Reaktion #72997

Reaktionsgleichung

Trichloroacetyl isocyanate

4-{[2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}tetrahydro-2H-pyran-4-ol

m-chloroperbenzoic acid

trichloroacetyl isocyanate

dichloromethane

→

4-{[4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}tetrahydro-2H-pyran-4-ol

Ausbeute 41.0%

Lösungsmittel

chloroform

methanol

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigethe solution was transferred to a separatory funnel
2. 2
   Waschenwashed with 10% Na2CO3 (100 mL)
3. 3
   ExtraktionThe aqueous layer was back-extracted with chloroform
4. 4
   Trocknendried over MgSO4
5. 5
   Filtrationfiltered
6. 6
   Einengenconcentrated under reduced pressure
7. 7
   Sonstigeto yield a light orange solid
8. 8
   workup.WAITAfter 1 h
9. 9
   workup.WAITAfter 1 h
10. 10
    Sonstigethe volatiles were removed under reduced pressure
11. 11
    workup.DISSOLUTIONthe residue was dissolved in methanol (30 mL)
12. 12
    workup.ADDITIONA solution of sodium methoxide in methanol (25%, 5.0 mL) was added
13. 13
    Einengenconcentrated under reduced pressure
14. 14
    SonstigeThe residue was partitioned between dichloromethane (100 mL) and water (100 mL)
15. 15
    ExtraktionThe aqueous layer was extracted with dichlormethane (2×100 mL)
16. 16
    Trocknendried over MgSO4
17. 17
    Filtrationfiltered
18. 18
    Einengenconcentrated under reduced pressure
19. 19
    SonstigeThe crude product was purified by flash chromatography (silica gel, eluted with 10% methanol/dichloromethane)
20. 20
    Sonstigeto afford a clear oil that
21. 21
    Sonstigewas triturated with isopropanol (50 mL)
22. 22
    Sonstigeto afford white crystals
23. 23
    Einengenconcentrated under reduced pressure
24. 24
    Sonstigedried in a vacuum oven at 80° C.

Vorschrift

To a solution of 4-{[2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}tetrahydro-2H-pyran-4-ol (3.0 g, 8.79 mmol) in chloroform (60 mL) at rt was added m-chloroperbenzoic acid (m-CPBA, 3.2 g, 10.5 mmol). After 2 h, the solution was transferred to a separatory funnel and washed with 10% Na2CO3 (100 mL). The aqueous layer was back-extracted with chloroform. The organic layers were combined, dried over MgSO4, filtered, and concentrated under reduced pressure to yield a light orange solid. To the solid was added dichloromethane (30 mL). Trichloroacetyl isocyanate (1.05 mL, 8.79 mL) was added dropwise. After 1 h, additional trichloroacetyl isocyanate (0.3 equivalent) was added. After 1 h, the volatiles were removed under reduced pressure and the residue was dissolved in methanol (30 mL). A solution of sodium methoxide in methanol (25%, 5.0 mL) was added and the solution stirred overnight at rt and concentrated under reduced pressure. The residue was partitioned between dichloromethane (100 mL) and water (100 mL). The aqueous layer was extracted with dichlormethane (2×100 mL). The organic layers were combined, dried over MgSO4, filtered, and concentrated under reduced pressure. The crude product was purified by flash chromatography (silica gel, eluted with 10% methanol/dichloromethane) to afford a clear oil that was triturated with isopropanol (50 mL) to afford white crystals. The crystals were dissolved in methanol, concentrated under reduced pressure, and dried in a vacuum oven at 80° C. to provide 4-{[4-amino-2-(ethoxymethyl)-1H-imidazo[4,5-c]quinolin-1-yl]methyl}tetrahydro-2H-pyran-4-ol (1.27 g, 41%) as a white frothy solid, mp 212-214° C. 1H NMR (300 MHz, DMSO-d6) δ 8.33 (dd, J=8.3, 1.1 Hz, 1H), 7.60 (dd, J=8.3, 1.2 Hz, 1H), 7.40 (ddd, J=8.3, 7.0, 1.4 Hz, 1H), 7.22 (ddd, J=8.3, 7.0, 1.4 Hz, 1H), 6.37 (br s, 2H), 4.90 (br s, 2H), 4.88 (s, 1H), 4.70 (br s, 2H), 3.62-3.47 (m, 6H), 1.87-1.74 (m, 2H), 1.28 (m, 2H), 1.14 (t, J=7.0 Hz, 3H); MS (APCI) m/z 357 (M+H)+; Anal. Calcd for C19H24N4O3: C, 64.03; H, 6.79; N, 15.72.

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