ratios (by weight) No. No. Control Agent C1-1 8 and Abamectin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-2 8 and Acetamiprid 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-3 8 and Amitraz 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-4 8 and Avermectin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-5 8 and Azadirachtin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-6 8 and Bensultap 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-7 8 and Beta-cyfluthrin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-8 8 and Bifenthrin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-9 8 and Buprofezin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-10 8 and Cartap 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-11 8 and Chlorantraniliprole 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-12 8 and Chlorfenapyr 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-13 8 and Chlorpyrifos 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-14 8 and Clothianidin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-15 8 and Cyantraniliprole 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-16 8 and Cyfluthrin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-17 8 and Cyhalothrin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-18 8 and Cypermethrin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-19 8 and Cyromazine 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-20 8 and Deltamethrin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-21 8 and Dieldrin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-22 8 and Dinotefuran 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-23 8 and Diofenolan 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-24 8 and Emamectin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-25 8 and Endosulfan 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-26 8 and Esfenvalerate 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-27 8 and Ethiprole 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-28 8 and Fenothiocarb 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-29 8 and Fenoxycarb 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-30 8 and Fenvalerate 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-31 8 and Fipronil 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-32 8 and Flonicamid 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-33 8 and Flubendiamide 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-34 8 and Flufenoxuron 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-35 8 and Hexaflumuron 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-36 8 and Hydramethylnon 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-37 8 and Imidacloprid 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-38 8 and Indoxacarb 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 Lambda- C1-39 8 and 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 cyhalothrin C1-40 8 and Lufenuron 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-41 8 and Metaflumizone 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-42 8 and Methomyl 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-43 8 and Methoprene 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-44 8 and Methoxyfenozide 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-45 8 and Nitenpyram 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-46 8 and Nithiazine 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-47 8 and Novaluron 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-48 8 and Oxamyl 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-49 8 and Phosmet 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-50 8 and Pymetrozine 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-51 8 and Pyrethrin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-52 8 and Pyridaben 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-53 8 and Pyridalyl 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-54 8 and Pyriproxyfen 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-55 8 and Ryanodine 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-56 8 and Spinetoram 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-57 8 and Spinosad 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-58 8 and Spirodiclofen 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-59 8 and Spiromesifen 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-60 8 and Spirotetramat 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-61 8 and Sulfoxaflor 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-62 8 and Tebufenozide 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-63 8 and Tefluthrin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-64 8 and Thiacloprid 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-65 8 and Thiamethoxam 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-66 8 and Thiodicarb 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-67 8 and Thiosultap-sodium 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-68 8 and Tolfenpyrad 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-69 8 and Tralomethrin 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-70 8 and Triazamate 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-71 8 and Triflumezopyrim 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 C1-72 8 and Triflumuron 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 Bacillus C1-73 8 and 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 thuringiensis Bacillus C1-74 8 and thuringiensis 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 delta-endotoxin NPV (e.g., C1-75 8 and 100:1 10:1 5:1 2:1 1:1 1:2 1:5 1:10 1:100 Gemstar) Table C2 Table C2 is identical to Table C1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 14. For example, the first weight ratio entry of the first line of Table C2 specifically discloses the mixture of Compound 14 with abamectin applied in a weight ratio of 100 parts Compound 1 to 1 part abamectin.
Table C3 Table C3 is identical to Table C1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 16. For example, the first weight ratio entry of the first line of Table C3 specifically discloses the mixture of Compound 16 with abamectin applied in a weight ratio of 100 parts Compound 1 to 1 part abamectin.
Table C4 Table C4 is identical to Table C1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 19. For example, the first weight ratio entry of the first line of Table C4 specifically discloses the mixture of Compound 19 with abamectin applied in a weight ratio of 100 parts Compound 1 to 1 part abamectin.
Table C5 Table C5 is identical to Table C1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 41. For example, the first weight ratio entry of the first line of Table C5 specifically discloses the mixture of Compound 41 with abamectin applied in a weight ratio of 100 parts Compound 1 to 1 part abamectin.
