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Insecticidal oximino and hydrazono derivatives of N-benzyl-4-benzhydryl-and N-benzyl-4-benzhydrol-piperidines

Patent 5939438 Issued on August 17, 1999. Estimated Expiration Date: Icon_subject September 9, 2018. Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.

Patent References

Insecticidal n-(substituted arylmethyl)-4-[bis(substituted phenyl) methyl]p i
Patent #: 5569664
Issued on: 10/29/1996
Inventor: Silverman, et al.

Insecticidal N-(substituted arylmethyl)-4-[bis(substituted phenyl)methyl]piperidines Patent #: 5639763
Issued on: 06/17/1997
Inventor: Silverman, et al.

Inventors

Assignee

Application

No. 150424 filed on 09/09/1998

US Classes:

514/331, Nitrogen attached indirectly to the piperidine ring by nonionic bonding546/229, Nitrogen attached indirectly to the piperidine ring by nonionic bonding546/231, Plural acyclic nitrogens bonded directly to the same carbon or single bonded directly to each other546/232, Chalcogen attached indirectly to the piperidine ring by nonionic bonding546/235The chalcogen, X, is in a -C(=X)- group

Examiners

Primary: Shah, Mukund J.
Assistant: Kifle, Bruck

Attorney, Agent or Firm

International Classes

A01N 043/40
C07D 211/26
C07D 211/28
C07D 211/18

Abstract

It has now been found that certain novel oximino and hydrazono derivatives of N-benzyl-4-benzhydryl- and 4-benhydrolpiperidines, and their corresponding N-oxides and agriculturally acceptable salts are useful as insecticides. These compounds are represented by Formula I: where R is hydrogen, halogen, alkyl, alkoxy, dialkylamino; R1 is hydrogen, alkyl, haloalkyl, alkoxyalkyl, alkylcarbonyl and alkylaminocarbonyl; X is oxygen, or NR2, Q is fluoro and hydroxy; Z is halogen, haloalkyl, haloalkoxy, pentahalothio, haloalkylthio, haloalkylsulfinyl, haloalkylsulfonyl, and --OCF2 O-- attached to two adjacent carbon atoms of the phenyl ring; n is 0 or 1; and, when X is NR2, R2 is hydrogen, alkyl, alkylcarbonyl, alkoxycarbonyl, or R1 and R2 taken together may be --Cm H2.spsb.m, or --C2 H4 OC2 H4 --, where m is 3-9. Preferred compounds include those where R is hydrogen; R1 is alkyl; Q is hydroxy; X is oxygen; and Z is trifluoromethyl or trifluoromethoxy.

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