ES2182779T3 - Azadioxacicloalquenos y su empleo para el combate de hongos nocivos y parasitos animales. - Google Patents
Azadioxacicloalquenos y su empleo para el combate de hongos nocivos y parasitos animales.Info
- Publication number
- ES2182779T3 ES2182779T3 ES00904871T ES00904871T ES2182779T3 ES 2182779 T3 ES2182779 T3 ES 2182779T3 ES 00904871 T ES00904871 T ES 00904871T ES 00904871 T ES00904871 T ES 00904871T ES 2182779 T3 ES2182779 T3 ES 2182779T3
- Authority
- ES
- Spain
- Prior art keywords
- carbon atoms
- alkyl
- halogenated
- alkoxy
- halogen
- Prior art date
- Legal status (The legal status 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 status listed.)
- Expired - Lifetime
Links
- 244000000054 animal parasite Species 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 44
- 125000000217 alkyl group Chemical group 0.000 abstract 17
- 125000003545 alkoxy group Chemical group 0.000 abstract 11
- 229910052736 halogen Inorganic materials 0.000 abstract 7
- 150000002367 halogens Chemical class 0.000 abstract 7
- 125000003342 alkenyl group Chemical group 0.000 abstract 4
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 4
- 125000001072 heteroaryl group Chemical group 0.000 abstract 4
- -1 nitro, hydroxy Chemical group 0.000 abstract 4
- 125000004414 alkyl thio group Chemical group 0.000 abstract 3
- 125000004122 cyclic group Chemical group 0.000 abstract 3
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 3
- 229910052739 hydrogen Inorganic materials 0.000 abstract 3
- 239000001257 hydrogen Substances 0.000 abstract 3
- 125000004433 nitrogen atom Chemical group N* 0.000 abstract 3
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 2
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 2
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 2
- 125000003282 alkyl amino group Chemical group 0.000 abstract 2
- 125000000304 alkynyl group Chemical group 0.000 abstract 2
- 125000005133 alkynyloxy group Chemical group 0.000 abstract 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 2
- 125000004435 hydrogen atom Chemical class [H]* 0.000 abstract 2
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 2
- 229910052760 oxygen Inorganic materials 0.000 abstract 2
- 239000001301 oxygen Substances 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000001424 substituent group Chemical group 0.000 abstract 2
- 229910052717 sulfur Inorganic materials 0.000 abstract 2
- 239000011593 sulfur Substances 0.000 abstract 2
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 abstract 1
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004457 alkyl amino carbonyl group Chemical group 0.000 abstract 1
- 125000004670 alkyl amino thio carbonyl group Chemical group 0.000 abstract 1
- 125000004448 alkyl carbonyl group Chemical group 0.000 abstract 1
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000002947 alkylene group Chemical group 0.000 abstract 1
- 125000005530 alkylenedioxy group Chemical group 0.000 abstract 1
- 125000004682 aminothiocarbonyl group Chemical group NC(=S)* 0.000 abstract 1
- 125000003118 aryl group Chemical group 0.000 abstract 1
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 1
- 229910052799 carbon Inorganic materials 0.000 abstract 1
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- 125000004473 dialkylaminocarbonyl group Chemical group 0.000 abstract 1
- 125000004671 dialkylaminothiocarbonyl group Chemical group 0.000 abstract 1
- 125000002485 formyl group Chemical group [H]C(*)=O 0.000 abstract 1
