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DK1746089T3 - PROCESS FOR THE PREPARATION OF 2-cyanopyridine derivatives - Google Patents

PROCESS FOR THE PREPARATION OF 2-cyanopyridine derivatives Download PDF

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Publication number
DK1746089T3
DK1746089T3 DK06120806.2T DK06120806T DK1746089T3 DK 1746089 T3 DK1746089 T3 DK 1746089T3 DK 06120806 T DK06120806 T DK 06120806T DK 1746089 T3 DK1746089 T3 DK 1746089T3
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DK
Denmark
Prior art keywords
cyanide
process according
salt
halogen
catalyst
Prior art date
Application number
DK06120806.2T
Other languages
Danish (da)
Inventor
Norman Dann
Peter Riordan
Mehul Amin
Michael Mellor
Original Assignee
Bayer Cropscience Sa
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
Priority claimed from GB0021066A external-priority patent/GB0021066D0/en
Priority claimed from GB0025616A external-priority patent/GB0025616D0/en
Application filed by Bayer Cropscience Sa filed Critical Bayer Cropscience Sa
Priority claimed from EP01982337A external-priority patent/EP1311483B1/en
Application granted granted Critical
Publication of DK1746089T3 publication Critical patent/DK1746089T3/en

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    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/24Heterocyclic 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 substituted hydrocarbon radicals attached to ring carbon atoms
    • C07D213/26Radicals substituted by halogen atoms or nitro radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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
    • C07D213/61Halogen atoms or nitro radicals
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic 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
    • C07D213/02Heterocyclic 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
    • C07D213/04Heterocyclic 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
    • C07D213/60Heterocyclic 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
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/84Nitriles

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  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyridine Compounds (AREA)
  • Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)

