AR066009A1 - 4-(3- aminobenzoil )-1- etilpirazoles y su utilizacion como herbicidas - Google Patents
4-(3- aminobenzoil )-1- etilpirazoles y su utilizacion como herbicidasInfo
- Publication number
- AR066009A1 AR066009A1 ARP080101482A ARP080101482A AR066009A1 AR 066009 A1 AR066009 A1 AR 066009A1 AR P080101482 A ARP080101482 A AR P080101482A AR P080101482 A ARP080101482 A AR P080101482A AR 066009 A1 AR066009 A1 AR 066009A1
- Authority
- AR
- Argentina
- Prior art keywords
- alkyl
- methanone
- hydroxy
- phenyl
- methyl
- Prior art date
Links
- 239000004009 herbicide Substances 0.000 title 1
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 8
- 150000002431 hydrogen Chemical class 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- UTQGIAXIIZNRAZ-UHFFFAOYSA-N (3-aminophenyl)-(1-ethylpyrazol-4-yl)methanone Chemical class C1=NN(CC)C=C1C(=O)C1=CC=CC(N)=C1 UTQGIAXIIZNRAZ-UHFFFAOYSA-N 0.000 abstract 1
- 125000004178 (C1-C4) alkyl group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- ONRRCAFLEFWSDP-UHFFFAOYSA-N C1=C(S(C)(=O)=O)C(NCC)=C(C)C(C(=O)C2=C(N(CC)N=C2)O)=C1 Chemical compound C1=C(S(C)(=O)=O)C(NCC)=C(C)C(C(=O)C2=C(N(CC)N=C2)O)=C1 ONRRCAFLEFWSDP-UHFFFAOYSA-N 0.000 abstract 1
- VFFLLZXBCJTKNF-UHFFFAOYSA-N C1=C(S(C)(=O)=O)C(NCCC)=C(C)C(C(=O)C2=C(N(CC)N=C2)O)=C1 Chemical compound C1=C(S(C)(=O)=O)C(NCCC)=C(C)C(C(=O)C2=C(N(CC)N=C2)O)=C1 VFFLLZXBCJTKNF-UHFFFAOYSA-N 0.000 abstract 1
- FVELVTSZPYNKOT-UHFFFAOYSA-N C1=C(S(C)(=O)=O)C(NCCCC)=C(C)C(C(=O)C2=C(N(CC)N=C2)O)=C1 Chemical compound C1=C(S(C)(=O)=O)C(NCCCC)=C(C)C(C(=O)C2=C(N(CC)N=C2)O)=C1 FVELVTSZPYNKOT-UHFFFAOYSA-N 0.000 abstract 1
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- GCINHYWVFJQUED-UHFFFAOYSA-N CCN1N=CC(C(=O)C=2C(=C(N(C)C)C(=CC=2)S(C)(=O)=O)C)=C1O Chemical compound CCN1N=CC(C(=O)C=2C(=C(N(C)C)C(=CC=2)S(C)(=O)=O)C)=C1O GCINHYWVFJQUED-UHFFFAOYSA-N 0.000 abstract 1
- XBTVVUGNPLYPML-UHFFFAOYSA-N CCN1N=CC(C(=O)C=2C(=C(NC(C)C)C(=CC=2)S(C)(=O)=O)C)=C1O Chemical compound CCN1N=CC(C(=O)C=2C(=C(NC(C)C)C(=CC=2)S(C)(=O)=O)C)=C1O XBTVVUGNPLYPML-UHFFFAOYSA-N 0.000 abstract 1
- CMQFZQROFBRDKC-UHFFFAOYSA-N CCN1N=CC(C(=O)C=2C(=C(NCCOC)C(=CC=2)S(C)(=O)=O)C)=C1O Chemical compound CCN1N=CC(C(=O)C=2C(=C(NCCOC)C(=CC=2)S(C)(=O)=O)C)=C1O CMQFZQROFBRDKC-UHFFFAOYSA-N 0.000 abstract 1
- PSJVBFPXAFQRRQ-UHFFFAOYSA-N CCN1N=CC(C=O)=C1O Chemical compound CCN1N=CC(C=O)=C1O PSJVBFPXAFQRRQ-UHFFFAOYSA-N 0.000 abstract 1
- -1 [2-methyl-4- (methylsulfonyl) -3- (prop -2-en-1-ylamino) -phenyl] methanone Chemical compound 0.000 abstract 1
- 125000003236 benzoyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C(*)=O 0.000 abstract 1
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 abstract 1
- 150000001875 compounds Chemical class 0.000 abstract 1
