KR101013147B1 - Novel allenyl sulfide compounds and synthesis of them - Google Patents
Novel allenyl sulfide compounds and synthesis of them Download PDFInfo
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- C07C321/24—Thiols, sulfides, hydropolysulfides, or polysulfides having thio groups bound to carbon atoms of six-membered aromatic rings
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Abstract
본 발명은 유기 황-인듐 착물을 이용한 신규의 알레닐 설파이드 유도체와 이의 제조방법에 관한 것으로서, 더욱 상세하게는 본 발명은 싸이올 (thiol)의 친핵성을 증가시키기 위해 새로운 형태의 반응 시약인 인듐 트라이(오가노싸이올레이트)와 삼차 프로파질 아세테이트가 교차-짝지움 반응을 하여 제조된 하기 화학식 1로 표시되는 신규의 알레닐 설파이드 유도체와 이의 제조방법에 관한 것이다.The present invention relates to a novel allenyl sulfide derivative using an organic sulfur-indium complex and a method for preparing the same. More particularly, the present invention relates to a new type of reaction reagent, indium, which is used to increase the nucleophilicity of thiol. The present invention relates to a novel allenyl sulfide derivative represented by the following Chemical Formula 1 prepared by cross-coupling tri (organothiolate) and tertiary propazyl acetate and a method of preparing the same.
[화학식 1][Formula 1]
상기 화학식 1에서, R1, R2, R3, R4 는 각각 발명의 상세한 설명에서 정의한 바와 같다.In Chemical Formula 1, R 1 , R 2 , R 3 , R 4 Are as defined in the detailed description of the invention, respectively.
알레닐 설파이드, 프로파질 아세테이트, 인듐 트라이(오가노싸이올레이트), 팔라듐, 교차-짝지움 반응 Allenyl sulfide, propazyl acetate, indium tri (organothiolate), palladium, cross-coupling reaction
Description
본 발명은 유기 황-인듐 착물을 이용한 신규의 알레닐 설파이드 유도체와 이의 제조방법에 관한 것으로서, 더욱 상세하게는 본 발명은 싸이올 (thiol)의 친핵성을 증가시키기 위해 새로운 형태의 반응 시약인 인듐 트라이(오가노싸이올레이트)와 삼차 프로파질 아세테이트가 교차-짝지움 반응을 하여 제조된 하기 화학식 1로 표시되는 신규의 알레닐 설파이드 유도체와 이의 제조방법에 관한 것이다.The present invention relates to a novel allenyl sulfide derivative using an organic sulfur-indium complex and a method for preparing the same. More particularly, the present invention relates to a new type of reaction reagent, indium, which is used to increase the nucleophilicity of thiol. The present invention relates to a novel allenyl sulfide derivative represented by the following Chemical Formula 1 prepared by cross-coupling tri (organothiolate) and tertiary propazyl acetate and a method of preparing the same.
[화학식 1][Formula 1]
[상기 화학식 1에서,[In Formula 1,
R1 및 R2는 서로 독립적으로 (C1-C10)알킬 또는 (C6-C12)아릴이거나, R1과 R2는 (C2-C7)알킬렌으로 연결되어 3원 내지 8원의 고리를 형성할 수 있으며;R 1 and R 2 are independently of each other (C1-C10) alkyl or (C6-C12) aryl, or R 1 and R 2 are linked with (C2-C7) alkylene to form a 3-8 membered ring. Can be;
R3는 (C1-C10)알킬 또는 (C6-C12)아릴이고;R 3 is (C1-C10) alkyl or (C6-C12) aryl;
R4는 수소 또는 (C1-C10)알킬이고;R 4 is hydrogen or (C 1 -C 10) alkyl;
상기 R1, R2, R3 및 R4의 알킬 또는 아릴은 (C1-C10)알킬, (C1-C10)알콕시, 할로겐, (C6-C12)아릴 및 아세틸로 이루어진 군으로부터 선택된 하나 이상의 치환기로 더 치환될 수 있다.]Alkyl or aryl of R 1 , R 2 , R 3 and R 4 may be selected from the group consisting of (C1-C10) alkyl, (C1-C10) alkoxy, halogen, (C6-C12) aryl and acetyl. May be further substituted.]
알렌(allene) 화합물은 다양한 물질을 제조할 수 있는 원료물질로 유용하므로, 이에 다양한 치환기가 도입된 알레닐 설파이드 화합물의 합성에 대하여 많은 관심의 대상이 되고 있다. Since allene compounds are useful as raw materials for preparing various materials, they are of great interest for the synthesis of allenyl sulfide compounds having various substituents introduced therein.
일반적으로 알려진 알레닐 설파이드 화합물의 합성방법들을 살펴보면, 알레닐 설폭사이드 화합물의 환원반응 (Cookson, R. Chem. Commun. 1978, 822, Mattay, J. Synthesis 1991, 1, 11), 리튬 알킬 싸이올레이트 유도체와 포스핀옥사이드, 알데하이드를 사용한 반응 (Huang, X. Tetrahedron Letters 2003, 44, 5913), 프로파질 할라이드 유도체와 금속촉매를 이용한 교차-짝지움 반응 ( Kakiuchi, K. Eur. J. Org. Chem. 2004, 504) 등이 알려져 있다.In general, known synthesis methods of allenyl sulfide compounds include reduction reactions of allenyl sulfoxide compounds (Cookson, R. Chem. Commun. 1978, 822, Mattay, J. Synthesis 1991, 1, 11), lithium alkyl thiols Reactions with late derivatives, phosphine oxides and aldehydes (Huang, X. Tetrahedron Letters 2003, 44, 5913), cross-coupling reactions with propazyl halide derivatives and metal catalysts (Kakiuchi, K. Eur. J. Org. Chem. 2004, 504).
상기 반응들은 시약제조과정이 까다롭고, 다양한 치환기의 도입에 제한이 있다. These reactions are difficult to prepare reagents and have limitations on the introduction of various substituents.
따라서, 보다 제조방법이 간편하고, 작용기의 선택이 광범위한 유기 금속 화합물을 사용하여 다양한 치환기가 도입된 알레닐 설파이드 화합물의 제조방법이 요구되고 있다.Therefore, there is a need for a method for producing an allenyl sulfide compound having a simpler manufacturing method and various substituents introduced using an organometallic compound having a wide selection of functional groups.
본 발명의 목적은, 신규의 알레닐 설파이드 유도체를 제공하는데 있다.An object of the present invention is to provide a novel allenyl sulfide derivative.
본 발명의 다른 목적은, 인듐 트라이(오가노싸이올레이트)와 삼차 프로파질 아세테이트가 교차-짝지움 반응시켜 알레닐 설파이드 유도체를 제조하는 신규한 방법을 제공하는데 있다.Another object of the present invention is to provide a novel method for preparing allenyl sulfide derivatives by cross-coupling indium tri (organothiolate) and tertiary propazyl acetate.
본 발명은 유기 황-인듐 착물을 이용한 신규의 알레닐 설파이드 유도체와 이의 제조방법에 관한 것으로서, 더욱 상세하게는 본 발명은 싸이올 (thiol)의 친핵성을 증가시키기 위해 새로운 형태의 반응 시약인 인듐 트라이(오가노싸이올레이트)와 삼차 프로파질 아세테이트가 팔라듐 촉매하에서 교차-짝지움 반응을 하여 제조된 하기 화학식 1로 표시되는 신규의 알레닐 설파이드 유도체와 이의 제조방법에 관한 것이다. The present invention relates to a novel allenyl sulfide derivative using an organic sulfur-indium complex and a method for preparing the same. More particularly, the present invention relates to a new type of reaction reagent, indium, which is used to increase the nucleophilicity of thiol. It relates to a novel allenyl sulfide derivative represented by the following formula (1) prepared by tri-organothiolate and tertiary propazyl acetate under a palladium catalyst and a method for preparing the same.
