JP2008221090A - Silicon lewis acid catalyst and reaction method using silicon lewis acid catalyst - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a technique capable of synthesizing γ-keto-α-amino acid compound and β-amino carbonyl compound without activating amide and ketone separately. <P>SOLUTION: The catalyst comprises a silicate presented by the general formula [I] and a basic compound. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention particularly relates to a silicon Lewis acid catalyst and a reaction method for synthesizing a γ-keto α-amino acid compound and a β-aminocarbonyl compound using the silicon Lewis acid catalyst.

In recent years, a so-called direct addition reaction in which a carbonyl compound is used without prior activation has been reported. However, the carbonyl compounds that can be used are limited to ketones and aldehydes with high α-position acidity.
N. Yoshikawa, YMA Yamada, J. Das, H. Sasai, M. Shibasaki J. Am. Chem. Soc. 1999, 121, 4168. B. List, RA Lerner, CFBarbas III J. Am. Chem. Soc. 2000, 122, 2395. AB Northrup, DWCMacMillan J. Am. Chem. Soc. 2002, 124, 6798. Letcka, T. et al. J. Am. Chem. Soc. 2002, 124, 67-77.

  By the way, the catalytic direct addition reaction of carbonyl compounds in the same oxidation state (amide or the like) as the ester or ester is not known. When considering further conversion of the product after the addition reaction, development of a direct addition reaction of a carbonyl compound in the same oxidation state (amide or the like) as that of an ester or an ester is desired.

  Therefore, the problem to be solved by the present invention is to provide a technique capable of synthesizing γ-keto α-amino acid compounds and β-aminocarbonyl compounds without separately activating amides and ketones.

The above issues are
A silicon salt represented by the following general formula [I]:
This is solved by a catalyst characterized by having a basic compound.

一般式［Ｉ］中、Ｒ^１，Ｒ^２，Ｒ^３は、各々、アルキル基およびトリアルキルシリル基の群の中から選ばれる何れかであり、同じでも異なるものでも良く、Ｒ^４はパーフルオロアルキル基である。
特に、好ましくは、Ｒ^１，Ｒ^２，Ｒ^３が炭素数１〜４のアルキル基およびトリアルキルシリル基の群の中から選ばれる何れかであり、Ｒ^４が炭素数１〜４のパーフルオロアルキル基である。更に好ましくは、Ｒ^１，Ｒ^２，Ｒ^３がメチル基、エチル基、及びトリメチルシリル基の群の中から選ばれる何れかであり、Ｒ^４がトリフルオロメチル基である。中でも、Ｒ^１，Ｒ^２，Ｒ^３がメチル基、Ｒ^４がトリフルオロメチル基である。 Formula [I]

In general formula [I], R ¹ , R ² , and R ³ are each selected from the group of an alkyl group and a trialkylsilyl group, and may be the same or different, and R ⁴ is perfluoro It is an alkyl group.
Particularly preferably, R ¹ , R ² and R ³ are any one selected from the group of an alkyl group having 1 to 4 carbon atoms and a trialkylsilyl group, and R ⁴ is a perfluoro having 1 to ⁴ carbon atoms. It is an alkyl group. More preferably, R ¹ , R ² and R ³ are any one selected from the group of a methyl group, an ethyl group and a trimethylsilyl group, and R ⁴ is a trifluoromethyl group. Among them, R ¹ , R ² and R ³ are methyl groups, and R ⁴ is a trifluoromethyl group.

  The basic compound is preferably a compound belonging to amines. Of these, compounds belonging to tertiary amines are preferred. For example, triethylamine or pyridine.

  Moreover, the said subject has a silicon salt represented with said general formula [I], and a basic compound, and this basic compound is 5-40 mass parts with respect to 100 mass parts of this silicon salt. Solved by a catalyst characterized by a proportion.

In addition, the above problem is
A silicon salt represented by the following general formula [X];
This is solved by a catalyst characterized by having a basic compound.