Table C6 Table C6 is identical to Table C1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 42. For example, the first weight ratio entry of the first line of Table C6 specifically discloses the mixture of Compound 42 with abamectin applied in a weight ratio of 100 parts Compound 1 to 1 part abamectin.
Table C7 Table C7 is identical to Table C1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 51. For example, the first weight ratio entry of the first line of Table C7 specifically discloses the mixture of Compound 51 with abamectin applied in a weight ratio of 100 parts Compound 1 to 1 part abamectin.
Table C8 Table C8 is identical to Table C1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 54. For example, the first weight ratio entry of the first line of Table C8 specifically discloses the mixture of Compound 54 with abamectin applied in a weight ratio of 100 parts Compound 1 to 1 part abamectin.
Table C9 Table C9 is identical to Table C1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 55. For example, the first weight ratio entry of the first line of Table C9 specifically discloses the mixture of Compound 55 with abamectin applied in a weight ratio of 100 parts Compound 1 to 1 part abamectin.
Table C10 Table C10 is identical to Table C1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 76. For example, the first weight ratio entry of the first line of Table C10 specifically discloses the mixture of Compound 76 with abamectin applied in a weight ratio of 100 parts Compound 1 to 1 part abamectin.
Listed below in Tables D1 to D10 are embodiments of specific compositions comprising a compound of Formula 1 (compound numbers (Cmpd. No.) refer to compounds in Index Tables A-N) and an additional fungicide.
Table D1 Mixture Cmpd. and Mixture No. Cmpd. and Fungicide Fungicide No. No. No.
D1-1 8 and Probenazole D1-17 8 and Difenoconazole D1-2 8 and Tiadinil D1-18 8 and Cyproconazole D1-3 8 and Isotianil D1-19 8 and Propiconazole D1-4 8 and Pyroquilon D1-20 8 and Fenoxanil D1-5 8 and Metominostrobin D1-21 8 and Ferimzone D1-6 8 and Flutolanil D1-22 8 and Fthalide D1-7 8 and Validamycin D1-23 8 and Kasugamycin D1-8 8 and Furametpyr D1-24 8 and Picoxystrobin D1-9 8 and Pencycuron D1-25 8 and Penthiopyrad D1-10 8 and Simeconazole D1-26 8 and Famoxadone D1-11 8 and Orysastrobin D1-27 8 and Cymoxanil D1-12 8 and Trifloxystrobin D1-28 8 and Proquinazid D1-13 8 and Isoprothiolane D1-29 8 and Flusilazole Mixture Cmpd. and Mixture No. Cmpd. and Fungicide Fungicide No. No. No.
D1-14 8 and Azoxystrobin D1-30 8 and Mancozeb D1-15 8 and Tricyclazole D1-31 8 and Copper hydroxide D1-16 8 and Hexaconazole D1-32 8 and (a) (a) 1-[4-[4-[5-(2,6-difluorophenyl)-4,5-dihydroisoxazolyl]thiazolyl]piperidinyl][5-methyl (trifluoromethyl)-1H-pyrazolyl]ethanone Table D2 Table D2 is identical to Table D1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 14. For example, the first mixture in Table D2 is designated D2-1 and is a mixture of compound 14 and the additional fungicide probenazole.
Table D3 Table D3 is identical to Table D1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 16. For example, the first mixture in Table D3 is designated D3-1 and is a mixture of compound 16 and the additional fungicide probenazole.
Table D4 Table D4 is identical to Table D1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 19. For example, the first mixture in Table D4 is designated D4-1 and is a mixture of compound 19 and the additional fungicide probenazole.
Table D5 Table D5 is identical to Table D1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 41. For example, the first mixture in Table D5 is designated D5-1 and is a mixture of compound 41 and the additional fungicide probenazole.
Table D6 Table D6 is identical to Table D1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 42. For example, the first mixture in Table D6 is designated D6-1 and is a mixture of compound 42 and the additional fungicide probenazole.
