IP Library Granted Patent US 9,073,912
Granted Patent B2
US 9,073,912 · App. 14/399,084 · Granted Jul 7, 2015

Azetidine derivatives as antiparasitic agents

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Quick Facts
Patent No.
US 9,073,912
App. No.
14/399,084
Granted
Jul 7, 2015
Kind
B2
Abstract

This invention recites substituted azetidine derivatives of Formula (1) stereoisomers thereof, veterinarily acceptable salts thereof, compositions thereof, and their use as a parasiticide in animals. The substituents A, B, R 1a , R 1b , R 1c , R 2 , R 3 , R 4 , R 6 , and n are as described herein.

Claims (138)

1. A compound of Formula (1)

wherein

A is phenyl, naphthyl, or heteroaryl where said heteroaryl contains 1 to 4 heteroatoms each independently selected from N, O and S;

B is

where in “ ” represents the point of attachment;

R 1a , R 1b , and R 1c are each independently hydrogen, halo, hydroxyl, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 0 -C 3 alkylC 3 -C 6 cycloalkyl, C 1 -C 6 haloalkoxy, —C(O)NH 2 , —SF 5 , or —S(O) p R;

R 2 is halo, cyano, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, nitro, hydroxyl, —C(O)NR a R b , C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, —S(O) p R, or —OR;

R 3 is hydrogen, halo, hydroxyl, cyano, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 0 -C 3 alkylC 3 -C 6 cycloalkyl, —C(O)NH 2 , nitro, —SC(O)R, —C(O)NR a R b , C 0 -C 3 alkylNR a R 4 , —NR a NR b R 4 , —NR a OR b , —ONR a R b , N 3 , —NHR 4 , —OR, or —S(O) p R;

R 4 is hydrogen, C 1 -C 6 alkyl, C 0 -C 6 alkylC 3 -C 6 cycloalkyl, —C(O)R 5 , —C(S)R 5 , —C(O)NR a R 5 , —C(O)C(O)NR a R 5 , —S(O) p R c , —S(O) 2 NR a R 5 , —C(NR 7 )R 5 , —C(NR 7 )NR a R 5 , C 0 -C 6 alkylphenyl, C 0 -C 6 alkylheteroaryl, or C 0 -C 6 alkylheterocycle;

R 5 is hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 0 -C 6 alkylC 3 -C 6 cycloalkyl, C 0 -C 6 alkylphenyl, C 0 -C 6 alkylheteroaryl, or C 0 -C 6 alkylheterocycle;

R 6 is cyano, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, —C(O)NR a R b , C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 2 -C 6 haloalkenyl, or C 2 -C 6 haloalkynyl;

R 7 is hydrogen, C 1 -C 6 alkyl, hydroxyl, cyano, nitro, —S(O) p R c , or C 1 -C 6 alkoxy;

R 8 is hydrogen, C 1 -C 6 alkyl, hydroxyl, cyano, —S(O) p R c , or C 1 -C 6 alkoxy;

R is C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl each optionally substituted by at least one halo;

R a is hydrogen, C 1 -C 6 alkyl, or C 0 -C 3 alkylC 3 -C 6 cycloalkyl; wherein the alkyl and alkylcycloalkyl is optionally substituted by cyano or at least one halo substituent;

R b is hydrogen, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 0 -C 3 alkylphenyl, C 0 -C 3 alkylheteroaryl, or C 0 -C 3 alkylheterocycle, each optionally substituted, where chemically possible, with at least one substituent selected from hydroxyl, cyano, halo, or —S(O) p R;

