反应详情

The title compound was prepared in 77% yield from 2-thieno[2,3-c]pyridin-3-yl-furo[2,3-c]pyridin]-7-ylamine by a procedure analogous to Intermediate 10, Step B. 1H NMR (300 MHz, CDCl3+CD3OD): δ 6.83 (s, 1H), 7.82 (s, 1H), 8.11 (d, J=5.6 Hz, 1H), 8.26 (s, 1H), 8.44 (d, J=5.8 Hz, 1H), 9.02 (s, 1H).