NZ627192A - Methods of producing methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate - Google Patents
Methods of producing methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylateInfo
- Publication number
- NZ627192A NZ627192A NZ627192A NZ62719212A NZ627192A NZ 627192 A NZ627192 A NZ 627192A NZ 627192 A NZ627192 A NZ 627192A NZ 62719212 A NZ62719212 A NZ 62719212A NZ 627192 A NZ627192 A NZ 627192A
- Authority
- NZ
- New Zealand
- Prior art keywords
- chloro
- methyl
- carboxylate
- fluoro
- pyridine
- 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
- C07D213/79—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
- C07D213/02—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
- C07D213/803—Processes of preparation
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic Table
- C07F5/02—Boron compounds
- C07F5/025—Boronic and borinic acid compounds
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Pyridine Compounds (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US201161582166P | 2011-12-30 | 2011-12-30 | |
| PCT/US2012/072071 WO2013102078A1 (en) | 2011-12-30 | 2012-12-28 | Methods of producing methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NZ627192A true NZ627192A (en) | 2015-09-25 |
Family
ID=48695351
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ627192A NZ627192A (en) | 2011-12-30 | 2012-12-28 | Methods of producing methyl 4-amino-3-chloro-6-(4-chloro-2-fluoro-3-methoxyphenyl)pyridine-2-carboxylate |
Country Status (16)
| Country | Link |
|---|---|
| US (1) | US8754110B2 (enExample) |
| EP (1) | EP2797890B1 (enExample) |
| JP (1) | JP6092250B2 (enExample) |
| KR (1) | KR102065543B1 (enExample) |
| AR (1) | AR089628A1 (enExample) |
| AU (1) | AU2012362268B2 (enExample) |
| BR (1) | BR112014015962B8 (enExample) |
| CA (1) | CA2861611C (enExample) |
| CO (1) | CO7010843A2 (enExample) |
| IL (1) | IL233412B (enExample) |
| IN (1) | IN2014DN05767A (enExample) |
| MX (1) | MX340947B (enExample) |
| NZ (1) | NZ627192A (enExample) |
| PL (1) | PL2797890T3 (enExample) |
| RU (1) | RU2616621C2 (enExample) |
| WO (1) | WO2013102078A1 (enExample) |
Families Citing this family (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP2797933B1 (en) * | 2011-12-30 | 2017-08-16 | Dow AgroSciences LLC | Methods of forming 4-chloro-2-fluoro-3-substituted-phenylboronic acid pinacol esters and methods of using the same |
| 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 |
| EP3041849A4 (en) | 2013-09-05 | 2017-04-19 | Dow AgroSciences LLC | Methods for producing borylated arenes |
| TW201625354A (zh) | 2014-06-16 | 2016-07-16 | 陶氏農業科學公司 | 用於製備氧硼基化芳烴之方法 |
| MX2017011447A (es) * | 2015-05-22 | 2018-06-18 | Dow Agrosciences Llc | Recuperacion y / o reuso de un catalizador de paladio despues de una reaccion de acoplamiento suzuki. |
| CN105851037B (zh) * | 2016-05-17 | 2018-09-07 | 陕西上格之路生物科学有限公司 | 一种含氟氯吡啶酯的三元除草组合物 |
| US10087164B2 (en) | 2016-05-19 | 2018-10-02 | Dow Agrosciences Llc | Synthesis of 6-aryl-4-aminopicolinates and 2-aryl-6-aminopyrimidine-4-carboxylates by direct Suzuki coupling |
Family Cites Families (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US7145040B2 (en) * | 2004-07-02 | 2006-12-05 | Bristol-Myers Squibb Co. | Process for the preparation of amino acids useful in the preparation of peptide receptor modulators |