[화학식 1][Formula 1]
[상기 화학식 1에서,[In Formula 1,
R1 및 R2는 서로 독립적으로 (C1-C10)알킬 또는 (C6-C12)아릴이거나, R1과 R2는 (C2-C7)알킬렌으로 연결되어 3원 내지 8원의 고리를 형성할 수 있으며;R 1 and R 2 are independently of each other (C1-C10) alkyl or (C6-C12) aryl, or R 1 and R 2 are linked with (C2-C7) alkylene to form a 3-8 membered ring. Can be;
R3는 (C1-C10)알킬 또는 (C6-C12)아릴이고;R 3 is (C1-C10) alkyl or (C6-C12) aryl;
R4는 수소 또는 (C1-C10)알킬이고;R 4 is hydrogen or (C 1 -C 10) alkyl;
상기 R1, R2, R3 및 R4의 알킬 또는 아릴은 (C1-C10)알킬, (C1-C10)알콕시, 할로겐, (C6-C12)아릴 및 아세틸로 이루어진 군으로부터 선택된 하나 이상의 치환기로 더 치환될 수 있다.]Alkyl or aryl of R 1 , R 2 , R 3 and R 4 may be selected from the group consisting of (C1-C10) alkyl, (C1-C10) alkoxy, halogen, (C6-C12) aryl and acetyl. May be further substituted.]
본 발명에서의 '알킬'은 탄소수 1 내지 10의 직쇄상 또는 분쇄상의 포화 탄소사슬을 포함한다."Alkyl" in the present invention includes a straight or pulverized saturated carbon chain having 1 to 10 carbon atoms.
구체적으로, 상기 R1 및 R2는 서로 독립적으로 메틸, 에틸, n-프로필, i-프로필, n-뷰틸, i-뷰틸, t-뷰틸, n-펜틸, i-펜틸, n-헥실, n-헵틸, n-옥틸, n-노닐, 2-에틸헥실, 데실, 트리플루오로메틸, 벤질, 페닐, 나프틸, 2-메틸페닐, 3-메틸페닐, 4-메틸페닐, 2-브로모페닐, 3-브로모페닐, 4-브로모페닐, 2-아세틸페닐, 3-아세틸페닐, 4-아세틸페닐, 2-메톡시페닐, 3-메톡시페닐, 4-메톡시페닐 또는 바이페닐이거나, C5 알킬렌으로 연결되어 6원의 고리를 형성할 수 있고; R3는 메틸, 에틸, n-프로필, i-프로필, n-뷰틸, i-뷰틸, t-뷰틸, n-펜틸, i-펜틸, n-헥실, n-헵틸, n-옥틸, n-노닐, 2-에틸헥실, 데실, 트리플루오로메틸, 벤질, 페닐, 나프틸, 2-메틸페닐, 3-메틸페닐, 4-메틸페닐, 2-브로모페닐, 3-브로모페닐, 4-브로모페닐, 2- 아세틸페닐, 3-아세틸페닐, 4-아세틸페닐, 2-메톡시페닐, 3-메톡시페닐, 4-메톡시페닐 또는 바이페닐이고; R4는 수소, 메틸, 에틸, n-프로필, i-프로필, n-뷰틸, i-뷰틸, t-뷰틸, n-펜틸, i-펜틸, n-헥실, n-헵틸, n-옥틸, n-노닐, 2-에틸헥실, 데실, 트리플루오로메틸 또는 벤질인 것을 특징으로 한다.Specifically, R 1 and R 2 are independently of each other methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl, n-pentyl, i-pentyl, n-hexyl, n -Heptyl, n-octyl, n-nonyl, 2-ethylhexyl, decyl, trifluoromethyl, benzyl, phenyl, naphthyl, 2-methylphenyl, 3-methylphenyl, 4-methylphenyl, 2-bromophenyl, 3- Bromophenyl, 4-bromophenyl, 2-acetylphenyl, 3-acetylphenyl, 4-acetylphenyl, 2-methoxyphenyl, 3-methoxyphenyl, 4-methoxyphenyl or biphenyl or C5 alkylene Can be linked to form a six-membered ring; R 3 is methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl, n-pentyl, i-pentyl, n-hexyl, n-heptyl, n-octyl, n-nonyl 2-ethylhexyl, decyl, trifluoromethyl, benzyl, phenyl, naphthyl, 2-methylphenyl, 3-methylphenyl, 4-methylphenyl, 2-bromophenyl, 3-bromophenyl, 4-bromophenyl, 2- acetylphenyl, 3-acetylphenyl, 4-acetylphenyl, 2-methoxyphenyl, 3-methoxyphenyl, 4-methoxyphenyl or biphenyl; R 4 is hydrogen, methyl, ethyl, n-propyl, i-propyl, n-butyl, i-butyl, t-butyl, n-pentyl, i-pentyl, n-hexyl, n-heptyl, n-octyl, n -Nonyl, 2-ethylhexyl, decyl, trifluoromethyl or benzyl.
상기 화학식 1의 알레닐 설파이드 유도체는 더욱 구체적으로는 R1은 페닐, 3-아세틸페닐 또는 4-브로모페닐이고; R2는 메틸이고; R1과 R2가 펜틸렌(-CH2CH2CH2CH2CH2-)으로 연결되어 6원의 고리인 사이클로헥실을 형성할 수 있고; R3는 n-프로필, 아이소프로필, t-뷰틸, 페닐, 4-메틸페닐 또는 4-메톡시페닐이고; R4는 수소원자, 메틸 또는 t-뷰틸인 화합물이다.More specifically, the allenyl sulfide derivative of Chemical Formula 1 is R 1 is phenyl, 3-acetylphenyl or 4-bromophenyl; R 2 is methyl; R 1 and R 2 may be linked to pentylene (—CH 2 CH 2 CH 2 CH 2 CH 2 —) to form a cyclohexyl which is a 6 membered ring; R 3 is n-propyl, isopropyl, t-butyl, phenyl, 4-methylphenyl or 4-methoxyphenyl; R 4 is a hydrogen atom, methyl or t-butyl.
본 발명에 따른 상기 화학식 1로 표시되는 알레닐 설파이드 유도체를 구체적으로 예시하면 다음과 같다: Specific examples of the allenyl sulfide derivative represented by Formula 1 according to the present invention are as follows:
(3-페닐-1,2-부타다이에닐)(4-메틸페닐) 설파이드,(3-phenyl-1,2-butadienyl) (4-methylphenyl) sulfide,
(3-페닐-1,2-부타다이에닐)(4-메톡시페닐) 설파이드, (3-phenyl-1,2-butadienyl) (4-methoxyphenyl) sulfide,
(3-페닐-1,2-부타다이에닐)(페닐) 설파이드, (3-phenyl-1,2-butadienyl) (phenyl) sulfide,
(3-페닐-1,2-부타다이에닐)(아이소프로필) 설파이드,(3-phenyl-1,2-butadienyl) (isopropyl) sulfide,
(3-페닐-1,2-부타다이에닐)(n-프로필) 설파이드, (3-phenyl-1,2-butadienyl) (n-propyl) sulfide,
(3-페닐-1,2-부타다이에닐)(tert-부틸) 설파이드, (3-phenyl-1,2-butadienyl) (tert-butyl) sulfide,
(3-(4-브로모페닐)-1,2-부타다이에닐)(4-메톡시페닐) 설파이드, (3- (4-bromophenyl) -1,2-butadienyl) (4-methoxyphenyl) sulfide,
(3-(4-브로모페닐)-1,2-부타다이에닐)(아이소프로필) 설파이드, (3- (4-bromophenyl) -1,2-butadienyl) (isopropyl) sulfide,
(3-(4-브로모페닐)-1,2-부타다이에닐)(페닐) 설파이드, (3- (4-bromophenyl) -1,2-butadienyl) (phenyl) sulfide,
(2-사이클로헥실리덴바이닐)(4-메틸페닐) 설파이드,(2-cyclohexylidenevinyl) (4-methylphenyl) sulfide,
(2-사이클로헬실리덴바이닐)(4-메톡시페닐) 설파이드, (2-cyclohelylidenevinyl) (4-methoxyphenyl) sulfide,
(2-사이클로헥실리덴바이닐)(페닐) 설파이드, (2-cyclohexylidenevinyl) (phenyl) sulfide,
(2-사이클로헥실리덴바이닐)(이소프로필) 설파이드, (2-cyclohexylidenevinyl) (isopropyl) sulfide,
3-(4-(페닐싸이오)부타-2,3-다이엔-2-일)페닐 아세테이트, 3- (4- (phenylthio) buta-2,3-dien-2-yl) phenyl acetate,
3-(4-(tert-부틸싸이오)부타-2,3-다이엔-2-일)페닐 아세테이트, 3- (4- (tert-butylthio) buta-2,3-dien-2-yl) phenyl acetate,
(4-메톡시페닐)(4-페닐펜타-2,3-다이엔-2-일) 설파이드, (4-methoxyphenyl) (4-phenylpenta-2,3-dien-2-yl) sulfide,
(아이소프로필)(4-페닐펜타-2,3-다이엔-2-일) 설파이드, (Isopropyl) (4-phenylpenta-2,3-dien-2-yl) sulfide,
(4-메톡시페닐)2-페닐옥타-2,3-다이엔-4-일) 설파이드, (4-methoxyphenyl) 2-phenylocta-2,3-dien-4-yl) sulfide,
(2-페닐옥타-2,3-다이엔-4-일)(n-프로필) 설파이드, (2-phenylocta-2,3-dien-4-yl) (n-propyl) sulfide,
(2-페닐옥타-2,3-다이엔-4-일)(페닐) 설파이드.(2-phenylocta-2,3-dien-4-yl) (phenyl) sulfide.
