AR002596A1 - SUBSTITUTED CARBONYLAMINPHENYLURACILES, PROCEDURE FOR THEIR OBTAINING, HERBICIDAL AGENT CONTAINING THEM, PROCEDURE FOR THE FIGHT AGAINST UNDESIRABLE PLANTS, USE OF SUCH COMPOUNDS FOR THE STRUGGLE AGAINST UNDESIRABLE PLANTS. - Google Patents
SUBSTITUTED CARBONYLAMINPHENYLURACILES, PROCEDURE FOR THEIR OBTAINING, HERBICIDAL AGENT CONTAINING THEM, PROCEDURE FOR THE FIGHT AGAINST UNDESIRABLE PLANTS, USE OF SUCH COMPOUNDS FOR THE STRUGGLE AGAINST UNDESIRABLE PLANTS.Info
- Publication number
- AR002596A1 AR002596A1 ARP960103312A AR10331296A AR002596A1 AR 002596 A1 AR002596 A1 AR 002596A1 AR P960103312 A ARP960103312 A AR P960103312A AR 10331296 A AR10331296 A AR 10331296A AR 002596 A1 AR002596 A1 AR 002596A1
- Authority
- AR
- Argentina
- Prior art keywords
- carbon atoms
- substituted
- chlorine
- cyano
- fluorine
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title 1
- 239000004009 herbicide Substances 0.000 title 1
- 125000004432 carbon atom Chemical group C* 0.000 abstract 8
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical group [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 7
- 229910052801 chlorine Chemical group 0.000 abstract 7
- 239000000460 chlorine Chemical group 0.000 abstract 7
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 5
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 5
- 125000000217 alkyl group Chemical group 0.000 abstract 5
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 5
- 229910052794 bromium Inorganic materials 0.000 abstract 5
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 5
- 229910052731 fluorine Inorganic materials 0.000 abstract 5
- 239000011737 fluorine Substances 0.000 abstract 5
- -1 thiocarbamoyl Chemical group 0.000 abstract 4
- 125000003917 carbamoyl group Chemical group [H]N([H])C(*)=O 0.000 abstract 2
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 2
- 125000000753 cycloalkyl group Chemical group 0.000 abstract 2
- 229910052739 hydrogen Inorganic materials 0.000 abstract 2
- 239000001257 hydrogen Substances 0.000 abstract 2
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 2
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 2
- 125000003342 alkenyl 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
- 125000004644 alkyl sulfinyl group Chemical group 0.000 abstract 1
- 125000004390 alkyl sulfonyl group Chemical group 0.000 abstract 1
- 125000004414 alkyl thio group Chemical group 0.000 abstract 1
- 125000000304 alkynyl group Chemical group 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
- CPPKAGUPTKIMNP-UHFFFAOYSA-N cyanogen fluoride Chemical group FC#N CPPKAGUPTKIMNP-UHFFFAOYSA-N 0.000 abstract 1
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 abstract 1
- 125000006263 dimethyl aminosulfonyl group Chemical group [H]C([H])([H])N(C([H])([H])[H])S(*)(=O)=O 0.000 abstract 1
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 abstract 1
- 125000001153 fluoro group Chemical group F* 0.000 abstract 1
- 125000002541 furyl group Chemical group 0.000 abstract 1
- 229910052736 halogen Inorganic materials 0.000 abstract 1
- 150000002367 halogens Chemical class 0.000 abstract 1
- 125000000842 isoxazolyl 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
- 125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 1
- 125000002971 oxazolyl group Chemical group 0.000 abstract 1
- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 abstract 1
- 125000003356 phenylsulfanyl group Chemical group [*]SC1=C([H])C([H])=C([H])C([H])=C1[H] 0.000 abstract 1
- 125000003226 pyrazolyl group Chemical group 0.000 abstract 1
- 125000004076 pyridyl group Chemical group 0.000 abstract 1
- 125000002943 quinolinyl group Chemical group N1=C(C=CC2=CC=CC=C12)* 0.000 abstract 1
- 125000003718 tetrahydrofuranyl group Chemical group 0.000 abstract 1
- 125000005958 tetrahydrothienyl group Chemical group 0.000 abstract 1
- 125000001544 thienyl group Chemical group 0.000 abstract 1
- 125000000876 trifluoromethoxy group Chemical group FC(F)(F)O* 0.000 abstract 1
- 125000002023 trifluoromethyl group Chemical group FC(F)(F)* 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D239/00—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
