反应详情

Following the procedure used to prepare 3-[4-(1-amino-cyclobutyl)-phenyl]-6-fluoro-2-phenyl-chromen-4-one, {1-[4-(6-methoxy-7-methyl-4-oxo-2-phenyl-4H-chromen-3-yl)-phenyl]-cyclobutyl}-carbamic acid tert-butyl ester (40 mg, 0.078 mmol) was reacted to give the title compound (28 mg, 88%). LCMS (Method E): RT=3.99 min, [M+H]+=412. 1H NMR (400 MHz, DMSO-d6): δ 7.55 (s, 1H), 7.37-7.24 (m, 8H), 7.06 (d, J=7.8 Hz, 2H), 3.86 (s, 3H), 2.35-2.16 (m, 7H), 2.07-1.87 (m, 3H), 1.64-1.53 (m, 1H).

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