Reacción #79076

Ecuación de reacción

NaHCO3

7-amino-4-methylthiopyrido[4,3-d]pyrimidine

4-aminobenzotrifluoride hydrochloride

4-aminobenzotrifluoride

→

7-amino-4-(4-trifluoromethylanilino)pyrido[4,3-d]pyrimidine

Rendimiento 63.2%

Disolventes

MeOH CHCl3

Condiciones de reacción

Tratamiento posterior

1. 1
   Otrodried onto alumina
2. 2
   Otrochromatographed over alumina (4-7% MeOH/CH2Cl2)

Procedimiento

A mixture of 7-amino-4-methylthiopyrido[4,3-d]pyrimidine (390 mg, 2.03 mmol), 4-aminobenzotrifluoride hydrochloride (0.40 g, 2.02 mmol) and 4-aminobenzotrifluoride (1.61 g, 10.0 mmol) is stirred at 180° C. for 2 min. The resulting product is neutralized with excess NaHCO3, dissolved in MeOH/CHCl3, dried onto alumina and chromatographed over alumina (4-7% MeOH/CH2Cl2) to give 7-amino-4-(4-trifluoromethylanilino)pyrido[4,3-d]pyrimidine (390 mg, 63) as a cream solid. Analytically pure material was obtained by further chromatography over silica gel (5% MeOH/CH2C2) to give pale yellow needles. 1H NMR (DMSO) δ 10.09 (1H, brs), 9.40 (1H, s), 8.48 (1H, s), 8.13 (2H, d, J 8.2 Hz), 7.74 (2H, d, J=8.7 Hz), 6.72 (2H, brs), 6.40 (1H, s).

Fuente