AR078623A1 - Compuestos herbicidas - Google Patents
Compuestos herbicidasInfo
- Publication number
- AR078623A1 AR078623A1 ARP100103736A ARP100103736A AR078623A1 AR 078623 A1 AR078623 A1 AR 078623A1 AR P100103736 A ARP100103736 A AR P100103736A AR P100103736 A ARP100103736 A AR P100103736A AR 078623 A1 AR078623 A1 AR 078623A1
- Authority
- AR
- Argentina
- Prior art keywords
- optionally substituted
- groups
- alkoxy
- alkyl
- amino
- Prior art date
Links
- 150000001875 compounds Chemical class 0.000 title abstract 4
- 230000002363 herbicidal effect Effects 0.000 title abstract 2
- 239000004009 herbicide Substances 0.000 title 1
- 125000004191 (C1-C6) alkoxy group Chemical group 0.000 abstract 7
- 229910052739 hydrogen Inorganic materials 0.000 abstract 7
- 239000001257 hydrogen Substances 0.000 abstract 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 abstract 7
- 125000006413 ring segment Chemical group 0.000 abstract 7
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical group N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 abstract 6
- 125000000041 C6-C10 aryl group Chemical group 0.000 abstract 6
- 229910052736 halogen Inorganic materials 0.000 abstract 6
- 150000002367 halogens Chemical group 0.000 abstract 6
- 229910052760 oxygen Inorganic materials 0.000 abstract 6
- 125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 6
- 229910052717 sulfur Chemical group 0.000 abstract 6
- 125000004453 alkoxycarbonyl group Chemical group 0.000 abstract 5
- 229910052757 nitrogen Inorganic materials 0.000 abstract 5
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 4
- 125000004890 (C1-C6) alkylamino group Chemical group 0.000 abstract 4
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 abstract 4
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical group [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 abstract 4
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 abstract 4
- 125000004432 carbon atom Chemical group C* 0.000 abstract 4
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 abstract 4
- 125000000000 cycloalkoxy group Chemical group 0.000 abstract 4
- -1 heterobicyclic carboxylic acid derivatives Chemical class 0.000 abstract 4
- 239000001301 oxygen Chemical group 0.000 abstract 4
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 4
- 239000011593 sulfur Chemical group 0.000 abstract 4
- 125000006273 (C1-C3) alkyl group Chemical group 0.000 abstract 3
- 125000006583 (C1-C3) haloalkyl group Chemical group 0.000 abstract 3
- 125000006619 (C1-C6) dialkylamino group Chemical group 0.000 abstract 3
- 150000001204 N-oxides Chemical class 0.000 abstract 3
- 125000003545 alkoxy group Chemical group 0.000 abstract 3
- 125000000217 alkyl group Chemical group 0.000 abstract 3
- 125000002619 bicyclic group Chemical group 0.000 abstract 3
- 229910052799 carbon Inorganic materials 0.000 abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 abstract 3
- 150000003839 salts Chemical class 0.000 abstract 3
- 125000000027 (C1-C10) alkoxy group Chemical group 0.000 abstract 2
- 125000006559 (C1-C3) alkylamino group Chemical group 0.000 abstract 2
- 125000006594 (C1-C3) alkylsulfony group Chemical group 0.000 abstract 2
- 125000004455 (C1-C3) alkylthio group Chemical group 0.000 abstract 2
- 125000006274 (C1-C3)alkoxy group Chemical group 0.000 abstract 2
- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 abstract 2
- 125000006552 (C3-C8) cycloalkyl group Chemical group 0.000 abstract 2
- 125000000882 C2-C6 alkenyl group Chemical group 0.000 abstract 2
- 125000003302 alkenyloxy group Chemical group 0.000 abstract 2
- 125000005196 alkyl carbonyloxy group Chemical group 0.000 abstract 2
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 abstract 2
- 125000004181 carboxyalkyl group Chemical group 0.000 abstract 2
- 125000004093 cyano group Chemical group *C#N 0.000 abstract 2
- 125000004438 haloalkoxy group Chemical group 0.000 abstract 2
- 125000001072 heteroaryl group Chemical group 0.000 abstract 2
- 239000000203 mixture Substances 0.000 abstract 2
- 125000002950 monocyclic group Chemical group 0.000 abstract 2
- QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 abstract 2
- 125000006698 (C1-C3) dialkylamino group Chemical group 0.000 abstract 1
- 125000000229 (C1-C4)alkoxy group Chemical group 0.000 abstract 1
- 125000006727 (C1-C6) alkenyl group Chemical group 0.000 abstract 1
- 125000004454 (C1-C6) alkoxycarbonyl group Chemical group 0.000 abstract 1
- 125000004739 (C1-C6) alkylsulfonyl group Chemical group 0.000 abstract 1
- 125000006592 (C2-C3) alkenyl group Chemical group 0.000 abstract 1
- 125000006656 (C2-C4) alkenyl group Chemical group 0.000 abstract 1
- SAPUJGILULUQBA-UHFFFAOYSA-N 2-(2-hydroxyphenyl)-9-(2-methoxyphenyl)purine-6-carboxamide Chemical compound COC1=CC=CC=C1N1C2=NC(C=3C(=CC=CC=3)O)=NC(C(N)=O)=C2N=C1 SAPUJGILULUQBA-UHFFFAOYSA-N 0.000 abstract 1
- GVDYOZNGVNCJBW-UHFFFAOYSA-N 2-(3-hydroxyphenyl)-8-(2-methoxyphenyl)-6-oxo-5,7-dihydropteridine-4-carboxamide Chemical compound COC1=CC=CC=C1N1C(N=C(N=C2C(N)=O)C=3C=C(O)C=CC=3)=C2NC(=O)C1 GVDYOZNGVNCJBW-UHFFFAOYSA-N 0.000 abstract 1
- REKXWQDSPQOUAG-UHFFFAOYSA-N 2-(3-hydroxyphenyl)-9-(2-methoxyphenyl)purine-6-carboxamide Chemical compound COC1=CC=CC=C1N1C2=NC(C=3C=C(O)C=CC=3)=NC(C(N)=O)=C2N=C1 REKXWQDSPQOUAG-UHFFFAOYSA-N 0.000 abstract 1
- BZNCKRJKHWOKQP-UHFFFAOYSA-N 2-chloro-9-methylpurine-6-carboxylic acid Chemical compound N1=C(Cl)N=C2N(C)C=NC2=C1C(O)=O BZNCKRJKHWOKQP-UHFFFAOYSA-N 0.000 abstract 1
- SCGSNFBPUFNJIR-UHFFFAOYSA-N 6-oxo-8-phenyl-2-pyridin-3-yl-5,7-dihydropteridine-4-carboxamide Chemical compound C1C(=O)NC=2C(C(=O)N)=NC(C=3C=NC=CC=3)=NC=2N1C1=CC=CC=C1 SCGSNFBPUFNJIR-UHFFFAOYSA-N 0.000 abstract 1
- GIVHHJHEQAVLRO-UHFFFAOYSA-N 6-oxo-8-phenyl-2-pyridin-4-yl-5,7-dihydropteridine-4-carboxamide Chemical compound C1C(=O)NC=2C(C(=O)N)=NC(C=3C=CN=CC=3)=NC=2N1C1=CC=CC=C1 GIVHHJHEQAVLRO-UHFFFAOYSA-N 0.000 abstract 1
- MWKDGWKQVQCNGG-UHFFFAOYSA-N 9-(2-hydroxyethyl)-2-phenylpurine-6-carboxamide Chemical compound N=1C=2N(CCO)C=NC=2C(C(=O)N)=NC=1C1=CC=CC=C1 MWKDGWKQVQCNGG-UHFFFAOYSA-N 0.000 abstract 1
- FBECNQNZSXSUKI-UHFFFAOYSA-N 9-(2-hydroxyethyl)-2-prop-1-enylpurine-6-carboxamide Chemical compound CC=CC1=NC(C(N)=O)=C2N=CN(CCO)C2=N1 FBECNQNZSXSUKI-UHFFFAOYSA-N 0.000 abstract 1
- OCXWDXMLAQPCKK-UHFFFAOYSA-N 9-benzylpurine-2,6-dicarboxamide Chemical compound C12=NC(C(=O)N)=NC(C(N)=O)=C2N=CN1CC1=CC=CC=C1 OCXWDXMLAQPCKK-UHFFFAOYSA-N 0.000 abstract 1
- AENLBSGSASHWDU-UHFFFAOYSA-N 9-phenyl-2-pyridin-3-ylpurine-6-carboxamide Chemical compound C1=NC=2C(C(=O)N)=NC(C=3C=NC=CC=3)=NC=2N1C1=CC=CC=C1 AENLBSGSASHWDU-UHFFFAOYSA-N 0.000 abstract 1