또한, 본 발명은 상기 화학식 1로 표시되는 알레닐 설파이드 유도체의 제조방법을 포함하며, 보다 상세하게는 팔라듐 촉매 및 포스핀 리간드 존재하에서, 싸이올 (thiol)의 친핵성을 증가시키기 위해 새로운 형태의 반응 시약인 인듐 트라이(오가노싸이올레이트) (화학식 3)와 삼차 프로파질 아세테이트(화학식 2)를 교차-짝지움 반응시켜 상기 화학식 1로 표시되는 신규의 알레닐 설파이드 유도체를 제 조한다(반응식 1).In addition, the present invention includes a method for preparing an allenyl sulfide derivative represented by Chemical Formula 1, and more specifically, in the presence of a palladium catalyst and a phosphine ligand, in order to increase the nucleophilicity of a thiol A novel allenyl sulfide derivative represented by Chemical Formula 1 is prepared by cross-coupling a reaction reagent, indium tri (organothiolate) (Formula 3), with tertiary propazyl acetate (Formula 2). One).
[반응식 1]Scheme 1
[상기 반응식 1에서, R1 및 R2는 서로 독립적으로 (C1-C10)알킬 또는 (C6-C12)아릴이거나, R1과 R2는 (C2-C7)알킬렌으로 연결되어 3원 내지 8원의 고리를 형성할 수 있으며; R3는 (C1-C10)알킬 또는 (C6-C12)아릴이고; R4는 수소 또는 (C1-C10)알킬이고; 상기 R1, R2, R3 및 R4의 알킬 또는 아릴은 (C1-C10)알킬, (C1-C10)알콕시, 할로겐, (C6-C12)아릴 및 아세틸로 이루어진 군으로부터 선택된 하나 이상의 치환기로 더 치환될 수 있다.][In Reaction Scheme 1, R 1 and R 2 are independently of each other (C1-C10) alkyl or (C6-C12) aryl, or R 1 and R 2 are connected to (C2-C7) alkylene and 3 to 8 Can form a ring of circles; R 3 is (C1-C10) alkyl or (C6-C12) aryl; R 4 is hydrogen or (C 1 -C 10) alkyl; Alkyl or aryl of R 1 , R 2 , R 3 and R 4 may be selected from the group consisting of (C1-C10) alkyl, (C1-C10) alkoxy, halogen, (C6-C12) aryl and acetyl. May be further substituted.]
본 발명의 제조방법에서 사용되는 반응 촉매로는 팔라듐 촉매를 사용하되, 팔라듐 촉매는 Pd2dba3CHCl3, Pd(OAc)2, (dppf)PdCl2, Pd(PPh3)4, (PPh3)2PdCl2, (DPEphos)PdCl2 및 PdCl2 로 이루어진 군에서 선택사용되며, 바람직하기로는 Pd2dba3CHCl3를 사용한다. 반응 리간드로는 포스핀 리간드를 사용하되, 포스핀 리간드는 비스(2-다이페닐포스피노페닐)에터[DPEphos; Bis(2- diphenylphosphinophenyl)ether], 4,5-비스(다이페닐포스피노)-9,9-다이메틸크산텐[Xantphos; 4,5-Bis(diphenylphosphino)-9,9-dimethylxanthene], 사이클로헥실 다이페닐 포스핀[(Biph)PCy2], 1,1'-비스(다이페닐포스피노)페로센[DPPF; 1,1'-Bis(diphenylphosohino)ferrocene], 1,2-비스(다이페닐포스피노)에터[DPPE; 1,2- Bis(diphenylphosohino)ether] 또는 1,3-비스(다이페닐포스피노)프로판[DPPP; 1,3- Bis(diphenylphosohino)propane]으로 이루어진 군으로부터 선택사용될 수 있으며, 팔라듐의 활성을 높여주는 최적의 리간드로는 DPEphos를 사용하는 것이 좋다. 반응용매로는 다이메틸포름아미드 (DMF) 또는 테트라하이드로퓨란 (THF) 등과 같은 통상의 유기용매를 사용하며, 바람직하게는 다이메틸포름아미드(DMF)를 사용하여 반응을 수행한다. 반응 온도는 25 ℃ 내지 사용된 용매의 환류 온도 범위를 유지하도록 하며, 바람직하기로는 25 ℃ 내지 100 ℃를 유지한다. 특히 바람직하기로는 다이메틸포름아미드 (DMF) 용매 하에 25 ℃ 내지 100 ℃를 유지하는 것이다. 반응시간은 반응물질, 용매의 종류 및 용매의 양에 따라 달라질 수 있으며, TLC 등을 통하여 출발물질이 모두 소모되었음을 확인 후 반응을 완결시키도록 한다. 반응이 완결되면, 추출과정을 통해 감압하에서 용매를 증류시킨 후 관 크로마토그래피 등의 통상의 방법을 통하여 목적물을 분리 정제할 수 있다.As the reaction catalyst used in the preparation method of the present invention, a palladium catalyst is used, but the palladium catalyst is Pd 2 dba 3 CHCl 3 , Pd (OAc) 2 , (dppf) PdCl 2 , Pd (PPh 3 ) 4 , (PPh 3 ) 2 PdCl 2 , (DPEphos) PdCl 2 and PdCl 2 are selected and used, preferably Pd 2 dba 3 CHCl 3 is used. Phosphine ligands are used as reaction ligands, but phosphine ligands are bis (2-diphenylphosphinophenyl) ether [DPEphos; Bis (2-diphenylphosphinophenyl) ether], 4,5-bis (diphenylphosphino) -9,9-dimethylxanthene [Xantphos; 4,5-Bis (diphenylphosphino) -9,9-dimethylxanthene], cyclohexyl diphenyl phosphine [(Biph) PCy 2 ], 1,1'-bis (diphenylphosphino) ferrocene [DPPF; 1,1'-Bis (diphenylphosohino) ferrocene], 1,2-bis (diphenylphosphino) ether [DPPE; 1,2-Bis (diphenylphosohino) ether] or 1,3-bis (diphenylphosphino) propane [DPPP; 1,3-Bis (diphenylphosohino) propane] can be selected from the group consisting of, DPEphos is recommended as the optimal ligand to increase the activity of palladium. As the reaction solvent, a conventional organic solvent such as dimethylformamide (DMF) or tetrahydrofuran (THF) is used, and preferably, the reaction is performed using dimethylformamide (DMF). The reaction temperature is maintained at 25 ° C. to the reflux temperature range of the solvent used, preferably from 25 ° C. to 100 ° C. Particular preference is given to maintaining 25 ° C. to 100 ° C. under dimethylformamide (DMF) solvent. The reaction time may vary depending on the reactants, the type of solvent, and the amount of the solvent, and then complete the reaction after confirming that all the starting materials are consumed through TLC. After the reaction is completed, the solvent may be distilled off under reduced pressure through the extraction process, and then the target product may be separated and purified through conventional methods such as column chromatography.
