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AR123526A1 - Un proceso para la síntesis de compuestos antranílicos de ácido / amida e intermediarios de los mismos - Google Patents

Un proceso para la síntesis de compuestos antranílicos de ácido / amida e intermediarios de los mismos

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Publication number
AR123526A1
AR123526A1 ARP210102573A ARP210102573A AR123526A1 AR 123526 A1 AR123526 A1 AR 123526A1 AR P210102573 A ARP210102573 A AR P210102573A AR P210102573 A ARP210102573 A AR P210102573A AR 123526 A1 AR123526 A1 AR 123526A1
Authority
AR
Argentina
Prior art keywords
formula
compound
hydrogen
alkyl
group
Prior art date
Application number
ARP210102573A
Other languages
English (en)
Inventor
Tridib Mahapatra
Pranab Kumar Patra
Sanjib Mal
Raju Sharma
Alexander G M Klausener
Original Assignee
Pi Industries Ltd
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 Pi Industries Ltd filed Critical Pi Industries Ltd
Publication of AR123526A1 publication Critical patent/AR123526A1/es

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    • 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
    • C07C221/00Preparation of compounds containing amino groups and doubly-bound oxygen atoms bound to the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C225/00Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones
    • C07C225/22Compounds containing amino groups and doubly—bound oxygen atoms bound to the same carbon skeleton, at least one of the doubly—bound oxygen atoms not being part of a —CHO group, e.g. amino ketones having amino groups bound to carbon atoms of six-membered aromatic rings of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/02Formation of carboxyl groups in compounds containing amino groups, e.g. by oxidation of amino alcohols
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C227/14Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof
    • C07C227/18Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton from compounds containing already amino and carboxyl groups or derivatives thereof by reactions involving amino or carboxyl groups, e.g. hydrolysis of esters or amides, by formation of halides, salts or esters
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C229/00Compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • C07C229/52Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton
    • C07C229/54Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton with amino and carboxyl groups bound to carbon atoms of the same non-condensed six-membered aromatic ring
    • C07C229/56Compounds containing amino and carboxyl groups bound to the same carbon skeleton having amino and carboxyl groups bound to carbon atoms of six-membered aromatic rings of the same carbon skeleton with amino and carboxyl groups bound to carbon atoms of the same non-condensed six-membered aromatic ring with amino and carboxyl groups bound in ortho-position
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/02Preparation of carboxylic acid amides from carboxylic acids or from esters, anhydrides, or halides thereof by reaction with ammonia or amines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C231/00Preparation of carboxylic acid amides
    • C07C231/10Preparation of carboxylic acid amides from compounds not provided for in groups C07C231/02 - C07C231/08
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C237/00Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups
    • C07C237/28Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton
    • C07C237/30Carboxylic acid amides, the carbon skeleton of the acid part being further substituted by amino groups having the carbon atom of at least one of the carboxamide groups bound to a carbon atom of a non-condensed six-membered aromatic ring of the carbon skeleton having the nitrogen atom of the carboxamide group bound to hydrogen atoms or to acyclic carbon atoms
    • 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
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C253/00Preparation of carboxylic acid nitriles
    • C07C253/30Preparation of carboxylic acid nitriles by reactions not involving the formation of cyano groups
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C255/00Carboxylic acid nitriles
    • C07C255/49Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton
    • C07C255/58Carboxylic acid nitriles having cyano groups bound to carbon atoms of six-membered aromatic rings of a carbon skeleton containing cyano groups and singly-bound nitrogen atoms, not being further bound to other hetero atoms, bound to the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D265/00Heterocyclic compounds containing six-membered rings having one nitrogen atom and one oxygen atom as the only ring hetero atoms
    • C07D265/041,3-Oxazines; Hydrogenated 1,3-oxazines
    • C07D265/121,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems
    • C07D265/141,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring
    • C07D265/241,3-Oxazines; Hydrogenated 1,3-oxazines condensed with carbocyclic rings or ring systems condensed with one six-membered ring with hetero atoms directly attached in positions 2 and 4
    • C07D265/26Two oxygen atoms, e.g. isatoic anhydride
    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02PCLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
    • Y02P20/00Technologies relating to chemical industry
    • Y02P20/50Improvements relating to the production of bulk chemicals
    • Y02P20/55Design of synthesis routes, e.g. reducing the use of auxiliary or protecting groups

