JP6261111B2

JP6261111B2 - Method for reducing arenesulfonamide and method for producing arenesulfonic acid

Info

Publication number: JP6261111B2
Application number: JP2013148664A
Authority: JP
Inventors: 石原　一彰; 一彰石原; 学波多野; 圭祐西川
Original assignee: Nagoya University NUC; Tokai National Higher Education and Research System NUC
Current assignee: Nagoya University NUC; Tokai National Higher Education and Research System NUC
Priority date: 2013-07-17
Filing date: 2013-07-17
Publication date: 2018-01-17
Anticipated expiration: 2033-07-17
Also published as: JP2015020961A

Description

本発明は、アレーンスルホンアミドの還元方法、アレーンスルホン酸の製法及びビナフチルジスルホン酸に関する。 The present invention relates to a method for reducing arenesulfonamide, a method for producing arenesulfonic acid, and binaphthyl disulfonic acid.

１，１’−ビナフチル−２，２’−ジスルホン酸（ＢＩＮＳＡ）は、アレーンスルホン酸の一種であるが、例えばピリジニウム塩として不斉マンニッヒ触媒として利用可能であることが知られている（特許文献１）。ＢＩＮＳＡの合成方法としては、ビナフトールの２，２’位のＯＨ基をＯ−チオカルバモイルに変換し、それを転移反応によってＳ−チオカルバモイルに変換後、スルホン酸基へ導くものが報告されている（非特許文献１）。 1,1′-binaphthyl-2,2′-disulfonic acid (BINSA) is a kind of arenesulfonic acid, and is known to be usable as an asymmetric Mannich catalyst, for example, as a pyridinium salt (Patent Document) 1). As a method for synthesizing BINSA, a method has been reported in which the OH group at the 2,2 ′ position of binaphthol is converted to O-thiocarbamoyl, which is converted to S-thiocarbamoyl by a transfer reaction and then led to a sulfonic acid group. (Non-Patent Document 1).

ところで、アレーンスルホンアミドは、化学的に安定であり、激しい反応条件に耐え得るため、アミンの保護基として、有機合成的に幅広く用いられている。スルホンアミドの保護の主体はアミンであるため、スルホンアミドの脱保護によりアミンを製造する方法は多数確立されている。スルホンアミドの脱保護には、例えば、強酸（ＨＢｒ，ＨＣｌＯ₄，トリフルオロ酢酸など）、強塩基（ＫＯＨ，ＮａＯＨなど）、ヨウ化サマリウム、塩化チタン（III）、Ｂｕ₃ＳｎＨ／ＡＩＢＮ、金属リチウム／ナフタレン、光反応、電気分解などが用いられる。これらは、スルホンアミドのスルホン部位を、例えば二酸化硫黄（ＳＯ₂）などに分解しながら脱保護するため、スルフィン酸やスルホン酸として取り出すことは原理的にできなかった。一方、スルホンアミドの脱保護をＫＰＰｈ₂によって行うことにより、スルフィン酸とアミンを得る例も報告されている（非特許文献２）。この非特許文献２では、スルフィン酸は不安定であるとして単離していない。更に、Ｎ−トリフリルアジリジンをＮａＡｌＨ₂（ＯＣ₂Ｈ₄ＯＣＨ₃）₂（Ｒｅｄ−Ａｌという）で還元してトリフリル基が脱保護されたアジリジンを得た例が報告されている（非特許文献３）。この非特許文献３では、スルホン部位については言及されていない。 By the way, arenesulfonamides are chemically stable and can withstand harsh reaction conditions, and thus are widely used as organic protecting groups for organic synthesis. Since the main component of sulfonamide protection is an amine, many methods for producing an amine by deprotection of the sulfonamide have been established. For deprotection of sulfonamide, for example, strong acid (HBr, HClO ₄ , trifluoroacetic acid, etc.), strong base (KOH, NaOH, etc.), samarium iodide, titanium (III) chloride, Bu ₃ SnH / AIBN, metallic lithium / Naphthalene, photoreaction, electrolysis, etc. are used. Since these deprotect the sulfone moiety of the sulfonamide while decomposing it into, for example, sulfur dioxide (SO ₂ ) or the like, it was not possible in principle to take it out as sulfinic acid or sulfonic acid. On the other hand, an example of obtaining sulfinic acid and an amine by deprotecting sulfonamide with KPPh ₂ has been reported (Non-patent Document 2). In this non-patent document 2, sulfinic acid is not isolated as being unstable. Furthermore, an example in which N-trifurylaziridine was reduced with NaAlH ₂ (OC ₂ H ₄ OCH ₃ ) ₂ (referred to as Red-Al) to obtain aziridine in which the trifuryl group was deprotected has been reported (Non-patent Document). 3). This Non-Patent Document 3 does not mention the sulfone moiety.

国際公開第２００９／５４２４０号パンフレットInternational Publication No. 2009/54240 Pamphlet

Angew. Chem., Int. Ed. 2009, vol48, p4363Angew. Chem., Int. Ed. 2009, vol48, p4363 J. Am. Chem. Soc. 2012, vol34, p19358J. Am. Chem. Soc. 2012, vol34, p19358 J. Org. Chem. 1972, vol37, p2208J. Org. Chem. 1972, vol37, p2208

上述したように、アレーンスルホンアミドの脱保護によりアミンを製造する方法は知られているものの、アレーンスルホンアミドからそれに対応するスルフィン酸などの還元体を製造する方法は知られていなかった。 As described above, although a method for producing an amine by deprotection of arenesulfonamide is known, a method for producing a corresponding reduced form such as sulfinic acid from arenesulfonamide has not been known.

本発明はこのような課題を解決するためになされたものであり、アレーンスルホンアミドから対応する還元体を収率よく得ることを主目的とする。 The present invention has been made to solve such problems, and a main object of the present invention is to obtain a corresponding reduced product from arenesulfonamide in a high yield.

上述した目的を達成するために、本発明者らは、Ｎ，Ｎ−ジメチル−２−ナフタレンスルホンアミドをモデル基質として用い、種々の還元剤を用いて還元反応を試みたところ、Ｒｅｄ−Ａｌを用いたときに、過剰還元によって生成するナフタレンの副生を抑制しつつ、対応する還元体が収率よく得られることを見いだし、本発明を完成するに至った。 In order to achieve the above-mentioned object, the present inventors tried reduction reaction using various reducing agents using N, N-dimethyl-2-naphthalenesulfonamide as a model substrate. When used, it was found that the corresponding reductant was obtained in good yield while suppressing the by-product of naphthalene produced by excessive reduction, and the present invention was completed.

即ち、本発明のアレーンスルホンアミドの還元方法は、ＡｒＳＯ₂ＮＲ¹Ｒ²（Ａｒは置換基を有していてもよいアレーンであり、Ｒ¹及びＲ²は同じでも異なっていてもよいアルキル基である）で表されるアレーンスルホンアミドを、ＭＡｌＨ_ｎＲ_４−ｎ（Ｍはアルカリ金属であり、ｎは１〜３のいずれかの整数であり、Ｒはアルコキシ基又はアルコキシアルコキシ基である）で表される還元剤で還元することにより、対応するスルフィン酸、スルフェン酸、ジスルフィド及びチオールの少なくとも１つの還元体を得るものである。 That is, in the method for reducing an arenesulfonamide of the present invention, ArSO ₂ NR ¹ R ² (Ar is an arene which may have a substituent, and R ¹ and R ² may be the same or different alkyl groups. MALH _n R _4-n (M is an alkali metal, n is an integer of 1 to 3, and R is an alkoxy group or an alkoxyalkoxy group) To obtain at least one reduced form of the corresponding sulfinic acid, sulfenic acid, disulfide and thiol.

本発明のアレーンスルホンアミドの還元方法によれば、アレーンスルホンアミドから対応する還元体を収率よく得ることができる。また、得られた還元体は、酸素又は過酸化水素で酸化することにより、対応するアレーンスルホン酸に容易に変換することができる。 According to the method for reducing an arenesulfonamide of the present invention, a corresponding reduced product can be obtained from the arenesulfonamide with a high yield. The obtained reduced product can be easily converted to the corresponding arenesulfonic acid by oxidation with oxygen or hydrogen peroxide.

本発明のアレーンスルホンアミドの還元方法では、ＡｒＳＯ₂ＮＲ¹Ｒ²で表されるアレーンスルホンアミドを反応基質として用いる。ここで、Ａｒは置換基を有していてもよいアレーンである。アレーンとしては、ベンゼン、１−ナフタレン、２−ナフタレン、１−アントラセン、２−アントラセン、９−アントラセン、１−フェナントレン、２−フェナントレン、３−フェナントレン、４−フェナントレン、９−フェナントレン、ビフェニル、ビナフチルなどが挙げられる。アレーンは１つ以上の置換基を有していてもよい。その場合、置換基としては、ハロゲン原子、アルキル基、アリール基、スルホン酸エステル基などが挙げられる。Ｒ¹及びＲ²は同じでも異なっていてもよいアルキル基である。アルキル基としては、メチル基、エチル基、プロピル基、イソプロピル基、ｎ−ブチル基、イソブチル基、ｓｅｃ−ブチル基、ｔｅｒｔ−ブチル基などが挙げられる。 In the arenesulfonamide reduction method of the present invention, arenesulfonamide represented by ArSO ₂ NR ¹ R ² is used as a reaction substrate. Here, Ar is an arene which may have a substituent. Examples of arenes include benzene, 1-naphthalene, 2-naphthalene, 1-anthracene, 2-anthracene, 9-anthracene, 1-phenanthrene, 2-phenanthrene, 3-phenanthrene, 4-phenanthrene, 9-phenanthrene, biphenyl, and binaphthyl. Is mentioned. The arene may have one or more substituents. In that case, examples of the substituent include a halogen atom, an alkyl group, an aryl group, and a sulfonate group. R ¹ and R ² are alkyl groups which may be the same or different. Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group.

本発明のアレーンスルホンアミドの還元方法では、ＭＡｌＨ_ｎＲ_４−ｎ（Ｍはアルカリ金属であり、ｎは１〜３のいずれかの整数であり、Ｒはアルコキシ基又はアルコキシアルコキシ基である）で表される還元剤を用いる。ここで、Ｍとしては、Ｌｉ，Ｎａ，Ｋなどが挙げられ、このうちＮａが好ましい。ｎは、２であることが好ましい。アルコキシ基としては、メトキシ基、エトキシ基、プロポキシ基、イソプロポキシ基、ｎ−ブトキシ基、イソブトキシ基、ｓｅｃ−ブトキシ基、ｔｅｒｔ−ブトキシ基などが挙げられる。アルコキシアルコキシ基としては、メトキシメトキシ基、２−メトキシエトキシ基、２−メトキシプロポキシ基、３−メトキシプロポキシ基などが挙げられ、このうち２−メトキシエトキシ基が好ましい。こうした還元剤としては、Ｒｅｄ−ＡｌすなわちＮａＡｌＨ₂（ＯＣ₂Ｈ₄ＯＣＨ₃）₂が好ましい。還元剤の使用量は、スルホンアミドに対して１〜２０当量の範囲で設定するのが好ましく、３〜１０当量の範囲で設定するのがより好ましく、５〜１０当量の範囲で設定するのが更に好ましい。 In the arenesulfonamide reduction method of the present invention, MAlH _n R _4-n (M is an alkali metal, n is an integer of 1 to 3, and R is an alkoxy group or an alkoxyalkoxy group). The reducing agent represented is used. Here, examples of M include Li, Na, K and the like, and among these, Na is preferable. n is preferably 2. Examples of the alkoxy group include a methoxy group, an ethoxy group, a propoxy group, an isopropoxy group, an n-butoxy group, an isobutoxy group, a sec-butoxy group, and a tert-butoxy group. Examples of the alkoxyalkoxy group include a methoxymethoxy group, a 2-methoxyethoxy group, a 2-methoxypropoxy group, and a 3-methoxypropoxy group, and among them, a 2-methoxyethoxy group is preferable. As such a reducing agent, Red-Al, that is, NaAlH ₂ (OC ₂ H ₄ OCH ₃ ) ₂ is preferable. The amount of the reducing agent used is preferably set in the range of 1 to 20 equivalents relative to the sulfonamide, more preferably in the range of 3 to 10 equivalents, and in the range of 5 to 10 equivalents. Further preferred.

本発明のアレーンスルホンアミドの還元方法では、溶媒を用いることが好ましい。溶媒としては、例えば、エーテル系溶媒が挙げられる。エーテル系溶媒としては、ジエチルエーテル、ジイソプロピルエーテル、メチル−ｔｅｒｔ−ブチルエーテル、テトラヒドロフラン、１，２−ジメトキシエタン、１，２−ジエトキシエタン、ジオキサン、シクロペンチルメチルエーテルなどが挙げられる。反応溶媒の使用量は、基質の濃度が０．００１〜０．５ｍｏｌ／Ｌとなるように設定するのが好ましく、０．０１〜０．１ｍｏｌ／Ｌとなるように設定するのがより好ましい。 In the method for reducing arenesulfonamide of the present invention, it is preferable to use a solvent. Examples of the solvent include ether solvents. Examples of the ether solvent include diethyl ether, diisopropyl ether, methyl-tert-butyl ether, tetrahydrofuran, 1,2-dimethoxyethane, 1,2-diethoxyethane, dioxane, cyclopentylmethyl ether and the like. The amount of reaction solvent used is preferably set so that the concentration of the substrate is 0.001 to 0.5 mol / L, and more preferably 0.01 to 0.1 mol / L.

本発明のアレーンスルホンアミドの還元方法では、反応温度は、−１０℃〜１００℃が好ましく、０〜５０℃がより好ましい。反応系の雰囲気は、窒素ガスやアルゴンガスなどの不活性雰囲気が好ましい。反応時間は、反応基質や還元剤、反応温度に応じて適宜設定すればよい。還元反応は、アレーンスルホンアミドが消失するまで行ってもよいが、副反応が起こりやすい場合には、アレーンスルホンアミドが消失する前に終了してもよい。 In the arenesulfonamide reduction method of the present invention, the reaction temperature is preferably -10 ° C to 100 ° C, more preferably 0 to 50 ° C. The atmosphere of the reaction system is preferably an inert atmosphere such as nitrogen gas or argon gas. What is necessary is just to set reaction time suitably according to a reaction substrate, a reducing agent, and reaction temperature. The reduction reaction may be performed until the arenesulfonamide disappears, but may be terminated before the arenesulfonamide disappears when side reactions are likely to occur.