Description

DESCRIPTION
[0001] This invention relates to novel process for the preparation of 2-cyanopyridines, which compounds are useful as intermediates for the production of pesticides.
[0002] There have been a number of procedures published for introducing a cyano group at the 2-position of a pyridine moiety. These typically involve substitution of a halogen, in particular bromine or fluorine, in a polar solvent, e.g. dimethyl sulphoxide or dimethylformamide. In addition, there are numerous methods starting from the activated pyridine N-oxide or /V-alkylpyridine. Many of these cyanation routes use heavy metal reagents, containing copper or nickel. For example, EP0034917 discloses the preparation of 2-cyano-3-chloro-5-trifluoromethylpyridine from the 2-bromo analogue by reaction with cuprous cyanide in dimethylformamide at 120°C.
[0003] However, many of these prior art processes suffer from one or more drawbacks, including poor yields, use of heavy metals which produce toxic effluents, or polar solvents which are difficult to recover. Further, methods which involve formation of the pyridine N-oxide or /V-alkylpyridine involve several steps. These drawbacks are more critical on scale-up to industrial scale.
[0004] International Patent Application WO 01/17970 describes the cyanation of 2-halopyridine compounds with an activating agent and a cyanide source in a polar solvent and thus avoids many of the above disadvantages. However there still remains with this procedure the need to recycle the activating agent and the aprotic solvent in order to minimise the costs for an industrial scale process.
[0005] US 4,851,539 discloses a process for the preparation of 2-cyano-3-chloro-5-trifluoromethylpyridine by cyanation of 2-fluoro-3-chloro-5-trifluoromethylpyridine using potassium cyanide in dimethyl sulfoxide as a cyanide source.
[0006] WO 92/18487 discloses pyrid-2-yl propenoic acid derivatives or pyrimidinyl propenoic acid derivatives and a process for their preparation. A process of cyanation by sodium or potassium cyanide in the presence of a trialkylamine and in an organic solvent is disclosed.
[0007] EP 0034917 discloses 2-cyano-3-halogeno-5-trifluoromethylpyridine compounds and a process for their production. A cyanation process in 2-position of a pyridine is disclosed in that document. The cyanation of a 2-bromo-3-halogeno-5-trifluoromethylpyridine is preferably carried out in a polar solvent.
[0008] We have now developed an alternative and improved process for the preparation of 2-cyanopyridines which is applicable to industrial scale processes.
[0009] Thus, according to the present invention, there is provided a process for the preparation of a compound of general formula (II) general formula (II):
(ID or a salt thereof, which comprises treating a compound of general formula (III):
m or a salt thereof with a cyanide source chosen as being hydrogen cyanide, an alkali metal cyanide, an alkaline earth metal cyanide or an optionally substituted ammonium cyanide and a phase transfer catalyst in an aqueous solvent or without solvent, wherein X is halogen; each Y, which may be the same or different, is halogen, haloalkyl, alkoxycarbonyl or alkylsulphonyl; n is 0 to 3.
[0010] In this invention halogen means a fluorine, chlorine or bromine atom. The preferred halogen atom is chlorine.
[0011] Haloalkyl typically means a Ci to C6 alkyl moiety substituted by one or more halogen atoms. For example the Ci to C6 alkyl moiety may be methyl, ethyl, n-propyl or i-propyl, preferably methyl. The C-| to C6 alkyl moiety is preferably substituted by one or more chlorine or fluorine atoms. A more preferred haloalkyl group is trifluoromethyl.
[0012] An alkoxycarbonyl group is typically Ci to C6 alkoxycarbonyl such as methoxycarbonyl, ethoxycarbonyl, n-propoxycarbonyl or i-propoxycarbonyl.
[0013] An alkylsulphonyl group is typically Ci to C6 alkylsulphonyl in which the Ci to C6 moiety is as defined above.
[0014] Preferably X is chlorine.
[0015] Preferably Y is halogen or haloalkyl (more preferably trifluoromethyl).
[0016] Compound (III) is preferably 3-chloro-2-fluoro-5-trifluoromethylpyridine.
[0017] The catalyst is generally a phase transfer catalyst such as a tetraalkyl ammonium salt such as benzyl trimethylammonium chloride, tricaprylylmethylammonium chloride, tetramethylammonium chloride, tetra-n-propylammonium bromide, n-dodecyl trimethylammonium chloride, tetra-n-butylammonium chloride, tetra-n-butylammonium bromide, tetra-n-octylammonium bromide or n-tetradecyl trimethylammonium bromide; or a tetraalkyl phosphonium salt such as tetra-n-butylphosphonium bromide or tetraphenylphosphonium bromide; or a crown ether or acyclic analogue thereof such as TDA-1 (tris[2-(2-methoxyethoxy)ethyl]amine); or an amine such as 4-dimethylaminopyridine.
[0018] Preferably the catalyst is selected from tricaprylylmethylammonium chloride and tetra-n-octylammonium bromide.
[0019] The amount of catalyst used is generally from about 0.01 to 10 mol %, preferably from about 0.1 to 5 mol %, more preferably from about 1 to 5 mol %.
[0020] The above process of the invention is a high yielding process for the preparation of 2-cyanopyridines, which is simple to perform and operates at moderate temperatures and does not suffer from the drawbacks of many prior art processes. In particular the process of the invention does not require heavy metal cyanides such as copper or nickel cyanide, which, when used on an industrial scale, produce toxic effluent streams and are difficult to recover. The process of the invention produces waste streams, which are readily treatable.
[0021] In addition, the process does not require the preparation of activated pyridine/V-oxide or W-alkylpyridine for high conversions, which is a requisite for many of the prior art processes. The process of the invention does not require an activating agent such as 4-dimethylaminopyridine and hence avoids additional recovery and recycling steps. A further advantage of the process of the invention is that organic solvents are not used in the reaction, thus avoiding the need to recycle expensive solvents such as dimethyl sulphoxide.
[0022] The cyanide source is preferably sodium cyanide or potassium cyanide, preferably potassium cyanide. The amount of cyanide source used is generally from about 1.0 to about 2.0 molar equivalents (however more may be used if desired), preferably from 1.0 to 1.5 molar equivalents, more preferably from 1.0 to 1.1 molar equivalents.
[0023] The reaction is generally and preferably performed using water as solvent, however it may also be carried out in the absence of solvent.
[0024] The reaction conditions typically comprise combining all reactants in a suitable reaction vessel and stirring at a temperature of from 10 to 60°C, preferably from 20 to 40°C.
[0025] The present invention thus provides a high yielding process for the preparation of 2-cyanopyridines. Since the reaction uses moderate reaction temperatures, simple and inexpensive reactors and downstream processing equipment is all that is required. Furthermore, since the reactants are readily available, the process is inexpensive to operate. In addition, the present process produces waste streams that are readily treatable.
[0026] The present invention is further illustrated by the following preparative examples:
Example 1 [0027] A solution of potassium cyanide (71,6g) in water (215g) was added during 1 hour to a stirred mixture of 3-chloro-2-fluoro-5-trifluoromethylpyridine (199.5g) and Aliquat 336 (tricaprylylmethylammonium chloride, 12.1g) at 30°C. Stirring was maintained at this temperature for 4 hours at which time the amount of starting fluoride was less than 1% by hplc. The lower organic phase was separated and washed with aqueous sodium chloride solution and distilled to give 3-chloro-2-cyano-5-trifluoromethylpyridine (185.8g, 90% yield) bp 90°C at 15mbar. The purity of this product was 98%.
Example 2 [0028] Solid sodium cyanide (0.29g) was added to a stirred mixture of 3-chloro-2-fluoro-5-trifluoromethylpyridine (0.8g) and tetrabutylammonium bromide (0.06g) at 20-25°C, and stirred for 23 hours to give 3-chloro-2-cyano-5-trifluoromethylpyridine (0.68g, 82% yield by hplc).
REFERENCES CITED IN THE DESCRIPTION
This list of references cited by the applicant is for the reader's convenience only. It does not form part of the European patent document. Even though great care has been taken in compiling the references, errors or omissions cannot be excluded and the EPO disclaims all liability in this regard.
Patent documents cited in the description • FP0034817A røOQ21 [00071 • WO0117970A [00041 • ΙΙ.°·4Ρ.51639Α fOOOSl • WQ9218487A [00061

