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2,4,6-Trimethylpyridine → 5-chloro-2'-pyridin-4-yl-5',6'-dihydro-3H,7'H-spiro[2-benzofuran-1,4'-[1]benzothiophene]-3,7'-dione

HRID 1615487
ノート
印刷プレビュー

反応式

HRID 1615487 の反応式
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]2[C:8]3([O:23][C:24](=[O:25])[C:4]=2[CH:3]=1)[C:13]1[CH:14]=[C:15]([C:17]2[CH:22]=[CH:21][N:20]=[CH:19][CH:18]=2)[S:16][C:12]=1[CH2:11][CH2:10][CH2:9]3.[O:26]1CCOCC1.S(OOS([O-])(=O)=O)([O-])(=O)=O.[K+].[K+].CC1C=C(C)N=C(C)C=1>O.CCOC(C)=O.O.O.O.O.O.S([O-])([O-])(=O)=O.[Cu+2].C(#N)C>[Cl:1][C:2]1[CH:7]=[CH:6][C:5]2[C:8]3([O:23][C:24](=[O:25])[C:4]=2[CH:3]=1)[C:13]1[CH:14]=[C:15]([C:17]2[CH:22]=[CH:21][N:20]=[CH:19][CH:18]=2)[S:16][C:12]=1[C:11](=[O:26])[CH2:10][CH2:9]3
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

9

反応物 4

HCID 79532,4,6-Trimethylpyridine2 回HCID 24412Potassium Persulfate2 回HCID 312751,4-Dioxane2 回HCID 681829575-chloro-2'-pyridin-4-yl-6',7'-dihydro-3H,5'H-spiro[2-benzofuran-1,4'-[1]benzothiophen]-3-one

生成物 1

HCID 569709015-chloro-2'-pyridin-4-yl-5',6'-dihydro-3H,7'H-spiro[2-benzofuran-1,4'-[1]benzothiophene]-3,7'-dione
収率 3%

試薬・触媒・溶媒 4

HCID 24463Copper sulfate pentahydrate触媒2 回HCID 962Water溶媒2 回HCID 6342Acetonitrile溶媒HCID 8857Ethyl Acetate溶媒

反応条件

温度
80 °C

実験手順

In a 100 mL round bottomed flask was placed 5-chloro-2′-pyridin-4-yl-6′,7′-dihydro-3H,5′H-spiro[2-benzofuran-1,4′-[1]benzothiophen]-3-one (0.714 g, 1.94 mmol) (including side product) along with 1,4-dioxane (20 mL) and acetonitrile (10 mL). To the mixture was added a suspension of potassium persulfate (1.85 g, 6.84 mmol) and copper (II) sulfate pentahydrate (180 mg, 0.72 mmol) in water (20 mL) followed by γ-collidine (0.897 mL, 6.79 mmol). The mixture was stirred for 3.5 hr at 80° C. Again, to the mixture was added a suspension of potassium persulfate (1.96 g, 7.25 mmol) and copper(II) sulfate pentahydrate (20 mg, 0.08 mmol) in water (20 mL, 1000 mmol) followed by γ-collidine (0.9 mL, 7 mmol) and 1,4-dioxane (10 mL, 100 mmol). The mixture was stirred for an additional 16 hr at 80° C. The mixture was allowed to cool to rt and then diluted with EtOAc (50 mL). Insoluble materials were removed by filtration through a celite pad and the aqueous phase was separated from the filtrate. The aqueous phase was extracted with EtOAc (50 mL). The combined organic phases were dried over anhydrous MgSO4. Insoluble materials were removed by filtration and the filtrate was concentrated under reduced pressure. The residue was purified by HPLC (FA) to obtain the title compound (22.5 mg; 3%) as an off-white crystalline solid. LCMS: (FA) ES+ 382, 384; 1H NMR (400 MHz, d6-DMSO) δ ppm 8.59 (dd, 2H), 8.07 (d, 1H), 7.89 (dd, 1H), 7.77 (d, 1H), 7.71 (dd, 2H), 7.46 (s, 1H), 2.47-3.05 (m, 4H).

後処理

  1. customIn a 100 mL round bottomed flask was placed
  2. additionTo the mixture was added
  3. additionAgain, to the mixture was added
  4. stirringThe mixture was stirred for an additional 16 hr at 80° C
  5. temperatureto cool to rt
  6. customInsoluble materials were removed by filtration through a celite pad
  7. customthe aqueous phase was separated from the filtrate
  8. extractionThe aqueous phase was extracted with EtOAc (50 mL)
  9. dry with materialThe combined organic phases were dried over anhydrous MgSO4
  10. customInsoluble materials were removed by filtration
  11. concentrationthe filtrate was concentrated under reduced pressure
  12. customThe residue was purified by HPLC (FA)

出典と根拠

ORDレコード
ord-523619b599b84fec8565f3680775040b
出典データセット
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08765746B2

反応ノート

読み込み中…

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