本発明のアレーンスルホンアミドの還元方法では、還元体としてアレーンスルホンアミドに対応するスルフィン酸（−ＳＯ₂Ｈ）を選択的に得ることが好ましい。スルフェン酸（−ＳＯＨ）やジスルフィド（−Ｓ−Ｓ−）やチオール（−ＳＨ）まで還元してしまうと、次に酸化でスルホン酸に変換する場合に酸化剤が多く必要になってしまうからである。スルフィン酸を選択的に得るには、例えば還元剤の使用量をスルホンアミドの５〜１０当量とするのが好ましい。こうすれば、過剰な還元反応を抑制することができる。 In the arenesulfonamide reduction method of the present invention, it is preferable to selectively obtain sulfinic acid (—SO ₂ H) corresponding to arenesulfonamide as a reduced form. If sulfenic acid (—SOH), disulfide (—S—S—), and thiol (—SH) are reduced, a large amount of oxidizing agent is required for the subsequent conversion to sulfonic acid by oxidation. is there. In order to selectively obtain sulfinic acid, for example, the amount of reducing agent used is preferably 5 to 10 equivalents of sulfonamide. In this way, excessive reduction reaction can be suppressed.

本発明のアレーンスルホン酸の製法では、上述したアレーンスルホンアミドの還元方法によって得られた前記還元体を、酸素又は過酸化水素で酸化することにより、対応するスルホン酸を得る。 In the process for producing arenesulfonic acid of the present invention, the corresponding sulfonic acid is obtained by oxidizing the reduced product obtained by the above-described method for reducing arenesulfonamide with oxygen or hydrogen peroxide.

酸素で酸化する場合、酸素ガスを用いてもよいし空気中の酸素を用いてもよいが、酸素ガスを用いることが好ましい。酸素圧は、特に限定するものではないが、例えば１〜１０ａｔｍの範囲で適宜設定すればよい。酸素で酸化する場合、溶媒は、酸素に不活性な溶媒であればよく、例えば、ＨＭＰＡやＤＭＦ、ＤＭＳＯ、アセトニトリル、アセトンなどの極性非プロトン性溶媒が挙げられる。また、水酸化カリウムなどの塩基の存在下で酸化を行ってもよい。過酸化水素で酸化する場合、過酸化水素水を用いることが好ましい。その場合、溶媒は、過酸化水素に不活性な溶媒であればよく、例えば、酢酸メチルや酢酸エチルなどのエステル系溶媒が挙げられる。反応温度は、−１０℃〜１００℃が好ましく、０〜５０℃がより好ましい。反応時間は、反応基質や酸化剤、反応温度に応じて適宜設定すればよい。酸化反応は、アレーンスルホンアミドの還元体が消失するまで行ってもよいが、副反応が起こりやすい場合には、還元体が消失する前に終了してもよい。 When oxidizing with oxygen, oxygen gas or oxygen in the air may be used, but oxygen gas is preferably used. The oxygen pressure is not particularly limited, but may be appropriately set within a range of 1 to 10 atm, for example. When oxidizing with oxygen, the solvent may be any solvent inert to oxygen, and examples thereof include polar aprotic solvents such as HMPA, DMF, DMSO, acetonitrile, and acetone. Moreover, you may oxidize in presence of bases, such as potassium hydroxide. When oxidizing with hydrogen peroxide, it is preferable to use aqueous hydrogen peroxide. In that case, the solvent may be any solvent inert to hydrogen peroxide, and examples thereof include ester solvents such as methyl acetate and ethyl acetate. The reaction temperature is preferably -10 ° C to 100 ° C, more preferably 0 to 50 ° C. What is necessary is just to set reaction time suitably according to a reaction substrate, an oxidizing agent, and reaction temperature. The oxidation reaction may be performed until the reduced form of arenesulfonamide disappears. However, if a side reaction is likely to occur, the oxidation reaction may be completed before the reduced form disappears.

本発明のアレーンスルホン酸の製法では、式（１）で表される光学活性スルホンアミドを、前記還元剤による還元とそれに続く酸化によって、式（２）で表される光学活性ジスルホン酸を得るようにしてもよい。式（２）で表される光学活性ジスルホン酸は、種々の有機合成反応の触媒としての利用が期待される。 In the process for producing arenesulfonic acid of the present invention, an optically active disulfonic acid represented by the formula (2) is obtained by reducing the optically active sulfonamide represented by the formula (1) with the reducing agent and subsequent oxidation. It may be. The optically active disulfonic acid represented by the formula (2) is expected to be used as a catalyst for various organic synthesis reactions.

式（１），（２）中、Ｒ¹及びＲ²は前述の通りである。Ｒ³はアルキル基である。アルキル基としては、メチル基、エチル基、プロピル基、イソプロピル基、ｎ−ブチル基、イソブチル基、ｓｅｃ−ブチル基、ｔｅｒｔ−ブチル基などが挙げられる。Ｒ⁴及びＲ⁵は同じであっても異なっていてもよく、水素原子、ハロゲン原子又は置換基を有していてもよいアリール基である。ハロゲン原子としては、塩素原子、臭素原子、ヨウ素原子などが挙げられる。アリール基としては、フェニル基、１−ナフチル基、２−ナフチル基、１−アントラセニル基、２−アントラセニル基、５−アントラセニル基、１−フェナントレニル基、２−フェナントレニル基、３−フェナントレニル基、４−フェナントレニル基、９−フェナントレニル基などが挙げられる。アリール基は１つ以上の置換基を有していてもよい。その場合、置換基としては、ハロゲン原子やアルキル基、アリール基、アルコキシ基などが挙げられる。これらの具体例については、既に説明したとおりである。 In formulas (1) and (2), R ¹ and R ² are as described above. R ³ is an alkyl group. Examples of the alkyl group include a methyl group, an ethyl group, a propyl group, an isopropyl group, an n-butyl group, an isobutyl group, a sec-butyl group, and a tert-butyl group. R ⁴ and R ⁵ may be the same or different and are a hydrogen atom, a halogen atom or an aryl group which may have a substituent. Examples of the halogen atom include a chlorine atom, a bromine atom, and an iodine atom. As the aryl group, phenyl group, 1-naphthyl group, 2-naphthyl group, 1-anthracenyl group, 2-anthracenyl group, 5-anthracenyl group, 1-phenanthrenyl group, 2-phenanthrenyl group, 3-phenanthrenyl group, 4- Examples thereof include a phenanthrenyl group and a 9-phenanthrenyl group. The aryl group may have one or more substituents. In that case, examples of the substituent include a halogen atom, an alkyl group, an aryl group, and an alkoxy group. These specific examples are as already described.

本発明のアレーンスルホン酸の製法によれば、３，３’位に種々の置換基（特にアリール基）を有する光学活性ビナフチルジスルホン酸を合成することができる。例えば、式（３）で表される新規なビナフチルジスルホン酸を合成することができる。 According to the process for producing arenesulfonic acid of the present invention, it is possible to synthesize optically active binaphthyl disulfonic acid having various substituents (particularly aryl groups) at the 3,3 ′ positions. For example, a novel binaphthyl disulfonic acid represented by the formula (3) can be synthesized.

［実施例１］
窒素置換した反応容器に、Ｎ，Ｎ−ジメチルナフタレン−２−スルホンアミド（２３．５ｍｇ，０．１０ｍｍｏｌ）とＴＨＦ（４ｍＬ）を加えて、０℃に冷却し、Ｒｅｄ−Ａｌ（６５ｗｔ％トルエン溶液、０．３０ｍＬ，１．０ｍｍｏｌ）を加えた。同混合物を４０℃で２２時間加熱した。反応終了をＴＬＣで確認し、０℃に冷却した後、激しく撹拌しながら硫酸ナトリウムの飽和水溶液を適量加え、酢酸エチル（１０ｍＬ×２）を用いて通常の分液処理を行った。抽出した有機層は飽和塩化ナトリウム水溶液（５ｍＬ）で洗浄し、硫酸マグネシウムで乾燥後、ろ過、濃縮した。得られた濃縮物は、精製せずにそのまま以降の操作を続けた。得られた濃縮物にヘキサメチルリン酸トリアミド（ＨＭＰＡ）（１ｍＬ）、水酸化カリウム（３３．７ｍｇ，０．６０ｍｍｏｌ）を加え、約５気圧（０．５ＭＰａ）の酸素を封入した。この混合物を８０℃で１０時間加熱した。反応終了後、室温まで冷却し、そのままシリカゲルカラムクロマトグラフィー（クロロホルム：メタノール＝１：１）にて生成物を分取し、目的の２−ナフタレンスルホン酸カリウム塩を収率７１％（１７．８ｍｇ）で得た。得られた２−ナフタレンスルホン酸カリウム塩のスペクトルデータは以下のとおり。 [Example 1]
N, N-dimethylnaphthalene-2-sulfonamide (23.5 mg, 0.10 mmol) and THF (4 mL) were added to the reaction vessel purged with nitrogen, cooled to 0 ° C., and Red-Al (65 wt% toluene solution). , 0.30 mL, 1.0 mmol) was added. The mixture was heated at 40 ° C. for 22 hours. After completion of the reaction was confirmed by TLC and cooled to 0 ° C., an appropriate amount of a saturated aqueous solution of sodium sulfate was added with vigorous stirring, and normal liquid separation treatment was performed using ethyl acetate (10 mL × 2). The extracted organic layer was washed with a saturated aqueous sodium chloride solution (5 mL), dried over magnesium sulfate, filtered and concentrated. The obtained concentrate was continued without further purification. Hexamethylphosphoric triamide (HMPA) (1 mL) and potassium hydroxide (33.7 mg, 0.60 mmol) were added to the obtained concentrate, and oxygen at about 5 atm (0.5 MPa) was enclosed. The mixture was heated at 80 ° C. for 10 hours. After completion of the reaction, the reaction mixture was cooled to room temperature, and the product was fractionated by silica gel column chromatography (chloroform: methanol = 1: 1) as it was to obtain the desired 2-naphthalenesulfonic acid potassium salt in a yield of 71% (17.8 mg). ). The spectrum data of the obtained 2-naphthalenesulfonic acid potassium salt are as follows.

¹H NMR (400 MHz, CD₃OD) δ 7.55 (m, 2H), 7.85-8.00 (m, 4H), 8.34 (s, 1H). ¹³C NMR (100 MHz, d₆-DMSO:D₂O = 3:1) δ 124.0, 126.0, 128.5, 129.0, 129.1, 129.8, 129.9, 133.1, 134.7, 143.1. IR (KBr) 3422, 1624, 1230, 1186, 1101, 1045 cm^-1. HRMS (FAB-) calcd for C₁₀H₇O₃S [M-K]^- 207.0116, found 207.0118. ¹ H NMR (400 MHz, CD ₃ OD) δ 7.55 (m, 2H), 7.85-8.00 (m, 4H), 8.34 (s, 1H). ¹³ C NMR (100 MHz, d ₆ -DMSO: D ₂ O = 3: 1) δ 124.0, 126.0, 128.5, 129.0, 129.1, 129.8, 129.9, 133.1, 134.7, 143.1.IR (KBr) 3422, 1624, 1230, 1186, 1101, 1045 cm ^-1 .HRMS (FAB-) _{_{_{calcd for C 10 H 7 O 3}}} S [MK] - 207.0116, found 207.0118.

［比較例１〜３］
実施例１のＲｅｄ−Ａｌの代わりに、比較例１ではＤＩＢＡＬ（水素化ジイソブチルアルミニウム）、比較例２ではＬｉＡｌＨ₄（水素化リチウムアルミニウム）、比較例３ではＡｌＨ₃（水素化アルミニウム）を用いた以外は、実施例１と同様にして反応を行った。具体的な反応条件及び結果を表１に示す。比較のために実施例１の反応条件及び結果も表１に示した。 [Comparative Examples 1-3]
In place of Red-Al of Example 1, DIBAL (diisobutylaluminum hydride) was used in Comparative Example 1, LiAlH ₄ (lithium aluminum hydride) was used in Comparative Example 2, and AlH ₃ (aluminum hydride) was used in Comparative Example 3. The reaction was carried out in the same manner as in Example 1 except that. Specific reaction conditions and results are shown in Table 1. For comparison, the reaction conditions and results of Example 1 are also shown in Table 1.

表１に示すように、還元剤としてＤＩＢＡＬを用いた比較例１では、還元反応が進行せず、未反応のスルホンアミドが定量的に回収された。また、還元剤としてＬｉＡｌＨ₄やＡｌＨ₃を用いた比較例２，３では、還元反応及びそれに続く酸化反応の後に、対応するスルホン酸カリウムがそれぞれ収率４６％，４９％で得られた。この比較例２，３では、還元反応でＣ−Ｓ結合が切断されたナフタレンが約３０％副生し、これがスルホン酸カリウムの収率を中程度にとどめた原因となった。これに対して、還元剤としてＲｅｄ−Ａｌを用いた実施例１では、ナフタレンの副生を約５％にまで抑制することができ、目的とするスルホン酸カリウムが収率７１％で得られた。 As shown in Table 1, in Comparative Example 1 using DIBAL as the reducing agent, the reduction reaction did not proceed and unreacted sulfonamide was quantitatively recovered. In Comparative Examples 2 and ₃ using LiAlH ₄ or AlH ₃ as the reducing agent, the corresponding potassium sulfonates were obtained in a yield of 46% and 49%, respectively, after the reduction reaction and the subsequent oxidation reaction. In Comparative Examples 2 and 3, about 30% of the naphthalene with the C—S bond cleaved by the reduction reaction was by-produced, which caused the yield of potassium sulfonate to be moderate. On the other hand, in Example 1 using Red-Al as the reducing agent, the by-product of naphthalene could be suppressed to about 5%, and the target potassium sulfonate was obtained in a yield of 71%. .

［実施例２〜５］
実施例２〜５では、Ｎ，Ｎ−ジメチルナフタレン−２−スルホンアミドを下記式に記載した条件で実施例１に準じて還元及び酸化を行い、更にアンバーライトでイオン交換を行うことにより、目的の２−ナフタレンスルホン酸を高収率で得た。 [Examples 2 to 5]
In Examples 2 to 5, N, N-dimethylnaphthalene-2-sulfonamide was reduced and oxidized according to Example 1 under the conditions described in the following formula, and further ion exchange was performed with amberlite. Of 2-naphthalenesulfonic acid was obtained in high yield.

［実施例６］
実施例６では、下記式に示すように、Ｎ，Ｎ−ジメチルナフタレン−２−スルホンアミドをＲｅｄ−Ａｌで還元して対応するスルフィン酸を単離し、その後、単離したスルフィン酸を酸素で酸化して対応するスルホン酸を得た。以下にその実験手順を説明する。 [Example 6]
In Example 6, as shown in the following formula, N, N-dimethylnaphthalene-2-sulfonamide was reduced with Red-Al to isolate the corresponding sulfinic acid, and then the isolated sulfinic acid was oxidized with oxygen. The corresponding sulfonic acid was obtained. The experimental procedure will be described below.

