ARTHROPODICIDAL AMIDES U.S. 4,070,365 discloses insecticidally active amides that do not, however, suggest the particular compounds of this invention.

SUMMARY OF THE INVENTION This invention pertains to amides of Formula I, including all geometric and stereoisomers, suitable salts thereof, compositions containing them and use of such compounds to control arthropods in both agronomic and nonagronomic environments. The term "compounds" will be understood to include all such isomers and salts thereof. The compounds are:

wherein

Q is selected from the group

0-3 Q-4

0-5 Q-6

Q-7 Q-8

Q-9

A is H;

E is selected from the group H and C^-Cs alkyl; E being other than H when Q is Q-7; or

A and E are taken together to form -CH ₂ -,-CH ₂ CH ₂ -, -0-, -S-, -S(O)-, -S(0) ₂ -, -NR ⁷ -, -0CH ₂ -, -SCH ₂ -, -N(R ⁷ )CH ₂ -, substituted -CH2-, and

substituted -CH ₂ CH ₂ -, the substituents independently selected from 1-2 halogen and 1-2 methyl;

M is selected from the group H and ^^ ₃ alkyl; or E and M are taken together as -CH ₂ CH ₂ -, -CH ₂ CH ₂ CH ₂ - or -CH ₂ CH ₂ CH ₂ CH ₂ -, each group optionally substituted with one or more members independently selected from the group halogen, N0 ₂ , CN, C _! -C ₃ alkyl, ^-0 ₃ haloalkyl, OH, OR ⁶ and C(0) ₂ R ¹⁹ ;

G is selected from the group

G-l G-2 G-3

G-4 G-5 G-6

X is selected from the group 0 and S; Y is selected from the group H; Ci-Cg alkyl; benzyl; C -C ₆ alkenyl; C -C ₆ alkynyl; C- _j^ -C ₈ alkyl substituted by halogen, C-JL-C3 alkoxy,

C _x -eZ _z haloalkoxy, CN, N0 ₂ , S(0) _r R ³⁰ , P(X) (OR ²⁵ ) ₂ , C(0)R ³⁰ , C(0) ₂ R ³⁰ and phenyl optionally substituted by halogen, CN, C ₁ -C haloalkyl and C _x -C ₂ haloalkoxy; C ₃ -C ₅ cycloalkyl; C ₃ -C ₆ halocycloalkyl; C -C ₆ cycloalkylalkyl; CHO; C ₂ -C ₆ alkylcarbonyl; C ₂ -C ₆ alkoxycarbonyl; C ₂ -C ₆ haloalkylcarbonyl; C(0)R ³³ ; C(0) ₂ R ³³ ; C(S)R ²⁶ ; C(S)R ³³ ; C(0)C(0) ₂ R ²⁵ ; C(0)CH ₂ C(0) ₂ R ²⁵ ; S(0) _r R ³⁰ ;

S(0) ₂ CH ₂ C(0) ₂ R ²⁵ ; P(X) (0R ²⁵ ) ₂ ; phenylthio; R ^1:L OC(0)N(R ¹² )S-; R ¹³ (R ¹⁴ )NS-; N=CR ⁹ R ¹⁰ ; OR ⁸ ; NR ⁸ R ⁹ ; and R ³⁸ ; Y being R ³⁸ when Q is Q-9; Y being other than N=CR ⁹ R ¹⁰ , OR ⁸ , and NR ⁸ R ⁹ when Q is Q-8 and A and E are taken together as -CH -;

Z is selected from the group CH ₂ , O, S and NR ²⁹ ; R is selected from the group H, halogen, 0-^-0 ₃ alkyl, ^-^ alkoxy, CN, and N0 ₂ ; R ¹ and R ² are independently selected from the group H, C^-Cg alkyl, C- _j^ -Cg haloalkyl, C ₂ -Cg alkenyl,

C ₂ -C ₆ haloalkenyl, C -Cg alkynyl, C ₃ -Cg halo- alkynyl, C ₂ -C ₆ alkoxyalkyl, C ₂ -C ₆ alkylthioalkyl, Ci-Cg nitroalkyl, C ₂ -C ₆ cyanoalkyl, C ₃ -C ₃ alkoxycarbonylalkyl, C ₃ ~C cycloalkyl, C ₃ -Cg halocycloalkyl, halogen, CN,

N ₃ , SCN, N0 ₂ , OR ¹⁶ , SR ¹⁶ , S(0)R ¹⁶ , S(O) ₂ R ¹⁶ , 0C(0)R ¹⁶ , OS(0) ₂ R ¹⁶ , C(0)R ¹⁶ , C(0) ₂ R ¹⁶ , C(0)NR ¹⁶ R ¹⁷ , S(0) ₂ NR ¹⁶ R ¹⁷ , NR ¹⁶ R ¹⁷ , NR ¹⁷ C(0)R ¹⁶ , OC(0)NHR ¹⁶ , NR ¹⁷ C(0)NHR ¹⁶ , NR ¹⁷ S(O) ₂ R ¹⁶ , phenyl optionally substituted with 1 to 3 substituents independently selected from , and benzyl optionally substituted with 1 to 3 substituents independently selected from ; or when m or n is 2, (R ¹ ) ₂ are taken together, or (R ² ) ₂ are taken together as -OCH ₂ 0-, -OCF ₂ 0-, -OCH ₂ CH ₂ 0-,

-CH ₂ C(CH ₃ ) ₂ 0-, -CF ₂ CF ₂ 0- or -OCF ₂ CF ₂ 0- to form a cyclic bridge; provided that when R ¹ or R ² is S(0)R ¹⁶ , S(0) ₂ R ¹⁶ , OC(0)R ¹⁶ , NR ¹⁷ S(O) ₂ R ¹⁶ or OS(0) ₂ R ¹⁶ then R ¹⁶ is other than H; R ³ is selected from the group H, J, N ₃ , N0 ₂ , halogen, N(R ²¹ )R ²² , C(R ³¹ )=N-0-R ³² , C^-Cg alkyl, Ci-C haloalkyl, C ₂ -C ₆ alkenyl, C ₂ -C ₆ haloalkenyl, C -Cg alkynyl, C ₂ -Cg alkoxyalkyl, C ₃ -C ₈ alkoxycarbonylalkyl, C(0)R ¹⁶ , C(0) ₂ R ¹⁶ , OR ¹⁸ , C(0)NR ¹⁶ R ¹⁷ , C(S)NR ¹⁶ R ¹⁷ , C(S)R ¹⁶ , ^'

C(S)SR ¹⁶ , CN, Si(R ²⁵ ) (R ²⁶ ) (R ²⁷ ), SR ²⁵ , S(0)R ²⁵ ,

S(0) ₂ R ²⁵ , P(0) (OR ²⁵ ) ₂ , phenyl optionally substituted with (R ¹⁵ )p, and benzyl optionally substituted with 1 to 3 substituents independently selected from ; or R ³ is C ₂ -C ₆ epoxyalkyl optionally substituted with one or more members independently selected from the group C ₁ -C ₃ alkyl, CN, C(0)R ²³ , C(0) ₂ R ²³ , and phenyl optionally substituted with W; or R ³ is C^-C alkyl substituted with one or more members independently selected from the group

C(0)N(R ²⁴ )R ³⁴ , C(0)R ²⁴ , SR ²⁵ , S(0)R ²⁵ , S(0) ₂ R ²⁵ , SCN, CN, C ₁ -C ₂ haloalkoxy. Si(R ²⁵ ) (R ²⁶ ) (R ²⁷ ) , N(R ²¹ )R ²² , N0 ₂ , OC(0)R ²⁴ , P(0) (0R ²⁵ ) ₂ , and J; R ³ being other than H when Q is Q-7; J is selected from the group saturated, partially unsaturated or aromatic 5- or 6-membered heterocyclic ring, bonded through carbon or nitrogen, containing 1-4 heteroatoms independently selected from the group consisting of 0-2 oxygen, 0-2 sulfur and 0-4 nitrogen, this substituent optionally containing one carbonyl and optionally substituted with one or more members independently selected from W; R ⁴ and R ⁵ are independently selected from the group H, C ₁ -C ₄ alkyl, C(0)R ¹⁹ and C ₂ -C ₄ alkoxycarbonyl; R ⁶ is selected from the group H, ^-0 ₄ alkyl, C(0)R ¹⁹ and C(0) ₂ R ¹⁹ ; R ⁷ is selected from the group H, C _! -C ₄ alkyl, C ₁ -C ₄ haloalkyl, C ₂ -C ₄ alkenyl, C -C ₄ haloalkenyl, SR ¹⁶ , S(0)R ¹⁶ , S(0) ₂ R ¹⁶ , C(0)R ¹⁶ , C(0) ₂ R ¹⁶ , C(0)NR ¹⁶ R ²⁰ , C(S)NR ¹⁶ R ²⁰ , C(S)R ¹⁶ , C(S)OR ¹⁶ , P(0) (OR ¹⁶ ) ₂ , P(S) (OR ¹⁶ ) ₂ , P(O) (R ¹⁶ )OR ¹⁶ , P(O) (R ¹⁶ )SR ²⁰ , optionally substituted phenyl, and optionally substituted benzyl wherein the

optional phenyl and benzyl substituents are independently selected from F, CI, Br, CH ₃ , CF ₃ and OCF ₃ ; provided that when R ⁷ is other than C(0)R ¹⁶ , C(0)NR ¹⁶ R ²⁰ or C(S)NR ¹⁶ R ²⁰ then R ¹⁶ is other than H;

R ⁸ is selected from the group H, 0 ₃ ^ ₄ alkyl, C ₁ -C ₄ haloalkyl, C ₂ -C alkenyl, C ₂ -C ₄ alkynyl, S(0) ₂ NR ¹⁷ R ¹⁸ , S(0) ₂ R ¹⁶ , C(0)R ¹⁶ , C(0) ₂ R ¹⁶ , C(0)NR ¹⁶ R ²⁰ , phenyl optionally substituted with halogen or C ₁ -C ₄ alkoxy, and benzyl optionally substituted with halogen; provided that when R ⁸ is S(0) ₂ R ¹⁶ , R ¹⁶ is other than H;

R ⁹ is selected from the group H, ^-^ ₄ alkyl and C(0)R ¹⁶ ; R ¹⁰ is selected from the group H, C _! -C ₄ alkyl, C ₁ -C ₄ haloalkyl and phenyl optionally substituted with one or more members independently selected from halogen, CN, N0 ₂ , CF ₃ and OCF ₃ ; or

R ⁹ and R ¹⁰ are taken together as -CH ₂ CH ₂ CH ₂ -, -CH ₂ CH ₂ CH ₂ CH ₂ r ^or -CH ₂ CH ₂ CH ₂ CH ₂ CH ₂ -;

R ¹¹ is Ci-Ciβ alkyl;

R ¹² is C _X -C ₄ alkyl;

R ¹³ and R ¹⁴ are independently ^-0 ₄ alkyl; or

R ¹³ and R ¹⁴ are taken together as -CH ₂ CH ₂ CH ₂ CH ₂ CH ₂ - or -CH ₂ CH ₂ OCH ₂ CH ₂ -;

R ¹⁵ is selected from the group C^C ₆ alkyl, Ci-C ₈ haloalkyl, C -C ₆ alkenyl, C ₂ -C ₆ haloalkenyl, C ₂ -C ₆ alkynyl, C^-Cg haloalkynyl, C -Cg alkoxyalkyl, C ₂ -Cg alkylthioalkyl, C^Cg nitroalkyl, C ₂ -Cg cyanoalkyl, C ₃ -C ₃ alkoxycarbonylalkyl, C ₃ -Cg cycloalkyl, C ₃ -C ₆ halocycloalkyl, halogen, CN, N ₃ , SCN, N0 , OR ¹⁶ , SR ¹⁶ , S(0)R ¹⁶ , S(0) ₂ R ¹⁶ , OC(0)R ¹⁶ , 0S(0) ₂ R ¹⁶ , C(0)R ¹⁶ , C(0) ₂ R ¹⁶ , C(0)NR ¹⁶ R ¹⁷ , S(0) ₂ NR ¹⁶ R ¹⁷ , NR ¹⁶ R ¹⁷ , NR ¹ C(0)R ¹⁶ , OC(0)NHR ¹⁶ ,

NR ¹⁷ C(0)NHR ¹⁶ , NR ¹⁷ S(0) ₂ R ¹⁶ , phenyl optionally

substituted with 1 to 3 substituents independently selected from , and benzyl optionally substituted with 1 to 3 substituents independently selected from W; or when p is 2, (R ¹⁵ . ₂ ^are taken together as -OCH ₂ 0-, -OCF ₂ 0-,

-OCH ₂ CH ₂ 0-, -CH ₂ C(CH ₃ ) ₂ 0-, -CF ₂ CF ₂ 0- or -0CF ₂ CF ₂ 0- to form a cyclic bridge; provided that when R ¹⁵ is S(0)R ¹⁶ , S(0) ₂ R ¹⁶ , 0C(0)R ¹⁶ , NR ¹⁷ S(0) ₂ R ¹⁶ or OS(0) ₂ R ¹⁶ then R ¹⁶ is other than H;

R ¹⁶ is selected from the group H, C-j _^ -C alkyl, ^-Cg haloalkyl, C ₂ -C ₆ alkenyl, C ₂ -C ₆ haloalkenyl, C ₂ -C ₆ alkynyl, C ₃ -C ₆ haloalkynyl, C ₂ -Cg alkoxyalkyl, C ₂ -Cg alkylthioalkyl, Ci-C nitroalkyl, C ₂ -C ₆ cyanoalkyl, C ₃ —C ₈ alkoxycarbonylalkyl, C ₃ -C ₆ cycloalkyl, C ₃ -C ₆ halocycloalkyl, optionally substituted phenyl and optionally substituted benzyl wherein the optional phenyl and benzyl substituents are 1 to 3 substituents independently selected from ; R ¹⁷ is selected from the group H and C ₁ -C ₄ alkyl; or R ¹⁶ and R ¹⁷ , when attached to the same atom, are taken together as -(CH ₂ ) ₄ -, -(CH ₂ ) ₅ -, or -CH ₂ CH ₂ 0CH ₂ CH ₂ -; R ¹⁸ is selected from the group H, C- _J .-C ₄ alkyl, C ₂ -C alkenyl, C ₂ -C ₄ alkynyl, C ₂ -C ₄ alkylcarbonyl, C ₂ -C ₄ alkoxyσarbonyl and C- _X -C ₄ alkylsulfonyl; R ¹⁹ is C- _J .-C ₃ alkyl;

R20 j_ _s selected from the group H, C^-^ alkyl, C ₂ -C ₄ alkenyl and C ₂ ~C ₄ alkynyl; R ²¹ is selected from the group H, C ₂ -C ₇ alkylcarbonyl, C ₂ -C ₇ alkoxycarbonyl, optionally substituted C ₁ -C ₄ alkyl, optionally substituted

C ₂ -C ₄ alkenyl, and optionally substituted C ₂ -C

alkynyl, all of these optional substituents being independently selected from C ₁ -C alkoxy,

CN, C(0)R ²⁸ and C(0) ₂ R ²⁵ ; R ²² is selected from the group H, C ₁ -C ₃ alkyl, phenyl optionally substituted with at least one member independently selected from , and benzyl optionally substituted with at least one member independently selected from W; R ²³ is selected from the group H, ^-0 ₄ alkyl, C ₂ -C ₄ alkenyl and C ₂ -C ₄ alkynyl;

R ²⁴ is selected from the group H and 0^-0 ₃ alkyl; R ²⁵ is selected from the group C- _JL -C ₃ alkyl and phenyl optionally substituted with at least one member independently selected from W; R ²⁶ is selected from the group C ₁ -C ₄ alkyl, ^^ ₄ haloalkyl, C ₁ -C alkoxy, and 0-^-0 ₄ haloalkoxy; R ²⁷ is C^C^ alkyl; R28 is selected from the group H, ^^ ₃ alkyl and phenyl optionally substituted with at least one member independently selected from ;

R29 i _s selected from the group H, CHO, C ₁ -C alkyl,

C ₂ -C alkylcarbonyl and C ₂ -C ₄ alkoxycarbonyl; R ³⁰ is selected from the group C ₁ -C ₃ alkyl and ^-0 ₃ haloalkyl; R ³¹ is selected from the group H, CI, C ₁ -C ₄ alkyl,

C ₁ -C ₄ alkoxy, C ₁ -C ₂ alkylthio and CN; R ³² is selected from the group H, C__- ι__ alkyl, C ₂ -C ₃ alkylcarbonyl and C ₂ -C ₃ alkoxycarbonyl; R33 i _s selected from the group C ₁ -C alkylthio, ^c ι~ ^c ₄ haloalkylthio, and phenyl optionally substituted with at least one member independently selected from W; R ³⁴ is selected from the group H and alkyl; R35 is selected from the group CHO; ^-0 ₄ alkyl substituted with substituents independently selected from halogen, C^^ alkoxy, C ₁ -C

haloalkoxy, CN, N0 ₂ , C ₂ -C ₄ alkylcarbonyl, C ₂ -C ₄ alkoxycarbonyl and N(R ³⁶ ) (R ³⁷ ) ; or R ³⁵ is C ₂ -C ₆ haloalkylcarbonyl; C ₃ ~C ₆ alkenyl; C ₃ ~C haloalkenyl; C ₃ -Cg alkynyl; C ₃ -C ₆ haloalkynyl; C ₃ -C ₆ cycloalkyl;. C(S)R ²⁶ ; C(S)R ³³ ;

C(0)C(0) ₂ R ²⁵ ; C(0)CH ₂ C(0) ₂ R ²⁵ ; S(0) _r R ³⁰ ; S(0) ₂ CH ₂ C(0) ₂ R ²⁵ ; P(X) (OR ²⁵ ) ₂ ; C(O)N(R ³⁶ ) (R ³⁷ ) ; S(0) _r N(R ¹³ )R ¹⁴ ; S(0) _r N(R ¹² )C(0)OR ^1:L ; S(0) _r N(R ¹² )CHO; J; CH ₂ J; C(0)J; C(0)Ph where the phenyl group is optionally substituted by a group independently selected from W; and benzyl optionally substituted by a group independently selected from W;

R ³⁶ is selected from the group H, C _] i-C ₄ alkyl, C^C, _} alkenyl, phenyl optionally substituted by a group independently selected from W, and benzyl optionally substituted by a group independently selected from W;

R ³⁷ is selected from the group C-^-C^ alkyl and C ₁ -C alkenyl;

R38 i _s selected from the group C(S)R ²⁶ , C(S)R ³³ ,

C(0)C(0)2R ²⁵ , C(0)CH ₂ C(0) ₂ R ²⁵ , S(0)R ³⁰ , S(0) ₂ R ³⁰ , S(0) ₂ CH ₂ C(0) ₂ R ²⁵ , P(X)(0R ²⁵ ) ₂ , C ₃ -C ₆ halo¬ alkynyl, and C- _jL —Cg alkyl substituted by P(X) (0R ²⁵ ) ₂ ;

W is selected from the group halogen, CN, N0 ₂ , C ₁ -C ₂ alkyl, C _! -C ₂ haloalkyl, C ₁ -C ₂ alkoxy, ^c i~ ^c ₂ haloalkoxy, C ₁ -C ₂ alkylthio, C ₁ -C ₂ haloalkylthio, C- _J .-C ₂ alkylsulfonyl, and C ₁ -C ₂ haloalkylsulfonyl; m is 1 to 3; n is 1 to 3; p is 1 to 3; and r is 0, 1 or 2. Exemplary values of J include:

J-4 J-5 J-6

J-7 J-8 J-9

J-10 J-11 J-12

J-13 J-14 J-15

10

J-16 J-17 J-18

J-19 j-20

Preferred for reasons including ease of synthesis and/or greater arthropodicidal efficacy are the following compounds, A through L: Compounds A are those wherein:

R ¹ is selected from the group H, haloalkyl, C ₂ ~C ₆ alkenyl, C ₂ -C ₆ haloalkenyl, C ₂ -C ₆ alkynyl, C ₃ -C ₆ haloalkynyl, C ₂ -C ₆ alkoxyalkyl, C ₂ -Cg alkylthioalkyl, Ci-C nitroalkyl, C ₂ -Cg cyanoalkyl, C ₃ -C ₃ alkoxycarbonylalkyl, C ₃ -C ₆ cycloalkyl, C ₃ -C ₆ halocycloalkyl, halogen, CN, SCN, N0 ₂ , OR ¹⁶ , SR ¹⁶ , S(0) ₂ R ¹⁶ , C(0)R ¹⁶ , C(0) ₂ R ¹⁶ , phenyl optionally substituted with 1 to 3 substituents independently selected from W, and benzyl optionally substituted with 1 to 3 substituents independently selected from ; with one R ¹ substituent in the 4-position, or when m is 2 then (R ¹ ) are taken together as -CH ₂ C(CH ₃ ) ₂ 0-,

-OCH ₂ CH ₂ 0-, -OCF ₂ CF ₂ 0-, or -CF CF ₂ 0- to form a 5- or 6-membered fused ring; R ² is selected from the group H, C^-Cg alkyl, C^-C haloalkyl, C ₂ -C ₆ alkenyl, C ₂ -Cg haloalkenyl, halogen, CN, SCN, N0 ₂ , OR ¹⁶ , SR ¹⁶ , S(0)R ¹⁶ ,

OC(0) ₂ R ¹⁶ , OS(0) ₂ R ¹⁶ , C(0)R ¹⁶ , C(0) ₂ R ¹⁶ , C(0)NR ¹⁶ R ¹⁷ , S(0) ₂ NR ¹⁶ R ¹⁷ , NR ¹⁶ R ¹⁷ ; R ³ is selected from the group H, C ₁ -C alkyl, C(0)R ¹⁶ , C(0) ₂ R ¹⁶ , and phenyl independently substituted by one or more substituents selected from (R ¹⁵ ) _D ;

R ¹⁵ is selected from the group C^-C alkyl, C^-C haloalkyl,. C ₂ -C ₆ alkenyl, C ₂ -C ₆ haloalkenyl, halogen, CN, SCN, N0 ₂ , OR ¹⁶ , SR ¹⁶ , S(0) ₂ R ¹⁶ , OC(0) ₂ R ¹⁶ , OS(0)R ¹⁶ , C(0)R ¹⁶ , C(0) ₂ R ¹⁶ , C(0)NR ¹⁶ R ¹⁷ , S(0) ₂ NR ¹⁶ R ¹⁷ , NR ¹⁶ R ¹⁷ , phenyl optionally substituted with 1 to 3 substituents independently selected from , and benzyl optionally substituted with 1 to 3 substituents independently selected from W; R ¹⁶ is selected from the group C^-C^ alkyl, C ₁ -C ₂ haloalkyl, C ₃ -C alkenyl and propargyl; R ¹⁷ is selected from the group H and CH ₃ ; R35 is selected from CHO, C__-C^ alkyl substituted with substituents independently selected from the group halogen, C ₁ -C ₂ alkoxy, C ₁ -C haloalkoxy, CN, N0 , C ₂ -C ₄ alkylcarbonyl, C -C alkoxycarbonyl and N(R ³⁵ ) (R ³⁶ ) ; or R ³⁵ is C ₂ -C ₆ haloalkylcarbonyl; C ₃ -C ₆ alkenyl; C ₃ -C ₆ haloalkenyl; C ₃ -C ₆ alkynyl; C(0)N(R ³⁵ ) (R ³⁶ ) ; R^OCfO.NfR ¹² )^-; R ¹³ (R ¹⁴ )NS-; C(0)Ph where the phenyl group is optionally substituted by a group independently selected from W; and benzyl optionally substituted by a group independently selected from W; R ³⁸ is selected from the group C(S)R ²⁶ , C(S)R ³³ ,

C(0)C(0) ₂ R ²⁵ , C(0)CH ₂ C(0) ₂ R ²⁵ , S(0)R ³⁰ , S(0) ₂ R ³⁰ , S(0) ₂ CH ₂ C(0) ₂ R ²⁵ , P(X) (OR ² ) ₂ , C ₃ -C ₆ haloalkynyl, and C- _j^ -Cg alkyl substituted by P(X) (OR ²⁵ ) ₂ ; and m is 1 or 2.

