Classifications

• • C—CHEMISTRY; METALLURGY
  • C07—ORGANIC CHEMISTRY
  • C07D—HETEROCYCLIC COMPOUNDS
  • C07D309/00—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings
  • C07D309/32—Heterocyclic compounds containing six-membered rings having one oxygen atom as the only ring hetero atom, not condensed with other rings having two double bonds between ring members or between ring members and non-ring members

Definitions

• the invention relates to an improved process for the preparation of dihydropyrones of the general formula I,
• radicals R 1 and R 2 may have the meanings given in the claims.
• Dihydropyrones are important as intermediates in drug synthesis.
• 5,6-dihydro-4-hydroxy ⁇ 6-phenethyl-6-propyl-2H-pyran-2-one is an important wipe product in the synthesis of tipranavir, an HIV protease inhibitor.
• the compounds of formula I and processes for their preparation are known from the prior art e.g. from the international patent application WO 98/19997 and from the "Journal of edicinal Chemistry, 1998, Vol. 41, No. 18".
• step a) is the reaction of a dianion of the methyl acetoacetic ester with 1-phenyl-3-hexanone and in a subsequent step b) the cyclization of the ⁇ -keto ester formed by means of alkaline hydrolysis and subsequent acidification.
• the process is carried out batchwise and achieves a yield of 72%.
• step a) is carried out continuously in a microreactor.
• the invention therefore relates to a method on a laboratory scale and also technically applicable for the preparation of a compound of the general formula
• R 1 for a C ⁇ Cs-alkyl, C 6 -C 10 aryl-C 1 -C 4 alkyl, or C -C 8 cycloalkyl-C 4 -C 4 alkyl radical
• R 2 represents a Ci-Cs-alkyl radical
• R 3 represents a CC 4 alkyl or benzyl radical
• microreactors suitable for the method according to the invention are known, for example, from "Microreactors; Wolfgang Ehrfeld, Volker Hessel, Holger Löwe; Wi! Ey-VCH; ISBN 3-527-29590-9; Chapter 3 Micromixers".
• Microreactors that can be used in the process according to the invention generally have a housing made of stainless steel, glass, titanium or metal alloys and an inlay or inlay structure made of thermally oxidized silicon, copper, aluminum, nickel, silver, metal alloys, and Foturan glass or metal-coated plastic, glass or ceramic materials.
• the mixing of the educt streams can be both turbulent and laminar, preferably laminar.
• the channel structures preferred for a laminar mixture generally include interdigital structures, star-shaped structures or structures of a caterpillar mixer.
• Microreactor types that can be used for the method according to the invention are available, for example, from the companies Institut für Mikrotechnik Mainz GmbH, Cellular Process Chemistry GmbH or Mikroglas AG.
• a method is particularly preferred in which a microreactor with an interdigital channel structure, particularly preferably a microreactor of the LIGA type (production method by means of lithography, electroforming, molding) with an interdigital channel structure, for example produced by the Institute for Microtechnology Mainz GmbH, is used for reaction step a) ,
• a process is particularly preferred in which a feed stream A containing the compound of formula (II) and a feed stream B containing an acetoacetic ester in the form of a dianion are continuously mixed with one another in the mixing element of a microreactor and the liquid reaction mixture is passed into a capillary, in particular a residence capillary , to be led.
• the capillary has a length of 0.1 to 10 m, preferably 0.3 to 8 m, preferably 0.5 to 6 m, particularly preferably 0.8 to 4 m, particularly preferably approximately 1 m and has an inner diameter of 0.05 to 5 mm, preferably 0.1 to 4 mm, preferably 0.3 to 3 mm, particularly preferably about 1 mm.
• step a) uses 1-phenyl-3-hexanone as the compound of the formula (II).
• acetoacetic ester is used as dilithium, monolithium monosodium or disodium salt in step a).
• step a) is carried out at a temperature of -78 to +85 ° C, preferably at -40 to +50 ° C, preferably at -30 to +20 ° C, particularly preferably at -25 to +10 ° C, particularly preferably at -20 to 0 ° C, very particularly preferably at -15 to -5 ° C, very preferably at about -10 ° C.
• step a) at a total flow rate, which is calculated by adding the flow rates of the compound of the formula II and the acetoacetic ester, from 1.5 to 5 ml / min, preferably at 1.8 to 4 ml / min, particularly preferably at 2 to 3.5 ml / min, particularly preferably at about 2.5 ml / min.
• a method is particularly preferred in which the flow rate of the compound of the formula (II) to that of the acetoacetic ester in a ratio of 1: 1 to 1: 2, preferably from 1: 1, 1 to 1: 1, 8, particularly preferably from 1: 1, 2 to 1: 1, 5, particularly preferably from about 1: 1, 3.
• low-pulsation pumps preferably rotary lobe pumps, preferably ceramic rotary lobe pumps or HPLC pumps
• the flow rates can be adapted to different reactor types in the sense of an optimal space / time yield.
• a method is furthermore particularly preferred, the reaction being carried out in a plurality of microreactors connected in series or in parallel.