一般式［Ｘ］中、Ｒ^４，Ｒ^５，Ｒ^６は、各々、アルキル基またはトリアルキルシリル基であり、同じでも異なるものでも良い。特に、好ましくは、Ｒ^４，Ｒ^５，Ｒ^６が炭素数１〜４のアルキル基およびトリアルキルシリル基の群の中から選ばれる何れかである。更に好ましくは、メチル基、エチル基、及びトリメチルシリル基の群の中から選ばれる何れかである。中でも、メチル基である。Ｒ^７,Ｒ^８，Ｒ^９，Ｒ^１０は電子吸引性置換基であり、同じでも異なるものでも良い。好ましくはパーフルオロアルキル基である。中でもペンタフルオロフェニル基（−Ｃ_６Ｆ_５）である。 Formula [X]

In the general formula [X], R ⁴ , R ⁵ and R ⁶ are each an alkyl group or a trialkylsilyl group, and may be the same or different. Particularly preferably, R ⁴ , R ⁵ and R ⁶ are any selected from the group consisting of an alkyl group having 1 to 4 carbon atoms and a trialkylsilyl group. More preferably, it is any one selected from the group of a methyl group, an ethyl group, and a trimethylsilyl group. Among them, it is a methyl group. R ⁷ , R ⁸ , R ⁹ and R ¹⁰ are electron-withdrawing substituents, and may be the same or different. A perfluoroalkyl group is preferred. Among them, a pentafluorophenyl group (—C ₆ F ₅ ).

  The basic compound is preferably a compound belonging to amines. Of these, compounds belonging to tertiary amines are preferred. For example, triethylamine or pyridine.

  Moreover, the said subject has a silicon salt represented with said general formula [I], and a basic compound, and this basic compound is 5-40 mass parts with respect to 100 mass parts of this silicon salt. Solved by a catalyst characterized by a proportion.

  Moreover, it is solved by the above catalyst, which is a silicon Lewis acid catalyst for synthesizing γ-keto α-amino acid compound or β-aminocarbonyl compound.

  Further, the catalyst is characterized in that it is used in the reaction of a compound represented by the following general formula [II] with a compound represented by the following general formula [III] or general formula [IV]. Solved by the catalyst.

一般式［ＩＩ］中、Ｒ^５は、置換基を有していても良いアルコキシカルボニル基又はアリール基であり、Ｒ^６は置換基を有していても良いアリール基である。
好ましいＲ^５は、炭素数１〜４のアルコキシカルボニル基、又は無置換もしくは一置換のアリール基である。中でも、エトキシカルボニル基やフェニル基である。好ましいＲ^６はｐ−トリル基である。 Formula [II]

In general formula [II], R ⁵ is an alkoxycarbonyl group or aryl group which may have a substituent, and R ⁶ is an aryl group which may have a substituent.
Preferred R ⁵ is an alkoxycarbonyl group having 1 to 4 carbon atoms, or an unsubstituted or monosubstituted aryl group. Among them, an ethoxycarbonyl group and a phenyl group. Preferred R ⁶ is a p-tolyl group.

一般式［ＩＩＩ］中、Ｒ^７は、Ｈ又は置換基を有していても良いアルキル基で、Ｒ^８，Ｒ^９との間で環を形成しても良く、Ｒ^８，Ｒ^９は、置換基を有していても良いアルキル基、アルコキシ基またはアリール基で、同じでも異なるものでも良い。
好ましいＲ^７はＨである。好ましいＲ^８，Ｒ^９は炭素数１〜４のアルキル基である。特に、メチル基である。 Formula [III]

In the general formula [III], ^{R 7} is H or an optionally substituted alkyl group ^may form a ring with the ^{R 8, R 9, R 8} , R 9 is The alkyl group, alkoxy group or aryl group which may have a substituent may be the same or different.
Preferred R ⁷ is H. Preferred R ⁸ and R ⁹ are alkyl groups having 1 to 4 carbon atoms. In particular, it is a methyl group.

