反应详情

To a 100 ml round-bottomed flask equipped with condenser and N2 inlet were added 1.0 g (3.88 mmol) of 6-(2-bromoethyl)benzothiazolone, 822 mg (3.88 mmol) N-(1-naphthyl)piperazine, 410 mg (3.88 mmol) sodium carbonate, and 50 ml methylisobutylketone. The reaction was refluxed for 24 hours, cooled, and was chromatographed on silica gel, eluting the byproducts with ethyl acetate (1 l) and the product with 4% methanol in ethyl acetate (1.5 l). The product fractions (Rf =0.2 in 5% methanol in ethyl acetate) were evaporated, taken up in methylene chloride, and precipitated by addition of ether saturated with HCl; the solid was filtered and washed with ether, dried, and washed with acetone. The latter was done by slurrying the solid with acetone and filtering. The title compound was obtained as a high melting, non-hygroscopic solid product, m.p. 288°-288.5° C., 0.78 g (59%).

1. customTo a 100 ml round-bottomed flask equipped with condenser and N2 inlet
2. temperatureThe reaction was refluxed for 24 hours
3. temperaturecooled
4. customwas chromatographed on silica gel
5. washeluting the byproducts with ethyl acetate (1 l)
6. customThe product fractions (Rf =0.2 in 5% methanol in ethyl acetate) were evaporated
7. customprecipitated by addition of ether saturated with HCl
8. filtrationthe solid was filtered
9. washwashed with ether
10. customdried
11. washwashed with acetone
12. filtrationfiltering