反应详情

温度

25 °C

2.61 g (4.67 mmol) (7R,8R,9R)-10-acetyl-3-bromo-7-(2-methoxyethoxy)-2-methyl-9-phenyl-8-pivaloyloxy-7.8.9.10-tetrahydroimidazo[1.2-h][1.7]naphthyridine, 0.63 g (5.14 mmol) phenylboronic acid, 0.89 g (15.4 mmol) KF (spray-dried), 0.14 g (0.15 mmol) Pd2(dba)3, 0.07g (0.36 mmol/10wt % solution in hexane)P(t-Bu)3 and THF (30 ml) are added to a Schlenk tube under argon. Afterwards the Schlenk tube is evacuated and refilled with argon in a freeze-pump-thaw cycles technique three times. The reaction mixture is stirred under argon for 2 d at 25° C. Subsequently the reaction is diluted by adding of ethyl acetate and then filtrated through silica gel. The concentrated crude product is purified by column chromatography (diethyl ether/petrol ether: 6/4) to give 1.80 g (3.24 mmol/70%) of the title compound as an amorphous colourless solid. 1H-NMR (200 MHz, [D6] DMSO): δ=1.20 (s, 9H), 2.20(s, 3H), 2.43(s, 3H), 3.30 (s, 3H), 3.40–3.57(m, 2H), 3.88 (t, 2H), 4.64 (d, 1H), 5.35 (t, 1H), 5.83(d, 1H), 7.00(d, 1H), 7.10–7.30(m, 5H), 7.41–7.68 (m, 5H), 8.24(d, 1H).

1. customAfterwards the Schlenk tube is evacuated
2. additionrefilled with argon in a freeze-pump-thaw cycles technique three times
3. additionSubsequently the reaction is diluted
4. additionby adding of ethyl acetate
5. filtrationfiltrated through silica gel
6. concentrationThe concentrated crude product
7. customis purified by column chromatography (diethyl ether/petrol ether: 6/4)