O-(Tetrahydropyran-2-yl)hydroxylamine → HCID 76652338、化合物
反応式
[CH2:1]([CH:8]1[CH2:12][O:11][C:10](=[O:13])[N:9]1[C:14](=[O:23])[C:15]([CH2:17][CH:18]1[CH2:22][CH2:21][CH2:20][CH2:19]1)=[CH2:16])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[O:24]1[CH2:29][CH2:28][CH2:27][CH2:26][CH:25]1[O:30][NH2:31]>>[CH2:1]([CH:8]1[CH2:12][O:11][C:10](=[O:13])[N:9]1[C:14](=[O:23])[CH:15]([CH2:17][CH:18]1[CH2:19][CH2:20][CH2:21][CH2:22]1)[CH2:16][NH:31][O:30][CH:25]1[CH2:26][CH2:27][CH2:28][CH2:29][O:24]1)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
3
反応条件
- 温度
- 45 °C
実験手順
4-Benzyl-3-(2-cyclopentylmethyl-acryloyl)-oxazolidin-2-one (22.90 g, 73.1 mmol) and O-(tetrahydro-2H-pyran-2-yl)-hydroxylamine (34.24 g, 292.3 mmol) is combined at stirred at 45° C. for 48 hours under nitrogen. The crude product is purified by flash chromatography (SiO2, 0→30% EtOAc in hexane), which gives 4-benzyl-3-[2-cyclopentylmethyl-3-(tetrahydro-pyran-2-yloxyamino)-propionyl]-oxazolidin-2-one (21.65 g, 69% yield) as an oil.
後処理
- customThe crude product is purified by flash chromatography (SiO2, 0→30% EtOAc in hexane), which