본 발명의 알레닐 설파이드 유도체는 다양한 치환기가 도입되어 있는 신규한 물질로, 다양한 물질을 제조할 수 있는 원료물질로 유용하고, 인듐 트리오가노 싸이올레이트와 삼차 프로파질 아세테이트를 교차-짝지움 반응시켜 제조되어진다. 상기 인듐 트라이(오가노싸이올레이트)는 싸이올 (thiol)의 친핵성을 증가시키기 위한 새로운 형태의 반응 시약으로, 알레닐 설파이드 유도체를 제조하는데 있어 종래의 방법에 비해 반응이 간단하고, 70%이상의 고수율로 알레닐 설파이드 유도체를 수득할 수 있다.The allenyl sulfide derivative of the present invention is a novel substance having various substituents introduced therein, which is useful as a raw material for preparing various substances, and cross-couples reaction of indium triorgano thioleate with tertiary propazyl acetate. To be manufactured. The indium tri (organothiolate) is a new type of reaction reagent for increasing the nucleophilicity of thiol, and the reaction is simple compared to the conventional method for preparing allenyl sulfide derivatives, and 70% Allenyl sulfide derivatives can be obtained with the above high yield.
이상에서 설명한 바와 같은 본 발명은 하기의 실시예를 통하여 더욱 상세히 설명하겠는 바, 하기의 실시예 들은 본 발명에 대한 이해를 돕기 위한 것으로서 본 발명의 범위가 여기에 국한된 것은 아니다. The present invention as described above will be described in more detail through the following examples, the following examples are intended to help the understanding of the present invention is not limited to the scope of the present invention.
[[ 실시예Example ]]
[실시예 1] (3-페닐-1,2-부타다이에닐)(4-메틸페닐)설파이드 [(3-phenyl-1,2-butadienyl)(4-methylphenyl)sulfide]의 제조Example 1 Preparation of (3-phenyl-1,2-butadienyl) (4-methylphenyl) sulfide [(3-phenyl-1,2-butadienyl) (4-methylphenyl) sulfide]
질소분위기 하에서 Pd2dba3CHCl3 (6.21 mg, 0.006 mmol)와 DPEphos (12.9 mg, 0.024 mmol)을 DMF (0.6 mL)를 사용하여 실온에서 10분간 교반시킨 후 2-페닐부타-3-인-2-일 아세테이트 (56.5 mg, 0.3 mmol)을 DMF (0.2 mL)에 녹여 첨가하고 1분간 교반시킨다. 이 용액에 In(S-p-Tol)3 (48.4 mg, 0.1 mmol)을 DMF (0.4 mL)에 녹여 첨가한다. 반응은 25℃에서 5시간 교반시킨 후 5% 염산수용액(1 mL)을 가해 반응을 종결시켰다. 이 혼합물은 Et2O (15 mL x 3)로 추출하고 포화 NH4Cl (10 mL), 포화 NaCl 수용액 (10 mL)로 씻어주었다. 추출한 유기물은 무수 MgSO4로 건조하고 여과하였다. 용매를 제거한 후 관 크로마토그래피로 분리하여 원하는 생성물을 57 mg (76%)을 얻었다.Under nitrogen atmosphere, Pd 2 dba 3 CHCl 3 (6.21 mg, 0.006 mmol) and DPEphos (12.9 mg, 0.024 mmol) were stirred for 10 minutes at room temperature using DMF (0.6 mL), followed by 2-phenylbuta-3-yne-. 2-yl acetate (56.5 mg, 0.3 mmol) is dissolved in DMF (0.2 mL) and added and stirred for 1 minute. To this solution, In (Sp-Tol) 3 (48.4 mg, 0.1 mmol) is added dissolved in DMF (0.4 mL). The reaction was stirred at 25 ° C. for 5 hours, and 5% aqueous hydrochloric acid solution (1 mL) was added to terminate the reaction. The mixture was extracted with Et 2 O (15 mL × 3) and washed with saturated NH 4 Cl (10 mL) and saturated aqueous NaCl solution (10 mL). The extracted organics were dried over anhydrous MgSO 4 and filtered. The solvent was removed and the residue was separated by column chromatography to give 57 mg (76%) of the desired product.
1H NMR (400 MHz, CDCl3): δ 7.39-7.21 (m, 7H), 7.10 (d, J = 7.7 Hz, 2H), 6.23 (q, J = 2.6 Hz, 1H), 2.31 (s, 3H), 2.10 (d, J = 2.8 Hz, 3H). 1 H NMR (400 MHz, CDCl 3 ): δ 7.39-7.21 (m, 7H), 7.10 (d, J = 7.7 Hz, 2H), 6.23 (q, J = 2.6 Hz, 1H), 2.31 (s, 3H ), 2.10 (d, J = 2.8 Hz, 3H).
[실시예 2] (3-페닐-1,2-부타다이에닐)(4-메톡시페닐)설파이드 [(3-phenyl-1,2-butadienyl)(4-methoxyphenyl)sulfide]의 제조Example 2 Preparation of (3-phenyl-1,2-butadienyl) (4-methoxyphenyl) sulfide [(3-phenyl-1,2-butadienyl) (4-methoxyphenyl) sulfide]
상기 실시예 1과 같은 방법으로 제조하였다. 다만, In(S-p-Tol)3 대신 In(S-p-methoxyphenyl)3 (53.2 mg, 0.1 mmol)을 사용하여 원하는 생성물 (70 mg, 86%)를 얻었다.It was prepared in the same manner as in Example 1. However, In (Sp-methoxyphenyl) 3 (53.2 mg, 0.1 mmol) was used instead of In (Sp-Tol) 3 to obtain the desired product (70 mg, 86%).
1H NMR (400 MHz, CDCl3): δ 7.39 (d, J = 8.9 Hz, 2H), 7.36-7.29 (m, 4H), 7.24-7.20 (m, 1H), 6.82 (d, J = 8.9 Hz, 2H), 6.19 (d, J = 2.7 Hz, 1H), 3.77 (s, 3H), 2.05 (d, J = 2.7 Hz, 3H). 1 H NMR (400 MHz, CDCl 3 ): δ 7.39 (d, J = 8.9 Hz, 2H), 7.36-7.29 (m, 4H), 7.24-7.20 (m, 1H), 6.82 (d, J = 8.9 Hz , 2H), 6.19 (d, J = 2.7 Hz, 1H), 3.77 (s, 3H), 2.05 (d, J = 2.7 Hz, 3H).
[실시예 3] (3-페닐-1,2-부타다이에닐)(페닐)설파이드 [(3-phenyl-1,2-butadienyl)(phenyl)sulfide]의 제조Example 3 Preparation of (3-phenyl-1,2-butadienyl) (phenyl) sulfide [(3-phenyl-1,2-butadienyl) (phenyl) sulfide]
상기 실시예 1과 같은 방법으로 제조하였다. 다만, In(S-p-Tol)3 대신 In(SPh)3 (44.2 mg, 0.1 mmol)을 사용하여 원하는 생성물 (59 mg, 83%)를 얻었다.It was prepared in the same manner as in Example 1. However, In (SPh) 3 (44.2 mg, 0.1 mmol) was used instead of In (Sp-Tol) 3 to obtain the desired product (59 mg, 83%).
