Réaction #2275696
ord-267c8bb64fe54009a84b95ec665bc546
Équation de réaction
Réactifs
Réactifs
Solvants
Conditions de réaction
Traitement
- 1workup.STIRRINGstirred 3 days
- 2ConcentrationThe reaction volume is partially concentrated under reduced pressure
- 3workup.ADDITIONthen diluted with EtOAc
- 4Lavagewashed with saturated aqueous NaHCO3 and saturated aqueous NaCl
- 5SéchageThe organic layer is dried (MgSO4)
- 6Filtrationfiltered
- 7Concentrationconcentrated under reduced pressure
- 8Autreto afford a yellow oil that
- 9Autreis purified over silica (EtOAc:heptane gradient 1:1 to 1:0)
Mode opératoire
To a solution of 3,5-bis-benzyloxy-pyridine-2-carboxylic acid HCl, 2, (8.06 g, 21.7 mmol) in DMF (100 mL) at 0° C. under N2 is added diisopropylethylamine (11.35 mL, 65.1 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide (EDCI) (6.23 g, 32.6 mmol) and 1-hydroxybenzotriazole (HOBt) (0.294 g, 2.2 mmol). The solution is stirred for 5 minutes and glycine methyl ester hydrochloride (4.09 g, 32.6 mmol) is added. The reaction is allowed to warm slowly to room temperature and stirred 3 days. The reaction volume is partially concentrated under reduced pressure then diluted with EtOAc and washed with saturated aqueous NaHCO3 and saturated aqueous NaCl. The organic layer is dried (MgSO4), filtered and concentrated under reduced pressure to afford a yellow oil that is purified over silica (EtOAc:heptane gradient 1:1 to 1:0) to afford 3.5 g (40% yield) of the desired product as a yellow oil. 1H NMR (400 MHz, CDCl3) δ ppm 8.12 (1H, t, J=4.9 Hz), 7.95 (1H, d, J=1.8 Hz), 7.38-7.44 (2H, m), 7.22-7.35 (8H, m), 6.85 (1H, d, J=2.6 Hz), 5.14 (2H, s), 5.03 (2H, s), 4.18 (2H, d, J=5.5 Hz), 3.69 (3H, s). HPLC-MS: m/z 407 [M+H]+.