- 125000003601 C2-C6 alkynyl group Chemical group 0.000 abstract 1
- 125000001313 C5-C10 heteroaryl group Chemical group 0.000 abstract 1
- 239000004480 active ingredient Substances 0.000 abstract 1
- 125000002252 acyl group Chemical group 0.000 abstract 1
- 125000004183 alkoxy alkyl group Chemical group 0.000 abstract 1
- 125000005278 alkyl sulfonyloxy group Chemical group 0.000 abstract 1
- 239000000729 antidote Substances 0.000 abstract 1
- 125000004391 aryl sulfonyl group Chemical group 0.000 abstract 1
- 125000004429 atom Chemical group 0.000 abstract 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 abstract 1
- 125000004663 dialkyl amino group Chemical group 0.000 abstract 1
- FMNUSOPQJITSQT-UHFFFAOYSA-N ethyl 2-chloro-9-(2-ethoxy-2-oxoethyl)purine-6-carboxylate Chemical compound N1=C(Cl)N=C2N(CC(=O)OCC)C=NC2=C1C(=O)OCC FMNUSOPQJITSQT-UHFFFAOYSA-N 0.000 abstract 1
- FFMOHDQBZUPRBN-UHFFFAOYSA-N ethyl 2-chloro-9-methylpurine-6-carboxylate Chemical compound CCOC(=O)C1=NC(Cl)=NC2=C1N=CN2C FFMOHDQBZUPRBN-UHFFFAOYSA-N 0.000 abstract 1
- 230000012010 growth Effects 0.000 abstract 1
- 125000000262 haloalkenyl group Chemical group 0.000 abstract 1
- 125000001188 haloalkyl group Chemical group 0.000 abstract 1
- 125000004995 haloalkylthio group Chemical group 0.000 abstract 1
- 125000000623 heterocyclic group Chemical group 0.000 abstract 1
- 230000008635 plant growth Effects 0.000 abstract 1
- 229920006395 saturated elastomer Polymers 0.000 abstract 1
- 125000004665 trialkylsilyl group Chemical group 0.000 abstract 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D471/00—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00
- C07D471/02—Heterocyclic compounds containing nitrogen atoms as the only ring hetero atoms in the condensed system, at least one ring being a six-membered ring with one nitrogen atom, not provided for by groups C07D451/00 - C07D463/00 in which the condensed system contains two hetero rings
- C07D471/04—Ortho-condensed systems
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Nitrogen And Oxygen Or Sulfur-Condensed Heterocyclic Ring Systems (AREA)
- Plural Heterocyclic Compounds (AREA)
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GBGB0917934.2A GB0917934D0 (en) | 2009-10-13 | 2009-10-13 | Herbicidal compounds |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| AR078623A1 true AR078623A1 (es) | 2011-11-23 |
Family
ID=41402971
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| ARP100103736A AR078623A1 (es) | 2009-10-13 | 2010-10-13 | Compuestos herbicidas |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US20120202690A1 (esLanguage) |
| EP (1) | EP2488518A2 (esLanguage) |
| CN (1) | CN102574849A (esLanguage) |
| AR (1) | AR078623A1 (esLanguage) |
| AU (1) | AU2010308158A1 (esLanguage) |
| BR (1) | BR112012008530A2 (esLanguage) |
| CA (1) | CA2773604A1 (esLanguage) |
| GB (1) | GB0917934D0 (esLanguage) |
| IN (1) | IN2012DN02075A (esLanguage) |
| TW (1) | TW201114768A (esLanguage) |
| WO (1) | WO2011045561A2 (esLanguage) |
Families Citing this family (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB0902474D0 (en) * | 2009-02-13 | 2009-04-01 | Syngenta Ltd | Chemical compounds |
| CN103271040B (zh) * | 2013-06-05 | 2015-03-11 | 江苏龙灯化学有限公司 | 一种协同除草组合物 |
| TW201625635A (zh) | 2014-11-21 | 2016-07-16 | 默沙東藥廠 | 作為可溶性鳥苷酸環化酶活化劑之三唑并吡基衍生物 |