1H NMR (400 MHz, CDCl3): δ 7.44-7.18 (m, 10H), 6.26 (q, J = 2.6 Hz, 1H), 2.11 (d, J = 2.6 Hz, 3H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.44-7.18 (m, 10H), 6.26 (q, J = 2.6 Hz, 1H), 2.11 (d, J = 2.6 Hz, 3H)
[실시예 4] (3-페닐-1,2-부타다이에닐)(아이소프로필)설파이드 [(3-phenyl-1,2-butadienyl)(isopropyl)sulfide]의 제조Example 4 Preparation of (3-phenyl-1,2-butadienyl) (isopropyl) sulfide [(3-phenyl-1,2-butadienyl) (isopropyl) sulfide]
상기 실시예 1과 같은 방법으로 제조하였다. 다만, In(S-p-Tol)3 대신 In(S-iso-Pr)3 (34.1 mg, 0.1 mmol)을 사용하여 원하는 생성물 (54 mg, 88%)를 얻었다.It was prepared in the same manner as in Example 1. However, In (S-iso-Pr) 3 (34.1 mg, 0.1 mmol) was used instead of In (Sp-Tol) 3 to obtain the desired product (54 mg, 88%).
1H NMR (400 MHz, CDCl3): δ 7.42 (d, J = 7.6 Hz, 2H), 7.33 (t, J = 7.6 Hz, 2H), 7.22 (t, J = 7.3 Hz, 1H), 6.09 (q, J =2.8 Hz, 1H), 3.10-3.00 (m, 1H), 2.16 (d, J = 2.8 Hz, 3H), 1.34 (d, J = 6.7 Hz, 3H), 1.28 (d, J = 6.7 Hz, 3H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.42 (d, J = 7.6 Hz, 2H), 7.33 (t, J = 7.6 Hz, 2H), 7.22 (t, J = 7.3 Hz, 1H), 6.09 ( q, J = 2.8 Hz, 1H), 3.10-3.00 (m, 1H), 2.16 (d, J = 2.8 Hz, 3H), 1.34 (d, J = 6.7 Hz, 3H), 1.28 (d, J = 6.7 Hz, 3H)
[실시예 5] (3-페닐-1,2-부타다이에닐)(n-프로필)설파이드 [(3-phenyl-1,2-butadienyl)(n-propyl)sulfide]의 제조Example 5 Preparation of (3-phenyl-1,2-butadienyl) (n-propyl) sulfide [(3-phenyl-1,2-butadienyl) (n-propyl) sulfide]
상기 실시예 1과 같은 방법으로 제조하였다. 다만, In(S-p-Tol)3 대신 In(S-n-Pr)3 (34.1 mg, 0.1 mmol)을 사용하여 원하는 생성물 (55 mg, 90%)를 얻었다.It was prepared in the same manner as in Example 1. However, In (Sn-Pr) 3 (34.1 mg, 0.1 mmol) was used instead of In (Sp-Tol) 3 to obtain the desired product (55 mg, 90%).
1H NMR (400 MHz, CDCl3): δ 7.43 (d, J = 7.6 Hz, 2H), 7.33 (t, J = 7.6 Hz, 2H), 7.2 (t, J = 7.3 Hz, 1H), 6.09 (q, J = 2.8 Hz, 1H), 2.64-2.52 (m, 2H), 2.16 (d, J = 2.8 Hz, 3H), 1.67-1.57 (m, 2H), 0.93 (t, J = 7.3 Hz, 3H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.43 (d, J = 7.6 Hz, 2H), 7.33 (t, J = 7.6 Hz, 2H), 7.2 (t, J = 7.3 Hz, 1H), 6.09 ( q, J = 2.8 Hz, 1H), 2.64-2.52 (m, 2H), 2.16 (d, J = 2.8 Hz, 3H), 1.67-1.57 (m, 2H), 0.93 (t, J = 7.3 Hz, 3H )
[실시예 6] (3-페닐-1,2-부타다이에닐)(tert-부틸)설파이드 [(3-phenyl-1,2-butadienyl)(tert-butyl)sulfide]의 제조Example 6 Preparation of (3-phenyl-1,2-butadienyl) (tert-butyl) sulfide [(3-phenyl-1,2-butadienyl) (tert-butyl) sulfide]
상기 실시예 1과 같은 방법으로 제조하였다. 다만, In(S-p-Tol)3 대신 In(S-tert-Bu)3 (38.2 mg, 0.1 mmol)을 사용하여 원하는 생성물 (56 mg, 86%)를 얻었다.It was prepared in the same manner as in Example 1. However, In (S-tert-Bu) 3 (38.2 mg, 0.1 mmol) was used instead of In (Sp-Tol) 3 to obtain the desired product (56 mg, 86%).
1H NMR (400 MHz, CDCl3): δ 7.42-7.20(m, 5H), 6.13 (d, J = 2.6Hz, 1H), 2.15 (d, J = 2.6 Hz, 3H), 1.41 (s, 9H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.42-7.20 (m, 5H), 6.13 (d, J = 2.6 Hz, 1H), 2.15 (d, J = 2.6 Hz, 3H), 1.41 (s, 9H )
[실시예 7] (3-(4-브로모페닐)-1,2-부타다이에닐)(4-메톡시페닐)설파이드 [(3-(4-bromophenyl)-1,2-butadienyl)(4-methoxyphenyl)sulfide]의 제조[Example 7] (3- (4-bromophenyl) -1,2-butadienyl) (4-methoxyphenyl) sulfide [(3- (4-bromophenyl) -1,2-butadienyl) ( 4-methoxyphenyl) sulfide]
상기 실시예 1과 같은 방법으로 제조하였다. 다만, 2-페닐부타-3-인-2-일 아세테이트 대신 2-(4-브로모페닐)부타-3-인-2-일 아세테이트 (80.1 mg, 0.3 mmol), In(S-p-Tol)3 대신 In(S-p-methoxyphenyl)3 (53.2 mg, 0.1 mmol)을 사용하여 원하는 생성물 (82.6 mg, 80%)를 얻었다. It was prepared in the same manner as in Example 1. 2- (4-bromophenyl) buta-3-yn-2-yl acetate (80.1 mg, 0.3 mmol), In (Sp-Tol) 3 instead of 2-phenylbuta-3-yn-2-yl acetate Instead, In (Sp-methoxyphenyl) 3 (53.2 mg, 0.1 mmol) was used to obtain the desired product (82.6 mg, 80%).
1H NMR (400 MHz, CDCl3): δ 7.41 (d, J = 8.7 Hz, 2H), 7.37 (d, J = 8.7 Hz, 2H), 7.18 (d, J = 8.6 Hz, 2H), 6.81 (d, J = 8.6 Hz, 2H), 6.19 (q, J = 2.6 Hz, 1H), 3.77 (s, 3H), 2.00 (d, J = 2.6 Hz, 3H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.41 (d, J = 8.7 Hz, 2H), 7.37 (d, J = 8.7 Hz, 2H), 7.18 (d, J = 8.6 Hz, 2H), 6.81 ( d, J = 8.6 Hz, 2H), 6.19 (q, J = 2.6 Hz, 1H), 3.77 (s, 3H), 2.00 (d, J = 2.6 Hz, 3H)
[실시예 8] (3-(4-브로모페닐)-1,2-부타다이에닐)(아이소프로필)설파이드 [(3-(4-bromophenyl)-1,2-butadienyl)(isopropyl)sulfide]의 제조Example 8 (3- (4-bromophenyl) -1,2-butadienyl) (isopropyl) sulfide [(3- (4-bromophenyl) -1,2-butadienyl) (isopropyl) sulfide Manufacture of
상기 실시예 1과 같은 방법으로 제조하였다. 다만, 2-페닐부타-3-인-2-일 아세테이트 대신 2-(4-브로모페닐)부타-3-인-2-일 아세테이트 (80.1 mg, 0.3 mmol), In(S-p-Tol)3 대신 In(S-iso-Pr)3 (34.1 mg, 0.1 mmol)을 사용하여 원하는 생성물 (74.6 mg, 88%)를 얻었다.It was prepared in the same manner as in Example 1. 2- (4-bromophenyl) buta-3-yn-2-yl acetate (80.1 mg, 0.3 mmol), In (Sp-Tol) 3 instead of 2-phenylbuta-3-yn-2-yl acetate Instead, In (S-iso-Pr) 3 (34.1 mg, 0.1 mmol) was used to give the desired product (74.6 mg, 88%).
