反应详情

A mixture of 0.5 g of 4-(2-naphthyl)-thiazol-2-ylamine hydrobromide with 0.34 g of 4-methoxy-benzenesulfonyl chloride was stirred for 3 hours with 2 ml of pyridine. The resulting, red colored suspension was poured into 30 ml of 1N hydrochloric acid and extracted with ethyl acetate. The organic phases were combined, dried with magnesium sulphate and freed from solvent. The residue was dissolved in a mixture of 25 ml of ethanol and 20 ml of 2N sodium hydroxide solution. After the addition of 0.5 g of active charcoal the mixture was stirred at room temperature for 30 minutes and subsequently the active charcoal was filtered off. The product separated upon neutralization with concentrated hydrochloric acid. Recrystallization from 10 ml of ethyl acetate and 15 ml of n-hexane yielded 0.19 g of 4-methoxy-N-(4-naphthalen-2-yl-thiazol-2-yl)-benzenesulfonamide as colorless crystals.

1. extractionextracted with ethyl acetate
2. dry with materialdried with magnesium sulphate
3. dissolutionThe residue was dissolved in a mixture of 25 ml of ethanol and 20 ml of 2N sodium hydroxide solution
4. additionAfter the addition of 0.5 g of active charcoal the mixture
5. filtrationsubsequently the active charcoal was filtered off
6. customThe product separated upon neutralization with concentrated hydrochloric acid
7. customRecrystallization from 10 ml of ethyl acetate and 15 ml of n-hexane