一般式［ＩＶ］中、Ｒ^１０は、Ｈ又は置換基を有していても良いアルキル基で、Ｒ^１１との間で環を形成しても良く、Ｒ^１１は、置換基を有していても良いアルキル基またはアリール基である。
好ましいＲ^１０はＨである。好ましいＲ^１１は置換基を有していても良いフェニル基である。 Formula [IV]

In the general formula [IV], R ¹⁰ is H or an optionally substituted alkyl group may form a ring with the R ^11, R ¹¹ is substituted It may be an alkyl group or an aryl group.
Preferred R ¹⁰ is H. Preferred R ¹¹ is a phenyl group which may have a substituent.

Further, the object is to react the compound represented by the general formula [II] with the compound represented by the general formula [III] in the presence of the catalyst. -Solved by the production method of keto α-amino acid compounds.

In addition, the above-described problem is characterized by reacting the compound represented by the general formula [II] with the compound represented by the general formula [IV] in the presence of the catalyst. -Solved by the process for the preparation of aminocarbonyl compounds.

  The present invention enables a nucleophilic addition reaction to an imine using an amide or ketone as a nucleophile. This addition reaction can be used directly without the need to activate amides and ketones separately. As a result, γ-keto α-amino acid compounds (derivatives) and β-aminocarbonyl compounds can be easily synthesized and are very useful in the field of fine chemicals such as pharmaceutical intermediates.

  In the present invention, the metal to be used is relatively harmless silicon, and the reaction can proceed with a catalytic amount of silicon salt, so that the burden on the environment is small.

The catalyst according to the present invention contains the silicon salt represented by the general formula [I] and a basic compound. In general formula [I], R ¹ , R ² , and R ³ are each selected from the group of alkyl groups and trialkylsilyl groups. Preferred R ¹ , R ² and R ³ are any selected from the group consisting of an alkyl group having 1 to 4 carbon atoms and a trialkylsilyl group. More preferably, it is any one selected from the group of a methyl group, an ethyl group, and a trimethylsilyl group. Among them, it is a methyl group. R ⁴ is a perfluoroalkyl group. Preferable R ⁴ is a perfluoroalkyl group having 1 to 4 carbon atoms. Of these, a trifluoromethyl group. Preferred basic compounds are compounds belonging to amines. Among these, compounds belonging to tertiary amines. For example, triethylamine or pyridine. The ratio of the silicon salt to the basic compound is preferably 5 to 40 parts by mass of the basic compound with respect to 100 parts by mass of the silicon salt.

The catalyst according to the present invention contains the silicon salt represented by the above general formula [X] and a basic compound. In the general formula [X], R ⁴ , R ⁵ and R ⁶ are each an alkyl group or a trialkylsilyl group, and may be the same or different. Particularly preferably, R ⁴ , R ⁵ and R ⁶ are any selected from the group consisting of an alkyl group having 1 to 4 carbon atoms and a trialkylsilyl group. More preferably, it is any one selected from the group of a methyl group, an ethyl group, and a trimethylsilyl group. Among them, it is a methyl group. R ⁷ , R ⁸ , R ⁹ and R ¹⁰ are electron-withdrawing substituents, and may be the same or different. A perfluoroalkyl group is preferred. Among them, a pentafluorophenyl group (—C ₆ F ₅ ). Preferred basic compounds are compounds belonging to amines. Among these, compounds belonging to tertiary amines. For example, triethylamine or pyridine. The ratio of the silicon salt to the basic compound is preferably 5 to 40 parts by mass of the basic compound with respect to 100 parts by mass of the silicon salt.

The catalyst of the present invention is particularly a silicon Lewis acid catalyst for synthesizing γ-keto α-amino acid compounds or β-aminocarbonyl compounds. Among them, the catalyst is used in the reaction of the compound represented by the general formula [II] (N-sulfonylimine) with the compound represented by the general formula [III] or the general formula [IV]. In general formula [II], R ⁵ represents an alkoxycarbonyl group or an aryl group which may have a substituent. Preferred R ⁵ is an alkoxycarbonyl group having 1 to 4 carbon atoms or an unsubstituted or monosubstituted aryl group having 5 to 10 carbon atoms. Among them, an ethoxycarbonyl group and a phenyl group. R ⁶ is an aryl group which may have a substituent. In particular, it is an aryl group having 5 to 10 carbon atoms. Among them, a p-tolyl group. In General Formula [III], R ⁷ is H or an alkyl group (preferably having 1 to 4 carbon atoms) which may have a substituent. Particularly preferred R ⁷ is H. R ⁸ and R ⁹ are an alkyl group, an alkoxy group or an aryl group which may have a substituent. It can be the same or different. Also, it may form a ring with the R ^7. Preferred R ⁸ and R ⁹ are alkyl groups having 1 to 4 carbon atoms. In particular, it is a methyl group. In general formula [IV], R ¹⁰ is H or an alkyl group (preferably having 1 to 4 carbon atoms) which may have a substituent. Particularly preferred R ¹⁰ is H. R ¹¹ is an alkyl group or an aryl group which may have a substituent. Then, they may form a ring with the R ^10. Preferred R ¹¹ is a phenyl group which may have a substituent.