R c is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkylC 3 -C 6 cycloalkyl, C 0 -C 3 alkylC 3 -C 6 cycloalkyl, C 0 -C 3 alkylphenyl, C 0 -C 3 alkylheteroaryl, or C 0 -C 3 alkylheterocycle each optionally substituted with at least one substituent selected from cyano, halo, hydroxyl, oxo, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 haloalkyl, —S(O) p R, —SH, —S(O) p NR a R b , —NR a R b , —NR a C(O)R b , —SC(O)R b , —SCN, or —C(O)NR a R b ;

each of R 4 and R 5 C 1 -C 6 alkyl or C 0 -C 6 alkylC 3 -C 6 cycloalkyl can be optionally and independently substituted by at least one substituent selected from C 1 -C 6 alkyl, cyano, halo, hydroxyl, C 1 -C 6 hydroxyalkyl, oxo, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, —S(O) p R c , —SH, —S(O) p NR a R b , —NR a R b , —NR a C(O)R b , —SC(O)R c , —SCN, or —C(O)NR a R b ; and

wherein R 4 and R 5 C 0 -C 6 alkylphenyl, C 0 -C 6 alkylheteroaryl, or C 0 -C 6 alkylheterocycle moiety can be further optionally substituted with at least one substituent selected from C 1 -C 6 alkyl, cyano, halo, oxo, ═S, ═NR 7 , hydroxyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, —SH, —S(O) p R, and C 1 -C 6 haloalkoxy;

n is the integer 0, 1, or 2, and when n is 2, each R 2 may be identical or different from each other; and

p is the integer 0, 1, or 2,

stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof.

2. The compound of claim 1 having Formula (2)

stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof.

3. The compound of claim 2 wherein A is phenyl, naphthyl, or pyridinyl;

R 1a , R 1b , and R 1c are each independently selected from hydrogen, halo, hydroxyl, and C 1 -C 6 haloalkyl;

R 2 is halo, cyano, hydroxyl, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, —C(O)NR a R b , or —OR; and wherein n is the integer 0, 1, or 2;

R 3 is hydrogen, halo, hydroxyl, N 3 , or cyano;

R 4 is —C(O)R 5 ; and

R 6 is C 1 -C 6 haloalkyl,

stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof.

4. The compound of claim 3 wherein A is phenyl;

R 1a , R 1b , and R 1c are each independently selected from hydrogen, halo, and CF 3 ;

R 3 is hydrogen, halo or hydroxyl;

R 6 is CF 3 ; and

n is the integer 0,

stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof.

5. The compound of claim 1 having Formula (5)

stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof.

6. The compound of claim 5 wherein A is phenyl, naphthyl, or pyridinyl;

R 1a , R 1b , and R 1c are each independently selected from hydrogen, halo, hydroxyl, and C 1 -C 6 haloalkyl;

R 2 is halo, cyano, hydroxyl, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, —C(O)NR a R b , or —OR; and wherein n is the integer 0, 1, or 2;

R 3 is hydrogen, halo, hydroxyl, N 3 , or cyano;

R 4 is —C(O)R 5 ; and

R 6 is C 1 -C 6 haloalkyl,

stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof.

7. The compound of claim 6 wherein A is phenyl;

R 1a , R 1b , and R 1c are each independently selected from hydrogen, halo, and CF 3 ;

R 3 is hydrogen, halo or hydroxyl;

R 6 is CF 3 ; and

n is the integer 0,

stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof.

8. The compound of claim 1 having Formula (6)

stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof.

9. The compound of claim 8 wherein A is phenyl, naphthyl, or pyridinyl;

R 1a , R 1b , and R 1c are each independently selected from hydrogen, halo, hydroxyl, and C 1 -C 6 haloalkyl;

R 2 is halo, cyano, hydroxyl, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, —C(O)NR a R b , or —OR; and wherein n is the integer 0, 1, or 2;

R 3 is hydrogen, halo, hydroxyl, N 3 , or cyano;

R 4 is —C(O)R 5 ; and

R 6 is C 1 -C 6 haloalkyl,

stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof.

10. The compound of claim 9 wherein A is phenyl;

R 1a , R 1b , and R 1c are each independently selected from hydrogen, halo, and CF 3 ;

R 3 is hydrogen, halo or hydroxyl;

R 6 is CF 3 ; and

n is the integer 0,

stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof.

