反应详情

Prepared in the same manner as described for example 1. A solution of 4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (0.70 g, 1.92 mmol, 1 eq.) in anhydrous THF was treated with 1,1′-carbonyldiimidazole (0.32 g, 1.96 mmol, 1.02 eq.) and warmed as described. The reaction was allowed to cool and then treated with N,N-dimethylethylenediamine (0.20 g, 2.35 mmol, 1.2 eq.). The reaction was treated as described in example 1 to give a yellow oil. The oil was purified by silica gel flash chromatography using 5% 2M NH3 in methanol in chloroform as the mobile phase. Fractions containing the product were pooled and the solvent removed in vacuo leaving 4′-(2-phenoxy-ethylsulfanylmethyl)-biphenyl-2-carboxylic acid (2-dimethylamino-ethyl)-amide (0.50 g, 60% yield) as a bright yellow oil.

1. customPrepared in the same manner
2. temperaturewarmed
3. temperatureto cool
4. additionThe reaction was treated
5. customto give a yellow oil
6. customThe oil was purified by silica gel flash chromatography
7. additionFractions containing the product
8. customthe solvent removed in vacuo