反应详情

To a stirred mixture of methyl 5-(2-pyrrolidinyl)methoxypyridine-2-carboxylate (370 mg, 1.57 mmol), 4-[N′-(2-bromophenyl)ureido]-3-methoxyphenylacetic acid (595 mg, 1.57 mmol), 4-DMAP (230 mg, 1.88 mmol) in DMF (10 ml) was added EDC.HCl (360 mg, 1.88 mmol) at room temperature. The resulting mixture was stirred at room temperature for 20 hr. The mixture was pored into ice-water. The solid was collected, washed with water and air-dried. The crude solid was purified by silica-gel (30 ml) column chromatography with CHCl3-EtOH (98:2, v/v) as eluent and crystallized with Et2O to give methyl 5-[1-[4-[N′-(2-bromophenyl)ureido]-3-methoxyphenyl acetyl]-2-pyrrolidinylmethoxy]pyridine-2-carboxylate (650 mg, 69%) as an amorphous solid. IR (KBr) n 3323, 1720, 1624, 1601, 1527 cm−1; 1H-NMR (CDCl3) δ 1.22 and 2.00 (each m, 4 H), 3.48–4.55 (series of s and m, 13 H which contains amide-isomers), 6.93–8.82 (series of s and m, 12 H which contains amide-isomers); MS (FAB) m/z 597 (M30 −1) and 599 (M++1); Anal. Calcd for C28H30BrN4O6.1.0×H2O: C, 54.55; H, 5.23; N, 9.09. Found: C, 54.13; H, 5.03; N, 9.33.

1. customThe solid was collected
2. washwashed with water
3. customair-dried
4. customThe crude solid was purified by silica-gel (30 ml) column chromatography with CHCl3-EtOH (98:2
5. customv/v) as eluent and crystallized with Et2O