［６−１］還元反応
窒素置換した反応容器に、Ｎ，Ｎ−ジメチルナフタレン−２−スルホンアミド（２３．５ｍｇ，０．１０ｍｍｏｌ）とＴＨＦ（４ｍＬ）を加えて、０℃に冷却し、Ｒｅｄ−Ａｌ（６５ｗｔ％トルエン溶液、０．１５ｍＬ，０．５０ｍｍｏｌ）を加えた。同混合物を室温で５時間撹拌した。反応終了をＴＬＣで確認し、０℃に冷却した後、激しく撹拌しながら硫酸ナトリウムの飽和水溶液を適量加え、酢酸エチル（１０ｍＬ×２）を用いて通常の分液処理を行った。抽出した有機層を飽和塩化ナトリウム水溶液（５ｍＬ）で洗浄し、硫酸マグネシウムで乾燥後、ろ過、濃縮し、目的の２−ナフタレンスルフィン酸を収率９５％（１８．４ｍｇ）で得た。得られた２−ナフタレンスルフィン酸のスペクトルデータは以下のとおり。 [6-1] Reduction Reaction N, N-dimethylnaphthalene-2-sulfonamide (23.5 mg, 0.10 mmol) and THF (4 mL) were added to a nitrogen-substituted reaction vessel, cooled to 0 ° C., and Red. -Al (65 wt% toluene solution, 0.15 mL, 0.50 mmol) was added. The mixture was stirred at room temperature for 5 hours. After completion of the reaction was confirmed by TLC and cooled to 0 ° C., an appropriate amount of a saturated aqueous solution of sodium sulfate was added with vigorous stirring, and normal liquid separation treatment was performed using ethyl acetate (10 mL × 2). The extracted organic layer was washed with a saturated aqueous sodium chloride solution (5 mL), dried over magnesium sulfate, filtered and concentrated to obtain the desired 2-naphthalenesulfinic acid in a yield of 95% (18.4 mg). The spectrum data of the obtained 2-naphthalenesulfinic acid are as follows.

¹H NMR (400 MHz, CD₃OD) δ 7.55 (m, 2H), 7.85-8.00 (m, 4H), 8.34 (s, 1H). ¹³C NMR (100 MHz, d₆-DMSO:D₂O = 3:1) δ 124.0, 126.0, 128.5, 129.0, 129.1, 129.8, 129.9, 133.1, 134.7, 143.1. ¹ H NMR (400 MHz, CD ₃ OD) δ 7.55 (m, 2H), 7.85-8.00 (m, 4H), 8.34 (s, 1H). ¹³ C NMR (100 MHz, d ₆ -DMSO: D ₂ O = 3: 1) δ 124.0, 126.0, 128.5, 129.0, 129.1, 129.8, 129.9, 133.1, 134.7, 143.1.

［６−２］酸化反応
続いて、窒素置換した反応容器に、２−ナフタレンスルフィン酸（９６．１ｍｇ，０．５０ｍｍｏｌ）、ジメチルホルムアミド（ＤＭＦ）（５ｍＬ）を加え、風船の酸素を封入した（１気圧）。この混合物を６０℃で２８時間加熱した。反応終了後、室温まで冷却し、溶媒を留去して、減圧乾燥（１〜２Ｔｏｒｒ）し、目的の２−ナフタレンスルホン酸を収率９５％（１００ｍｇ）で得た。 [6-2] Oxidation Reaction Subsequently, 2-naphthalenesulfinic acid (96.1 mg, 0.50 mmol) and dimethylformamide (DMF) (5 mL) were added to a nitrogen-substituted reaction vessel, and balloon oxygen was sealed ( 1 atm). The mixture was heated at 60 ° C. for 28 hours. After completion of the reaction, the reaction mixture was cooled to room temperature, the solvent was distilled off, and the residue was dried under reduced pressure (1-2 Torr) to obtain the desired 2-naphthalenesulfonic acid in a yield of 95% (100 mg).

［実施例７］
下記式にしたがって、ジスルホンイミド（化合物１０）を出発物質として、目的とする３，３’−ジフェニル−１，１’−ビナフチル−２，２’ジスルホン酸（化合物２２）を合成した。なお、化合物１０は文献Eur. J. Org. Chem. 2010, p4181の記載にしたがって合成した。 [Example 7]
According to the following formula, the target 3,3′-diphenyl-1,1′-binaphthyl-2,2′disulfonic acid (Compound 22) was synthesized using disulfonimide (Compound 10) as a starting material. Compound 10 was synthesized as described in the literature Eur. J. Org. Chem. 2010, p4181.

［７−１］ステップ１
窒素置換したシュレンク反応容器に、化合物１０（Ｒ体、３２８．６ｍｇ，０．６０ｍｍｏｌ）、炭酸カリウム（２４９ｍｇ，１．８０ｍｍｏｌ）、塩化メチレン（１０ｍＬ）を加えて、０℃に冷却した。トリメチルオキソニウムテトラフルオロボラート（２６６．２ｍｇ，１．８０ｍｍｏｌ）を加えた後、室温まで昇温し、４時間撹拌した。反応終了をＴＬＣで確認した後、飽和塩化アンモニウム水溶液（５ｍＬ）を加え、酢酸エチル（１５ｍＬ×２）を用いて通常の分液処理を行った。抽出した有機層を飽和塩化ナトリウム水溶液（１０ｍＬ）で洗浄し、硫酸マグネシウムで乾燥後、ろ過、濃縮した。得られた濃縮物から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＝３：１）にて生成物を分取し、目的の化合物１２（Ｒ体）を収率＞９９％（３３７．０ｍｇ）で得た。化合物１２のスペクトルデータは以下のとおり。 [7-1] Step 1
To a Schlenk reaction vessel purged with nitrogen, compound 10 (R-form, 328.6 mg, 0.60 mmol), potassium carbonate (249 mg, 1.80 mmol), and methylene chloride (10 mL) were added, and the mixture was cooled to 0 ° C. Trimethyloxonium tetrafluoroborate (266.2 mg, 1.80 mmol) was added, and the mixture was warmed to room temperature and stirred for 4 hours. After confirming the completion of the reaction by TLC, a saturated aqueous ammonium chloride solution (5 mL) was added, and normal liquid separation treatment was performed using ethyl acetate (15 mL × 2). The extracted organic layer was washed with a saturated aqueous sodium chloride solution (10 mL), dried over magnesium sulfate, filtered and concentrated. The product was fractionated from the obtained concentrate by silica gel column chromatography (hexane: ethyl acetate = 3: 1) to obtain the desired compound 12 (R form) in a yield> 99% (337.0 mg). It was. The spectral data of Compound 12 is as follows.

¹H NMR (400 MHz, CDCl₃) δ 2.95 (s, 3H), 7.25 (d, J = 8.2 Hz, 2H), 7.39-7.48 (m, 12H), 7.68 (t, J = 7.3 Hz, 2H), 7.98 (d, J = 8.2 Hz, 2H), 8.06 (s, 2H). ¹³C NMR (100 MHz, CDCl₃) δ 30.7, 127.3 (2C), 127.8 (2C), 127.9 (2C), 128.3 (2C), 128.4 (2C), 128.5 (2C), 128.7 (2C), 130.0 (2C), 130.4 (2C), 131.8 (2C), 132.2 (2C), 133.8 (2C), 134.5 (2C), 138.0 (2C), 139.0 (2C), 139.8 (2C). M.p. 278℃ (decomposed). IR (KBr) 3056, 2932, 1366, 1349, 1176, 1029 cm^-1. [α]_D ²⁴= 38.8 (c 1.0, CHCl₃, (R)). HRMS (FAB+) calcd for C₃₃H₂₄NO₄S₂ [M+H]⁺ 562.1147, found 562.1150. ¹ H NMR (400 MHz, CDCl ₃ ) δ 2.95 (s, 3H), 7.25 (d, J = 8.2 Hz, 2H), 7.39-7.48 (m, 12H), 7.68 (t, J = 7.3 Hz, 2H) , 7.98 (d, J = 8.2 Hz, 2H), 8.06 (s, 2H). 13 C NMR (100 MHz, CDCl 3) δ 30.7, 127.3 (2C), 127.8 (2C), 127.9 (2C), 128.3 ( 2C), 128.4 (2C), 128.5 (2C), 128.7 (2C), 130.0 (2C), 130.4 (2C), 131.8 (2C), 132.2 (2C), 133.8 (2C), 134.5 (2C), 138.0 ( 2C), 139.0 (2C), 139.8 (2C). Mp 278 ° C (decomposed). IR (KBr) 3056, 2932, 1366, 1349, 1176, 1029 cm ^-1 . [Α] _D ²⁴ = 38.8 (c 1.0, CHCl ₃ , (R)). HRMS (FAB +) calcd for C ₃₃ H ₂₄ NO ₄ S ₂ [M + H] ⁺ 562.1147, found 562.1150.

［７−２］ステップ２
化合物１２（５６１．１ｍｇ，１．０ｍｍｏｌ）に対して、水酸化ナトリウム（８．０ｇ，２００ｍｍｏｌ）、メタノール（１００ｍＬ）を加えた。同反応溶液を７０℃で１５時間加熱した。室温に冷却し、反応終了をＴＬＣで確認した後、メタノールを減圧留去したのち、酢酸エチル（３０ｍＬ）と飽和塩化アンモニウム水溶液（２０ｍＬ）を加え、酢酸エチル（１５ｍＬ×２）を用いて通常の分液処理を行った。抽出した有機層を飽和塩化ナトリウム水溶液（１０ｍＬ）で洗浄し、硫酸マグネシウムで乾燥後、ろ過、濃縮した。得られた濃縮物からシリカゲルカラムクロマトグラフィー（クロロホルム：メタノール＝５：１）にて生成物を分取し、目的の化合物１４（Ｒ体）を収率９９％（６０１．７ｍｇ）で得た。化合物１４のスペクトルデータは以下のとおり。 [7-2] Step 2
Sodium hydroxide (8.0 g, 200 mmol) and methanol (100 mL) were added to compound 12 (561.1 mg, 1.0 mmol). The reaction solution was heated at 70 ° C. for 15 hours. After cooling to room temperature and confirming the completion of the reaction by TLC, methanol was distilled off under reduced pressure, and then ethyl acetate (30 mL) and a saturated aqueous ammonium chloride solution (20 mL) were added, followed by normal use with ethyl acetate (15 mL × 2). Liquid separation treatment was performed. The extracted organic layer was washed with a saturated aqueous sodium chloride solution (10 mL), dried over magnesium sulfate, filtered and concentrated. The product was fractionated from the obtained concentrate by silica gel column chromatography (chloroform: methanol = 5: 1) to obtain the target compound 14 (R form) in a yield of 99% (601.7 mg). The spectral data of Compound 14 is as follows.

¹H NMR (400 MHz, CD₃OD) δ 2.30 (s, 3H), 6.96 (d, J = 8.7 Hz, 1H), 7.16-7.38 (m, 6H), 7.39-7.48 (m, 4H), 7.51 (t, J = 7.3 Hz, 1H), 7.57-7.69 (m, 4H), 7.76 (s, 1H), 7.80 (s, 1H), 7.85 (d, J = 9.1 Hz, 1H), 7.87 (d, J = 8.2 Hz, 1H). ¹³C NMR (100 MHz, CD₃OD) δ 28.9, 127.3, 127.4, 127.7, 127.9, 128.2, 128.4, 128.5, 128.6, 129.4, 130.9, 131.2, 131.3, 132.8, 134.0, 134.5, 134.7, 135.4, 136.1, 138.7, 140.3, 140.4, 142.4, 142.7, 144.6. M.p. 273 ℃ (decomposed). IR (KBr) 3376, 1494, 1326, 1170, 1041 cm^-1. [α]_D ²³ = 155 (c 1.0, CH₃OH, (R)). HRMS (FAB+) calcd forC₃₃H₂₄NNa₂O₅S₂ [M+Na]⁺624.0891, found 624.0899. ¹ H NMR (400 MHz, CD ₃ OD) δ 2.30 (s, 3H), 6.96 (d, J = 8.7 Hz, 1H), 7.16-7.38 (m, 6H), 7.39-7.48 (m, 4H), 7.51 (t, J = 7.3 Hz, 1H), 7.57-7.69 (m, 4H), 7.76 (s, 1H), 7.80 (s, 1H), 7.85 (d, J = 9.1 Hz, 1H), 7.87 (d, J = 8.2 Hz, 1H). ¹³ C NMR (100 MHz, CD ₃ OD) δ 28.9, 127.3, 127.4, 127.7, 127.9, 128.2, 128.4, 128.5, 128.6, 129.4, 130.9, 131.2, 131.3, 132.8, 134.0, 134.5, 134.7, 135.4, 136.1, 138.7, 140.3, 140.4, 142.4, 142.7, 144.6. Mp 273 ° C (decomposed). IR (KBr) 3376, 1494, 1326, 1170, 1041 cm ^-1 . [Α] _D ²³ = 155 (c 1.0, CH ₃ OH, (R)). HRMS (FAB +) calcd forC ₃₃ H ₂₄ NNa ₂ O ₅ S ₂ [M + Na] ⁺ 624.0891, found 624.0899.

［７−３］ステップ３
化合物１４（１２０．３ｍｇ，０．２０ｍｍｏｌ）に、炭酸カリウム（６９．１ｍｇ，０．５０ｍｍｏｌ）、塩化メチレン（７．５ｍＬ）を加えて、０℃に冷却した。トリエチルオキソニウムテトラフルオロボラート（１Ｍ塩化メチレン溶液、０．５０ｍＬ，０．５０ｍｍｏｌ）を加えた後、室温まで昇温し、２０時間撹拌した。反応終了をＴＬＣで確認した後、飽和塩化アンモニウム水溶液（５ｍＬ）を加え、酢酸エチル（１５ｍＬ×２）を用いて通常の分液処理を行った。抽出した有機層を飽和塩化ナトリウム水溶液（１０ｍＬ）で洗浄し、硫酸マグネシウムで乾燥後、ろ過、濃縮した。得られた濃縮物から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＝４：１）にて生成物を分取し、目的の化合物１６（Ｒ体）を収率９８％（１１９．３ｍｇ）で得た。化合物１６のスペクトルデータは以下のとおり。 [7-3] Step 3
To compound 14 (120.3 mg, 0.20 mmol), potassium carbonate (69.1 mg, 0.50 mmol) and methylene chloride (7.5 mL) were added and cooled to 0 ° C. After adding triethyloxonium tetrafluoroborate (1M methylene chloride solution, 0.50 mL, 0.50 mmol), the mixture was warmed to room temperature and stirred for 20 hours. After confirming the completion of the reaction by TLC, a saturated aqueous ammonium chloride solution (5 mL) was added, and normal liquid separation treatment was performed using ethyl acetate (15 mL × 2). The extracted organic layer was washed with a saturated aqueous sodium chloride solution (10 mL), dried over magnesium sulfate, filtered and concentrated. The product was fractionated from the obtained concentrate by silica gel column chromatography (hexane: ethyl acetate = 4: 1) to obtain the target compound 16 (R form) in a yield of 98% (119.3 mg). . The spectral data of Compound 16 is as follows.