Table D7 Table D7 is identical to Table D1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 51. For example, the first mixture in Table D7 is designated D7-1 and is a mixture of compound 51 and the additional fungicide probenazole.
Table D8 Table D8 is identical to Table D1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 54. For example, the first mixture in Table D8 is designated D8-1 and is a mixture of compound 54 and the additional fungicide probenazole.
Table D9 Table D9 is identical to Table D1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 55. For example, the first mixture in Table D9 is designated D9-1 and is a mixture of compound 55 and the additional fungicide probenazole.
Table D10 Table D10 is identical to Table D1, except that each reference to compound 8 in the column headed “Cmpd. No.” is replaced by a reference to compound 76. For example, the first mixture in Table D10 is designated D10-1 and is a mixture of compound 76 and the additional fungicide probenazole.
Invertebrate pests are controlled in agronomic and nonagronomic applications by applying one or more compounds of this invention, typically in the form of a composition, in a biologically effective amount, to the environment of the pests, including the agronomic and/or nonagronomic locus of infestation, to the area to be protected, or directly on the pests to be controlled.
Thus the present invention comprises a method for controlling an invertebrate pest in agronomic and/or nonagronomic applications, comprising contacting the invertebrate pest or its environment with a biologically effective amount of one or more of the compounds of the invention, or with a composition comprising at least one such compound or a composition comprising at least one such compound and a biologically effective amount of at least one additional biologically active compound or agent. Examples of suitable compositions comprising a compound of the invention and a biologically effective amount of at least one additional biologically active compound or agent include granular compositions wherein the additional active compound is present on the same granule as the compound of the invention or on granules separate from those of the compound of the invention.
To achieve contact with a compound or composition of the invention to protect a field crop from invertebrate pests, the compound or composition is typically applied to the seed of the crop before planting, to the foliage (e.g., leaves, stems, flowers, fruits) of crop plants, or to the soil or other growth medium before or after the crop is planted.
One embodiment of a method of contact is by spraying. Alternatively, a granular composition comprising a compound of the invention can be applied to the plant foliage or the soil. Compounds of this invention can also be effectively delivered through plant uptake by contacting the plant with a composition comprising a compound of this invention applied as a soil drench of a liquid formulation, a granular formulation to the soil, a nursery box treatment or a dip of transplants. Of note is a composition of the present invention in the form of a soil drench liquid formulation. Also of note is a method for controlling an invertebrate pest comprising contacting the invertebrate pest or its environment with a biologically effective amount of a compound of the present invention or with a composition comprising a biologically effective amount of a compound of the present invention. Of further note is this method wherein the environment is soil and the composition is applied to the soil as a soil drench formulation. Of further note is that compounds of this invention are also effective by localized application to the locus of infestation. Other methods of contact include application of a compound or a composition of the invention by direct and residual sprays, aerial sprays, gels, seed coatings, microencapsulations, systemic uptake, baits, ear tags, boluses, foggers, fumigants, aerosols, dusts and many others. One embodiment of a method of contact is a dimensionally stable fertilizer granule, stick or tablet comprising a compound or composition of the invention. The compounds of this invention can also be impregnated into materials for fabricating invertebrate control devices (e.g., insect netting).
Compounds of the invention are useful in treating all plants, plant parts and seeds.
Plant and seed varieties and cultivars can be obtained by conventional propagation and breeding methods or by genetic engineering methods. Genetically modified plants or seeds (transgenic plants or seeds) are those in which a heterologous gene (transgene) has been stably integrated into the plant's or seed's genome. A transgene that is defined by its particular location in the plant genome is called a transformation or transgenic event.