- 125000005843 halogen group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 125000005844 heterocyclyloxy group Chemical group 0.000 abstract 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 1
- 125000001624 naphthyl group Chemical group 0.000 abstract 1
- 229910052757 nitrogen Inorganic materials 0.000 abstract 1
- 125000002071 phenylalkoxy group Chemical group 0.000 abstract 1
- 125000003884 phenylalkyl group Chemical group 0.000 abstract 1
- 125000006413 ring segment Chemical group 0.000 abstract 1
- 125000004434 sulfur atom Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—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
- A01N43/82—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 three ring hetero atoms
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—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
- A01N43/88—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 six-membered rings with three ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D231/00—Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
- 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
- C07D231/18—One oxygen or sulfur atom
- C07D231/20—One oxygen atom attached in position 3 or 5
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D249/00—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms
- C07D249/02—Heterocyclic compounds containing five-membered rings having three nitrogen atoms as the only ring hetero atoms not condensed with other rings
- C07D249/08—1,2,4-Triazoles; Hydrogenated 1,2,4-triazoles
- 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
- C07D249/12—Oxygen or sulfur atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/14—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing three or more hetero rings
Abstract
Azadioxacicloalquenos de la fórmula I **(Fórmula)** en la que los substituyentes y el índice tienen el siguiente significado: Y N o CRa, representando Ra hidrógeno, halógeno, o alquilo con 1 a 4 átomos de carbono; n 0, 1, 2, 3 o 4, pudiendo ser diferentes los substituyentes R1, si n es mayor que 1; R1 nitro, ciano, halógeno, alquilo con 1 a 6 átomos de carbono o, para el caso de que n sea mayor que 1, adicionalmente un puente enlazado en dos átomos de anillo adyacentes, que contiene tres a cuatro eslabones seleccionados a partir del grupo: 3 o 4 átomos de carbono, 2 o 3 átomos de carbono y 1 o 2 átomos de nitrógeno, oxígeno y/o azufre, pudiendo formar este puente un resto insaturado parcialmente o aromático junto con el anillo al que está unido, y además los átomos de carbono del puente pueden estar parcial o completamente substituidos por átomos de halógeno o grupos metilo; R2 hidrógeno, nitro, ciano, halógeno, alquilo con 1 a 4 átomos de carbono, alquilo halogenado con 1 a 4 átomos de carbono, alcoxi con 1 a 4 átomos de carbono, alquiltio con 1 a 4 átomos de carbono o alcoxi con 1 a 4 átomos de carbono - carbonilo; R3 alquilo con 1 a 6 átomos de carbono, que está halogenado parcial o completamente, o puede portar uno a tres grupos Rb, Rb halógeno, ciano, nitro, hidroxi, alquilo con 1 a 6 átomos de carbono, alquilo halogenado con 1 a 6 átomos de carbono, alquilo con 1 a 6 átomos de carbono - carbonilo, cicloalquilo con 3 a 6 átomos de carbono, alcoxi con 1 a 6 átomos de carbono, alcoxi halogenado con 1 a 6 átomos de carbono, alcoxi con 1 a 6 átomos de carbono - carbonilo, alquiltio con 1 a 6 átomos de carbono, alquilamino con 1 a 6 átomos de carbono, dialquilo con 1 a 6 átomos de carbono amino, alquenilo con 