HRID10826

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CC(=O)NC[C@H]1CN(c2ccc(I)c(F)c2)C(=O)O1

HCID11222662

N-{[(5S)-3-(3-Fluoro-4-iodophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide

C12H12FIN2O3

结构：CC(C)(C)OC(=O)NC[C@H]1CN(c2ccc(I)cc2)C(=O)O1

HCID86591790

未命名化合物

PRODUCTS

生成物

结构：CC(=O)NC[C@H]1CN(c2ccc(C3CCC(=O)NC3)cc2)C(=O)O1

HCID10314631

未命名化合物

PROCEDURE

实验过程

N-({(5S)-2-oxo-3-[4-(6-oxopiperidin-3-yl)phenyl]-1,3-oxazolidin-5-yl}methyl)acetamide is prepared by the route described in Example 1 substituting tert-butyl [(5S)-3-(4-iodophenyl)-2-oxo-1,3-oxazolidin-5-yl]methylcarbamate for N-{[(5S)-(3-fluoro-4-iodophenyl)-2-oxo-1,3-oxazolidin-5-yl]methyl}acetamide. 1H-NMR (DMSO) δ: 8.24, 7.51, 7.47, 7.33, 4.71, 4.10, 3.72, 3.40, 3.18, 3.14, 2.97, 2.28, 1.94, 1.83