USE OF ARYL DERIVATIVES FOR CONTROLLING ECTOPARASITES
The present invention relates to the use of compounds of formula (I), wherein the variables are as defined in the description, in the free form or in salt form, for the manufacture of a medicament for controlling ectoparasites on a warm-blooded animal, wherein said medicament is administered orally to the animal at a dose of from 0.1 to 100 mg/kg from 30 minutes before to 3 hours after feeding the animal with an animal food.
1 . A method for controlling ectoparasites on a warm-blooded animal, said method comprising orally administering to the animal a compound of formula
including all geometric and stereoisomers, N-oxides, S-oxides and salts thereof,
wherein, R′, R″ and R′″ are each independently hydrogen, halogen, cyano, C 1 -C 2 -alkyl, halo-C 1 -C 2 -alkyl, C 1 -C 2 -alkoxy or C 1 -C 2 -haloalkoxy, subject to the proviso that at least one of R′, R″ and R′″ is not hydrogen;
*—Y—** is a radical of formula
A 1 is O, S or NR 1 ′, A 2 is CH 2 , O or S, and A 3 is O, S or NR 1 ′;
R 1 ′ independently is as defined as R 1 below;
R 2 is H, methyl, halogen, hydroxy or methylsulfonyl;
and X is
(a) a radical of formula
wherein R 5 is H, C 1 -C 2 -alkyl, C 1 -C 2 -haloalkyl, halogen, nitro or cyano and Q is
(i) a 5- or 6-membered heteroaromatic ring comprising 1 to 3 same or different heteroatoms selected from the group consisting of O, S and N which is further unsubstituted or substituted; or is
(ii) a group —C(O)N(R 1 )-T, wherein R 1 is H, C 1 -C 4 -alkyl, C 2 -C 4 -alkylcarbonyl or C 2 -C 4 -alkoxycarbonyl and T is C 1 -C 6 -alkyl which is unsubstituted or substituted by C 3 -C 6 -cycloalkyl, halogen, cyano, nitro, amino, hydroxy, C 1 -C 6 -alkoxy, C 1 -C 6 -haloalkoxy, C 1 -C 6 -alkylthio, C 1 -C 6 -haloalkylthio, C 1 -C 6 -alkylsulfinyl, C 1 -C 6 -haloalkylsulfinyl, C 1 -C 5 -alkylsulfonyl, C 1 -C 6 -haloalkylsulfonyl, carboxy, carbamoyl, C 1 -C 6 -alkylcarbonylamino, C 1 -C 6 -haloalkylcarbonylamino, C 1 -C 6 -alkoxycarbonyl, sulfonamido, N-mono- or N,N, di-C 1 -C 4 -alkylsulfonamido, C 2 -C 6 -alkanoyl, unsubstituted or in the alkyl portion by halogen, cyano, ethenyl or ethynyl substituted N—C 1 -C 6 -alkylaminocarbonyl, or unsubstituted or halogen-, C 1 -C 2 -alkyl-, C 1 -C 2 -haloalkyl or cyano-substituted 4- to 6-membered heterocyclyl; or T is C 3 -C 6 -cycloalkyl or 4- to 6-membered heterocyclyl, which is each unsubstituted or substituted by halogen, C 1 -C 2 -alkyl, C 1 -C 2 -haloalkyl or cyano; or is
(iii) a radical —C(O)NH—C═N—O—C 1 -C 2 -alkyl, a radical —C(O)N═C—N-di-C 1 -C 2 -alkyl or a radical —C(O)N═C(NH 2 )—O—C 1 -C 2 -alkyl; or is
(iv) a group —CH(R 3 )—N(R 4 )—C(O)-T 1 , wherein R 3 is H, C 1 -C 6 -alkyl, C 1 -C 6 -haloalkyl, halogen or cyano, R 4 is H; C 1 -C 4 -alkyl C 2 -C 4 -alkylcarbonyl or C 2 -C 4 -alkoxycarbonyl, and T 1 is independently defined as T above;
(b) a radical of formula
wherein R 5 is H, C 1 -C 2 -alkyl, C 1 -C 2 -haloalkyl, halogen, nitro or cyano, and Q is as defined above;
(c) a radical of formula
wherein Q is as defined above;
(d) a radical of formula
wherein n is 1 or 2 and Q′ is a group —N(R 3 )—C(O)-T 2 , wherein T 2 independently has the meaning of T above and R 4 is as defined above; or
(e) a radical of formula
wherein A 4 is O or S and Q and R 5 are each as defined above, and wherein one of Q and R 5 is located in the 2-position and the other one in the 3-position;
wherein said compound of formula i is administered orally to the animal at a dose of from 0.1 to 100 mg/kg from 30 minutes before to 3 hours after feeding the animal with an animal food.
