Acetic Acid → Diisopropyl Ether

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Reaction Steps

The procedure used in Example 216 is followed. In a 10 ml round-bottomed flask under an argon atmosphere, dissolve 229 mg of 4-{5-[(3-dimethylaminopropyl)aminocarbonyl]-1H-benzimidazol-2-yl}-9H-fluoren-9-one oxime (Z,E), obtained in the previous stage, in a mixture of 1.2 ml of ethanol, 1.2 ml of water and 1.2 ml of acetic acid. At room temperature, add 136 mg of zinc in three stages. Between each addition, stir for approximately one hour to two hours. Add Celite and filter. The filtrate is concentrated under pressure. The crude product is purified by flash chromatography on silica gel (40-63 μm), eluting with a mixture of dichloromethane and ammonia as a 7N solution in methanol (9/1 by volume). After formation of the paste with diisopropyl ether, in this way we obtain 150 mg of 4-{5-[(3-dimethylaminopropyl)aminocarbonyl]-1H-benzimidazol-2-yl}-9H-fluorene-9(R,S)-amine, in the form of an off-white powder, which is used as it is in the following stage, with the following characteristics:

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