• alkyl stands for a straight-chain or branched alkyl group having 1 to 8 C atoms, preferably 2 to 7 C atoms, preferably 3 to 6 C atoms. Methyl, ethyl, n-propyl, iso-propyl, n-butyl, iso-butyl, sec. Butyl, tert-butyl, n-pentyl, iso-pentyl or neo-pentyl are particularly preferred.
• aryl stands for an aromatic hydrocarbon radical having 6 to 10 carbon atoms, preferably phenyl or naphthyl, particularly preferably phenyl, which can be substituted by one or more alkyl groups.
• Cyclopryl radicals with 3 to 8 carbon atoms are cyclopryl, cyclobutyl, cyclopentyl, cyclohexyl, cycloheptyl or cyclooctyl.
• R 1 is preferably phenylmethyl, phenylethyl or phenylpropyl, particularly preferably 2-phenylethyl,
• R 2 is preferably methyl, ethyl, n-propyl or n-butyl, particularly preferably n-propyl.
• R 3 is preferably methyl, ethyl, n-propyl or benzyl, particularly preferred
• Metal hydrides, metal organyls, metal amides, metal dialkylamides or metal hexamethyldisilazanes are preferably used as strong bases.
• Metal cations are, for example, lithium, sodium, potassium, rubidium, cesium, magnesium, calcium, titanium, silicon, tin and lanthanides, preferably lithium or sodium, particularly preferably lithium.
• Very particularly preferred bases are sodium hydride, lithium diethylamide, butyllithium, lithium diisopropylamide, othiumhexamethyldisilazane, sodium hexamethyldisilazane or potassium hexamethyldisilazane or combinations of these.
• 2 or more equivalents of these bases are used, preferably 1.8 to 3.0, in particular 1.9 to 2.5 equivalents.
• the acetoacetic ester is generally in the form of a dianion of the formula III.
• the process according to the invention is generally carried out in the presence of an inert diluent.
• diluents are non-polar organic solvents such as e.g. aliphatic or aromatic hydrocarbons, ethers or mixtures thereof.
• the diluent is selected from the group consisting of dimethoxyethane, diethyl ether, te / f-butyl methyl ether, tetrahydrofuran, n-hexane, cyclohexane, toluene, xylene or a mixture of these solvents, in particular tetrahydrofuran and dimethoxyethane.
• the reaction mixture can also contain one or more amines such as, for example, diethylamine, diisopropylamine or tetramethylethylene diamine.
• the advantage of the process according to the invention lies in the high purity and the unexpectedly high yield of dihydropyranone of over 90%, which results from the continuous microreactor process of step a).
• the compound of formula IV can be processed as a product of the microreactor process without further purification.
• Example 1 5.6-Dihvdro-4-hvdroxy- ⁇ -dhenethyl-6-proDyl-2H-pyran-2-one
• Step a) A mixture I of 81.9 g of 1-phenyl-3-hexanone and 840 ml of tetrahydrofuran and a mixture II of 72.9 g of ethyl are placed in a microreactor from the Institut für Mikrotechnik Mainz GmbH (type Liga with interdigital channel structure) - Acetoacetic ester, 117 ml of diethylamine and 450 ml of n-butyllithium in n-hexane (2.5 molar) in 361 ml of tetrahydrofuran at -10 ° C pumped together and mixed.
• the volume flow of mixture I is set at 1 ml / min and the volume flow of mixture II at 1.1 ml / min.
• the product solution is passed through a capillary (length 1 m, diameter 1 mm) and then in saturated ammonium chloride solution. Hydrochloric acid solution collected at a pH of 5 - 6.
• 140 g of the crude ⁇ -keto ester resulting from step a) are taken up in 200 ml of methanol at 5 to 10 ° C.
• Solid potassium hydroxide is added with stirring at 5 to 10 ° C. and then stirred for about 15 hours at room temperature.
• the methanol is distilled off and 500 ml of water are added to the residue. It is extracted twice with 200 ml of toluene. After the organic phase has been separated off, 400 ml of fresh toluene are again added to the aqueous phase. This is with conc. Acidified sulfuric acid up to pH 1.9.
• the aqueous phase is separated off and the organic phase is extracted 3 times with water.
• the organic phase is evaporated to dryness in vacuo (60 mbar) at 40 ° C.
• the crude product is dissolved in 200 ml of toluene at 60 ° C and then filtered.
• 200 ml of n-octane are slowly added dropwise to the filtrate at 40 ° C. with stirring. It is seeded with 5,6-dihydro-4-hydroxy-6-phenethyl-6-propyl-2H-pyran-2-one crystals and stirred for about 15 hours at room temperature.
• 400 ml of n-octane are added dropwise to the resulting crystal mass and the mixture is cooled to 0-5 ° C. After stirring for about 1 hour at 0 - 5 ° C, the crystals are filtered off, washed with n-octane and dried. The yield is 92%.

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• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
• Pyrane Compounds (AREA)
• Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

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Citations (6)

• 2001
  • 2001-02-22 DE DE2001108471 patent/DE10108471C1/de not_active Expired - Fee Related
• 2002
  • 2002-02-20 EP EP02719875.3A patent/EP1368331B1/de not_active Expired - Lifetime
  • 2002-02-20 JP JP2002567917A patent/JP4335529B2/ja not_active Expired - Fee Related
  • 2002-02-20 MX MXPA03007531A patent/MXPA03007531A/es active IP Right Grant
  • 2002-02-20 CA CA2438878A patent/CA2438878C/en not_active Expired - Fee Related
  • 2002-02-20 WO PCT/EP2002/001772 patent/WO2002068403A1/de not_active Ceased

Patent Citations (6)

Non-Patent Citations (10)

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