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US4568684A Expired / Lapsed US ⏱️ 0.0 years remaining

N-Substituted 2-methylnaphthylamides, their preparation, and fungicides containing these compounds

Assignee: BASF SE
•
Filing: 1984-12-17
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Granted: 1986-02-04
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Expires: 2004-12-17
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Abstract

Abstract N-substituted 2-methylnaphthylamides of the general formula I ##STR1## where R is an unsubstituted or substituted furyl, isoxazolyl, oxazolyl, isothiazolyl, thiazolyl, 1,2,4-oxadiazol-3-yl, 1,2,4-thiadiazol-3-yl, 1,2,4-thiadiazol-5-yl, 1,2,5-thiadiazol-3-yl, 1,3,4-thiadiazol-2-yl or C 1 -C 5 -alkyl radical, or the group --CH 2 --Y--R 1 , where Y is oxygen or sulfur and R 1 is C 1 -C 6 -alkoxyethyl or C 1 -C 6 -alkoxyethoxyethyl, or R is C 2 -C 5 -alkenyl, C 2 -C 5 -alkynyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkoxycarbonyl or C 3 -C 7 -cycloalkyl, and fungicides containing these compounds.

Inventors

  • 👤 Costin Rentzea
  • 👤 Karl Eicken
  • 👤 Hans Theobald
  • 👤 Bernd Zeeh
  • 👤 Ernst-Heinrich Pommer
  • 👤 Eberhard Ammermann

Bibliographic Details

Application Number —
Jurisdiction US
Data Source google_patents
Last Synchronized 2026-11-06 19:56
CPC Classifications
C; C07; C07D; C07D275/00; C07D275/02; C07D275/03; A; A01; A01N; A01N37/00; A01N37/44; A01N37/46; A01N43/00; A01N43/02; A01N43/04; A01N43/06; A01N43/08; A01N43/48; A01N43/50; A01N43/56; A01N43/64; A01N43/647; A01N43/653; A01N43/72; A01N43/74; A01N43/80; A01N43/82; A01N47/00; A01N47/08; A01N47/10; A01N47/20; A01N53/00; C07D231/00; C07D231/02; C07D231/10; C07D231/12; C07D233/00; C07D233/54; C07D233/56; C07D249/00; C07D249/02; C07D249/08; C07D261/00; C07D261/02; C07D261/06; C07D261/10; C07D261/18; C07D277/00; C07D277/02; C07D277/20; C07D277/32; C07D277/56; C07D285/00; C07D285/01; C07D285/02; C07D285/04; C07D285/06; C07D285/10; C07D307/00; C07D307/02; C07D307/34; C07D307/56; C07D307/68

Claims Analysis

Total Claims: 7
Claim 1
Independent Claim 65 words
An N-substituted 2-methylnaphthylamide of the formula ##STR28## where R is C 1 -C 5 -alkyl which is unsubstituted or substituted by halogen, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, imidazol-1-yl, pyrazol-1-yl or 1,2,4-triazol-1-yl, or R is C 2 -C 5 -alkenyl, C 2 -C 5 -alkynyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkoxycarbonyl or C 3 -C 7 -cycloalkyl.
Claim 2
Dependent Claim 65 words
An N-substituted 2-methylnaphthylamide of the formula ##STR28## where R is C 1 -C 5 -alkyl which is unsubstituted or substituted by halogen, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, imidazol-1-yl, pyrazol-1-yl or 1,2,4-triazol-1-yl, or R is C 2 -C 5 -alkenyl, C 2 -C 5 -alkynyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkoxycarbonyl or C 3 -C 7 -cycloalkyl.
Claim 3
Dependent Claim 89 words
A process for combating fungi, wherein the fungi or the objects to be protected against fungus attack are treated with an effective amount of an N-substituted 2-methylnaphthylamide of the formula ##STR29## where R is C 1 -C 5 -alkyl which is unsubstituted or substituted by halogen, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, imidazol-1-yl, pyrazol-1-yl or 1,2,4-triazol-1-yl, or R is C 2 -C 5 -alkenyl, C 2 -C 5 -alkynyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkoxycarbonyl or C 3 -C 7 -cycloalkyl.
Claim 4
Dependent Claim 89 words
A process for combating fungi, wherein the fungi or the objects to be protected against fungus attack are treated with an effective amount of an N-substituted 2-methylnaphthylamide of the formula ##STR29## where R is C 1 -C 5 -alkyl which is unsubstituted or substituted by halogen, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, imidazol-1-yl, pyrazol-1-yl or 1,2,4-triazol-1-yl, or R is C 2 -C 5 -alkenyl, C 2 -C 5 -alkynyl, C 1 -C 5 -alkoxy, C 1 -C 5 -alkoxycarbonyl or C 3 -C 7 -cycloalkyl.
Claim 5
Dependent Claim 41 words
An N-substituted 2-methylnaphthylamide as claimed in claim 1, wherein R is methoxymethyl, ethoxymethyl, methylthiomethyl, ethylthiomethyl, methoxyethyl, imidazol-1-ylmethyl, pyrazol-1-ylmethyl, 1,2,4-triazol-1-ylmethyl, methyl, ethyl, propyl, chloromethyl, bromomethyl, 1-chloroethyl, 2-chloroethyl, 1-chloropropyl, 3-chloropropyl, 4-chlorobutyl, vinyl, propenyl, ethynyl, methoxy, ethoxy, propoxy, methoxycarbonyl, ethoxycarbonyl, propoxycarbonyl, cyclopropyl or cyclohexyl.
Claim 6
Dependent Claim 28 words
An N-substituted 2-methylnaphthylamide as set forth in claim 1, wherein R is C 1 -C 5 alkyl substituted by halogen or substituted by C 1 -C 4 alkoxy.
Claim 7
Dependent Claim 13 words
An N-substituted 2-methylnaphthylamide as set forth in claim 1, wherein R is methylmethoxy.

References Cited (Backward Citations)

US4430336A Cited

USPTO Annuity & Maintenance Windows

Annuity Stage Window Opens Payment Deadline Surcharge Period Until Estimated Fee Status
3.5 Years (Year 4) 1989-02-03 1989-08-05 1990-02-04 $2000.00 Window Closed / Lapsed
7.5 Years (Year 8) 1993-02-03 1993-08-05 1994-02-04 $3760.00 Window Closed / Lapsed
11.5 Years (Year 12) 1997-02-03 1997-08-05 1998-02-04 $7700.00 Window Closed / Lapsed

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