Genetically modified plant and seed cultivars which can be treated according to the invention include those that are resistant against one or more biotic stresses (pests such as nematodes, insects, mites, fungi, etc.) or abiotic stresses (drought, cold temperature, soil salinity, etc.), or that contain other desirable characteristics. Plants and seeds can be genetically modified to exhibit traits of, for example, herbicide tolerance, insect-resistance, modified oil profiles or drought tolerance. Useful genetically modified plants and seeds containing single gene transformation events or combinations of transformation events are listed in Table Z. Additional information for the genetic modifications listed in Table Z can be obtained from the following databases: http://www2.oecd.org/biotech/byidentifier.aspx http://www.aphis.usda.go http://gmoinfo.jrc.ec.europa.eu The following abbreviations are used in Table Z which follows: tol. is tolerance, res. is resistance, SU is sulfonylurea, ALS is acetolactate synthase, HPPD is 4- Hydroxyphenylpyruvate Dioxygenase, NA is Not Available? Table Z Crop Event Name Event Code Trait(s) Gene(s) Alfalfa J101 MON8 Glyphosate tol. cp4 epsps (aroA:CP4) Alfalfa J163 MON-ØØ163-7 Glyphosate tol. cp4 epsps (aroA:CP4) Canola* 2317 (Event CGN2 High lauric acid oil te Canola* 23-198 (Event 23) CGN2 High lauric acid oil te Canola* 61061 DP-Ø61Ø61-7 Glyphosate tol. gat4621 Canola* 73496 DP-Ø73496-4 Glyphosate tol. gat4621 Canola* GT200 (RT200) MON2 Glyphosate tol. cp4 epsps (aroA:CP4); goxv247 Canola* GT73 (RT73) MON-ØØØ73-7 Glyphosate tol. cp4 epsps (aroA:CP4); goxv247 Canola* HCN10 (Topas NA Glufosinate tol. bar 19/2) Canola* HCN28 (T45) ACS-BNØØ8-2 Glufosinate tol. pat (syn) Canola* HCN92 (Topas ACS-BNØØ7-1 Glufosinate tol. bar 19/2) Canola* MON88302 MON-883Ø2-9 Glyphosate tol. cp4 epsps (aroA:CP4) Canola* MPS961 NA Phytate breakdown phyA Canola* MPS962 NA Phytate breakdown phyA Canola* MPS963 NA Phytate breakdown phyA Canola* MPS964 NA Phytate breakdown phyA Canola* MPS965 NA Phytate breakdown phyA Canola* MS1 (B91-4) ACS-BNØØ4-7 Glufosinate tol. bar Canola* MS8 ACS-BNØØ5-8 Glufosinate tol. bar Canola* OXY-235 ACS-BNØ11-5 Oxynil tol. bxn Canola* PHY14 NA Glufosinate tol. bar Canola* PHY23 NA Glufosinate tol. bar Canola* PHY35 NA Glufosinate tol. bar Canola* PHY36 NA Glufosinate tol. bar Canola* RF1 (B93-101) ACS-BNØØ1-4 Glufosinate tol. bar Canola* RF2 (B94-2) ACS-BNØØ2-5 Glufosinate tol. bar Canola* RF3 ACS-BNØØ3-6 Glufosinate tol. bar Bean EMBRAPA 5.1 EMB-PV051-1 Disease res. ac1 (sense and antisense) Brinjal EE-1 Insect res. cry1Ac (Eggplant) Carnation 11 (7442) FLO4 SU tol..; modified flower surB; dfr; hfl (f3'5'h) color Carnation 11363 (1363A) FLO1 SU tol.; modified flower surB; dfr; bp40 (f3'5'h) color Carnation 1226A (11226) FLO8 SU tol.; modified flower surB; dfr; bp40 (f3'5'h) color Carnation 123.2.2 (40619) FLO-4Ø619-7 SU tol.; modified flower surB; dfr; hfl (f3'5'h) color Carnation 123.2.38 (40644) FLO-4Ø644-4 SU tol.; modified flower surB; dfr; hfl (f3'5'h) color Carnation 123.8.12 FLO-4Ø689-6 SU tol.; modified flower surB; dfr; bp40 (f3'5'h) color Carnation 123.8.8 (40685) FLO-4Ø685-1 SU tol.; modified flower surB; dfr; bp40 (f3'5'h) color Carnation 1351A (11351) FLO7 SU tol.; modified flower surB; dfr; bp40 (f3'5'h) color Carnation 1400A (11400) FLO-114ØØ-2 SU tol.; modified flower surB; dfr; bp40 (f3'5'h) color Carnation 15 FLO-ØØØ15-2 SU tol.; modified flower surB; dfr; hfl (f3'5'h) color Carnation 16 FLO-ØØØ16-3 SU tol.; modified flower surB; dfr; hfl (f3'5'h) color Carnation 4 FLO-ØØØØ4-9 SU tol.; modified flower surB; dfr; hfl (f3'5'h) color Carnation 66 FLO-ØØØ66-8 SU tol.; delayed senescence surB; acc Carnation 959A (11959) FLO3 SU tol.; modified flower surB; dfr; bp40 (f3'5'h) color Carnation 988A (11988) FLO7 SU tol.; modified flower surB; dfr; bp40 (f3'5'h) color Carnation 26407 IFD2 SU tol.; modified flower surB; dfr; bp40 (f3'5'h) color Carnation 25958 IFD3 SU tol.; modified flower surB; dfr; bp40 (f3'5'h) color Chicory RM3-3 NA Glufosinate tol. bar Chicory RM3-4 NA Glufosinate tol. bar Chicory RM3-6 NA Glufosinate tol. bar Cotton 19-51a DD-Ø1951A-7 ALS herbicide tol. S4-HrA Cotton 281236 DAS5 Glufosinate tol.; insect res. pat (syn); cry1F Cotton 300623 DAS-21Ø23-5 Glufosinate tol.; insect res. pat (syn); cry1Ac Cotton 31707 NA Oxynil tol.; insect res. bxn; cry1Ac Cotton 31803 NA Oxynil tol.; insect res. bxn; cry1Ac Cotton 31807 NA Oxynil tol.; insect res. bxn; cry1Ac Cotton 31808 NA Oxynil tol.; insect res. bxn; cry1Ac Cotton 42317 NA Oxynil tol.; insect res. bxn; cry1Ac Cotton BNLA-601 NA Insect res. cry1Ac Cotton BXN10211 BXN10211-9 Oxynil tol. bxn; cry1Ac Cotton BXN10215 BXN10215-4 Oxynil tol. bxn; cry1Ac Cotton BXN10222 BXN10222-2 Oxynil tol. bxn; cry1Ac Cotton BXN10224 BXN10224-4 Oxynil tol. bxn; cry1Ac Cotton COT102 SYN-IR102-7 Insect res. vip3A(a) Cotton COT67B SYN-IR67B-1 Insect res. cry1Ab Cotton COT202 Insect res. vip3A Cotton Event 1 NA Insect res. cry1Ac Cotton GMF Cry1A GTL-GMF311- Insect res. cry1Ab-Ac Cotton GHB119 BCS-GH005-8 Insect res. cry2Ae Cotton GHB614 BCS-GH002-5 Glyphosate tol. 2mepsps Cotton GK12 NA Insect res. cry1Ab-Ac Cotton LLCotton25 ACS-GH001-3 Glufosinate tol. bar Cotton MLS 9124 NA Insect res. cry1C Cotton MON1076 MON2 Insect res. cry1Ac Cotton MON1445 MON2 Glyphosate tol. cp4 