JO2140B1 - Benzazoles benzoxazole benzthiazole and benzimidazole derivatives - Google Patents

Benzazoles benzoxazole benzthiazole and benzimidazole derivatives

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Publication number
JO2140B1
JO2140B1 JO19992140A JOP19992140A JO2140B1 JO 2140 B1 JO2140 B1 JO 2140B1 JO 19992140 A JO19992140 A JO 19992140A JO P19992140 A JOP19992140 A JO P19992140A JO 2140 B1 JO2140 B1 JO 2140B1
Authority
JO
Jordan
Prior art keywords
sub
alkyl
optionally substituted
sup
substituted phenyl
Prior art date
Application number
JO19992140A
Other languages
Arabic (ar)
Inventor
كريستوفر جون ماثيوس
روسيل فينر
سوزان باتريشيا بارنيت
جون ارتش كريستوفر
ستيفن كريستوفر سميث
باتريك جيلف كراولي
ويليام جاي ويتنجهام
بول هيني ستيفن
جون ويليامز
ايوجهان ماكليود توركويل
دانيال كليرك ايريك
ديفيد جون هيوجهز
سارا ارمسترونغ
نيجل جون بارنيز
جون ويتل الان
ليسلي بيلكينغتون بريان
Original Assignee
سينجنتا ليمتد
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by سينجنتا ليمتد filed Critical سينجنتا ليمتد
Priority to JO19992140A priority Critical patent/JO2140B1/en
Application granted granted Critical
Publication of JO2140B1 publication Critical patent/JO2140B1/en

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  • Plural Heterocyclic Compounds (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