1H NMR (400 MHz, CDCl3): δ 7.45 (d, J = 8.6 Hz, 2H), 7.28 (d, J = 8.6 Hz, 2H), 6.10 (q, J = 2.8 Hz, 1H), 3.06-3.0 (m, 1H), 2.13 (d, J = 2.8 Hz, 3H), 1.34 (d, J = 6.7 Hz, 3H), 1.27 (d, J = 6.7 Hz, 3H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.45 (d, J = 8.6 Hz, 2H), 7.28 (d, J = 8.6 Hz, 2H), 6.10 (q, J = 2.8 Hz, 1H), 3.06- 3.0 (m, 1H), 2.13 (d, J = 2.8 Hz, 3H), 1.34 (d, J = 6.7 Hz, 3H), 1.27 (d, J = 6.7 Hz, 3H)
[실시예 9] (3-(4-브로모페닐)-1,2-부타다이에닐)(페닐)설파이드 [(3-(4-bromophenyl)-1,2-butadienyl)(phenyl)sulfide]의 제조Example 9 (3- (4-bromophenyl) -1,2-butadienyl) (phenyl) sulfide [(3- (4-bromophenyl) -1,2-butadienyl) (phenyl) sulfide] Manufacture
상기 실시예 1과 같은 방법으로 제조하였다. 다만, 2-페닐부타-3-인-2-일 아 세테이트 대신 2-(4-브로모페닐)부타-3-인-2-일 아세테이트 (80.1 mg, 0.3 mmol), In(S-p-Tol)3 대신 In(SPh)3 (44.2 mg, 0.1 mmol)을 사용하여 원하는 생성물 (77 mg, 81%)를 얻었다.It was prepared in the same manner as in Example 1. However, 2- (4-bromophenyl) buta-3-yn-2-yl acetate (80.1 mg, 0.3 mmol), In (Sp-Tol) instead of 2-phenylbuta-3-yn-2-yl acetate ) 3 instead of in (SPh) 3 (using the 44.2 mg, 0.1 mmol) to give the desired product (77 mg, 81%).
1H NMR (400 MHz, CDCl3): δ 7.44 (d, J = 8.6 Hz, 2H), 7.32-7.25 (m, 5 H), 7.22 (d, J = 8.6 Hz, 2H), 6.26 (q, J = 2.6 Hz, 1H), 2.07 (s, 3H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.44 (d, J = 8.6 Hz, 2H), 7.32-7.25 (m, 5H), 7.22 (d, J = 8.6 Hz, 2H), 6.26 (q, J = 2.6 Hz, 1H), 2.07 (s, 3H)
[실시예 10] (3-(4-(페닐싸이오)부타-2,3-다이엔-2-일)페닐) 아세테이트 [3-(4-(phenylthio)buta-2,3-dien-2-yl)phenyl acetate]의 제조Example 10 (3- (4- (phenylthio) buta-2,3-dien-2-yl) phenyl) acetate [3- (4- (phenylthio) buta-2,3-dien-2 -yl) phenyl acetate]
상기 실시예 1과 같은 방법으로 제조하였다. 다만, 2-페닐부타-3-인-2-일 아세테이트 대신 2-(3-아세틸페닐)부타-3-인-2-일 아세테이트 (73.9 mg, 0.3 mmol), In(S-p-Tol)3 대신 In(SPh)3 (44.2 mg, 0.1 mmol)을 사용하여 원하는 생성물 (69.2 mg, 78 %)를 얻었다.It was prepared in the same manner as in Example 1. Instead of 2-phenylbuta-3-yn-2-yl acetate, instead of 2- (3-acetylphenyl) buta-3-yn-2-yl acetate (73.9 mg, 0.3 mmol), In (Sp-Tol) 3 In (SPh) 3 (44.2 mg, 0.1 mmol) was used to give the desired product (69.2 mg, 78%).
1H NMR (400 MHz, CDCl3): δ 7.43 (d, J = 7.6 Hz, 2H), 7.34-7.19 (m, 5H), 7.07 (t, J = 1.7 Hz, 1H), 6.96 (d, J = 8.2 Hz, 1H), 6.28 (q, J = 2.6 Hz, 1H), 2.30 (s, 3H), 2.07 (s, 3H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.43 (d, J = 7.6 Hz, 2H), 7.34-7.19 (m, 5H), 7.07 (t, J = 1.7 Hz, 1H), 6.96 (d, J = 8.2 Hz, 1H), 6.28 (q, J = 2.6 Hz, 1H), 2.30 (s, 3H), 2.07 (s, 3H)
[실시예 11] 3-(4-(tert-부틸싸이오)부타-2,3-다이엔-2-일)페닐 아세테이트 [3-(4-(tert-butylthio)buta-2,3-dien-2-yl)phenyl acetate]의 제조Example 11 3- (4- (tert-butylthio) buta-2,3-dien-2-yl) phenyl acetate [3- (4- (tert-butylthio) buta-2,3-dien -2-yl) phenyl acetate]
상기 실시예 1과 같은 방법으로 제조하였다. 다만, 2-페닐부타-3-인-2-일 아세테이트 대신 2-(3-아세틸페닐)부타-3-인-2-일 아세테이트 (73.9 mg, 0.3 mmol), In(S-p-Tol)3 대신 In(S-tert-Bu)3 (38.2 mg, 0.1 mmol)을 사용하여 원하는 생성물 (64mg, 75%)를 얻었다.It was prepared in the same manner as in Example 1. Instead of 2-phenylbuta-3-yn-2-yl acetate, instead of 2- (3-acetylphenyl) buta-3-yn-2-yl acetate (73.9 mg, 0.3 mmol), In (Sp-Tol) 3 In (S-tert-Bu) 3 (38.2 mg, 0.1 mmol) was used to give the desired product (64 mg, 75%).
1H NMR (400 MHz, CDCl3): δ 7.33 (t, J = 7.8 Hz, 1H), 7.27 (d, J = 6.8 Hz, 1H), 7.10 (t, J = 1.9 Hz, 1H), 6.95 (d, J = 7.8 Hz, 1H), 6.14 (q, J = 2.6 Hz, 1H), 2.29 (s, 3H), 2.13 (d, J = 2.6 Hz, 3H), 1.40 (s, 9H). 1 H NMR (400 MHz, CDCl 3 ): δ 7.33 (t, J = 7.8 Hz, 1H), 7.27 (d, J = 6.8 Hz, 1H), 7.10 (t, J = 1.9 Hz, 1H), 6.95 ( d, J = 7.8 Hz, 1H), 6.14 (q, J = 2.6 Hz, 1H), 2.29 (s, 3H), 2.13 (d, J = 2.6 Hz, 3H), 1.40 (s, 9H).
