反応 #2487431

ord-c64fe51a91f24ffcb1cb9ed17498f300

反応条件

詳細条件
See reaction.notes.procedure_details.

実験手順

Compound 8 was prepared in a similar manner to compound 1 from 2-bromo-5-methoxypyridine to afford a tan solid (28 mg, 10%). 1H NMR (500 MHz, CDCl3): δ 8.74 (s, 1H), 8.19 (s, 1H), 7.63 (br s, 1H), 7.51 (d, J=8.5 Hz, 1H), 7.34-7.33 (m, 1H), 7.24-7.23 (m, 1H), 6.75-6.74 (m, 1H), 6.67-6.66 (m, 1H), 5.58 (d, J=14.0 Hz, 1H), 5.07 (d, J=14.0 Hz, 1H), 3.88 (s, 3H). MS(ESI): m/z 382 [M+−1]. HPLC: 92.37%.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US08796001B2uspto-grants-2014_08