Реакция #220948

ord-a56dc0aef1554be0b435d57bd541f38f

Уравнение реакции

CC(=O)Nc1ccc(O)cc1
4-acetamidophenol
Cc1cc(NC(=O)C2(C)CO2)ccc1F
2-methyloxirane-2-carboxylic acid (4-fluoro-3-methylphenyl)amide
CC(=O)Nc1ccc(OCC(C)(O)C(=O)Nc2ccc(F)c(C)c2)cc1
3-(4-Acetylaminophenoxy)-N-(4-fluoro-3-methylphenyl)-2-hydroxy-2-methylpropionamide

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Методика

3-(4-Acetylaminophenoxy)-N-(4-fluoro-3-methylphenyl)-2-hydroxy-2-methylpropionamide was prepared as described in Example 61 c starting from 4-acetamidophenol and 2-methyloxirane-2-carboxylic acid (4-fluoro-3-methylphenyl)amide. 1H NMR (400 MHz, DMSO-d6): 1.40 (3H, s), 2.00 (3H, s), 2.20 (3H, s), 3.90 (1H, d, J=9.5 Hz), 4.15 (1H, d, J=9.5 Hz), 6.03 (1H, s), 6.84 (2H, d, J=8.7 Hz), 7.03-7.08 (1H, m), 7.44 (2H, d, J=8.7 Hz), 7.54-7.57 (1H, m), 7.67-7.69 (1H, m), 9.62 (1H, s), 9.75 (1H, s).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07390923B2uspto-grants-2008_06