反应详情

To a stirred mixture 4-cyclopentyl-4-oxo-2-benzylsulfonylmethyl-butyric acid (169.5 mg, 0.5 mmol), 2-amino-1-(5-ethyl-1,3,4-oxadiazole-2-yl)-1-pentanol HCl salt (117.5 mg), and HOBt (91.8 mg, 0.6 mmol) in MeCl2 5 ml), was added EDC (144 mg, 0.75 mmol) and N-methylmorpholine (0.3 ml) at room temperature. After stirring for 14 hours, the reaction mixture was extracted with ethyl acetate. The organic layer was washed with saturated NaHCO3, brine, dried with MgSO4 and concentrated to yield 240 mg of crude product. The crude product was treated with Dess-Martin periodinane (343 mg, 0.693 mmol) at room temperature in 5 mls of MeCl2. After stirring for 1 hour, 5 mls of saturated Na2S2O3—NaHCO3 were added. After a further 0.5 hours, the reaction mixture was extracted with ethyl acetate, washed with brine, dried with MgSO4 and concentrated. The residue was purified with silica gel column chromatography to yield 145 mg of N-[1-(5-Ethyl-[1,3,4]oxadiazole-2-carbonyl)-butyl]-4-oxo-2-benzylsulfonyl-methyl-4-pyrrolidin-1-yl-butyramide; H1NMR(DMSO-d): 8.85 (½H, d, NH, diastereomeric), 8.78 (½H, d, NH, diastereomeric), 7.5–7.3(5H, m), 5.1–4.95(1H, m), 4.5–4.3 (2H, m), 3.5–3.2 (8H, m), 3.2–3(1H, m), 2.82(2H, m), 2–1.8(6H, m), 1.6–1.3(2H, m), 1.24(3H, m), 0.9–0.8(3H, m); MS: 518.2(M−1), 519.7 (M+1).

1. extractionthe reaction mixture was extracted with ethyl acetate
2. washThe organic layer was washed with saturated NaHCO3, brine
3. dry with materialdried with MgSO4
4. concentrationconcentrated
5. customto yield 240 mg of crude product
6. stirringAfter stirring for 1 hour
7. waitAfter a further 0.5 hours
8. extractionthe reaction mixture was extracted with ethyl acetate
9. washwashed with brine
10. dry with materialdried with MgSO4
11. concentrationconcentrated
12. customThe residue was purified with silica gel column chromatography