| WO2007082076A1 (en) | 2006-01-13 | 2007-07-19 | Dow Agrosciences Llc | 2-(poly-substituted aryl)-6-amino-5-halo-4-pyrimidinecarboxylic acids and their use as herbicides |
| CN101360713B (zh) * | 2006-01-13 | 2012-08-15 | 美国陶氏益农公司 | 6-(多取代芳基)-4-氨基吡啶甲酸酯及其作为除草剂的用途 |
| PL2327694T3 (pl) * | 2007-10-02 | 2013-12-31 | Dow Agrosciences Llc | Podstawione kwasy 4-aminopikolinowe i ich zastosowanie jako herbicydów |
| CN105254652A (zh) * | 2008-01-11 | 2016-01-20 | 陶氏益农公司 | 对1-氟-2-取代的-3-氯苯选择性脱质子化和官能化的方法 |
| GB0902474D0 (en) * | 2009-02-13 | 2009-04-01 | Syngenta Ltd | Chemical compounds |
| US8252938B2 (en) * | 2009-06-08 | 2012-08-28 | Dow Agrosciences, Llc. | Process for the preparation of 6-(aryl)-4-aminopicolinates |
| CA2780203A1 (en) * | 2009-11-19 | 2011-05-26 | Lexicon Pharmaceuticals, Inc. | Process for the preparation of substituted phenylalanines |
| EP2797933B1 (en) * | 2011-12-30 | 2017-08-16 | Dow AgroSciences LLC | Methods of forming 4-chloro-2-fluoro-3-substituted-phenylboronic acid pinacol esters and methods of using the same |
| 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 |
-
2012
- 2012-12-28 BR BR112014015962A patent/BR112014015962B8/pt active IP Right Grant
- 2012-12-28 KR KR1020147020894A patent/KR102065543B1/ko active Active
- 2012-12-28 AU AU2012362268A patent/AU2012362268B2/en active Active
- 2012-12-28 PL PL12862450T patent/PL2797890T3/pl unknown
- 2012-12-28 JP JP2014550511A patent/JP6092250B2/ja active Active
- 2012-12-28 CA CA2861611A patent/CA2861611C/en active Active
- 2012-12-28 WO PCT/US2012/072071 patent/WO2013102078A1/en not_active Ceased
- 2012-12-28 RU RU2014131451A patent/RU2616621C2/ru active
- 2012-12-28 MX MX2014008019A patent/MX340947B/es active IP Right Grant
- 2012-12-28 US US13/729,995 patent/US8754110B2/en active Active
- 2012-12-28 EP EP12862450.9A patent/EP2797890B1/en active Active
- 2012-12-28 NZ NZ627192A patent/NZ627192A/en unknown
- 2012-12-28 IN IN5767DEN2014 patent/IN2014DN05767A/en unknown
-
2013
- 2013-01-02 AR ARP130100011A patent/AR089628A1/es active IP Right Grant
-
2014
- 2014-06-26 IL IL233412A patent/IL233412B/en active IP Right Grant
- 2014-07-18 CO CO14156063A patent/CO7010843A2/es unknown
Also Published As
| Publication number | Publication date |
|---|---|
| AU2012362268B2 (en) | 2016-11-17 |
| RU2014131451A (ru) | 2016-02-20 |
| BR112014015962B1 (pt) | 2019-12-17 |
| JP6092250B2 (ja) | 2017-03-08 |
| CA2861611C (en) | 2020-04-21 |
| RU2616621C2 (ru) | 2017-04-18 |
| EP2797890A4 (en) | 2015-09-23 |
| BR112014015962A2 (pt) | 2017-06-13 |
| KR20140117444A (ko) | 2014-10-07 |
| EP2797890A1 (en) | 2014-11-05 |
| IL233412A0 (en) | 2014-08-31 |
| PL2797890T3 (pl) | 2017-06-30 |
| US8754110B2 (en) | 2014-06-17 |
| WO2013102078A1 (en) | 2013-07-04 |
| US20130172566A1 (en) | 2013-07-04 |
| JP2015504059A (ja) | 2015-02-05 |
| CA2861611A1 (en) | 2013-07-04 |
| AU2012362268A1 (en) | 2014-07-31 |
| AR089628A1 (es) | 2014-09-03 |
| KR102065543B1 (ko) | 2020-01-13 |
| BR112014015962B8 (pt) | 2022-10-11 |
| MX340947B (es) | 2016-08-01 |
| MX2014008019A (es) | 2014-12-08 |
| EP2797890B1 (en) | 2016-10-05 |
