ECSP045032A - CARBOXYL ACID FENETILAMIDE DERIVATIVES a-OXYGENATED OR a-TIOLATED - Google Patents
CARBOXYL ACID FENETILAMIDE DERIVATIVES a-OXYGENATED OR a-TIOLATEDInfo
- Publication number
- ECSP045032A ECSP045032A ECSP045032A ECSP045032A EC SP045032 A ECSP045032 A EC SP045032A EC SP045032 A ECSP045032 A EC SP045032A EC SP045032 A ECSP045032 A EC SP045032A
- Authority
- EC
- Ecuador
- Prior art keywords
- alkyl
- optionally substituted
- alkenyl
- alkynyl
- alkoxy
- Prior art date
Links
- -1 CARBOXYL Chemical class 0.000 title abstract 3
- 239000002253 acid Substances 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 abstract 10
- 125000003342 alkenyl group Chemical group 0.000 abstract 8
- 125000000304 alkynyl group Chemical group 0.000 abstract 8
- 229910052739 hydrogen Inorganic materials 0.000 abstract 6
- 239000001257 hydrogen Substances 0.000 abstract 6
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 5
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 5
- 229910052736 halogen Inorganic materials 0.000 abstract 4
- 150000002367 halogens Chemical group 0.000 abstract 4
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 3
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 125000005082 alkoxyalkenyl group Chemical group 0.000 abstract 2
- 125000005018 aryl alkenyl group Chemical group 0.000 abstract 2
- 125000003710 aryl alkyl group Chemical group 0.000 abstract 2
- 125000005015 aryl alkynyl group Chemical group 0.000 abstract 2
- 125000005160 aryl oxy alkyl group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 229910052717 sulfur Chemical group 0.000 abstract 2
- 239000011593 sulfur Chemical group 0.000 abstract 2
- 241000233866 Fungi Species 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 206010061217 Infestation Diseases 0.000 abstract 1
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 1
- 125000003545 alkoxy group Chemical group 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000003282 alkyl amino group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 1
- 125000001589 carboacyl group Chemical group 0.000 abstract 1
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000000232 haloalkynyl group Chemical group 0.000 abstract 1
- 125000005347 halocycloalkyl group Chemical group 0.000 abstract 1
- 125000001072 heteroaryl group Chemical group 0.000 abstract 1
- 125000004447 heteroarylalkenyl group Chemical group 0.000 abstract 1
- 125000004446 heteroarylalkyl group Chemical group 0.000 abstract 1
- 125000005312 heteroarylalkynyl group Chemical group 0.000 abstract 1
- 244000005700 microbiome Species 0.000 abstract 1
- 239000000203 mixture Substances 0.000 abstract 1
- 230000003287 optical effect Effects 0.000 abstract 1
- 230000003032 phytopathogenic effect Effects 0.000 abstract 1
- 230000002265 prevention Effects 0.000 abstract 1
- 230000001681 protective effect Effects 0.000 abstract 1
- 125000003107 substituted aryl group Chemical group 0.000 abstract 1
Landscapes
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
La invención se refiere a derivados de fenetilamida de ácido carboxílico a-oxigenados o a-tiolados de fórmula general I incluyendo sus isómeros ópticos y mezclas de tales isómeros, en donde A representa arilo optativamente sustituido o heteroarilo optativamente sustituido; X es oxígeno o azufre; Y es oxígeno o azufre; R1 es hidrógeno, alquilo, alquenilo, alquinilo, cicloalquilo, haloalquilo, haloalquenilo, haloalquinilo o halocicloalquilo; R2 es hidrógeno, alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquil-alquilo, alcoxi-alquilo, alcoxi-alquenilo, alcoxi-alquinilo, en donde todos los grupos alquilo, alquenilo, alquinilo o cicloalquilo pueden estar optativamente sustituidos con halógeno; o aril-alquilo optativamente sustituido, aril-alquenilo optativamente sustituido, aril-alquinilo optativamente sustituido o ariloxi-alquilo optativamente sustituido; R3 es hidrógeno, alquilo, alquenilo, alquinilo, cicloalquilo, cicloalquil-alquilo, alcoxi-alquilo, alcoxi-alquenilo, alcoxi-alquinilo, en donde todos los grupos alquilo, alquenilo, alquinilo o cicloalquilo pueden estar optativamente sustituidos con halógeno; o es aril-alquilo optativamente sustituido, aril-alquenilo optativamente sustituido, aril-alquinilo optativamente sustituido, ariloxi-alquilo optativamente