4-Methylmorpholine → Lysylthreonine

HRID 1058192ノート

反応式

HRID 1058192 の反応式
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]

参加物

7

実験手順

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, 4H), 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).

後処理

  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

出典と根拠

ORDレコード
ord-8a69d571f6cd4b5c8084fd480b1418ec
出典データセット
uspto-grants-2003_02
特許番号
US06515173B1

反応ノート

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