- C07D239/02—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
- C07D239/24—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three or more double bonds between ring members or between ring members and non-ring members
- C07D239/28—Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having three 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, directly attached to ring carbon atoms
- C07D239/46—Two or more oxygen, sulphur or nitrogen atoms
- C07D239/52—Two oxygen atoms
- C07D239/54—Two oxygen atoms as doubly bound oxygen atoms or as unsubstituted hydroxy radicals
-
- 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
- A01N43/54—1,3-Diazines; Hydrogenated 1,3-diazines
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/14—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing three or more hetero rings
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Life Sciences & Earth Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Plural Heterocyclic Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Catching Or Destruction (AREA)
Abstract
La invención se refiere a carbonilaminofeniluracilos de la fórmula general (I), en la que: R1 significa hidrógeno, ciano, fluor o cloro; R2 significaciano, fluor, cloro o bromo; R3 significa cicloalquilo o cicloalquilalquilo, sustituidos respectivamente en caso dado por ciano, por fluor, por cloro, porbromo o por alquilo con 1 a 4 átomos de carbono, con 3 a 8 átomos de carbono en la parte cicloalquilo y en caso dado de 1 a 4 átomos de carbono en la partealquilo; R3 significa además fenilo, naftilo, bencilo, feniletilo, furilo, tetrahidrofurilo, tienilo, tetrahidrotienilo, oxazolilo, isoxazolilo,pirazolilo, piridinilo o quinolinilo sustituidos respectivamente en caso dado por fluor, por cloro, por bromo, por ciano, por nitro, porcarboxi, porcarbamoilo, por tiocarbamoilo, por alquilo con 1 a 4 átomos de carbono, por alcoxi con 1 a 4 átomos de carbono, por alquiltio con 1 a 4 átomos de carbono,por alquilsulfinilo con 1 a 4 átomos de carbono o por alquilsulfonilo con 1 a 4átomos de carbono (que están sustituidos respectivamente en caso dado por fluory/o por cloro), por dimetilaminosulfonilo o por dietilaminosulfonilo, por alxoxi-carbonilo con 1 a 4 átomos de carbono (que está sustituido en caso dadopor fluor, por cloro, por bromo, por ciano, por metoxi o por etoxi), por fenilo, por feniloxi o por feniltio (que están substituidos respectivamente encaso dado por fluor, por cloro, por bromo, por ciano, por metilo, por metoxi por trifluormetilo y/o por trifluormetoxi); R4 significa hidrógeno significaalquilo, alquenilo o alquinilo con respectivamente hasta 10 átomos de carbono sustituidos respectivamente en caso dado por ciano, por carboxi, porcarbamoilo, por tiocarbamoilo, por halógeno, por alquilo con 1 a 4 átomos de carbono o por alcoxi-carbonilo con 1 a 4 átomos de carbono; R4 significa ademásThe invention relates to carbonylaminophenyluracils of the general formula (I), in which: R1 represents hydrogen, cyano, fluorine or chlorine; R2 signifier, fluorine, chlorine or bromine; R3 denotes cycloalkyl or cycloalkylalkyl, substituted respectively by cyano, by fluorine, by chlorine, by bromine or by alkyl with 1 to 4 carbon atoms, with 3 to 8 carbon atoms in the cycloalkyl part and optionally 1 to 4 carbon atoms in the alkyl part; R3 also represents phenyl, naphthyl, benzyl, phenylethyl, furyl, tetrahydrofuryl, thienyl, tetrahydrothienyl, oxazolyl, isoxazolyl, pyrazolyl, pyridinyl or quinolinyl substituted respectively by fluorine, by chlorine, by bromine, by cyano, by nitro, by carboxy, By carbamoyl, by thiocarbamoyl, by C 1 to 4 alkyl, by C 1 to 4 alkoxy, by C 1 to 4 alkylthio, by C 1 to 4 alkylsulfinyl or by C 1 to 4 alkylsulfonyl 4 carbon atoms (which are respectively substituted by fluor and / or chlorine), by dimethylaminosulfonyl or by diethylaminosulfonyl, by alxoxycarbonyl with 1 to 4 carbon atoms (which is substituted by fluorine, by chlorine, by bromine if necessary , by cyano, by methoxy or by ethoxy), by phenyl, by phenyloxy or by phenylthio (which are substituted respectively by fluorine, by chlorine, by bromine, by cyano, by methyl, by methoxy by trifluoromethyl and / or po r trifluoromethoxy); R4 represents hydrogen means alkyl, alkenyl or alkynyl with in each case up to 10 carbon atoms substituted in each case by cyano, by carboxy, by carbamoyl, by thiocarbamoyl, by halogen, by alkyl with 1 to 4 carbon atoms or by alkoxycarbonyl with 1 to 4 carbon atoms; R4 also means