[실시예 12] (2-사이클로헥실리덴바이닐)(4-메틸페닐)설파이드 [(2-cyclohexylidenevinyl)(4-methylphenyl)sulfide]의 제조Example 12 Preparation of (2-cyclohexylidenevinyl) (4-methylphenyl) sulfide [(2-cyclohexylidenevinyl) (4-methylphenyl) sulfide]
질소분위기 하에서 Pd2dba3CHCl3 (6.21 mg, 0.006 mmol)와 DPEphos (12.9 mg, 0.024 mmol)을 DMF (0.6 mL)를 사용하여 실온에서 10분간 교반시킨 후 1-에티닐사 이클로헥실 아세테이트 (49.9 mg, 0.3 mmol)을 DMF (0.2 mL)에 녹여 첨가하고 1분간 교반시킨다. 이 용액에 In(S-p-Tol)3 (48.4 mg, 0.1 mmol)을 DMF (0.4 mL)에 녹여 첨가한다. 반응은 100℃에서 1시간 교반 시킨 후 5% 염산수용액 (1 mL)을 가해 반응을 종결시켰다. 이 혼합물은 Et2O (15 mL x 3)로 추출하고 포화 NH4Cl (10 mL), 포화 NaCl 수용액 (10 mL)로 씻어주었다. 추출한 유기물은 무수 MgSO4로 건조하고 여과하였다. 용매를 제거한 후 관 크로마토그래피로 분리하여 원하는 생성물을 57.6 mg (83%)을 얻었다.Under nitrogen atmosphere, Pd 2 dba 3 CHCl 3 (6.21 mg, 0.006 mmol) and DPEphos (12.9 mg, 0.024 mmol) were stirred for 10 minutes at room temperature using DMF (0.6 mL), followed by 1-ethynylcyclohexyl acetate ( 49.9 mg, 0.3 mmol) is added dissolved in DMF (0.2 mL) and stirred for 1 minute. To this solution, In (Sp-Tol) 3 (48.4 mg, 0.1 mmol) is added dissolved in DMF (0.4 mL). The reaction was stirred at 100 ° C. for 1 hour, and 5% aqueous hydrochloric acid solution (1 mL) was added to terminate the reaction. The mixture was extracted with Et 2 O (15 mL × 3) and washed with saturated NH 4 Cl (10 mL) and saturated aqueous NaCl solution (10 mL). The extracted organics were dried over anhydrous MgSO 4 and filtered. The solvent was removed and then separated by column chromatography to give 57.6 mg (83%) of the desired product.
1H NMR (400 MHz, CDCl3): δ 7.29 (d, J = 8.0 Hz, 2H), 7.11 (d, J = 8.0 Hz, 2H), 5.77-5.75 (m, 1H), 2.32 (s, 3H), 2.13-2.10 (m, 4H), 1.57-1.48 (m, 6H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.29 (d, J = 8.0 Hz, 2H), 7.11 (d, J = 8.0 Hz, 2H), 5.77-5.75 (m, 1H), 2.32 (s, 3H ), 2.13-2.10 (m, 4H), 1.57-1.48 (m, 6H)
[실시예 13] (2-사이클로헥실리덴바이닐)(4-메톡시페닐)설파이드 [(2-cyclohexylidenevinyl)(4-methoxyphenyl)sulfide]의 제조Example 13 Preparation of (2-cyclohexylidenevinyl) (4-methoxyphenyl) sulfide [(2-cyclohexylidenevinyl) (4-methoxyphenyl) sulfide]
상기 실시예 12과 같은 방법으로 제조하였다. 다만, In(S-p-Tol)3 대신 In(S-p-methoxyphenyl)3 (53.2 mg, 0.1 mmol)을 사용하여 원하는 생성물 (59 mg, 80%)를 얻었다.It was prepared in the same manner as in Example 12. However, In (Sp-methoxyphenyl) 3 (53.2 mg, 0.1 mmol) was used instead of In (Sp-Tol) 3 to obtain the desired product (59 mg, 80%).
1H NMR (400 MHz, CDCl3): δ 7.36 (d, J = 8.8 Hz, 2H), 6.86 (d, J = 8.8 Hz, 2H), 5.74-5.72 (m, 1H), 3.80 (s, 3H), 2.09-2.06 (m, 4H), 1.57-1.51 (m, 2H), 1.48-1.41 (m, 4H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.36 (d, J = 8.8 Hz, 2H), 6.86 (d, J = 8.8 Hz, 2H), 5.74-5.72 (m, 1H), 3.80 (s, 3H ), 2.09-2.06 (m, 4H), 1.57-1.51 (m, 2H), 1.48-1.41 (m, 4H)
[실시예 14] (2-사이클로헥실리덴바이닐)(페닐)설파이드 [(2-cyclohexylidenevinyl)(phenyl)sulfide]의 제조Example 14 Preparation of (2-cyclohexylidenevinyl) (phenyl) sulfide [(2-cyclohexylidenevinyl) (phenyl) sulfide]
상기 실시예 12과 같은 방법으로 제조하였다. 다만, In(S-p-Tol)3 대신 In(SPh)3 (53.2 mg, 0.1 mmol)을 사용하여 원하는 생성물 (54.5 mg, 84%)를 얻었다. It was prepared in the same manner as in Example 12. However, In (SPh) 3 (53.2 mg, 0.1 mmol) was used instead of In (Sp-Tol) 3 to obtain the desired product (54.5 mg, 84%).
1H NMR (400 MHz, CDCl3): δ 7.39 (d, J = 7.8 Hz, 2H), 7.30 (t, J = 7.7 Hz, 2H), 7.20 (t, J = 7.3 Hz, 1H), 5.80-5.78 (m, 1H), 2.17-2.10 (m, 4H), 1.62-1.46 (m, 6H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.39 (d, J = 7.8 Hz, 2H), 7.30 (t, J = 7.7 Hz, 2H), 7.20 (t, J = 7.3 Hz, 1H), 5.80- 5.78 (m, 1H), 2.17-2.10 (m, 4H), 1.62-1.46 (m, 6H)
[실시예 15] (2-사이클로헥실리덴바이닐)(아이소프로필)설파이드 [(2-cyclohexylidenevinyl)(isopropyl)sulfide]의 제조Example 15 Preparation of (2-cyclohexylidenevinyl) (isopropyl) sulfide [(2-cyclohexylidenevinyl) (isopropyl) sulfide]
상기 실시예 12과 같은 방법으로 제조하였다. 다만, In(S-p-Tol)3 대신 In(S-iso-Pr)3 (34.1 mg, 0.1 mmol)을 사용하여 원하는 생성물 (45.1 mg, 82%)를 얻었다.It was prepared in the same manner as in Example 12. However, In (S-iso-Pr) 3 (34.1 mg, 0.1 mmol) was used instead of In (Sp-Tol) 3 to obtain the desired product (45.1 mg, 82%).
1H NMR (400 MHz, CDCl3): δ 5.62-5.60 (m, 1H), 3.08-2.97 (m, 1H), 2.19-2.14 (m, 4H), 1.65-1.52 (m, 6H), 1.31 (s, 3H), 1.30 (s, 3H) 1 H NMR (400 MHz, CDCl 3 ): δ 5.62-5.60 (m, 1H), 3.08-2.97 (m, 1H), 2.19-2.14 (m, 4H), 1.65-1.52 (m, 6H), 1.31 ( s, 3H), 1.30 (s, 3H)
[실시예 16] (4-메톡시페닐)(4-페닐펜타-2,3-다이엔-2-일)설파이드 [(4-methoxyphenyl)(4-phenylpenta-2,3-dien-2-yl) sulfide]의 제조Example 16 (4-methoxyphenyl) (4-phenylpenta-2,3-dien-2-yl) sulfide [(4-methoxyphenyl) (4-phenylpenta-2,3-dien-2-yl ) sulfide]
상기 실시예 12과 같은 방법으로 제조하였다. 다만, 1-에티닐사이클로헥실 아세테이트 대신 2-페닐펜타-3-인-2-일 아세테이트 (60.7 mg, 0.3 mmol), In(S-p-Tol)3 대신 In(S-p-methoxyphenyl)3 (53.2 mg, 0.1 mmol)을 사용하여 원하는 생성물 (70 mg, 83%)를 얻었다.It was prepared in the same manner as in Example 12. 2-phenylpenta-3-yn-2-yl acetate (60.7 mg, 0.3 mmol) instead of 1-ethynylcyclohexyl acetate, In (Sp-methoxyphenyl) 3 (53.2 mg, instead of In (Sp-Tol) 3 0.1 mmol) was used to give the desired product (70 mg, 83%).