Claims (12)

1. Fremgangsmåde til fremstillling af en forbindelse med generel formel (II)A process for the preparation of a compound of general formula (II) (Π) eller et salt deraf, hvilken fremgangsmåde omfatter behandling af en forbindelse med generel formel (III):(Π) or a salt thereof, comprising the treatment of a compound of general formula (III): (ΙΠ) eller et salt deraf med en cyanidkilde, der er udvalgt blandt hydrogencyanid, et alkalimetalcyanid, et jordalkalimetalcyanid eller et eventuelt substitueret ammoniumcyanid; og en faseoverførselskatalysator; i et vandigt opløsningsmiddel eller uden opløsningsmiddel, hvor X er halogen; hvert Y, som kan være ens eller forskellige, er halogen, haloalkyl, alkoxycarbonyl eller alkylsulfonyl; n er 0 til 3.(ΙΠ) or a salt thereof with a cyanide source selected from hydrogen cyanide, an alkali metal cyanide, an alkaline earth metal cyanide or an optionally substituted ammonium cyanide; and a phase transfer catalyst; in an aqueous solvent or without solvent where X is halogen; each Y, which may be the same or different, is halogen, haloalkyl, alkoxycarbonyl or alkylsulfonyl; n is 0 to 3. 2. Fremgangsmåde ifølge krav 1, hvor X er chlor.The process of claim 1, wherein X is chlorine. 3. Fremgangsmåde ifølge krav 1 eller 2, hvor Y er halogen eller haloalkyl.The process of claim 1 or 2, wherein Y is halogen or haloalkyl. 4. Fremgangsmåde ifølge krav 3, hvor Y er trifluormethyl.The process of claim 3, wherein Y is trifluoromethyl. 5. Fremgangsmåde ifølge krav 4, hvor forbindelsen med formel (III) er 3-chlor-2-fluor-5-trifluormethylpyridin.The process of claim 4, wherein the compound of formula (III) is 3-chloro-2-fluoro-5-trifluoromethylpyridine. 6. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 5, hvor katalysatoren er et tetraalkylammoniumsalt eller et tetrraalkylphosphoniumsalt.A process according to any one of claims 1 to 5, wherein the catalyst is a tetraalkylammonium salt or a tetraalkylphosphonium salt. 7. Fremgangsmåde ifølge krav 6, hvor katalysatoren er udvalgt blandt tricaprylylmethylammoniumchlorid og tetra-n-octylammoniumbromid.The process of claim 6, wherein the catalyst is selected from tricaprylyl methylammonium chloride and tetra-n-octylammonium bromide. 8. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 7, hvor den anvendte mængde af katalysator er fra 0,01 til 10 mol-%.A process according to any one of claims 1 to 7, wherein the amount of catalyst used is from 0.01 to 10 mol%. 9. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 8, hvor cyanidkilden er kaliumcyanid.A process according to any one of claims 1 to 8, wherein the cyanide source is potassium cyanide. 10. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 9, hvor den anvendte mængde af cyanidkilde er fra 1,0 til 2,0 molækvivalenter.A process according to any one of claims 1 to 9, wherein the amount of cyanide source used is from 1.0 to 2.0 molar equivalents. 11. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 10, hvor opløsningsmidlet er vand.A process according to any one of claims 1 to 10, wherein the solvent is water. 12. Fremgangsmåde ifølge et hvilket som helst af kravene 1 til 11, hvor temperaturen er fra 10 til 60 °C.A process according to any one of claims 1 to 11, wherein the temperature is from 10 to 60 ° C.
DK06120806.2T 2000-08-25 2001-08-21 PROCESS FOR THE PREPARATION OF 2-cyanopyridine derivatives DK1746089T3 (en)