- 125000006317 cyclopropyl amino group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000004170 methylsulfonyl group Chemical group [H]C([H])([H])S(*)(=O)=O 0.000 abstract 1
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
- 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 1
- 150000003839 salts Chemical class 0.000 abstract 1
Classifications
-
- 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
-
- 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
- A01N43/48—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with two nitrogen atoms as the only ring hetero atoms
- A01N43/56—1,2-Diazoles; Hydrogenated 1,2-diazoles
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P13/00—Drugs for disorders of the urinary system
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/55—Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Pest Control & Pesticides (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Plant Pathology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Urology & Nephrology (AREA)
- Medicinal Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
Abstract
Reivindicacion 1: 4-(3-Aminobenzoil)-1-etilpirazoles de la formula (1) o sus sales en que R1 significa hidrogeno, alquilo C1-6 o alcoxi C1-4-alquilo C1-6, R2 significa alquilo C1-6, alquenilo C2-6, alquinilo C2-6, alcoxi C1-4-alquilo C1-6, di-aIcoxiC1-4-alquilo C1-6, alcoxi C1-4-alcoxi C1-4-alquilo C1-6, cicloalquilo C3-6 o cicloalquil C3-6-alquilo C1-6; Y significa hidrogeno, alquil C1-6-sulfonilo, alcoxi C1-4-alquil C1-6- sulfonilo, o fenilsulfonilo, tiofenil-2-sulfonilo, benzoilo, alquil C1-4-benzoil-alquilo C1-6 o bencilo sustituido en cada caso con m radicales iguales o diferentes tomados del conjunto que se compone de halogeno, alquilo C1-4 y alcoxi C1-4, m significa 0, 1, 2 o 3, debiendo de estar excluidos los compuestos (1-etil-5-hidroxi-1H-pirazol-4-il)-[2-metil-3-(metilamino)-4-(metilsulfonil)fenil]-metanona, [3-(etilamino)-2-metil-4-(metilsulfonil)fenil](1-etil5-hidroxi-1H-pirazol-4-il) metanona, (1-etil-5-hidroxi-1H-pirazol-4-il)[2-metil-4-(metilsulfonil)-3-(propilamino)fenil]- metanona, (1-etil-5-hidroxi-1H-pirazol-4-il){2-metil-3-[(1-metiletil)amino]-4-(metil-sulfonil)-fenil}metanona; [3-(butilamino)-2-metil-4-(metilsulfonil)fenil](1-etil-5-hidroxi-1H-pirazol-4-il)-metanona, (1-etil-5-hidroxi-1H-pirazol-4-il){3-[(2-metoxietil)amino]-2-metil-4-(metilsulfonil)-fenil}metanona, [3-(cicIopropilamino)-2-metiI-4-(metilsulfonil)fenil](1-etil-5-hidroxi-1H-pirazol-4-il)metanona, (1-etil-5-hidroxi-1H-pirazol-4-iI)[2-metil-4-(metilsulfonil)-3-(prop-2-en-1-ilamino)-fenil]metanona y [3-(dimetilamino)2-metil-4-(metilsulfonil)fenil](1-etil-5-hidroxi-1H-pirazol-4-il)-metanona.