A compound of formula (1): wherein X is O or S; n is 0 or 1; Y is O, S or NR.sup.7 ; R.sup.1 is hydrogen, halogen, C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 alkoxy, C.sub.1-6 haloalkoxy, C.sub.1-6 alkylthio, C.sub.1-6 haloalkylthio, C.sub.3-6 cycloalkyl, C.sub.1-6 alkoxy(C.sub.1-6)alkyl or SF.sub.5 ; R.sup.2 is hydrogen, halogen, C.sub.1-6 alkyl, C.sub.1-6 alkoxy, C.sub.1-6 haloalkoxy, C.sub.1-6 alkylthio, C.sub.1-6 haloalkylthio, C.sub.1-6 alkylsulfinyl, C.sub.1-6 haloalkylsulfinyl, C.sub.1-6 alkylsulfonyl, C.sub.1-6 haloalkylsulfonyl, C.sub.1-6 haloalkyl, cyano, nitro, CHO, CH.dbd.NOR.sup.5, C.sub.1-6 alkylcarbonyl, C.sub.1-6 alkoxycarbonyl or SF.sub.5 ; or together R.sup.1 and R.sup.2 form a five or six membered saturated or unsaturated carbocyclic ring, optionally substituted by one or two C.sub.1-6 alky groups; R.sup.3, is hydrogen, C.sub.1-6 alkyl, CH.sub.2 (C.sub.1-4 haloalkyl), C.sub.1-6 cyanoalkyl, C.sub.3-6 alkenyl, C.sub.3-6 alkynyl, C.sub.1-6 -alkoxy(C.sub.1-6)alkyl, C.sub.1-6 alkylthio(C.sub.1-6)alkyl, C.sub.1-6 alkoxy(C.sub.1-6)alkoxy(C.sub.1-6)alkyl, C.sub.1-6 alkylcarbonyl, C.sub.1-6 alkoxycarbonyl, formyl, C.sub.1-6 alkylcarbonyl(C.sub.1-6)alkyl, C.sub.1-6 alkoxycarbonyl(C.sub.1-6)alkyl, C.sub.1-6 alkylaminocarbonyl, di(C.sub.1-6)alkylaminocarbonyl, optionally substituted phenoxycarbonyl, optionally substituted phenyl(C.sub.1-4)alkyl or S(O).sub.q R.sup.6 ; R.sup.4 is hydrogen, halogen, cyano, C.sub.1-8 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 cyanoalkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.3-7 cycloalkyl, C.sub.3-7 halocycloalkl, C.sub.3-7 cyanocycloalkyl, C.sub.1-3 alkyl(C.sub.3-7)cycloalkyl, C.sub.1-3 alkyl(C.sub.3-7)halocycloalkyl, C.sub.3-6 cycloalkyl(C.sub.1-6)alkyl, C.sub.5-6 cycloalkenyl, C.sub.5-6 cycloalkenyl(C.sub.1-6)alkyl, C.sub.2-6 haloalkenyl, C.sub.1-6 cyanoalkenyl, C.sub.1-6 alkoxy(C.sub.1-6)alkyl, formyl, C.sub.1-6 carboxyalkyl, C.sub.1-6 alkylcarbonyl(C.sub.1-6)alkyl, C.sub.1-6 alkoxycarbonyl(C.sub.1-6)alkyl, C.sub.1-6 alkylthio(C.sub.1-6)alkyl, C.sub.1-6 alkylsulfinyl(C.sub.1-6)alkyl, C.sub.1-6 alkylsulfonyl(C.sub.1-6 alkyl, aminocarbonyl(C.sub.1-6)alkyl, C.sub.1-6 alkylaminocarbonyl(C.sub.1-6)alkyl, di(C.sub.1-6)alkylaminocarbonyl(C.sub.1-6)alkyl, C.sub.1-6 alkoxycarbonyl, C.sub.1-6 alkylcarbonyl, aminocarbonyl, C.sub.1-6 alkylaminocarbonyl, di(C.sub.1-6)alkylaminocarbonyl, optionally substituted phenyl, optionally substituted phenyl(C.sub.1-4)alkyl, optionally substituted phenyl(C.sub.2-4)alkenyl, optionally substituted heteroaryl, optionally substituted heteroaryl(C.sub.1-4)alkyl, optionally substituted heterocyclyl, optionally substituted heterocyclyl(C.sub.1-4)alkyl, a group OR.sup.8, a group SH, a group S(O).sub.p R.sup.9, a group NR.sup.10 R.sup.11 or a group C(R.sup.12).dbd.NOR.sup.13 ; R.sup.5 is hydrogen, C.sub.1-6 alkyl, optionally substituted phenyl or optionally substituted phenyl(C.sub.1-4)alkyl; R.sup.6 is C.sub.1-6 alkyl, C.sub.1-6 haloalkyl or optionally substituted phenyl; R.sup.7 is hydrogen, cyano, C.sub.1-8 alkyl, C.sub.1-6 haloalkyl, C.sub.1-6 cyanoalkyl, C.sub.2-6 alkenyl, C.sub.2-6 alkynyl, C.sub.3-7 cycloalkyl, C.sub.2-6 haloalkenyl, C.sub.3-6 cycloalkyl(C.sub.1-6)alkyl, C.sub.1-6 alkoxy(C.sub.1-6)alkyl, C.sub.1-6 alkoxycarbonyl, C.sub.1-6 alkylcarbonyl, C.sub.1-6 alkylaminocarbonyl, di(C.sub.1-6)alkylaminocarbonyl, optionally substituted phenyl or optionally substituted heteroaryl; R.sup.8 is hydrogen, C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.3-6 alkenyl, C.sub.1-4 cyanoalkyl, C.sub.1-6 alkoxycarbonyl(C.sub.1-6)alkyl, optionally substituted phenyl, optionally substituted phenyl(C.sub.1-4)alkyl, optionally substituted heteroaryl, N.dbd.C(CH.sub.3).sub.2 ; R.sup.9 is C.sub.1-6 alkyl, C.sub.1-6 haloalkyl, C.sub.3-6 alkenyl, cyano, C.sub.1-4 cyanoalkyl, C.sub.1-6 alkoxycarbonyl(C.sub.1-6)alkyl, optionally substituted phenyl, optionally substituted phenyl(C.sub.1-4)alkyl or optionally substituted heteroaryl; R.sup.10 and R.sup.11 are, independently, hydrogen, C.sub.1-8 alkyl, C.sub.3-7, cycloalkyl, C.sub.3-6 alkenyl, C.sub.3-6 alkynyl, C.sub.2-6 haloalkyl, C.sub.1-6 alkoxy(C.sub.1-6)alkyl, C.sub.1-6 alkoxycarbonyl, optionally substituted phenoxycarbonyl, formyl, C.sub.1-6 alkylcarbonyl, C.sub.1-6 alkylSO.sub.2, optionally substituted phenylSO.sub.2 or optionally substituted phenyl(C.sub.1-4)alkyl; R.sup.12 is C.sub.1-3 alkyl R.sup.13 is C.sub.1-6 alkyl, optionally substituted phenyl(C.sub.1-2)alkyl; and p and q are, independently, 0, 1 or 2, processes for preparing these compounds, compositions comprising them, methods of using them to combat fungal diseases and methods of using them to combat or control insect, acarine, mollusc and nematode pests.
JO19992140A 1999-08-14 1999-08-14 Benzazoles benzoxazole benzthiazole and benzimidazole derivatives JO2140B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JO19992140A JO2140B1 (en) 1999-08-14 1999-08-14 Benzazoles benzoxazole benzthiazole and benzimidazole derivatives

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JO19992140A JO2140B1 (en) 1999-08-14 1999-08-14 Benzazoles benzoxazole benzthiazole and benzimidazole derivatives

Publications (1)

Publication Number Publication Date
JO2140B1 true JO2140B1 (en) 2002-08-07

Family

ID=48093530

Family Applications (1)

Application Number Title Priority Date Filing Date
JO19992140A JO2140B1 (en) 1999-08-14 1999-08-14 Benzazoles benzoxazole benzthiazole and benzimidazole derivatives

Country Status (1)

Country Link
JO (1) JO2140B1 (en)

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