Compounds B are those of Preferred A wherein G is G-3, R ⁴ is H and R ⁵ is H.

Compounds C are of Preferred B wherein Q is Q-l.

Compounds D are of Preferred B wherein Q is Q-2. Compounds E are of Preferred B wherein Q is Q-7.

Compounds F are of Preferred B wherein Q is Q-8.

Compounds G are of Preferred B wherein Q is Q-9. Specifically preferred are those compounds of Preferred B:

(H) 3,4-bis (4-chlorophenyl)-4,5-dihydro-N-[4- (trifluoromethyl)phenyl]-lH-pyrrole-1- carboxamide, (I) methyl 2,3-dihydro-7-(trifluoromethyl)-2-[[ [4- (trifluoromethyl)phenylamino]carbonyl]- [l]benzopyrano[3,4-c]pyrrole-3a(4H)- carboxylate,

(J) methyl 7-chloro-3,9-dihydro-3-[ [ [4-(trifluoro¬ methoxy)phenylamino]carbonyl]indeno[l,2-e]-l,3- oxazine-9a(2H)-carboxylate, (K) methyl 7-chloro-4-formyl-2,3,4,5-tetrahydro-2- [ [4-(trifluoromethoxy)phenylamino]carbonyl]-

4aH-indeno[2,l-e]-l,2,4-triazine-4a- carboxylate, and (L) methyl 4-formyl-2,3,4,5-tetrahydro-7-(2,2,2- trifluoroethoxy)-2-[ [4-(trifluoromethoxy)- phenylamino]carbonyl]- H-indeno[2,1—e]—1,2,4- triazole-4a-carboxylate. In the above definitions, the term "alkyl", used either alone or in compound words such as "alkylthio" or "haloalkyl", denotes straight chain or branched alkyl, such as methyl, ethyl, n-propyl, isopropyl and the different butyl, pentyl, and hexyl isomers. "Alkoxy" denotes methoxy, ethoxy, n-propoxy, isopropoxy and the different butoxy and pentoxy isomers. "Alkenyl" denotes straight chain or branched alkenes, such as vinyl, 1-propenyl, 2-propenyl, 3-propenyl and the different butenyl, pentenyl, and hexenyl isomers. "Alkynyl" denotes straight chain or branched alkynes, such as ethynyl, 1-propynyl, 3-propynyl and the different butynyl, pentynyl, and hexynyl isomers. "Alkylthio" denotes methylthio, ethylthio and the different propylthio, butylthio, pentylthio, and

hexylthio isomers. "Alkylsulfinyl", "alkylsulfonyl", "alkylamino", and.the like, are defined analogously to the above examples. "Cycloalkyl" denotes cyclopropyl, cyclobutyl, cyclopentyl, and cyclohexyl. The term "halogen", either alone or in compound words such as "haloalkyl", denotes fluorine, chlorine, bromine or iodine. Further, when used in compound words such as "haloalkyl" said alkyl can be partially or fully substituted with halogen atoms, which can be the same or different. Examples of haloalkyl include CH ₂ CH ₂ F, CF ₂ CF ₂ and CH ₂ CHFC1. The terms "halocycloalkyl", "haloalkenyl" and "haloalkynyl" are defined analogously to the term "haloalkyl".

The total number of carbon atoms in a substituent group is indicated by the "Ci-C _j " prefix where i and j are numbers from 1 to 8. For example, C^-^ alkylsulfonyl designates methylsulfonyl through propylsulfonyl; C ₂ alkylcarbonyl includes C(0)CH ₃ ' and C ₄ alkylcarbonyl includes C(0)CH ₂ CH ₂ CH ₃ and C(0)CH(CH ₃ ) ₂ ; C ₂ alkoxycarbόnyl designates C(0)0CH ₃ and C ₄ alkoxycarbonyl designates C(0)0CH ₂ CH ₂ CH ₃ and ■ C(0)0CH(CH ₃ ) ₂ ; and as a final example, C ₃ alkoxycarbonylalkyl includes CH C(0) CH ₃ and C alkoxycarbonylalkyl includes CH ₂ CH ₂ C(0.) ₂ CH ₃ , CH ₂ C(0) ₂ CH ₂ CH ₃ and CH(CH ₃ )C(O) ₂ CH ₃ .

Compounds of Formula I can exist as one or more stereoisomers. The various stereoisomers include enantiomers, diastereomers and geometric isomers. One skilled in the art will appreciate that one stereoisomer may be the more active. One skilled in the art knows how to separate said enantiomers, diastereomers and geometric isomers. Accordingly, the present invention ^" comprises racemic mixtures, individual stereoisomers,and optically active mixtures.

DETAILS OF THE INVENTION

Compounds of Formula I are prepared as described in Schemes 1 through 28 with substituents as previously defined, unless otherwise noted. Compounds of Formula I (Q-1) where R is H and X is 0 or S can be prepared by the reaction of Formula II compounds in the presence of a conventional organic solvent such as benzene, toluene, xylene, acetonitrile and the like. This transformation can be performed optionally in the presence of an acid catalyst (0 to 1 equivalents) .

Typical acid catalysts include p-toluenesulfonic acid, pyridine p-toluenesulfonate, hydrochloric acid or sulf ric acid. The reaction temperature can range from about -10 to 200°C with 35 to 120°C being preferred. The reaction is generally complete after 24 hours. Scheme 1 illustrates this transformation.

■Scheme 1

¹¹ I (Q-1)

Compounds of Formula II can be prepared by the reaction of Formula III compounds with an oxidizing agent such as pyridine-sulfur trioxide complex/dimethyl sulfoxide, oxalyl chloride/dimethyl sulfoxide or pyridinium chlorochromate. These oxidation procedures are well documented in the literature. A typical reaction involves combination of Formula III compounds with the oxidizing agent in a solvent such as methylene

chloride, chloroform, benzene or toluene. The reaction can be run in the -presence of a base such as triethyl- amine. The reaction temperatures can range from about -78 to 200°C. The reaction time can range from 30 minutes to 24 hours. Scheme 2 illustrates this trans ormation.

Scheme 2

Compounds of Formula III where X is O or S can be prepared by the reaction of Formula IV compounds with isocyanates of Formula V. Typical reactions involve the combination of equimolar amounts of IV and V in a conventional organic solvent such as ethyl acetate, methylene chloride, chloroform, benzene and toluene. A base such as an alkali metal, alkali metal alkoxide or metal hydride can be used. The reaction temperatures can vary from 0°C to the reflux temperature of the particular solvent being used. The reaction is usually complete in less than 24 hours. Scheme 3 illustrates this transformation.

Scheme 3

IV

Compounds of Formula IV can be prepared by the reduction of Formula VI compounds. Typical reactions involve combinations of an excess in molar amounts of a reducing agent (1 to 10 equivalents) such as lithium aluminum hydride, with one equivalent of a Formula VI compound in a solvent such as tetrahydrofuran or ether. The reaction temperature can vary from 0°C to the reflux temperature of the particular solvent being used and the reaction is usually complete in 24 hours. This transformation is illustrated in Scheme 4.

Scheme 4

Compounds of Formula VI can be prepared using procedures known to the art (J ^" . Med. Chem . 1991, 34, 2557; Org. Syn . 1952, 32, 86). Compounds of Formula I (Q-2) where R is H, X is 0 or S and Z is CH ₂ can be prepared from Formula VII compounds utilizing analogous procedures described for Schemes 1 through 4 (see Scheme 5) .

Scheme 5

II

Compounds of Formula VII are known in the art or can be obtained by methods analogous to known procedures (Synth . Commun . 1985, 15, 899) .

Compounds of Formula I (Q-3, where R is H and X is 0; and Q—4, where R is H, X is O and Z is CH ₂ ) can be prepared by reaction of acid chloride VIII with a substituted amine of Formula IX in equimolar proportions in the presence of an excess of an acid scavenger, such as tertiary alkylamines or pyridines in an aprotic organic solvent such as ether, tetrahydrofuran, chloroform, methylene chloride, benzene or toluene. _The reaction temperature can vary between 0 to 50°C and the reaction is usually complete in less than 24 hours. Scheme 6 illustrates this transformation.

Scheme 6

CI

VIII IX a is 1 or 2

Compounds of Formula VIII can be prepared from compounds of Formula X through conventional methodology

generally used for the conversion of esters to their corresponding acid chlorides as illustrated in Scheme 7.

Scheme 7

COOCH3

X a is 1 or 2

Compounds of Formula X can be readily prepared by the dehydration of alcohols of Formula XI (see Scheme 8) . For a general review of dehydration reactions, see March, "Advanced Organic Chemistry", 3rd ed, pp. 901 to 903.

Scheme 8

COOMe

XI a is 1 or 2

Compounds of Formula XI can be prepared by the reduction of Formula XII compounds. A typical reaction involves combination of an excess in molar amounts of a reducing agent such as sodium borohydride (1.1 equivalent to 3 equivalents) with a Formula XII compound. Conventional organic solvents such as methanol, ethanol, dimethoxyethane, ether or

tetrahydrofuran can be used. Typical reaction time varies from 2 to 2 hours. This transformation is illustrated in Scheme 9.

XII a is 1 or 2

Compounds of Formula XII can be prepared from Formula XIII compounds (see Scheme 10) . This is typically done by treatment of a Formula XIII compound with a strong base such as lithium diisopropylamide at low temperatures in the range of 0 to -78°C in a solvent such as tetrahydrofuran. An electrophile such as XIV is then added ^" to the anion affording, after workup with acid, compounds of Formula XII. The reaction is usually complete in less than 24 hours.

Literature precedence for Schemes 8 through 10 can be found in Tetrahedron Lett . 1991, 32, 6481.

Scheme 10

a is 1 or 2

Compounds of Formula XIII can be prepared from compounds of Formula XV. Typically, Formula XV

compounds are prepared by refluxing in a suitable solvent such as to.luene, benzene, methanol or ethanol in the presence of a catalytic amount (0.1 to 0.5 equivalents) of a metal alkoxide such as sodium methoxide. Typical reaction times vary from 30 minutes to 4 hours. Scheme 11 illustrates this transformation.

COOMe

XV a is 1 or 2

Compounds of Formula XV where E is H can be prepared by reductive amination of the ketoester XVII with an appropriately substituted aniline XVI (see March, "Advanced Organic Chemistry", 3rd ed. pp. 798-800 and Tetrahedron Lett . 1990, 31, 5547) . This transformation is illustrated in Scheme 12.

COOMe

XVI XVII a is 1 or 2

Compounds of Formula I (Q-5) can be prepared by reaction of compounds of Formula XVIII with compounds of Formula IX. Typical reactions involve the

combination of equimolar amounts of XVIII and IX in a conventional organic solvent such as ethyl acetate, methylene chloride, chloroform, benzene or toluene. A base such as an alkali metal, tertiary amine, alkali metal alkoxide or metal hydride can be used. Scheme 13 illustrates this transformation.

Scheme 13

XVIII IX

Compounds of the Formula XVIII (X = 0) can be prepared by the Curtius rearrangement of compounds of the Formula XIX by procedures well known to the art (J. Jim . Chem . Soc. 1927, 45, 2528) . The reaction is usually performed in_an organic solvent such as benzene at temperatures of about 80°C. Scheme 14 illustrates this transformation.

XVIII

XIX

Compounds of Formula XVIII (X = S) can be prepared from compounds of Formula XX (Chem . Zuesti 1974, 28, 848) by reaction with thiophosgene in a conventional organic solvent such as dichloroethane, followed by treatment with triethyl amine, by procedures known to

the art; ( J. Org. Chem . 1965, 30, 1926) . Scheme 15 illustrates this transformation.

Scheme 15

XVIII

Compounds of Formula XIX can be prepared from compounds of Formula XXI by known procedures. Two carbon homologations are known (Wittig reaction, Synthesis 1979, 633) . Suitable functionality can be introduced (e.g., an ester) in this way, such that azides of Formula XIX can be prepared by procedures that are known (Fieser & Fieser, "Reagents for Organic Synthesis," Vol. VI, 1967). Scheme 16 illustrates this transformation.

Scheme 16

XI > ^NaN 3

The starting ketones of Formula XXI are known in the art or can be obtained by methods analogous to known procedures. Those skilled in the art will recognize Formula XXI compounds to include deoxy- benzoins, tetralones, chromanones, thiochromanones, benzofuran-3-ones, isochromanones, and others.

Compounds of Formula I (Q-6) can be prepared by the reaction of compounds of Formula XXII with a 1,3-dicarboιιyl compound (or suitable equivalent) by known procedures (J ^" . Jϊet. Chem . 1969, 77, and references cited therein) . Scheme 17 illustrates the transformation.

Scheme 17

H

XXII

Compounds of Formula XXII are known and can be prepared by known procedures.

Compounds of Formula I (Q-7) can be prepared by the reaction of compounds of Formula XXIII with compounds of Formula IX. Typical reactions involve the combination of equimolar amounts of XXIII and IX in a conventional organic ^" solvent such as ethyl acetate, dichloromethane or ether. A base such as triethyl— amine, pyridine, sodium amide, sodium methoxide or 2-hydroxypyridine can be added to the reaction. The compound IX can optionally be pretreated with an organometallic reagent such as trimethylaluminium or a Grignard reagent, prior to reaction with XXIII. The compound XXIII (L = OH) can be optionally pretreated with a reagent such as 1,l'-carbonyldiimidazole. Compounds of Formula XXIII (L = OH, CI, imidazole) are readily prepared from compounds of Formula XXIII (L = OMe or OEt) by methods known to those skilled in the art. Scheme 18 illustrates this transformation.

Scheme 18

is OH, CI, OCH ₃ , OCH ₂ CH ₃ or

Compounds of Formula XXIII can be prepared from compounds of Formula XXIV by a two-step sequence.

Reaction of ammonia with iminoyl chlorides is known to those skilled in the art ( Ukr. Khim . Zh . (Russ. Ed.) 1979, 45(7), 624). Accordingly, treatment of compounds of Formula XXIV with ammonia in benzene at 80°C affords an intermediate aminal. This intermediate can be dehydrated directly By treatment with a suitable reagent such as phosphorus pentoxide in a conventional organic solvent such as dichloromethane. The reaction is usually complete in about 20 h at ambient temperature, although elevated temperatures in the range of 40-150°C can be used. Scheme 19 illustrates this transformation.

Scheme 19

XXIII

XXIV -OMe, OEt

Compounds of F.ormula XXIV can be prepared from compounds of Formula XXV by a two-step sequence known to those skilled in the art. These are: A: Preparation of an amide by addition of an oxalyl chloride derivative in a conventional organic solvent such as dichloromethane, in the presence of a suitable base such as triethylamine.

B: Preparation of an imidoyl chloride from an amide by use of a reagent such as 0 ₃ P/CC1 , PC1 ₅ and the like. A conventional organic solvent such as ' dichloromethane or benzene can be used, and elevated temperatures up to 130°C can be used. Typically, the reaction is complete after a few hours at 40°C. Scheme 20 illustrates this transformation.

Scheme 20

Compounds of Formula XXV can be prepared by the reaction of compounds of Formula XXVI with compounds of Formula XXVII by procedures similar to those described in the art (Synthesis 1991, 327) . The conditions for this reaction are the combination of compounds of Formula XXVI with a small excess (1.1-1.5 eq.) of Formula XXVII derivatives in the presence of a base as a catalyst such as 1,4-diazabicyclooctane[2.2.2]octane (DABCO) , 1,5-diazabicyclo[5,4,0]-undec-5-ene (DBU) , lithium diisopropylamide, sodium hydroxide and the like. Suitable solvents include toluene,

tetrahydrofuran, dioxane and water. Scheme 21 illustrates this transformation.

Scheme 21

XXVI

XXVII (M - H)

Compounds of Formula I (Q-8, R ³⁵ =CHO) , where A and E are taken together, can be prepared by reaction of compounds of Formula I (Q-8, R ³⁵ =H) with acetic-formic anhydride; (see Reagents for Organic Synthesis, Fieser & Fieser, Vol 1, page 4) . The compounds are combined in the absence of solvent, usually employing a large excess of acetic-formic anhydride, and the reaction is usually complete after 6 h. Scheme 22 illustrates the transformation.

Scheme 22

Compounds of Formula I (Q-8) where R ³⁵ is other than CHO, can be prepared by standard alkylation, acylation, and sulfenylation reactions.

Alternatively, compounds of Formula I (Q-8) can be prepared by treatment of Formula XXVIII compounds with

a slight excess of a reagent such as Eschermoser's salt, or a suitably substituted equivalent such as formaldehyde in a conventional organic solvent such as tetrahydrofuran. Reactions are usually complete within 24 h. Scheme 23 illustrates this tranformation.

Compounds of Formula XXVIII can be prepared by the reaction of compounds of Formula XXV with semicarbazides of Formula XXIX. Conditions for this reaction require an acid catalyst such as hydrochloric, sulfuric or p-toluene sulfonic acid. Reaction temperatures can range from 0° to 150°C with the reflux temperature of the solvent used, generally preferred. Suitable solvents include methanol, ethanol, isopropanol, tetrahydrofuran and dioxane. Scheme 24 illustrates this transformation.

Scheme 24

XXVIII

Compounds of Formula I (Q-9) (Y=R ³⁸ and C ₂ -C alkoxycarbonyl) can be prepared by treatment of compounds of Formula XXX with phosphorus pentoxide and

dimethoxymethane in a conventional organic solvent such as dichloromethane, chloroform, 1,2-dichloroethane, or tetrahydrofuran. Typically, the reaction is complete in a few hours at 50°C, but can be conducted at temperatures between 25°-80°C with longer reaction times being experienced for lower temperatures. Scheme 25 illustrates this transformation.

Scheme 25

XXX L»=OMe, OEt

Compounds of Formula XXX can be prepared from compounds of Formula XXXI by methods known to those skilled in the art; see Fieser & Fieser, "Reagents for Organic Synthesis" (e.g., by use of phosphorus pentoxide/dimethoxymethane, or sodium hydride/chloromethyl methyl ether) . Scheme 26 illustrates this transformation.

Scheme 26

Compounds of Formula XXXI can be prepared by reacting compounds of Formula XXXII with compounds of Formula XXXIII in the presence of a suitable base such as triethylamine or sodium carbonate. The reaction is conducted in a conventional organic solvent such as dichloromethane, benzene, toluene, ether, or glyme and is usually complete in a few hours at ambient temperature. Scheme 27 illustrates this transformation.

Scheme 27

XXXII XXXIII

Compounds of Formula XXXII are known; see WO 92/11249. Compounds of Formula XXXIII can be prepared by treatment of compounds of Formula XXXIV with phosgene or phosgene equivalents in a conventional organic solvent such as benzene. Compounds of Formula XXXIV can optionally be treated with a base such as sodium hydride, sodium ethoxide or N,N-dieth laniline to facilitate the reaction with phosgene. The reaction is usually complete in a few hours at ambient temperature, but can be conducted at elevated temperatures if shorter reaction times are desirable. Scheme 28 illustrates this transformation.

Scheme 28

Phosgene

HNG XXXIII

Y

XXXIV

Alternatively., compounds of Formula I (Q-9) where Y is other than H, can be prepared by standard alkylation, acylation, or sulfenylation reactions by known methods.

It is recognized that in many of the trans¬ formations described it will be necessary to utilize appropriate protecting groups to prevent unwanted side reactions or use reagents that do not affect functionality other than that desired. One skilled in the art will be able to select appropriate protecting groups and reagents to this end.