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| EP07007491A EP1980554A1 (de) | 2007-04-12 | 2007-04-12 | 4-(3-Aminobenzoyl)-1-ehtylpyrazole und ihre Verwendung als Herbizide |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR066009A1 true AR066009A1 (es) | 2009-07-15 |
Family
ID=38515360
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP080101482A AR066009A1 (es) | 2007-04-12 | 2008-04-10 | 4-(3- aminobenzoil )-1- etilpirazoles y su utilizacion como herbicidas |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US7939467B2 (es) |
| EP (2) | EP1980554A1 (es) |
| JP (1) | JP2010523607A (es) |
| CN (1) | CN101657426A (es) |
| AR (1) | AR066009A1 (es) |
| AU (1) | AU2008238384B2 (es) |
| BR (1) | BRPI0810834A8 (es) |
| CA (1) | CA2683588C (es) |
| CL (1) | CL2008001051A1 (es) |
| TW (1) | TW200901882A (es) |
| WO (1) | WO2008125212A1 (es) |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US11155284B2 (en) | 2016-07-14 | 2021-10-26 | L.B. Foster Rail Technologies, Corp. | Rail port insert |
| CN112409263B (zh) * | 2019-08-23 | 2024-04-05 | 东莞市东阳光农药研发有限公司 | 取代的苯甲酰类化合物及其应用 |
Family Cites Families (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| AR012142A1 (es) * | 1997-03-24 | 2000-09-27 | Dow Agrosciences Llc | Compuestos de 1-alquil-4-benzoil-5-hiroxipirazol, composiciones herbicidas que los contienen; metodo para controlar vegetacion no deseada y compuestosintermediarios utiles para preparar dichos compuestos |
| JPH11292849A (ja) * | 1998-04-03 | 1999-10-26 | Nippon Soda Co Ltd | ベンゾイルピラゾール化合物および除草剤 |
| DE10325659A1 (de) * | 2003-06-06 | 2004-12-23 | Bayer Cropscience Gmbh | Herbizide Mittel enthaltend 3-Aminobenzoylpyrazole und Safener |
-
2007
- 2007-04-12 EP EP07007491A patent/EP1980554A1/de not_active Withdrawn
-
2008
- 2008-04-01 AU AU2008238384A patent/AU2008238384B2/en not_active Expired - Fee Related
- 2008-04-01 WO PCT/EP2008/002566 patent/WO2008125212A1/de not_active Ceased
- 2008-04-01 JP JP2010502445A patent/JP2010523607A/ja active Pending
- 2008-04-01 BR BRPI0810834A patent/BRPI0810834A8/pt not_active Application Discontinuation
- 2008-04-01 CN CN200880011822A patent/CN101657426A/zh active Pending
- 2008-04-01 CA CA2683588A patent/CA2683588C/en not_active Expired - Fee Related
- 2008-04-01 EP EP08734918A patent/EP2137159A1/de not_active Withdrawn
- 2008-04-10 TW TW097113055A patent/TW200901882A/zh unknown
- 2008-04-10 AR ARP080101482A patent/AR066009A1/es unknown
- 2008-04-10 US US12/101,062 patent/US7939467B2/en not_active Expired - Fee Related
- 2008-04-11 CL CL200801051A patent/CL2008001051A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| BRPI0810834A2 (pt) | 2014-10-29 |
| US7939467B2 (en) | 2011-05-10 |
| CA2683588C (en) | 2015-03-31 |
| EP2137159A1 (de) | 2009-12-30 |
| TW200901882A (en) | 2009-01-16 |
| CN101657426A (zh) | 2010-02-24 |
| CL2008001051A1 (es) | 2008-08-08 |
| AU2008238384A1 (en) | 2008-10-23 |
| JP2010523607A (ja) | 2010-07-15 |
| AU2008238384B2 (en) | 2013-01-24 |
| CA2683588A1 (en) | 2008-10-23 |
| US20080254991A1 (en) | 2008-10-16 |
| EP1980554A1 (de) | 2008-10-15 |
| BRPI0810834A8 (pt) | 2016-04-26 |
| WO2008125212A1 (de) | 2008-10-23 |
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| Date | Code | Title | Description |
|---|---|---|---|
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