Reaktion #988732

Reaktionsgleichung

5-bromo-3-[4-(3-piperidin-1-yl-propoxy)-phenyl]-1H-pyrrolo[2,3-b]pyridine hydrochloride

sodium bicarbonate

sodium carbonate

2-[3-Methoxy-4-(4-methoxy-benzyloxy)-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane

→

2-methoxy-4-{3-[4-(3-piperidin-1-yl-propoxy)-phenyl]-1H-pyrrolo[2,3-b]pyridin-5-yl}-phenol

Ausbeute 8.3%

Lösungsmittel

dichloromethane

acetonitrile

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONwere added
2. 2
   SonstigeThe mixture was irradiated in a Personal Chemistry® microwave reactor to 165° C. for 1200 sec
3. 3
   ExtraktionThe aqueous layer was extracted three times with dichloromethane
4. 4
   Trocknenthe combined organic phases were dried over sodium sulfate
5. 5
   Sonstigeevaporated
6. 6
   SonstigeThe crude product was purified by flash chromatography on amine functionalized silica gel (ISCO RediSep® amine column)
7. 7
   workup.DISSOLUTIONThe resulting intermediate was dissolved in 30 ml of dichloromethane
8. 8
   workup.ADDITION750 mg (1.06 mmol) of PS-thiophenol (Argonaut Technologies) was added
9. 9
   workup.ADDITIONTo this was added 1.5 ml of trifluoroacetic acid
10. 10
    FiltrationThe resin was filtered off
11. 11
    Waschenwashed with dichloromethane
12. 12
    WaschenThe filtrate was washed with a saturated aqueous solution of sodium bicarbonate
13. 13
    Trocknendried over sodium sulfate
14. 14
    Sonstigeevaporated
15. 15
    SonstigeThe residue was triturated with 20 ml of dichloromethane
16. 16
    Sonstigedried by suction

Vorschrift

100 mg (0.24 mmol) of 5-bromo-3-[4-(3-piperidin-1-yl-propoxy)-phenyl]-1H-pyrrolo[2,3-b]pyridine hydrochloride, 120 mg (0.33 mmol) of 2-[3-Methoxy-4-(4-methoxy-benzyloxy)-phenyl]-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane and 10 mg (5 mol %) of dichlorobis(triphenylphosphino)palladium(II) were placed in a vial and 1.5 ml of acetonitrile and 1.5 ml of a 2 M aqueous solution of sodium carbonate were added. The mixture was irradiated in a Personal Chemistry® microwave reactor to 165° C. for 1200 sec. The resulting mixture was distributed between dichloromethane and a saturated aqueous solution of sodium bicarbonate. The aqueous layer was extracted three times with dichloromethane and the combined organic phases were dried over sodium sulfate and evaporated. The crude product was purified by flash chromatography on amine functionalized silica gel (ISCO RediSep® amine column) using a gradient of ethyl acetate in hexanes. The resulting intermediate was dissolved in 30 ml of dichloromethane and 750 mg (1.06 mmol) of PS-thiophenol (Argonaut Technologies) was added. To this was added 1.5 ml of trifluoroacetic acid and the mixture was stirred at room temperature for 2 hours. The resin was filtered off and washed with dichloromethane. The filtrate was washed with a saturated aqueous solution of sodium bicarbonate, dried over sodium sulfate and evaporated. The residue was triturated with 20 ml of dichloromethane and dried by suction to afford 9 mg (20 μmol, 8% yield) of 2-methoxy-4-{3-[4-(3-piperidin-1-yl-propoxy)-phenyl]-1H-pyrrolo[2,3-b]pyridin-5-yl}-phenol as a beige powder. 1H-NMR (d6-DMSO) δ: 11.83 [1H] d, 9.06 [1H] s, 8.50 [1H] d, 8.28 [1H] d, 7.76 [1H], 7.67 [2H] d(m), 7.25 [1H] d, 7.12 [1H] dd, 7.01 [2H] d(m), 6.88 [1H] d, 4.02 [2H] t, 3.87 [3H] s, 2.39 [2H] t, 2.34 [4H] (m),br, 1.88 [2H] t, 1.50 [4H] qui, 1.38 [2H] (m). MS m/z: 458 [MH+].

Quelle