¹H NMR (400 MHz, CDCl₃) δ 0.93 (t, J = 7.2 Hz, 3H), 2.33 (d, J = 5.0 Hz, 3H), 3.29 (q, J = 5.0 Hz, 1H), 3.70 (dq, J = 9.6, 6.9 Hz, 1H), 3.86 (dq, J = 9.6, 6.9 Hz, 1H), 7.25 (d, J = 8.2 Hz, 1H), 7.29 (d, J = 8.7 Hz, 1H), 7.37-7.55 (m, 8H), 7.57-7.74 (m, 5H), 7.79 (m, 1H), 7.91 (d, J = 8.2 Hz, 2H), 7.93 (s, 1H), 7.94 (s 1H). ¹³C NMR (100 MHz, CDCl₃) δ 14.4, 28.8, 66.2, 127.2, 127.54, 127.56, 127.61, 127.91, 127.94, 128.0, 128.3, 128.5, 128.8, 129.1, 129.1, 130.0, 132.1, 132.3, 132.5, 132.6, 132.7, 133.5, 133.9, 134.8, 136.1, 137.4, 138.5, 139.6, 140.0, 140.6. M.p. 140-142℃. IR (KBr) 3372, 3055, 1332, 1183, 1000 cm^-1. [α]_D ²⁵ = 186.4 (c 1.0, CHCl₃, (R)). HRMS (FAB+) calcd for C₃₃H₃₀NO₅S₂ [M+H]⁺ 608.1565, found 608.1555. ¹ H NMR (400 MHz, CDCl ₃ ) δ 0.93 (t, J = 7.2 Hz, 3H), 2.33 (d, J = 5.0 Hz, 3H), 3.29 (q, J = 5.0 Hz, 1H), 3.70 (dq , J = 9.6, 6.9 Hz, 1H), 3.86 (dq, J = 9.6, 6.9 Hz, 1H), 7.25 (d, J = 8.2 Hz, 1H), 7.29 (d, J = 8.7 Hz, 1H), 7.37 -7.55 (m, 8H), 7.57-7.74 (m, 5H), 7.79 (m, 1H), 7.91 (d, J = 8.2 Hz, 2H), 7.93 (s, 1H), 7.94 (s 1H). 13 C NMR (100 MHz, CDCl ₃ ) δ 14.4, 28.8, 66.2, 127.2, 127.54, 127.56, 127.61, 127.91, 127.94, 128.0, 128.3, 128.5, 128.8, 129.1, 129.1, 130.0, 132.1, 132.3, 132.5, 132.6, 132.7, 133.5, 133.9, 134.8, 136.1, 137.4, 138.5, 139.6, 140.0, 140.6. Mp 140-142 ℃. IR (KBr) 3372, 3055, 1332, 1183, 1000 cm ^-1 . [Α] _D ²⁵ = 186.4 (c 1.0, CHCl ₃ , (R)). HRMS (FAB +) calcd for C ₃₃ H ₃₀ NO ₅ S ₂ [M + H] ⁺ 608.1565, found 608.1555.

［７−４］ステップ４
化合物１６（３０．４ｍｇ，０．０５０ｍｍｏｌ）に、炭酸カリウム（１３．８ｍｇ，１．０ｍｍｏｌ）、１，２−ジクロロエタン（２ｍＬ）を加えて、０℃に冷却した。トリメチルオキソニウムテトラフルオロボラート（１４．８ｍｇ，０．１０ｍｍｏｌ）を加えた後、９０℃まで昇温し、５２時間撹拌した。反応終了をＴＬＣで確認した後、飽和塩化アンモニウム水溶液（５ｍＬ）を加え、酢酸エチル（１０ｍＬ×２）を用いて通常の分液処理を行った。抽出した有機層を飽和塩化ナトリウム水溶液（１０ｍＬ）で洗浄し、硫酸マグネシウムで乾燥後、ろ過、濃縮した。得られた濃縮物から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＝４：１）にて生成物を分取し、目的の化合物１８（Ｒ体）を収率８５％（２６．６ｍｇ）で得た。化合物１８のスペクトルデータは以下のとおり。 [7-4] Step 4
To compound 16 (30.4 mg, 0.050 mmol), potassium carbonate (13.8 mg, 1.0 mmol) and 1,2-dichloroethane (2 mL) were added and cooled to 0 ° C. Trimethyloxonium tetrafluoroborate (14.8 mg, 0.10 mmol) was added, and then the temperature was raised to 90 ° C. and stirred for 52 hours. After confirming the completion of the reaction by TLC, a saturated aqueous ammonium chloride solution (5 mL) was added, and normal liquid separation treatment was performed using ethyl acetate (10 mL × 2). The extracted organic layer was washed with a saturated aqueous sodium chloride solution (10 mL), dried over magnesium sulfate, filtered and concentrated. The product was fractionated from the obtained concentrate by silica gel column chromatography (hexane: ethyl acetate = 4: 1) to obtain the target compound 18 (R form) in a yield of 85% (26.6 mg). . The spectral data of Compound 18 is as follows.

¹H NMR (400 MHz, CDCl₃) δ 0.94 (t, J = 7.3 Hz, 3H), 2.10 (s, 6H), 3.73 (m, 1H), 3.90 (m, 1H), 7.27-7.32 (m, 2H), 7.33-7.50 (m, 8H), 7.53-7.78 (m, 6H), 7.86 (s, 1H), 7.88 (d, J = 8.6 Hz, 1H), 7.90 (d, J = 8.6 Hz, 1H), 7.94 (s, 1H). ¹³C NMR (100 MHz, CDCl₃) δ 14.5, 34.5, 66.3, 127.2, 127.3, 127.4, 127.5, 127.6, 127.7, 127.8, 127.9, 128.4, 128.9, 129.2, 129.8, 132.1, 132.2, 132.5, 132.6, 133.1, 133.7, 134.1, 135.1, 137.5, 137.7, 139.6, 139.9, 140.7, 141.4. IR (KBr) 3057, 2927, 1355, 1325, 1183, 1137 cm^-1. [α]_D ²⁴ = 337.5 (c 1.0, CHCl₃, (R)). HRMS (FAB+) calcd for C₃₆H₃₃NO₅S₂ [M+H]⁺ 622.1722, found 622.1711. ¹ H NMR (400 MHz, CDCl ₃ ) δ 0.94 (t, J = 7.3 Hz, 3H), 2.10 (s, 6H), 3.73 (m, 1H), 3.90 (m, 1H), 7.27-7.32 (m, 2H), 7.33-7.50 (m, 8H), 7.53-7.78 (m, 6H), 7.86 (s, 1H), 7.88 (d, J = 8.6 Hz, 1H), 7.90 (d, J = 8.6 Hz, 1H ), 7.94 (s, 1H) . 13 C NMR (100 MHz, CDCl 3) δ 14.5, 34.5, 66.3, 127.2, 127.3, 127.4, 127.5, 127.6, 127.7, 127.8, 127.9, 128.4, 128.9, 129.2, 129.8, 132.1, 132.2, 132.5, 132.6, 133.1, 133.7, 134.1, 135.1, 137.5, 137.7, 139.6, 139.9, 140.7, 141.4. IR (KBr) 3057, 2927, 1355, 1325, 1183, 1137 cm ^-1 . [Α] _D ²⁴ = 337.5 (c 1.0, CHCl ₃ , (R)). HRMS (FAB +) calcd for C ₃₆ H ₃₃ NO ₅ S ₂ [M + H] ⁺ 622.1722, found 622.1711.

［７−５］ステップ５
化合物１８（６９．７ｍｇ，０．１１２ｍｍｏｌ）にＴＨＦ（４ｍＬ）を加えて、０℃に冷却し、Ｒｅｄ−Ａｌ（６５ｗｔ％トルエン溶液、０．３０ｍＬ，１．０ｍｍｏｌ）を加えた。同混合物を４０℃で６時間加熱した。反応終了をＴＬＣで確認し、０℃に冷却した後、激しく撹拌しながら硫酸ナトリウムの飽和水溶液を適量加え、酢酸エチル（１０ｍＬ×２）を用いて通常の分液処理を行った。抽出した有機層を飽和塩化ナトリウム水溶液（５ｍＬ）で洗浄し、硫酸マグネシウムで乾燥後、ろ過、濃縮した。得られた濃縮物は、精製せずにそのまま以降の操作を続けた。得られた濃縮物にヘキサメチルリン酸トリアミド（ＨＭＰＡ）（１ｍＬ）、水酸化カリウム（３３．７ｍｇ，０．６０ｍｍｏｌ）を加え、約５気圧（０．５ＭＰａ）の酸素を封入した。この混合物を８０℃で１０時間加熱した。反応終了後、室温まで冷却し、そのままシリカゲルカラムクロマトグラフィー（クロロホルム：メタノール＝１：１）にて生成物を分取し、目的の化合物２０（Ｒ体）を収率５３％（３８．２ｍｇ）で得た。化合物２０のスペクトルデータは以下のとおり。 [7-5] Step 5
THF (4 mL) was added to compound 18 (69.7 mg, 0.112 mmol), cooled to 0 ° C., and Red-Al (65 wt% toluene solution, 0.30 mL, 1.0 mmol) was added. The mixture was heated at 40 ° C. for 6 hours. After completion of the reaction was confirmed by TLC and cooled to 0 ° C., an appropriate amount of a saturated aqueous solution of sodium sulfate was added with vigorous stirring, and normal liquid separation treatment was performed using ethyl acetate (10 mL × 2). The extracted organic layer was washed with a saturated aqueous sodium chloride solution (5 mL), dried over magnesium sulfate, filtered and concentrated. The obtained concentrate was continued without further purification. Hexamethylphosphoric triamide (HMPA) (1 mL) and potassium hydroxide (33.7 mg, 0.60 mmol) were added to the obtained concentrate, and oxygen at about 5 atm (0.5 MPa) was enclosed. The mixture was heated at 80 ° C. for 10 hours. After completion of the reaction, the reaction mixture was cooled to room temperature, and the product was fractionated as it was by silica gel column chromatography (chloroform: methanol = 1: 1) to obtain the target compound 20 (R form) in a yield of 53% (38.2 mg). I got it. The spectral data of Compound 20 is as follows.

¹H NMR (400 MHz, CD₃OD) δ 7.06 (d, J = 8.6 Hz, 2H), 7.18 (t, J = 8.0 Hz, 2H), 7.26-7.35 (m, 6H), 7.41 (t, J = 7.6 Hz, 2H), 7.66 (d, J = 7.6 Hz, 4H), 7.69 (s, 2H), 7.81 (d, J = 8.2 Hz, 2H). ¹³C NMR (100 MHz, CD₃OD) δ 127.0 (2C), 127.1 (2C), 127.6 (4C), 127.8 (2C), 128.3 (2C), 129.2 (2C), 131.4 (4C), 132.2 (2C), 134.2 (2C), 134.3 (2C), 138.1 (2C), 140.3 (2C), 140.4 (2C), 145.2 (2C). IR (KBr) 3056, 1231, 1186, 1038 cm^-1. [α]_D ²⁴ = 91.3 (c 0.80, CH₃OH, (R)). HRMS (FAB+) calcd for C₃₂H₂₁Na₂O₆S₂ [M-2K+2Na+H]⁺611.0575, found 611.0584; (FAB-) calcd for C₃₂H₂₀NaO₆S₂ [M-2K+Na]^-587.0599, found 587.0608. ¹ H NMR (400 MHz, CD ₃ OD) δ 7.06 (d, J = 8.6 Hz, 2H), 7.18 (t, J = 8.0 Hz, 2H), 7.26-7.35 (m, 6H), 7.41 (t, J = 7.6 Hz, 2H), 7.66 (d, J = 7.6 Hz, 4H), 7.69 (s, 2H), 7.81 (d, J = 8.2 Hz, 2H). ¹³ C NMR (100 MHz, CD ₃ OD) δ 127.0 (2C), 127.1 (2C), 127.6 (4C), 127.8 (2C), 128.3 (2C), 129.2 (2C), 131.4 (4C), 132.2 (2C), 134.2 (2C), 134.3 (2C), 138.1 (2C), 140.3 (2C), 140.4 (2C), 145.2 (2C). IR (KBr) 3056, 1231, 1186, 1038 cm ^-1 . [Α] _D ²⁴ = 91.3 (c 0.80, CH ₃ OH, (R)). HRMS (FAB +) calcd for C ₃₂ H ₂₁ Na ₂ O ₆ S ₂ [M-2K + 2Na + H] ⁺ 611.0575, found 611.0584; (FAB-) calcd for C ₃₂ H ₂₀ NaO ₆ S ₂ ^{[M-2K + Na] -} 587.0599, found 587.0608.

［７−６］ステップ６
化合物２０（３７．９ｍｇ，０．０５９ｍｍｏｌ）を陽イオン交換樹脂（アンバーライトＩＲ１２０Ｈ、１００ｃｍ³）に通した。次いで、回収液からメタノールを減圧留去し、トルエンにて共沸脱水を行った。その後、１〜２Ｔｏｒｒにて１２時間減圧乾燥し、化合物２２（Ｒ体）を収率＞９９％（３４．４ｍｇ）で得た。化合物２２のスペクトルデータは以下のとおり。 [7-6] Step 6
Compound 20 (37.9 mg, 0.059 mmol) was passed through a cation exchange resin (Amberlite IR120H, 100 cm ³ ). Subsequently, methanol was distilled off from the recovered liquid under reduced pressure, and azeotropic dehydration was performed with toluene. Then, it dried under reduced pressure at 1-2 Torr for 12 hours, and obtained compound 22 (R body) with yield> 99% (34.4 mg). The spectral data of Compound 22 is as follows.

