IP Library Granted Patent US 9,089,137
Granted Patent B2
US 9,089,137 · App. 14/372,979 · Granted Jul 28, 2015

Phenyl-substituted ketoenols for controlling fish parasites

Inventors: Jan Koesling (Bejing, CN); Reiner Fischer (Monheim, DE)
Assignee: Bayer Intellectual Property GmbH
A01N43/90A01N43/08A01N43/10A01N43/16A01N43/36A01N43/40A01N43/56A01N43/72A01N43/86
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Quick Facts
Patent No.
US 9,089,137
App. No.
14/372,979
Granted
Jul 28, 2015
Kind
B2
Abstract

The present invention relates to the control of fish parasites, especially Copepodae, by means of phenyl-substituted ketoenols.

Claims (49)

1. A method of controlling parasitic Copepodae comprising administering to a fish a compound of the formula (I)

in which

W is hydrogen, alkyl, halogen, haloalkyl, alkoxy or haloalkoxy,

X is alkyl, alkenyl, alkynyl, halogen, alkoxy, haloalkyl, haloalkoxy or cyano,

Y is hydrogen, alkyl, alkoxy or halogen,

Z is hydrogen, halogen, alkyl, alkoxy, haloalkyl, haloalkoxy or optionally singly or multiply substituted phenyl,

CKE is one of the groups

in which

U is —S—, —S(O)—, —S(O) 2 —, —O—,

 or an S═N—, S(O)═N— or

or is optionally Q 3 and Q 4 -substituted C 1 -C 4 -alkylene which may optionally be interrupted by oxygen,

A is hydrogen, or is in each case optionally halogen-substituted alkyl, alkenyl, alkoxyalkyl, alkylthioalkyl, saturated or unsaturated, optionally substituted cycloalkyl, in which optionally at least one ring atom has been replaced by a heteroatom, or is in each case optionally halogen-, alkyl-, haloalkyl-, alkoxy-, haloalkoxy-, cyano- or nitro-substituted aryl, arylalkyl or hetaryl,

B is hydrogen, alkyl or alkoxyalkyl, or

A and B together with the carbon atom to which they are attached are a saturated or unsaturated, unsubstituted or substituted ring system optionally containing at least one heteroatom,

D is hydrogen or an optionally substituted radical from the series alkyl, alkenyl, alkynyl, alkoxyalkyl, saturated or unsaturated cycloalkyl, in which optionally one or more ring members have been replaced by heteroatoms, or is in each case optionally substituted arylalkyl, aryl, hetarylalkyl or hetaryl, or

A and D together with the atoms to which they are attached are a saturated or unsaturated ring system which optionally contains at least one (when CKE=8 and 11 one further) heteroatom and which is unsubstituted or substituted in the A,D moiety, or

A and Q 1 together are in each case optionally substituted alkanediyl or alkenediyl which may optionally be interrupted by at least one heteroatom,

an

 or substituted

or,

B and Q 2 together with the atoms to which they are attached are a saturated or unsaturated ring system which optionally contains at least one heteroatom and which is unsubstituted or substituted in the B, Q 2 moiety, or

D and Q 1 together with the atoms to which they are attached are a saturated or unsaturated ring system which optionally contains at least one heteroatom and which is unsubstituted or substituted in the D, Q 1 moiety,

Q 1 is hydrogen, alkyl, alkoxyalkyl, optionally substituted cycloalkyl, in which optionally a methylene group has been replaced by oxygen or sulphur, or is optionally substituted phenyl,

Q 2 , Q 4 , Q 5 and Q 6 independently of one another are hydrogen or alkyl,

Q 3 is hydrogen, or is in each case optionally substituted alkyl, alkoxy, alkylthio, alkoxyalkyl, alkylthioalkyl, optionally substituted cycloalkyl, in which optionally one or two methylene groups have been replaced by oxygen or sulphur, or is optionally substituted phenyl, or

Q 1 and Q 2 together with the carbon atom to which they are attached are an unsubstituted or substituted ring system optionally comprising a heteroatom, or

