反应详情

A solution of 2-amino-5-(2-bromoacetyl)benzenesulphonamide (0.5 g), N-(1-methyl-3-phenylpropyl)-N-(phenylmethyl) amine (0.45 g) and propylene oxide (2.5 ml) in 2-butanone (30 ml) was heated under reflux for 3 hours. The solution was then concentrated to a red-brown oil (0.7 g) which was dissolved in absolute ethanol (30 ml) and treated with sodium borohydride (258 mg) at room temperature during 2 hours. Excess borohydride was then destroyed with 2N hydrochloric acid and the ethanol was removed under reduced pressure. The residue was basified with 8% sodium bicarbonate and extracted with ethyl acetate (3 × 50 ml). The extracts were washed with water (100 ml), dried and concentrated to an orange oil (0.63 g). The oil was dissolved in acetone (10 ml) and re-precipitated as an orange solid (340 mg) by addition of petroleum ether (b.p. 60°-80°). Chromatographic purification of this solid on silica plates [Merck St17; elution with chloroform: methanol (5:1 )] and conversion of the product into a hydrochloride salt gave the title compound, 0.2 g, m.p. 133°-136°.

1. temperatureunder reflux for 3 hours
2. concentrationThe solution was then concentrated to a red-brown oil (0.7 g) which
3. dissolutionwas dissolved in absolute ethanol (30 ml)
4. additiontreated with sodium borohydride (258 mg) at room temperature during 2 hours
5. customExcess borohydride was then destroyed with 2N hydrochloric acid
6. customthe ethanol was removed under reduced pressure
7. extractionextracted with ethyl acetate (3 × 50 ml)
8. washThe extracts were washed with water (100 ml)
9. customdried
10. concentrationconcentrated to an orange oil (0.63 g)
11. dissolutionThe oil was dissolved in acetone (10 ml)
12. customre-precipitated as an orange solid (340 mg) by addition of petroleum ether (b.p. 60°-80°)
13. customChromatographic purification of this solid
14. washon silica plates [Merck St17; elution with chloroform: methanol (5:1 )] and conversion of the product into a hydrochloride salt