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Benzoxazolyl-glyoxylonitrile-2-oxime ether derivatives

Assignee: Novartis Corp
•
Filing: 1979-08-28
•
Granted: 1982-08-31
•
Expires: 1999-08-28
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Abstract

Abstract A process for protecting cultivated plants against aggressive agricultural chemicals is described in which oxime derivatives of the formula ##STR1## are used as antidotes. Either the cultivated area for the cultivated plants or the cultivated plants themselves or parts of the plant (seeds, tubers, stem parts and the like), as desired, can be treated with these oxime derivatives, which are used as a dressing.

Inventors

  • 👤 Alfons Lukaszczyk
  • 👤 Henry Martin
  • 👤 Peter J. Diel
  • 👤 Werner Fory
  • 👤 Karl Gatzi
  • 👤 Haukur Kristinsson
  • 👤 Beat Muller
  • 👤 Rene Muntwyler
  • 👤 Johannes P. Pachlatko
  • 👤 Hermann Rempfler
  • 👤 Rolf Schurter
  • 👤 Henry Szczepanski

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-04 01:24
CPC Classifications
C; C07; C07D; C07D213/00; C07D213/02; C07D213/04; C07D213/24; C07D213/44; C07D213/53; C07D213/60; C07D213/61; C07D213/62; C07D213/63; C07D213/64; C07D213/65; C07D213/69; C07D213/70; C07D213/78; C07D213/79; C07D215/00; C07D215/02; C07D215/16; C07D215/20; C07D215/24; C07D215/26; C07D215/32; C07D215/34; C07D233/00; C07D233/04; C07D233/20; C07D233/26; C07D233/54; C07D233/66; C07D233/86; C07D235/00; C07D235/02; C07D235/04; C07D235/06; C07D235/14; C07D235/16; C07D249/00; C07D249/02; C07D249/04; C07D249/06; C07D263/00; C07D263/52; C07D263/54; C07D263/56; C07D277/00; C07D277/60; C07D277/62; C07D277/64; C07D285/00; C07D285/01; C07D285/02; C07D285/04; C07D285/12; C07D285/125; C07D285/13; C07D307/00; C07D307/02; C07D307/04; C07D307/18; C07D307/20; C07D307/34; C07D307/38; C07D307/52; C07D309/00; C07D309/16; C07D309/20; C07D309/32; C07D311/00; C07D311/02; C07D311/04; C07D311/58; C07D317/00; C07D317/08; C07D317/44; C07D317/46; C07D317/48; C07D317/50; C07D317/58; C07D335/00; C07D335/04; C07D335/06; C07D339/00; C07D339/02; C07D339/06; C07D339/08; Y; Y10; Y10S; Y10S47/00; Y10S47/03

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 26 words
A compound of the formula ##STR70## wherein R 35 is methyl, tert.butyl or chloro, and Q is hydrogen, cyanomethyl, methallyl or --CON(CH 3 ) 2 .
Claim 2
Dependent Claim 26 words
A compound of the formula ##STR70## wherein R 35 is methyl, tert.butyl or chloro, and Q is hydrogen, cyanomethyl, methallyl or --CON(CH 3 ) 2 .
Claim 3
Dependent Claim 20 words
The compound according to claim 1 in which R 35 is chloro and Q is --CON(CH 3 ) 2 .
Claim 4
Dependent Claim 26 words
A compound of the formula ##STR71## wherein R 36 is methyl or nitro, and Q is hydrogen, cyanomethyl, allyl, propargyl or --CON(CH 3 ) 2 .
Claim 5
Dependent Claim 26 words
A compound of the formula ##STR71## wherein R 36 is methyl or nitro, and Q is hydrogen, cyanomethyl, allyl, propargyl or --CON(CH 3 ) 2 .
Claim 6
Dependent Claim 77 words
A compound of the formula ##STR72## wherein Q is hydrogen; methyl; cyanomethyl; propargyl; benzyl; alkylcarbonyl in which the alkyl group has from 1 to 4 carbon atoms; chloromethylcarbonyl; alkoxycarbonyl in which the alkyl group has from 1 to 4 carbon atoms; ethylthiocarbonyl; alkenylcarbonyl in which the alkenyl group has 2 or 3 carbon atoms; phenylcarbonyl mono-substituted by methyl, methoxy, or nitro, or mono- or di-substituted by chlorine; N-methylcarbamoyl; N-chloromethylcarbamoyl; N-(2'-chloroethyl)-carbamoyl; N-dichlorophenylcarbamoyl; N-allylcarbamoyl; N,N-dimethylcarbamoyl; N-methyl-N-methoxycarbamoyl; 2-furanoyl; or methylsulfonyl.
Claim 7
Dependent Claim 77 words
A compound of the formula ##STR72## wherein Q is hydrogen; methyl; cyanomethyl; propargyl; benzyl; alkylcarbonyl in which the alkyl group has from 1 to 4 carbon atoms; chloromethylcarbonyl; alkoxycarbonyl in which the alkyl group has from 1 to 4 carbon atoms; ethylthiocarbonyl; alkenylcarbonyl in which the alkenyl group has 2 or 3 carbon atoms; phenylcarbonyl mono-substituted by methyl, methoxy, or nitro, or mono- or di-substituted by chlorine; N-methylcarbamoyl; N-chloromethylcarbamoyl; N-(2'-chloroethyl)-carbamoyl; N-dichlorophenylcarbamoyl; N-allylcarbamoyl; N,N-dimethylcarbamoyl; N-methyl-N-methoxycarbamoyl; 2-furanoyl; or methylsulfonyl.

References Cited (Backward Citations)

US3927005A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1985-08-30 1986-03-01 1986-08-31 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1989-08-30 1990-03-01 1990-08-31 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1993-08-30 1994-03-01 1994-08-31 $7700.00 Window Closed / Lapsed

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