2 . A method according to claim 1 wherein the compound of formula I comprises a compound of formula (Ia),
wherein R′, R″, R′″ and X are as defined.
3 . A method according to claim 1 , wherein R′, R″ and R′″ are each independently of the other H, halogen or trifluoromethyl, subject to the proviso, that at least one of R′, R″ and R′″ is not H.
4 . A method according to claim 1 comprising a compound of formula
wherein R′, R″ and R′″ are each independently of the other H, halogen or trifluoromethyl, subject to the proviso, that at least one of R′, R″ and R′″ is not H, R 5 is methyl, halogen, CF 3 or cyano, and Q is as defined in claim 1 .
5 . A method according to claim 1 comprising a compound of formula
wherein R′, R″ and R′″ are each independently of the other H, halogen or trifluoromethyl, subject to the proviso, that at least one of R′, R″ and R′″ is not H, R 5 ′ is methyl, halogen, CF 3 or cyano, and A 4 , Q and R 5 are as defined in claim 1 .
6 . A method according to claim 5 , wherein A 4 is S, Q is located in the 2-position, R 5 is located in the 3-position.
7 . A method according to claim 4 , wherein R 5 is methyl, halogen, CF 3 or cyano, in particular methyl.
8 . A method according to claim 1 comprising a compound of formula
wherein R′, R″ and R′″ are each independently of the other H, halogen or trifluoromethyl, subject to the proviso, that at least one of R′, R″ and R′″ is not H, and Q is as defined in claim 1 .
9 . A method according to claim 4 , wherein Q is
(i) a radical
(ii) a radical —C(O)N(R 1 )-T, wherein R 1 is H, methyl, ethyl or acetyl and T is C 1 -C 2 -alkyl; C 1 -C 2 -haloalkyl; C 1 -C 2 -alkoxycarbonyl-C 1 -C 2 -alkyl; C 1 -C 2 -alkyl which is substituted by pyridyl, pyrimidinyl, thiazolyl, oxazolyl, tetrahydrofuranyl, thietanyl or oxetanyl; C 1 -C 2 -alkyl which is substituted by N—C 1 -C 2 -alkylaminocarbonyl or by N—C 1 -C 2 -alkylaminocarbonyl substituted in the alkyl moiety by halogen, cyano, ethenyl or ethynyl; pyridyl; pyrimidyl; thiazolyl; oxazolyl; tetrahydrofuranyl; thietanyl; or oxetanyl;
(iii) a radical —C(O)NH—C═N—O—CH 3 , —C(O)N═C—N-di-CH 3 or —C(O)N═C(NH 2 )—O—CH 3 ; or
(iv) a group —CH(R 3 )—N(R 4 )—C(O)-T 1 wherein R 3 is H, C 1 -C 6 -alkyl, or cyano, R 4 is H; methyl, ethyl or acetyl and T 1 is straight-chain or branched C 1 -C 4 -alkyl or C 1 -C 4 -alkyl which is substituted by cyclopropyl, halogen, cyano, C 1 -C 2 -alkoxy, C 1 -C 2 -haloalkoxy, C 1 -C 2 -alkylthio, C 1 -C 2 -alkylsulfinyl, C 1 -C 2 -alkylsulfonyl, C 1 -C 2 -haloalkylcarbonylamino, pyridyl, pyrimidyl, thiazolyl, oxazolyl, thietanyl, oxetanyl, dioxolanyl, methyldioxolanyl, dioxanyl or tetrahydrofuryl.