epsps (aroA:CP4) Cotton MON15985 MON7 Insect res. cry1Ac; cry2Ab2 Cotton MON1698 MON1 Glyphosate tol. cp4 epsps (aroA:CP4) Cotton MON531 MON6 Insect res. cry1Ac Cotton MON757 MON7 Insect res. cry1Ac Cotton MON88913 MON8 Glyphosate tol. cp4 epsps (aroA:CP4) Cotton Nqwe Chi 6 Bt NA Insect res. NA? Cotton SKG321 NA Insect res. cry1A; CpTI Cotton T303-3 BCS-GH003-6 Insect res.; glufosinate tol. cry1Ab; bar Cotton T304-40 BCS-GH004-7 Insect res.; glufosinate tol. cry1Ab; bar Cotton CE43-67B Insect res. cry1Ab Cotton CE46-02A Insect res. cry1Ab Cotton CE44-69D Insect res. cry1Ab Cotton 1143-14A Insect res. cry1Ab Cotton 1143-51B Insect res. cry1Ab Cotton T342-142 Insect res. cry1Ab Cotton PV-GHGT07 Glyphosate tol. cp4 epsps (aroA:CP4) (1445) Cotton EE-GH3 Glyphosate tol. mepsps Cotton EE-GH5 Insect res. cry1Ab Cotton MON88701 MON3 Dicamba & glufosinate tol. Modified dmo; bar Cotton OsCr11 Anti-allergy Modified Cry j Creeping ASR368 SMG-368ØØ-2 Glyphosate tol. cp4 epsps (aroA:CP4) Bentgrass Eucalyptus 20-C Salt tol. codA Eucalyptus 12-5C Salt tol. codA Eucalyptus 12-5B Salt tol. codA Eucalyptus 107-1 Salt tol. codA Eucalyptus 1/9/2001 Salt tol. codA Eucalyptus 2/1/2001 Salt tol. codA Eucalyptus Cold tol. des9 Flax FP967 CDC-FL001-2 ALS herbicide tol. als Lentil RH44 Imidazolinone tol. als Maize 3272 SYN-E3272-5 Modified alpha-amylase amy797E Maize 5307 SYN1 Insect res. ecry3.1Ab Maize 59122 DAS7 Insect res.; glufosinate tol. cry34Ab1; cry35Ab1; Maize 676 PH7 Glufosinate tol.; pollination pat; dam control Maize 678 PH9 Glufosinate tol.; pollination pat; dam control Maize 680 PH2 Glufosinate tol.; pollination pat; dam control Maize 98140 DP6 Glyphosate toll; ALS gat4621; zm-hra herbicide tol.
Maize Bt10 NA Insect res.; glufosinate tol. cry1Ab; pat Maize Bt176 (176) SYN-EV176-9 Insect res.; glufosinate tol. cry1Ab; bar Maize BVLA430101 NA Phytate breakdown phyA2 Maize CBH-351 ACS-ZM004-3 Insect res.; glufosinate tol. cry9C; bar Maize DAS40278-9 DAS40278-9 2,4-D tol. aad-1 Maize DBT418 DKB9 Insect res.; glufosinate tol. cry1Ac; pinII; bar Maize DLL25 (B16) DKB5 Glufosinate tol. bar Maize GA21 MON9 Glyphosate tol. mepsps Maize GG25 Glyphosate tol. mepsps Maize GJ11 Glyphosate tol. mepsps Maize Fl117 Glyphosate tol. mepsps Maize GAT-ZM1 Glufosinate tol. pat Maize LY038 REN3 Increased lysine cordapA Maize MIR162 SYN-IR162-4 Insect res. vip3Aa20 Maize MIR604 SYN-IR604-5 Insect res. mcry3A Maize MON801 MON801 Insect res.; glyphosate tol. cry1Ab; cp4 epsps (MON80100) (aroA:CP4); goxv247 Maize MON802 MON7 Insect res.; glyphosate tol. cry1Ab; cp4 epsps (aroA:CP4); goxv247 Maize MON809 PH-MON2 Insect res.; glyphosate tol. cry1Ab; cp4 epsps (aroA:CP4); goxv247 