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Toxicology (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Hydrogenated Pyridines (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

Reivindicación 1: Un proceso para la preparación de un compuesto de fórmula (Z) o su sal, en donde, R¹ y R² se seleccionan independientemente entre el grupo que comprende hidrógeno, halógeno, alquilo C₁₋₄, haloalquilo C₁₋₄ o cicloalquilo C₃₋₆; R³ se selecciona entre el grupo que comprende hidrógeno, halógeno, ciano, haloalquilo C₁₋₄ o cicloalquilo C₃₋₆; R se selecciona entre el grupo que comprende hidrógeno o COR¹¹; en donde R¹¹ se selecciona entre el grupo que comprende alcoxi C₁₋₄, O-bencilo u O-fenilo; R¹⁰ se selecciona entre el grupo que comprende CX₃, OR⁹ o NR⁴ᵃR⁴ᵇ; en donde X representa halógeno; R⁹ se selecciona entre el grupo que comprende hidrógeno o alquilo C₁₋₄; R⁴ᵃ y R⁴ᵇ se seleccionan independientemente entre el grupo que comprende hidrógeno, alquilo C₁₋₄, cicloalquilo C₃₋₆, cicloalquil C₃₋₆-alquilo C₁₋₄; o NR⁴ᵃR⁴ᵇ representa -N=S(R⁷R⁸)=(O)ₙ; n representa un número entero de 0 - 1; R⁷ y R⁸ se seleccionan independientemente entre el grupo que comprende alquilo C₁₋₄, haloalquilo C₁₋₄, cicloalquilo C₃₋₆ o cicloalquil C₃₋₆-alquilo C₁₋₄; que comprende una o más de las siguientes etapas de a) a f): a) hacer reaccionar una anilina sustituida de fórmula (II) con un trihaloacetonitrilo de fórmula (IX) para obtener un compuesto de fórmula (Z), en donde R¹⁰ es CX₃; o i. hacer reaccionar una anilina sustituida de fórmula (II) con acetonitrilo para obtener una 2-aminoacetofenona sustituida de fórmula (III), y ii. halogenar el compuesto de fórmula (III) usando un reactivo de halogenación para obtener un compuesto de fórmula (Z), en donde R¹⁰ es CX₃; b) hidrolizar el compuesto de fórmula (Z), en donde R¹⁰ es CX₃, con una base o un ácido para obtener un compuesto de fórmula (Z), en donde R¹⁰ es OR⁹ y R⁹ es hidrógeno; o convertir el compuesto de fórmula (III) en un compuesto de fórmula (Z), en donde R¹⁰ es OR⁹ y R⁹ es hidrógeno, sin aislar el compuesto de fórmula (Z) en donde R¹⁰ es CX₃; c) convertir el compuesto de fórmula (Z), en donde R¹⁰ es CX₃, en un compuesto de fórmula (Z), en donde R¹⁰ es OR⁹ y R⁹ es alquilo; con una base o un ácido y en presencia de un disolvente alcohólico; d) hacer reaccionar el compuesto de fórmula (Z), en donde R¹⁰ es CX₃, con una amina sustituida de fórmula (VIII) para obtener un compuesto de fórmula (Z), en donde R¹⁰ es NR⁴ᵃR⁴ᵇ; e) hacer reaccionar el compuesto de fórmula (Z), en donde R¹⁰ es OR⁹ y R⁹ es hidrógeno; con una amina sustituida de fórmula (VIII) y un reactivo de acoplamiento o reactivos de halogenación y opcionalmente en presencia de una base para obtener un compuesto de fórmula (Z), en donde R¹⁰ es NR⁴ᵃR⁴ᵇ; o i. hacer reaccionar el compuesto de fórmula (Z), en donde R¹⁰ es OR⁹ y R⁹ es hidrógeno; con un ácido para obtener un compuesto de fórmula (IVa), y ii. hacer reaccionar el compuesto de fórmula (IVa) con una amina sustituida de fórmula (VIII) para obtener compuesto de fórmula (Z), en donde R¹⁰ es NR⁴ᵃR⁴ᵇ; f) hacer reaccionar el compuesto de fórmula (Z), en donde R¹⁰ es OR⁹ y R⁹ es alquilo C₁₋₄; con una amina sustituida de fórmula (VIII) en presencia de una base para obtener un compuesto de fórmula (Z), en donde R¹⁰ es NR⁴ᵃR⁴ᵇ; en donde R, R¹, R², R³, R⁴ᵃ y R⁴ᵇ son como se han definido anteriormente.
ARP210102573A 2020-09-17 2021-09-16 Un proceso para la síntesis de compuestos antranílicos de ácido / amida e intermediarios de los mismos AR123526A1 (es)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IN202011040285 2020-09-17

