RU2018144344A - Синтез 6-арил-4-аминопиколинатов и 2-арил-6-аминопиримидин-4-карбоксилатов прямым сочетанием сузуки - Google Patents

Синтез 6-арил-4-аминопиколинатов и 2-арил-6-аминопиримидин-4-карбоксилатов прямым сочетанием сузуки Download PDF

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RU2018144344A
RU2018144344A RU2018144344A RU2018144344A RU2018144344A RU 2018144344 A RU2018144344 A RU 2018144344A RU 2018144344 A RU2018144344 A RU 2018144344A RU 2018144344 A RU2018144344 A RU 2018144344A RU 2018144344 A RU2018144344 A RU 2018144344A
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catalyst
alkyl
suzuki coupling
alkoxy
aryl
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RU2018144344A
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Russian (ru)
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RU2018144344A3 (cg-RX-API-DMAC10.html
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Джейсон С. ФИСК
Сяоюн ЛИ
Марк МЮЛЬФЕЛЬД
Роберт С. БАУМАН
Джоссиан Оппенхаймер
Сыюй ТУ
Марк А. НИТЦ
Ритам ЧАКРАБАРТИ
Шон Д. ФЕЙСТ
Джеймс В. РИНГЕР
Рональд Б. ЛЕНГ
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ДАУ АГРОСАЙЕНСИЗ ЭлЭлСи
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Publication of RU2018144344A3 publication Critical patent/RU2018144344A3/ru

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    • 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
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J35/00—Catalysts, in general, characterised by their form or physical properties
    • B01J35/30—Catalysts, in general, characterised by their form or physical properties characterised by their physical properties
    • B01J35/391—Physical properties of the active metal ingredient
    • 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
    • C07D213/79—Acids; Esters
    • 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
    • C07D213/90—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 more than three double bonds between ring members or between ring members and non-ring members
    • 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
    • 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
    • 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
    • C07D239/32—One oxygen, sulfur or nitrogen atom
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
    • B01J2231/40—Substitution reactions at carbon centres, e.g. C-C or C-X, i.e. carbon-hetero atom, cross-coupling, C-H activation or ring-opening reactions
    • B01J2231/42—Catalytic cross-coupling, i.e. connection of previously not connected C-atoms or C- and X-atoms without rearrangement
    • B01J2231/4205—C-C cross-coupling, e.g. metal catalyzed or Friedel-Crafts type
    • B01J2231/4211—Suzuki-type, i.e. RY + R'B(OR)2, in which R, R' are optionally substituted alkyl, alkenyl, aryl, acyl and Y is the leaving group
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
    • B01J2531/80—Complexes comprising metals of Group VIII as the central metal
    • B01J2531/82—Metals of the platinum group
    • B01J2531/824—Palladium
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
    • B01J31/02—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides
    • B01J31/04—Catalysts comprising hydrides, coordination complexes or organic compounds containing organic compounds or metal hydrides containing carboxylic acids or their salts

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Pyridine Compounds (AREA)
RU2018144344A 2016-05-19 2017-05-19 Синтез 6-арил-4-аминопиколинатов и 2-арил-6-аминопиримидин-4-карбоксилатов прямым сочетанием сузуки RU2018144344A (ru)

Applications Claiming Priority (5)

Application Number Priority Date Filing Date Title
US201662338562P 2016-05-19 2016-05-19
US62/338562 2016-05-19
US201662416811P 2016-11-03 2016-11-03
US62/416811 2016-11-03
PCT/US2017/033489 WO2017201377A1 (en) 2016-05-19 2017-05-19 Synthesis of 6-aryl-4-aminopicolinates and 2-aryl-6-aminopyrimidine-4-carboxylates by direct suzuki coupling

Publications (2)

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RU2018144344A true RU2018144344A (ru) 2020-06-19
RU2018144344A3 RU2018144344A3 (cg-RX-API-DMAC10.html) 2021-02-18