11. The compound of claim 1 having Formula (3) or Formula (4)

R 1a , R 1b , and R 1c are each independently selected from hydrogen, halo, hydroxyl, and C 1 -C 6 haloalkyl;

R 2 is halo, cyano, hydroxyl, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, —C(O)NR a R b , or —OR; and wherein n is the integer 0, 1, or 2;

R 3 is hydrogen, halo, hydroxyl, N 3 , or cyano;

R 4 is —C(O)R 5 ; and

R 6 is C 1 -C 6 haloalkyl,

stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof.

12. A compound of claim 1 selected from the group consisting of:

1-(3-{4-[4-(3,5-dichloro-phenyl)-4-trifluoromethyl-4,5-dihydro-3H-pyrrol-2-yl]-phenyl}-3-fluoro-azetidin-1-yl)-2-methanesulfonyl-ethanone;

1-(3-{4-[4-(3,5-dichloro-phenyl)-4-trifluoromethyl-4,5-dihydro-3H-pyrrol-2-yl]-phenyl}-3-fluoro-azetidin-1-yl)-2-methyl-propan-1-one;

3-(3,5-dichloro-4-fluorophenyl)-5-(4-{3-fluoro-1-[(methylsulfonyl)-acetyl]azetidin-3-yl}phenyl)-3-(trifluoromethyl)-3,4-dihydro-2H-pyrrole;

3-(3,5-dichloro-4-fluorophenyl)-5-[4-(3-fluoro-1-isobutyrylazetidin-3-yl)phenyl]-3-(trifluoromethyl)-3,4-dihydro-2H-pyrrole;

1-(3-fluoro-3-{4-[4-(3,4,5-trichloro-phenyl)-4-trifluoromethyl-4,5-dihydro-3H-pyrrol-2-yl]-phenyl}-azetidin-1-yl)-2-methanesulfonyl-ethanone;

5-[4-(3-fluoro-1-isobutyrylazetidin-3-yl)phenyl]-3-(3,4,5-trichloro-phenyl)-3-(trifluoromethyl)-3,4-dihydro-2H-pyrrole;

1-(3-{4-[5-(3,5-dichloro-4-fluoro-phenyl)-5-trifluoromethyl-[1,4,2]dioxazol-3-yl]-phenyl}-3-fluoro-azetidin-1-yl)-2-methanesulfonyl-ethanone;

1-(3-{4-[5-(3,5-dichloro-4-fluoro-phenyl)-5-trifluoromethyl-[1,4,2]dioxazol-3-yl]-phenyl}-3-fluoro-azetidin-1-yl)-2-methyl-propan-1-one;

1-(3-{4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-[1,4,2]dioxazol-3-yl]-phenyl}-3-fluoro-azetidin-1-yl)-2-methanesulfonyl-ethanone;

1-(3-{4-[5-(3,5-dichloro-phenyl)-5-trifluoromethyl-[1,4,2]dioxazol-3-yl]-phenyl}-3-fluoro-azetidin-1-yl)-2-methyl-propan-1-one;

1-(3-fluoro-3-{4-[5-(3,4,5-trichloro-phenyl)-5-trifluoromethyl-[1,4,2]dioxazol-3-yl]-phenyl}-azetidin-1-yl)-2-methanesulfonyl-ethanone;

1-(3-fluoro-3-{4-[5-(3,4,5-trichloro-phenyl)-5-trifluoromethyl-[1,4,2]dioxazol-3-yl]-phenyl}-azetidin-1-yl)-2-methyl-propan-1-one;

1-(3-fluoro-3-{4-[5-(3,4,5-trichloro-phenyl)-5-trifluoromethyl-4,5-dihydro-1H-pyrazol-3-yl]-phenyl}-azetidin-1-yl)-2-methyl-propan-1-one;

1-(3-{4-[5-(3,5-dichloro-4-fluoro-phenyl)-5-trifluoromethyl-4,5-dihydro-1H-pyrazol-3-yl]-phenyl}-3-fluoro-azetidin-1-yl)-2-methyl-propan-1-one;