EXAMPLE 1 Step A: 4-chloro-oc-f (4-chlorophenylimethylene!-acetic: acid

A mixture of 17.0 g (0.1 mol) of 4-chlorophenyl- acetic acid, 16.9 g (0.12 mol) of 4-chlorobenzaldehyde, 25 mL of triethylamine and 25 mL of acetic anhydride was heated at reflux for 1 1/2 hours. Ice was added to the mixture after cooling and the pH adjusted to 6 with concentrated hydrochloric acid. The resulting mixture was extracted twice with ether, and the ether solution concentrated. The residue was dissolved in IN sodium hydroxide and washed with ether:hexanes (1:1) . The pH of the aqueous layer was adjusted to 3 with concentrated hydrochloric acid and extracted twice with ether. The combined ether extracts was dried over anhydrous magnesium sulfate, filtered and concentrated to give an oily solid. Recrystallization from ethanol:water (1:1) afforded 23.5 g of a light yellow solid, 178-180°C. ^X H NMR (CDC1 ₃ ) δ 7.88 (s, IH) , 7.35-6.98, (2dd, 8H) . Step B: methyl 4-chloro-oc-r .4-chlorophenyl.methylene ^" !-

. acetate To a suspension of 10.0 g (0.034 mol) of the product of Step A in 70 mL methanol was added 5 mL of

thionyl chloride. The reaction was heated at reflux for 45 min. Afte.r cooling, it was carefully poured into saturated aqueous sodium bicarbonate solution. The mixture was extracted twice with ether and the 5 combined ether extracts washed with brine, dried over anhydrous magnesium sulfate, filtered and concentrated to give 10.06 g of a white solid, 87-88°C. ^-H NMR (CDC1 ₃ ) δ 7.80 (s, IH) 7.36-6.96 (2dd, 8H) , 3.80 (s, 3H) . 10 Step C: methyl 4-πhloro-oc-T t4-chlorophenylϊ-β- tnit.ro- methyl.benzene propanoate A mixture of 8.52 g (0.028 mol) of the product of Step B and 2.2 mL of triton B (40% in methanol) in 55 mL of nitromethane was heated at reflux for 4 hours. 15 After cooling, the mixture was made acidic with IN hydrochloric acid. Water was added and the mixture . extracted three times with methylene chloride. The combined methylene chloride extracts was washed with IN hydrochloric acid, brine, dried over anhydrous ^* 20 magnesium sulfate, filtered, and concentrated to give an oil which was purified by chromatography on silica gel (ethyl acetate:hexanes 1:8) to give 2.6 g of a brown solid, 132-135°C. ^-H NMR (CDC1 ₃ ) δ 7.40-7.23 ( , 8H), 4.40 (dd, IH) , 4.25 (dd, IH) , 4.18 (m, IH) , 3.94 25 (d, IH) , 3.45 (s, 3H) .

Step D: methyl 4-chloro-χ-r (4-chloropheny1.-β- (amino- methyl.benzene propanol To a suspension of 2.97 g (0.078 mol) of lithium aluminum hydride in 30 mL of tetrahydrofuran at 0°C was 30 added dropwise a solution of 2.88 g (0.0078 mol) of the product of Step C in 30 mL of tetrahydrofuran. The mixture was heated at reflux for 2 hours, then stirred at ambient temperature for 2 days. Excess lithium aluminum hydride was carefully quenched with water. 35 50% aqueous sodium hydroxide was added to dissolve aluminum salts, and the mixture extracted three times

with ethyl acetate. The combined ethyl acetate extracts was washed with brine, dried over anhydrous magnesium sulfate, filtered, and concentrated to give an oil which solidified on standing. The solid was triturated with ether:hexanes (1:1) to give 2.37 g of an off-white solid, 139-145°C. -Ε. NMR (CDC1 ₃ ) δ 7.35-7.30 (m, 8H) , 4.05 (m, 2H) , 3.75 (m, 2H) , 3.55 (m, 2H) , 2.14 (bs, 3H) . Step E: N- r2. 3-bi .<- 4-πhlorophenyl , -4-hγdroxybutyl1 -N' - f4-(trifluoromethyl ) henyl1urea

To a suspension of 1.0 g (0.Q032 mol) of the product of Step D in 5.5 mL tetrahydrofuran was added 0.603 g (0.0032 mol) of 4-trifluoromethylphenyl- isocyanate. The reaction was stirred at ambient temperature for 30 min., concentrated and the residue triturated with methylene chloride to give 1.18 g of a white solid. ^X H NMR (DMSO-d ₆ ) δ 8.70 (s, IH) , 7.49-7.20 (m, 12H) , 5.70 (t, IH) , 3.60-2.80 (m, 6H) . Step F: 3,4-bis(4-chlorophenyl.-4.5-dihydro-N-T4-tri- fluoromethyl. henyll-lH-pγrrole-1-carboxamide

To a solution of 0.836 g (0.0017 mol) of the product of Step E and 1.7 mL of triethylamine in 2.5 L of dimethyl sulfoxide was added a solution of 1.68 g (0.011 mol) of sulfur trioxide-pyridine complex in 5 mL of dimethyl sulfoxide. The reaction mixture was stirred at ambient temperature for 4 hours, poured into ice and the resulting solid filtered. The solid was washed several times with water and transferred into a flask. 50 mL of toluene was added and the mixture refluxed in a Dean-Starke trap to remove water. 17 mg of pyridine p-toluene sulfonate was added and refluxing continued for another hour. The reaction was concentrated and the residue purified by column chromatography on silica gel (methylene chloride: hexanes 4:1) to give 0.230 g of a white solid.

Trituration with hexanes afforded 0.213 g of a white

solid, 206-208°C. ^-H NMR (DMSO-dg) δ 9.10 (s, IH) , 7.87-7.30 (m, 13HJ , 4.74 (dd, IH) , 4.38 (t, IH) , 3.84 (dd, IH) .

EXAMPLE 2 Step A: methyl 2-amino-5-chloro-2.3-dihydro-l-oxo-lH- indene-2-carboxylate hydrochloride An ice cold solution of hydroxylamine-o-sulfonic • acid (11.4 g, 100.8 mmol) in water (102 mL) and sodium hydroxide solution (50 mL, 2N) was added in one portion to a mixture of cyclohexanone (10 g, 102 mmol) , toluene (180 mL) , and sodium hydroxide solution (50 mL, 2N) at 0°C. The mixture was stirred for 10 minutes. The organic layer was removed and dried over magnesium sulfate. Methyl 5-chloro-2,3-dihydro-l-oxo-2-lH- indene—2-carboxylate (7 g, 31.3 mmol) was added in one portion to a portion (155 mL) of the toluene solution. DABCO (0.1 g, 0.89 mmol) was added in one portion and the mixture was stirred for 1 h at 5°C. The mixture was washed with hydrochloric acid (2x50 mL, IN). The acid washings were evaporated under reduced pressure to give the product (4.37 g) , as a solid; m.p. 145-148°C (dec); ^-H NMR (free base) (CDC1 ₃ ) δ 7.73 (d, IH) , 7.48 (s, IH) , 7.41 (d, IH) , 3.69 (s, 3H) , 3.68 (1/2 ABq, IH) , and 3.05 (1/2 ABq, IH) . Step B: methyl 2-amino-5-chloro-2.3-dihydro-l-. f f-4- r ri luoromethoxy. henylamino!carbonyl!- hydrazono!-lH-indene-2-carboxylate A mixture of the product (2 g, 7.24 mmol) from Step A and 4-(4—trifluoromethoxy)phenylsemicarbazide (1.83 g, 7.78 mmol) in ethanol (18 mL) was boiled for 2 h. The mixture was allowed to cool and was stirred at room temperature overnight. The mixture was poured into sodium bicarbonate solution (200 mL, saturated) and then extracted with ethyl acetate (3x100 mL) . The combined extracts were dried and evaporated and the material washed with ether to give 1.0 g of an

off-white solid, of which a small portion was further purified by chromatography on silica gel (ethyl acetate/ethanol 5:1), m.p. 156.5 to 158°C (dec). ^-H NMR (CDC1 ₃ ) δ 8.4 (s, IH) , 8.20 (s, IH) , 7.83 (d, IH) , 7.56 (d, 2H), 7.42-7.18 (m, 4H) , 3.73-3.65 (m, 4H) , 3.05 (1/2 ABq, IH) . Step C: methyl 7-chloro-2.3.4.5-tetrahydro-2-r T4-

■ ri luoromethoxy.phenylamino!carbonyl1-4aH- indeno.2■1-e!-1.2.4-triazine-4a-carboxylat-.fi Esthermoser's salt (0.8 g, 4.32 mmol) and the product (1.97 g, 4.31 mmol) from Step B were added to tetrahydrofuran (35 mL) and the mixture was stirred for 20 h at room temperature. The mixture was poured into water and was extracted with ethyl acetate (2x100 mL) . The combined organic extracts were dried and evaporated. The product was purified by chromatography on silica gel (eluted with ethyl acetate/hexanes (3:2)) and afforded 0.87 g (43%) as a white solid; m.p. 183-187°C; IR (Mineral Oil) 3368, 3291, 1752, 1665, 1639, 1603, 1563, 15.35, 1416, 1316, 1275, 1226, 1200, 1174, 1068, 1009, 945, 914, 890, 828 cm ^-1 ; ΛH NMR (CDCI ₃ ) δ 8.42 (s, IH), 7.63-7.14 (m, 7H) , 5.38 (1/2 ABq, IH) , 4.42-4.32 (m, IH) , 3.70 (s, 3H) , 3.52 (1/2 ABq, IH) , 3.07 (1/2, IH ABq) , 2.43 (br s, IH) . Step D: methyl 7-chloro-4-formyl-2.3.4.5-te rahyr.ro- ?. T T4- ttrifluoromethoxy.phenylamino!carbonyl!- 4aH-indeno \2.1-e!-1.2.4-triazine-4a-carboxylat-.e Acetic anhydride (0.6 mL) was added in one portion to formic acid (0.5 g) . When the mixture had cooled to room temperature, the product from Step C (0.12 g,

2.56 mmol) was added in one portion. After 2 h, the mixture was poured into sodium bicarbonate solution (100 L, saturated) , and the solution was extracted with ethyl acetate (3x50 mL) . The combined extracts were dried and evaporated to give the product ^' (0.12 g, 94%) as a solid; m.p. 204-206°C; IR (Mineral oil) 3301,

1741, 1691, 1664, 1604, 1562, 1533, 1416, 1319, 1262, 1240, 1219, 1193,.1163, 1091, 1012, 883, 831, 805 cm" ¹ ; ^-H NMR (CDC1 ₃ ) 9.63 (s, ~0.6H) , 9.55 (s, -0.4H), 8.49 (s, -0.6H), 8.45 (s, -0.4H), 7.98-7.33 (m, 7H) , 5.82 (1/2 ABq, -0.7H), 5.76 (1/2 ABq, -0.3H), 4.69 (1/2

ABq, IH), 4.0 (1/2 ABq, -0.7H), 3.83 (1/2 ABq, -0.3H), 3.77 (1/2 ABq, -0.3H), 3.61 (s, ~1H) , 3.53 (s, ~2H) , 3.36 (1/2 ABq, ~0.7H). (Two conformations are apparent by NMR, and by integration the ratio appears to be 2.3-1.5:1).

EXAMPLE 3 Step A: 2-amino-6-chloro- .4-dihydro-2-methyl-l .2H.- napthalenone hydrochloride Ice cold sodium hydroxide solution (75 mL, 2N) was added to hydroxylamine-O-sulfonic acid (17.1 g,

0.15 mol) in water (150 mL) at 0°C. When the solution had cooled to about 5°C it was added in one portion to a mixture of sodium hydroxide solution (75 mL, 2N) , cyclohexanone (15 g, 0.15 mol) and toluene (270 mL) at 0°C. The mixture was stirred for 10 min. The organic layer was separated, dried and decanted from the drying agent. This afforded a solution of the cyclohexane- spiro-3'-oxaziridine which was used directly. The oxyaziridine solution prepared as above (540 L) was added in one portion to an enolate (previously prepared by addition of 2-methyl-6-chlorotetralone (18.07 g, 92.9 mmol) in THF (40 mL) to lithium diisopropylamide (10.4 g, 97.1 mmol) in THF/hexanes (60 mL/40 mL) at -50°C. When the addition was complete, the mixture was stirred for 1 h at -50°C) . The reaction was stirred for 1 h, and was allowed to warm to 0°C. The mixture was poured into water (500 mL) , and the organic layer was separated. The aqueous layer was further extracted with dichloromethane (3x250 mL) . The combined extracts ^' were dried, hydrochloric acid (about 10 mL, cone.) was added, and the mixture was evaporated. Ether (250 mL)

was added and hydrochloric acid (about 10 mL, cone.) was added. The mixture was stirred overnight and was filtered to give the product as a solid (19.18 g, 83%) . ^ NMR (free base) (CDC1 ₃ ) 8.00 (d, IH) , 7.32-7.25 (m, 2H) , 3.19-2.89 (m, 2H) , 2.18-1.98 (m, 2H) , 1.29 (s, 3H) .

Step B: methylr t6-chloro-3.4-dihydro-2-methyl-l-oxo^ 2 (lH)-naphthalenyl.amino!oxoacetate Methyl oxalyl chloride (2.55 g, 20.8 mmol) was added to the product of Step A (5.15 g, 20.8 mmol) and triethylamine (4.2 g, 41.5 mmol) in dichloromethane (20 mL) . After 20 min, the mixture was poured into water (100 mL) , and the organic layer was removed. The aqueous layer was further extracted with ethyl acetate (2x20 mL) . The combinated extracts were dried and evaporated. Crystallization from hexanes/ether afforded 4 g (65%) of a solid: m.p. 128-129.5°C. IR (Mineral oil) : 3310, 1743, 1710, 1681, 1592, 1565, 1525, 1411, 1348, 1310, 1286, 1244, 1227, 1114, 1006, 977, 961, 937, 895, 865 and 849 cm" ¹ . --H NMR (CDC1 ₃ ) δ 8.32 (s, IH), 8.0 (d, IH), 7.34 (d, IH) , 7.27 (s, IH) , 3.91 (s, 3H), 3.19-2.93 (m, 3H) , 2.30-2.22 (m, IH) , 1.61 (s, 3H) . Step C: methyl chloro T (6-chloro- .4-dihydro-2-methyl-l- oxo-2 t i -naphthalenyl . imino! acetaf.e

Triphenylphosphine (1.95 g, 7.44 mmol) was added to the product from Step B (2 g, 6.77 mmol) and carbon tetrachloride (1.15 g, 7.46 mmol) in dichloromethane (14 mL) . The mixture was boiled for about 3 h. A further portion of carbon tetrachloride (0.12 g,

0.78 mmol) and triphenylphosphine (0.2 g, 0.67 mmol) was added. The mixture was boiled for about 1 h. The mixture was allowed to cool and stirred at room temperature overnight. The mixture was diluted with ether (100 ml) and filtered. The filtrate was evaporated to dryness to give 3.84 g of a solid. A

portion (0.2 g) of the solid was purified by chromatography on silica gel (eluted with ethyl acetate/hexanes 1:1) to give 0.05 g of a yellow solid. IR (mineral oil) : 1744, 1678, 1593, 1566, 1548, 1512, 1442, 1372, 1333, 1295, 1271, 1226, 1082, 1031, 969, 910, 897, 868, 831 cm ^-1 . --E NMR (CDC1 ₃ ) δ 8.01 (d, IH) , 7.35-7.26 (m, 2H) , 3.90 (s, 3H) , 3.06 (t, 2H) , 2.75-2.60 (m, IH) , 2.23-2.10 (m, IH) , 1.68 (s, 3H) . Step D: methyl 7-πhloro-3a.5-dihydro-3a-methyl-4H- napt l ^~ 1.2-d!imida7.o!e-?-carboxylate

Ammonia was passed through the product from Step C (2.94 g, 9.36 mmol) in boiling benzene (100 mL) . After about 5 h, the mixture was allowed to cool and was diluted with ethyl acetate (100 mL) . The mixture was extracted with hydrochloric acid (IN, 2x60 mL) . The combined acidic extracts were made basic by addition of sodium carbonate solution. The mixture was extracted with ethyl acetate (3x60 L) , and the combined extracts were dried and evaporated. Crystallization from ether/hexane gave 0.9 g of a solid product. Phosphorus pentoxide was added to a portion (0.07 g, 0.23 mmol) of this product in dichloromethane (5 mL) . The mixture was stirred at room temperature overnight, and was poured into a mixture of sodium carbonate solution (100 mL) and ice. The mixture was extracted with ethyl acetate (3x20 mL) and the combined extracts were dried and evaporated. Chromatography on silica gel (eluted with ethyl acetate) afforded 20 mg (30%) of a white crystalline solid. IR (mineral oil) : 1736, 1592, 1539, 1185, 1132, 889, 838, 809 cm" ¹ . --E NMR (CDC1 ₃ ) δ 8.06 (d, IH), 7.37-7.33 (m, 2H) , 7.04 (s, 3H) , 3.25 (1/2 AB of ABX, IH) , 3.06 (1/2 AB of ABX, IH) , 2.65 (1/2 AB of ABX, IH) , 1.84-1.66 (m, IH) , 1.36 (s, 3H) . MS m/e 276(M) .

Step E : 7-chloro-3a . 5-dihydro-3a-methyl-N- ( (4- ltrifluoromethoxy ) henyl ) )-4H-napth ( 11 . 2- Ω) . imidazole-2-oarboxamide The compound, 4-trifluoromethoxy aniline (0.51 g, 2.88 mmol), in THF (3 mL) was added dropwise to methyl magnesium chloride (0.96 mL, 3M) in THF (1 mL) . When all effervescence had ceased, a portion (about 2 mL, about 1.16 mmol) of the solution was added dropwise to a portion (0.16 g, 0.57 mmol) of the product from Step D in THF (6 mL) . The mixture was poured into hydrochloric acid (50 mL, IN) , and the aqueous mixture was extracted with ethyl acetate (1x50 mL) . The organic extracts were washed with sodium bicarbonate solution (1x50 mL) , dried and evaporated. Crystallization from _. ether/hexanes gave 0.12 g (50%) of a white solid: m.p. 109-110.5°C. IR (mineral oil) : 3321, 1669, 1598, 1579, 1549, 1411, 1267, 1221, 1178, 1095, 1018, 993, 952, 901, 876, 824 cm" ¹ . ¹ .H NMR (CDC1 ₃ ) δ 9.33 (s, IH), 8.05 (s, IH) , 7.80 (d, IH) , 7.38-7.36 (m, 2H) , 7_.25 (d, IH) , 3.36-3.27 (m, IH) , 3.14-3.05 (m, IH) , 2.68-2.63 (m, IH) ,.1.82-1.73 (m, IH) , 1.39 (s, IH) . MS m/e 421(M).

Key for Tables κ=

K-l κ-2

K-3 K-4

K-5 K-6

K-7 K-8

K-9 K-10

K-ll K-12

K-13 K-14

K-15 K-16

K-17 K-18

K-19 K-20

K-23 K-24

By the procedures described herein, the following compounds of Tables 1-24 can be prepared. The compounds in Table 1, line 1 can be referred to as 1-1 and 1-2 (as designated by line and column) . The four separate compounds in Table 22, line 1 are compounds wherein K=K-22, R ² =6-C1, R ³⁵ =CHO, Y=H, and R ³ is one of C0 ₂ Me, C0 ₂ Et, 4-F-Ph, or 4-Cl-Ph. Thus, the four compounds of Table 22, line 1 are 1-1 (R ³ =C0 ₂ Me) , 1-2 (R ³ =C0 ₂ Et) , 1-3 (R ³ =4-F-Ph) , and 1-4 (R ³ =4-Cl-Ph) . The other lines 2-510 describe four separate compounds per line similarly to line 1.