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US (3) US10087164B2 (cg-RX-API-DMAC10.html)
EP (1) EP3458442B1 (cg-RX-API-DMAC10.html)
JP (2) JP7113762B2 (cg-RX-API-DMAC10.html)
KR (1) KR20190007048A (cg-RX-API-DMAC10.html)
CN (1) CN109415319A (cg-RX-API-DMAC10.html)
AU (2) AU2017268424B2 (cg-RX-API-DMAC10.html)
BR (1) BR112018073348B8 (cg-RX-API-DMAC10.html)
CA (1) CA3023935A1 (cg-RX-API-DMAC10.html)
IL (1) IL263075A (cg-RX-API-DMAC10.html)
MX (1) MX2018014174A (cg-RX-API-DMAC10.html)
RU (1) RU2018144344A (cg-RX-API-DMAC10.html)
WO (1) WO2017201377A1 (cg-RX-API-DMAC10.html)

Families Citing this family (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA3023935A1 (en) * 2016-05-19 2017-11-23 Dow Agrosciences Llc Synthesis of 6-aryl-4-aminopicolinates and 2-aryl-6-aminopyrimidine-4-carboxylates by direct suzuki coupling
CN113015721B (zh) * 2018-09-19 2025-07-25 科迪华农业科技有限责任公司 毒莠定卤素类似物的制备
WO2020133403A1 (zh) * 2018-12-29 2020-07-02 青岛清原化合物有限公司 取代的嘧啶芳酯衍生物及其制备方法、除草组合物和应用
BR112022018513A2 (pt) 2020-03-18 2022-11-01 Corteva Agriscience Llc Síntese melhorada de 6-aril-4-aminopicolinatos
WO2021188639A1 (en) 2020-03-18 2021-09-23 Corteva Agriscience Llc Improved synthesis of 4-amino-6-(heterocyclic)picolinates
CN115551833A (zh) * 2020-05-11 2022-12-30 科迪华农业科技有限责任公司 具有杀有害生物活性的化合物的制备
WO2023248174A1 (en) * 2022-06-22 2023-12-28 Hetero Labs Limited An improved process for preparation of voxelotor
CN115819334B (zh) * 2022-06-28 2025-03-18 安徽众邦生物工程有限公司 一种氯氟吡啶酯的制备方法
EP4762927A1 (en) 2024-12-20 2026-06-24 Bayer Aktiengesellschaft Herbicidal combinations