Q 3 and Q 4 together with the carbon atom to which they are attached are a saturated or unsaturated, unsubstituted or substituted ring system optionally comprising at least one heteroatom, or

A and Q 3 together with the carbon atom to which they are attached are a saturated or unsaturated, unsubstituted or substituted ring system optionally comprising at least one heteroatom, or

A and Q 5 together with the carbon atom to which they are attached are a saturated or unsaturated, unsubstituted or substituted ring system optionally comprising at least one heteroatom,

G is hydrogen (a) or is one of the groups

in which

E is a metal ion equivalent or an ammonium ion,

L is oxygen or sulphur,

M is oxygen or sulphur,

R 1 is in each case optionally halogen-substituted alkyl, alkenyl, alkoxyalkyl, alkylthioalkyl, polyalkoxyalkyl, or is optionally halogen-, alkyl- or alkoxy-substituted cycloalkyl, which may be interrupted by at least one heteroatom, or is in each case optionally substituted phenyl, phenylalkyl, hetaryl, phenoxyalkyl or hetaryloxyalkyl,

R 2 is in each case optionally halogen-substituted alkyl, alkenyl, alkoxyalkyl, polyalkoxyalkyl, or is in each case optionally substituted cycloalkyl, phenyl or benzyl,

R 3 , R 4 and R 5 independently of one another are in each case optionally halogen-substituted alkyl, alkoxy, alkylamino, dialkylamino, alkylthio, alkenylthio, cycloalkylthio or are in each case optionally substituted phenyl, benzyl, phenoxy or phenylthio,

R 6 and R 7 independently of one another are hydrogen, or are in each case optionally halogen-substituted alkyl, cycloalkyl, alkenyl, alkoxy, alkoxyalkyl, or are optionally substituted phenyl, or are optionally substituted benzyl, or together with the N atom to which they are bonded are a ring system optionally interrupted by oxygen or sulphur.

2. The method according to claim 1 , wherein the parasitic Copepodae are from the genus Caligidae.

3. The method according to claim 1 , wherein the parasitic Copepodae are from the genus Lepeophtheirus.

4. The method according to claim 3 , wherein the parasitic Copepodae is Lepeoptheirus salmonis.

5. The method according to claim 1 , wherein the fish is a salmonid fish ( Salmonidae ).

6. The method according to claim 1 , wherein the fish is a carp.

7. The method according to claim 1 , wherein the fish is a seabass ( Dicentrarchus labrax ).

8. The method according to claim 1 , wherein the fish is an amberjack ( Seriola spp.).

9. The method according to claim 4 , wherein the fish is a salmonid fish ( Salmonidae ).

10. The method according to claim 4 , wherein the fish is a carp.

11. The method according to claim 4 , wherein the fish is a seabass ( Dicentrarchus labrax ).

12. The method according to claim 4 , wherein the fish is an amberjack ( Seriola spp.).

Assignments (7)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 10, 2025
From: ELANCO ANIMAL HEALTH GMBH
To: INTERVET INC.
Reel/Frame 070456/0400 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 27, 2024
From: KOESLING, JAN, DR.
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 067944/0544 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 8, 2024
From: BAYER INTELLECTUAL PROPERTY GMBH
To: ELANCO ANIMAL HEALTH GMBH (F/K/A BAYER ANIMAL HEALTH GMBH)
Reel/Frame 067342/0990 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded May 8, 2024
From: REINER FISCHER
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 067348/0897 →
CHANGE OF NAME Recorded Feb 22, 2024
From: BAYER ANIMAL HEALTH GMBH
To: ELANCO ANIMAL HEALTH GMBH
Reel/Frame 066645/0469 →
NUNC PRO TUNC ASSIGNMENT Recorded Feb 21, 2024
From: BAYER INTELLECTUAL PROPERTY GMBH
To: BAYER ANIMAL HEALTH GMBH
Reel/Frame 066517/0950 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 15, 2015
From: KOESLING, JAN, DR.; FISCHER, REINER, DR.
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 034720/0905 →
Priority Claims (1)
EP 12152614 · Jan 26, 2012 · regional
Continuity (1)
Related Publication 20150005358A1 · Jan 1, 2015