¹H NMR (400 MHz, CD₃OD) δ 7.07 (d, J = 8.6 Hz, 2H), 7.25 (t, J = 7.3 Hz, 2H), 7.29-7.43 (m, 6H), 7.50 (t, J = 6.9 Hz, 2H), 7.61 (d, J = 7.0 Hz, 4H), 7.80 (s, 2H), 7.89 (d, J = 7.8 Hz, 2H). ¹³C NMR (100 MHz, CD₃OD) δ 127.5 (2C), 127.6 (2C), 127.9 (4C), 128.6 (2C), 128.7 (2C), 129.0 (2C), 131.0 (4C), 132.8 (2C), 134.0 (2C), 134.5 (2C), 138.4 (2C), 138.6 (2C), 140.0 (2C), 144.2 (2C). IR (KBr) 3420, 3053, 1229, 1182, 1035 cm^-1. [α]_D ²⁴ = 121 (c 1.0, MeOH, (R)). HRMS (FAB+) calcd for C₃₂H₂₂O₆S₂ [M]⁺ 566.0858, found 566.0862.
［７−７］ステップ７
窒素置換したシュレンク反応容器に、化合物２２（３１．０ｍｇ，０．０５５ｍｍｏｌ）、炭酸カリウム（６９．１ｍｇ，０．５０ｍｍｏｌ）、塩化メチレン（２ｍＬ）を加えて、０℃に冷却した。トリエチルオキソニウムテトラフルオロボラート（１Ｍ塩化メチレン溶液、０．５０ｍＬ，０．５０ｍｍｏｌ）を加えた後、室温まで昇温し、１５時間撹拌した。反応終了をＴＬＣで確認した後、飽和塩化アンモニウム水溶液（５ｍＬ）を加え、酢酸エチル（１５ｍＬ×２）を用いて通常の分液処理を行った。抽出した有機層を飽和塩化ナトリウム水溶液（１０ｍＬ）で洗浄し、硫酸マグネシウムで乾燥後、ろ過、濃縮した。得られた濃縮物から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＝３：１）にて生成物を分取し、目的の化合物２４（Ｒ体）を収率８４％（２８．８ｍｇ）で得た。化合物２４の光学純度は、ＨＰＬＣで決定し、＞９９％ｅｅであることを確認した［ダイセルキラルカラムＩＡ，ヘキサン：イソプロパノール＝９：１，１．０ｍＬ／ｍｉｎ，ｔ_R＝９．０ｍｉｎ（Ｓ），１６．９ｍｉｎ（Ｒ）]。化合物２４のスペクトルデータは以下のとおり。 ¹ H NMR (400 MHz, CD ₃ OD) δ 7.07 (d, J = 8.6 Hz, 2H), 7.25 (t, J = 7.3 Hz, 2H), 7.29-7.43 (m, 6H), 7.50 (t, J = 6.9 Hz, 2H), 7.61 (d, J = 7.0 Hz, 4H), 7.80 (s, 2H), 7.89 (d, J = 7.8 Hz, 2H). ¹³ C NMR (100 MHz, CD ₃ OD) δ 127.5 (2C), 127.6 (2C), 127.9 (4C), 128.6 (2C), 128.7 (2C), 129.0 (2C), 131.0 (4C), 132.8 (2C), 134.0 (2C), 134.5 (2C), 138.4 (2C), 138.6 (2C), 140.0 (2C), 144.2 (2C). IR (KBr) 3420, 3053, 1229, 1182, 1035 cm ^-1 . [Α] _D ²⁴ = 121 (c 1.0, MeOH, (R)). HRMS (FAB +) calcd for C ₃₂ H ₂₂ O ₆ S ₂ [M] ⁺ 566.0858, found 566.0862.
[7-7] Step 7
Compound 22 (31.0 mg, 0.055 mmol), potassium carbonate (69.1 mg, 0.50 mmol), and methylene chloride (2 mL) were added to a nitrogen-substituted Schlenk reaction vessel and cooled to 0 ° C. After adding triethyloxonium tetrafluoroborate (1M methylene chloride solution, 0.50 mL, 0.50 mmol), the mixture was warmed to room temperature and stirred for 15 hours. After confirming the completion of the reaction by TLC, a saturated aqueous ammonium chloride solution (5 mL) was added, and normal liquid separation treatment was performed using ethyl acetate (15 mL × 2). The extracted organic layer was washed with a saturated aqueous sodium chloride solution (10 mL), dried over magnesium sulfate, filtered and concentrated. The product was separated from the obtained concentrate by silica gel column chromatography (hexane: ethyl acetate = 3: 1) to obtain the target compound 24 (R form) in a yield of 84% (28.8 mg). . The optical purity of compound 24 was determined by HPLC and confirmed to be> 99% ee [Daicel chiral column IA, hexane: isopropanol = 9: 1, 1.0 mL / min, t _R = 9.0 min (S) , 16.9 min (R)]. The spectral data of Compound 24 is as follows.

¹H NMR (400 MHz, CDCl₃) δ 0.94 (t, J = 6.9 Hz, 6H), 3.66-3.75 (m, 2H), 3.79-3.88 (m, 2H), 7.25 (d, J = 8.7 Hz, 2H), 7.39-7.75 (m, 14H), 7.92 (d, J = 8.2 Hz, 2H), 7.96 (s, 2H).¹³C NMR (100 MHz, CDCl₃) δ14.5, 66.3, 127.5, 127.8, 127.9, 128.1, 129.3, 129.7, 130.3, 132.2, 132.7, 133.0, 134.1, 137.7, 138.9, 140.6. IR (KBr) 3056, 2984, 2256, 1580, 1493, 1444, 1354, 1185, 1001 cm^-1. [α]_D ²⁴ = 112.0 (c 0.20, CHCl₃, (R)). HRMS (FAB+) calcd for C₃₆H₃₁O₆S₂ [M+H]⁺ 623.1562, found 623.1563. ¹ H NMR (400 MHz, CDCl ₃ ) δ 0.94 (t, J = 6.9 Hz, 6H), 3.66-3.75 (m, 2H), 3.79-3.88 (m, 2H), 7.25 (d, J = 8.7 Hz, 2H), 7.39-7.75 (m, 14H ), 7.92 (d, J = 8.2 Hz, 2H), 7.96 (s, 2H). 13 C NMR (100 MHz, CDCl 3) δ14.5, 66.3, 127.5, 127.8 , 127.9, 128.1, 129.3, 129.7, 130.3, 132.2, 132.7, 133.0, 134.1, 137.7, 138.9, 140.6.IR (KBr) 3056, 2984, 2256, 1580, 1493, 1444, 1354, 1185, 1001 cm ^-1 . [α] _D ²⁴ = 112.0 (c 0.20, CHCl ₃ , (R)). HRMS (FAB +) calcd for C ₃₆ H ₃₁ O ₆ S ₂ [M + H] ⁺ 623.1562, found 623.1563.

［比較例４〜７］
表２に示すように、前出の化合物１０，１２，１４，１６につき、実施例７のステップ５，６と同様の還元・酸化反応及びイオン交換反応を試みたところ、目的とする化合物２２は全く得られなかった。 [Comparative Examples 4 to 7]
As shown in Table 2, when the same reduction / oxidation reaction and ion exchange reaction as in Steps 5 and 6 of Example 7 were tried for the above-mentioned compounds 10, 12, 14, and 16, the target compound 22 was It was not obtained at all.

［実施例８］
下記式にしたがって、ジスルホンイミド（化合物２６（Ｓ体））を出発物質として、目的とする３，３’−ジアリール−１，１’−ビナフチル−２，２’ジスルホン酸（化合物４０ａ〜４０ｃ）を合成した。なお、化合物２６は文献Eur. J. Org. Chem. 2010, p4181の記載にしたがって合成した。 [Example 8]
According to the following formula, starting from disulfonimide (compound 26 (S form)), the desired 3,3′-diaryl-1,1′-binaphthyl-2,2′disulfonic acid (compounds 40a to 40c) is obtained. Synthesized. Compound 26 was synthesized as described in the literature Eur. J. Org. Chem. 2010, p4181.

［８−１］ステップ１
窒素置換したシュレンク反応容器に、化合物２６（２７．７ｍｇ，０．０５０ｍｍｏｌ）、炭酸カリウム（２０．７ｍｇ，０．１５ｍｍｏｌ）、塩化メチレン（２ｍＬ）を加えて、０℃に冷却した。トリメチルオキソニウムテトラフルオロボラート（２２．２ｍｇ，０．１５ｍｍｏｌ）を加えた後、室温まで昇温し、２０時間撹拌した。反応終了をＴＬＣで確認した後、飽和塩化アンモニウム水溶液（５ｍＬ）を加え、クロロホルム（１５ｍＬ×２）を用いて通常の分液処理を行った。抽出した有機層を飽和塩化ナトリウム水溶液（１０ｍＬ）で洗浄し、硫酸マグネシウムで乾燥後、ろ過、濃縮した。得られた濃縮物から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＝６：１〜３：１）にて生成物を分取し、目的の化合物２８（Ｓ体）を収率＞９９％（２８．３ｍｇ）で得た。化合物２８のスペクトルデータは以下のとおり。 [8-1] Step 1
Compound 26 (27.7 mg, 0.050 mmol), potassium carbonate (20.7 mg, 0.15 mmol), and methylene chloride (2 mL) were added to a Schlenk reaction vessel purged with nitrogen, and cooled to 0 ° C. After adding trimethyloxonium tetrafluoroborate (22.2 mg, 0.15 mmol), the mixture was warmed to room temperature and stirred for 20 hours. After confirming the completion of the reaction by TLC, a saturated aqueous ammonium chloride solution (5 mL) was added, and normal liquid separation treatment was performed using chloroform (15 mL × 2). The extracted organic layer was washed with a saturated aqueous sodium chloride solution (10 mL), dried over magnesium sulfate, filtered and concentrated. The product was fractionated from the obtained concentrate by silica gel column chromatography (hexane: ethyl acetate = 6: 1 to 3: 1) to obtain the desired compound 28 (S form) in a yield> 99% (28. 3 mg). The spectral data of Compound 28 is as follows.

¹HNMR (400 MHz, CDCl₃) δ 3.36 (s, 3H), 7.00 (d, J = 8.7 Hz, 2H), 7.36 (t, J = 7.3 Hz, 2H), 7.66 (t, J = 7.6 Hz, 2H), 7.91 (d, J = 8.1 Hz, 2H), 8.51 (s, 2H). ¹³CNMR (100 MHz, CDCl₃) δ 31.5, 114.1 (2C), 127.6 (2C), 128.4 (2C), 128.7 (2C), 130.7 (2C), 131.2 (2C), 135.5 (2C), 137.3 (4C), 140.8 (2C). M.p. 283℃ (decomposed). IR (KBr) 3419, 1551, 1372, 1348, 1183, 1156, 1132, 1044 cm^-1. [α]_D ²⁵ = 131.2 (c 0.20, CHCl₃, (S)). HRMS (EI+) calcd for C₂₁H₁₃Br₂NO₄S₂ [M+H]⁺564.8653, found 564.8657. ¹ HNMR (400 MHz, CDCl ₃ ) δ 3.36 (s, 3H), 7.00 (d, J = 8.7 Hz, 2H), 7.36 (t, J = 7.3 Hz, 2H), 7.66 (t, J = 7.6 Hz, 2H), 7.91 (d, J = 8.1 Hz, 2H), 8.51 (s, 2H). 13 CNMR (100 MHz, CDCl 3) δ 31.5, 114.1 (2C), 127.6 (2C), 128.4 (2C), 128.7 (2C), 130.7 (2C), 131.2 (2C), 135.5 (2C), 137.3 (4C), 140.8 (2C). Mp 283 ° C (decomposed). IR (KBr) 3419, 1551, 1372, 1348, 1183, 1156, 1132, 1044 cm ^-1 . [Α] _D ²⁵ = 131.2 (c 0.20, CHCl ₃ , (S)). HRMS (EI +) calcd for C ₂₁ H ₁₃ Br ₂ NO ₄ S ₂ [M + H] ⁺ 564.8653, found 564.8657.

［８−２］ステップ２
窒素置換した反応容器に、化合物２８（５６７ｍｇ，１．０ｍｍｏｌ）、フェニルボロン酸（３６６ｍｇ，３ｍｍｏｌ）テトラキス（トリフェニルホスフィン）パラジウム（０）（１１６ｍｇ，０．１ｍｍｏｌ）、炭酸カリウム（１．３８ｇ，１０ｍｍｏｌ）、ＴＨＦ（２０ｍＬ），水（５ｍＬ）を加えて、８５℃に加熱して１２時間撹拌した。反応終了をＴＬＣで確認した後、飽和塩化アンモニウム水溶液（２０ｍＬ）を加え、クロロホルム（３０ｍＬ×２）を用いて通常の分液処理を行った。抽出した有機層を飽和塩化ナトリウム水溶液（３０ｍＬ）で洗浄し、硫酸ナトリウムで乾燥後、ろ過、濃縮した。得られた濃縮物から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＝６：１〜３：１）にて生成物を分取し、目的の化合物３０ａ（Ｓ体）を収率８７％（４９０ｍｇ）で得た。また、化合物３０ｂ（Ｓ体），３０ｃ（Ｓ体）については、フェニルボロン酸の代わりに、それぞれ４−ビフェニルボロン酸及び３，５−ジフェニルフェニルボロン酸を用いることにより、収率８９％及び９０％で得た。化合物３０ｂ，３０ｃのスペクトルデータは以下のとおり。 [8-2] Step 2
In a reaction vessel purged with nitrogen, compound 28 (567 mg, 1.0 mmol), phenylboronic acid (366 mg, 3 mmol), tetrakis (triphenylphosphine) palladium (0) (116 mg, 0.1 mmol), potassium carbonate (1.38 g, 10 mmol), THF (20 mL), and water (5 mL) were added, and the mixture was heated to 85 ° C. and stirred for 12 hours. After confirming the completion of the reaction by TLC, a saturated aqueous ammonium chloride solution (20 mL) was added, and normal liquid separation treatment was performed using chloroform (30 mL × 2). The extracted organic layer was washed with a saturated aqueous sodium chloride solution (30 mL), dried over sodium sulfate, filtered and concentrated. The product was fractionated from the obtained concentrate by silica gel column chromatography (hexane: ethyl acetate = 6: 1 to 3: 1) to obtain the target compound 30a (S form) in a yield of 87% (490 mg). Obtained. For compounds 30b (S-form) and 30c (S-form), instead of phenylboronic acid, 4-biphenylboronic acid and 3,5-diphenylphenylboronic acid were used, respectively, yields of 89% and 90%. %. The spectrum data of compounds 30b and 30c are as follows.

