JP2006070001A - Chiral phase transfer catalyst with spiro skeleton, its preparation method and catalytic asymmetric reaction using the same - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a chiral phase transfer catalyst with a spiro skeleton, its preparation method and catalytic asymmetric reaction using the same. <P>SOLUTION: The catalytic asymmetric reaction is performed by using an optically active crown ether derivative with the spiro ring skeleton of formula (1) (wherein n is an integer of 0-2) as the phase transfer catalyst. The derivative can be synthesized from a specific spiro compound and a polyol through Williamson ether synthesis. <P>COPYRIGHT: (C)2006,JPO&NCIPI

Description

  The present invention relates to an asymmetric catalytic reaction that provides an optically active compound useful as a synthetic intermediate for pharmaceuticals, agricultural chemicals, and the like, an optically active crown ether derivative that is a catalyst thereof, and a method for producing the catalyst.

  In recent years, asymmetric phase transfer catalysts have been actively researched for the development of environmentally friendly asymmetric reactions, many of which are optically active quaternary ammonium salts, which are organic salts. As examples other than the optically active quaternary ammonium salt, those using optically active crown ethers have been reported (see, for example, Non-Patent Documents 1-6), and to asymmetric Michael addition reactions and asymmetric aldol reactions. Examples of development are known.

Cram, D.C. J. et al. Et al. Chem. Soc. , Chem. Commun. 625 (1981). Koga, K .; Et al .: Tetrahedron Lett. , 30, 7229 (1989). Brunet, F.M. Et al: Tetrahedron Asymmetry, 5, 935 (1994). Toke, L.M. Et al .: Tetrahedron Lett. 36, 5951 (1995). Kobayashi, S .; Et al: Org. Lett. , 3, 165 (2001). Akiyama, T .; Et al .: Chem. Commun. , 1734 (2003).

  By the way, these asymmetric phase transfer catalysts are required to have various diversification according to the purpose of the reaction. Regarding optically active crown ether derivatives having a spiro skeleton, examples of their synthesis and their catalytic action are also reported. There was no.

（式中、ｎは０〜２の整数を表す。） The present inventors have found that an optically active crown ether derivative having a rigid spiro skeleton works effectively as a catalyst for an asymmetric synthesis reaction, and has completed the present invention.
That is, the present invention is an optically active crown ether derivative having a spiro ring skeleton represented by the following formula (1).

(In the formula, n represents an integer of 0 to 2.)

で表される光学活性なスピロ化合物と、下記式（３）

（式中、ｎは上記に同じ。Ｘ_１は脱離基を表す。）
で表されるポリエーテルを、塩基存在下で作用させることを特徴とする、式（１）

（式中、ｎは上記に同じ。）
で表されるスピロ環骨格を有する光学活性クラウンエーテル誘導体の製造法に関する。 The present invention also provides the following formula (2):

An optically active spiro compound represented by formula (3):

(In the formula, n is the same as above. X ₁ represents a leaving group.)
Wherein the polyether represented by formula (1) is allowed to act in the presence of a base.

(Wherein n is the same as above)
And a method for producing an optically active crown ether derivative having a spiro ring skeleton.

  Furthermore, the present invention relates to the use of an optically active crown ether derivative having a spiro ring skeleton represented by the formula (1) as a phase transfer catalyst in an asymmetric catalytic reaction.

  The optically active crown ether derivative having a spiro ring skeleton obtained by the present invention has a function as a phase transfer catalyst, and can be used for asymmetric catalytic reaction to obtain an optically active compound with high optical purity in a high yield. it can.

