Réaction #2329002

ord-1ab4a75401a34a8dbd13634582e825f0

Conditions de réaction

Conditions détaillées
See reaction.notes.procedure_details.

Mode opératoire

The title compound was synthesised according to the procedure described for 4-(6-methoxy-1,3-benzoxazol-2-yl)-N-methylaniline starting from 5-bromo-N-methylpyrimidin-2-amine. 1H NMR δ ppm 8.84-9.02 (m, 2H) 7.95 (d, 1H) 7.61 (d, 1H) 7.37 (d, 1H) 6.97 (dd, 1 H) 3.83 (s, 3H) 2.89 (d, 3H); ES-MS m/z 257 (M+H).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07670591B2uspto-grants-2010_03