反应详情

To a solution of 4-methoxyquinoline-2-carboxylic acid and DMF (50 μL) in DCM at 0° C. was added dropwise oxalyl chloride (1.2 eq). The cooling bath was removed and the mixture was stirred for 2 hr at RT, then the solvent was removed under reduced pressure. The residue was dissolved in THF/MeCN (1:1) and cooled to 0° C., a pre-cooled solution (0° C.) of TMSCHN2 (1.2 eq) and Et3N (1.2 eq) was added dropwise and the resulting mixture was stirred for 2 hr at 0° C. An excess of 2M HCl solution in Et2O was added and the reaction was stirred for further hour at 0° C. and then partitioned between sat. aq. NaHCO3 solution and DCM. The organic phase was separated, dried (Na2SO4), and concentrated under reduced pressure to afford a dark brown solid which was used as such in the next step. 1H NMR (300 MHz, CDCl3) δ: 8.47 (1H, d, J=8.0 Hz), 8.09 (1H, d, J=8.4 Hz), 7.81-7.73 (1H, m), 7.66-7.58 (1H, m), 7.51 (1H, s), 5.31 (2H, s), 4.13 (3H, s). MS (ES) Cl2H10ClNO2 requires: 235, found: 236 (M+H)+.

1. customThe cooling bath was removed
2. customthe solvent was removed under reduced pressure
3. dissolutionThe residue was dissolved in THF/MeCN (1:1)
4. temperaturecooled to 0° C.
5. stirringthe resulting mixture was stirred for 2 hr at 0° C
6. stirringthe reaction was stirred for further hour at 0° C.
7. custompartitioned between sat. aq. NaHCO3 solution and DCM
8. customThe organic phase was separated
9. dry with materialdried (Na2SO4)
10. concentrationconcentrated under reduced pressure
11. customto afford a dark brown solid which