Reaktion #638288

Reaktionsgleichung

Bromoacetonitrile

6-methyl-4H-imidazo[1,5,4-de]quinoxaline-2,5(1H,6H)-dione

Intermediate 23

6-methyl-4H-imidazo[1,5,4-de]quinoxaline-2,5(1H,6H)-dione

sodium hydride

→

title compound

(6-Methyl-2,5-dioxo-5,6-dihydro-4H-imidazo[1,5,4-de]quinoxalin-1(2H)-yl)acetonitrile

Lösungsmittel

DMF

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONin was added dropwise
2. 2
   Sonstigequenched with H2O (20 mL)
3. 3
   ExtraktionThe mixture was extracted with EtOAc (2×30 mL)
4. 4
   Waschenthe combined organic extracts were washed with brine (10 mL)
5. 5
   Trocknendried over Na2SO4
6. 6
   Filtrationfiltered
7. 7
   Einengenconcentrated in vacuo
8. 8
   SonstigeThe crude product was partially purified by silica gel chromatography
9. 9
   Wascheneluting with a gradient of CH2Cl2

Vorschrift

To a stirred solution of 6-methyl-4H-imidazo[1,5,4-de]quinoxaline-2,5(1H,6H)-dione (296 mg, 1.46 mmol, described in Intermediate 23) in DMF (5 mL) at 0° C. was added sodium hydride (60% dispersion in mineral oil; 78 mg, 1.96 mmol) and the resulting mixture was stirred for 5 min Bromoacetonitrile (0.122 mL, 1.75 mmol) in was added dropwise and the reaction mixture was allowed to warm to ambient temperature and was stirred for 3 h, then quenched with H2O (20 mL). The mixture was extracted with EtOAc (2×30 mL) and the combined organic extracts were washed with brine (10 mL), then dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was partially purified by silica gel chromatography, eluting with a gradient of CH2Cl2:MeOH—100:0 to 95:5, followed by trituration with CH2Cl2 to give the title compound. MS: m/z=243 (M+1).

Quelle