FI75815B - Nya n-arylbenzamidderivat. - Google Patents

Nya n-arylbenzamidderivat. Download PDF

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Publication number
FI75815B
FI75815B FI812875A FI812875A FI75815B FI 75815 B FI75815 B FI 75815B FI 812875 A FI812875 A FI 812875A FI 812875 A FI812875 A FI 812875A FI 75815 B FI75815 B FI 75815B
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alkyl
dimethoxybenzamide
formula
ethyl
hydrogen
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FI812875A
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English (en)
Finnish (fi)
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FI812875L (fi
FI75815C (sv
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Jr Kenneth Wayne Burow
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Lilly Co Eli
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    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
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    • A01N43/64—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with three nitrogen atoms as the only ring hetero atoms
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    • A01N43/80—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms five-membered rings with one nitrogen atom and either one oxygen atom or one sulfur atom in positions 1,2
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    • C07D231/02—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members
    • C07D231/14—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings having two or three double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D231/40—Acylated on said nitrogen atom
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    • C07D233/66—Heterocyclic compounds containing 1,3-diazole or hydrogenated 1,3-diazole rings, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D249/10—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D261/10—Heterocyclic compounds containing 1,2-oxazole or hydrogenated 1,2-oxazole rings not condensed with other rings having two or more double bonds between ring members or between ring members and non-ring members with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/06—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles
    • C07D271/07—1,2,4-Oxadiazoles; Hydrogenated 1,2,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
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    • C07D271/02—Heterocyclic compounds containing five-membered rings having two nitrogen atoms and one oxygen atom as the only ring hetero atoms not condensed with other rings
    • C07D271/10—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles
    • C07D271/113—1,3,4-Oxadiazoles; Hydrogenated 1,3,4-oxadiazoles with oxygen, sulfur or nitrogen atoms, directly attached to ring carbon atoms, the nitrogen atoms not forming part of a nitro radical
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    • C07D275/02—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings
    • C07D275/03—Heterocyclic compounds containing 1,2-thiazole or hydrogenated 1,2-thiazole rings not condensed with other rings with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
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    • C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
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    • C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
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    • C07D285/04—Thiadiazoles; Hydrogenated thiadiazoles not condensed with other rings
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Claims (25)

