Pyridine → HCID 12458458, 화합물
반응식
N1[CH:6]=[CH:5]C=CC=1.[CH:7](=[N:9]/[OH:10])\[CH3:8].C([CH2:14][C:15]([O-:17])=[O:16])C#C.[CH2:18](N(CC)CC)C>C(Cl)(Cl)Cl>[C:15]([O:17][CH2:5][C:6]1[O:10][N:9]=[C:7]([CH3:18])[CH:8]=1)(=[O:16])[CH3:14]참가 물질
6
실험 절차
To a suspension of N-chlorosuccimide (71.5 g, 535 mmol) in CHCl3 (360 mL) and pyridine (1.61 g, 20.3 mmol) was added a solution of (E)-acetaldehyde oxime (31.6 g, 535 mmol). After a period of 1 h, propargylacetate (35.0 g, 357 mmol) in a minimum of CHCl3 was added to the previous mixture. Triethylamine (114 g, 1124 mmol) was then added dropwise and the reaction mixture was cooled in a water bath in order to maintain the internal temperature below the boiling point. After a period of 1 h, the reaction mixture was concentrated in vacuo followed by the addition of EtOAc. The mixture was filtered on a glass filter and the solid washed with EtOAc, the combined filtrates were evaporated. After evaporation, additional EtOAc was added and the previous process repeated. The EtOAc was evaporated and the crude product was purified on a on Biotage system (isocratic elution 40% EtOAc:60% Hexanes) and the fractions followed by LC/MS to provide the titled compound as a clear oil. LC/MS m/z 156 [M+H]+.