The abbreviations, Me, Et, i-Pr, Ac, and Ph have the following meaning: Me = -CH ₃ ; Et = -CH ₂ CH ₃ ; n-Pr - CH ₂ CH ₂ CH ₃ ; i-Pr - -CH(CH ₃ ) ₂ ;

Ac = -C(0)CH ₃ ; and

1Δ£I-E-_1

κ-κ-1 R ¹ -OCF ₃ , R ³ =C0 ₂ Me; Y-H; R - R ¹ -0CF ₃ , R ³ -C0 ₂ Et; Y-H; _R 2. R ¹ -0CF ₃ , R ³ -Ph; Y-H; _R 2. R ¹ -OCF ₃ , R ³ -4-F-Ph; Y-H; R ¹ =OCF ₃ , R ³ -4-Cl-P ; Y-H; R ¹ -OCF ₃ , R ³ -C0 ₂ Me; Y-Me; _R 2- R!-0CF ₃ , R ³ -C0 ₂ Et; Y-Me; _R 2- R ¹ -OCF ₃ , R ³ -Ph; Y-Me; _R 2- R ¹ -0CF ₃ , R ³ -4-F-Ph; Y-Me; _R 2- R ¹ -OCF ₃ , R ³ -4-Cl-P ; Y-Me; _R 2- R ¹ -0CF ₃ , R ³ -C0 ₂ Me; Y=C0 ₂ Me; _R 2- R ¹ -0CF ₃ , R ³ -C0 ₂ Et; Y-C0 ₂ Me; R2- R ¹ -0CF ₃ , R ³ -Ph; Y-C0 ₂ Me; _R 2- R ¹ -OCF ₃ , R ³ -4-F-Ph; Y-C0 ₂ Me; R2- R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y=C0 ₂ Me; R2- R ¹ -OCF ₃ , R ³ -C0 ₂ Me; Y-COMe; _R 2- R ¹ -OCF ₃ , R ³ -C0 ₂ Et; Y-COMe; _R 2- R ¹ -OCF ₃ , "R ³ -C0 ₂ Me; Y-COMe; R2- R1-OCF ₃ , R ³ -C0 ₂ Et; Y-COMe; _R 2- R ¹ -OCF ₃ , R ³ -Ph; Y-COMe; R2- R ¹ -OCF ₃ , R ³ -4-F-P ; Y-COMe; R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-COMe; _R 2-

R ¹ -OCF ₃ , R ³ -C0 ₂ Me; Y-H; R2-

R ¹ -OCF ₃ , R ³ -C0 ₂ Et; Y-H; R2-

R ¹ -OCF ₃ , R ³ -P ; Y-H; _R 2-

R ¹ -OCF ₃ , R -4-F-Ph; Y-H; _R 2-

R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-H; R2-

R ¹ -OCF ₃ , R ³ -C0 ₂ Me; Y-H; _R 2=

R1-0CF ₃ , R ³ -C0 ₂ Et; Y-H; _R -

R1«OCF ₃ , R ³ -P ; Y-H;

R1=0CF ₃ , R ³ -4-F-Ph; Y-H; R ¹ =OCF ₃ , R ³ -4-Cl-Ph; Y-H;

κ-κ- R-Cl; E-H; R ¹ -OCF ₃ , R ³ -C0 ₂ Me; Y-H; R-Cl; E-H; R ¹ -OCF ₃ , R ³ =C0 ₂ Et; Y-H; R-Cl; E-H; R ¹ -0CF ₃ , R ³ -Ph; Y-H; l2_ R-Cl; E-H; R ¹ -0CF ₃ , R ³ -4-F-P ; Y-H; R=C1; E-H; R ¹ =0CF ₃ , R ³ -4-Cl-Ph; Y-H; R=OMe; E-H; R ¹ -OCF ₃ , R ³ -C0 ₂ Me; Y-H; R-OMe; E-H; R ¹ -OCF ₃ , R ³ -C0 ₂ Et; Y-H; *2- R-OMe; E-H; R ¹ -0CF ₃ , R -P ; Y-H; R-OMe; E-H; R ¹ -0CF ₃ , R ³ -4-F-Ph; Y-H; R-OMe; E-H; R ¹ -0CF ₃ , R ³ -4-Cl-Ph; Y-H;

ΔE E_

K-K-2

R ¹ -CF ₃ , R ³ -COOMe; Y-H; ^2- R ¹ -CF ₃ , R ³ -COOEt; Y-H; ■l2- R ¹ -CF ₃ , R ³ -Ph; Y-H; R2. R ¹ -CF ₃ , R -.4_ _F _ h; Y-H; R2- R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-H; R ¹ -CF ₃ , R ³ -COOMe; Y-Me; R ¹ -CF ₃ , R ³ -COOEt; Y-Me; *2« R ³ -P ; Y-Me; R ¹ -CF ₃ , R ³ -4-F-Ph; Y-Me; R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-Me; l2_ R^CFs, R ³ -COOMe; Y-COOMe; R ¹ =CF ₃ , R ³ -COOEt ; Y-COOMe; R ¹ -CF ₃ , R ³ -P ; Y-COOMe; R2- R ¹ =CF ₃ , R ³ -4-F-P ; Y-COOMe; R2- R ¹ =CF ₃ , R ³ =4-Cl-P ; Y=COOMe; _R 2= R ¹ =CF _3r R ³ =COOMe; Y=COMe; 2- R ¹ -CF ₃ , R ³ -COOEt; Y-COMe; R ¹ =CF ₃ , R ³ -P ; Y-COMe;

K-K-2 R-H; E-H; R ¹ -CF ₃ , R ³ -4-F-P ; Y-COMe; _R 2. R-H; E-H; R-T-CF3, R ³ -4-Cl-Ph; Y-COMe; R2. R ¹ -CF ₃ , R ³ -Me; Y-H; R ¹ -CF ₃ , R ³ -i-Pr; Y-H; * - R ¹ -CF ₃ , R ³ -Ph; Y-H; R ¹ -CF ₃ , R ³ -4-F-Ph; Y-H; _R 2. R ¹ -CF ₃ , R ³ -4-Cl-P ; Y-H; . R ¹ -CF ₃ , R ³ -Me; Y-H; _R 2. R ¹ -CF ₃ , R ³ -i-Pr; Y-H; l2- R ¹ -CF ₃ , R ³ -P ; Y-H; ^ _ R ¹ -CF ₃ , R ³ -4-F-Ph; Y-H; R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-H; R ^X -CF ₃ , R ³ -Me; Y-H; R ¹ -CF ₃ , R ³ -i-Pr; Y-H; R ¹ -CF ₃ , R ³ -Ph; Y-H; *.--- R ¹ -CF ₃ , R ³ -4-F-Ph; Y-H; R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-H; R-OMe; E-H R ¹ -CF ₃ ,_ R ³ -Me; Y-H; R-OMe; E-H R ¹ -CF ₃ , R ³ -i-Pr; Y-H; R-OMe; E-H R ¹ -CF ₃ , R ³ -P ; Y-H; R-OMe; E-H R ¹ -CF ₃ , R ³ -4-F-P ; Y-H; R-OMe; E-H R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-H;

X&&I£_3.

K-K-3

R ¹ =OCF ₃ , RR ³³ --PP1 ; Y-H; R ¹ =OCF ₃ , R ³ -4-F-Ph; Y=H; R2-

R ₃ 1- ^L «=OCF ₃ , R ³ °=-4-ι--rC.lι --Pv h; Y-H; R2-

R1=OCF ₃ , R ³ =Ph; Y-Me; ,2 ₌

R1-=OCF ₃ , R ³ -4-F-Ph; Y-Me; R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-Me;

^■ K-K-3 R-H; E-H; R ¹ -OCF ₃ , R ³ -Ph; Y-COOMe; R2- R-H; E-H; R ¹ =OCF ₃ , R ³ -4-F-Ph; Y-COOMe; R2- R-H; E-H; R ¹ =OCF ₃ , R ³ -4-Cl-Ph; Y-COOMe; R2- R-H; E-H; R ¹ =OCF ₃ , R ³ -Ph; Y-COMe; R-H; E-H; R ¹ =OCF ₃ , R ³ -4-F-Ph; Y-COMe; R-H; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-P ; Y-COMe; R-Me; E-H; R ¹ -OCF ₃ , R ³ -4-F-P ; Y-H; R-Me; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-P ; Y-H; R-CN; E-H; R ¹ -OCF ₃ , R ³ -4-F-P ; Y-H; _R 2- R-CN; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-H; R2- R-Cl; E-H; R ¹ =OCF ₃ , R ³ -P ; Y-H; _R 2- R-Cl; E-H; R ¹ -OCF ₃ , R ³ -4-F-P ; Y-H; R2- R-Cl; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-H; R2- R-OMe; E-H; R ¹ -OCF ₃ , R ³ -4-F-Ph; Y-H; R2« R-OMe; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-H;

1-----E---

K-K-4 R ¹ =CF ₃ , R ³ -Ph; Y-H; _R 2. R ¹ -CF ₃ , R ³ -4-F-Ph; Y-H; _R 2. R ¹ -CF ₃ , R ³ -4-Cl-Plι; Y-H; _R 2. R ¹ -CF ₃ , R ³ -P ; Y-Me; *2« R ¹ -CF ₃ , R ³ -4-F-P ; Y-Me; R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-Me; R ¹ =CF ₃ , R ³ -Ph; Y-COOMe; R ¹ -CF ₃ , R ³ -4-F-Ph; Y-COOMe; _R 2- R ¹ -CF ₃ , R ³ -4-Cl-P ; Y-COOMe; 2= R ¹ =CF ₃ , R ³ -Ph; Y=COMe; _R 2= R ¹ =CF ₃ , R ³ =4-F-Ph; Y=COMe; R2- R ¹ =CF ₃ , R ³ -4-Cl-Ph; Y-COMe; ; R ¹ =CF ₃ , R ³ -4-F-P ; Y-H;

K-K-4 R-Me; E-H R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-H; R-CN; E-H R ³ -4-F-P ; Y-H; R-CN; E-H R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-H; R-Cl; E-H R ¹ -CF ₃ , R ³ -Ph; Y-H; R2- R-Cl; E-H R ¹ -CF ₃ , R ³ -4-F-Ph; Y-H; _R 2- R-Cl; E-H R ¹ -CF ₃ , R ³ -4-Cl-P ; Y-H; R2- R-OMe; E-H; R ¹ -CF ₃ , R ³ -4-F-Ph; Y-H; R-OMe; E-H; R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-H;

ZΔB E_≥

K-K-5 R ¹ -OCF ₃ , R ³ -Ph; Y-H; R2- R ¹ -OCF ₃ , R ³ -4-F-P ; Y-H; R2- R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-H; R2- R ¹ -OCF ₃ , R ³ -Ph; Y-Me; R2- R ¹ -OCF ₃ , R ³ -4-F-Ph; Y-Me; _R 2- R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-Me; R2- R ¹ -OCF ₃ , R ³ -P ; Y-C0 ₂ Me; R ² -

R ¹ -0CF ₃ , R ³ -4-F-P ; Y-C0 ₂ Me; R ² - R ¹ -0CF ₃ , R ³ -4-Cl-P ; Y-C0 ₂ Me; R ² - R ¹ -OCF ₃ , R ³ -4-F-Ph; Y-COMe; R ² -

R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-COMe; R ² -

R ¹ -OCF ₃ , R ³ -4-F-Ph; Y-H; R ² -

R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-H; R ² -

R ¹ -OCF ₃ , R ³ -Ph; Y-H; R ² =

R ¹ -OCF ₃ , R ³ -4-F-Ph; Y-H; _R 2-

R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-H; _R 2-

R ¹ =OCF ₃ , R ³ =P ; Y-H; R2-

R ¹ -OCF ₃ , R ³ -4-F-Ph; Y-H; R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-H; R=OMe; E-H; R ¹ -OCF ₃ , R ³ =P ; Y-H;

- K-K-5 R-OMe; E-H; R ¹ -OCF ₃ , R ³ -4-F-P ; Y-H; R ² - R-OMe; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-P ; Y-H; R ² =

TABLE 6

K-K-6 R ¹ -CF ₃ , R ³ -Ph; Y-H; _R 2- R1-CF ₃ , R ³ -4-F-Ph; Y-H; R2- R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-H; R2- R ¹ =CF ₃ , R ³ -Ph; Y-Me; _R 2- R ¹ -CF ₃ , R ³ -4-F-P ; Y-Me; _R 2= R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-Me; R ¹ =CF ₃ , R ³ -Ph; Y-COOMe; R ^X -CF ₃ , R ³ -4-F-Ph; Y-COOMe; R ¹ -CF ₃ , R ³ -4-Cl-P ; Y-COOMe; R ¹ -CF ₃ , R ³ -4-F-Ph; Y-COMe; R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-COMe; _R 2.

R1-CF ₃ , R ³ -4-F-Ph; Y-H; _R 2.

R ¹ -CF ₃ , R ³ -4-Cl-P ; Y-H; R2.

R.I-CF3, R ³ -ph; Y-H; i2-

R ¹ -CF ₃ , R ³ -4-F-Ph; Y-H; _R 2.

R ¹ -CF ₃ , R ³ -4-Cl-P ; Y-H; R2-

R ¹ -CF ₃ , R ³ -Ph; Y-H; R .

R ¹ -CF ₃ , R ³ -4-F-P ; Y-H; R ¹ -CF ₃ , R ³ -4-Cl-Ph.; Y-H; R-OMe; E-H; R ¹ -CF ₃ , R ³ -P ; Y-H; _R 2. R-OMe; E-H; R ¹ -CF ₃ , R ³ -4-F-Ph; Y-H; _R 2. R-OMe; E-H; R ¹ -CF ₃ , R ³ -4-Cl-P ; Y-H; R2=

κ-κ-7 R-H; E-H; R ¹ -OCF ₃ , R ³ -Ph; Y-H; 3-C1 3-F 3-CF3 R-H; E-H; R ¹ -OCF ₃ , R ³ -4-F-Ph; Y-H; 3-Cl 3-F 3-CF3 R-H; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-H; 3-Cl 3-F 3-CF3 R-H; E-H; R ¹ -OCF ₃ , R ³ -P ; Y-Me; 3-Cl 3-F 3-CF3 R=H; E-H; R ¹ -OCF ₃ , R ³ -4-F-P ; Y-Me; _R 2= 3-Cl 3-F 3-C 3 R-H; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-P ; Y-Me; 3-Cl 3-F 3-CF3 R-H; E-H; R ¹ -OCF ₃ , R ³ -Ph; Y-C0 ₂ Me; 3-Cl 3-F 3-CF3 R-H; E-H; R ¹ -OCF ₃ , R ³ «4-F-P ; Y-C0 Me; 3-Cl 3-F 3-CF3 R-H; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-C0 ₂ Me; *2. 3-Cl 3-F 3-CF3 R-H; E-H; R ¹ -OCF ₃ , R ³ -4-F-Ph; Y-COMe; 3-Cl 3-F 3-CF3 R-H; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-COMe; R - 3-Cl 3-F 3-CF3 R-Me; E-H; 3-Cl 3-F 3-CF3 R-Me; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-P ; Y-H; _R 2- 3-Cl 3-F 3-CF3 R-CN; E-H; R ¹ -OCF ₃ , R ³ -P ; Y-H; R2- 3-Cl 3-F 3-CF3 R-CN; E-H; R ¹ -OCF ₃ , R ³ -4-F-Ph; Y-H; 3-Cl 3-F 3-CF3 R-CN; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-H; *2_ 3-Cl 3-F 3-CF3 R-Cl ; E-H; R ¹ -OCF ₃ , .--R ³ -Ph; Y-H; 3-Cl 3-F 3-CF3 R-Cl; E-H; R ¹ -OCF ₃ , R ³ -4-F-P ; Y-H; _R 2- 3-Cl 3-F 3-CF3 R-Cl; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-Ph; Y-H; _R 2- 3-Cl 3-F 3-CF3 R-OMe; E-H; R ¹ - OCF3, R ³ -Ph; Y-H; _R 2- 3-Cl 3-F 3-CF ₃ R-OMe; E-H; R ¹ -OCF ₃ , R ³ -4-F-Ph; Y-H; 3-Cl 3-F 3-CF3 R=OMe; E-H; R ¹ -OCF ₃ , R ³ -4-Cl-P ; Y-H; 3-Cl 3-F 3-CF

TABLE 8

K-K-8 R=H E-H R ¹ -CF ₃ , R ³ -Ph; Y-H; R-H E-H R ¹ -CF ₃ , R ³ -4-F-Ph; Y-H; R-H E-H R ¹ =CF ₃ , R ³ =4-Cl-P ; Y-H; R-H E-H R ¹ =CF ₃ , R ³ -p ; Y-Me; R-H E-H R ¹ =CF ₃ , R ³ -4-F-Ph; Y-Me;

• -κ-8 R ¹ =CF ₃ , R ³ -4-Cl-Ph; Y-Me; R ¹ -CF ₃ , R ³ -Ph; Y-COOMe; R ¹ -CF ₃ , R ³ -4-F-P ; Y-COOMe; *2« R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-COOMe; R ¹ =CF ₃ , R ³ -4-F-Ph; Y=COMe; R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-COMe; * ² -

R ¹ -CF ₃ , R ³ -4-F-Ph; Y-H;

R ¹ =CF ₃ , R ³ -4-Cl-Ph; Y-H;

R ¹ -CF ₃ , R ³ -Ph; Y-H;

R ¹ -CF ₃ , R ³ -4-F-Ph; Y-H; ^ ² -

R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-H;

R ¹ -CF ₃ , R ³ -P ; Y-H; R ² -

R ¹ -CF ₃ , R ³ -4-F-P ; Y-H; R ² - R ¹ -CF ₃ , R ³ -4-Cl-P ; Y-H;

20 R-OMe; E-H; R ¹ -CF ₃ , R ³ -Ph; Y-H;

21 R-OMe; E-H; R ^X -CF ₃ , R ³ -4-F-Ph; Y-H;

22 R-OMe; E-H; R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-H;

K-K-9

A-0 R-H; R ¹ -CF ₃ R ³ -Me; Y-H; A=0 R-H; R ¹ -CF ₃ R ³ -i-Pr; Y-H; A-0 R-H; R ¹ -CF ₃ R ³ -COOMe; Y-H; A=0 R-H; R ¹ =CF ₃ R ³ -Ph; Y-H; A-O R-H; R ¹ -CF _{3 l} R3_4_ _F _ ; Y-H; R2- A-O R-H; R ¹ =CF _{3 l} R ³ -4-Cl-P ; Y-H; _R 2- A-O R-H; R ¹ =CF ₃ R ³ -Me; Y-Me; R2- A-O R-H; R1=CF ₃ R ³ =i-Pr; Y-Me; _R 2= A=0 R-H; R ¹ =CF ₃ R ³ =COOMe; Y=Me; A=0 R-H; R ¹ =CF ₃ R ³ -4-F-P ; Y-Me; _R 2= A-O R-H; R ¹ =CF ₃ R ³ -4-Cl-Ph; Y-Me; _R 2=

K-K-9

R ¹ =CF ₃ R ³ -Me; Y-COOMe; R ¹ -CF ₃ R ³ =i-Pr; Y-COOMe; R1»CF3 R ³ =COOMe; Y-COOMe; R ¹ =CF ₃ R ³ «4-F-Ph; γ-C00Me; R ¹ -CF ₃ R ³ -4-Cl-Ph; Y-COOMe; R ¹ -CF ₃ R ³ -Me; Y-COMe; R ² - R ¹ =CF ₃ R ³ -i-Pr; Y-COMe; R = R1-CF ₃ R ³ -COOMe; Y-COMe; R ¹ -CF ₃ R ³ -4-F-P ; Y-COMe; R!-CF ₃ R ³ -4-Cl-Ph; Y-COMe; »NH; R-H; R ¹ -CF ₃ ; R ³ -i-Pr; Y-H; _R 2- »NH; R-H; R ¹ -CF ₃ ; R ³ -COOMe; Y-H; R ² - >NH R-H; R ¹ -CF ₃ ; R ³ -4-F-Ph; Y-H; R ² - »NH; R-H; R ¹ -CF ₃ ; R ³ -4-Cl-Ph; Y-H; R ² -

>CH ₂ ; R-H R ¹ -CF ₃ ; R ³ -C0OMe; Y-H; R ² - R ³ -4-F-Ph; Y-H; R ² -

■CH ₂ ; R-H R ¹ -CF ₃ ; R ³ -4-Cl-Ph; Y-H; R ² -

■CH ₂ ; R-H R ¹ -CF ₃ ; R ³ -COOMe; Y-Me; R ² -

■CH ₂ ; R-H R ¹ -CF ₃ ; R ³ -4-F-P ; Y-Me; R ² -

=CH ₂ ; R-H R ¹ -CF ₃ ; R ³ -4-Cl-Ph; Y-Me; R ² -

R ¹ -CF ₃ ; R ³ -Me; Y-H; R ² -

R1-CF ₃ R ³ -i-Pr; Y-H; R ² - R ¹ -CF ₃ R ³ -COOMe; Y-H; _R 2- R ¹ -CF ₃ R3_4_ _F _p _h . y_ _H . R ² - R ¹ -CF ₃ R3_4_ _c i-Ph; Y-H; R ² - R ¹ -CF ₃ R ³ -Me; Y-H; R ² - R ¹ -CF ₃ R ³ -i-Pr; Y-H; R ² - R ¹ -CF ₃ R ³ -COOMe; Y-H; R ¹ -CF ₃ R ³ -4-F-Ph; Y-H; R = R ¹ =CF ₃ R ³ =4-Cl-P ; Y-H; _R 2= R ¹ -CF ₃ R ³ -Me; Y-H; _R 2= R ¹ =CF ₃ R ³ =i-Pr; Y-H; p2 ₌

K-K-9 A=0 R-Cl; R ¹ =CF ₃ ; R ³ -COOMe; Y-H; A-O R-Cl; R ¹ -CF ₃ ; R ³ -4-F-P ; Y-H; A-O R-Cl; R ¹ -CF ₃ ; R ³ -4-Cl-P ; Y-H; A-O R-OMe; R ¹ =CF ₃ ; R ³ -Me; Y-H; A-O R-OMe; R ¹ -CF ₃ ; R ³ -i-Pr; Y-H; A-O R-OMe; R ¹ -CF ₃ ; R ³ -COOMe; Y-H; A-O R-OMe; R ¹ =CF ₃ ; R ³ -4-F-P ; Y-H; A-O R-OMe; R ¹ -CF ₃ ; R ³ -4-Cl-Ph; Y-H; A-O R-H; R ¹ -OCF ₃ ; R ³ -Me; Y-H; A-O R-H R ¹ -OCF ₃ R ³ -i-Pr; Y-H; A-O R-H R ¹ -OCF ₃ R ³ -COOMe; Y-H; A-O R-H R ³ -Ph; Y-H; A-O R-H R ¹ -OCF ₃ R ³ -4-F-Ph; Y-H; A-O R-H R ¹ -OCF ₃ R ³ -4-Cl-P ; Y-H; A-O R-H, R1-0CF ₃ R ³ -Me; Y-Me; A-O R-H R ¹ =OCF ₃ R ³ -i-Pr; Y-Me; A-O R-H R ¹ -OCF ₃ R ³ -COQMe; Y-Me; A-O R-H R ¹ -OCF ₃ R3« ₄ _ _Fr ; γ-Me; A-O R-H R ¹ -OCF ₃ R ³ -4-Cl-Ph; Y-Me; A-O R-H R ¹ -OCF ₃ R ³ -Me; Y-COOMe; A-O R-H R ¹ -OCF ₃ R ³ -i-Pr; Y-COOMe; A-O R-H R ¹ -OCF ₃ R ³ -COOMe; Y-COOMe; A-O R-H R ¹ -OCF ₃ R ³ -4-F-P ; Y-COOMe; A-O R-H R ¹ -OCF ₃ R ³ -4-Cl-P ; Y-COOMe; A-O R-H R ¹ =OCF ₃ R ³ -Me; Y-COMe; A-O R-H R ¹ -OCF ₃ R ³ -i-Pr; Y-COMe; A-O R-H R ¹ -OCF ₃ R ³ -COOMe; Y-COMe; A-O R-H R ¹ =OCF ₃ R ³ -4-F-Ph; γ=COMe; A-O A-NH; R-H; R ¹ -OCF ₃ ; R ³ -i-Pr; Y-H; A-NH; R-H; R ¹ =OCF ₃ ; R ³ =COOMe; Y-H; A-NH; R-H; R ¹ =OCF ₃ ; R ³ «4-F-Ph; Y-H;