1-(3-fluoro-3-(4-(5-(3,4,5-trichlorophenyl)-5-(trifluoromethyl)-4,5-dihydro-1H-pyrazol-3-yl)phenyl)azetidin-1-yl)-2-(methylsulfonyl)ethanone;

1-(3-(4-(5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydro-1H-pyrazol-3-yl)phenyl)-3-fluoroazetidin-1-yl)-2-(methylsulfonyl)ethanone;

1-(3-(4-(5-(3,5-dichlorophenyl)-5-(trifluoromethyl)-4,5-dihydro-1H-pyrazol-3-yl)phenyl)-3-fluoroazetidin-1-yl)-2-methylpropan-1-one; and

1-(3-(4-(5-(3,5-dichloro-4-fluorophenyl)-5-(trifluoromethyl)-4,5-dihydro-1H-pyrazol-3-yl)phenyl)-3-fluoroazetidin-1-yl)-2-(methylsulfonyl)ethanone, stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof.

13. A pharmaceutical or veterinary composition comprising a therapeutic amount of a compound of Formula (1)

wherein

A is phenyl, naphthyl, or heteroaryl where said heteroaryl contains 1 to 4 heteroatoms each independently selected from N, O and S;

B is

where in “ ” represents the point of attachment;

R 1a , R 1b , and R 1c are each independently hydrogen, halo, hydroxyl, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 0 -C 3 alkylC 3 -C 6 cycloalkyl, C 1 -C 6 haloalkoxy, —C(O)NH 2 , —SF 5 , or —S(O) p R;

R 2 is halo, cyano, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, nitro, hydroxyl, —C(O)NR a R b , C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, —S(O) p R, or —OR;

R 3 is hydrogen, halo, hydroxyl, cyano, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 0 -C 3 alkylC 3 -C 6 cycloalkyl, —C(O)NH 2 , nitro, —SC(O)R, —C(O)NR a R b , C 0 -C 3 alkylNR a R 4 , —NR a NR b R 4 , —NR a OR b , —ONR a R b , N 3 , —NHR 4 , —OR, or —S(O) p R;

R 4 is hydrogen, C 1 -C 6 alkyl, C 0 -C 6 alkylC 3 -C 6 cycloalkyl, —C(O)R 5 , —C(S)R 5 , —C(O)NR a R 5 , —C(O)C(O)NR a R 5 , —S(O) p R c , —S(O) 2 NR a R 5 , —C(NR 7 )R 5 , —C(NR 7 )NR a R 5 , C 0 -C 6 alkylphenyl, C 0 -C 6 alkylheteroaryl, or C 0 -C 6 alkylheterocycle;

R 5 is hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 0 -C 6 alkylC 3 -C 6 cycloalkyl, C 0 -C 6 alkylphenyl, C 0 -C 6 alkylheteroaryl, or C 0 -C 6 alkylheterocycle;

R 6 is cyano, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, —C(O)NR a R b , C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 2 -C 6 haloalkenyl, or C 2 -C 6 haloalkynyl;

R 7 is hydrogen, C 1 -C 6 alkyl, hydroxyl, cyano, nitro, —S(O) p R c , or C 1 -C 6 alkoxy;

R 8 is hydrogen, C 1 -C 6 alkyl, hydroxyl, cyano, —S(O) p R c , or C 1 -C 6 alkoxy;

R is C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl each optionally substituted by at least one halo;

R a is hydrogen, C 1 -C 6 alkyl, or C 0 -C 3 alkylC 3 -C 6 cycloalkyl; wherein the alkyl and alkylcycloalkyl is optionally substituted by cyano or at least one halo substituent;

R b is hydrogen, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 0 -C 3 alkylphenyl, C 0 -C 3 alkylheteroaryl, or C 0 -C 3 alkylheterocycle, each optionally substituted, where chemically possible, with at least one substituent selected from hydroxyl, cyano, halo, or —S(O) p R;