Maize MON810 MON6 Insect res.; glyphosate tol. cry1Ab; cp4 epsps (aroA:CP4); goxv247 Maize MON832 NA Glyphosate tol. cp4 epsps (aroA:CP4); goxv247 Maize MON863 MON5 Insect res. cry3Bb1 Maize MON87427 MON7 Glyphosate tol. cp4 epsps (aroA:CP4) Maize MON87460 MON4 Drought tol. cspB Maize MON88017 MON3 Insect res.; glyphosate tol. cry3Bb1; cp4 epsps (aroA:CP4) Maize MON89034 MON3 Insect res. cry2Ab2; cry1A.105 Maize MS3 ACS-ZM001-9 Glufosinate tol.; pollination bar; barnase control Maize MS6 ACS-ZM005-4 Glufosinate tol.; pollination bar; barnase control Maize NK603 MON6 Glyphosate tol. cp4 epsps (aroA:CP4) Maize T14 ACS-ZM002-1 Glufosinate tol. pat (syn) Maize T25 ACS-ZM003-2 Glufosinate tol. pat (syn) Maize TC1507 DAS1 Insect res.; glufosinate tol. cry1Fa2; pat Maize TC6275 DAS8 Insect res.; glufosinate tol. mocry1F; bar Maize VIP1034 Insect res.; glufosinate tol. vip3A; pat Maize 43A47 DP-043A47-3 Insect res.; glufosinate tol. cry1F; cry34Ab1; cry35Ab1; pat Maize 40416 DP8 Insect res.; glufosinate tol. cry1F; cry34Ab1; cry35Ab1; pat Maize 32316 DP8 Insect res.; glufosinate tol. cry1F; cry34Ab1; cry35Ab1; pat Maize 4114 DP3 Insect res.; glufosinate tol. cry1F; cry34Ab1; cry35Ab1; pat Melon Melon A NA Delayed ripening/senescence sam-k Melon Melon B NA Delayed ripening/senescence sam-k Papaya 55-1 CUH-CP551-8 Disease res. prsv cp Papaya 63-1 CUH-CP631-7 Disease res. prsv cp Papaya Huanong No. 1 NA Disease res. prsv rep Papaya X17-2 UFL-X17CP-6 Disease res. prsv cp Petunia Petunia-CHS NA Modified product quality CHS suppres.sion Plum C-5 ARS-PLMC5-6 Disease res. ppv cp Canola** ZSR500 NA Glyphosate tol. cp4 epsps (aroA:CP4); goxv247 Canola** ZSR502 NA Glyphosate tol. cp4 epsps (aroA:CP4); goxv247 Canola** ZSR503 NA Glyphosate tol. cp4 epsps (aroA:CP4); goxv247 Poplar Bt poplar NA Insect res. cry1Ac; API Poplar Hybrid poplar NA Insect res. cry1Ac; API clone 741 Poplar trg300-1 High cellulose AaXEG2 Poplar trg300-2 High cellulose AaXEG2 Potato 1210 amk NA Insect res. cry3A Potato 2904/1 kgs NA Insect res. cry3A Canola** ZSR500 NA Glyphosate tol. cp4 epsps (aroA:CP4); goxv247 Canola** ZSR502 NA Glyphosate tol. cp4 epsps (aroA:CP4); goxv247 Potato ATBT04-27 NMK8 Insect res. cry3A Potato ATBT04-30 NMK2 Insect res. cry3A Potato ATBT04-31 NMK9 Insect res. cry3A Potato ATBT04-36 NMK1 Insect res. cry3A Potato ATBT04-6 NMK6 Insect res. cry3A Potato BT06 NMK3 Insect res. cry3A Potato BT10 NMK5 Insect res. cry3A Potato BT12 NMK8 Insect res. cry3A Potato BT16 NMK6 Insect res. cry3A Potato BT17 NMK9 Insect res. cry3A Potato BT18 NMK7 Insect res. cry3A Potato BT23 NMK1 Insect res. cry3A Potato EH921 BPS9 Modified starch/carbohydrate gbss (antisense) Potato