The present invention will be described in further detail.
Although the crown ether having a spiro ring skeleton represented by the formula (1) has no asymmetric carbon, it has C ₂ symmetric central chirality generated by the arrangement of substituents. This spiro skeleton is rigid and becomes an analog of a compound having axial chirality with a relatively high degree of freedom. Since it has a crown ether structure, it functions as an asymmetric phase transfer catalyst by using each enantiomer. In the optically active crown ether derivative having a spiro ring skeleton represented by the above formula (1), n represents an integer of 0 to 2, particularly preferably n = 1.
In addition, the hydrogen atom on the crown ether having a spiro ring skeleton represented by the formula (1) in the present invention may be substituted with another functional group without departing from the gist of the present invention.

Next, a method for producing an optically active crown ether derivative having a spiro ring skeleton represented by the formula (1) will be described in detail.
The optically active crown ether derivative having a spiro ring skeleton represented by the formula (1) can be produced by a generally known Williamson ether synthesis method.

  1,1′-spirobiindane-7,7′-diol, which is a spiro compound represented by the formula (2), can be obtained according to literature (Vladimir, BB et al .: Tetrahedron Asymmetry, 10, 125). (1999).).

In the polyether represented by the formula (3), n represents an integer of 0 to 2, and particularly preferably n = 1. X ₁ means a leaving group, and preferred examples include halogen such as chloro, bromo and iodo, and sulfonyl such as tosyl, mesyl and trifluoromethanesulfonyl. Particularly preferred is tosyl.

  Usable as a base are carbonates such as potassium carbonate, sodium carbonate, potassium bicarbonate, sodium bicarbonate, alkali metal hydroxides such as sodium hydroxide and potassium hydroxide, sodium hydride, potassium hydride, Examples include alkali metal or alkaline earth metal hydrides such as calcium hydride, alkali metal alcoholates such as sodium methylate, sodium ethylate and potassium tert-butoxide, with potassium tert-butoxide being particularly preferred.

  The solvent that can be used is not particularly limited as long as it is aprotic, but ethers such as THF, dimethyl sulfoxide, N, N-dimethylformamide, N, N-dimethylacetamide and the like are preferably used. Although there is no restriction | limiting in particular in reaction temperature, Preferably it is the range of 0-100 degreeC.

  There is no restriction | limiting in particular in reaction concentration, The one where it is as thin as possible exists in the tendency for a yield to improve, Preferably it is 0.001-1M, More preferably, it is the range of 0.01-0.1M.

Next, the asymmetric catalytic reaction using the optically active crown ether derivative having a spiro ring skeleton represented by the formula (1) will be described in detail.
The type of asymmetric catalytic reaction is not particularly limited as long as it is a reaction using an optically active crown ether having a spiro ring skeleton represented by the formula (1) as a phase transfer catalyst, preferably an asymmetric alkylation reaction, More preferably, it is an asymmetric alkylation reaction of a glycine derivative represented by the following formula (4). In this reaction, hydrogen in the α-position of the carbonyl group of the glycine derivative is substituted with an alkyl group using an electrophile (R ₂ -X ₂ ) in the presence of an optically active phase transfer catalyst and a base, and the following formula (5) This is a reaction for introducing an asymmetry by inducing a glycine derivative addition product.

（式中、Ｒ_２は置換もしくは非置換の、飽和もしくは不飽和の脂肪族炭化水素基を意味し、Ｘ_２は脱離基を意味する。）

(Wherein R ₂ represents a substituted or unsubstituted, saturated or unsaturated aliphatic hydrocarbon group, and X ₂ represents a leaving group.)

