C([N:4]1[CH:10]([CH3:11])[C:9]2[CH:12]=[CH:13][CH:14]=[CH:15][C:8]=2[NH:7][C:6](=[O:16])[CH:5]1[CH:17]=[CH:18][C:19]1C=CC=CC=1)C=C.Cl>CCOCC.C=CC1C=CC=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.C1C=CC(P(C2C=CC=CC=2)C2C=CC=CC=2)=CC=1.Cl[Ru]Cl>[CH3:11][CH:10]1[N:4]2[CH2:19][CH:18]=[CH:17][CH:5]2[C:6](=[O:16])[NH:7][C:8]2[CH:15]=[CH:14][CH:13]=[CH:12][C:9]1=2The product of Example 15 (103 mg, 0.32 mmol) was first converted to the HCl salt with excess 1M HCl in ether, and all of the volatiles were removed. The resulting solid was then dissolved in dry dichloromethane (15 mL) and bis(tricyclohexylphosphine)benzylidine ruthenium(IV) dichloride (132 mg, 0.16 mmol) was added, and the flask was flushed with Ar(g). The reaction was allowed to proceed at room temperature for three days, after which time, the reaction was diluted with an additional 10 mL of dichloromethane, and transferred to a separatory funnel. The organic layer was washed with a saturated solution of sodium bicarbonate (3×15 mL), the aqueous layers were then combined and extracted with dichloromethane (2×10 mL). The organic layers were then combined, washed once with brine (15 mL), dried over magnesium sulfate, filtered and evaporated to yield a crude residue which was purified by flash column chromatography using ethyl acetate-hexane (3:1) to yield 32 mg (61% yield) of a dark oil. 1H NMR (360 MHz, CDCl3) δ 7.60 (bs, 1H), 7.42 (d, J=7.6 Hz, 1H), 7.32-7.19 (m, 2H), 7.00-6.95 (m, 1H), 6.16-6.10 (m, 1H), 5.88-5.82 (m, 1H), 4.34 (bs, 1H), 3.96-3.81 (m, 2H), 3.55-3.46 (m, 1H), 1.58 (d, J=6.5 Hz, 3H).
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