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE19523640A DE19523640A1 (en) | 1995-06-29 | 1995-06-29 | Substituted carbonylaminophenyluracile |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR002596A1 true AR002596A1 (en) | 1998-03-25 |
Family
ID=7765542
Family Applications (2)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP960103312A AR002596A1 (en) | 1995-06-29 | 1996-06-25 | SUBSTITUTED CARBONYLAMINPHENYLURACILES, PROCEDURE FOR THEIR OBTAINING, HERBICIDAL AGENT CONTAINING THEM, PROCEDURE FOR THE FIGHT AGAINST UNDESIRABLE PLANTS, USE OF SUCH COMPOUNDS FOR THE STRUGGLE AGAINST UNDESIRABLE PLANTS. |
| ARP970100841A AR006084A1 (en) | 1995-06-29 | 1997-03-03 | SUBSTITUTED AMINOFENILURACILOS AND THEIR USE OF THEM FOR THE FIGHT AGAINST UNDESIRABLE PLANTS |
Family Applications After (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP970100841A AR006084A1 (en) | 1995-06-29 | 1997-03-03 | SUBSTITUTED AMINOFENILURACILOS AND THEIR USE OF THEM FOR THE FIGHT AGAINST UNDESIRABLE PLANTS |
Country Status (10)
| Country | Link |
|---|---|
| EP (1) | EP0835247A1 (en) |
| JP (1) | JPH11508545A (en) |
| KR (1) | KR19990028225A (en) |
| CN (1) | CN1193319A (en) |
| AR (2) | AR002596A1 (en) |
| AU (1) | AU6304396A (en) |
| BR (1) | BR9609319A (en) |
| CA (1) | CA2225828A1 (en) |
| DE (1) | DE19523640A1 (en) |
| WO (1) | WO1997001542A1 (en) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6077812A (en) | 1997-02-26 | 2000-06-20 | Fmc Corporation | Cycloimido-substituted benzofused heterocyclic herbicides |
| DE19830694A1 (en) | 1998-07-09 | 2000-01-13 | Bayer Ag | Substituted acylaminophenyl uracile |
| IL139899A (en) | 1999-12-07 | 2005-06-19 | Sumitomo Chemical Co | Uracil compounds and use thereof |
| IL167955A (en) | 2000-02-04 | 2007-10-31 | Sumitomo Chemical Co | Heteroaryl substituted anilines |
| MY138097A (en) * | 2000-03-22 | 2009-04-30 | Du Pont | Insecticidal anthranilamides |
| CN101165057B (en) * | 2006-10-19 | 2011-04-27 | 湖南化工研究院 | Herbicidal N3-Substituted Phenyluracils |
| CN101704790B (en) * | 2006-10-19 | 2011-09-28 | 湖南化工研究院 | Phytocidal N-uracil-substituted phenyl aryloxy-alkyl amide compound |
| BR112020000553A2 (en) | 2017-07-11 | 2020-07-21 | Vertex Pharmaceuticals Incorporated | carboxamides as sodium channel modulators |
| WO2020146612A1 (en) | 2019-01-10 | 2020-07-16 | Vertex Pharmaceuticals Incorporated | Esters and carbamates as modulators of sodium channels |
| US12441703B2 (en) | 2019-01-10 | 2025-10-14 | Vertex Pharmaceuticals Incorporated | Carboxamides as modulators of sodium channels |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP3089621B2 (en) * | 1990-12-17 | 2000-09-18 | 日産化学工業株式会社 | Uracil derivatives |
-
1995
- 1995-06-29 DE DE19523640A patent/DE19523640A1/en not_active Withdrawn
-
1996
- 1996-06-17 JP JP9504139A patent/JPH11508545A/en active Pending
- 1996-06-17 AU AU63043/96A patent/AU6304396A/en not_active Abandoned
- 1996-06-17 CN CN96196296A patent/CN1193319A/en active Pending
- 1996-06-17 EP EP96922007A patent/EP0835247A1/en not_active Withdrawn
- 1996-06-17 BR BR9609319A patent/BR9609319A/en not_active Application Discontinuation
- 1996-06-17 CA CA002225828A patent/CA2225828A1/en not_active Abandoned
- 1996-06-17 WO PCT/EP1996/002612 patent/WO1997001542A1/en not_active Ceased
- 1996-06-17 KR KR1019970709536A patent/KR19990028225A/en not_active Withdrawn
- 1996-06-25 AR ARP960103312A patent/AR002596A1/en unknown
-
1997
- 1997-03-03 AR ARP970100841A patent/AR006084A1/en unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU6304396A (en) | 1997-01-30 |
| CN1193319A (en) | 1998-09-16 |
| AR006084A1 (en) | 1999-08-11 |
| EP0835247A1 (en) | 1998-04-15 |
| DE19523640A1 (en) | 1997-01-02 |
| BR9609319A (en) | 1999-07-06 |
| CA2225828A1 (en) | 1997-01-16 |
| JPH11508545A (en) | 1999-07-27 |
| WO1997001542A1 (en) | 1997-01-16 |
| KR19990028225A (en) | 1999-04-15 |
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