1. N-arylbensamidderivat med formeln (I) eller ett i lantbrukshänseende godtagbart salt därav,
5 RV+*\ 5 •C ΰ-ΊΗ-*4 (I) V j^q kännetecknad därav, att Z är syre eller svavel; R^ är väte, halogen, C,-C4- alkyl eller C^-C^-alkoxi; R är väte, halogen, C^-C,-alkyl, C^-C^-alkoxi, C^-C^-alkyltio eller trifluormetyl; är väte, halogen, C^-C^-alkyl, C^-C^-alkoxi eller C^-C^-alkyl- tio; under förutsättning att dä nägon av R^, R2 eller R2 är alkyl, är den ena eller vardera av de aterstäende fenyl- 2 substltuenterna annat än väte; och da R är trifluormetyl Ί o 4 är den ena eller vardera av Rx och R-5 annat än väte; R är en arylgrupp som valts bland grupperna 20 -FT*· -Tt.· -Tl·· VÄ, , V" . V ” 4T-- /“X· \x ·“" x_x H R R 3Q väri A är CH eller N och B är CH eller N, under förutsättning att nägondera av grupperna A och B är CH och den andra är N; X är NH, 0 eller S; R är väte eller C^C^alkyl; R5 är väte _6 Rs R _1_-,1 -C-R7 eller J/ -U?lC
35 R8 /i2—(inj K l03\ “= y ' 1 eller 2 ne 75815 väri y är ett heltal frän O tili 5; R6, R7 och R® är oberoende av varandra väte, C^-C^-alkyl,halogen-Ci“Cj3-alkyl, C2~Ci3~alkenyl, C^-C-^-alkynyl, C^-C4-alkoxi-C^-Cg-alkyl, C-^-C^-alkyltio-C^-Cg-alkyl, C^-Cg-alkoxi,
5 C2-C4~alkanoyloxi-C^-Cg-alkyl/ C^-Cg-alkyltio eller / \ . x , /~V' '1 eller 2 X~vCH -(0) -(CH } - (CH \ / Λ , X I / 2 Y n ' sm y /*-(0.4 ) - i» -K \X0 väri m är ett heltal frän 0 tili 4; n är 0 eller 1; 9 10 och R och R är oberoende av varandra väte, halogen, 15 12 C^-C^-alkyl eller C^-C^-alkenyl; Q och Q är oberoende av varandra CH2, O, S, CH20 eller CH2S, under förutsätt- ning att da Q1 och Q1 2 vardera är annat än CH9, är y ej 5 4 0; med villkor att R är väte endast da R är 20 H Λ Jk och med villkor att R^ och RJ är annat än väte da R3 är 25 -5Γ-4-r4 .. \χ eller \f^ S H 30 N-arylbensamidderivat med formeln (I) enligt 2 patentkravet 1, kännetecknat därav, att Z är 3 4 .. 4 syre, R ar 119 7581 5 -4- _u—35 JL 4^4 \>< \X R 5 —It —J—R5 X X \XB eller \_x* H R 10 ..... 5 .. .. varx R ar vate; R ar vate, R6 _1_# -C-R7 eller /--R1C
15 R8 /*-Xy 1 eller 2 6 7 väri R och R oberoende av varandra är väte, C^-C^-alkyl, C2~C^-alkenyl eller C2-C/j-alkynyl; y är ett heltal frän 20 0 till 4; R® är väte, C^-C-^-alkyl, halo-C^-C-^-alkyl, C2-Ci3-alkenyl, ^-C^-alkynyl, C^-C^-alkoxi-C^-Cg-alkyl, C^-C^-alkyltio-C-^-Cg-alkyl, 25 // (CH ) -(0) —(CH ) — eller /7 z y n s m R1 " . t eller 2 30 (CHX\X • V'° vari m är ett heltal frän 0 till 4; n är 0 eller 1; och 35 r^ och R^ är oberoende av varandra väte, halogen, C^—C4 — alkyl eller C2~C^-alkenyl. 120 7 5 81 5
3. N-arylbensamidderivat med foonein (I) enligt patentkravet 1 eller 2, kännetecknat därav, att 4 Z är syre och R är s '1—1 II I s II II ' yV · 5 0 « 1~1 /**\ . /~\ \/\= eller V
4. N-arylbensamidderivat med formeln (1) enligt 15 nägot av patentkraven 1-3, kännetecknat därav, 1 2 3 att R är väte och R och R är C^-C^-alkoxi.
5. N-arylbensamidderivat med formeln (I) enligt 2 patentkravet 4, kännetecknat därav, att R 3 är en 2-metoxi- och R är en 6-metoxisubstituent. 20 6. N-arylbensamidderivat med formeln (I) enligt nä- got av patentkraven 1-5, kännetecknat därav, att R8 är en steriskt hindrad eller stor grupp.
7. N-arylbensamidderivat med formeln (I) enligt patentkravet 6, kännetecknat därav, att R8 är en 25 grupp med formeln R6 -C-R7 ;« 30 6 7 väri R är väte eller C^-C^-alkyl, R är C^-C^-alkyl och R8 är C1-C13-alkyl.
8. N-arylbensamidderivat med formeln (I) enligt patentkravet 7, kännete cknat därav, att R8 är 35 1-etyl-l-metylpropyl. »1 75815
9. N-arylbensamidderivat med formeln (I) enligt patentkravet 6, kännetecknat därav, att är en grupp med formeln 5 f A—?’ / —*1C /O2—(k)y * 1 eller 2 10 väri R^ är C.-C.-alkyl; R^ och R^ är oberoende av var- 12 andra väte eller C^-C^-alkyl; Q och Q är och y är ett heltal frän 0 till 4.
10. N-arylbensamidderivat med formeln (I) enligt pa-tentkravet 9, kännetecknat därav, att R5 är 1-etylcyklohexyl.
11. N-/3-(1-etyl-l-metylpropyl)-5-isoxazolyl/- 2.6- dimetoxibensamid.
12. N—/3—(1,1-dimetyletyl)-5-isoxazolyl7-2,6-di-7 Ω metoxibensamid.
13. N-/3-(1-etylcyklohexyl)-5-isoxazoly1/-2,6-dime toxibensamid.
14. N-/6-(1,1-dimetyletyl)pyridazin-3-yl7~2,6-dimetoxibensamid. 2 5 15. N-/?-(1-etyl-l-metylpropyl) pyridazin—3-yl/— 2.6- dimetoxibensamid.
16. N-arylbensamidderivat med formeln (I), eller ett i lantbrukshänseende godtagbart salt därav enligt nägot av patentkraven 1-15, kännetecknat där- 30 av, att det används som en herbicid.
17. Herbicidkomposition, kännetecknad därav, att den som en aktiv ingrediens omfattar ett N-aryl-bensamidderivat med formeln (I), eller ett i lantbrukshänseende godtagbart sait därav, enligt nägot av patentkraven 35 1-15, i förening med i lantbrukshänseende godtagbara bärare eller utspädningsmedel.
FI812875A 1980-09-16 1981-09-15 Nya N-arylbenzamidderivat FI75815C (sv)