2 a 6 átomos de carbono, alqueniloxi con 2 a 6 átomos de carbono, alquiniloxi con 3 a 6 átomos de carbono y alquilendioxi con 1 a 4 átomos de carbono, que puede estar halogenado, cicloalquilo con 3 a 6 átomos de carbono, fenilo, naftilo, heteroarilo de 5 eslabones, que contiene uno a cuatro átomos de nitrógeno, o uno a tres átomos de nitrógeno y un átomo de azufre u oxígeno, o heteroarilo de 6 eslabones, que contiene uno a cuatro átomos de nitrógeno; pudiendo los sistemas cíclicos estar parcial o completamente halogenados, o portar uno a tres grupos Rc, Rc halógeno, ciano, nitro, hidroxi, mercapto, amino, carboxilo, aminocarbonilo, aminotiocarbonilo, alquilo, alquilo halogenado, alquenilo, alqueniloxi, alquiniloxi, alcoxi, alcoxi halogenado, alquiltio, alquilamino, dialquilamino, formilo, alquilcarbonilo, alquilsulfonilo, alquilsulfoxilo, alcoxicarbonilo, alquilcarboniloxi, alquilaminocarbonilo, dialquilaminocarbonilo, alquilaminotiocarbonilo, dialquilaminotiocarbonilo, conteniendo los grupos alquilo en estos restos 1 a 6 átomos de carbono, y conteniendo los citados grupos alquenilo o alquinilo en estos restos 2 a 8 átomos de carbono; C(=NORd) - P1 - Rd'', representando Rd hidrógeno o alquilo con 1 a 6 átomos de carbono, P oxígeno, azufre o NRd, y siendo 1igual a 0 o 1; y/o uno a tres de los siguientes restos: cicloalquilo, cicloalcoxi, heterociclilo, heterocicliloxi, conteniendo los sistemas cíclicos 3 a 10 eslabones de anillo; fenilo, fenoxi, feniltio, fenil - alcoxi con 1 a 6 átomos de carbono, fenil alquilo con 1 a 6 átomos de carbono, hetarilo, hetariloxi, hetariltio, conteniendo los restos hetarilo 5 o 6 eslabones de anillo, pudiendo los sistemas cíclicos estar parcial o completamente halogenados, o substituidos por uno a tres grupos Rb, A =N - OR4, =CH - OR4=CH - SR4 o =CH - R5, significando R4 alquilo con 1 a 4 átomos de carbono o alquilo halogenado con 1 a 4 átomos de carbono, R5 halógeno o un grupo R4, y W alquileno con 1 a 3 átomos de carbono, que no está substituido, o está substituido por uno o dos grupos Re, Re halógeno, ciano, alquilo con 1 a 4 átomos de carbono, alquilo halogenado con 1 a 4 átomos de carbono, alquenilo con 2 a 4 átomos de carbono, alquenilo halogenado con 2 a 4 átomos de carbono, alquinilo con 2 a 4 átomos decarbono o alquinilo halogenado con 1 a 4 átomos de carbono, alcoxi con 1 a 4 átomos de carbono, alcoxi halogenado con 1 a 4 átomos de carbono, alquenoxi con 2 a 4 átomos de carbono, alquenoxi halogenado con 2 a 4 átomos de carbono, alquinoxi con 2 a 4 átomos de carbono o alquinoxi halogenado con 2 a 4 átomos de carbono, alquilo con 1 a 4 átomos de carbono - carboniloxi.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19900892 | 1999-01-13 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| ES2182779T3 true ES2182779T3 (es) | 2003-03-16 |
Family
ID=7894052
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ES00904871T Expired - Lifetime ES2182779T3 (es) | 1999-01-13 | 2000-01-04 | Azadioxacicloalquenos y su empleo para el combate de hongos nocivos y parasitos animales. |
Country Status (9)
| Country | Link |
|---|---|
| US (1) | US6451790B1 (es) |
| EP (1) | EP1140926B1 (es) |
| JP (1) | JP2002534522A (es) |
| AT (1) | ATE222907T1 (es) |
| AU (1) | AU2661800A (es) |
| DE (1) | DE50000412D1 (es) |
| ES (1) | ES2182779T3 (es) |
| PT (1) | PT1140926E (es) |
| WO (1) | WO2000042039A1 (es) |
Families Citing this family (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2001044238A1 (de) * | 1999-12-13 | 2001-06-21 | Bayer Aktiengesellschaft | Pyrazolylbenzylether |
