Реакция #56937

ord-9298de7aabad4d458588f6019ad29763

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

Following the method described in Example 165, 2-[2-amino-6-(4-chloro-phenylamino) pyrimidin-4-yl]-4-bromo-phenol and 4-methoxy-benzyl chloride provided the title compound (50% yield). 1H NMR (CD3OD) δ 3.76 (s, 3H, CH3), 5.16 (s, 2H, CH2), 6.37 (s, 1H, Ar), 6.89-6.92 (m, 2H, Ar), 7.28-7.30 (m, 3H, Ar), 7.39-7.42 (m, 2H, Ar), 7.69-7.32 (m, 4H, Ar).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07419984B2uspto-grants-2008_09