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US18767580A 1980-09-16 1980-09-16
US18767580 1980-09-16

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FI812875L FI812875L (fi) 1982-03-17
FI75815B true FI75815B (fi) 1988-04-29
FI75815C FI75815C (sv) 1988-08-08

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KR (1) KR850001951B1 (sv)
AU (1) AU544567B2 (sv)
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BR (1) BR8105900A (sv)
CA (1) CA1179345A (sv)
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DE (2) DE3167845D1 (sv)
DK (1) DK163509C (sv)
DO (1) DOP1981004105A (sv)
EG (1) EG15899A (sv)
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GB (1) GB2084140B (sv)
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IE51515B1 (en) 1987-01-07
EG15899A (en) 1989-01-30
CS682981A2 (en) 1987-01-15
GB2084140B (en) 1984-06-27
BG48682A3 (en) 1991-04-15
NZ198358A (en) 1985-04-30
DK163509B (da) 1992-03-09
IL63839A0 (en) 1981-12-31
AU544567B2 (en) 1985-06-06
ES8302010A1 (es) 1983-01-01
MA19269A1 (fr) 1982-04-01
CA1179345A (en) 1984-12-11
MY8600354A (en) 1986-12-31
ZA816393B (en) 1983-04-27
KR830007593A (ko) 1983-11-04
NO159054B (no) 1988-08-22
PL127767B1 (en) 1983-11-30
JPS5781467A (en) 1982-05-21
GB2084140A (en) 1982-04-07
FI812875L (fi) 1982-03-17
PT73672A (en) 1981-10-01
GR75017B (sv) 1984-07-12
EP0049071B1 (en) 1984-12-19
PT73672B (en) 1982-12-20
SU1160932A3 (ru) 1985-06-07
DE3167845D1 (de) 1985-01-31
AU7525781A (en) 1982-03-25
DOP1981004105A (es) 1988-04-05
UA7145A1 (uk) 1995-06-30
HU191037B (en) 1986-12-28
CY1315A (en) 1986-03-28
NO813142L (no) 1982-03-17
IE812144L (en) 1982-03-16
RO83401A (ro) 1984-04-02
IL63839A (en) 1984-12-31
YU221681A (en) 1983-10-31
PH17881A (en) 1985-01-14
RO83401B (ro) 1984-04-30
RO88495A (ro) 1986-01-30
FI75815C (sv) 1988-08-08
SU1375111A3 (ru) 1988-02-15
DE49071T1 (de) 1984-01-05
OA06900A (fr) 1983-04-30
PL233031A1 (sv) 1982-04-26
DD206930A5 (de) 1984-02-15
DK163509C (da) 1992-08-24
HK17586A (en) 1986-03-21
JPH05386B2 (sv) 1993-01-05
BR8105900A (pt) 1982-06-08
EP0049071A1 (en) 1982-04-07
ES505517A0 (es) 1983-01-01
CS252456B2 (en) 1987-09-17
NO159054C (no) 1988-11-30
KR850001951B1 (ko) 1985-12-31
DK410781A (da) 1982-03-17

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