化合物３０ｂ：¹H NMR (400 MHz, CDCl₃) δ 3.00 (s, 3H), 7.27 (d, J = 8.7 Hz, 2H), 7.35 (t, J = 7.3 Hz, 2H), 7.39-7.49 (m, 6H), 7.51-7.60 (m, 4H), 7.62-7.74 (m, 10H), 8.00 (d, J = 8.2 Hz, 2H), 8.07 (s, 2H). ¹³C NMR (100 MHz, CDCl₃) δ 30.7, 125.8, 126.5, 127.1, 127.4, 128.2, 128.4, 128.7, 129.1, 129.9, 130.8, 131.6, 131.9, 133.8, 134.4, 137.5, 138.7, 138.9, 140.3, 140.5. M.p. 194-196℃. IR (KBr) 3028, 1576, 1487, 1369, 1349, 1177 cm^-1. [α]_D ²³ = 12.8 (c 0.50, CHCl₃, (S)). HRMS (FAB+) calcd for C₄₅H₃₁NO₄S₂ [M]⁺ 713.1694, found 713.1702. Compound 30b: ¹ H NMR (400 MHz, CDCl ₃ ) δ 3.00 (s, 3H), 7.27 (d, J = 8.7 Hz, 2H), 7.35 (t, J = 7.3 Hz, 2H), 7.39-7.49 (m , 6H), 7.51-7.60 (m, 4H), 7.62-7.74 (m, 10H), 8.00 (d, J = 8.2 Hz, 2H), 8.07 (s, 2H). ¹³ C NMR (100 MHz, CDCl ₃ ) δ 30.7, 125.8, 126.5, 127.1, 127.4, 128.2, 128.4, 128.7, 129.1, 129.9, 130.8, 131.6, 131.9, 133.8, 134.4, 137.5, 138.7, 138.9, 140.3, 140.5. Mp 194-196 ° C. IR ( KBr) 3028, 1576, 1487, 1369, 1349, 1177 cm ^-1 . [Α] _D ²³ = 12.8 (c 0.50, CHCl ₃ , (S)). HRMS (FAB +) calcd for C ₄₅ H ₃₁ NO ₄ S ₂ [M] ⁺ 713.1694, found 713.1702.

化合物３０ｃ：¹H NMR (400 MHz, CDCl₃) δ 3.00 (s, 3H), 7.30-7.40 (m, 6H), 7.40-7.50 (m, 10H), 7.66-7.76 (m, 14H), 7.87 (m, 2H), 8.01 (d, J = 8.2 Hz, 2H), 8.16 (s, 2H). ¹³CNMR (100 MHz, CDCl₃) δ 30.7, 125.3, 126.4, 127.2, 127.4, 127.5, 127.6, 128.2, 128.3, 128.8, 128.9, 130.0, 131.7, 132.0, 133.9, 134.4, 137.6, 139.1, 140.6, 140.7, 141.2. M.p. 194-196℃. IR (KBr) 2940, 1593, 1574, 1496, 1370, 1349, 1177, 1028 cm^-1. [α]_D ²⁴ = -30.0 (c 0.50, CHCl₃, (S)). HRMS (EI+) calcd for C₅₇H₃₉NNaO₄S₂ [M]⁺ 865.2321, found 865.2336. Compound 30c: ¹ H NMR (400 MHz, CDCl ₃ ) δ 3.00 (s, 3H), 7.30-7.40 (m, 6H), 7.40-7.50 (m, 10H), 7.66-7.76 (m, 14H), 7.87 ( m, 2H), 8.01 (d , J = 8.2 Hz, 2H), 8.16 (s, 2H). 13 CNMR (100 MHz, CDCl 3) δ 30.7, 125.3, 126.4, 127.2, 127.4, 127.5, 127.6, 128.2, 128.3, 128.8, 128.9, 130.0, 131.7, 132.0, 133.9, 134.4, 137.6, 139.1, 140.6, 140.7, 141.2. Mp 194-196 ° C. IR (KBr) 2940, 1593, 1574, 1496, 1370, 1349, 1177, 1028 cm ^-1 . [Α] _D ²⁴ = -30.0 (c 0.50, CHCl ₃ , (S)). HRMS (EI +) calcd for C ₅₇ H ₃₉ NNaO ₄ S ₂ [M] ⁺ 865.2321, found 865.2336.

［８−３］ステップ３
実施例７のステップ２と同様にして、化合物３０ａ〜３０ｃから化合物３２ａ〜３２ｃ（いずれもＳ体）をそれぞれ収率９３％，９６％，９０％で得た。化合物３２ｂ，３２ｃのスペクトルデータは以下のとおり。 [8-3] Step 3
In the same manner as in Step 2 of Example 7, Compounds 32a to 32c (both S forms) were obtained from Compounds 30a to 30c in yields of 93%, 96%, and 90%, respectively. The spectrum data of the compounds 32b and 32c are as follows.

化合物３２ｂ：¹H NMR (400 MHz, d8-THF) δ 2.10 (s, 3H), 4.30 (br, 1H), 6.90 (d, J = 8.6 Hz, 1H), 7.12 (t, J = 7.3 Hz, 1H), 7.16-7.22 (m, 2H), 7.23-7.32 (m, 2H), 7.32-7.46 (m, 6H), 7.55-7.84 (m, 16H). ¹³C NMR (100 MHz, d8-THF) δ 28.8, 126.1, 126.3 126.9, 127.3, 127.6, 128.1, 128,2, 128.4, 129.0, 129.4, 129.6, 131.0, 131.4, 131.7, 132.5, 132.6, 133.8, 134.2, 134.4, 135.5, 135.9, 137.6, 139.3, 139.8, 140.8, 141.1, 141.2, 141.3, 141.9, 142.7, 144.0. M.p. 284-286℃. IR (KBr) 3373, 3065, 1486, 1393, 1329, 1229, 1203, 1042 cm^-1. [α]_D ²² = -81.9 (c 0.20, CHCl₃, (S)). HRMS (ESI-) calcd for C₄₅H₃₂NO₅S₂ [M-Na]^- 730.1727, found 7301723. Compound 32b: ¹ H NMR (400 MHz, d8-THF) δ 2.10 (s, 3H), 4.30 (br, 1H), 6.90 (d, J = 8.6 Hz, 1H), 7.12 (t, J = 7.3 Hz, 1H), 7.16-7.22 (m, 2H), 7.23-7.32 (m, 2H), 7.32-7.46 (m, 6H), 7.55-7.84 (m, 16H). ¹³ C NMR (100 MHz, d8-THF) δ 28.8, 126.1, 126.3 126.9, 127.3, 127.6, 128.1, 128,2, 128.4, 129.0, 129.4, 129.6, 131.0, 131.4, 131.7, 132.5, 132.6, 133.8, 134.2, 134.4, 135.5, 135.9, 137.6, 139.3, 139.8, 140.8, 141.1, 141.2, 141.3, 141.9, 142.7, 144.0. Mp 284-286 ° C. IR (KBr) 3373, 3065, 1486, 1393, 1329, 1229, 1203, 1042 cm ^-1 . [Α] _D ²² _{= -81.9 (c 0.20, CHCl 3} , (S)) HRMS (ESI-) calcd for C 45 H 32 NO 5 S 2 [M-Na] -. 730.1727, found 7301723.

化合物３２ｃ：¹H NMR (400 MHz, d8-THF) δ 2.18 (s, 3H), 4.10 (br, 1H), 7.03 (d, J = 8.7 Hz, 1H), 7.14 (m, 2H), 7.20 (t, J = 7.8 Hz, 1H), 7.24-7.50 (m, 14H), 7.68-8.05 (m, 18H). ¹³CNMR (100 MHz, d8-THF) δ 28.9, 124.4, 125.6, 127.3, 127.6, 127.9, 128.0, 128.1, 128.3, 128.4, 129.0, 129.4, 129.6, 129.7, 132.6, 133.1, 134.0, 134.2, 134.3, 136.3, 136.5, 138.3, 139.5, 139.9, 140.8, 141.4, 141.7, 141.9, 142.2, 143.7, 145.2. M.p. 282-284℃. IR (KBr) 3374, 3058, 1593, 1496, 1330, 1232, 1169, 1040 cm^-1. [α]_D ²³ = -125.2 (c 0.20, CHCl₃, (S)). HRMS (ESI-) calcd for C₅₇H₄₀NO₅S₂ [M-Na]^- 882.2353, found 882.2367. Compound 32c: ¹ H NMR (400 MHz, d8-THF) δ 2.18 (s, 3H), 4.10 (br, 1H), 7.03 (d, J = 8.7 Hz, 1H), 7.14 (m, 2H), 7.20 ( t, J = 7.8 Hz, 1H ), 7.24-7.50 (m, 14H), 7.68-8.05 (m, 18H). 13 CNMR (100 MHz, d8-THF) δ 28.9, 124.4, 125.6, 127.3, 127.6, 127.9 , 128.0, 128.1, 128.3, 128.4, 129.0, 129.4, 129.6, 129.7, 132.6, 133.1, 134.0, 134.2, 134.3, 136.3, 136.5, 138.3, 139.5, 139.9, 140.8, 141.4, 141.7, 141.9, 142.2, 143.7, 145.2 Mp 282-284 ℃. IR (KBr) 3374, 3058, 1593, 1496, 1330, 1232, 1169, 1040 cm ^-1 . [Α] _D ²³ = -125.2 (c 0.20, CHCl ₃ , (S)). _{HRMS (ESI-) calcd for C 57} H 40 NO 5 S 2 [M-Na] - 882.2353, found 882.2367.

［８−４］ステップ４
実施例７のステップ３と同様にして、化合物３２ａ〜３２ｃから化合物３４ａ〜３４ｃ（いずれもＳ体）をそれぞれ収率６８％，７８％，７８％で得た。化合物３４ｂ，３４ｃのスペクトルデータは以下のとおり。 [8-4] Step 4
In the same manner as in Step 3 of Example 7, compounds 34a to 34c (all of the S isomers) were obtained from compounds 32a to 32c in yields of 68%, 78%, and 78%, respectively. The spectrum data of the compounds 34b and 34c are as follows.

化合物３４ｂ：¹H NMR (400 MHz, CDCl₃) δ 0.95 (t, J = 7.8 Hz, 3H), 2.38 (d, J = 4.9 Hz, 3H), 3.48 (q, J = 5.0 Hz, 1H), 3.77 (dq, J = 10.1, 7.1 Hz, 1H), 3.92 (dq, J = 10.1, 7.1 Hz, 1H), 7.25-7.53 (m, 10H), 7.60-7.83 (m, 13H), 7.88 (d, J = 7.8 Hz, 1H), 7.94 (d, J = 8.2 Hz, 2H), 7.99 (s, 1H), 8.01 (s, 1H). ¹³C NMR (100 MHz, CDCl₃) δ 14.9, 28.8, 66.3, 126.0, 126.6, 126.9, 127.1, 127.2, 127.3, 127.4, 127.6, 127.7, 127.8, 128.0, 128.1, 128.8, 128.9, 129.0, 129.2, 129.6, 130.6, 132.2, 132.4, 132.7, 132.8, 133.6, 134.1, 134.8, 135.9, 137.2, 138.7, 139.1, 139.8, 140.0, 140.3, 140.7, 141.2. M.p. 163-165℃. IR (KBr) 3373, 3030, 1487, 1353, 1331, 1183 cm^-1. [α]_D ²³ = -76.0 (c 0.20, CHCl₃, (S)). HRMS (FAB+) calcd for C₄₇H₃₈NO₅S₂ [M+H]⁺ 760.2191, found 760.2203. Compound 34b: ¹ H NMR (400 MHz, CDCl ₃ ) δ 0.95 (t, J = 7.8 Hz, 3H), 2.38 (d, J = 4.9 Hz, 3H), 3.48 (q, J = 5.0 Hz, 1H), 3.77 (dq, J = 10.1, 7.1 Hz, 1H), 3.92 (dq, J = 10.1, 7.1 Hz, 1H), 7.25-7.53 (m, 10H), 7.60-7.83 (m, 13H), 7.88 (d, J = 7.8 Hz, 1H), 7.94 (d, J = 8.2 Hz, 2H), 7.99 (s, 1H), 8.01 (s, 1H). ¹³ C NMR (100 MHz, CDCl ₃ ) δ 14.9, 28.8, 66.3 , 126.0, 126.6, 126.9, 127.1, 127.2, 127.3, 127.4, 127.6, 127.7, 127.8, 128.0, 128.1, 128.8, 128.9, 129.0, 129.2, 129.6, 130.6, 132.2, 132.4, 132.7, 132.8, 133.6, 134.1, 134.8 , 135.9, 137.2, 138.7, 139.1, 139.8, 140.0, 140.3, 140.7, 141.2. Mp 163-165 ° C. IR (KBr) 3373, 3030, 1487, 1353, 1331, 1183 cm ^-1 . [Α] _D ²³ = -76.0 (c 0.20, CHCl ₃ , (S)). HRMS (FAB +) calcd for C ₄₇ H ₃₈ NO ₅ S ₂ [M + H] ⁺ 760.2191, found 760.2203.

化合物３４ｃ：¹H NMR (400 MHz, CDCl₃) δ 0.85 (t, J = 7.0 Hz, 3H), 2.40 (d, J = 5.0 Hz, 3H), 3.56 (q, J = 5.5 Hz, 1H), 3.75 (m, 1H), 3.86 (m, 1H), 7.29-7.54 (m, 16H), 7.59-7.67 (m, 2H), 7.70-7.80 (m, 8H), 7.82-8.00 (m, 7H), 8.03 (m, 1H), 8.08 (s, 1H), 8.10 (s 1H). ¹³C NMR (100 MHz, CDCl₃) δ 14.6, 29.2, 66.4, 125.3, 126.2, 126.9, 127.5, 127.7, 127.9, 128.5, 128.6, 129.2, 129.3, 129.4, 129.6, 132.6, 132.8, 132.9, 133.0, 133.9, 134.3, 135.2, 136.3 137.6, 139.0, 140.1, 140.3, 140.4, 140.8, 141.0, 141.1, 141.2, 141.4, 141.7, 141.8, 142.0. M.p. 193-194℃. IR (KBr) 3376, 3034, 1593, 1496, 1330, 1182 cm^-1. [α]_D ²² = -112.0 (c 0.20, CHCl₃, (S)). HRMS (FAB+) calcd for C₅₉H₄₆NO₅S₂ [M+H]⁺ 912.2817, found 912.2814. Compound 34c: ¹ H NMR (400 MHz, CDCl ₃ ) δ 0.85 (t, J = 7.0 Hz, 3H), 2.40 (d, J = 5.0 Hz, 3H), 3.56 (q, J = 5.5 Hz, 1H), 3.75 (m, 1H), 3.86 (m, 1H), 7.29-7.54 (m, 16H), 7.59-7.67 (m, 2H), 7.70-7.80 (m, 8H), 7.82-8.00 (m, 7H), 8.03 (m, 1H), 8.08 (s, 1H), 8.10 (s 1H). 13 C NMR (100 MHz, CDCl 3) δ 14.6, 29.2, 66.4, 125.3, 126.2, 126.9, 127.5, 127.7, 127.9, 128.5 , 128.6, 129.2, 129.3, 129.4, 129.6, 132.6, 132.8, 132.9, 133.0, 133.9, 134.3, 135.2, 136.3 137.6, 139.0, 140.1, 140.3, 140.4, 140.8, 141.0, 141.1, 141.2, 141.4, 141.7, 141.8, 142.0. Mp 193-194 ℃. IR (KBr) 3376, 3034, 1593, 1496, 1330, 1182 cm ^-1 . [Α] _D ²² = -112.0 (c 0.20, CHCl ₃ , (S)). HRMS (FAB + ) calcd for C ₅₉ H ₄₆ NO ₅ S ₂ [M + H] ⁺ 912.2817, found 912.2814.