R ₂ of the electrophile used in the formula (4) means a substituted or unsubstituted saturated or unsaturated aliphatic hydrocarbon group. A saturated or unsaturated aliphatic hydrocarbon group is a saturated aliphatic hydrocarbon group, that is, an alkyl group such as methyl, ethyl, propyl, isopropyl, butyl, isobutyl, t-butyl, pentyl, cyclopropyl, carbon-carbon, etc. An aliphatic hydrocarbon group having a carbon-carbon unsaturated group such as a carbon-carbon double bond or a carbon-carbon triple bond, that is, an alkenyl group such as vinyl, allyl, prenyl, methallyl, or an alkynyl group such as ethynyl, propynyl, etc. These may be linear, branched or cyclic. The aliphatic hydrocarbon group may have an aromatic group as a substituent, that is, an aralkyl group. Examples of aralkyl include benzyl, phenethyl and the like. The aromatic group may contain a heterocyclic group such as pyridyl, furyl, thienyl, osazolyl. Other substituents for aliphatic hydrocarbon groups include halo, haloformyl, hydroxy, alkoxy, oxo, oxycarbonyl, carbamoyl, phosphino, amino, imino, thio, mercapto, sulfo, sulfenyl, sulfonyl, cyano, nitro, nitroso And groups or atoms commonly known in organic chemistry, such as azo, diazo, azide, hydrazino, isocyanato, silyl or organometallic. Particularly preferred is benzyl.

  Although the carbon number of the said aliphatic hydrocarbon group does not have a restriction | limiting in particular, Preferably it is 1-30, More preferably, it is 1-20. The number of cycloaliphatic hydrocarbon groups is preferably 3 to 10, more preferably 5 to 7.

X ₂ of the electrophile used in the formula (4) means a leaving group like X ₁ described above. Therefore, halogen such as chloro, bromo and iodo, and sulfonyl such as tosyl, mesyl and trifluoromethanesulfonyl. Can be preferably used. Particularly preferred is bromo.

  Examples of the base used herein include alkali metal hydroxides such as sodium hydroxide and potassium hydroxide, alkali metal or alkaline earth metal hydrides such as sodium hydride, potassium hydride and calcium hydride, and sodium methylate. , Alkali metal alcoholates such as sodium laurate and potassium tert-butoxide, and potassium hydroxide is particularly preferred.

  As a solvent, what is normally used as a solvent, such as toluene, ether, a methylene chloride, acetone, alcohol, water, can be used. Alternatively, a two-phase system such as toluene-water may be used.

  Although there is no restriction | limiting in particular in reaction temperature, Preferably it is the range of -50-50 degreeC.

  The amount of the optically active crown ether derivative (1) having a spiro ring skeleton, which is the compound of the present invention, used in this reaction is preferably 0.5 mol% to 50 mol% with respect to the glycine derivative (4) as a substrate. Preferably they are 1 mol%-15 mol%.

（Ｒ）−１，１’−スピロビインダンー７，７’−ジオール（２）（２２３ｍｇ；０．８８ｍｍｏｌ）およびペンタエチレングリコールジトシレート（３）（５３５ｍｇ，０．９８ｍｍｏｌ）をＴＨＦ１２ｍＬに溶解させ、カリウムtert-ブトキシド（２１０ｍｇ，１．８７ｍｍｏｌ）を加えた後、１２時間還流した。その後、水を加え、塩化メチレンで抽出した。硫酸ナトリウムにて溶媒乾燥を行い、減圧濃縮後、シリカゲルカラムクロマトグラフィー（ヘキサン／酢酸エチル＝１／１）にて精製を行い、（Ｒ−１）を収量２６４ｍｇ、収率６６％で得た。
¹H-NMR(CDCl₃):
δ2.05-2.11 (m,2H), 2.18-2.25 (m,2H), 2.88-2.94 (m,4H), 3.13-3.26 (m,4H),
3.39-3.58 (m,8H), 3.78-3.83 (m,2H), 3.93-3.99 (m,2H), 6.59 (d,J=7.8Hz,2H), 6.75
(d,J=7.3Hz,2H), 6.98-7.03 (m,2H); ¹³C-NMR(CDCl₃):δ31.5,
38.3, 59.1, 67.7, 69.2, 70.4, 70.7, 70.8, 109.6, 116.7, 127.3, 137.1, 145.0,
155.3; MS:m/z 454. EXAMPLES Hereinafter, although an Example is given and this invention is demonstrated further more concretely, this invention is not limited to these Examples.
[Example 1]
Synthesis of (R) -7,7 ′-(1,1′-spirobiindanyl) -21-crown-6 (R-1)

