Pyridine → L-Tryptophanamide
反応式
Cl.CO[C:4](=[O:17])[C@H:5]([CH2:7][C:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[NH:10][CH:9]=1)[NH2:6].[N:18]1C=CC=CC=1>ClCCl>[NH2:6][C@H:5]([C:4]([NH2:18])=[O:17])[CH2:7][C:8]1[C:16]2[C:11](=[CH:12][CH:13]=[CH:14][CH:15]=2)[NH:10][CH:9]=1参加物
4
実験手順
A solution of the active ester VIII (0.035 g, 0.06 mmol), L-tryptophan methyl ester hydrochloride (0.049 g, 0.19 mmol) and pyridine (0.015 g, 0.19 mmol) in dichloromethane (20 ml) was stirred overnight. The solvent was removed under reduced pressure and the residue purified by column chromatography (ethyl acetate elution) to yield the trytophan amide as a dark red crystalline solid.
後処理
- customThe solvent was removed under reduced pressure
- customthe residue purified by column chromatography (ethyl acetate elution)
出典と根拠
- ORDレコード
- ord-1b4fd1c1137a43baa4c47018ac7cf7d7
- 出典データセット
- uspto-grants-2000_12
- 特許番号
- US06166202
反応ノート
読み込み中…