［８−５］ステップ５
実施例７のステップ４と同様にして、化合物３４ａ〜３４ｃから化合物３６ａ〜３６ｃ（いずれもＳ体）をそれぞれ収率９１％，＞９９％，９８％で得た。化合物３６ｂ，３６ｃのスペクトルデータは以下のとおり。 [8-5] Step 5
In the same manner as in Step 4 of Example 7, Compounds 36a to 36c (both S forms) were obtained from Compounds 34a to 34c in yields of 91%,> 99%, and 98%, respectively. The spectrum data of the compounds 36b and 36c are as follows.

化合物３６ｂ：¹H NMR (400 MHz, CDCl₃) δ 0.97 (t, J = 6.9 Hz, 3H), 2.16 (s, 6H), 3.79 (dq, J = 10.1, 7.3 Hz, 1H), 3.79 (dq, J = 10.1, 7.3 Hz, 1H), 7.30-7.52 (m, 10H), 7.58-7.80 (m, 14H), 7.79-7.96 (m, 3H), 7.99 (s, 1H). ¹³C NMR (100 MHz, CDCl₃) δ 14.5, 34.5, 66.3, 126.0, 126.4, 126.9, 127.1, 127.4, 127.5, 127.6, 127.7, 127.9, 128.0, 128.8, 128.9, 129.2, 130.3, 132.2, 132.3, 132.5, 132.8, 133.1, 133.7, 134.1, 135.2, 137.1, 137.4, 139.8, 139.9, 140.1, 140.3, 140.4, 140.5, 140.7. M.p. 171-173℃. IR (KBr) 3029, 1487, 1355, 1324, 1136, 1067 cm^-1. [α]_D ²⁴ = -91.9 (c 0.20, CHCl₃, (S)). HRMS (FAB+) calcd for C₄₈H₄₀NO₅S₂ [M+H]⁺ 774.2348, found 774.2359. Compound 36b: ¹ H NMR (400 MHz, CDCl ₃ ) δ 0.97 (t, J = 6.9 Hz, 3H), 2.16 (s, 6H), 3.79 (dq, J = 10.1, 7.3 Hz, 1H), 3.79 (dq , J = 10.1, 7.3 Hz, 1H), 7.30-7.52 (m, 10H), 7.58-7.80 (m, 14H), 7.79-7.96 (m, 3H), 7.99 (s, 1H). ¹³ C NMR (100 MHz, CDCl ₃ ) δ 14.5, 34.5, 66.3, 126.0, 126.4, 126.9, 127.1, 127.4, 127.5, 127.6, 127.7, 127.9, 128.0, 128.8, 128.9, 129.2, 130.3, 132.2, 132.3, 132.5, 132.8, 133.1, 133.7, 134.1, 135.2, 137.1, 137.4, 139.8, 139.9, 140.1, 140.3, 140.4, 140.5, 140.7. Mp 171-173 ° C. IR (KBr) 3029, 1487, 1355, 1324, 1136, 1067 cm ^-1 . α] _D ²⁴ = -91.9 (c 0.20, CHCl ₃ , (S)). HRMS (FAB +) calcd for C ₄₈ H ₄₀ NO ₅ S ₂ [M + H] ⁺ 774.2348, found 774.2359.

化合物３６ｃ：¹H NMR (400 MHz, CDCl₃) δ 0.86 (t, J = 6.9 Hz, 3H), 2.20 (s, 6H), 3.77 (m, 1H), 3.90 (m, 1H), 7.30-7.52 (m, 16H), 7.59-7.68 (m, 2H), 7.70-8.03 (m, 17H), 8.09 (s, 1H). ¹³CNMR (100 MHz, CDCl₃) δ 14.4, 34.8, 66.2, 124.7, 125.1, 126.0, 127.2, 127.3, 127.4, 127.5, 127.7, 127.9, 128.0, 128.9, 129.0, 129.1, 129.3, 132.3, 132.7, 133.1, 133.7, 134.1, 135.2, 137.3, 137.4, 139.9, 140.1, 140.6, 140.8, 140.9, 141.2, 141.6, 142.3. M.p. 189-191℃. IR (KBr) 3035, 1593, 1576, 1497, 1355, 1322, 1183, 1137 cm^-1. [α]_D ²³ = -93.9 (c 0.20, CHCl₃, (S)). HRMS (FAB+) calcd for C₆₀H₄₈NO₅S₂ [M+H]⁺ 926.2974, found 926.2969. Compound 36c: ¹ H NMR (400 MHz, CDCl ₃ ) δ 0.86 (t, J = 6.9 Hz, 3H), 2.20 (s, 6H), 3.77 (m, 1H), 3.90 (m, 1H), 7.30-7.52 (m, 16H), 7.59-7.68 ( m, 2H), 7.70-8.03 (m, 17H), 8.09 (s, 1H). 13 CNMR (100 MHz, CDCl 3) δ 14.4, 34.8, 66.2, 124.7, 125.1 , 126.0, 127.2, 127.3, 127.4, 127.5, 127.7, 127.9, 128.0, 128.9, 129.0, 129.1, 129.3, 132.3, 132.7, 133.1, 133.7, 134.1, 135.2, 137.3, 137.4, 139.9, 140.1, 140.6, 140.8, 140.9 , 141.2, 141.6, 142.3. Mp 189-191 ℃. IR (KBr) 3035, 1593, 1576, 1497, 1355, 1322, 1183, 1137 cm ^-1 . [Α] _D ²³ = -93.9 (c 0.20, CHCl ₃ HRMS (FAB +) calcd for C ₆₀ H ₄₈ NO ₅ S ₂ [M + H] ⁺ 926.2974, found 926.2969.

［８−６］ステップ６
実施例７のステップ５と同様にして、化合物３６ａ〜３６ｃから化合物３８ａ〜３８ｃ（いずれもＳ体）をそれぞれ収率５５％，６６％，５７％で得た。化合物３８ｂ，３８ｃのスペクトルデータは以下のとおり。また、このステップ６の別例として、Ｒｅｄ−Ａｌによる還元反応をＴＨＦ中、４０℃で行い、続く酸化反応をＤＭＦ中、水酸化カリウム存在下、約１気圧（０．１ＭＰａ）の酸素を封入して６０℃で２４時間行った。そうしたところ、化合物３６ａ〜３６ｃから化合物３８ａ〜３８ｃ（いずれもＳ体）がそれぞれ収率３９％，５２％，４３％で得られた。このように汎用性の高いＤＭＦを用いて１気圧という緩和した条件で酸化反応を行った場合でも、円滑に反応が進行することがわかった。 [8-6] Step 6
In the same manner as in Step 5 of Example 7, compounds 38a to 38c (all of S isomers) were obtained from compounds 36a to 36c in yields of 55%, 66%, and 57%, respectively. The spectrum data of the compounds 38b and 38c are as follows. As another example of Step 6, a reduction reaction with Red-Al is carried out in THF at 40 ° C., and the subsequent oxidation reaction is encapsulated with oxygen at about 1 atm (0.1 MPa) in DMF in the presence of potassium hydroxide. And performed at 60 ° C. for 24 hours. As a result, compounds 38a to 38c (all in S form) were obtained from compounds 36a to 36c in yields of 39%, 52%, and 43%, respectively. Thus, it was found that the reaction proceeds smoothly even when the oxidation reaction is performed under the relaxed condition of 1 atm using the versatile DMF.

化合物３８ｂ：¹H NMR (400 MHz, CD₃OD) δ 7.04 (m, 2H), 7.18 (t, J = 8.2 Hz, 2H), 7.30 (t, J = 7.3 Hz, 2H), 7.42 (t, J = 7.6 Hz, 6H), 7.59 (d, J = 8.2 Hz, 4H), 7.66 (d, J = 7.8 Hz, 4H), 7.72-7.81 (m, 6H), 7.83 (d, J = 7.8 Hz, 2H). ¹³C NMR (100 MHz, CD₃OD) δ 126.4, 127.2, 127.9, 128.0, 128.1, 128.4, 129.2, 129.7, 131.7, 132.3, 134.2, 134.4, 138.3, 139.8, 140.2, 142.7, 144.2. IR (KBr) 3371, 1620, 1485, 1220, 1175, 1036 cm^-1. [α]_D ²³ = -10.0 (c 0.20, CH3OH, (S)). HRMS (FAB-) calcd for C₄₄H₂₈NaO₆S₂ [M-2K+Na]^- 739.1225, found 739.1205. Compound 38b: ¹ H NMR (400 MHz, CD ₃ OD) δ 7.04 (m, 2H), 7.18 (t, J = 8.2 Hz, 2H), 7.30 (t, J = 7.3 Hz, 2H), 7.42 (t, J = 7.6 Hz, 6H), 7.59 (d, J = 8.2 Hz, 4H), 7.66 (d, J = 7.8 Hz, 4H), 7.72-7.81 (m, 6H), 7.83 (d, J = 7.8 Hz, ¹³ C NMR (100 MHz, CD ₃ OD) δ 126.4, 127.2, 127.9, 128.0, 128.1, 128.4, 129.2, 129.7, 131.7, 132.3, 134.2, 134.4, 138.3, 139.8, 140.2, 142.7, 144.2.IR (KBr) 3371, 1620, 1485, 1220, 1175, 1036 cm ^-1 . [Α] _D ²³ = -10.0 (c 0.20, CH3OH, (S)). HRMS (FAB-) calcd for C ₄₄ H ₂₈ NaO ₆ _{S 2 [M-2K + Na} ] - 739.1225, found 739.1205.

化合物３８ｃ：¹H NMR (400 MHz, CD₃OD) δ 7.10 (m, 2H), 7.24 (t, J = 7.3 Hz, 2H), 7.32 (t, J = 7.3 Hz, 4H), 7.40-7.53 (m, 10H), 7.73-7.85 (m, 10H), 7.86-8.00 (m, 8H). ¹³CNMR (100 MHz, CD₃OD) δ 124.8, 127.4, 128.1, 128.4, 128.5, 129.2, 129.3, 129.7, 132.5, 134.3, 134.4, 138.3, 139.8, 141.4, 143.0, 146.0. IR (KBr) 3406, 1594, 1215, 1182, 1038 cm^-1. [α]_D ²³ = -72.0 (c 0.20, CH₃OH, (S)). HRMS (FAB-) calcd for C₅₆H₃₆NaO₆S₂ [M-2K+Na]^- 891.1851, found 891.1841. Compound 38c: ¹ H NMR (400 MHz, CD ₃ OD) δ 7.10 (m, 2H), 7.24 (t, J = 7.3 Hz, 2H), 7.32 (t, J = 7.3 Hz, 4H), 7.40-7.53 ( m, 10H), 7.73-7.85 (m , 10H), 7.86-8.00 (m, 8H). 13 CNMR (100 MHz, CD 3 OD) δ 124.8, 127.4, 128.1, 128.4, 128.5, 129.2, 129.3, 129.7, 132.5, 134.3, 134.4, 138.3, 139.8, 141.4, 143.0, 146.0. IR (KBr) 3406, 1594, 1215, 1182, 1038 cm ^-1 . [Α] _D ²³ = -72.0 (c 0.20, CH ₃ OH, ( . S)) HRMS (FAB-) calcd for C 56 H 36 NaO 6 S 2 [M-2K + Na] - 891.1851, found 891.1841.

［８−７］ステップ７
実施例７のステップ６と同様にして、化合物３８ａ〜３８ｃから化合物４０ａ〜４０ｃ（いずれもＳ体）をいずれも収率＞９９％で得た。化合物４０ｂ，４０ｃのスペクトルデータは以下のとおり。 [8-7] Step 7
In the same manner as in Step 6 of Example 7, compounds 40a to 40c (both S forms) were obtained from compounds 38a to 38c in a yield> 99%. The spectrum data of compounds 40b and 40c are as follows.

化合物４０ｂ：¹H NMR (400 MHz, CD₃OD) δ 7.10 (d, J = 8.6 Hz, 2H), 7.27 (t, J = 7.0 Hz, 2H), 7.33 (t, J = 7.3 Hz, 2H), 7.44 (t, J = 7.8 Hz, 4H), 7.51 (t, J = 7.8 Hz, 2H), 7.62-7.67 (m, 4H), 7.68-7.74 (m, 8H), 7.86 (s, 2H), 7.91 (d, J = 8.2 Hz, 2H). ¹³CNMR (100 MHz, CD₃OD) δ 126.5, 127.7, 127.9, 128.1, 128.7, 128.8, 129.1, 129.8, 131.6, 132.9, 134.1, 134.6, 138.5, 138.7, 139.7, 140.6, 142.4, 143.3. IR (KBr) 3382, 1697, 1486, 1220, 1164, 1033 cm^-1. [α]_D ²² = -20.8 (c 1.0, MeOH, (S)). HRMS (FAB-) calcd for C₄₄H₂₉O₆S₂ [M-H]^- 717.1406, found 717.1391. Compound 40b: ¹ H NMR (400 MHz, CD ₃ OD) δ 7.10 (d, J = 8.6 Hz, 2H), 7.27 (t, J = 7.0 Hz, 2H), 7.33 (t, J = 7.3 Hz, 2H) , 7.44 (t, J = 7.8 Hz, 4H), 7.51 (t, J = 7.8 Hz, 2H), 7.62-7.67 (m, 4H), 7.68-7.74 (m, 8H), 7.86 (s, 2H), 7.91 (d, J = 8.2 Hz , 2H). 13 CNMR (100 MHz, CD 3 OD) δ 126.5, 127.7, 127.9, 128.1, 128.7, 128.8, 129.1, 129.8, 131.6, 132.9, 134.1, 134.6, 138.5, 138.7 , 139.7, 140.6, 142.4, 143.3. IR (KBr) 3382, 1697, 1486, 1220, 1164, 1033 cm ^-1 . [Α] _D ²² = -20.8 (c 1.0, MeOH, (S)). HRMS (FAB _{_{-) calcd for C 44 H 29}} O 6 S 2 [MH] - 717.1406, found 717.1391.

