Reaktion #8890

Reaktionsgleichung

iodomethane

product

1-[3-Amino-5-(4-chlorophenyl)-6-(2,4-dichlorophenyl)furo[2,3-b]pyridin-2-yl]-2,2-dimethylpropan-1-one

sodium hydride

DMF

→

title compound

1-[5-(4-Chlorophenyl)-6-(2,4-dichlorophenyl)-3-(dimethylamino)furo[2,3-b]pyridin-2-yl]-2,2-dimethylpropan-1-one

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.ADDITIONAfter the addition
2. 2
   TemperaturThe reaction was warmed to room temperature
3. 3
   workup.STIRRINGstirred for 2 hours
4. 4
   SonstigeThe reaction was quenched with saturated NaHCO3 solution
5. 5
   SonstigeThe reaction mixture was partitioned between ethyl acetate and saturated NaHCO3 solution
6. 6
   WaschenThe organic layer was washed twice with saturated NaHCO3 solution, brine
7. 7
   Trocknendried (Na2SO4)
8. 8
   Filtrationfiltered
9. 9
   Einengenconcentrated in vacuo
10. 10
    SonstigePurification by MPLC (silica gel; 0% to 20% ethyl acetate:hexane gradient)

Vorschrift

A solution of 0.050 g (0.106 mmol) of the product from Example 17 in DMF (1 mL) at 0° C. was treated with sodium hydride (0.010 g; 60% dispersion; 0.232 mmol). After the addition, the reaction mixture was stirred for 20 minutes at 0° C., and then treated with iodomethane (26 μL; 0.424 mmol). The reaction was warmed to room temperature and stirred for 2 hours. The reaction was quenched with saturated NaHCO3 solution. The reaction mixture was partitioned between ethyl acetate and saturated NaHCO3 solution. The organic layer was washed twice with saturated NaHCO3 solution, brine, dried (Na2SO4), filtered, and concentrated in vacuo. Purification by MPLC (silica gel; 0% to 20% ethyl acetate:hexane gradient) gave the title compound. HPLC/MS: 501.0 (M+1), 503.0 (N+3); Rt=5.08 min.

Quelle