(R) -1,1′-spirobiindane-7,7′-diol (2) (223 mg; 0.88 mmol) and pentaethylene glycol ditosylate (3) (535 mg, 0.98 mmol) are dissolved in 12 mL of THF. After adding potassium tert-butoxide (210 mg, 1.87 mmol), the mixture was refluxed for 12 hours. Then, water was added and extracted with methylene chloride. The solvent was dried over sodium sulfate, concentrated under reduced pressure, and purified by silica gel column chromatography (hexane / ethyl acetate = 1/1) to obtain (R-1) in a yield of 264 mg and a yield of 66%.
¹ H-NMR (CDCl ₃ ):
δ2.05-2.11 (m, 2H), 2.18-2.25 (m, 2H), 2.88-2.94 (m, 4H), 3.13-3.26 (m, 4H),
3.39-3.58 (m, 8H), 3.78-3.83 (m, 2H), 3.93-3.99 (m, 2H), 6.59 (d, J = 7.8Hz, 2H), 6.75
(d, J = 7.3Hz, 2H), 6.98-7.03 (m, 2H); ¹³ C-NMR (CDCl ₃ ): δ31.5,
38.3, 59.1, 67.7, 69.2, 70.4, 70.7, 70.8, 109.6, 116.7, 127.3, 137.1, 145.0,
155.3; MS: m / z 454.

[Example 2]
Asymmetric alkylation reaction of glycine derivative using optically active spiro crown ether as phase transfer catalyst 18 mg (0.06 mmol) of glycine derivative (4a), 2.05 mg (0.003 mmol) of (R-1) and 60.5 mg of KOH (1 .08 mmol) To a mixture of 0.16 mL of toluene, 21 μL (0.18 mmol) of benzyl bromide was added dropwise at 0 ° C. and stirred at the same temperature for 16 hours. Water was added and extracted with ether. The organic phase was washed with brine, dried over magnesium sulfate, filtered, and the filtrate was evaporated under reduced pressure. The residue was purified by column chromatography (ether / hexane = 1/10) to obtain an addition product (R-5a) as a target adduct in a yield of 79% and 50% ee. The optical purity was determined by HPLC analysis (Chiral Cell OD: IPA / hexane = 1/99 manufactured by Daicel Corporation).

  The present invention can be used for asymmetric catalysis using a phase transfer catalyst.

Claims (6)

An optically active crown ether derivative having a spiro ring skeleton represented by the following formula (1).

(In the formula, n represents an integer of 0 to 2.)   An optically active crown ether derivative having a spiro ring skeleton in which n = 1 in formula (1). Following formula (2)

An optically active spiro compound represented by formula (3):

(In the formula, n is the same as above. X ₁ represents a leaving group.)
Wherein the polyether represented by formula (1) is allowed to act in the presence of a base.

(Wherein n is the same as above)
A process for producing an optically active crown ether derivative having a spiro ring skeleton represented by the formula:   Use of an optically active crown ether derivative having a spiro ring skeleton represented by formula (1) according to claim 1 or 2 as a phase transfer catalyst in an asymmetric catalytic reaction.   Use according to claim 4, characterized in that the asymmetric catalytic reaction is an asymmetric alkylation reaction. The optically active crown ether derivative having a spiro ring skeleton represented by the formula (1) according to claim 1 or 2 is used as a phase transfer catalyst, and the glycine derivative represented by the following formula (4) is used in the presence of a base. A method of producing an optically active alkyl-substituted glycine derivative represented by the following formula (5) by carrying out an asymmetric alkylation reaction using an electrophile (R ₂ -X ₂ ).

(Wherein R ₂ represents a substituted or unsubstituted, saturated or unsaturated aliphatic hydrocarbon group, and X ₂ represents a leaving group.)