HLMT15-15 NA Insect & disease res. cry3A; pvy cp Potato HLMT15-3 NA Insect & disease res. cry3A; pvy cp Potato HLMT15-46 NA Insect & disease res. cry3A; pvy cp Potato RBMT15-101 NMK6 Insect & disease res. cry3A; pvy cp Potato RBMT21-129 NMK1 Insect & disease res. cry3A; plrv orf1; plrv orf2 Potato RBMT21-152 NA Insect & disease res. cry3A; plrv orf1; plrv orf2 Potato RBMT21-350 NMK6 Insect & disease res. cry3A; plrv orf1; plrv orf2 Potato RBMT22-082 NMK6 Insect & disease res.; cry3A; plrv orf1; plrv Glyphosate tol. orf2; cp4 epsps (aroA:CP4) Potato RBMT22-186 NA Insect & disease res.; cry3A; plrv orf1; plrv Glyphosate tol. orf2; cp4 epsps (aroA:CP4) Potato RBMT22-238 NA Insect & disease res.; cry3A; plrv orf1; plrv Glyphosate tol. orf2; cp4 epsps (aroA:CP4) Potato RBMT22-262 NA Insect & disease res.; cry3A; plrv orf1; plrv Glyphosate tol. orf2; cp4 epsps (aroA:CP4) Potato SEMT15-02 NMK9 Insect & disease res. cry3A; pvy cp Potato SEMT15-07 NA Insect & disease res. cry3A; pvy cp Potato SEMT15-15 NMK4 Insect & disease res. cry3A; pvy cp Potato SPBT02-5 NMK1 Insect res. cry3A Potato SPBT02-7 NMK5 Insect res. cry3A Rice 7Crp#2427 Anti-allergy 7crp Rice 7Crp#10 NA Anti-allergy 7crp Rice GM Shanyou 63 NA Insect res. cry1Ab; cry1Ac Rice Huahui-1/TT51-1 NA Insect res. cry1Ab; cry1Ac Rice LLRICE06 ACS-OS001-4 Glufosinate tol. bar Rice LLRICE601 BCS-OS003-7 Glufosinate tol. bar Rice LLRICE62 ACS-OS002-5 Glufosinate tol. bar Rice Tarom molaii + NA Insect res. cry1Ab (truncated) cry1Ab Rice GAT-OS2 Glufosinate tol. bar Rice GAT-OS3 Glufosinate tol. bar Rice PE-7 Insect res. Cry1Ac Rice 7Crp#10 NA Anti-allergy 7crp Rice KPD627-8 High tryptophan OASA1D Rice KPD722-4 High tryptophan OASA1D Rice KA317 High tryptophan OASA1D Rice HW5 High tryptophan OASA1D Rice HW1 High tryptophan OASA1D Rice B1-18 Erect leaves semidwarf Δ OsBRI1 Rice G3-22 Semidwarf OSGA2ox1 Rice AD77 Disease res. DEF Rice AD51 Disease res. DEF Rice AD48 Disease res. DEF Rice AD41 Disease res. DEF Rice 13pNasNaatAprt1 Low iron tol. HvNAS1; HvNAAT-A; APRT Rice 13pAprt1 Low iron tol. APRT Rice gHvNAS1- Low iron tol. HvNAS1; HvNAAT-A; gHvNAAT-1 HvNAAT-B Rice gHvIDS3-1 Low iron tol. HvIDS3 Rice gHvNAAT1 Low iron tol. HvNAAT-A; HvNAAT-B Rice gHvNAS1-1 Low iron tol. HvNAS1 Rice NIA-OS006-4 Disease res. WRKY45 Rice NIA-OS005-3 Disease res. WRKY45 Rice NIA-OS004-2 Disease res. WRKY45 Rice NIA-OS003-1 Disease res. WRKY45 Rice NIA-OS002-9 Disease res. WRKY45 Rice NIA-OS001-8 Disease res. WRKY45 Rice OsCr11 Anti-allergy Modified Cry j Rice 17053 Glyphosate tol. cp4 epsps (aroA:CP4) Rice 17314 Glyphosate tol. cp4 epsps (aroA:CP4) Rose WKS
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