Family Cites Families (25)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
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
US7300907B2 (en) * 2006-01-13 2007-11-27 Dow Agrosciences Llc 2-(Poly-substituted aryl)-6-amino-5-halo-4-pyrimidinecarboxylic acids and their use as herbicides
CN101778829B (zh) * 2007-08-13 2013-07-31 陶氏益农公司 2-(2-氟-取代的苯基)-6-氨基-5-氯-4-嘧啶羧酸衍生物及其作为除草剂的用途
AU2008293462B2 (en) * 2007-08-30 2013-08-15 Corteva Agriscience Llc 2-(substituted phenyl)-6-amino-5-alkoxy, thioalkoxy and aminoalkyl-4-pyrimidinecarboxylates and their use as herbicides
EP2327694B1 (en) * 2007-10-02 2013-07-24 Dow AgroSciences LLC Substituted 4-amino-picolinic acids and their use as herbicides
CA2720848C (en) * 2008-04-18 2014-02-11 Dow Agrosciences Llc 2-(substituted phenyl)-6-hydroxy or alkoxy-5-substituted-4-pyrimidinecarboxylates and their use as herbicides
GB0808664D0 (en) * 2008-05-13 2008-06-18 Syngenta Ltd Chemical compounds
GB0902474D0 (en) * 2009-02-13 2009-04-01 Syngenta Ltd Chemical compounds
GB0907625D0 (en) * 2009-05-01 2009-06-10 Syngenta Ltd Method of controlling undesired vegetation
TWI547482B (zh) 2011-01-25 2016-09-01 陶氏農業科學公司 增加可回收之3-氯-4,5,6-三氟-2-氰吡啶之量的改良方法
EP2667717A4 (en) * 2011-01-25 2015-10-14 Dow Agrosciences Llc 6-AMINO-2-SUBSTITUTED-5-VINYLSILYLPYRIMIDIN-4-CARBOXYLIC ACIDS AND ESTERS AND 4-AMINO-6-SUBSTITUTED-3-VINYLSILYLPYRIDINE-2-CARBOXYLIC ESTERS AS HERBICIDES
TWI529163B (zh) * 2011-01-25 2016-04-11 陶氏農業科學公司 用於製備4-胺基-5-氟-3-鹵素-6-(經取代之)吡啶甲酸酯的方法
TWI592401B (zh) * 2011-01-25 2017-07-21 陶氏農業科學公司 用於製備4-胺基-3-氯-5-氟-6-(經取代的)吡啶甲酸酯的方法(一)
EP2736897B1 (de) * 2011-07-27 2015-11-25 Bayer Intellectual Property GmbH Substituierte picolinsäuren und pyrimidin-4-carbonsäuren, verfahren zu deren herstellung sowie deren verwendung als herbizide und pflanzenwachstumsregulatoren
JP6068501B2 (ja) 2011-12-30 2017-01-25 ダウ アグロサイエンシィズ エルエルシー (4−クロロ−2−フルオロ−3−置換フェニル)ボロネートを単離する方法ならびにそれを使用する方法
NZ627192A (en) 2011-12-30 2015-09-25 Dow Agrosciences Llc Methods of producing methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate
AR091856A1 (es) * 2012-07-24 2015-03-04 Dow Agrosciences Llc Proceso para la preparacion de 4-amino-5-fluor-3-halo-6-(substituido) picolinatos
CN102875456B (zh) * 2012-10-23 2013-12-11 西华大学 3,6-二氯-2-氨基吡啶的化学合成方法
US20140170058A1 (en) * 2012-12-13 2014-06-19 Dow Agrosciences Llc Process for the removal of palladium from 4-amino-3-halo-5-fluoro-6-(aryl) pyridine-2-carboxylates and 4-amino-3-halo-6-(aryl)pyridine-2-carboxylates
US9113629B2 (en) 2013-03-15 2015-08-25 Dow Agrosciences Llc 4-amino-6-(4-substituted-phenyl)-picolinates and 6-amino-2-(4-substituted-phenyl)-pyrimidine-4-carboxylates and their use as herbicides
US9637505B2 (en) * 2013-03-15 2017-05-02 Dow Agrosciences Llc 4-amino-6-(heterocyclic)picolinates and 6-amino-2-(heterocyclic)pyrimidine-4-carboxylates and their use as herbicides
KR20210125575A (ko) 2013-03-15 2021-10-18 코르테바 애그리사이언스 엘엘씨 4-아미노-6-(헤테로시클릭)피콜리네이트 및 6-아미노-2-(헤테로시클릭)피리미딘-4-카르복실레이트 및 제초제로서의 그의 용도
CN105208859A (zh) * 2013-03-15 2015-12-30 美国陶氏益农公司 作为除草剂的新型的4-氨基吡啶和6-氨基嘧啶羧酸酯
EP2970186B1 (en) 2013-03-15 2020-06-10 Dow AgroSciences LLC 4-amino-6-(heterocyclic)picolinates and 6-amino-2-(heterocyclic) pyrimidine-4-carboxylates and their use as herbicides
CA3023935A1 (en) * 2016-05-19 2017-11-23 Dow Agrosciences Llc Synthesis of 6-aryl-4-aminopicolinates and 2-aryl-6-aminopyrimidine-4-carboxylates by direct suzuki coupling

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CN109415319A (zh) 2019-03-01
JP2022141912A (ja) 2022-09-29
US10544121B2 (en) 2020-01-28
US10570114B2 (en) 2020-02-25
EP3458442A1 (en) 2019-03-27
EP3458442B1 (en) 2022-12-28
CA3023935A1 (en) 2017-11-23
KR20190007048A (ko) 2019-01-21
JP7113762B2 (ja) 2022-08-05
JP2019516708A (ja) 2019-06-20
US10087164B2 (en) 2018-10-02
WO2017201377A1 (en) 2017-11-23
NZ747932A (en) 2022-03-25
US20180334445A1 (en) 2018-11-22
IL263075A (en) 2018-12-31
EP3458442A4 (en) 2020-04-22
AU2017268424B2 (en) 2021-07-15
AU2021203233A1 (en) 2021-06-10
BR112018073348A2 (pt) 2019-03-06
BR112018073348B1 (pt) 2023-01-24
AU2017268424A1 (en) 2018-11-22
US20180334444A1 (en) 2018-11-22
MX2018014174A (es) 2019-03-14
BR112018073348B8 (pt) 2023-05-16
US20170334878A1 (en) 2017-11-23
RU2018144344A3 (cg-RX-API-DMAC10.html) 2021-02-18

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