| BR112019013266B1 (pt) | 2016-12-27 | 2022-10-11 | Nihon Nohyaku Co., Ltd | Composto de 4h-pirrolopiridina ou o sal deste, uso do mesmo, métodos para uso de um inseticida agrícola e hortícola e para controle de pragas agrícolas e hortícolas, composição compreendendo o dito composto e seu uso |
| WO2020035138A1 (en) * | 2018-08-14 | 2020-02-20 | Cmblu Projekt Ag | Redox-active compounds and uses thereof |
| BR112021010715A2 (pt) * | 2018-12-20 | 2021-11-16 | Ksq Therapeutics Inc | Pirazolopirimidinas substituídas e purinas substituídas e seu uso como inibidores de protease de processamento ubiquitina-específica 1 (usp1) |
| WO2021019537A1 (en) * | 2019-07-30 | 2021-02-04 | Adama Agan Ltd. | Process and intermediates for the preparation of pyroxasulfone |
| CN111763220B (zh) * | 2020-07-13 | 2021-06-01 | 湖南科技大学 | 一种9,10-二取代-3,1-苯并噁嗪并咪唑啉酮类化合物及其制备方法和用途 |
| TW202233621A (zh) | 2020-10-30 | 2022-09-01 | 美商Ｋｓｑ治療公司 | 經取代吡唑并嘧啶之固態形式及其用途 |
| CN114044796A (zh) * | 2021-11-18 | 2022-02-15 | 鄂尔多斯应用技术学院 | 一种四取代烯丙基叠氮化合物的立体选择性合成方法 |
Family Cites Families (26)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| BR8600161A (pt) | 1985-01-18 | 1986-09-23 | Plant Genetic Systems Nv | Gene quimerico,vetores de plasmidio hibrido,intermediario,processo para controlar insetos em agricultura ou horticultura,composicao inseticida,processo para transformar celulas de plantas para expressar uma toxina de polipeptideo produzida por bacillus thuringiensis,planta,semente de planta,cultura de celulas e plasmidio |
| US4834908A (en) | 1987-10-05 | 1989-05-30 | Basf Corporation | Antagonism defeating crop oil concentrates |
| CA2005658A1 (en) | 1988-12-19 | 1990-06-19 | Eliahu Zlotkin | Insecticidal toxins, genes encoding these toxins, antibodies binding to them and transgenic plant cells and plants expressing these toxins |
| EP0427529B1 (en) | 1989-11-07 | 1995-04-19 | Pioneer Hi-Bred International, Inc. | Larvicidal lectins and plant insect resistance based thereon |
| UA48104C2 (uk) | 1991-10-04 | 2002-08-15 | Новартіс Аг | Фрагмент днк, який містить послідовність,що кодує інсектицидний протеїн, оптимізовану для кукурудзи,фрагмент днк, який забезпечує направлену бажану для серцевини стебла експресію зв'язаного з нею структурного гена в рослині, фрагмент днк, який забезпечує специфічну для пилку експресію зв`язаного з нею структурного гена в рослині, рекомбінантна молекула днк, спосіб одержання оптимізованої для кукурудзи кодуючої послідовності інсектицидного протеїну, спосіб захисту рослин кукурудзи щонайменше від однієї комахи-шкідника |
| CN1098717A (zh) * | 1993-06-01 | 1995-02-15 | 日本曹达株式会社 | 嘧啶衍生物 |
| US5530195A (en) | 1994-06-10 | 1996-06-25 | Ciba-Geigy Corporation | Bacillus thuringiensis gene encoding a toxin active against insects |
| PL186631B1 (pl) | 1996-03-15 | 2004-02-27 | Syngenta Participations Ag | Synergistyczna kompozycja herbicydowa oraz sposóbzwalczania niepożądanych roślin |
| ES2368326T3 (es) | 2000-01-14 | 2011-11-16 | Dow Agrosciences Llc | 4-aminopicolinatos y su uso como herbicidas. |
| AR031027A1 (es) | 2000-10-23 | 2003-09-03 | Syngenta Participations Ag | Composiciones agroquimicas |
| AR037228A1 (es) | 2001-07-30 | 2004-11-03 | Dow Agrosciences Llc | Compuestos del acido 6-(aril o heteroaril)-4-aminopicolinico, composicion herbicida que los comprende y metodo para controlar vegetacion no deseada |