1H NMR (400 MHz, CDCl3): δ 7.35 (d, J = 8.8 Hz, 2H), 7.30-7.26 (m, 4H), 7.20-7.17 (m, 1H), 6.75 (d, J = 8.8 Hz, 2H), 3.73 (s, 3H), 2.01 (s, 3H), 1.92 (s, 3H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.35 (d, J = 8.8 Hz, 2H), 7.30-7.26 (m, 4H), 7.20-7.17 (m, 1H), 6.75 (d, J = 8.8 Hz , 2H), 3.73 (s, 3H), 2.01 (s, 3H), 1.92 (s, 3H)
[실시예 17] (이소프로필)(4-페닐펜타-2,3-다이엔-2-일)설파이드 [(isopropyl)(4-phenylpenta-2,3-dien-2-yl)sulfide]의 제조Example 17 Preparation of (Isopropyl) (4-phenylpenta-2,3-dien-2-yl) sulfide [(isopropyl) (4-phenylpenta-2,3-dien-2-yl) sulfide]
상기 실시예 12과 같은 방법으로 제조하였다. 다만, 1-에티닐사이클로헥실 아세테이트 대신 2-페닐펜타-3-인-2-일 아세테이트 (60.7 mg, 0.3 mmol), In(S-p-Tol)3 대신 In(S-iso-Pr)3 (34.1 mg, 0.1 mmol)을 사용하여 원하는 생성물 (54.4 mg, 84%)를 얻었다. It was prepared in the same manner as in Example 12. 2-phenylpenta-3-yn-2-yl acetate (60.7 mg, 0.3 mmol) instead of 1-ethynylcyclohexyl acetate, In (S-iso-Pr) 3 (34.1 instead of In (Sp-Tol) 3 mg, 0.1 mmol) was used to give the desired product (54.4 mg, 84%).
1H NMR (400 MHz, CDCl3): δ 7.42 (d, J = 7.5 Hz, 2H), 7.33 (t, J = 7.7 Hz, 2H), 7.21 (t, J = 7.3 Hz, 1H), 3.37-3.33 (m, 1H), 2.25 (s, 3H), 1.96 (s, 3H), 1.34 (d, J = 6.8 Hz, 6H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.42 (d, J = 7.5 Hz, 2H), 7.33 (t, J = 7.7 Hz, 2H), 7.21 (t, J = 7.3 Hz, 1H), 3.37- 3.33 (m, 1H), 2.25 (s, 3H), 1.96 (s, 3H), 1.34 (d, J = 6.8 Hz, 6H)
[실시예 18] (4-메톡시페닐)(2-페닐옥타-2,3-다이엔-4-일)설파이드 [(4-methoxyphenyl)(2-phenylocta-2,3-dien-4-yl)sulfide]의 제조Example 18 (4-methoxyphenyl) (2-phenylocta-2,3-dien-4-yl) sulfide [(4-methoxyphenyl) (2-phenylocta-2,3-dien-4-yl ) sulfide]
상기 실시예 12과 같은 방법으로 제조하였다. 다만, 1-에티닐사이클로헥실 아세테이트 대신 2-페닐옥타-3-인-2-일 아세테이트 (73.3 mg, 0.3 mmol), In(S-p-Tol)3 대신 In(S-p-methoxyphenyl)3 (53.2 mg, 0.1 mmol)을 사용하여 원하는 생성물 (69.7 mg, 72%)를 얻었다.It was prepared in the same manner as in Example 12. 2-phenylocta-3-yn-2-yl acetate (73.3 mg, 0.3 mmol) instead of 1-ethynylcyclohexyl acetate, In (Sp-methoxyphenyl) 3 (53.2 mg, instead of In (Sp-Tol) 3 0.1 mmol) was used to give the desired product (69.7 mg, 72%).
1H NMR (400 MHz, DMSO): δ 7.35-7.20 (m, 7H), 6.86 (d, J = 8.7 Hz, 2H), 3.71 (s, 3H), 2.22 (td, J = 7.4, 2.2 Hz, 2H), 1.92 (s, 3H), 1.51-1.44 (m, 2H), 1.36-1.28 (m, 2H), 0.82 (t, J = 7.3 Hz, 3H) 1 H NMR (400 MHz, DMSO): δ 7.35-7.20 (m, 7H), 6.86 (d, J = 8.7 Hz, 2H), 3.71 (s, 3H), 2.22 (td, J = 7.4, 2.2 Hz, 2H), 1.92 (s, 3H), 1.51-1.44 (m, 2H), 1.36-1.28 (m, 2H), 0.82 (t, J = 7.3 Hz, 3H)
[실시예 19] (2-페닐옥타-2,3-다이엔-4-일)(페닐)설파이드 [(2-phenylocta-2,3-dien-4-yl)(phenyl)sulfide]의 제조Example 19 Preparation of (2-phenylocta-2,3-dien-4-yl) (phenyl) sulfide [(2-phenylocta-2,3-dien-4-yl) (phenyl) sulfide]
상기 실시예 12과 같은 방법으로 제조하였다. 다만, 1-에티닐사이클로헥실 아세테이트 대신 2-페닐옥타-3-인-2-일 아세테이트 (73.3 mg, 0.3 mmol), In(S-p-Tol)3 대신 In(SPh)3 (44.2 mg, 0.1 mmol)을 사용하여 원하는 생성물 (72 mg, 82 %)를 얻었다.It was prepared in the same manner as in Example 12. 2-phenylocta-3-yn-2-yl acetate (73.3 mg, 0.3 mmol) instead of 1-ethynylcyclohexyl acetate, In (SPh) 3 (44.2 mg, 0.1 mmol instead of In (Sp-Tol) 3 ) To give the desired product (72 mg, 82%).
1H NMR (400 MHz, CDCl3): δ 7.41-7.18 (m, 10H), 2.33-2.28 (m, 2H), 1.99 (s, 3H), 1.59-1.50 (m, 2H), 1.43-1.31 (m, 2H), 0.87 (t, J = 7.4 Hz, 3H) 1 H NMR (400 MHz, CDCl 3 ): δ 7.41-7.18 (m, 10H), 2.33-2.28 (m, 2H), 1.99 (s, 3H), 1.59-1.50 (m, 2H), 1.43-1.31 ( m, 2H), 0.87 (t, J = 7.4 Hz, 3H)
[실시예 20] (2-페닐옥타-2,3-다이엔-4-일)(n-프로필)설파이드 [(2-phenylocta-2,3-dien-4-yl)(n-propyl)sulfide]의 제조Example 20 (2-phenylocta-2,3-dien-4-yl) (n-propyl) sulfide [(2-phenylocta-2,3-dien-4-yl) (n-propyl) sulfide Manufacture of
상기 실시예 12과 같은 방법으로 제조하였다. 다만, 1-에티닐사이클로헥실 아세테이트 대신 2-페닐옥타-3-인-2-일 아세테이트 (73.3 mg, 0.3 mmol), In(S-p-Tol)3 대신 In(S-n-Pr)3 (34.1 mg, 0.1 mmol)을 사용하여 원하는 생성물 (73.3 mg, 81%)를 얻었다.It was prepared in the same manner as in Example 12. However, instead of 1-cyclohexyl-2-phenyl acetate ethynyl-3-octanoyl-2-yl acetate in (73.3 mg, 0.3 mmol), In (Sp-Tol) 3 instead of In (Sn-Pr) 3 ( 34.1 mg, 0.1 mmol) was used to give the desired product (73.3 mg, 81%).
1H NMR (400 MHz, DMSO): δ 7.40-7.34 (m, 4H), 7.26-7.22 (m, 1H), 2.47 (t,d, J = 7.2, 2.2 Hz, 2H), 2.21 (t,d, J = 7.3, 2.8 Hz, 2H), 2.11 (s, 3H), 1.52-1.43 (m, 4H), 1.38-1.31 (m, 2H), 0.85 (t, J = 7.2 Hz, 3H), 0.82 (t, J = 7.3 Hz, 3H). 1 H NMR (400 MHz, DMSO): δ 7.40-7.34 (m, 4H), 7.26-7.22 (m, 1H), 2.47 (t, d, J = 7.2, 2.2 Hz, 2H), 2.21 (t, d , J = 7.3, 2.8 Hz, 2H), 2.11 (s, 3H), 1.52-1.43 (m, 4H), 1.38-1.31 (m, 2H), 0.85 (t, J = 7.2 Hz, 3H), 0.82 ( t, J = 7.3 Hz, 3H).
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