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AR069838A1 - Proceso para la preparacion de derivados de acido 2-amino-5-cianobenzoico - Google Patents

Proceso para la preparacion de derivados de acido 2-amino-5-cianobenzoico

Info

Publication number
AR069838A1
AR069838A1 ARP080105556A ARP080105556A AR069838A1 AR 069838 A1 AR069838 A1 AR 069838A1 AR P080105556 A ARP080105556 A AR P080105556A AR P080105556 A ARP080105556 A AR P080105556A AR 069838 A1 AR069838 A1 AR 069838A1
Authority
AR
Argentina
Prior art keywords
alkyl
formula
compound
independently
preparing
Prior art date
Application number
ARP080105556A
Other languages
English (en)
Inventor
Donald J Dumas
Albert Loren Casalnuovo
Original Assignee
Du Pont
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Du Pont filed Critical Du Pont
Publication of AR069838A1 publication Critical patent/AR069838A1/es

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D401/00Heterocyclic 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
    • C07D401/02Heterocyclic 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
    • C07D401/04Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/14Preparation of carboxylic acid nitriles by reaction of cyanides with halogen-containing compounds with replacement of halogen atoms by cyano groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic 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
    • C07D231/14Heterocyclic 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D231/00Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings
    • C07D231/02Heterocyclic compounds containing 1,2-diazole or hydrogenated 1,2-diazole rings not condensed with other rings
    • C07D231/10Heterocyclic 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
    • C07D231/14Heterocyclic 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
    • C07D231/16Halogen atoms or nitro radicals

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Toxicology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
  • Catalysts (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Reivindicacion 1: Un método para preparar un compuesto caracterizado porque responde a la formula 1 donde: R1 es NHR3 o OR4; R2 es CH3 o CI; R3 es H, C1-4 alquilo ciclopropilo, ciclopropilciclopropilo, ciclopropilmetilo o metilciclopropilo; y R4 es H o C1-4 alquilo; que comprende poner en contacto (1) un compuesto de formula 2 donde X es Br o CI; con (2) un reactivo de cianuro metálico, (3) un reactivo sal de cobre(l), (4) un reactivo sal yoduro y (5) al menos un compuesto de formula 3 donde cada R5, R6, R7, R8 y R9 es independientemente H, C1-12 alquilo, C1-6 alcoxi o NR10R11 y cada R10 y R11 es independientemente H o C1-6 alquilo; o un par de R10 y R11 unidos al mismo nitrogeno se toman juntos como -CH2CH2CH2-, -CH2CH2CH2CH2-, -CH2(CH2)3CH2-, -CH2CH2OCH2CH2-, -CH2CH2N(R16)CH2CH2- o -CH2CH2S(O)nCH2CH2, cada uno opcionalmente sustituido con hasta 4 sustituyentes seleccionados independientemente entre C1-4 alquilo; cada R16 es independientemente H o C1-12 alquilo; y cada n es independientemente 0, 1 o 2; con la salvedad de que cuando X es CI, luego R2 es metilo. Reivindicacion 17: Un método para preparar un compuesto caracterizado porque responde a la formula 4 donde R2 es CH3 o CI; R3 es H, C1-4 alquilo, ciclopropilo, ciclopropilciclopropilo, ciclopropilmetilo, o metilciclopropilo; Z es CR15 o N; R12 es CI, Br, CF3, OCF2H o OCH2CF3; R13 es F, CI o Br; R14 es H, F o CI; y R15 es H, F, CI o Br; usando un compuesto de formula 1 donde R1 es NHR3 o OR4; y R4 es H o C1-4 alquilo; caracterizado por: preparar dicho compuesto de formula 1 mediante el método de la reivindicacion 1.
ARP080105556A 2007-12-19 2008-12-19 Proceso para la preparacion de derivados de acido 2-amino-5-cianobenzoico AR069838A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US845807P 2007-12-19 2007-12-19

Publications (1)

Publication Number Publication Date
AR069838A1 true AR069838A1 (es) 2010-02-24

Family

ID=40521896

Family Applications (1)

Application Number Title Priority Date Filing Date
ARP080105556A AR069838A1 (es) 2007-12-19 2008-12-19 Proceso para la preparacion de derivados de acido 2-amino-5-cianobenzoico

Country Status (15)

Country Link
US (1) US8247570B2 (es)
EP (1) EP2231592B1 (es)
JP (1) JP5398734B2 (es)
KR (1) KR101587296B1 (es)
CN (1) CN101970397B (es)
AR (1) AR069838A1 (es)
AU (1) AU2008343227B2 (es)
BR (1) BRPI0819568B1 (es)
CA (1) CA2709952A1 (es)
CL (1) CL2008003756A1 (es)
CO (1) CO6300860A2 (es)
IL (1) IL206390A (es)
RU (1) RU2010129913A (es)
TW (1) TWI432421B (es)
WO (1) WO2009085816A1 (es)

