反応 #866

ord-b4a1a9f06c874053b3ad0f85aaa15884

反応方程式

CC[C@H](NC(=O)[C@H](NC(=O)[C@@H](NC(=O)OCc1ccccc1)C(Cc1ccccc1)C(=O)O)[C@H](C)CC)c1ccccc1
N-benzyloxycarbonyl-β-benzyl-L-aspartyl-D-isoleucine (S)-α-ethylbenzylamide
CC[C@H](NC(=O)[C@H](NC(=O)[C@@H](N)CC(=O)O)[C@H](C)CC)c1ccccc1
α-L-aspartyl-D-isoleucine (S)-α-ethylbenzylamide
収率 72.3%

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    その他The catalyst was removed by filtration
  2. 2
    濃縮the resulting filtrate was concentrated under reduced pressure
  3. 3
    その他The crystals thus precipitated
  4. 4
    ろ過were taken out by filtration
  5. 5
    その他dried

実験手順

To a suspension of 2.81 g (4.7 mmols) of N-benzyloxycarbonyl-β-benzyl-L-aspartyl-D-isoleucine (S)-α-ethylbenzylamide in 150 ml of methanol and 50 ml of water was added 2.0 g of 10% Pd-carbon (water content 50%). The mixture was reduced under hydrogen at room temperature for 5 hours. The catalyst was removed by filtration, and the resulting filtrate was concentrated under reduced pressure to be 20 ml. The crystals thus precipitated were taken out by filtration and dried to obtain 1.22 g (3.4 mmols) of α-L-aspartyl-D-isoleucine (S)-α-ethylbenzylamide.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US05723165uspto-grants-1998_03