4-Methylmorpholine → Lysylthreonine

HRID 1006729Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1006729
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]

Komponenten

7

Versuchsvorschrift

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).

Aufarbeitung

  1. washwashed once with saturated aqueous ammonium chloride solution, once with saturated aqueous sodium bicarbonate solution, once with brine
  2. dry with materialdried (MgSO4)
  3. concentrationconcentrated
  4. customThe crude product was purified by flash chromatography on silica gel
  5. washeluting with 40% ethyl acetate-hexanes

Quellen und Nachweise

ORD-Eintrag
ord-89516119c5ee4a1b8255400dc49c95b6
Quelldatensatz
uspto-grants-2004_09
Patentnummer
US06790989B2

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