Реакция #48945

ord-fd321fd2741843669cb3731128632eca

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

The title compound was prepared from methyl 2-bromoacetate and 4-(3,5-dichloropyridin-4-ylamino)-8-hydroxy-7-methoxy-2H-chromen-2-one (Example 29) following the procedure outlined in Example 25. 1H NMR (400 MHz, DMSO-d6): δ 9.54 (s, 1H), 8.83 (s, 2H), 7.97 (d, 1H), 7.23 (d, 1H), 4.73 (s, 2H), 4.66 (s, 1H), 3.92 (s, 3H), 3.69 (s, 3H); MS (ESI): 424.8.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07745646B2uspto-grants-2010_06