反应 #2192498

ord-ac76415a5cea459fab2507d31cbd3445

反应条件

详细条件
See reaction.notes.procedure_details.

实验过程

The title compound was prepared in 58% yield from 2-chloro-5-bromo-3H-pyrimidin-4-one (Example 1A) and 2-bromomethyl-thiophene-3-carbonitrile according to the general procedure outlined for Example 1B. 1H NMR (400 MHz, CDCl3): δ 8.10 (s, 1H), 7.40 (d, 1H, J=5.6 Hz), 7.21 (d, 1H, J=5.6 Hz), 5.74 (s, 2H). MS (ES) [m+H] calc'd for C10H5N3OSBrCl, 330, 332; found 330, 332.

来源

DOI: 10.6084/m9.figshare.5104873.v1专利: US07579357B2uspto-grants-2009_08