2,6-Dimorpholin-4-ylpyridin-4-amine → N4-(5-chlorobenzo[d][1,3]dioxol-4-yl)-N2-(2,6-dimorpholinopyridin-4-yl)-N4-methylpyrimidine-2,4-diamine

Participants

Reaction Steps

2,6-Dimorpholinopyridin-4-amine (160 mg, 0.60 mmol) and 2-chloro-N-(5-chlorobenzo[d][1,3]dioxol-4-yl)-N-methylpyrimidin-4-amine (180 mg, 0.60 mmol) were reacted according to the procedure in Example 1 to give N4-(5-chlorobenzo[d][1,3]dioxol-4-yl)-N2-(2,6-dimorpholinopyridin-4-yl)-N4-methylpyrimidine-2,4-diamine (80 mg, 25.2%) as a pale yellow foam. NMR Spectrum (CDCl3) 3.23-3.58 (m, 11H), 3.72-3.90 (m, 8H), 5.65 (s, 1H), 6.03 (s, 2H), 6.50 (s, 2H), 6.79 (d, 1H), 6.99 (d, 1H), 7.17 (s, 1H), 7.90 (s, 1H); Mass spectrum: MH+ 526.

Provenance & Evidence