R c is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkylC 3 -C 6 cycloalkyl, C 0 -C 3 alkylC 3 -C 6 cycloalkyl, C 0 -C 3 alkylphenyl, C 0 -C 3 alkylheteroaryl, or C 0 -C 3 alkylheterocycle each optionally substituted with at least one substituent selected from cyano, halo, hydroxyl, oxo, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 haloalkyl, —S(O) p R, —SH, —S(O) p NR a R b , —NR a R b , —NR a C(O)R b , —SC(O)R b , —SCN, or —C(O)NR a R b ;

each of R 4 and R 5 C 1 -C 6 alkyl or C 0 -C 6 alkylC 3 -C 6 cycloalkyl can be optionally and independently substituted by at least one substituent selected from C 1 -C 6 alkyl, cyano, halo, hydroxyl, C 1 -C 6 hydroxyalkyl, oxo, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, —S(O) p R c , —SH, —S(O) p NR a R b , —NR a R b , —NR a C(O)R b , —SC(O)R b , —SCN, or —C(O)NR a R b ; and

wherein R 4 and R 5 C 0 -C 6 alkylphenyl, C 0 -C 6 alkylheteroaryl, or C 0 -C 6 alkylheterocycle moiety can be further optionally substituted with at least one substituent selected from C 1 -C 6 alkyl, cyano, halo, oxo, ═S, ═NR 7 , hydroxyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, —SH, —S(O) p R, and C 1 -C 6 haloalkoxy;

n is the integer 0, 1, or 2, and when n is 2, each R 2 may be identical or different from each other; and

p is the integer 0, 1, or 2;

stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof.

14. The pharmaceutical or veterinary composition of claim 13 further comprising a pharmaceutically or veterinarily acceptable excipient, diluent, or carrier, and optionally comprising at least one additional veterinary agent selected from the group consisting of abamectin, ivermectin, avermectin, moxidectin, emamectin, eprinomectin, selamectin, doramectin, nemadectin, albendazole, cambendazole, fenbendazole, flubendazole, mebendazole, oxfenbendazole, oxibendazole, parbendazole, tetramisole, levamisole, pyrantel pamoate, oxantel, morantel, indoxacarb, closantel, triclabendazole, clorsulon, refoxanide, niclosamide, praziquantel, epsiprantel, 2-desoxoparaherquamide, pyripole, pyrafluprole, lufenuron, spiromesifen, tebufenozide, spinosad, spinetoram, imidacloprid, dinotefuran, metaflumizone, thibendiamide, chlorantraniliprole, indoxacarb, pyridalyl, deltamethrin, pyrimidifen, pyrifluquinazon, milbemycin oxime, milbemycin, demiditraz, amitraz, fipronil, S-methoprene, hydroprene, pyriproxyfen, permethrin, and pyrethrin, or mixtures thereof.

15. A method for the treatment of an animal with a parasitic infection or infestation comprising administering to said animal in need thereof an effective amount of a compound of Formula (1)

wherein

A is phenyl, naphthyl, or heteroaryl where said heteroaryl contains 1 to 4 heteroatoms each independently selected from N, O and S;

B is

where in “ ” represents the point of attachment, and “*” represents a chiral carbon;

R 1a , R 1b , and R 1c are each independently hydrogen, halo, hydroxyl, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy, C 0 -C 3 alkylC 3 -C 6 cycloalkyl, C 1 -C 6 haloalkoxy, —C(O)NH 2 , —SF 5 , or —S(O) p R;

R 2 is halo, cyano, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, nitro, hydroxyl, —C(O)NR a R b , C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, —S(O) p R, or —OR;

R 3 is hydrogen, halo, hydroxyl, cyano, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 0 -C 3 alkylC 3 -C 6 cycloalkyl, —C(O)NH 2 , nitro, —SC(O)R, —C(O)NR a R b , C 0 -C 3 alkylNR a R 4 , —NR a NR b R 4 , —NR a OR b , —ONR a R b , N 3 , —NHR 4 , —OR, or —S(O) p R;

