UY32242A - ACIDS OF 2 - [(1-CIANOPROPIL) CARBAMOIL] -5-NICOTINIC METOXIMETHYL AND ITS USE FOR THE MANUFACTURE OF HERBICIDE IMIDAZOLINONES - Google Patents
ACIDS OF 2 - [(1-CIANOPROPIL) CARBAMOIL] -5-NICOTINIC METOXIMETHYL AND ITS USE FOR THE MANUFACTURE OF HERBICIDE IMIDAZOLINONESInfo
- Publication number
- UY32242A UY32242A UY32242A UY32242A UY32242A UY 32242 A UY32242 A UY 32242A UY 32242 A UY32242 A UY 32242A UY 32242 A UY32242 A UY 32242A UY 32242 A UY32242 A UY 32242A
- Authority
- UY
- Uruguay
- Prior art keywords
- hydrogen
- imidazolinones
- acids
- metoximethyl
- cianopropil
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/60—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom 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
- C07D213/78—Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
- C07D213/81—Amides; Imides
-
- 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
- C07D401/04—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 directly linked by a ring-member-to-ring-member bond
Abstract
Ácidos 2-[(1-cianopropil)carbamoil]-5-metoximetil nicotínicos de la fórmula (I) en donde Z es hidrógeno o halógeno; Z1 es hidrógeno, halógeno, ciano o nitro; R1 es C1-C4 alquilo; R2 es C1-C4 alquilo, C3-C6 cicloalquilo o R1 y R2, cuando se los toma junto con el átomo al cual están unidos, representan un grupo C3-C6 cicloalquilo opcionalmente sustituido con metilo y R3 es hidrogeno o un catión seleccionado preferentemente del grupo que consiste en metales alcalinos, metales alcalinotérreos, manganeso, cobre, hierro, zinc, cobalto, plomo, plata, níquel, amonio y amonio orgánico; son intermediarios útiles para la síntesis de imidazolinonas herbicidas.2 - [(1-Cyanopropyl) carbamoyl] -5-methoxymethyl nicotinic acids of the formula (I) wherein Z is hydrogen or halogen; Z1 is hydrogen, halogen, cyano or nitro; R1 is C1-C4 alkyl; R2 is C1-C4 alkyl, C3-C6 cycloalkyl or R1 and R2, when taken together with the atom to which they are attached, represent a C3-C6 cycloalkyl group optionally substituted with methyl and R3 is hydrogen or a cation preferably selected from group consisting of alkali metals, alkaline earth metals, manganese, copper, iron, zinc, cobalt, lead, silver, nickel, ammonium and organic ammonium; they are useful intermediates for the synthesis of herbicidal imidazolinones.
Applications Claiming Priority (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US11422308P | 2008-11-13 | 2008-11-13 | |
US11423008P | 2008-11-13 | 2008-11-13 | |
US12061308P | 2008-12-08 | 2008-12-08 | |
US12095708P | 2008-12-09 | 2008-12-09 | |
US14250609P | 2009-01-05 | 2009-01-05 |
Publications (1)
Publication Number | Publication Date |
---|---|
UY32242A true UY32242A (en) | 2010-05-31 |
Family
ID=41507836
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
UY32242A UY32242A (en) | 2008-11-13 | 2009-11-13 | ACIDS OF 2 - [(1-CIANOPROPIL) CARBAMOIL] -5-NICOTINIC METOXIMETHYL AND ITS USE FOR THE MANUFACTURE OF HERBICIDE IMIDAZOLINONES |
Country Status (4)
Country | Link |
---|---|
AR (1) | AR074329A1 (en) |
TW (1) | TW201021702A (en) |
UY (1) | UY32242A (en) |
WO (1) | WO2010055042A1 (en) |