Applications Claiming Priority (4)

Application Number Priority Date Filing Date Title
GB0021066A GB0021066D0 (en) 2000-08-25 2000-08-25 Novel process
GB0025616A GB0025616D0 (en) 2000-10-19 2000-10-19 Novel process
EP01420128A EP1199305A1 (en) 2000-10-19 2001-06-07 Process for the preparation of 2-aminomethylpyridines
EP01982337A EP1311483B1 (en) 2000-08-25 2001-08-21 Process for the preparation of 2-aminomethyl-halogen-pyridines

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DK1746089T3 true DK1746089T3 (en) 2015-08-24

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JP (1) JP4922534B2 (en)
KR (1) KR100818566B1 (en)
BR (2) BR0117363B1 (en)
DK (1) DK1746089T3 (en)
ES (1) ES2545477T3 (en)
IL (2) IL154014A (en)
RU (1) RU2266900C2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP3088390A1 (en) * 2015-04-30 2016-11-02 Bayer CropScience AG Catalytic hydrogenation of substituted cyanopyridines
EP3489221A1 (en) * 2017-11-22 2019-05-29 Bayer AG Process for the preparation of fluopicolide

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US4159382A (en) * 1978-06-28 1979-06-26 The Dow Chemical Company Process for preparing picolylamine
JPS5663949A (en) * 1979-10-29 1981-05-30 Kuraray Co Ltd Preparation of nitrile compound
JPS56118066A (en) * 1980-02-21 1981-09-16 Ishihara Sangyo Kaisha Ltd 2-cyano-3-halogeno-5-trifluoromethylpyridine and its preparation
EP0034917B1 (en) * 1980-02-21 1984-08-08 Ishihara Sangyo Kaisha Ltd. 2-substituted-5-trifluoromethylpyridines and a process for producing the same
IL68822A (en) * 1982-06-18 1990-07-12 Dow Chemical Co Pyridyl(oxy/thio)phenoxy compounds,herbicidal compositions and methods of using them
US4851539A (en) * 1982-06-18 1989-07-25 The Dow Chemical Company 2,3-Difluoropyridine and 3-fluoro-2-pyridinyloxyphenol compounds
JPH06749B2 (en) * 1985-04-30 1994-01-05 広栄化学工業株式会社 Method for producing aminomethylpyridine
US4766219A (en) * 1985-06-03 1988-08-23 The Dow Chemical Company Preparation of 2-cyano-6-chloropyridine compounds
AT391693B (en) * 1988-11-15 1990-11-12 Cl Pharma METHOD FOR PRODUCING 3-5-DIMETHYL-4METHOXYPYRIDINE DERIVATIVES AND NEW INTERMEDIATE PRODUCT THEREFOR
NZ242290A (en) * 1991-04-15 1994-12-22 Zeneca Ltd Pyridyl and pyrimidinyl substituted oxime-o-benzyl ether derivatives; preparatory processes, fungicidal compositions and an intermediate
DE4132808A1 (en) * 1991-10-02 1993-04-08 Hoechst Ag PROCESS FOR THE PREPARATION OF 2-AMINOMETHYLPIPERIDINE
DE19529973A1 (en) * 1995-08-16 1997-02-20 Hoechst Ag Process for the preparation of ortho-nitrobenzonitriles
TW575562B (en) * 1998-02-19 2004-02-11 Agrevo Uk Ltd Fungicides

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IL154014A (en) 2010-11-30
BR0117362B1 (en) 2013-08-27
BR0117363B1 (en) 2013-08-27
IL190807A0 (en) 2008-11-03
JP4922534B2 (en) 2012-04-25
IL190807A (en) 2011-06-30
JP2004506716A (en) 2004-03-04
RU2266900C2 (en) 2005-12-27
ES2545477T3 (en) 2015-09-11
KR20030024911A (en) 2003-03-26
KR100818566B1 (en) 2008-04-01

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