反应详情

The title compound was prepared by the method of Example 89 step C from tert-butyl(6aS,10aR)-2-bromo-4,5,7,8,10,10a-hexahydropyrido[4,3-b]pyrrolo[3,2,1-hi]indole-9(6aH)carboxylate (189 mg, 0.5 mmol) and 4-methoxy-2-(trifluoromethyl)phenylboronic acid (248 mg, 1.0 mmol) to afford after chromatographic purification the title compound (196 mg, 83%). 1H NMR (CDCl3, 300 MHz) δ 7.21–7.26 (m,2H), 7.01–7.05 (m, 1H), 6.86 (s, 1H), 6.82 (s, 1H), 3.90–4.30 (m, 3H), 3.86 (s, 3H), 3.3.64–3.75 (m, 1H), 3.25–3.50 (m, 4H), 3.05–3.12 (m, 1H), 2.85–2.95 (m, 1H), 1.80–1.90 (m, 2H), 1.47 (s, 9H) ppm. MS-ApCI: 475 [M+H+].

1. customto afford
2. customafter chromatographic purification the title compound (196 mg, 83%)