Families Citing this family (22)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2010535156A (ja) 2007-08-03 2010-11-18 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング ウイルスポリメラーゼ阻害剤
US8476257B2 (en) 2007-12-19 2013-07-02 Boehringer Ingelheim International Gmbh Viral polymerase inhibitors
TWI431000B (zh) 2008-03-05 2014-03-21 Du Pont 製備2-胺基-5-氰基苯甲酸衍生物之方法
TW201247631A (en) 2011-04-28 2012-12-01 Du Pont Herbicidal pyrazinones
DK2729444T3 (en) * 2011-07-08 2017-12-04 Bayer Ip Gmbh METHOD FOR PREPARING 2-AMINO-5-CYANO-N, 3-DIMETHYLBENZAMIDE
EP2742027A1 (en) 2011-08-12 2014-06-18 Basf Se N-thio-anthranilamide compounds and their use as pesticides
AR087515A1 (es) 2011-08-12 2014-03-26 Basf Se Compuestos de n-tio-antranilamida y sus usos como plaguicidas
MX2014001609A (es) 2011-08-12 2014-05-01 Basf Se Compuestos de n-tio-antranilamida y sus usos como plaguicidas.
IN2014CN01025A (es) 2011-08-12 2015-04-10 Basf Se
BR112014015531A8 (pt) 2011-12-21 2017-07-04 Basf Se compostos, composição agrícola ou veterinária, métodos, semente e utilização d eum composto
WO2013113789A1 (en) 2012-02-02 2013-08-08 Basf Se N-thio-anthranilamide compounds and their use as pesticides
CN109970707A (zh) 2012-02-07 2019-07-05 拜耳知识产权有限责任公司 取代的邻氨基苯甲酸衍生物的制备方法
CN104003976B (zh) * 2014-05-07 2016-03-16 肇庆市真格生物科技有限公司 多取代吡啶基吡唑酰胺及其制备方法和用途
TWI678354B (zh) * 2014-05-29 2019-12-01 新加坡商艾佛艾姆希農業新加坡有限公司 藉空氣氧化製備3-甲基-2-硝基苯甲酸之製程
CN105461683B (zh) * 2015-11-18 2019-01-15 江苏省农用激素工程技术研究中心有限公司 邻氨基苯甲酰胺化合物的制备方法
WO2020117493A1 (en) * 2018-12-03 2020-06-11 Fmc Corporation Method for preparing n-phenylpyrazole-1-carboxamides
WO2020170092A1 (en) 2019-02-18 2020-08-27 Pi Industries Ltd. A process for preparing anthranilic diamides and intermediates thereof
US11718584B2 (en) 2019-02-22 2023-08-08 Pi Industries Ltd. Process for the synthesis anthranilic diamide compounds and intermediates thereof
TW202222162A (zh) 2020-09-26 2022-06-16 印度商皮埃企業有限公司 鄰胺苯甲酸/醯胺化合物及其中間體的合成方法
EP4380363A1 (en) 2021-08-05 2024-06-12 Syngenta Crop Protection AG Method for controlling diamide resistant pests & compounds therefor
WO2024038436A1 (en) 2022-08-16 2024-02-22 Adama Makhteshim Ltd. Process for preparing cyantraniliprole via amino-cyano-benzene derivative
WO2024116197A1 (en) * 2022-11-30 2024-06-06 Natco Pharma Limited An improved process for the preparation of intermediate of cyantraniliprole

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP2005534700A (ja) 2002-08-02 2005-11-17 マサチューセッツ インスティテュート オブ テクノロジー 銅触媒による炭素−ヘテロ原子および炭素−炭素結合の形成
IN243219B (es) 2003-01-28 2010-10-01 Du Pont
MY140912A (en) * 2004-07-26 2010-01-29 Du Pont Mixtures of anthranilamide invertebrate pest control agents
TWI363756B (en) * 2004-12-07 2012-05-11 Du Pont Method for preparing n-phenylpyrazole-1-carboxamides
DE102006042439A1 (de) 2006-09-09 2008-03-27 Saltigo Gmbh Verfahren zur katalytischen Herstellung von aromatischen oder heteroaromatischen Nitrilen
TWI415827B (zh) * 2006-12-21 2013-11-21 Du Pont 製備2-胺基-5-氰基苯甲酸衍生物之方法
TWI431000B (zh) 2008-03-05 2014-03-21 Du Pont 製備2-胺基-5-氰基苯甲酸衍生物之方法

Also Published As

Publication number Publication date
TWI432421B (zh) 2014-04-01
CO6300860A2 (es) 2011-07-21
AU2008343227A1 (en) 2009-07-09
CN101970397A (zh) 2011-02-09
CL2008003756A1 (es) 2009-11-27
KR20100098443A (ko) 2010-09-06
TW200934770A (en) 2009-08-16
EP2231592B1 (en) 2016-02-17
JP5398734B2 (ja) 2014-01-29
BRPI0819568B1 (pt) 2018-02-06
AU2008343227B2 (en) 2013-08-01
KR101587296B1 (ko) 2016-01-21
CN101970397B (zh) 2014-04-16
US20120130080A1 (en) 2012-05-24
IL206390A (en) 2014-06-30
EP2231592A1 (en) 2010-09-29
IL206390A0 (en) 2010-12-30
JP2011507872A (ja) 2011-03-10
US8247570B2 (en) 2012-08-21
BRPI0819568A2 (pt) 2017-07-04
RU2010129913A (ru) 2012-01-27
CA2709952A1 (en) 2009-07-09
WO2009085816A1 (en) 2009-07-09

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