| CO7010843A2 (es) | 2014-07-31 |
| BR112014015962A8 (pt) | 2017-07-04 |
| IN2014DN05767A (enExample) | 2015-04-10 |
| IL233412B (en) | 2019-01-31 |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Phapale et al. | Nickel-catalysed Negishi cross-coupling reactions: scope and mechanisms | |
| Moragas et al. | Metal‐catalyzed reductive coupling reactions of organic halides with carbonyl‐type compounds | |
| CA2539174C (en) | Process for reduction of carbon dioxide with organometallic complex | |
| Rana et al. | Ni-Catalyzed dehydrogenative coupling of primary and secondary alcohols with methyl-N-heteroaromatics | |
| CA2861631C (en) | Methods of forming 4-chloro-2-fluoro-3-substituted-phenylboronic acid pinacol esters and methods of using the same | |
| RU2014131451A (ru) | Способы получения метил 4-амино-3-хлор-6-(4-хлор-2-фтор-3-метоксифенил)пиридин-2-карбоксилата | |
| CN105017043B (zh) | α‑烷基支链取代的α‑氨基酸衍生物的合成方法 | |
| Chen et al. | CO2 Fixation into Useful Aromatic Carboxylic Acids via C (sp2)–X Bonds Functionalization | |
| CN104447519B (zh) | 一种制备3-取代-2-溴-6-三氟甲基吡啶的方法 | |
| CN111747975B (zh) | 贝达喹啉消旋体及其中间体的制备方法 | |
| CN104151231A (zh) | 一种2,2’-联吡啶的制备方法 | |
| CN107892699A (zh) | 一种吡啶‑4‑硼酸的合成工艺 | |
| CN103483267B (zh) | 多样性的芳基并咪唑类季铵盐及其制备方法和应用 | |
| CN110015987B (zh) | 一种2,3’-二甲氧基-[2,4’]联吡啶的制备方法 | |
| CN105693567A (zh) | 一种制备芳基亚磺酸盐的方法 | |
| TH153165A (th) | วิธีการผลิตเมธิล 4-อะมิโน-3-คลอโร-6-(4-คลอโร-2-ฟลูออโร-3-เมธอกซิเฟนิล)พิริดีน-2-คาร์บอกซิเลท | |
| LU509186B1 (en) | Method for synthesizing photocatalytic organogermanium compounds | |
| CN103497083B (zh) | 一种制备烷基取代芳烃的方法 | |
| CN121226238A (zh) | 氨基吡啶类化合物及其制备方法和应用 | |
| CN115677569B (zh) | 基于铁催化芳基卤代物与烷基卤代物还原偶联反应的吡啶类和取代苯类化合物合成方法 | |
| CN105837633A (zh) | 一种抗菌化合物的制备方法 | |
| CN104030930B (zh) | 一种反式-（1r,2s）-2-（3,4-二氟苯基）环丙胺盐酸盐的合成方法 | |
| CN119874710A (zh) | 一种嘧啶并吡咯类化合物的制备方法 | |
| Bera et al. | Electrochemical functionalization of pyridines | |
| CN102002056A (zh) | 一种普拉格雷中间体的制备方法 |
Legal Events
| Date | Code | Title | Description |
|---|---|---|---|
| PSEA | Patent sealed | ||
| RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 28 DEC 2017 BY CPA GLOBAL Effective date: 20161111 |
|
| RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 28 DEC 2018 BY CPA GLOBAL Effective date: 20171116 |
|
| RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 28 DEC 2019 BY CPA GLOBAL Effective date: 20181115 |
|
| RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 28 DEC 2020 BY CPA GLOBAL Effective date: 20191114 |
|
| RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 28 DEC 2021 BY CPA GLOBAL Effective date: 20201112 |
|
| RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 28 DEC 2022 BY CPA GLOBAL Effective date: 20211111 |
|
| RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 28 DEC 2023 BY CPA GLOBAL Effective date: 20221111 |
|
| RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 28 DEC 2024 BY MAXVAL GROUP INC. Effective date: 20231205 |
|
| RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 28 DEC 2025 BY MAXVAL GROUP INC. Effective date: 20241210 |
|
| RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 28 DEC 2026 BY MAXVAL GROUP INC. Effective date: 20251209 |