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US4692468A Expired / Lapsed US ⏱️ 0.0 years remaining

Control of colonial insects employing o-phenylenediamines

Assignee: Eli Lilly and Co
•
Filing: 1982-09-09
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Granted: 1987-09-08
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Expires: 2002-09-09
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Abstract

Abstract This invention is directed to the use of a class of N-(2,2-difluoroalkanoyl)-o-phenylenediamines as an agent for the control of certain colonial insects, i.e., ants and termites.

Inventors

  • 👤 Rudolph J. Boisvenue

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 08:26
CPC Classifications
A; A01; A01N; A01N37/00; A01N37/18; A01N37/22; A01N37/24; A01N25/00; A01N25/002; A01N25/006

Claims Analysis

Total Claims: 8
Claim 1
Independent Claim 198 words
Method for eradicating a fire ant colony, which comprises supplying to the colony an effective amount of an active agent which is a compound of the formula ##STR7## wherein R 1 represents (1) halo, (2) CF 3 , (3) CF 2 H, or (4) CF 2 Cl; one of R 2 and R 3 represents a 2,2-difluoroalkanoyl radical of the formula ##STR8## wherein R 4 represents (1) H, (2) Cl, (3) F, (4) difluoromethyl, or (5) trifluoromethyl; and the other of R 2 and R 3 represents (1) H, (2) the same 2,2-difluoroalkanoyl radical represented by the first of R 2 and R 3 , (3) a radical of the formula ##STR9## wherein R 5 represents loweralkyl of C 1 -C 4 or phenyl, (4) lower alkanoyl of C 2 -C 5 , (5) benzoyl, or (6) halogenated lower alkanoyl of C 2 -C 5 , subject to the limitation that the alpha position bears at least one substituent selected from the group consisting of hydrogen and halogen of atomic weight from 35 to 127, both inclusive; subject to the further limitation that when R 3 represents a 2,2-difluoroalkanoyl radical, R 2 is a group other than H.
Claim 2
Dependent Claim 198 words
Method for eradicating a fire ant colony, which comprises supplying to the colony an effective amount of an active agent which is a compound of the formula ##STR7## wherein R 1 represents (1) halo, (2) CF 3 , (3) CF 2 H, or (4) CF 2 Cl; one of R 2 and R 3 represents a 2,2-difluoroalkanoyl radical of the formula ##STR8## wherein R 4 represents (1) H, (2) Cl, (3) F, (4) difluoromethyl, or (5) trifluoromethyl; and the other of R 2 and R 3 represents (1) H, (2) the same 2,2-difluoroalkanoyl radical represented by the first of R 2 and R 3 , (3) a radical of the formula ##STR9## wherein R 5 represents loweralkyl of C 1 -C 4 or phenyl, (4) lower alkanoyl of C 2 -C 5 , (5) benzoyl, or (6) halogenated lower alkanoyl of C 2 -C 5 , subject to the limitation that the alpha position bears at least one substituent selected from the group consisting of hydrogen and halogen of atomic weight from 35 to 127, both inclusive; subject to the further limitation that when R 3 represents a 2,2-difluoroalkanoyl radical, R 2 is a group other than H.
Claim 3
Dependent Claim 49 words
The method of claim 1 wherein the active agent is a compound of the formula ##STR10## wherein R 6 represents chloro or trifluoromethyl; R 7 represents a 2,2-difluoroalkanoyl radical as defined in claim 1; and R 8 represents H or the same 2,2-difluoroalkanoyl radical represented by R 7 .
Claim 4
Dependent Claim 13 words
The method of claim 2 wherein the active agent is 3-nitro-5-(trifluoromethyl)-N 1 -(2,2,3,3-tetrafluoropropionyl)-o-phenylenediamine.
Claim 5
Dependent Claim 13 words
The method of claim 2 wherein the active agent is 3-nitro-5-(trifluoromethyl)-N 1 -(pentafluoropropionyl)-o-phenylenediamine.
Claim 6
Dependent Claim 15 words
The method of claim 2 wherein the active agent is 3-nitro-5-(trifluoromethyl)-N 1 ,N 2 -bis(trifluoroacetyl)-o-phenylenediamine.
Claim 7
Dependent Claim 15 words
The method of claim 2 wherein the active agent is 3-nitro-5-chloro-N 1 ,N 2 -bis(trifluoroacetyl)-o-phenylenediamine.
Claim 8
Dependent Claim 15 words
The method of claim 2 wherein the active agent is 3-nitro-5-(trifluoromethyl)-N 1 ,N 2 -bis(2,2,3,3-tetrafluoropropionyl)-o-phenylenediamine.

References Cited (Backward Citations)

US29508A Cited
US3557211A Cited
US4011341A Cited
USRE29508E Cited
US4108631A Cited
US3989840A Cited
US4122165A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1990-09-07 1991-03-09 1991-09-08 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1994-09-07 1995-03-09 1995-09-08 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1998-09-07 1999-03-09 1999-09-08 $7700.00 Window Closed / Lapsed

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