| DE10132687A1 (de) * | 2001-07-05 | 2003-01-16 | Bayer Cropscience Ag | Pyrazolylbenzylthioether |
| CN108530402B (zh) * | 2018-04-10 | 2020-06-26 | 浙江工业大学 | 一种(R)-3-丙基-γ-丁内酯的制备方法 |
Family Cites Families (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE2933985A1 (de) | 1979-08-22 | 1981-04-09 | Bayer Ag, 5090 Leverkusen | Neue 4-fluor-3-phenoxy-benzyl-ether und verfahren zu deren herstellung sowie neue zwischenprodukte hierfuer und verfahren zu deren herstellung |
| NZ213630A (en) | 1984-10-19 | 1990-02-26 | Ici Plc | Acrylic acid derivatives and fungicidal compositions |
| DE3623921A1 (de) | 1986-07-16 | 1988-01-21 | Basf Ag | Oximether und diese enthaltende fungizide |
| DE3836581A1 (de) | 1988-10-27 | 1990-05-03 | Basf Ag | Heterocyclisch substituierte (alpha)-aryl-acrylsaeuremethylester und ihre verwendung |
| DE4305502A1 (de) | 1993-02-23 | 1994-08-25 | Basf Ag | Ortho-substituierte 2-Methoxyiminophenylessigsäuremethylamide |
| ZW8594A1 (en) * | 1993-08-11 | 1994-10-12 | Bayer Ag | Substituted azadioxacycbalkenes |
| IL113414A (en) | 1994-05-03 | 2000-08-13 | Basf Ag | Substituted methyl alpha-phenylbutenoates their preparation and use for combating harmful fungi and animal pests |
| IL118086A0 (en) | 1995-05-24 | 1996-08-04 | Basf Ag | 2-[2-hetaryloxymethylene phenyl] crotonates their preparation and their use as pesticides |
| TR199701672T1 (xx) | 1995-06-22 | 1998-05-21 | Novartis Ag | Zararl� bitki ve hayvanlar� �ld�r�c� trioksimino heterosiklik bile�ikler. |
| JPH0989653A (ja) | 1995-09-26 | 1997-04-04 | Matsushita Electric Works Ltd | 赤外線検出装置 |
| DE19602095A1 (de) | 1996-01-22 | 1997-07-24 | Bayer Ag | Halogenpyrimidine |
| TW492962B (en) | 1996-05-30 | 2002-07-01 | Bayer Ag | Process for preparing 3-(1-hydroxyphenyl-1-alkoximinomethyl)dioxazines |
| DE19642864A1 (de) | 1996-10-17 | 1998-04-23 | Bayer Ag | Oximderivate |
| DE19706396A1 (de) | 1996-12-09 | 1998-06-10 | Bayer Ag | Verfahren zur Herstellung von 3-(l-Hydroxiphenyl-l-alkoximinomethyl)dioxazinen |
| DE19739982A1 (de) | 1996-12-10 | 1998-06-18 | Bayer Ag | Fungizide Wirkstoffkombinationen |
| DE19709874A1 (de) | 1997-03-11 | 1998-09-17 | Bayer Ag | Acrylsäurephenylesterderivate |
| DE19710355A1 (de) | 1997-03-13 | 1998-09-17 | Bayer Ag | Alkoximinomethyldioxazinderivate |
| DE19713762A1 (de) | 1997-04-03 | 1998-10-08 | Bayer Ag | Methoximinomethyldioxazine |
-
2000
- 2000-01-04 JP JP2000593607A patent/JP2002534522A/ja not_active Withdrawn
- 2000-01-04 ES ES00904871T patent/ES2182779T3/es not_active Expired - Lifetime
- 2000-01-04 AT AT00904871T patent/ATE222907T1/de not_active IP Right Cessation
- 2000-01-04 WO PCT/EP2000/000013 patent/WO2000042039A1/de active IP Right Grant
- 2000-01-04 DE DE50000412T patent/DE50000412D1/de not_active Expired - Lifetime
- 2000-01-04 AU AU26618/00A patent/AU2661800A/en not_active Abandoned
- 2000-01-04 EP EP00904871A patent/EP1140926B1/de not_active Expired - Lifetime
- 2000-01-04 PT PT00904871T patent/PT1140926E/pt unknown
-
2001
- 2001-01-04 US US09/889,164 patent/US6451790B1/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| JP2002534522A (ja) | 2002-10-15 |
| PT1140926E (pt) | 2003-01-31 |
| EP1140926B1 (de) | 2002-08-28 |
| DE50000412D1 (de) | 2002-10-02 |
| US6451790B1 (en) | 2002-09-17 |
| ATE222907T1 (de) | 2002-09-15 |
| AU2661800A (en) | 2000-08-01 |
| WO2000042039A1 (de) | 2000-07-20 |
| EP1140926A1 (de) | 2001-10-10 |
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