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ChemicalBook CAS DataBase List Linezolid

Linezolid synthesis

8synthesis methods
-

Yield:165800-03-3 98%

Reaction Conditions:

with triethylamine in dichloromethane at 20; for 3 h;

Steps:

8. Synthesis of compound 1, Linezolid

Compound 9 (100 mg, 0.34 mmol) was dissolved into 5 mL of anhydrous dicholoromethane in a 25 mL round bottom flask. The mixture was treated with Ac2O (0.2 mL, 1.59 mmol) and TEA (0.28 mL, 2.0 mmol) at room temperature. After 3 hours, dilute the mixture with EtOAc (40 mL).Wash the mixture with HCl (0.1 M, 5 mL), Sat. NaHCO3 (10) and brine (10 mL).Dry the organic layer with Na2SO4. Filter the organic layer and concentrate the organic layer at reduced pressure, the desired product was purified by silica gel column. Yield, 129 mg, 98%. 1H NMR (400 MHz, DMSO-d6) δ 8.27 (s, 1H), 7.49 (d, J = 15.0 Hz, 1H), 7.18 (d, J = 8.6 Hz, 1H), 7.04 (t, J = 9.2 Hz, 1H), 4.72 (s, 1H), 4.08 (t, J = 8.8 Hz, 1H), 3.71 (m, 4H), 2.95 (m, 4H), 1.85 (s, 3H). 13C NMR (101 MHz, DMSO-d6) δ 170.51, 156.26, 154.51, 153.83, 135.96 (d, J = 8.8 Hz), 133.89 (d, J = 10.6 Hz), 119.60 (d, J = 4.0 Hz), 114.42 (d, J = 2.6 Hz), 107.16, 106.90, 72.03, 66.61, 51.14, 47.73, 41.88, 22.87. 19F NMR (376 MHz, DMSO) δ -121.26.

References:

Wang, Keyin;Chen, Yinzhe;Wang, Siyuan;Zhang, Qian [Tetrahedron Letters,2022,vol. 105,art. no. 154050] Location in patent:supporting information

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