K-K-,9

76 A-NH; R-H; R ¹ -OCF ₃ ; R ³ -4-Cl-Ph; Y-H; 77 A=CH ₂ R-H R ¹ =OCF ₃ ; R ³ =COOMe; Y-H; _R 2= 78 A=CH ₂ R-H R ¹ -OCF ₃ ; R ³ -4-F-Ph; Y-H; R2- 79 A-CH ₂ R-H R ¹ -OCF ₃ ; R ³ -4-Cl-P ; Y-H; _R 2- 80 A=CH ₂ R-H R ¹ -OCF ₃ ; R ³ -COOMe; Y-Me; 81 A=CH ₂ R-H R!-OCF ₃ ; R ³ -4-F-Ph; Y-Me; _R 2. 82 A=CH ₂ R-H R ¹ -OCF ₃ ; R ³ -4-Cl-P ; Y-Me; R2- 83 A-O R-Me R ¹ -OCF ₃ R ³ -Me; Y-H; _R 2. 84 A-O R-Me R ¹ -OCF ₃ R ³ -i-Pr; Y-H; 85 A-O R-Me R ¹ -OCF ₃ R ³ -COOMe; Y-H; 86 A=0 R-Me R ¹ -OCF ₃ R ³ «4-F-P ; -H; 87 A-O R-Me R ¹ -OCF ₃ R ³ -4-Cl-Ph; Y-H; 88 A-O R-CN R ¹ -OCF ₃ R ^J -Me; Y-H; 89 A-O R-CN R -OCF 3 R ³ -j.-Pr; Y-H; _R 2- 90 A-O R-CN R ¹ -OCF ₃ R ³ -COOMe; Y-H; R2- 91 A-O R-CN R ¹ -OCF ₃ R ³ -4-F-Ph; Y-H; R ² - 92 A-O R-CN RI-OCF3 R ³ -4-Cl-P ; Y-H; R ² - 93 A-O R-Cl R ¹ -OCF ₃ R ³ -Me.j Y-H; R ² - 94 A-O R-Cl R ¹ -OCF ₃ R ³ -i-Pr; Y-H; R ² - 95 A-O R-Cl R ¹ -OCF ₃ R ³ -COOMe; Y-H; 96 A-O R-Cl R ¹ =OCF ₃ R ³ -4-F-Ph; Y-H; 97 A-O R-Cl R ¹ -OCF ₃ R ³ -4-Cl-Ph; Y-H; R ² - 98 A-O R-OMe; R ¹ -OCF ₃ ; R ³ -Me; Y-H; 99 A-O R-OMe; R ¹ -OCF ₃ ; R ³ -i-Pr; Y-H; 100 A-O R-OMe; R ³ -COOMe; Y-H; 101 A-O R-OMe; R ¹ -OCF ₃ ; R ³ -4-F-Ph; Y-H; 102 A-O R-OMe; R ¹ -OCF ₃ ; R ³ -4-Cl-Ph; Y-H;

TABLE IQ

K-K-1Q A-O; R-H; R ¹ =OCF ₃ ; R ³ -Me; Y-H; R ² - A-O; R-H; R ¹ -OCF ₃ ; R ³ -i~Pr; Y-H; R ² . A-O; R-H; R ¹ =OCF ₃ ; R ³ -COOMe; Y-H; R ² - A-O; R-H; R ¹ -OCF ₃ ; R ³ -4-F-P ; Y-H; R ² = A-O; R-H; R ¹ -OCF ₃ ; R ³ -4-Cl-P ; Y-H; A-NH; R-H; R ¹ -OCF ₃ ; R ³ -i-Pr; Y-H; R ² - A-NH; R-H; R ¹ -OCF ₃ ; R ³ -COOMe; Y-H; R ² - A-NH; R-H; R ¹ -OCF ₃ ; R ³ -4-F-Ph; Y-H; R ² - A-NH; R-H; R ¹ -OCF ₃ ; R ³ -4-Cl-P ; Y-H; R ² - A-O; R-H; R ¹ -CF ₃ ; R ³ -Me; Y-H; A-O; R-H; R ¹ -CF ₃ ; R ³ «A-Pr; Y-H; A-O; R-H; R ¹ -CF ₃ ; R ³ -COOMe; Y-H; R ² - R ³ -4-F-P ; Y-H; R ² = A-O; R-H; R ¹ -CF ₃ ; R ³ -4-Cl-Ph; Y-H; R ² - A-NH; R-H; R ¹ -CF ₃ ; R ³ -i-Pr; Y-H; R ² - A-NH; R-H; R ¹ -CF ₃ ; R ³ -COOMe; Y-H; R ² - A-NH; R-H; R ¹ -CF ₃ ; R ³ -4L-F-Ph; Y-H; A-NH; R-H; R ¹ -CF ₃ ; R ³ -4-Cl-P ; Y-H; * ² -

TABLE 11

K K-11 R-H R ¹ -CF ₃ R ³ -i-Pr; Y-H; R-H R ¹ =CF ₃ R ³ -COOMe; Y-H; R-H R ¹ -CF ₃ , R ³ -4-F-P ; Y-H; R ² - R-H R ¹ -CF ₃ , R ³ -4-Cl-Ph; Y-H; R ² - R-H R ¹ =CF ₃ R ³ =i-Pr; Y-Me; R ² = R-H R ¹ =CF ₃ i R ³ =COOMe; Y-Me; _R 2= R-H R ¹ -CF ₃ R-H, R ¹ -CF ₃ R ³ =ϊ-Pr; Y-COOMe; _R 2= R-H R ¹ -CF ₃ R ³ =COOMe; Y-COOMe;

K-K-ll R-H R ¹ =CF ₃ ; R ³ -4-F-Ph; Y-COOMe; _R 2. R-H R ¹ -CF ₃ ; R ³ -4-Cl-P ; Y-COOMe; _R 2. R-H R ^X -CF3; R ³ =i-Pr; Y-COMe; _R 2. R-H R ¹ =CF ₃ ; R ³ =COOMe; Y-COMe; R-H R ¹ -CF ₃ ; R ³ -4-F-Ph; Y-COMe; R-H R ¹ -CF ₃ ; R ³ =4-Cl-P ; Y-COMe; _R 2= R-Me R ¹ -CF ₃ ; R ³ -i-Pr; Y-H; _R 2. R-Me R!-CF ₃ R ³ -COOMe; Y-H; _R = R-Me R ¹ -CF ₃ 3.,4_ _F _p _h; γ_H; R2. R-Me R!-CF ₃ R ³ -4-Cl-Ph; Y-H; R = R-CN R ¹ -CF ₃ R ³ -i-Pr; Y-H; R-CN R!-CF ₃ R ³ -COOMe; Y-H; R-CN R ¹ -CF ₃ R ³ -4-F-Ph; Y-H; R-CN R ¹ -CF ₃ R ³ -4-Cl-P ; Y-H; R-Cl R ¹ -CF ₃ R ³ -i-Pr; Y-H; _R 2. R-Cl R ¹ -CF ₃ R ³ -COOMe; Y-H; _R 2. R-Cl R ³ -4-F-Ph; Y-H; R-Cl R ¹ -CF ₃ R ³ -4-Cl-=Ph; Y-H; R-OMe; R-T—CFs; R ³ -±-Pr; Y-H; R" R-OMe; R ¹ -CF ₃ ; R ³ -COOMe; Y-H; R-OMe; R ¹ -CF ₃ ; R ³ -4-F-Ph; Y-H;

TABLE 12

K-K-12

R-H R1-CF ₃ ; R ³ -i-Pr; Y-H; R-H R ¹ -CF ₃ ; R ³ =COOMe; Y-H; R-H R ¹ -CF ₃ ; R ³ -4-F-P ; Y-H; R=H R ¹ =CF ₃ ; R ³ =4-Cl-P ; Y=H; _R 2= R-H R ¹ -CF ₃ ; R ³ =i-Pr; Y-Me; _R 2= R-H R ¹ =CF ₃ ; R ³ -COOMe; Y-Me; R ² -

K-K-12 R ³ -4-Cl-P ; Y-Me; R3___ _P _ . γ-C00Me; R ³ -COOMe; Y-COOMe; R ³ -4-F-Ph; Y-COOMe; R ³ -4-Cl-P ; Y-COOMe; _R 2- R ³ -i-Pr; Y-COMe; R2- R ³ -COOMe; Y-COMe; R2- R ³ -4-F-Ph; Y-COMe; R ² - R ³ -4-Cl-Ph.; Y-COMe; _R 2-

R ³ -i-Pr; Y-H; R ² -

R ³ -COOMe; Y-H; R ² -

R3»4_ _F _p _h; Y-H; R ² -

R ³ -4-Cl-P ; Y-H; R ³ -i-Pr; Y-H; R ² - R ³ -COOMe; Y-H; R ² - R ³ -4-F-Ph; Y-H; R ³ -4-Cl-P ; Y-H; R ³ -i-Pr^_ Y-H; R ² - R ³ -COOMe; Y-H; R ² - R ³ -4- _F -Ph; Y-H; R2- R ³ -4-Cl-Ph; Y-H; _R 2- R-OMe; R ¹ -CF ₃ ; R ³ -i-Pr; Y-H; R-OMe; R ¹ -CF ₃ ; R ³ -COOMe; Y-H; R-OMe; R ¹ -CF ₃ ; R ³ -4-F-Ph; Y-H;

TABLE 13

K-K-13 R-H; R ¹ -CF ₃ ; R ³ =COOMe; Y-H; _R 2= R-H; R ¹ -CF ₃ ; R ³ =4-F-P ; Y=H; R2-

K-K-13 R ³ -4-Cl-P ; Y-H; R ³ -i-Pr; Y-Me; R ³ -COOMe; Y-Me; R ³ -4-Cl-Ph; Y-Me; R ³ -i-Pr; Y-COOMe; R ³ -COOMe; Y-COOMe; R3_. ₄ _ _F _ph; γ-C00Me;

R ³ -4-Cl-P ; Y-COOMe; R ³ -i-Pr; Y-COMe; R ³ =COOMe; Y-COMe; R ³ -4-F-Ph; γ-C0Me; R ³ -4-Cl-P ; Y-COMe;

R ³ -i-Pr; Y-H;

R ³ -COOMe; Y-H;

R ³ -4-F-Ph; Y-H;

R ³ -4-Cl-Ph; Y-H;

R ³ -i-Pr; Y-H;

R ³ -COOMe; Y-H;

R3-4_ _F _p ; Y-H;

R ³ -4-Cl-P ; Y-H;

R ³ -±-Pr; Y-H;

R ³ -COOMe; Y-H;

R ³ -4-F-Ph; γ_H; R3-4_ci-Ph; Y-H; R-OMe; R ¹ -CF ₃ ; R ³ -i-Pr; Y-H; R-OMe; R ¹ -CF ₃ ; R ³ -COOMe; Y-K; R=OMe; R ¹ =CF ₃ ; R ³ -4-F-P ; Y-H;

TABLE 14

K-K-14 R ³ -Me; R ⁶ -H; M-H; Y-H; R ¹ -OCF ₃ ; R ³ -i-Pr; R ⁶ -H; M-H; Y-H; R ¹ -OCF ₃ ; 2« R -4-F-Ph; R6« _H . M«H; Y-H; R ¹ -OCF ₃ ; R ³ -4-Cl-Ph; R ⁶ -H; M-H; Y-H; R ¹ -OCF ₃ ; R ³ -Me; R ⁶ -H; M-H; Y-Me; R ¹ -OCF ₃ ; R ³ -i-Pr; R ⁶ -H; M-H; Y-Me; R ¹ -OCF ₃ ; R R ³ «4-F-Ph; R6. _H; M.H; Y-Me; R ¹ -OCF ₃ ; R ² > R ³ -4-Cl-P ; R ⁶ -H; M-H; Y-Me; R ¹ -OCF ₃ ; R ² R ³ -Me; R ⁶ -H; M-H; Y-Ac; R ¹ -OCF ₃ ; R ² < R ³ -i-Pr; R ⁶ -H; M-H; Y-Ac; R ¹ -OCF ₃ ; R ² - R ³ -4-F-P ; R6» _H ; M-H; Y-Ac; R ¹ -OCF ₃ ; R ² R ³ -4-Cl-Ph; R6_ _H ; -H; Y-Ac; R ¹ -OCF ₃ ; R ³ ^Me; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -OCF ₃ ; 2. R ³ -i-Pr; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -OCF ₃ ; R ² R3-. ₄ _ _F _p _h . R6_ _H . !^H; γ-C0 Me; R ¹ -OCF ₃ ; R ² R ³ -4-Cl-Ph; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -OCF ₃ ; R ² R ³ -Me; R ⁶ -H; 1--H; Y-H; R ¹ -CF ₃ ; R ² - R ³ -i-Pr; R ⁶ -H; M-H; Y-H; R ¹ -CF ₃ ; R ² - R3_4_ _F _p _h; R6_ _H; !^H; Y-H; R ¹ -CF ₃ ; R ² - R ³ -4-Cl-P ; R ⁶ -H; M-H; Y-H; R ¹ -CF ₃ ; R ³ -Me; R ⁶ -H; M-H; Y-Me; R ¹ -CF ₃ ; R ² - R ³ -i-Pr; R ⁶ -H; M-H; Y-Me; R ¹ -CF ₃ ; R ² - R ³ -4-F-P ; R ⁶ -H; M-H; Y-Me; R ³ -4-Cl-Ph; R ⁶ -H; M-H; Y-Me; R ¹ -CF ₃ ; R ³ -4de; R ⁶ -H; M-H; Y-Ac; R ¹ -CF ₃ ; R ³ -i-Pr; R ⁶ -H; M-H; Y-Ac; R ¹ -CF ₃ ; R ² - R ³ -4- _F -P ; R6-H; M-H; Y-Ac; R ¹ -CF ₃ ; R ² - R ³ -4-Cl-Ph; R ⁶ -H; M-H; Y-Ac; R ¹ =CF ₃ ; R ² - R ³ -Me; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -CF ₃ ; R ² - R ³ =i-Pr; R ⁶ -H; M-H; Y=C0 ₂ Me; R ¹ =CF ₃ ; R ² =

-K-14 R=H; R ³ =4-F-Ph; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ =CF ₃ ; R ² « R-H; R ³ =4-Cl-Ph; R ⁶ -H; M-H; Y=C0 ₂ Me; R ¹ -CF ₃ ; R ² - ^,

TABLE 15

K-K-15 R ³ -Me; R ⁶ -H; M-H; Y-H; R ¹ -OCF ₃ ; R ³ -i-Pr; R ⁶ -H; M-H; Y-H; R ¹ -OCF ₃ ; R ² - R3-4_ _F _ ; R ⁶ -H; M-H; Y-H; R ¹ -OCF ₃ ; R ² « R ³ -4-Cl-Ph; R ⁶ -H; M-H; Y-H; R ¹ -OCF ₃ ; R ² - R ³ -Me; R ⁶ -H; M-H; Y-Me; R ¹ -OCF ₃ ; R ² - R ³ -i-Pr; R ⁶ -H; M-H; Y-Me; R ¹ =OCF ₃ ; R ³ -4- _F -P ; R ⁶ -H; M-H; Y-Me; R ¹ =OCF ₃ ; R ³ -4-Cl-Ph; R ⁶ -H; M-H; Y-Me; R ¹ -OCF ₃ ; R ² R ³ -Me; R ⁶ -H; M-H; Y-Ac; R ¹ - OCF ₃ ; R ² R ³ -i-Pr; R ⁶ -H; M-H; Y-Ac; R ¹ -OCF ₃ ; R ² . R ³ -4-F-Ph; R ⁶ -H; M-H; Y-Ac; R ¹ -OCF ₃ ; R ² < R ³ -4-Cl-Ph; R- ⁶ -H; M-H; Y-Ac; R ¹ -OCF ₃ ; R ² R ³ -Me; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -OCF ₃ ; R ² R ³ -i-Pr; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -OCF ₃ ; R ²

R ³ -4-F-Ph; R6-H; M-H; Y-C0 Me; R ¹ =OCF ₃ ; R ² R ³ -4-Cl-P ; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -OCF ₃ ; R ² R ³ -Me; R ⁶ -H; M-H; Y-H; R ¹ -CF ₃ ; R ² - R ³ -i-Pr; R ⁶ -H; M-H; Y-H; R ¹ -CF ₃ ; R ² - R ³ =4-F-Ph; Rδ^H; M=H; Y-H; R ¹ =CF ₃ ; R ³ -4-Cl-P ; R ⁶ -H; M-H; Y-H; R ¹ -CF ₃ ; R ³ -Me; R ⁶ -H; M-H; Y-Me; R ¹ =CF ₃ ;

? ³ — i i —-Pr; R°-H; M-H; Y-Me; R l==rCF ₃ ; R ³ =4-F-Ph; R ⁶ =H; M-H; Y-Me; R ^X -CF3; R ³ =4-Cl-Ph; R ⁶ =H; M=H; Y-Me; R ¹ =CF ₃ ; R2= R ³ -Me; R ⁶ =H; M-H; Y-Ac; R ¹ =CF ₃ ; R2= R ³ =A-Pr; R ⁶ -H; M-H; Y-Ac; R ¹ =CF ₃ ; R2.

K-K-15 R-H R ³ =4-F-P ; R ⁶ -H; M-H; Y-Ac; R ¹ -CF ₃ ; R ² - R-H R ³ -4-Cl-Ph; R ⁶ -H; M-H; Y-Ac; R ¹ -CF ₃ ; _R 2. R-H R ³ -Me; R ⁶ -H; M-H; Y=C0 ₂ Me; R ¹ -CF ₃ ; _R . R-H R ³ =i-Pr; R ⁶ -H; M-H; Y=C0 ₂ Me; R ¹ =CF ₃ ; 2. R-H R ³ -4-F-Ph; R6-H; M-H; Y-C0 ₂ Me; R ¹ =CF ₃ ; _R 2. R-H R ³ -4-Cl-Ph; R ⁶ -H; M-H; Y=C0 ₂ Me; R ¹ "CF ₃ i _R 2.

TABLE 16

K-K-16 R ³ -Me; R ⁶ -H; M-H; Y-H; R ¹ -0CF ₃ ; R ² - R ³ -i-Pr; R ⁶ -H; M-H; Y-H; R ¹ -OCF ₃ ; R2- R ³ -4-F-Ph; R6« _H ; M-H; Y-H; R ¹ -OCF ₃ ; R2- 3»4_ _C ι-Ph; R ⁶ -H; M-H; Y-H; R ¹ -OCF ₃ ; _R 2- R ³ -Me; R ⁶ -H; M-H; Y-Me; R ¹ -OCF ₃ ; _R 2- R ³ -i-Pr; R ⁶ -H; M-H; Y-Me; R ¹ -OCF ₃ ; R ² - R ³ -4-F-P ; R ⁶ -H; M-H; Y-Me; R ¹ -OCF ₃ ; R ² - R ³ -4-Cl-Ph; R-?-H; M-H; Y-Me; R ¹ -OCF ₃ ; R ² - R ³ -Me; R ⁶ -H; M-H; Y-Ac; R ¹ -OCF ₃ ; R ² - R ³ -i-Pr; R ⁶ -H; M-H; Y-Ac; R ¹ - OCF ₃ ; R ² - R3_ _ _F _ph; R6-H; M-H; Y-Ac; R ¹ -OCF ₃ ; R ² - R3_4_cι-Ph; R ⁶ -H; M-H; Y-Ac; R ¹ -OCF ₃ ; R ³ -Me; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -OCF ₃ ; R ² - R ³ -i-Pr; R ⁶ -H; M-H; Y-C0 Me; R ¹ -OCF ₃ ; R ² - R3- _ _F _p ; R6-H; M-H; Y-C0 ₂ Me; R ¹ -OCF ₃ ; R ² R ³ -4-Cl-Ph; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -OCF ₃ ; R ² R ³ -Me; R ⁶ -H; M-H; Y-H; R ¹ -CF ₃ ; R ²

R ³ -i-Pr; R ⁶ -H; M-H; Y-H; R ¹ =CF ₃ ; R ²

R3 ₌ _ _F _ h; R ⁶ -H; M-H; Y-H; R ¹ =CF ₃ ; R ² = R3„4_ i-P ; R ⁶ -H; M-H; Y-H; R ¹ -CF ₃ ; R ³ -Me; R ⁶ =H; M-H; Y-Me; R ¹ -CF ₃ ; R ³ -i-Pr; R ⁶ -H; M-H; Y-Me; R ¹ -CF ₃ ;

K-K-16 R3«4_ _F _ph; R6_ _H ; M-. _H ; γ-Me; R ¹ -CF ₃ ; R ³ -4-Cl-P ; R ⁶ -H; M-H; Y-Me; R ³ -Me; R ⁶ -H; M-H; Y-Ac; R ¹ -CF ₃ ; R ³ -i-Pr; R ⁶ -H; M-H; Y-Ac; R ¹ -CF ₃ ; R3„4_ _F _p _h ; R6« _H; M^H; γ-Ac; R ¹ -CF ₃ ; R ³ -4-Cl-Ph; R ⁶ -H; M-H; Y-Ac; R ¹ =CF ₃ ; _R 2- R ³ -Me; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -CF ₃ ; R ² - R ³ -i-Pr; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -CF ₃ ; R ² - R3- _ _F _ph; R6-H; M-H; Y-C0 ₂ Me; R ¹ -CF ₃ ; _R 2-

