반응식
N(C(OCC1C2C(=CC=CC=2)C2C1=CC=CC=2)=O)[C@H:2]([C:4](O)=[O:5])C.O.O[N:26]1[C:30]2[CH:31]=[CH:32][CH:33]=CC=2N=N1.C[N:36]1[CH2:41][CH2:40][O:39]CC1.Cl.C[N:44](C)CCCN=C=NCC.[C:54]([O:57]CC)(=[O:56])[CH3:55]>ClCCl>[CH3:2][C@@H:4]([OH:5])[C@H:55]([NH:44][C:40]([C@@H:41]([NH2:36])[CH2:33][CH2:32][CH2:31][CH2:30][NH2:26])=[O:39])[C:54]([OH:57])=[O:56]참가 물질
반응물 5
생성물 1
시약·촉매·용매 1
실험 절차
Amine 6 (790 mg, 1.68 mmol) and Fmoc-Ala-OH (578 mg, 1.86 mmol) were dissolved in 40 mL of dry dichloromethane. 1-Hydroxybenzotriazole hydrate (342 mg, 2.53 mmol) was added to this solution, followed by the addition of 4-methylmorpholine (0.30 mL, 2.7 mmol) and 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (391 mg, 2.04 mmol), and the resulting mixture was stirred at room temperature for 16 hours. The reaction mixture was diluted with ethyl acetate, washed once with saturated aqueous ammonium chloride solution, once with saturated aqueous sodium bicarbonate solution, once with brine, dried (MgSO4), and concentrated. The crude product was purified by flash chromatography on silica gel, eluting with 40% ethyl acetate-hexanes, to give 1.17 g (91%) of 7 as a white solid. 1H-NMR (300 MHz, CDCl3): d 7.76 (d, J=7 Hz, 2H), 7.62-7.55 (m, 2H), 7.40 (t, J=7 Hz, 2H), 7.35-7.28 (m, 7H), 6.95-6.46 (m, 2H), 5.45-5.25 (m, 1H), 5.11-5.05 (m, 2H), 4,75-4.30 (m, 5H), 4.28-4.04 (m, 4H), 3.94-3.76 (m, 1H), 3.50-3.36 (m, 1H), 2.95-2.61 (m, 2H), 1.82-1.65 (m, 2H), 1.54-1.41 (m, 4H), 1.39-1.32 (m, 3H).
후처리
- washwashed once with saturated aqueous ammonium chloride solution, once with saturated aqueous sodium bicarbonate solution, once with brine
- dry with materialdried (MgSO4)
- concentrationconcentrated
- customThe crude product was purified by flash chromatography on silica gel
- washeluting with 40% ethyl acetate-hexanes
출처 및 근거
- ORD 기록
- ord-89516119c5ee4a1b8255400dc49c95b6
- 출처 데이터셋
- uspto-grants-2004_09
- 특허 번호
- US06790989B2
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