  The method for producing a γ-keto α-amino acid compound of the present invention is represented by the compound represented by the above general formula [II] and the above general formula [III] in an organic solvent in the presence of the above catalyst. This is a method of reacting with a compound.

  The method for producing a β-aminocarbonyl compound of the present invention comprises a compound represented by the above general formula [II] and a compound represented by the above general formula [IV] in the presence of the above catalyst in an organic solvent. Is a method of reacting.

  Hereinafter, although a specific example is given and demonstrated, it is obvious for those skilled in the art that this invention is not limited to a following example.

1H
NMR (CDCl₃) δ＝7.86 (d, 2H), 7.76 (d, 2H), 7.58 (t, 1H), 7.42 (t,
2H), 7.22 (d, 2H), 5.79 (d, 1H), 4.22 (m, 1H), 4.03 (q, 2H), 3.60 (m, 2H), 2.39
(s. 3H), 1.08 (t, 3H) [Example 1]
A solution of ethyl-N-tosylimino ester (102 mg) in methylene chloride (1.0 mL) was mixed with a solution of acetophenone (97 mg) in methylene chloride (1.0 mL) and a solution of pyridine in methylene chloride (0.080 mol / L, 1.0 mL). ), Methylene chloride solution of silyl trifluoromethanesulfonate (0.080 mol / L, 1.0 mL) was sequentially added, and the mixture was stirred at room temperature in an argon atmosphere for 2 hours.
The reaction product thus obtained was purified by silica gel column chromatography to obtain ethyl 4-oxo-4-phenyl-2-tosylaminobutyrate (136 mg, yield 92%).

1H
NMR (CDCl ₃ ) δ = 7.86 (d, 2H), 7.76 (d, 2H), 7.58 (t, 1H), 7.42 (t,
2H), 7.22 (d, 2H), 5.79 (d, 1H), 4.22 (m, 1H), 4.03 (q, 2H), 3.60 (m, 2H), 2.39
(s. 3H), 1.08 (t, 3H)

1H
NMR (CDCl₃):δ＝7.72−7.67 (2H, m), 7.23−7.18 (2H, m), 5.87 (1H, d, J =
8.0 Hz), 4.09−4.04 (1H, m), 3.95−3.88 (2H, m), 3.1 (1H, dd, J = 16.7, 3.4 Hz),
2.87 (3H, s), 2.83 (3H, s), 2.80 (1H, dd, J = 16.7, 4.4 Hz), 2.34 (3H, s), 0.99
(3H, t, J = 7.2 Hz). [Example 2]
To a solution of tosylimino ester (51.0 mg, 0.20 mmol), N, N-dimethylacetamide (35.2 mg, 0.40 mmol), triethylamine (0.060 mmol) in tetrahydrofuran (1.0 mL) was added silyl trifluoromethanesulfonate. Of methylene chloride (0.120 mol / L, 0.5 mL) was added, and the mixture was stirred at room temperature in an argon atmosphere for 24 hours.
The reaction product thus obtained was purified by silica gel column chromatography to obtain ethyl 3-dimethylcarbamoyl-2-tosylaminopropionate (48.5 mg, 71% yield).