R3»4_cι-Ph; R6-H; M-H; Y-C0 ₂ Me; R ¹ -CF ₃ ; R ² -

TABLE 17

K-K-17 R ³ -Me; R ⁶ -H; M-H; Y-H; R ¹ -OCF ₃ ; R ³ -i-Pr; R ⁶ -H; M-H; Y-H; R ¹ =OCF ₃ ; ² - R ³ -4-F-P ; R ⁶ -H; M-H; Y-H; R ¹ -OCF ₃ ; R ² - R ³ -4-Cl-Ph; R-S-H; M-H; Y-H; R ¹ -OCF ₃ ; R ² - R ³ -Me; R ⁶ -H; M-H; Y-Me; R -<,CF ₃ ; _R 2- R ³ -i-Pr; R ⁶ -H; M-H; Y-Me; R2- R ³ -4- _F -Ph; Rδ-H; M-H; Y-Me; R ¹ -OCF ₃ ; R2- R ³ -4-Cl-Ph; R ⁶ -H; M-H; Y-Me; R ¹ -OCF ₃ ; _R 2- R ³ -Me; R ⁶ =H; M-H; Y-Ac; R ¹ -OCF ₃ ; _R 2- R ³ -i-Pr; R ⁶ -H; M-H; Y-Ac; R ¹ -OCF ₃ ; _R 2- R3-4_ _F _ph _; R6«. _H ; M-H; Y-Ac; R ¹ -OCF ₃ ; _R 2- R3-4_cι-Ph; R ⁶ -H; M-H; Y-Ac; R ¹ -OCF ₃ ; R ³ -Me; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -OCF ₃ ; R2- R ³ -i-Pr; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ =OCF ₃ ; R2- R3«=4_ _F _ ; R6=H; M-H; Y=C0 ₂ Me; R ¹ =0CF ₃ ; R ² ^ R ³ -4-Cl-P ; R ⁶ =H; M-H; Y-C0 ₂ Me; R ¹ =OCF ₃ ; R ² ^ R ³ -Me; R ⁶ -H; M-H; Y-H; R ^X =CF3; R ² R ³ =i-Pr; R ⁶ -H; M-H; Y-H; R ²

-κ-17 R3 ₌ -4_ _F _ _h; R ⁶ -H; M-H; Y-H; R ¹ =CF ₃ ; R ³ =4-Cl-Ph.; R ⁶ -H; M-H; Y-H; R ¹ -CF ₃ ; R ³ -Me; R ⁶ -H; M-H; Y-Me; R ¹ -CF ₃ ; R2- R ³ =i-Pr; R ⁶ -H; M-H; Y-Me; R ¹ -CF ₃ ; _R 2- R3«4_ _F _ph; R ⁶ -H; M-H; Y-Me; R ¹ -CF ₃ ; R ² .. R ³ -4-Cl-Ph; R ⁶ -H; M-H; Y-Me; R ¹ -CF ₃ ; R ³ -Me; R ⁶ -H; M-H; Y-Ac; R ¹ -CF ₃ ; R ³ -i-Pr; R ⁶ -H; M-H; Y-Ac; R ¹ -CF ₃ ; R2- R ³ -4-F-Ph; R ⁶ -H; M-H; Y-Ac; R ¹ -CF ₃ ; R2- R ³ -4-Cl-P ; R ⁶ -H; M-H; Y-Ac; R ¹ -CF ₃ ; R ² - R ³ -Me; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -CF ₃ ; R2- R ³ -i-Pr; R ⁶ -H; M-H; Y-C0 ₂ Me; R ^X -CF ₃ ; R ² - R ³ -4-F-Ph; R ⁶ -H; M-H; Y-C0 ₂ Me; R ¹ -CF ₃ ; R ² - R ³ -4-Cl-Ph; R ⁶ -H; M-H; Y=C0 ₂ Me; R ¹ -CF ₃ ;

TABLE 18

K-K-18 R ³ -4-F-P ; Y-C0 ₂ Me; R ³ =4-Cl-Ph; Y=C0 ₂ Me; R^- _R 3--,j_p _r; γ_ _H ;

R ³ -C0.-Me; Y-H; _R 3«4_ _F _ _Ph; γ_ _H ;

R ³ -4-Cl-Ph; Y-H; R ³ -i-Pr; Y-Me; ' 2.., R ³ -C0 ₂ Me; Y-Me; R ³ -4-F-Ph; Y-Me; R ³ -4-F-C1; γ-Me; R ³ -=i-Pr; Y-Ac; R ³ -C0 Me; Y-Ac; R ³ -4-F-Ph; Y-Ac; R ³ -4-Cl-P ; Y-Ac; R ³ -i-Pr; Y-C0 ₂ Me; R ³ -C0 ₂ Me; Y-C0 ₂ Me; R3_4_ _F _p _h ; γ-co ₂ Me; R ¹ -OCF ₃ R ³ -4-Cl-Ph; Y-C0 ₂ Me;

TABLE 19

K—K—19

R ¹ -CF _{3 R} 3«^_ _r . γ«H; R ¹ -CF ₃ R ³ -C0 ₂ -Me; Y-H; R ¹ -CF ₃ R ³ -4- -P ; Y-H; R ¹ -CF ₃ R3« ₄ _cι-Ph; Y-H; R1=C ₃ R ³ -C0 ₂ Me; Y-Me; R ¹ =CF ₃ R3 ₌ _ _F _p _h; γ-Me; _R 2= R ¹ =CF ₃ 3-=4_ _C1; γ=Me; R2= R ¹ =CF ₃ S^-pr; γ-=Ac; _R 2= R ¹ =CF ₃ R ³ =C0 ₂ Me; Y«Ac;

K-K-19 R -4-F-P ; Y-Ac; R ³ -4-Cl-P ; γ-Ac; Y-C0 ₂ Me; R ³ =C0 ₂ Me; Y-C0 ₂ Me; R ³ -4-F-Ph; γ-C0 ₂ Me; R ³ -4-Cl-Ph; Y-C0 ₂ Me;

R ³ -Ϊ-Pr; Y-H;

R ³ -C0 -Me; Y-H;

R ³ -4-F-Ph; Y-H; R .

R ³ -4-Cl-P ; Y-H; R2-

R ³ =±-Pr; Y-Me; R2.

R ³ -C0 ₂ Me; Y-Me; R2-

R3_4_ _F _ph; γ-Me; R2-

R3«4_ _F _CI _; γ-Me; »2-

R ³ -Ϊ-Pr; Y-Ac;

R ³ -C0 ₂ Me; Y-Ac; *2-

R ³ -4-F-Ph; Y-Ac;

R ³ -4-Cl-Ph.; Y-Ac;

R ³ -±-Pr; Y-C0 ₂ Me;

R ³ «C0 ₂ Me; Y-C0 ₂ Me; * -

R ³ -4- -Ph; Y-C0 ₂ Me; R ¹ =OCF ₃ R ³ -4-Cl-Ph; Y-C0 ₂ Me;

TABLE 2Q

K-K-20 R ¹ -CF ₃ ; R ³ =i-Pr; Y-H; R ¹ =CF ₃ ; R ³ =C0 ₂ -Me; Y-H; _R 2= R ¹ =CF ₃ ; R ³ =4-F-P ; Y-H; R ² = R ¹ =CF ₃ ; R ³ =4-Cl-Ph; Y-H; _R = R ¹ =CF ₃ ; R ³ =i-Pr; Y-Me; _R 2. R ¹ -CF ₃ ; R ³ =C0 ₂ Me; Y-Me;

K.K-20 R ¹ -CF ₃ R ³ -4-F-Ph; Y-Me; R ¹ -CF ₃ R ³ -4-F-Cl; γ-Me; R ¹ =CF ₃ R ³ -Ϊ-Pr; Y-Ac; _R 2= R ¹ =CF ₃ R ³ =C0 ₂ Me; Y-Ac; R ¹ -CF ₃ R3»«4_ _F _ _h ; γ-Ac; R ¹ =CF ₃ R3 ₌₄ _ci-P ; Y-Ac; .2 ₌ R ¹ -CF ₃ R ³ -i-Pr; Y-C0 Me; R ¹ -CF _3l R ³ -C0 Me; Y-C0 ₂ Me; R ¹ -CF ₃ R3_4_ _F _ph; Y=C0 ₂ Me; R ¹ =CF ₃ R ³ -4-Cl-Ph; Y-C0 ₂ Me; R ¹ -OCF ₃ R ³ -irPr; Y-H; -"-iOCF ₃ R ³ -CQ ₂ '-Me; Y-H; R ¹ -OCF ₃ R ³ -4- _F -P ; Y-H; R ¹ -OCF ₃ R3-4_ci-Ph; Y-H; R ^X -OCF ₃ R ³ - -Pr; Y-Me; _R 2. R ¹ -OCF ₃ , R ³ -C0 Me; Y-Me; R2- R ¹ -0CF ₃ R3«4- _F _p ; γ-Me; R ² - R ³ -4- _F -Clt Y-Me; R ¹ -OCF _3l R ³ -Ϊ-Pr; Y-Ac; R ¹ =OCF ₃ R ³ -C0 ₂ Me; Y-Ac; R ¹ -OCF ₃ R ³ -4-F-P ; Y-Ac; R ¹ -OCF ₃ R ³ -4-Cl-P ; Y-Ac; R ¹ -OCF ₃ R ³ =i-Pr; Y-C0 ₂ Me; R ¹ -OCF ₃ R ³ =C0 ₂ Me; Y=C0 ₂ Me; _R 2= R ¹ -OCF ₃ R3-.4-. _F _ph; γ-C0 ₂ Me; R^- R ¹ -OCF ₃ R ³ -4-Cl-Ph; Y-C0 ₂ Me;

TABLE 21

K-K-21

1 R ¹ =CF ₃ ; R ¹⁵ -F; E-Me; Y-H;

2 R ¹ =CF ₃ ; R ¹⁵ -F; E-Me; Y-Me;

3 R ¹ -CF ₃ ; R ¹⁵ -F; E-Me; Y-Ac;

4 R ¹ -CF ₃ ; R ¹⁵ -F; E-Me; Y-C0 ₂ Me; *2-

5 R ¹ =OCF ₃ ; R ¹⁵ -F; E-Me; Y-H; R^

6 R ¹ -OCF ₃ ; R ¹⁵ -F; E-Me; Y-Me;

7 R ¹ -OCF ₃ ; R ¹⁵ -F; E-Me; Y-Ac;

8 R ¹ -OCF ₃ ; R ¹⁵ -F; E-Me; Y-C0 Me;

9 R ¹ =CF ₃ ; R ¹⁵ -C1; E-Me; Y-H;

10 R ¹ -CF ₃ ; R ¹⁵ -C1; E-Me; Y-Me;

11 R ¹ =CF ₃ ; R ¹⁵ =C1; E-Me; Y-Ac;

12 R ¹ =CF ₃ ; R ¹⁵ -C1; E-Me; Y-C0 ₂ Me;

13 R ¹ -OCF ₃ ; R ¹⁵ -C1; E-Me; Y-H;

14 R ¹ -OCF ₃ ; R ¹⁵ -C1; E-Me; Y-Me;

15 R ¹ -OCF ₃ ; R ¹⁵ -C1; E-Me; Y-Ac;

16 R ¹ -OCF ₃ ; R ¹⁵ -C1; E-Me; Y-C0 ₂ Me;

TABLE 22

K-K-22 R ² -6-Cl; R ³⁵ -CHO; Y-H; R ³ - R ² -6-Cl; R ³⁵ =CHO; Y-H; R ³ = R ² =6-C1; R ³⁵ -CHO; Y-Me; R ³ - R ² -6-Cl; R ³⁵ -CHO; Y-Me; R ³ - R ² -6-Cl; R ³⁵ -CHO; Y-C0 ₂ Me; R ³ - R ² -6-Cl; R ³⁵ =CH0; Y=C0 ₂ Me; R ³ - R ² -6-Cl; R ³⁵ =CHO; Y-C0 ₂ Et; R ³ = R ² =6-C1; R ³⁵ =CH0; Y=C0 ₂ Et; R ³ =

K-K-22

,2 _=fi _ Cl R ³⁵ =CHO Y-Ac; _R 3= R^-6- I R ³⁵ -CHO Y-Ac; R = R ² =7- CI R ³⁵ -CHO Y-H; _R 3= R ² =7- ^• CI R ³⁵ =CHO Y-H; R3= R ² =7- ^• CI R ³⁵ =CHO Y-Me; R3- R ² =7- CI R ³⁵ -CHO Y-Me; _R 3= R ² =7- ^■ CI R ³⁵ -CHO Y-C0 ₂ Me; _R 3-

^ ² -7- ^■ ιCI R ³⁵ -CHO Y=C0 Me; R ³ - R ² -7- CI R ³⁵ -CHO Y-C0 ₂ Et; R ³ - R2=7- CI R ³⁵ =CHO Y-C0 ₂ Et; R ³ - R ² =7- ^■ CI R ³⁵ -CHO Y-Ac; R ³ = R ² =7-ι CI R ³⁵ -CHO Y-Ac; R ³ = R ² =6- ^■ F R ³⁵ =CHO Y-H; R ³ =

R ² =6- ^■ F R ³⁵ -CHO Y-H; R ³ - R ² =6- ^• F R ³⁵ -CHO Y-Me; R ³ - R2-6- ^• F R ³⁵ -CHO Y-Me; R ³ - R2— f-— ^{• ■} F R ³⁵ -CHO Y-C0 ₂ Me; R ³ -

^■ F R35-CHO Y-C0 ₂ Me; „ R ³ -

R ² -6- ^• F R ³⁵ -CHO Y-C0 ₂ Et; R3-

R ² -6- ^• F R ³⁵ -CHO Y-C0 ₂ Et; _R 3-

R ² =6- •F R ³⁵ -CHO Y-Ac; _R 3- R ² -6- ^• F R35-CHO Y-Ac; _R 3- R ² -7- ^• F R35-CHO Y-H; _R 3= R ² -7- ^• F R ³⁵ =CHO Y-H; _R 3- R ² =7- ^• F R ³⁵ -CHO Y-Me; R3- R ² =7- ^• F R ³⁵ -CHO Y-Me; _R 3- R ² =7- ^• F R ³⁵ -CHO Y=C0 ₂ Me; R3- R ² =7- ^• F R ³⁵ -CHO Y=C0 Me; _R 3= 2= ₇ - ^■ F R ³⁵ =CHO Y=C0 ₂ Et; _R 3= R2=7- ^■ F R ³⁵ =CHO Y=C0 ₂ Et; R ³ = R ² =7- ^• F R ³⁵ =CHO Y-Ac; _R 3= R ² =7- ^■ F R ³⁵ =CHO Y-Ac; _R 3-

- -

K"K-22

105 R ² -6-- ; R ³⁵ -C(O)NHMe; ^• Y-C0 ₂ Me; R ³ - 106 R ² -6--F; R ³⁵ -C(0)NHMe; Y-C0 ₂ Me; R ³ = 107 R ² =6- R ³⁵ =C(0)NHMe; Y=C0 ₂ Et; R ³ « 108 R ² -6- R ³ -5-c(0)NHMe; Y-C0 ₂ Et; R ³ - 109 R ² -6- R ³⁵ -C(0)NHMe; Y-Ac; R ³ - 110 R ² =6- R ³⁵ =C(0)NHMe; Y-Ac; R ³ - 111 R ² =7- R ³⁵ =C(0)NHMe; Y-H; R ³ . 112 R2-7- R ³⁵ -C(0)NHMe; Y-H; I ³ - 113 R2=7- R ³⁵ =C(0)NHMe; Y-Me; 114 R ² -7- R ³⁵ -C(0)NHMe; Y-Me; R-3- 115 R2-7 -F R ³⁵ -C{0)NHMe; Y-C0 ₂ Me; R ³ - 116 R2-7 -F R35_ _C (O)NHMe; Y-C0 ₂ Me; R ³ - 117 R ² -7--F; R ³⁵ -C(0)NHMe; Y-C0 ₂ Et; R ³ - 118 R ² -7- ^■ F; R ³⁵ -C(0)NHMe; Y-C0 ₂ Et; R ³ - 119 R ² -7- -F; R - ^3d5 - —C ( ₁ 0 _V ), NHM Aex,, Y -.--A„c; R ³ - 120 R ² -7 -F, - ³⁵ -C (0) NHMe; Y-Ac; _R 3- 121 R2-6 -CI; R ³ " ⁵ -S ^" 0- ₂ M ^" e Y-H; R ³ - 122 R ² -6 ^• CI R ³⁵ -S0 ₂ Me, Y-H; R ³ - 123 R ² =6- -CI R ³ -5-so ₂ Me Y-eie; R ³ - 124 R ² -6- -CI R35_ _sθ2Me . γ_ e; R ³ - 125 R ² -6- -CI 35_ _sθ2Me . γ_co ₂ Me; R ³ - 126 R ² -6- -CI, R ³⁵ -S0 ₂ Me; Y-C0 ₂ Me; R3- 127 R ² -6- -CI R35-. _sθ2Me . γ_co ₂ Et; _R 3- 128 R ² -6- -CI R ³⁵ «S0 ₂ Me; Y-C0 ₂ Et; R3- 129 R ² =6- -ci -A _C ; R ³ = 130 R ² -6- -CI R35--. _S o _2Me; γ-Ac; R ³ - 131 R ² =7- -CI R ³⁵ =S0 ₂ Me; Y-H; _R 3- 132 R2=7- -cι R ³⁵ =S0 ₂ Me; Y-H; _R 3= 133 R ² -7- •CI; R ³⁵ -S0 ₂ Me; Y-Me; _R 3= 134 R ² =7- ^■ CI; R ³⁵ =S0 ₂ Me; Y-Me; R3- 135 R ² -7 -CI; RR ³³⁵⁵ ==SS00 ₂ MMee; Y=C0 ₂ Me; _R 3= 136 R ² =7--CI;

K-K-22

169 6-C1 R ⁵ -COPh; Y-Ac; 170 6-C1 R ³⁵ -COPh Y-Ac; _R 3- 171 7-Cl R ³⁵ -COPh Y-H; R3- 172 7-Cl R 5_ oPh, Y-H; _R 3- 173 *2- 7-Cl R ³⁵ -COPh, Y-Me; R3- 174 =7-Cl Y-Me; _R 3- 175 '7-Cl R ³⁵ -COPh, Y-C0 ₂ Me; R ³ - 176 ■7-Cl R ³ 5-COPh Y-C0 ₂ Me; R ³ - 177 R^ ■7-Cl R ³ -5-C0Ph; Y-C0 ₂ Et; R3- 178 '7-Cl R ³⁵ =COPh; Y-C0 ₂ Et; R ³ - 179 ■7-Cl R ³ 5-c0Ph; Y-Ac; R ³ - 180 _R 2. 7-Cl R ³⁵ -COPh; Y-Ac; R ³ - 181 _R 2. '6-F R ³ 5-cθPh; Y-H; R ³ - 182 R. ■6-F R ³ -5-C0Ph; γ„- _H; R ³ - 183 6-F R ³ -5-C0Ph; Y-Me; R ³ - 184 6-F R ³⁵ -COPh; Y-Me; R ³ - 185 '6-F. R35_ _COPh . γ-co ₂ Me; R ³ - 186 R2. 6-F R ³ -5-C0Ph; Y-C0 ₂ MβL R ³ - 187 _R 2. 6- R ³⁵ -C0Ph Y-C0 ₂ Et; R ³ - 188 R2. 6-F R35--, _COPh . γ-co ₂ Et; R ³ - 189 R2. 6-F R ³⁵ -COPh; Y-Ac; R ³ - 190 R2. 6-F R35-«coPh; Y-Ac; R ³ - 191 _R 2= 7-F R35- _=COPh . « _H . R ³ - 192 _R . 7-F R35 _=C 0Ph; Y-H; R ³ - 193 R2. 7-F R ³⁵ -C0Ph; Y-Me; R ³ - 194 R ² - 7- R ³⁵ -C0Ph; Y-Me; R ³ - 195 R2. 7- R ³ 5-coPh; Y=C0 ₂ Me; R ³ - 196 R2- 7-F R ³ 5-cOPh; Y-C0 ₂ Me; R ³ - 197 R ² - 7-F R ³⁵ =COPh; Y=C0 ₂ Et; R ³ = 198 R ² - 7- R ³⁵ =COPh; Y=C0 ₂ Et; R ³ = 199 7-F R ³ 5«COPh; Y-Ac; 200 7-F R ³ -5-C0Ph, Y-Ac;

K=K-22

201 202 6-C1 R35=S0 ₂ CH ₂ C0 Me 203 6-C1 R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me 204 6-C1 R ³⁵ =S0 ₂ CH ₂ C0 ₂ Me 205 *2= 6-C1 R ³⁵ -S0 ₂ CH ₂ C0 Me

206 R- 6-C1 R35 _=sθ2 H ₂ C0 ₂ Me

207 R- 6-C1 R35--,so ₂ CH ₂ C0 ₂ Me

208 R ² 6-C1 R ³⁵ =S0 ₂ CH ₂ C0 ₂ Me

209 R ² 6-C1 R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me

210 R ² 6-C1 R ³ 5-so ₂ CH ₂ C0 ₂ Me

211 R ² 7-Cl R ³ -5=so ₂ CH ₂ C0 ₂ Me

212 R ² 7-Cl R35_ _sθ2 cH ₂ C0 ₂ Me 213 R2- 7-Cl R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me

214 R ² 7-Cl R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me

215 R ² 7-Cl R ³ -5-so ₂ CH ₂ C0 ₂ Me

216 R ² 7-Cl R ³⁵ =S0 CH ₂ C0 ₂ Me

217 R ² 7-Cl R ³ 5-so ₂ CH ₂ C0 Me

218 R ² 7-Cl R ³ -5-S0 CH ₂ C0 ₂ Me

219 R ² 7-Cl R ³ 5-so ₂ CH ₂ C0 ₂ Me

220 R ² 7-Cl R ³⁵ -S0 ₂ CH ₂ C0 Me

221 R ² 6-F R ³ 5-so CH ₂ C0 ₂ Me

222 R ² '6-F R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me

223 R ² 6-F R ³ -5-so ₂ CH ₂ C0 ₂ Me

224 R ² 6-F R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me

225 R ² 6-F R ³ 5»-.S0 ₂ CH ₂ C0 ₂ Me

226 R ^: 2. 6-F

227 R ² = 6-F R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me

228 R 2- _« 6-F R ³⁵ =S0 CH ₂ C0 ₂ Me

229 R ² = 6-F R ³⁵ =S0 ₂ CH ₂ C0 ₂ Me

230 R ² = 6-F R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me

231 R ² 7-F R ³⁵ =S0 ₂ CH ₂ C0 ₂ Me

232 R ² 7-F R ³ -5=so ₂ CH ₂ C0 ₂ Me

K-K-22 R ³⁵ =S0 ₂ CH ₂ C0 ₂ Me; Y.---M..-.-e■=;- R ³ -5»so ₂ CH ₂ C0 ₂ Me; Y-Me; _R 3- R ³⁵ =S0 ₂ CH ₂ C0 ₂ Me; Y-C0 ₂ Me; _R 3= R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me; Y»C0 ₂ Me; _R 3- R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me; Y-C0 ₂ Et; _R 3- R ³ 5-sθ ₂ CH ₂ C0 ₂ Me; Y-C0 ₂ Et; R ³ - R ³ 5«so ₂ CH ₂ C0 ₂ Me; Y-Ac; R3- R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me; Y-Ac; R ³ -