sustituido, heteroaril-alquilo optativamente sustituido, heteroaril-alquenilo optativamente sustituido o heteroaril-alquinilo optativamente sustituido; R4 es alquilo, alquenilo, alquinilo, alcoxi-alquilo, alcoxi, alqueniloxi, alquiniloxi, alquiltio, alcanoílo, alquilamino, dialquilamino, alcoxicarbonilo, en donde todos los grupos alquilo, alquenilo o alquinilo pueden estar optativamente sustituidos con halógeno; o es halógeno, ciano, nitro, amino, formilo o carboxilo; R5 es hidrógeno, alquilo, alquenilo o alquinilo; n es un número entero 0, 1, 2, 3 o 4; B1 representa un miembro puente -(CR10R11)q- o -(CHR10R11)r-Z-(CR12R13)s, en donde q es un número entero 2, 3 o 4; r es un número entero 0, 1, 2, 3; s es un número entero 1, 2 o 3, siempre que (r + s) sea 1, 2 o 3; Z es -O-, -S-, -SO-, -SO2-, NR6-, -CO-, -OOC-, -COO-, -NR6-CO- o -CO-NR6-; R6 es hidrógeno o alquilo; R10, R11, R12 y R13 independientemente entre sí son hidrógeno o alquilo; y B2 es un puente alquileno. Estos compuestos poseen propiedades protectoras útiles y pueden emplearse en forma ventajosa en la práctica agrícola para el control o prevención de la infestación de plantas por microorganismos fitopatógenos, especialmente hongos.The invention relates to a-oxygenated or a-thiolated carboxylic acid phenethylamide derivatives of general formula I including their optical isomers and mixtures of such isomers, wherein A represents optionally substituted aryl or optionally substituted heteroaryl; X is oxygen or sulfur; And it is oxygen or sulfur; R1 is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, haloalkyl, haloalkenyl, haloalkynyl or halocycloalkyl; R2 is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkyl-alkyl, alkoxy-alkyl, alkoxy-alkenyl, alkoxy-alkynyl, wherein all alkyl, alkenyl, alkynyl or cycloalkyl groups may be optionally substituted with halogen; or optionally substituted aryl-alkyl, optionally substituted aryl-alkenyl, optionally substituted aryl-alkynyl or optionally substituted aryloxy-alkyl; R3 is hydrogen, alkyl, alkenyl, alkynyl, cycloalkyl, cycloalkyl-alkyl, alkoxy-alkyl, alkoxy-alkenyl, alkoxy-alkynyl, wherein all alkyl, alkenyl, alkynyl or cycloalkyl groups may be optionally substituted with halogen; or is optionally substituted aryl-alkyl, optionally substituted aryl-alkenyl, optionally substituted aryl-alkynyl, optionally substituted aryloxy-alkyl, optionally substituted heteroaryl-alkyl, optionally substituted heteroaryl-alkenyl or optionally substituted heteroaryl-alkynyl; R4 is alkyl, alkenyl, alkynyl, alkoxy-alkyl, alkoxy, alkenyloxy, alkynyloxy, alkylthio, alkanoyl, alkylamino, dialkylamino, alkoxycarbonyl, wherein all alkyl, alkenyl or alkynyl groups may be optionally substituted with halogen; or is halogen, cyano, nitro, amino, formyl or carboxyl; R5 is hydrogen, alkyl, alkenyl or alkynyl; n is an integer 0, 1, 2, 3 or 4; B1 represents a bridge member - (CR10R11) q- or - (CHR10R11) r-Z- (CR12R13) s, where q is an integer 2, 3 or 4; r is an integer 0, 1, 2, 3; s is an integer 1, 2 or 3, provided that (r + s) is 1, 2 or 3; Z is -O-, -S-, -SO-, -SO2-, NR6-, -CO-, -OOC-, -COO-, -NR6-CO- or -CO-NR6-; R6 is hydrogen or alkyl; R10, R11, R12 and R13 independently of each other are hydrogen or alkyl; and B2 is an alkylene bridge. These compounds have useful protective properties and can be used advantageously in agricultural practice for the control or prevention of plant infestation by phytopathogenic microorganisms, especially fungi.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ECSP045032 ECSP045032A (en) | 2004-03-24 | 2004-03-24 | CARBOXYL ACID FENETILAMIDE DERIVATIVES a-OXYGENATED OR a-TIOLATED |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| ECSP045032 ECSP045032A (en) | 2004-03-24 | 2004-03-24 | CARBOXYL ACID FENETILAMIDE DERIVATIVES a-OXYGENATED OR a-TIOLATED |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ECSP045032A true ECSP045032A (en) | 2004-04-28 |
Family
ID=40435083
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ECSP045032 ECSP045032A (en) | 2004-03-24 | 2004-03-24 | CARBOXYL ACID FENETILAMIDE DERIVATIVES a-OXYGENATED OR a-TIOLATED |
Country Status (1)
| Country | Link |
|---|---|
| EC (1) | ECSP045032A (en) |
-
2004
- 2004-03-24 EC ECSP045032 patent/ECSP045032A/en unknown
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