1H
NMR (CDCl ₃ ): δ = 7.72-7.67 (2H, m), 7.23-7.18 (2H, m), 5.87 (1H, d, J =
8.0 Hz), 4.09−4.04 (1H, m), 3.95−3.88 (2H, m), 3.1 (1H, dd, J = 16.7, 3.4 Hz),
2.87 (3H, s), 2.83 (3H, s), 2.80 (1H, dd, J = 16.7, 4.4 Hz), 2.34 (3H, s), 0.99
(3H, t, J = 7.2 Hz).

1H
NMR (CDCl₃):δ＝7.62−7.57 (2H, m), 7.28−7.12 (7H, m), 6.74 (1H, d, J =
6.9 Hz), 4.67 (1H, q, J = 5.8 Hz), 2.86−2.78 (1H, m), 2.80 (3H, s), 2.73 (3H,
s), 2.67 (1H, dd, J = 15.6, 5.0 Hz), 2.36 (3H, s).
［実施例４］
トリフェニルカルボニウムテトラキスペンタフルオロフェニルボラート（９２．２ｍｇ、０．１０ｍｍｏｌ）のＮ，Ｎ−ジメチルアセトアミド（１８５μＬ，２．０ｍｍｏｌ）溶液にトリストリメチルシリルシラン（２９μＬ，０．１１ｍｍｏｌ）を加え、よく撹拌する。そして、このように調製されたトリストリメチルシリルシリルテトラキスペンタフルオロフェニルボラートに、トリエチルアミン（１４μＬ，０．１０ｍｍｏｌ）、フェニルトシルメタンイミン（２５９ｍｇ，１．０ｍｍｏｌ）を順に加え、２４時間攪拌した。
このようにして得られた反応物をシリカゲルカラムクロマトグラフィーにて精製し、Ｎ，Ｎ−ジメチル−３−フェニル−３−トシルアミノプロピオンアミド（３４５ｍｇ，収率１００％）を得た。

尚、ＮＭＲのデータは日本電子社製のものを用い、テトラメチルシランを内部標準物質として測定したものである。カラムクロマトグラフィーには Silica gel 60 (Merck社製) を使用した。

代 理 人 宇 高 克 己 [Example 3]
A solution of phenyltosylmethanimine (259 mg, 1.0 mmol), triethylamine (28 μL, 0.20 mmol) in N, N-dimethylacetamide (185 μL, 2.0 mmol) in silyl trifluoromethanesulfonate (36 μL,
0.20 mmol) was added, and the mixture was stirred at room temperature in an argon atmosphere for 24 hours.
The reaction product thus obtained was purified by silica gel column chromatography to obtain N, N-dimethyl-3-phenyl-3-tosylaminopropionamide (178 mg, yield 51%).

1H
NMR (CDCl ₃ ): δ = 7.62-7.57 (2H, m), 7.28-7.12 (7H, m), 6.74 (1H, d, J =
6.9 Hz), 4.67 (1H, q, J = 5.8 Hz), 2.86−2.78 (1H, m), 2.80 (3H, s), 2.73 (3H,
s), 2.67 (1H, dd, J = 15.6, 5.0 Hz), 2.36 (3H, s).
[Example 4]
Add tristrimethylsilylsilane (29 μL, 0.11 mmol) to a solution of triphenylcarbonium tetrakispentafluorophenylborate (92.2 mg, 0.10 mmol) in N, N-dimethylacetamide (185 μL, 2.0 mmol) and stir well. To do. Then, triethylamine (14 μL, 0.10 mmol) and phenyltosylmethanimine (259 mg, 1.0 mmol) were sequentially added to the tristrimethylsilylsilyltetrakispentafluorophenylborate thus prepared, and stirred for 24 hours.
The reaction product thus obtained was purified by silica gel column chromatography to obtain N, N-dimethyl-3-phenyl-3-tosylaminopropionamide (345 mg, yield 100%).

The NMR data was obtained from JEOL Ltd. and measured using tetramethylsilane as an internal standard substance. Silica gel 60 (Merck) was used for column chromatography.