R ³⁵ -C0CO ₂ Me; Y-H; R ³ -

R ³⁵ -COC0 ₂ M Mee; Y-H; R ³ -

R ³⁵ -C0C0 ₂ Miee; Y-Me;

R ³⁵ -COC0 ₂ Me; Y-Me; R ³ -

R ³ 5-c0C0 ₂ Me; Y-C0 ₂ Me; R ³ -

R ³⁵ -COC0 ₂ Me; Y-C0 ₂ Me; R ³ -

R ³⁵ -COC0 ₂ Me; Y-C0 ₂ Et; R ³ -

R35--:C0C0 ₂ Me; Y-C0 ₂ Et; R ³ -

R ³ 5-coC0 ₂ M Λee; Y-Ac; R ³ - l ³ -5-c0C0 ₂ Me Y-Ac; R ³ - R ³ 5-coC0 ₂ Me; Y-H; R ³ - R ³ -5-C0C0 ₂ Mfe(; Y-H; R ³ - R35-COC0 ₂ Ml<e Y-Me; R ³ -

R ³ 5-cocθ ₂ Me Y-Me; R ³ - R35,cocθ ₂ e Y-C0 ₂ Me; _R 3- R ³ 5-c0C0 ₂ Me Y-C0 ₂ Me; R3-

R ³ -5-C0C0 ₂ Me; Y-C0 ₂ Et; R3-

R ³ 5-coC0 ₂ Me; Y-C0 ₂ Et; R ³ -

R ³ 5-coC0 ₂ Me; Y-Ac; R ³ -

R ³ 5-c0C0 ₂ Me; Y-Ac; R3- R ³ 5=coC0 ₂ Me; Y-H; R3- R ³ 5-c0C0 ₂ Me; Y-H; R ³ = R ³ 5=c0C0 ₂ Me; Y-Me; R ³ = R ³ 5-c0C0 ₂ Me; Y-Me;

19

K-K-22

361 =-7-0CF ₃ R35_ _S o _2Me Y-H; 362 •7-0CF ₃ R35_ _sθ2Me Y-H; 363 R2= ;7-0CF ₃ R35,-- _Sθ2Me Y-Me; R ³ - 364 =7-OCF ₃ R35- _« , _sθ2Me Y-Me; R ³ - 365 ■7-OCF ₃ R ³⁵ -S0 ₂ Me Y-C0 ₂ Me; R ³ - 366 >7-OCF ₃ R ³ -5-so ₂ Me Y-C0 ₂ Me; R ³ - 367 ■7-OCF ₃ R -5-so ₂ Me Y-C0 ₂ Et; R ³ - 368 =7-OCF ₃ R35. ■S0 ₂ Me Y-C0 ₂ Et; R ³ - 369 •7-OCF ₃ -.35.<S0 ₂ Me Y-Ac; R3 ₌ 370 <7-OCF ₃ R ³⁵ -S0 ₂ Me Y-Ac; R3- 371 •7-OCH ₂ CF ₃ R ³⁵ -S0 ₂ Me Y-H; R ³ - 372 •7-0CH ₂ CF ₃ R35,-. _sθ2Me Y-H; R ³ - 373 >7-OCH ₂ CF ₃ R ³⁵ -S0 ₂ Me Y-Me; R ³ - 374 ■7-0CH ₂ CF ₃ R ^3< 5-S0 ₂ Me Y-Me; R ³ - 375 =7-OCH ₂ CF ₃ R35-so ₂ Me Y-C0 ₂ Me; R3. 376 >7-OCH ₂ CF ₃ R35« _S o ₂ Me Y-C0 ₂ Me; R ³ 377 -7-OCH ₂ CF ₃ R ³⁵ -S0 ₂ Me Y-C0 ₂ Et; R ³ 378 ■7-OCH ₂ CF ₃ R ^< 35-so ₂ Me ϊ-C0 ₂ Et; R ³ 379 _R 2. ■7-OCH ₂ CF ₃ R ³ 5-so ₂ Me Y-Ac; R ³ 380 _R 2. >7-OCH ₂ CF ₃ R ³⁵ -S0 ₂ Me Y-Ac; R ³ -

381 R2« '6-C1; R ³⁵ -COCF ₃ Y-H R ³ -

382 -^ ■6-Cl; R ³⁵ -COCF ₃ Y-H; R ³ -

383 R 2«6-Cl; R ³⁵ -COCF ₃ Y-Me; R ³ -

384 R ^: 2_6-Cl; R ³⁵ -COCF ₃ Y-Me; R ³ -

385 _R 2.6-Cl; R ³⁵ =COCF ₃ Y-C0 ₂ Me; R ³ = 386 R2.6-Cl; R ³⁵ -COCF ₃ Y-C0 ₂ Me; _R 3. 387 R ² -6-Cl; R ³⁵ -C0CF ₃ Y-C0 ₂ Et; R3= 388 R2.6-Cl; R ³⁵ =COCF ₃ Y=C0 ₂ Et; _R 3= 389 _R 2.6-Cl; R 5-C0CF ₃ Y-Ac; R3. 390 R . ■6-Cl; R3 ^J 5 ³ =COCF ₃ Y-Ac; _R 3= 391 392 R ² =7-C1; R ³⁵ =COCF ₃ Y-H; _R 3=

K-K-22

393 .2 ₌ 7-C1 R ³⁵ =COCF ₃ Y-Me; R ³ 394 7-Cl *35. COCF ₃ Y-Me; R ³ ' 395 7-Cl ,35.■COCF ₃ Y-C0 ₂ Me; R ³ ' 396 R-2. ^■ 7-Cl R35- ₌ C0CF ₃ Y-C0 ₂ Me; R 397 _R 2= ■7-Cl R3-"5,=C0CF ₃ Y=C0 Et; R ³ ' 398 ■7-Cl R 3-"5,-COCF ₃ Y-C0 ₂ Et; R ³ ' 399 <7-Cl R35, =COCF ₃ Y-Ac; R ³ ' 400 7-Cl R-3 ⁵³ 5-, C0CF ₃ Y-Ac; R ³ ' 401 _R 2. ■6-F R ³⁵ -COCF ₃ Y-H; R ³ ' 402 R2- 6-F R ³⁵ =COCF ₃ Y-H; R ³ ' 403 R2. '6-F R ³ -5-COCF ₃ Y-Me; R ³ ' 404 _R 2. ^■ 6-F R ³ 5-C0CF ₃ Y-Me; R ³ ' 405 _R 2. 6-F R ³⁵ -COCF ₃ Y-C0 Me; R ³ ' 406 _R 2. 6-F R35' COCF ₃ Y-C0 ₂ Me; 3, 407 R2. 6-F R35, COCF ₃ Y-C0 ₂ Et; R ³ ' 408 _R 2. 6-F R ³ 5-C0CF ₃ Y-C0 ₂ Et; R ³ ' 409 6-F R ³⁵ -COCF ₃ Y-Ac; R ³ ' 410 6-F R-35-coCF ₃ Y-Ac; _ R ³ ' 411 7-F R35-C0CF ₃ Y-H; R ³ ' 412 7-F R ³⁵ -COCF ₃ Y-H; R ³ ' 413 7-F R ³ 5-cόCF ₃ Y-Me; R3, 414 7-F R ³ 5. =C0CF ₃ Y-Me; R ³ 415 7-F R ³ 5«=COCF ₃ Y=C0 ₂ Me; R ³ ' 416 7-F R35.■COCF ₃ Y-C0 ₂ Me; R3. 417 7-F _R 35.■COCF ₃ Y-C0 ₂ Et; R ³ 418 7-F R ³ 5-C0CF ₃ Y=C0 ₂ Et; R ^: 419 7-F *35.=COCF ₃ Y-Ac; R ³ 420 _R 2- 7-F .35,=COCF ₃ Y-Ac; R ³ 421 =7-OCF ₂ H; R ³⁵ =COCF ₃ ; Y-H; R ³ = 422 _R 2= 7-OCF ₂ H; R ³⁵ =COCF ₃ ; Y=H; R ³ = 423 R ² -7-OCF ₂ H; R ³⁵ -COCF ₃ ; Y-Me; R ³ = 424 R ² =7-OCF ₂ H; R ³⁵ -COCF ₃ ; Y-Me; R ³ -

K-K-22

425 R2. *7-OCF ₂ H; R ³⁵ -COCF ₃ ; Y-C0 ₂ Me; R ³ -

426 R ² . -7-OCF ₂ H; R ³⁵ -COCF ₃ ; Y-C0 ₂ Me; R ³ -

427 R ² . *7-OCF ₂ H; R ³⁵ -COCF ₃ ; Y-C0 ₂ Et; R ³ -

428 R ² ' -7-0CF ₂ H; R ³⁵ -C0CF ₃ ; Y-C0 ₂ Et; R ³ -

429 R ² < -7-OCF ₂ H; R ³⁵ -COCF ₃ ; Y-Ac; R ³ -

430 R ² ' =7-OCF ₂ H; R ³⁵ -COCF ₃ ; Y-Ac; R ³ -

431 R2. ■7-OCF ₃ R ³ 5-C0CF ₃ Y-H; R3. 432 _R 2. ■7-OCF ₃ R ³⁵ -COCF ₃ Y-H; R ³ - 433 R . =7-OCF _{3 t} 35- ■COCF ₃ Y-Me; R ³ - 434 R2. ■7-OCF ₃ .35. ■COCF ₃ Y-Me; R ³ - 435 R ² - =7-OCF ₃ R35_ _C 0CF ₃ Y-C0 ₂ Me; 436 R ² - =7-OCF ₃ R 5-COCF ₃ Y=C0 ₂ Me; _R 3= 437 _R 2. ■7-OCF R35_ OC ₃ Y-C0 ₂ Et; _R 3- 438 R ² - ■7-OCF ₃ R35_ _C 0CF ₃ Y-C0 ₂ Et; R ³ - 439 =7-OCF ₃ R ³⁵ -COCF ₃ Y-Ac; R ³ -

440 R ² = ■7-OCF ₃ R ³ -5-C0CF Y-Ac; R ³ -

441 R ² - ■7-OCH ₂ CF ₃ R35_COCF ₃ Y-H; R ³ -

442 R ² " ■7-OCH ₂ CF ₃ R ³⁵ -COCF ₃ Y--H; R ³ -

443 ² ι ■7-OCH ₂ CF ₃ R ³ -5-C0CF ₃ Y-Me; R-3-

444 R . ■7-OCH ₂ CF ₃ R ³⁵ -C0CF ₃ Y-Me; R ³ -

445 R ² « 7-OCH ₂ CF ₃ R35. C0CF ₃ Y-C0 ₂ Me; _R 3.

446 R ² ' ■7-OCH ₂ CF ₃ R35. COCF ₃ Y-C0 ₂ Me; R3-

447 R ² - ■7-OCH ₂ CF ₃ R35-C0CF ₃ Y-C0 ₂ Et; R ³ '

448 R ² > ■7-OCH ₂ CF ₃ *35. COCF ₃ Y-C0 ₂ Et; R ³ '

449 R ² . ■7-OCH ₂ CF ₃ *35. =COCF ₃ Y-Ac; R ³ -

450 R ² - ■7-OCH ₂ CF ₃ R35--, 0CF ₃ Y-Ac; R ³ -

451 R ² . 7-CF ₃ ; R .3°5°,-CHO; Y-H; R ³ -

452 R ² = 7-CF ₃ ; R ³⁵ =CHO; Y-H; R ³ -

453 R ² = 7-CF ₃ ; R ³⁵ =CHO; Y-Me; R ³ =

454 R2= 7-CF ₃ ; R ³⁵ =CHO; Y-Me; _R 3=

455 R ² - 7-CF ₃ ; R ³⁵ =CHO; Y=C0 ₂ Me; R ³ =

456 R ² - 7-CF ₃ ; R ³⁵ -CHO; Y=C0 ₂ Me;

K-K-22

489 R ² -7-Br R ³⁵ -CHO; Y- -Ac; R ³ . 490 R ² =7-Br R ³⁵ =CHO; Y« *Ac; R ³ « 491 R ² -6-Br R ³⁵ =C0CF ₃ Y-H; _R 3= 492 R ² =6-Br R ³⁵ -COCF ₃ Y-H; _R 3= 493 R ² =6-Br R35 _X=COCF3 Y-Me; 494 R ² =6-Br R35»COCF ₃ Y-Me; R ³ - 495 R ² -6-Br R ³⁵ -C0CF ₃ Y-C0 ₂ Me; R ³ - 496 R ² =6-Br R ³⁵ -C0CF ₃ Y-C0 Me; R ³ = 497 R ² =6-Br R35- _=C 0CF ₃ , Y=C0 ₂ Et; R ³ - 498 R ² -6-Br R35_COCF ₃ Y-C0 ₂ Et; R ³ - 499 R ² =6-Br R35 _=C 0CF ₃ Y-Ac; R ³ - 500 R ² -6-Br R ³⁵ -COCF ₃ Y-Ac; R ³ - 501 R ² -7-Br R ³ 5-C0CF ₃ Y-H; R ³ - 502 R ² -7-Br R35-- _! COCF ₃ , Y-H; R ³ - 503 R ² -7-Br R ³⁵ -COCF ₃ , Y-Me; R ³ - 504 R ² -7-Br R35-« oCF ₃ Y-Me; 505 R ² -7-Br R35-C0CF ₃ Y-C0 ₂ Me; 506 R ² -7-Br R35-C0CF ₃ , Y-C0 ₂ Me; R ³ ' 507 R ² -7-B R ³⁵ «COCF ₃ Y-C0 ₂ Et; R ³ ' 508 R -7-Br R ³⁵ -COCF ₃ Y-C0 ₂ Et; R ^: 509 R ² -7-Br R ³ 5-C0CF ₃ Y-Ac; R 510 R ² -7-Br R ³ -5«C0CF ₃ Y-Ac; R

TABLE. 23

κ-κ-23

- -

R ³ = R ³ - R ³ = R ³ - R ³ - R ³ - R ³ - R ³ - R ³ - R ³ - R ³ - R ³ - R ³ - R ³ - R ³ - R ³ - R ³ - R ³ - R ³ - R ³ - R ³ = _R 3- _R 3- _R 3- _R 3- R3- R ³ - R ³ = R ³ = R ³ = R ³ -

K-K-23 R ³⁵ =C(0 ))NNHHMMet-; _r Y.-=C0 ₂ Me; R ³ = R ³⁵ =C(0)NHMe; Y-C0 ₂ Me; R ³ - R ³⁵ =C(0)NHMe; Y=C0 ₂ Et; R ³ - R ³⁵ -C(0)NHMe; Y-C0 ₂ Et; R ³ - R ³⁵ -C(0)NHMe; Y-Ac; R ³ - R ³⁵ -C(0)NHMe; Y-Ac; R ³ - R ³⁵ -C(0)NHMe; Y-H; R ³ - R ³⁵ =C(O) HMe; Y-H; R ³ - R ³⁵ -C(0)NHMe; Y-Me; R ³ - R ³⁵ -C(O) HMe; Y-Me; R3- R ³⁵ -C(O)NHMe; Y-C0 ₂ Me; _R 3- R ³⁵ -C(0)NHMe; Y-C0 ₂ Me; R3- R ³⁵ -C(0)NHMe; Y-C0 ₂ Et; R ³ - R ³⁵ -C(0)NHMe; Y-C0 ₂ Et; R ³ - R ³⁵ -C(0)NHMe; Y-Ac; R ³ -. R ³⁵ -C(0)NHMe; Y-Ac; R ³ -

R ³⁵ -S0 ₂ Me; Y-H; R3-

R ³⁵ -S0 ₂ Me ^■ H; _ R ³ -

R ³⁵ -S0 ₂ Me Y-Me; R ³ -

R ³⁵ -S0 ₂ Me Y-Me; R ³ - R35_, _sc , _2Me Y-C0 ₂ Me; R ³ -

R ³⁵ -S0 ₂ Me Y-C0 ₂ Me; R3-

R ³⁵ -S0 ₂ Me Y-C0 ₂ Et; _R 3-

R ³⁵ -S0 ₂ Me Y-C0 ₂ Et; _R 3-

R ³ 5- _S o ₂ M «ce Y-Ac; R3-

R ³⁵ -S0 ₂ M ήe. Y-Ac; _R 3=

R ³ 5=SO ₂ M( Y-H; _R 3-

R ³ 5_sθ ₂ Me Y-H; R3- _R 35--. _sθ2Me Y-Me; _R 3=

R ³⁵ =S0 ₂ Me Y-Me; _R 3= R ³⁵ =S0 ₂ Me Y=C0 ₂ Me; R3- RZ^S _Q ^ _Q Y=C0 ₂ Me; _R 3-

K-K-23

169 R ² -6-Cl R ³ -5=C0Ph; Y-Ac; R ³ - 170 R ² -6-Cl R -5=C0Ph Y-Ac; R ³ - 171 R ² -7-Cl R ³⁵ =COPh Y-H; R ³ - 172 R ² -7-Cl R ³⁵ -COPh Y-H; R ³ - 173 R ² -7-Cl R-35-cOPh Y-Me; R ³ - 174 R2-7-C1 R ³⁵ -C0Ph, Y-Me; R ³ - 175 R ² -7-Cl R ³⁵ -COPh Y-C0 ₂ Me; R ³ - 176 R ² -7-Cl R35 _« - _COPh Y-C0 ₂ Me; R ³ - 177 R ² -7-Cl R - ³ 5- -CXM0Ph ₍ , Y-C0 ₂ Et; R ³ - 178 R ² -7-Cl . ³ -5-c0Ph; Y-C0 ₂ Et; R ³ - 179 R2-7-C1 R ³ 5-coPh; Y-Ac; R ³ - 180 R ² -7-Cl R35--, _COPh . γ-Ac; R ³ - 181 R ² -6-F R ³⁵ -C0Ph; Y-H; R ³ - 182 R ² -6-F R35-« oP ; Y-H; R ³ - 183 R ² -6-F R35_, _COPh; γ--M _β ; R3- 184 R ² -6-F R ³⁵ -COPh; Y-Me; R3- 185 R ² -6-F R35 _mCO p _h . γ-co ₂ Me; _R 3- 186 R ² -6- R ³ 5-C0Ph; Y-C0 ₂ Mej R ³ - 187 R ² -6-F R ³ -5-C0Ph; Y-C0 ₂ Et; R ³ - 188 R ² -6-F R35_, _COPh . γ-co ₂ Et; R ³ - 189 R ² -6-F R ³ 5-cOPh Y-Ac; R3- 190 R ² -6-F R ³ 5-cθPh, Y-Ac; R ³ - 191 R ² -7-F _R 35-. _COPh Y-H; R ³ - 192 R --7_ _F Y-H; R3- 193 R ² -7-F _R 35«- _CO p _h . γ^ie; _R 3- 194 R2-.7_ _F R ³⁵ -COPh; Y>→le; R3- 195 R ² -7-F R ³ -5«cOPh; Y=C0 ₂ Me; _R 3- 196 R--7_F R35-« _CO p _h . γ-co ₂ Me; _R 3- 197 R2_. ₇ _ _F R35_. _C 0Ph; Y-C0 ₂ Et; _R 3= 198 R2=7_ _F R35 _=CO p _h; γ-co ₂ Et; R ³ = 199 R ² -7-F R ³⁵ -C0Ph; Y-Ac; R ³ -

^• 3 C — _ 200 R2-. ₇ _F R ³⁵ -COPh, Y-Ac;

92

K-K-23

R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me; Y-Me

R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me; Yι-τMiee;,- - -_3- ⁵ mm-.S-r0> ₂ τ.rCH ₂ τ.mC0 _2^ MMae;f vY—«mC0 ₂ «MMee;.<

RK ³³⁵ -S0 ₂ CH C0 ₂ Me; Y-C0 ₂ Et; R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me; Y-C0 ₂ Et; R ³ -5-S0 ₂ CH ₂ C0 ₂ Me; ; ^γ Y--AAec;: R ³⁵ -S0 ₂ CH ₂ C0 ₂ Me; Y-Ac;

R ³ 5-c0C0 ₂ Me; Y- •H;

R ³⁵ -C0C0 ₂ Me; Y-H;

R ³⁵ -C0C0 ₂ Me; Y-Me;

R ³⁵ -C0C0 ₂ Me; Y-41e;

R ³ 5-coco ₂ Me; Y-C0 ₂ Me;

R ³⁵ -C0C0 ₂ Me; Y-C0 ₂ Me; Y-C0 Et;

RSS-^oco^e- Y-C0 ₂ Et;

R ³⁵ -C0C0 ₂ Me; Y-Ac; R35-_ _cocθ2Me . Y-Ac;-

R ³⁵ -C0C0 ₂ Me; Y-H; R ³ -5-c0C0 ₂ Me; Y-H; R ³ -5-c0C0 ₂ Me; Y-Me; R35-« _cocθ2Me; Y-Me;