化合物４０ｃ：¹H NMR (400 MHz, CD₃OD) δ 7.16 (br, 2H), 7.27 (t, J = 7.3 Hz, 2H), 7.32 (t, J = 7.3 Hz, 4H), 7.40-7.53 (m, 10H), 7.73-7.85 (m, 10H), 7.86-8.00 (m, 8H). ¹³CNMR (100 MHz, CD₃OD) δ 124.9, 127.6, 128.2, 128.4, 128.5, 128.6, 129.2, 129.3, 129.7, 132.7, 134.2, 134.5, 139.9, 141.5, 142.8, 145.4. IR (KBr) 3389, 1497, 1218, 1186, 1035 cm^-1. [α]_D ²³ = -69.2 (c 0.20, CH₃OH, (S)). HRMS (FAB-) calcd for C₅₆H₃₇O₆S₂ [M-H]^- 869.2032, found 869.2014. Compound 40c: ¹ H NMR (400 MHz, CD ₃ OD) δ 7.16 (br, 2H), 7.27 (t, J = 7.3 Hz, 2H), 7.32 (t, J = 7.3 Hz, 4H), 7.40-7.53 ( m, 10H), 7.73-7.85 (m , 10H), 7.86-8.00 (m, 8H). 13 CNMR (100 MHz, CD 3 OD) δ 124.9, 127.6, 128.2, 128.4, 128.5, 128.6, 129.2, 129.3, 129.7, 132.7, 134.2, 134.5, 139.9, 141.5, 142.8, 145.4.IR (KBr) 3389, 1497, 1218, 1186, 1035 cm ^-1 . [Α] _D ²³ = -69.2 (c 0.20, CH ₃ OH, ( . S)) HRMS (FAB-) calcd for C 56 H 37 O 6 S 2 [MH] - 869.2032, found 869.2014.

［実施例９］
実施例８のステップ６の代わりに、下記式のように、ステップ１で化合物３６ａ〜３６ｃのスルホン酸エステルをスルホン酸ナトリウム塩（化合物３７ａ〜３７ｃ）に変換し、そのナトリウム塩を単離せず、ステップ２でＲｅｄ−Ａｌによる還元反応をＴＨＦ中、３５℃で行い、更に酸化反応をＤＭＦ中、水酸化カリウム存在下、約１気圧（０．１ＭＰａ）の酸素を封入して６０℃で３８時間行うことにより、化合物３８ａ〜３８ｃを得た。なお、ステップ２は、実施例８のステップ６の別例と同様である。ステップ３では、実施例８のステップ７（実施例７のステップ６）と同様にして、化合物４０ａ〜４０ｃを得た。以下には、ステップ１の手順について、化合物３６ａを化合物３７ａに変換する場合を例に挙げて説明する。 [Example 9]
Instead of Step 6 of Example 8, the sulfonate esters of compounds 36a-36c were converted to sodium sulfonate salts (compounds 37a-37c) in step 1 as shown below, and the sodium salt was not isolated, In Step 2, the reduction reaction with Red-Al is carried out in THF at 35 ° C., and the oxidation reaction is further carried out in DMF in the presence of potassium hydroxide with about 1 atm (0.1 MPa) of oxygen sealed at 60 ° C. for 38 hours. This gave compounds 38a-38c. Step 2 is the same as another example of step 6 of the eighth embodiment. In Step 3, in the same manner as in Step 7 of Example 8 (Step 6 of Example 7), compounds 40a to 40c were obtained. Hereinafter, the procedure of Step 1 will be described with reference to an example in which compound 36a is converted to compound 37a.

反応容器に、化合物３６ａ（１２４．４ｍｇ，０．２０ｍｍｏｌ）と水酸化ナトリウム（１．６０ｇ，４０ｍｍｏｌ）とメタノール（２０ｍＬ）を加えて、７０℃に加熱し、５時間撹拌した。溶媒を減圧留去し、２Ｍ塩酸で中和した。酢酸エチル（２０ｍＬ×３）を用いて通常の分液処理を行った。抽出した有機層は硫酸マグネシウムで乾燥後、ろ過、濃縮し、目的とする化合物３７ａをほぼ定量的に得た。この化合物３７ａは精製せずに次の反応（連続的還元・酸化）に用いた。化合物３７ｂ，３７ｃもこれと同様にして得た。化合物３７ａ〜３７ｃのスペクトルデータは以下のとおり。 To the reaction vessel, compound 36a (124.4 mg, 0.20 mmol), sodium hydroxide (1.60 g, 40 mmol) and methanol (20 mL) were added, heated to 70 ° C. and stirred for 5 hours. The solvent was distilled off under reduced pressure and neutralized with 2M hydrochloric acid. Ordinary liquid separation treatment was performed using ethyl acetate (20 mL × 3). The extracted organic layer was dried over magnesium sulfate, filtered and concentrated to obtain the target compound 37a almost quantitatively. This compound 37a was used for the next reaction (continuous reduction / oxidation) without purification. Compounds 37b and 37c were obtained in the same manner. The spectrum data of the compounds 37a to 37c are as follows.

化合物３７ａ：¹H NMR (400 MHz, CD₃OD) δ 2.12 (s, 6H), 6.98 (d, J = 8.7 Hz, 1H), 7.20-7.39 (m, 7H), 7.40-7,50 (m, 3H), 7.51-7.60 (m, 3H), 7.63 (d, J = 6.9 Hz, 2H), 7.75 (s, 1H), 7.76 (s, 1H), 7.87 (d, J = 7.9 Hz, 1H), 7.88 (d, J = 8.2 Hz, 1H). ¹³C NMR (100 MHz, CD₃OD) Many peaks overlapped. δ 35.5, 127.3, 127.4, 127.7, 128.0, 128.1, 128.2, 128.3, 128.4, 128.5, 128.7, 129.5, 129.6, 130.5, 130.9, 131.4, 132.8, 133.3, 133.7, 134.3, 134.5, 135.0, 135.6, 136.1, 139.2, 140.5, 143.4, 143.8, 144.6. M.p. 283℃ (decomposed). IR (KBr) 3444, 3054, 2923, 1491, 1322, 1188, 1135, 1042 cm^-1. [α]_D ²²= 88.8 (c 1.0, CH₃OH, (R)). HRMS (FAB-) calcd for C₃₄H₂₆NO₅S₂ [M-Na]^- 592.1252, found 592.1252. Compound 37a: ¹ H NMR (400 MHz, CD ₃ OD) δ 2.12 (s, 6H), 6.98 (d, J = 8.7 Hz, 1H), 7.20-7.39 (m, 7H), 7.40-7,50 (m , 3H), 7.51-7.60 (m, 3H), 7.63 (d, J = 6.9 Hz, 2H), 7.75 (s, 1H), 7.76 (s, 1H), 7.87 (d, J = 7.9 Hz, 1H) , 7.88 (d, J = 8.2 Hz, 1H). 13 C NMR (100 MHz, CD 3 OD) Many peaks overlapped. δ 35.5, 127.3, 127.4, 127.7, 128.0, 128.1, 128.2, 128.3, 128.4, 128.5, 128.7 , 129.5, 129.6, 130.5, 130.9, 131.4, 132.8, 133.3, 133.7, 134.3, 134.5, 135.0, 135.6, 136.1, 139.2, 140.5, 143.4, 143.8, 144.6.Mp 283 ℃ (decomposed). IR (KBr) 3444, 3054, 2923, 1491, 1322, 1188, 1135, 1042 cm ^-1 . [Α] _D ²² = 88.8 (c 1.0, CH ₃ OH, (R)). HRMS (FAB-) calcd for C ₃₄ H ₂₆ NO ₅ _{^{S 2 [M-Na] -}} 592.1252, found 592.1252.

化合物３７ｂ： ¹H NMR (400 MHz, d₈-THF) δ 1.91 (s, 6H), 6.77 (br, 1H), 6.90 (d, J = 8.7 Hz, 1H), 7.09-7.27 (m, 8H), 7.30-7.39 (m, 5H), 7.42-7.47 (m, 4H), 7.52-7.53 (m, 4H), 7.60-7.65 (m, 2H), 7.78-7.85 (m, 4H). ¹³C NMR (100 MHz, d₈-THF) Many peaks overlapped. δ 33.9, 124.9, 125.8, 126.5, 126.6, 126.7, 126.8, 127.1, 127.5, 127.7, 128.3, 128.4, 128.7, 130.8, 131.4, 131.7, 131.9, 132.8, 133.0, 133.9, 134.3, 134.8, 137.8, 138.7, 138.9, 140.3, 140.5, 140.8, 141.4, 142.8, 143.0. M.p. 289-292℃ (decomposed). IR (KBr) 3422, 3029, 1619, 1487, 1322, 1190, 1041 cm^-1. HRMS (FAB-) calcd for C₄₆H₃₄NO₅S₂[M-Na]^- 744.1878, found 744.1878. Compound 37b: ¹ H NMR (400 MHz, d ₈ -THF) δ 1.91 (s, 6H), 6.77 (br, 1H), 6.90 (d, J = 8.7 Hz, 1H), 7.09-7.27 (m, 8H) , 7.30-7.39 (m, 5H), 7.42-7.47 (m, 4H), 7.52-7.53 (m, 4H), 7.60-7.65 (m, 2H), 7.78-7.85 (m, 4H). ¹³ C NMR ( 100 MHz, d ₈ -THF) Many peaks overlapped.δ 33.9, 124.9, 125.8, 126.5, 126.6, 126.7, 126.8, 127.1, 127.5, 127.7, 128.3, 128.4, 128.7, 130.8, 131.4, 131.7, 131.9, 132.8, 133.0 , 133.9, 134.3, 134.8, 137.8, 138.7, 138.9, 140.3, 140.5, 140.8, 141.4, 142.8, 143.0. Mp 289-292 ° C (decomposed). IR (KBr) 3422, 3029, 1619, 1487, 1322, 1190, ^{. 1041 cm -1 HRMS (FAB-)} calcd for C 46 H 34 NO 5 S 2 [M-Na] - 744.1878, found 744.1878.

化合物３７ｃ： ¹H NMR (400 MHz, d₈-THF) δ2.00 (s, 6H), 6.98 (d, J = 8.7 Hz, 1H), 7.14-7.34 (m, 13H), 7.37-7.45 (m, 4H), 7.66-7.88 (m, 18H), 7.95 (br, 1H). ¹³C NMR (100 MHz, d₈-THF) Many peaks overlapped. δ34.5, 123.2, 124.0, 126.0, 126.6, 126.9, 127.1, 127.1, 127.3, 127.5, 128.2, 128.5, 128.7, 129.0, 131.9, 132.7, 133.1, 133.3, 133.7, 135.0, 137.6, 138.7, 139.8, 140.0, 140.5, 140.7, 140.9, 141.1, 141.5, 142.8, 143.2, 144.7. M.p. 293-296℃ (decomposed). IR (KBr) 3407, 3057, 3033, 2923, 1594, 1497, 1319, 1188, 1041 cm^-1. HRMS (FAB-) calcd for C₅₈H₄₂NO₅S₂ [M-Na]^-896.2504, found 896.2504. Compound 37c: ¹ H NMR (400 MHz, d ₈ -THF) δ2.00 (s, 6H), 6.98 (d, J = 8.7 Hz, 1H), 7.14-7.34 (m, 13H), 7.37-7.45 (m , 4H), 7.66-7.88 (m, 18H), 7.95 (br, 1H). 13 C NMR (100 MHz, d 8 -THF) Many peaks overlapped. δ34.5, 123.2, 124.0, 126.0, 126.6, 126.9, 127.1, 127.1, 127.3, 127.5, 128.2, 128.5, 128.7, 129.0, 131.9, 132.7, 133.1, 133.3, 133.7, 135.0, 137.6, 138.7, 139.8, 140.0, 140.5, 140.7, 140.9, 141.1, 141.5, 142.8, 143.2, 144.7. Mp 293-296 ℃ (decomposed). IR (KBr) 3407, 3057, 3033, 2923, 1594, 1497, 1319, 1188, 1041 cm ^-1 .HRMS (FAB-) calcd for C ₅₈ H ₄₂ NO ₅ S _{^{2 [M-Na] - 896.2504}} , found 896.2504.

化合物３６ａ〜３６ｃから化合物３８ａ〜３８ｃへの変換効率は、実施例８よりも実施例９の方が高い。その理由は、以下のように考えられる。化合物３６ａ〜３６ｃのＲｅｄ−Ａｌによる還元反応では、ビナフチル化合物のスルホンアミド部位はスルフィン酸に、スルホン酸エステル部位はスルホン酸に変換されるのが、次の酸化反応で最も効率よく酸化される。しかし、実際には、Ｒｅｄ−Ａｌによる還元反応では、スルホン酸エステル部位はチオールやジスルフィドに変換されてしまうことが確認されている。実施例９では、スルホン酸エステル部位をスルホン酸ナトリウム塩にすることで、これらの還元反応が抑制され、スルホン酸への選択的な変換効率が上がったと考えれる。 The conversion efficiency from compounds 36a to 36c to compounds 38a to 38c is higher in Example 9 than in Example 8. The reason is considered as follows. In the reduction reaction of compounds 36a to 36c with Red-Al, the sulfonamide site of the binaphthyl compound is converted to sulfinic acid, and the sulfonic acid ester site is converted to sulfonic acid, which is most efficiently oxidized by the subsequent oxidation reaction. However, in practice, it has been confirmed that in the reduction reaction with Red-Al, the sulfonic acid ester moiety is converted to thiol or disulfide. In Example 9, it is considered that these reduction reactions were suppressed by making the sulfonic acid ester moiety a sulfonic acid sodium salt, and the selective conversion efficiency to sulfonic acid was increased.

本発明によって得られるアリールスルホンアミドの還元体は、対応するアリールスルホン酸の合成中間体として有用である。また、アリールスルホン酸は、例えば有機合成反応の触媒などに利用可能である。 The reduced form of arylsulfonamide obtained by the present invention is useful as a synthetic intermediate for the corresponding arylsulfonic acid. Aryl sulfonic acid can be used, for example, as a catalyst for organic synthesis reaction.

Claims

ArSO _² NR ¹ R ₂ (Ar is aryl which may have a substituent, R ¹ and R ² are an alkyl group which may be the same or different) arene sulfonamide represented by, NaAlH _A method for reducing arenesulfonamides, wherein the corresponding sulfinic acid is obtained by reduction with a reducing agent represented by ₂ (OC ₂ H ₄ OCH ₃ ) ₂ .

A process for producing arenesulfonic acid , wherein the sulfinic acid obtained by the method for reducing arenesulfonamide according to claim 1 is oxidized with oxygen or hydrogen peroxide to obtain the corresponding sulfonic acid.

The method for producing arenesulfonic acid according to claim 2 , wherein the optically active sulfonamide represented by the formula (1) is used as the arenesulfonamide to obtain the optically active disulfonic acid represented by the formula (2).
(In the formulas (1) and (2), R ¹ and R ² are as described above, R ³ is an alkyl group, R ⁴ and R ⁵ may be the same or different, and may be a hydrogen atom, A halogen atom or an aryl group optionally having a substituent)