Families Citing this family (9)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP2370410B1 (en) | 2008-11-13 | 2013-10-23 | Basf Se | 2-[(1-cyanopropyl)carbamoyl]-5-chloromethyl nicotinic acids and the use thereof in manufacturing herbicidal imidazolinones |
WO2010054954A1 (en) | 2008-11-13 | 2010-05-20 | Basf Se | Process for manufacturing 5-chloromethyl-2,3-pyridine dicarboxylic acid anhydrides |
WO2010055139A1 (en) | 2008-11-13 | 2010-05-20 | Basf Se | Process for manufacturing substituted 3-pyridylmethyl ammonium bromides |
JP5570524B2 (en) | 2008-12-09 | 2014-08-13 | ビーエーエスエフ ソシエタス・ヨーロピア | Process for producing 5-formyl-pyridine-2,3-dicarboxylic acid ester |
CN105777623A (en) * | 2016-02-29 | 2016-07-20 | 北京颖泰嘉和生物科技股份有限公司 | Method for preparing pyridine side chain methyl quaternary ammonium compound |
WO2018091964A1 (en) | 2016-11-21 | 2018-05-24 | Adama Agan Ltd. | Process for preparing methoxy methyl pyridine dicarboxylate |
CN107216286B (en) * | 2017-06-27 | 2020-03-31 | 江苏省农用激素工程技术研究中心有限公司 | Preparation method of 5-bromomethyl-2, 3-pyridine dimethyl dicarboxylate |
RU2707043C1 (en) * | 2019-03-25 | 2019-11-21 | Акционерное общество "Щелково Агрохим" | Method of producing imazamox herbicide |
CN113620928A (en) * | 2021-08-16 | 2021-11-09 | 辽宁先达农业科学有限公司 | Synthesis method of imazamox sodium salt |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4518780A (en) * | 1982-05-25 | 1985-05-21 | American Cyanamid Company | Process for the preparation of 2-(5,5-disubstituted-4-oxo-2-imidazolin-2-yl)nicotinic acids and quinoline-3-carboxylic acids |
US4719303A (en) * | 1983-11-21 | 1988-01-12 | American Cyanamid Company | Preparation of substituted and unsubstituted 2-[(1-carbamoyl-1,2-dimethylpropyl)-carbamoyl]-3-quinolinecarboxylic, nicotinic and benzoic acids |
US4709036A (en) * | 1985-06-13 | 1987-11-24 | American Cyanamid Company | Process for the preparation of herbicidal 2-(4,4-disubstituted-5-oxo-2-imidazolin-2-yl)benzoic, nicotinic and quinoline-3-carboxylic acids, esters and salts |
US5334576A (en) * | 1986-07-28 | 1994-08-02 | American Cyanamid Company | 5 (and/or 6) substituted 2-(2-imidazolin-2-yl)nicotinic acids, esters and salts, useful as herbicidal agents and novel intermediates for the preparation of said nicotinic acids, esters and salts |
EP0322616A3 (en) * | 1987-12-31 | 1989-10-18 | American Cyanamid Company | Novel 5(and/or 6)substituted 2-(2-imidazolin-2-yl)nicotinic acids, esters and salts, useful as herbicidal agents and nivel intermediates for the preparation of said nicotinic acids, esters and salts |
US5973154A (en) * | 1999-05-03 | 1999-10-26 | American Cyanamid Company | Process for the preparation of chiral imidazolinone herbicides |
US6339158B1 (en) * | 1999-05-03 | 2002-01-15 | American Cyanamid Co. | Process for the preparation of chiral nicotinic, quinolinic or benzoic acid imidazolinone herbicides |
-
2009
- 2009-11-11 WO PCT/EP2009/064950 patent/WO2010055042A1/en active Application Filing
- 2009-11-13 TW TW98138670A patent/TW201021702A/en unknown
- 2009-11-13 UY UY32242A patent/UY32242A/en unknown
- 2009-11-13 AR ARP090104387 patent/AR074329A1/en unknown
Also Published As
Publication number | Publication date |
---|---|
AR074329A1 (en) | 2011-01-05 |
TW201021702A (en) | 2010-06-16 |
WO2010055042A1 (en) | 2010-05-20 |
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