| AR037856A1 (es) | 2001-12-17 | 2004-12-09 | Syngenta Participations Ag | Evento de maiz |
| SE0201980D0 (sv) | 2002-06-24 | 2002-06-24 | Astrazeneca Ab | Novel compounds |
| UA82358C2 (uk) | 2003-04-02 | 2008-04-10 | Дау Агросайенсиз Ллс | 6-алкіл або алкеніл-4-амінопіколінати гербіцидна композиція, спосіб боротьби з небажаною рослинністю |
| UA81177C2 (uk) | 2003-08-04 | 2007-12-10 | Дау Агросайєнсіз Ллс | 6-(1,1-дифторалкіл)-4-амінопіколінати та їх використання як гербіцидів |
| TWI355894B (en) | 2003-12-19 | 2012-01-11 | Du Pont | Herbicidal pyrimidines |
| WO2006062979A1 (en) | 2004-12-06 | 2006-06-15 | E.I. Dupont De Nemours And Company | Herbicidal 6-cyclopropyl-substitute 4-aminopicolinic acid derivatives |
| CN100344628C (zh) * | 2005-03-29 | 2007-10-24 | 沈阳化工研究院 | 吡唑并嘧啶酮类化合物及其应用 |
| CN100335481C (zh) * | 2005-10-11 | 2007-09-05 | 华中师范大学 | 一类具有杀菌除草活性的多取代吡啶并[4,3－d]嘧啶及制备 |
| TWI396505B (zh) | 2006-01-13 | 2013-05-21 | Dow Agrosciences Llc | ２-（聚-經取代芳基）-６-胺-５-鹵-４-嘧啶羧酸及其作為除草劑之用途 |
| BRPI0717773A2 (pt) * | 2006-10-19 | 2013-11-05 | Signal Pharm Llc | Composto, composição farmacêutica, e, métodos para tratar ou prevenir câncer, uma condição inflamatória, uma condição imunológica ou uma condição metabólica, e para inibir uma quinase em uma célula que expressa a dita quinase |
| EP2181098B1 (en) | 2007-08-30 | 2011-03-02 | Dow AgroSciences LLC | 2-(substituted phenyl)-6-amino-5-alkoxy, thioalkoxy and aminoalkyl-4-pyrimidinecarboxylates and their use as herbicides |
| GB0718433D0 (en) * | 2007-09-21 | 2007-10-31 | Vernalis R&D Ltd | New chemical compounds |
| PL2193120T3 (pl) | 2007-10-02 | 2017-01-31 | Dow Agrosciences Llc | Kwasy 2'podstowione-6-amino-5-alkilo-, alkenylo- lub alkinylo-4-pirymidynokarboksylowe i kwasy 6-podstawione-4-amino-3-alkilo-, alkenylo- lub alkinylopikolinowe oraz ich zastosowanie jako herbicydy |
| GB0725218D0 (en) | 2007-12-24 | 2008-02-06 | Syngenta Ltd | Chemical compounds |
| GB0902474D0 (en) | 2009-02-13 | 2009-04-01 | Syngenta Ltd | Chemical compounds |
-
2009
- 2009-10-13 GB GBGB0917934.2A patent/GB0917934D0/en not_active Ceased
-
2010
- 2010-10-07 TW TW099134166A patent/TW201114768A/zh unknown
- 2010-10-08 IN IN2075DEN2012 patent/IN2012DN02075A/en unknown
- 2010-10-08 WO PCT/GB2010/001890 patent/WO2011045561A2/en not_active Ceased
- 2010-10-08 CN CN2010800462265A patent/CN102574849A/zh active Pending
- 2010-10-08 AU AU2010308158A patent/AU2010308158A1/en not_active Abandoned
- 2010-10-08 EP EP10763404A patent/EP2488518A2/en not_active Withdrawn
- 2010-10-08 CA CA2773604A patent/CA2773604A1/en not_active Abandoned
- 2010-10-08 US US13/502,054 patent/US20120202690A1/en not_active Abandoned
- 2010-10-08 BR BR112012008530A patent/BR112012008530A2/pt not_active IP Right Cessation
- 2010-10-13 AR ARP100103736A patent/AR078623A1/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| CA2773604A1 (en) | 2011-04-21 |
| GB0917934D0 (en) | 2009-11-25 |
| CN102574849A (zh) | 2012-07-11 |
| WO2011045561A2 (en) | 2011-04-21 |
| US20120202690A1 (en) | 2012-08-09 |
| WO2011045561A3 (en) | 2011-06-16 |
| BR112012008530A2 (pt) | 2015-09-22 |
| TW201114768A (en) | 2011-05-01 |
| EP2488518A2 (en) | 2012-08-22 |
| AU2010308158A1 (en) | 2012-04-05 |
| IN2012DN02075A (esLanguage) | 2015-08-21 |
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