Representative Katsumi Udaka

Claims (14)

A silicon salt represented by the following general formula [I]:
A catalyst comprising a basic compound.
Formula [I]

[In the general formula [I], R ¹ , R ² and R ³ are each an alkyl group or a trialkylsilyl group, which may be the same or different, and R ⁴ is a perfluoroalkyl group. ] R ¹ , R ² , R ³ in the general formula [I] are any one selected from the group of an alkyl group having 1 to 4 carbon atoms and a trialkylsilyl group, and R ⁴ is perfluoro having 1 to ⁴ carbon atoms. The catalyst according to claim 1, which is a silicon salt of an alkyl group.   The catalyst according to claim 1 or 2, wherein the basic compound is a compound belonging to amines.   The catalyst according to claim 1 or 2, wherein the basic compound is a compound belonging to tertiary amines. The catalyst according to any one of claims 1 to 4, wherein the basic compound is in a proportion of 5 to 40 parts by mass with respect to 100 parts by mass of the silicon salt. A silicon salt represented by the following general formula [X];
A catalyst comprising a basic compound.
Formula [X]

[In general formula [X], R ⁴ , R ⁵ and R ⁶ are each an alkyl group or a trialkylsilyl group, and may be the same or different. R ⁷ , R ⁸ , R ⁹ and R ¹⁰ are electron-withdrawing substituents, and may be the same or different. ]   The catalyst according to claim 6, wherein the basic compound is a compound belonging to amines.   The catalyst according to claim 6 or 7, wherein the basic compound is a compound belonging to a tertiary amine. The catalyst according to any one of claims 6 to 8, wherein the basic compound is in a proportion of 5 to 40 parts by mass with respect to 100 parts by mass of the silicon salt. The catalyst according to any one of claims 1 to 9, which is a silicon Lewis acid catalyst for synthesizing a γ-keto α-amino acid compound or a β-aminocarbonyl compound. The catalyst according to any one of claims 1 to 9, wherein the catalyst is used in the reaction of a compound represented by the following general formula [II] with a compound represented by the following general formula [III]. .
Formula [II]

[In General Formula [II], R ⁵ is an alkoxycarbonyl group or an aryl group which may have a substituent, and R ⁶ is an aryl group which may have a substituent. ]
Formula [III]

In the General Formula [III], ^{R 7} is H or an optionally substituted alkyl group ^may form a ring with the ^{R 8, R 9, R 8} , R 9 is The alkyl group, alkoxy group or aryl group which may have a substituent may be the same or different. ] The catalyst according to any one of claims 1 to 9, which is a catalyst used in the reaction of a compound represented by the following general formula [II] and a compound represented by the following general formula [IV]: .
Formula [II]

[In General Formula [II], R ⁵ is an alkoxycarbonyl group or an aryl group which may have a substituent, and R ⁶ is an aryl group which may have a substituent. ]
Formula [IV]

[In the general formula [IV], R ¹⁰ is H or an optionally substituted alkyl group may form a ring with the R ^11, R ¹¹ has a substituent An alkyl group or an aryl group which may be present. ] A compound represented by the following general formula [II] and a compound represented by the following general formula [III] are reacted in the presence of the catalyst according to any one of claims 1 to 9. A method for producing a γ-keto α-amino acid compound.
Formula [II]

[In General Formula [II], R ⁵ is an alkoxycarbonyl group or an aryl group which may have a substituent, and R ⁶ is an aryl group which may have a substituent. ]
Formula [III]

In the General Formula [III], ^{R 7} is H or an optionally substituted alkyl group ^may form a ring with the ^{R 8, R 9, R 8} , R 9 is The alkyl group, alkoxy group or aryl group which may have a substituent may be the same or different. ] A compound represented by the following general formula [II] and a compound represented by the following general formula [IV] are reacted in the presence of the catalyst according to any one of claims 1 to 9. A method for producing a β-aminocarbonyl compound.
Formula [II]

[In General Formula [II], R ⁵ is an alkoxycarbonyl group or an aryl group which may have a substituent, and R ⁶ is an aryl group which may have a substituent. ]
Formula [IV]

[In the general formula [IV], R ¹⁰ is H or an alkyl group, may form a ring with the R ^11, R ¹¹ is an optionally substituted alkyl group or an aryl group It is. ]