Reaktion #68948

Reaktionsgleichung

2-Amino-5-cyanopyrazine

sodium tert-butoxide

1-(4-methoxybenzyl)-6-bromo-1H-imidazo[4,5-c]pyridine

→

title compound

Ausbeute 40.0%

5-(1-(4-methoxybenzyl)-1H-imidazo[4,5-c]pyridin-6-ylamino)pyrazine-2-carbonitrile

Ausbeute 40.0%

Lösungsmittel

DMF toluene

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigethe resulting mixture was degassed under a stream of nitrogen gas for 10 minutes
2. 2
   Sonstigethe mixture was degassed for a further 5 minutes
3. 3
   Sonstigemicrowave irradiation
4. 4
   SonstigeThe reaction mixture was partitioned between water and dichloromethane
5. 5
   ExtraktionThe aqueous phase extracted with dichloromethane
6. 6
   TrocknenThe combined organic layers were dried (Na2SO4)
7. 7
   Einengenconcentrated
8. 8
   workup.DISSOLUTIONThe residue was dissolved in methanol
9. 9
   Einengenconcentrated
10. 10
    SonstigeThe product was purified

Vorschrift

Palladium (II) acetate (3.5 mg, 16 μmol) was added to (±)-2,2″-bis(diphenylphosphino)-1,1″-binaphthalene (59 mg, 94 μmol) in DMF/toluene (1:2) and the resulting mixture was degassed under a stream of nitrogen gas for 10 minutes. 2-Amino-5-cyanopyrazine (19 mg, 0.16 mmol), sodium tert-butoxide (45 mg, 0.47 mmol) and 1-(4-methoxybenzyl)-6-bromo-1H-imidazo[4,5-c]pyridine (50 mg, 0.16 mmol) were added and the mixture was degassed for a further 5 minutes before heating at 150° C. for 30 minutes using microwave irradiation. The reaction mixture was partitioned between water and dichloromethane. The aqueous phase extracted with dichloromethane. The combined organic layers were dried (Na2SO4) and concentrated. The residue was dissolved in methanol, passed through a PS-Thiol column and concentrated. The product was purified using preparative HPLC to give the title compound (22.4 mg, 40%). 1H NMR (d6-DMSO, 400 MHz) δ 10.84 (br s, 1H), 8.77 (d, 1H, J=1.3 Hz), 8.74 (m, 2H), 8.49 (s, 1H), 8.17 (s, 1H), 7.34 (m, 2H), 5.41 (s, 2H), 3.72 (s, 3H). LCMS (2) Rt=2.32 min; m/z (ESI+) 358 (MH+), (ESI−) 356 (M−H).

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