Tetramethylene sulfoxide → 2-Chloro-5-[(1-oxidotetrahydrothien-2-yl)methyl]-pyridine

HRID 1171879

Reaktionsgleichung

Reaktionsgleichung von HRID 1171879
[CH2:1]1[S:5](=[O:6])[CH2:4][CH2:3][CH2:2]1.[Li]CCCC.CCCCCC.[Cl:18][C:19]1[N:24]=[CH:23][C:22]([CH2:25]Cl)=[CH:21][CH:20]=1.FC(F)(F)C(O)=O>C1COCC1.O>[Cl:18][C:19]1[CH:20]=[CH:21][C:22]([CH2:25][CH:1]2[CH2:2][CH2:3][CH2:4][S:5]2=[O:6])=[CH:23][N:24]=1

Komponenten

8

Reaktionsbedingungen

Temperatur
-70 °C

Versuchsvorschrift

Tetramethylene sulfoxide (6.5 g, 62 mmol) was dissolved in 30 mL anhydrous THF, stirred and cooled to −70° C. and then treated with 2.5 M n-BuLi in hexane (24 mL, 61 mmol) over a period of 10 min. The temperature was raised to −20 to −30° C. (Liquid N2/o-xylene bath) and the mixture was stirred for a further 30 min. The mixture was cooled to −70° C. and treated dropwise with a solution of 6-chloro-3-chloromethylpyridine in 15 mL THF. The reaction was stirred for 2 h at −70° C. and then treated dropwise with trifluoroacetic acid (8.0 g, 70 mmol). The mixture was warmed to room temperature, poured into 75 mL water and extracted with dichloromethane (2×50 mL). The combined organic extracts were washed with dilute sodium bicarbonate and saturated NaCl, dried over Na2SO4 and concentrated. The residue was chromatographed on silica gel with 5% methanol in dichloromethane to give 2.5 g of the desired sulfoxide as a brown oil in 35% yield.

Aufarbeitung

  1. temperatureThe temperature was raised to −20 to −30° C. (Liquid N2/o-xylene bath)
  2. stirringthe mixture was stirred for a further 30 min
  3. temperatureThe mixture was cooled to −70° C.
  4. stirringThe reaction was stirred for 2 h at −70° C.
  5. temperatureThe mixture was warmed to room temperature
  6. extractionextracted with dichloromethane (2×50 mL)
  7. washThe combined organic extracts were washed with dilute sodium bicarbonate and saturated NaCl
  8. dry with materialdried over Na2SO4
  9. concentrationconcentrated
  10. customThe residue was chromatographed on silica gel with 5% methanol in dichloromethane

Quellen und Nachweise

ORD-Eintrag
ord-2d74740455234539909bee02973e30df
Quelldatensatz
uspto-grants-2010_11
Patentnummer
US07829719B2

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