Sulfur Dioxide → 6-Bromo-2,3-dihydro-1,2-benzothiazole-1,1,3-trione

温度

0 °C

A solution of methyl 2-amino-4-bromobenzoate (4.5 g, 20 mmol) in 20% hydrochloric acid (30 mL) was stirred until all solids were dissolved. The solution was cooled to 0° C. and a solution of sodium nitrite (1.4 g, 0.020 mol) in water (20 mL) was added dropwise at such a rate that the internal reaction temperature did not exceed 5° C. The mixture was stirred at 0° C. for 45 minutes. Sulfur dioxide was bubbled into a mixture of acetic acid (50 mL) and water (5 mL) at 0° C. until the solution was saturated. Copper (I) chloride (2.0 g, 0.020 mol) was then added to the saturated sulfur dioxide solution. The mixture was cooled to 0° C. To this mixture was added the diazonium salt solution dropwise with vigorous stirring over a period of 30 minutes. The reaction mixture was stirred at 0° C. for 1 hour and then the mixture was allowed to warm to room temperature. The mixture was stirred at room temperature for 2 h before it was poured into ice water (250 mL) and extracted with EtOAc (3×50 mL). The organics were washed with sat. NaHCO3 solution and dried over anhydrous Na2SO4. The solvent was removed in vacuo to afford an oily residue which was dissolved in tetrahydrofuran (40 mL) and cooled to 0° C. To this mixture was added a cold (0° C.) solution of ammonium hydroxide (28%, 40 mL) portion-wise at such a rate that the internal reaction temperature was maintained below 10° C. The mixture was allowed to warm to room temperature and was then stirred at room temperature for 1 h. The solvent was removed in vacuo and the residue was dissolved in saturated aqueous sodium bicarbonate (40 mL) and washed with diethyl ether (50 mL). The aqueous layer was acidified with concentrated hydrochloric acid to pH 1. The resulting precipitate was collected by filtration and was dried under vacuum to produce of 6-Bromo-1,1-dioxo-1,2-dihydro-1λ6-benzo[d]isothiazol-3-one (500 mg, 10% yield). 1H NMR (400 MHz, DMSO) δ 8.44 (d, J=1.5, 1H), 8.04 (dd, J=8.1, 1.5, 1H), 7.81 (d, J=8.0, 1H).

1. dissolutionwere dissolved
2. customdid not exceed 5° C
3. customSulfur dioxide was bubbled into a mixture of acetic acid (50 mL) and water (5 mL) at 0° C. until the solution
4. temperatureThe mixture was cooled to 0° C
5. stirringwith vigorous stirring over a period of 30 minutes
6. stirringThe reaction mixture was stirred at 0° C. for 1 hour
7. temperatureto warm to room temperature
8. stirringThe mixture was stirred at room temperature for 2 h before it
9. extractionextracted with EtOAc (3×50 mL)
10. washThe organics were washed with sat. NaHCO3 solution
11. dry with materialdried over anhydrous Na2SO4
12. customThe solvent was removed in vacuo
13. customto afford an oily residue which
14. temperaturecooled to 0° C
15. temperaturewas maintained below 10° C
16. temperatureto warm to room temperature
17. stirringwas then stirred at room temperature for 1 h
18. customThe solvent was removed in vacuo
19. dissolutionthe residue was dissolved in saturated aqueous sodium bicarbonate (40 mL)
20. washwashed with diethyl ether (50 mL)
21. filtrationThe resulting precipitate was collected by filtration
22. customwas dried under vacuum

ORDレコード

ord-5d32a1f5a70c403086bda27141f8a86f

出典データセット

uspto-grants-2010_03

DOI

10.6084/m9.figshare.5104873.v1

特許番号

US07671221B2