R 4 is hydrogen, C 1 -C 6 alkyl, C 0 -C 6 alkylC 3 -C 6 cycloalkyl, —C(O)R 5 , —C(S)R 5 , —C(O)NR a R 5 , —C(O)C(O)NR a R 5 , —S(O) p R c , —S(O) 2 NR a R 5 , —C(NR 7 )R 5 , —C(NR 7 )NR a R 5 , C 0 -C 6 alkylphenyl, C 0 -C 6 alkylheteroaryl, or C 0 -C 6 alkylheterocycle;

R 5 is hydrogen, C 1 -C 6 alkyl, C 2 -C 6 alkenyl, C 0 -C 6 alkylC 3 -C 6 cycloalkyl, C 0 -C 6 alkylphenyl, C 0 -C 6 alkylheteroaryl, or C 0 -C 6 alkylheterocycle;

R 6 is cyano, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, —C(O)NR a R b , C 2 -C 6 alkenyl, C 2 -C 6 alkynyl, C 2 -C 6 haloalkenyl, or C 2 -C 6 haloalkynyl;

R 7 is hydrogen, C 1 -C 6 alkyl, hydroxyl, cyano, nitro, —S(O) p R c , or C 1 -C 6 alkoxy;

R 8 is hydrogen, C 1 -C 6 alkyl, hydroxyl, cyano, —S(O) p R c , or C 1 -C 6 alkoxy;

R is C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl each optionally substituted by at least one halo;

R a is hydrogen, C 1 -C 6 alkyl, or C 0 -C 3 alkylC 3 -C 6 cycloalkyl; wherein the alkyl and alkylcycloalkyl is optionally substituted by cyano or at least one halo substituent;

R b is hydrogen, C 1 -C 6 alkyl, C 3 -C 6 cycloalkyl, C 0 -C 3 alkylphenyl, C 0 -C 3 alkylheteroaryl, or C 0 -C 3 alkylheterocycle, each optionally substituted, where chemically possible, with at least one substituent selected from hydroxyl, cyano, halo, or —S(O) p R;

R c is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 haloalkylC 3 -C 6 cycloalkyl, C 0 -C 3 alkylC 3 -C 6 cycloalkyl, C 0 -C 3 alkylphenyl, C 0 -C 3 alkylheteroaryl, or C 0 -C 3 alkylheterocycle each optionally substituted with at least one substituent selected from cyano, halo, hydroxyl, oxo, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 haloalkyl, —S(O) p R, —SH, —S(O) p NR a R b , —NR a R b , —NR a C(O)R b , —SC(O)R b , —SCN, or —C(O)NR a R b ;

each of R 4 and R 5 C 1 -C 6 alkyl or C 0 -C 6 alkylC 3 -C 6 cycloalkyl can be optionally and independently substituted by at least one substituent selected from C 1 -C 6 alkyl, cyano, halo, hydroxyl, C 1 -C 6 hydroxyalkyl, oxo, C 1 -C 6 alkoxy, C 1 -C 6 haloalkoxy, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, —S(O) p R c , —SH, —S(O) p NR a R b , —NR a R b , —NR a C(O)R b , —SC(O)R c , —SCN, or —C(O)NR a R b ; and

wherein R 4 and R 5 C 0 -C 6 alkylphenyl, C 0 -C 6 alkylheteroaryl, or C 0 -C 6 alkylheterocycle moiety can be further optionally substituted with at least one substituent selected from C 1 -C 6 alkyl, cyano, halo, oxo, ═S, ═NR 7 , hydroxyl, C 1 -C 6 hydroxyalkyl, C 1 -C 6 alkoxy, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, —SH, —S(O) p R, and C 1 -C 6 haloalkoxy;

n is the integer 0, 1, or 2, and when n is 2, each R 2 may be identical or different from each other; and

p is the integer 0, 1, or 2;

stereoisomers thereof, and pharmaceutically or veterinarily acceptable salts thereof, and optionally, at least one additional veterinary agent.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 13, 2015
From: ZOETIS LLC
To: ZOETIS SERVICES LLC
Reel/Frame 035651/0817 →