10 . A method according to claim 4 , wherein Q is a radical
(q10) —C(O)NH—CH 2 —C(O)NH—CH 2 CF 3
(q11) —C(O)NH—CH 2 —C(O)NH—CH 2 CN
(q12) —C(O)NH—CH 2 —C(O)NH—CH 2 C≡CH
(q13) —C(O)NH—C═N—O—CH 3
(q14) —C(O)N═C—N(CH 3 ) 2
(q15) —C(O)N═C(NH 2 )—O—CH 3
(q16) —CH 2 —NH—C(O)—C 1 -C 3 -alkyl
(q17) —CH 2 —NH—C(O)-cyclopropyl
(q18) —CH 2 —NH—C(O)-cyclobutyl
(q19) —CH 2 —NH—C(O)—C 1 -C 2 -haloalkyl
(q20) —CH 2 —NH—C(O)—(CH 2 ) 1-2 —S—C 1 -C 2 -alkyl
(q21) —CH 2 —NH—C(O)—)—(CH 2 ) 1-2 —S(O) 2 —C 1 -C 2 -alkyl
(q22) —CH 2 —NH—C(O)—(CH 2 ) 1-2 —O—C 1 -C 2 -alkyl
(q23) .—CH 2 —NH—C(O)—(CH 2 ) 1-2 —CN
11 . A method according to claim 1 comprising a compound of formula
wherein R′, R″ and R′″ are each independently of the other H, halogen or trifluoromethyl, subject to the proviso, that at least one of R′, R″ and R′″ is not H, n is 1 or 2, and Q″ is as defined in claim 1 .
12 . A method according to claim 10 , wherein n is 1 and Q″ is a radical
(q26) —NH—C(O)—C 1 -C 3 -alkyl,
(q27) —NH—C(O)-cyclopropyl,
(q28) —NH—C(O)-cyclobutyl,
(q29) —NH—C(O)—C 1 -C 2 -haloalkyl,
(q30) —NH—C(O)—(CH 2 ) 1-2 —S—C 1 -C 2 -alkyl,
(q31) —NH—C(O)—(CH 2 ) 1-2 —S(O) 2 —C 1 -C 2 -alkyl,
(q32) —NH—C(O)—(CH 2 ) 1-2 —O—C 1 -C 2 -alkyl,
(q33) —NH—C(O)—(CH 2 ) 1-2 —CN,
13 . (canceled)
14 . A method according to claim 1 , wherein the aryl isoxazoline compound is administered at a dose of from 0.5 to 60 mg/kg and in particular from 1 to 25 mg/kg of animal.
15 . A method according to claim 1 , wherein the aryl isoxazoline compound is administered in form of a tablet or chewable treat.
16 . A method according to claim 1 , wherein the aryl isoxazoline compound is administered in liquid form.
17 . A method according to claim 1 , wherein the aryl isoxazoline compound is administered concurrently with up to 1 hour after feeding and in particular concurrently with up to 30 minutes after feeding the animal with the animal food.
18 . A method according to claim 1 , wherein the animal food comprises from 30 to 100%, in particular from 50 to 100%, of the animal's daily ratio of fat and protein.
19 . A method according to claim 1 , wherein the animal food represents the animal's main meal of the day.
20 . A method according to claim 1 , wherein the aryl oxazoline compound is administered once a week or less, preferably once every two weeks or less, and in particular once every four weeks or less.