Water → HCID 178464708, compound

Participants

Reaction Steps

The compound was prepared in a manner similar as to that described above (R)-4-[6-(4-Cyclopentyl-cyclohexyloxy)-5-trifluoromethyl-naphthalen-2-yl]-4-methyl-oxazolidin-2-one (15 mg, 0.000032 mol), (0.14 g, 0.0030 mol), 4.2 M lithium hydroxide, monohydrate in water (0.13 mL, 0.00055 mol) to give 12 mg of the desired product as a white solid (81%). ESI-MS: 419 (M−16)+. 1H NMR (400 MHz, MeOD) δ=8.64-8.50 (m, 1H), 8.17-7.98 (m, 2H), 7.98-7.87 (m, 1H), 7.73-7.62 (m, 1H), 7.50-7.40 (m, 1H), 4.84-4.76 (m, 2H), 3.80-3.58 (m, 2H), 2.12-1.96 (m, 2H), 1.85-1.42 (m, 18H), 1.21-1.05 (m, 2H).

Provenance & Evidence