Publications (1)

Publication Number Publication Date
AR123526A1 true AR123526A1 (es) 2022-12-14

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Family Applications (1)

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ARP210102573A AR123526A1 (es) 2020-09-17 2021-09-16 Un proceso para la síntesis de compuestos antranílicos de ácido / amida e intermediarios de los mismos

Country Status (10)

Country Link
US (1) US20230339844A1 (es)
EP (1) EP4214188A1 (es)
KR (1) KR20230069945A (es)
CN (1) CN116670115A (es)
AR (1) AR123526A1 (es)
CA (1) CA3191827A1 (es)
IL (1) IL301271A (es)
MX (1) MX2023003173A (es)
UY (1) UY39425A (es)
WO (1) WO2022058916A1 (es)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2024038436A1 (en) 2022-08-16 2024-02-22 Adama Makhteshim Ltd. Process for preparing cyantraniliprole via amino-cyano-benzene derivative
WO2024105700A1 (en) * 2022-11-18 2024-05-23 Pi Industries Ltd. A method for the synthesis of anthranilic amide compounds and intermediates thereof
WO2025057193A1 (en) * 2023-09-13 2025-03-20 Pi Industries Ltd. A method for the synthesis of substituted anthranilic amide compounds, intermediates and salts thereof
WO2025134143A1 (en) 2023-12-19 2025-06-26 Pi Industries Ltd. A method for the synthesis of substituted anthranilic amide compounds, intermediates and salts thereof

Family Cites Families (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
AR036872A1 (es) 2001-08-13 2004-10-13 Du Pont Compuesto de antranilamida, composicion que lo comprende y metodo para controlar una plaga de invertebrados
MY142967A (en) 2001-08-13 2011-01-31 Du Pont Method for controlling particular insect pests by applying anthranilamide compounds
IN243219B (es) 2003-01-28 2010-10-01 Du Pont
EP1717237B1 (en) 2004-02-18 2010-12-29 Ishihara Sangyo Kaisha, Ltd. Anthranilamides, process for the production thereof, and pest controllers containing the same
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
JP2009543861A (ja) * 2006-07-19 2009-12-10 イー・アイ・デュポン・ドウ・ヌムール・アンド・カンパニー 3−置換2−アミノ−5−ハロベンズアミドの製造方法
WO2010069502A2 (de) 2008-12-18 2010-06-24 Bayer Cropscience Ag Tetrazolsubstituierte anthranilsäureamide als pestizide
DK2582694T3 (en) 2010-06-15 2015-10-26 Bayer Ip Gmbh Method of producing tetrazol-substituted anthranilsyrediamidderivater and new crystalline modification of these derivatives
CN103328434A (zh) 2011-01-28 2013-09-25 纳幕尔杜邦公司 制备2-氨基苯甲酰胺衍生物的方法
JP6124012B2 (ja) 2011-05-26 2017-05-10 日産化学工業株式会社 1−(2−アミノ−置換フェニル)−2−ハロ−2,2−ジフルオロエタノン化合物及び1−(置換フェニル)−2−ハロ−2,2−ジフルオロエタノン化合物の製造方法
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Publication number Publication date
US20230339844A1 (en) 2023-10-26
TW202222773A (zh) 2022-06-16
WO2022058916A1 (en) 2022-03-24
UY39425A (es) 2022-03-31
CN116670115A (zh) 2023-08-29
CA3191827A1 (en) 2022-03-24
IL301271A (en) 2023-05-01
MX2023003173A (es) 2023-04-12
EP4214188A1 (en) 2023-07-26
KR20230069945A (ko) 2023-05-19

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