反应详情

7-fluorobenzo[d]thiazole 25D (500 mg, 3.26 mmol) was added dropwise to chlorosulfonic acid (2.5 mmol) at 0° C. After the addition was complete, the mixture was stirred at room temperature for 0.5 h and then heated at 105° C. and stirred overnight. The resulting mixture was cooled to −10° C. and quenched by pouring on crushed ice slowly. The resulting mixture was extracted with EtOAc (20 mL×2). The combined organic phase was washed with brine, dried over anhy. Na2SO4 and concentrated in vacuo. Column chromatography (15% PE/EtOAc) afforded 200 mg of title compound. 1H NMR (CHLOROFORM-d) δ: 9.44 (s, 1H), 8.32 (dd, J=8.6, 4.6 Hz, 1H), 7.38 (t, J=8.5 Hz, 1H).

1. additionAfter the addition
2. temperatureheated at 105° C.
3. stirringstirred overnight
4. temperatureThe resulting mixture was cooled to −10° C.
5. customquenched
6. additionby pouring
7. customon crushed ice slowly
8. extractionThe resulting mixture was extracted with EtOAc (20 mL×2)
9. washThe combined organic phase was washed with brine
10. customdried over anhy
11. concentrationNa2SO4 and concentrated in vacuo