R ³⁵ -C0C0 ₂ Me; Y-C0 ₂ Me;

R35-C0C0 ₂ Me; Y-C0 ~ _2Δ Me;,

R35-. _C 0C0 ₂ Me; Y-C0 ₂ Et;

R ³⁵ -C0C0 ₂ Me; Y-C0 ₂ Et;

RSS. oco^e; Y-Ac;

R35-c0C0 ₂ Me; Y-Ac; R ³⁵ -C0C0 ₂ Me; Y-H; R ³ 5-=c0C0 ₂ Me; Y=H; R 5-c0C0 ₂ Me; Y-Me; R ³ 5-c0C0 ₂ Me; Y-Me;

K-K-22

JO JO JO JO JO JO JO JO rø O JO JO JO JO rø rø JO JO JO JO JO JO JO JO to to to ω io ω io io lo to ω ω co ω io to lo io io to ω to io i R II II II H II R R H R fl II I I R R I I I R fl fl R II

K-K-23

393 R ² =7- ^■ Cl ,35. C0CF-. Y-Me; R ³ - 394 R ² -7- ^■ CI .35. ■C0CF ₃ Y-Me; R ³ - 395 R ² -7- ^■ CI .35. ■C0CF-. Y=C0 ₂ Me; R ³ = 396 R ² -7- ^■ CI R35_ _COCF3 Y-C0 Me; R3- 397 R ² =7- ^■ CI R35-C0CF ₃ Y-C0 ₂ Et; R ³ - 398 R ² =7- ^■ CI R35_ _COCF;3 Y-C0 ₂ Et; R ³ « 399 R ² =7- ^• CI R35«. _CO CF ₃ Y-Ac; R ³ - 400 R ² =7- ^• CI R35-C0CF ₃ Y-Ac; R ³ - 401 R ² =6- ^• F R ^ ^j 3 ^a 5-, C0CF ₃ Y-H; R ³ - 402 R ² -6- ^■ F R ³ 5-C0CF ₃ Y-H; R-3- 403 R ² -6- ^• F R ³ 5-C0CF ₃ Y-Me; R3- 404 R ² -6- ^• F R ³ 5-C0CF 3 Y-Me; R3- 405 R ² -6- ^■ F _R 35,=COCF ₃ Y-C0 ₂ Me; R - 406 R ² -6- ^• F R ^-3"5-, C0CF ₃ Y-C0 ₂ Me; 3- 407 R ² -6- ^■ F R ³ 5-C0CF ₃ Y-C0 ₂ Et; R-3- 408 R ² -6- •F R ³ 5-c0CF ₃ Y-C0 Et; R-3- 409 R ² -6- ^■ F R ³ 5_C0CF ₃ Y-Ac; R ³ - 410 R ² -6- ^■ F R35-, _CO CF ₃ Y-Ac; _ R3- 411 R ² -7- ^• F R ³ 5-C0CF ₃ Y-H; R3- 412 R ² -7- ^■ F R ³ 5-C0CF ₃ Y-H; 413 R -7- ^■ F R35..COCF3 Y-Me; _R 3- 414 R ² -7- ^• F R ³ 5_C0CF ₃ Y-Me; R ³ - 415 R ² -7- ^■ F R ³ 5_C0CF ₃ Y-C0 ₂ Me; R ³ - 416 R ² -7- ^• F R ³ -5-C0CF ₃ Y-C0 ₂ Me; R ³ - 417 R ² =7- ^■ F R35.. _COCF3 Y-C0 ₂ Et; R ³ - 418 R ² =7- ^• F R35. ■COCF3 Y-C0 ₂ Et; R ³ - 419 R ² -7- ^• F _R 35. ■COCF3 Y-Ac; _R 3- 420 R ² -7- ^■ F _P 35. COCF3 Y-Ac; R3- 421 R ² -7 -OCF ₂ H; 422 R ² =7- OCF ₂ H; R ³⁵ =COCF ₃ ; Y-H; R3- 423 R ² =7- OCF ₂ H; R ³⁵ =COCF ₃ ; Y-Me; R3- 424 R ² =7-OCF ₂ H; R ³⁵ -COCF ₃ ; Y-Me; R3-

- -

K-K-23

489 R ² -7-Br, R ³⁵ -CHO; Y- -Ac; R3- 490 R ² =7-Br R ³ =CHO; Y--Ac; R ³ = 491 R ² =6-Br R ³ 5=cOCF ₃ Y-H; R ³ - 492 R ² -6-Br R ³ 5-C0CF ₃ Y-H; R3- 493 R ² -6-Br R ³⁵ =C0CF ₃ Y-Me; R3- 494 R ² -6-Br R ³⁵ =COCF ₃ Y-Me; R ³ - 495 R ² =6-B R ³⁵ -COCF ₃ Y-C0 ₂ Me; R ³ - 496 R ² -6-Br R ³⁵ -COCF ₃ Y-C0 ₂ Me; R ³ - 497 R ² =6-Br R ³⁵ =COCF ₃ Y=C0 ₂ Et; R ³ - 498 R ² =6-Br R ³⁵ =COCF ₃ Y-C0 ₂ Et; R ³ - 499 R ² -6-Br R ³ 5-C0CF ₃₍ Y-Ac; R ³ - 500 R ² =6-Br R ³⁵ =C0CF ₃ Y-Ac; R ³ - 501 R ² -7-Br R ³⁵ -COCF ₃ Y-H; R ³ - 502 R ² -7-Br R ³⁵ -COCF ₃ Y-H; R ³ - 503 R ² =7-Br ³ 5-C0CF ₃ Y«44e; R ³ - 504 R ² -7-Br R ³⁵ -C0CF ₃ Y«44e; R ³ - 505 R ² -7-Br R ³ 5-C0CF ₃ Y-C0 ₂ Me; R ³ - 506 R ² -7-Br R35-C0CF ₃ Y-C0 ₂ Me; R ³ - 507 R ² -7-Br R35-C0CF ₃ Y-C0 ₂ Et; R ³ - 508 R ² -7-Br R ³⁵ -COCF ₃ Y-C0 ₂ Et; R ³ - 509 R ² -7-Br R35 C0CF ₃ Y-Ac; R ³ = 510 R ² -7-Br R35_ _C0CF3 Y-Ac; R ³ -

TABLE 24

K-K-2

1 R ¹ -OCF ₃ ; R ² -C1; R ³ -C0 ₂ Me; Y-

2 R ¹ =0CF ₃ ; R ² =C1; R ³ -4-F-Ph; Y=

3 R ¹ =0CF ₃ ; R ² =C1; R ³ -Me; Y=

4 R ¹ =OCF ₃ ; R ² =C1; R ³ -iPr; Y=

K-K-24

5 R ⁱ -0CF ₃ R2-=7_ _Br; R3-co ₂ Me; Y-

6 R ¹ -0CF ₃ R ² -7-Br; R ³ -4-F-Ph; Y-

7 R ¹ -0CF ₃ R ² -7-Br; R ³ -Me; Y-

8 R ¹ -0CF ₃ R ² =7-Br; R ³ -iPr; Y=

9 R ¹ =0CF ₃ R ² -7-F; R ³ -C0 ₂ Me; Y=

10 R ¹ -0CF ₃ R ² -7-F; R ³ -4-F-Ph; Y-

11 R ¹ -OCF ₃ R ² -7-F; R ³ -Me; Y=

12 R ¹ -0CF ₃ R ² -7-F; R ³ -iPr; Y-

13 R ¹ -CF ₃ R ² =C1; R ³ -C0 ₂ Me; Y=

14 R ¹ =CF ₃ R ² -C1; R ³ -4-F-Ph; Y=

15 R ¹ »CF ₃ R ² -C1; R ³ -Me; Y-

16 R ¹ -CF ₃ R ² -C1; R ³ -±Pr; Y-

17 R ¹ -CF ₃ R ² -7-Br; R ³ -C0 ₂ Me; Y-

18 R ¹ -CF ₃ R ² -7-Br; R ³ -4-F-Ph; Y-

19 R ¹ -CF ₃ R ² -7-Br; R ³ -Me; Y-

20 R ¹ -CF ₃ -7_B _Γ ; R ³ -iPr; Y-

21 R ¹ -CF ₃ R2-7_ _F; R3-co ₂ Me; Y-

22 R ¹ -CF ₃ R2«7_ _F - R ³ -4- -P ; Y-

23 *2_ ₇ 7_-F; R-'-Me; Y-

24 R ¹ -CF ₃ R «7_ _F; R ³ -iPr; Y-

Formulation/Utility

Compounds of this invention will generally be used in formulation with an agriculturally suitable carrier comprising a liquid or solid diluent or an organic solvent. Useful formulations include dusts, granules, baits, pellets, solutions, suspensions, emulsions, wettable powders, emulsifiable concentrates, dry flowables and the like, consistent with the physical properties of the active ingredient, mode of application and environmental factors such as soil type, moisture and temperature. Sprayable formulations can be extended in suitable media and used at spray volumes from about .one to several hundred liters per

hectare . High strength compositions are primarily used as intermediates for further formulation . The formulations - will typically contain effective amounts of active ingredient, diluent and surfactant within the following approximate ranges which add up to 100 weight percent .

Weight Percent

Wettable Powders

Oil Suspensions, Emulsions, Solutions, (including E ulsifiable Concentrates)

Dusts

Granules, Baits and Pellets

High Strength Compositions

Typical solid diluents are described in Watkins, et al.. Handbook of Insecticide Dust Diluents and

Carriers, 2nd Ed., Dorland Books, Caldwell, New Jersey. Typical liquid diluents and solvents are described in Marsden, Solvents Guide, 2nd Ed., Interscience, New York, 1950. McCutcheon 's Detergents and Emulsifiers Annual, Allured Publ. Corp., Ridgewood, New Jersey, as well as Sisely and Wood, Encyclopedia of Surface Active Agents, Chemical Publ. Co., Inc., New York, 1964, list surfactants and recommended uses. All ormulations can contain minor amounts of additives to reduce foam, caking, corrosion, microbiological growth, and the like. Solutions are prepared by simply mixing the ingredients. Fine solid compositions are made by blending and, usually, grinding as in a hammer mill or fluid energy mill. Water-dispersible granules can be produced by agglomerating a fine powder composition; see for example, Cross et al., Pesticide Formulations, Washington, D.C., 1988, pp 251-259. Suspensions are prepared by wet-milling; see, for example, U.S.

3,060,084. Granules and pellets can be made by spraying the active material upon preformed granular carriers or by agglomeration techniques. See Browning, "Agglomeration", Chemical Engineering, December 4, 1967, pp 147—148, 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 by blending, grinding in a hammer mill, and compacting into pellets as further described in U.S. 4,172,714. Water-dispersible and water-soluble granules can be prepared as well-known to one skilled in the art. For further information regarding the art of formulation, see 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, IVeed Control as a Science, John Wiley and Sons, Inc., New York, 1961, pp 81-96; and Hance et al., Weed Control Handbook, 8th Ed., Blackwell Scientific Publications, Oxford, 1989.

In the following Examples, all percentages are by weight and all formulations are worked up in conventional ways. Compound numbers refer to compounds in Index Table A.

Example A Wettable Powder

Compound 5 65.0% dodecylphenol polyethylene glycol ether 2.0% sodium ligninsulfonate 4.0% sodium silicoaluminate 6.0% montmorillonite (calcined) 23.0%

Example B Granule

Compound 5 10.0%

attapulgite granules (low volatile matter, 0.71/Q.30 mm; U.S.S. No.

25-50 sieves) 90.0%

Example C Extruded Pallfl

Compound 5 25.0% anhydrous sodium sulfate 10.0% crude calcium ligninsulfonate 5.0% sodium alkylnaphthalenesulfonate 1.0% calcium/magnesium bentonite 59.0%

Example D E ulsifiablP. Concentrate

Compound 5 20.0% blend of oil soluble sulfonates and polyoxyethylene ethers 10.0% isopho one 70.0%

The compounds of this invention exhibit activity against a wide spectrum of foliar-feeding, fruit- feeding, seed-feeding, aquatic and soil—inhabiting arthropods (term includes insects, mites and nematodes) which- are pests of growing and stored agronomic crops, forestry, greenhouse crops, ornamentals, nursery crops, stored food and fiber products, livestock, household, and public and animal health. Those skilled in the art will appreciate that not all compounds are equally effective against all pests. Nevertheless, all of the compounds of this invention display activity against pests that include: eggs, larvae and adults of the Order Lepidoptera; eggs, foliar-feeding, fruit-feeding, root-feeding, seed-feeding larvae and adults of the Order Coleoptera; eggs, immatures and adults of the Orders Hemiptera and Homoptera; eggs, larvae, nymphs and adults of the Order Acari; eggs, immatures and adults of the Orders Thysanoptera, Orthoptera and Dermaptera; eggs, immatures and adults of the Order

Diptera; and eggs, juveniles and adults of the Phylum

Nemata. The compounds of this invention are also active against pests of the Orders Hymenoptera, Isoptera, Phthiraptera, Siphonoptera, Blattaria, Thysanaura and Pscoptera; pests belonging to the Class Arachnida and Phylum Platyhelminthes. The compounds are particularly active against southern corn rootworm (Diabrotica undecimpunctata howardi), aster leafhopper (Mascrosteles fascifrons), boll weevil (Anthonomus grandis), two-spotted spider mite (Tetranychus urticae) , fall armyworm (Spodoptera frugiperda), black bean aphid (Aphis fabae), tobacco budworm (Heliothis virescens), rice water weevil (Lissorhoptrus oryzophilus), rice leaf beetle (Oulema oryzae), whitebacked planthopper (Sogatella furcifera) , green leafhopper (Nephotettix cincticeps), brown planthopper (Nilaparvata lugens) , small brown planthopper (Laodelphax striatellus) , rice stem borer (Chilo suppressalis), rice leafroller (Cnaphalocrocis medinalis) , black rice stink bug (Scotinophara lurida), rice stink bug (Lagynotomus elongatus), slender rice bug (Cletus puntiger), and southern green stink bug (Nezara viridula) . See WO 90/10623 and WO 92/00673 for more detailed pest descriptions.

Compounds of this invention can also be mixed with one or more other insecticides, fungicides, nematoσides, baσtericides, acaricides, semiochemicals, repellants, attractants, pheromones, feeding stimulants or other biologically active compounds to form a multi- component pesticide giving an even broader spectrum of agricultural protection. Examples of other agricultural protectants with which compounds of this invention can be formulated are: insecticides such as monocrotophos, carbofuran, tetrachlorvinphos, malathion, parathion—methyl, methomyl, chlordimeform, diazinon, deltamethrin, oxamyl, fenvalerate, esfenvalerate, permethrin, profenofos, sulprofos,

triflumuron, diflubenzuron, methoprene, buprofezin, thiodicarb, acephate, azinphosmethyl, chlorpyrifos, dimethoate, fipronil, flufenprox, fonophos, isofenphos, methidathion, methamidophos, phosmet, phosphamidon, phosalone, pirimicarb, phorate, terbufos, trichlorfon, methoxychlor, bifenthrin, biphenate, cyfluthrin, fenpropathrin, fluvalinate, flucythrinate, tralomethrin, metaldehyde and rotenone; fungicides such as carbendazim, thiuram, dodine, maneb, chloroneb, benomyl, cymoxanil, fenpropidine, fenpropimorph, triadimefon, captan, thiophanate-methyl, thiabendazole, phosethyl—Al, chlorothalonil, dichloran, metalaxyl, captafol, iprodione, oxadixyl, vinclozolin, kasugamycin, myclobutanil, tebuconazole, difenoconazole, diniconazole, fluquinconazole, ipconazole, metconazole, penconazole, propiconazole, uniconzole, flutriafol, prochloraz, pyrifenox, fenarimol, triadimenol, diclobutrazol, copper oxychloride, furalaxyl, folpet, flusilazol, blasticidin S, diclomezine, edifenphos, isoprothiolane, iprobenfos, epronil, neo-asozin, pencycuron, probenazole, pyroquilon, tricyclazole, validamycin, and flutolanil; nematocides such as aldoxycarb, fenamiphos and fosthietan; bactericides such as oxytetracyline, streptomycin and tribasic copper sulfate; acaricides such as binapacryl, oxythioquinox, chlorobenzilate, dicofol, dienochlor, cyhexatin, hexythiazox, amitraz, propargite, tebufenpyrad and fenbutatin oxide; and biological agents such as Bacillus thuringiensis, baculovirus and avermectin B.

In certain instances, combinations with other arthropodicides having a similiar spectrum of control but ^' a different mode of action will be particularly advantageous for resistance management. Arthropod pests are controlled and protection of agronomic crops, animal and human health is achieved by

applying one or more of the compounds of this invention, in an 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. A preferred method of application is by spraying. Alternatively, granular formulations of these compounds can be applied to the plant foliage or the soil. Other methods of application include direct and residual sprays, aerial sprays, systemic uptake, baits, eartags, boluses, foggers, fumigants, aerosols, and many others. The compounds can be incorporated into baits that are consumed by the arthropods or in devices such as traps and the like. The compounds of this invention can be applied in their pure state, but most often application will be of a formulation comprising one or more compounds with suitable carriers, diluents, and surfactants and possibly in combination with a food depending on the contemplated end use^ A preferred method of application involves spraying a water dispersion or refined oil solution of the compounds. Combinations with spray oils, spray oil concentrations, spreader stickers, adjuvants, and synergists and other solvents such as piperonyl butoxide often enhance compound efficacy.

The rate of application required for effective control will depend on such factors as the species of arthropod to be controlled, the pest's life cycle, life stage, its size, location, time of year, host crop or animal, feeding behavior, mating behavior, ambient moisture, temperature, and the like. Under normal circumstances, application rates of about 0.01 to 2 kg of active ingredient per hectare are sufficient to control pests in agronomic ecosystems, but as little as 0.001 kg/hectare may be sufficient or as much as 8 kg

hectare may be required. For nonagronomic applications, effective use rates will range from about 1.0 to 50 mg/square meter but as little as 0.1 mg/square meter may be sufficient or as much as 150 mg/square meter may be required.

The following Tests demonstrate the control efficacy of compounds of this invention on specific pests. The pest control protection a orded by the compounds is not limited, however, to these species. See Index Tables A-E for compound descriptions.

Index Table A

Cmpd 1 CF ₃ H 2 CF ₃ CI 3 OCF ₃ CI 4 Br CI

Ill Index Table C

Cmpd 54 OCF.

Cmpd 55 OCF ₃

Cmpd 14

Fall Armyworm

Test units, each consisting of an 8-ounce (230 L) plastic cup containing a layer of wheat germ diet, approximately 0.5 cm thick, were prepared. Ten third- instar larvae of fall armyworm .Spodoptera ruyi ^ ra. were placed into a cup. Solutions of each of the test

compounds (acetone/distilled water 75/25 solvent) were sprayed into the .pups, a single solution per set of three cups. Spraying was accomplished by passing the cups, on a conveyer belt, directly beneath a flat fan hydraulic nozzle which discharged the spray at a rate of 0.138 kg/ha of active ingredient per acre (about 0.125 pounds per hectare) at 30 p.s.i. (207 kPa) . The cups were then covered and held at 27°C and 50% relative humidity for 72 hours, after which time readings were taken. Of the compounds tested, the following resulted in greater than or equal to 80% mortality: 1, 3*, 4*, 5, 6, 1 , 8, 9, 10, 11, 12, 14, 15, 16, 17, 18, 19, 20, 21, 22, 23, 24, 25, 27,28, 29, 30, 31, 42 and 43. IEES_Γ_E

Tobacco Budworm

The test procedure of Test A was repeated for efficacy against third-instar larvae of the tobacco budworm (Heliothis virescens) except that mortality was assessed at 48 hours _Λ Of the compounds tested, the following resulted in greater than or equal to 80% mortality: 3*, 4*, 7, 8, 9, 10, 11, 12, 15, 16, 19, 20, 21, 22, 23, 25, 27, 28, 29, 30, 31 and 42.

TEST C Southern Corn Rootworm

Test units, each consisting of an 8-ounce (230 mL) plastic cup containing 1 sprouted corn seed, were prepared. Sets of three test units were sprayed as described in Test A with individual solutions of the test compounds. After the spray on the cups had dried, five third-instar larvae of the southern corn rootworm (Diabrotica undecimpunctata h ardi) were placed into each cup. A moistened dental wick was inserted into each cup to prevent drying and the cups were then covered. The cups were then held at 27°C and 50% relative humidity for 48 hours, after which time

mortality readings were taken. Of the compounds tested, the following resulted in greater than or equal to 80% mortality: 5, 6, 7, 8, 9, 10, 11, 14, 15, 16,

17, 18, 19, 20, 21, 22, 23, 24, 25, 27, 28, 29, 30, 31, 42 and 43.

_Ϊ E£T__E

Aster Leafhopper

Test units were prepared from a series of 12-ounce (350 mL) cups, each containing oat (Avena sativa) seedlings in a 1-inch (2.54 cm) layer of sterilized soil. The test units were sprayed as described in Test A with individual solutions of the below-listed compounds. After the oats had dried from the spraying, between 10 and 15 adult aster leafhoppers (Mascrosteles fascifrons) were aspirated into each of the covered cups. The cups were held at 27°C and 50% relative humidity for 48 hours, after which time mortality readings were taken. Of the compounds tested, the following resulted in greater than or equal to 80% mortality: 5, 7, 8,_9, 10, 11, 12, 25, 30, 31, 42 and 43.

.IE≤T_E Boll Weevil

Five adult boll weevils t nthonomus ςrrandis. were placed into each of a series of 9 ounce (260 mL) cups. The test procedure employed was then otherwise the same as in Test A with three cups per treatment. Mortality readings were taken 48 hours after treatment. Of the compounds tested, the following resulted in greater than or equal to 80% mortality: 5, 6, 7, 8, 12, 17,

18, 19, 20, 21, 22, 23, 25, 27,28, 29, 30 and 42.

* Tested at 0.55 kg/ha.