Reacción #3542

Ecuación de reacción

4-Amino-2-phenylamino-pyrimidine-5-carbonitrile

formic acid

→

title compound

4-Amino-2-phenylamino-pyrimidine-5-carboxaldehyde

Disolventes

water

Condiciones de reacción

Tratamiento posterior

1. 1
   FiltraciónThe reaction was filtered
2. 2
   Concentraciónthe filtrate was concentrated in vacuo
3. 3
   Extracciónextracted with ethyl acetate three times
4. 4
   FiltraciónThe aqueous layer was filtered through a fiberglass
5. 5
   Filtraciónfilter
6. 6
   workup.ADDITIONto disperse the emulsion that
7. 7
   LavadoThe aqueous filtrate was washed with ethyl acetate
8. 8
   Filtraciónfiltered
9. 9
   Lavadowashed with saturated sodium chloride
10. 10
    Secadodried with magnesium sulfate
11. 11
    Concentraciónconcentrated in vacuo
12. 12
    LavadoChromatography down silica gel, eluting with ethyl acetate:hexane (2:1)

Procedimiento

4-Amino-2-phenylamino-pyrimidine-5-carbonitrile (2.00 g) obtained from Example 71 was combined with wet Raney nickel (2.00 g), 98% formic acid (60 mL) and water (40 mL) in a Parr shaker. The reaction was placed under hydrogen (42 psi) and shaken for 20 minutes. The reaction was filtered, and the filtrate was concentrated in vacuo. The residue was suspended in water, made basic with saturated sodium bicarbonate, and extracted with ethyl acetate three times. The aqueous layer was filtered through a fiberglass filter to disperse the emulsion that was present. The aqueous filtrate was washed with ethyl acetate. The ethyl acetate washes were combined, filtered, washed with saturated sodium chloride, dried with magnesium sulfate and concentrated in vacuo. Chromatography down silica gel, eluting with ethyl acetate:hexane (2:1) gave 0.73 g of the title compound, CIMS (1% NH3 in CH4): 243=M+ +C2H5, 215=M+ +H (Base), 214=M+.

Fuente