Реакция #310181

ord-3a0c1fa5d4d5426aab91e81c2390b35d

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

The title compound was prepared from 3-[8-(2,6-difluorophenyl)-2-(methylsulfinyl)-7-oxo-7,8-dihydropyrido[2,3-d]pyrimidin-4-yl]-4-methyl-N-1,3-thiazol-2-ylbenzamide and N-(1-methylethyl)-1,2-ethanediamine by following the procedures in Example 79c. LC-MS m/z 576 (M+H)+; 1H-NMR (MeOD) 1.02 (d, J=6.0 Hz, 6H), 2.31 (m, 3H), 2.72 (m, 3H), 3.23 (m, 1H), 3.55 (m, 1H), 6.36 (d, J=8.8 Hz, 1H), 7.13 (m, 1H), 7.24 (m, 2H), 7.47 (m, 2H), 7.56 (m, 2H), 8.00 (s, 1H), 8.10 (d, J=7.6 Hz, 1H).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US08207176B2uspto-grants-2012_06