Trityl chloride → 3-(Trityl-amino)-piperidin-2-one
反応式
[C:1]1([C:7](Cl)([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl.Cl.[NH2:23][CH:24]1[CH2:29][CH2:28][CH2:27][NH:26][C:25]1=[O:30].C(N(CC)CC)C>O1CCCC1>[C:7]([NH:23][CH:24]1[CH2:29][CH2:28][CH2:27][NH:26][C:25]1=[O:30])([C:14]1[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=1)([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:1]1[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1参加物
実験手順
Add triphenylmethyl chloride (35.11 g, 126.0 mmol) to a suspension of 3-amino-piperidin-2-one dihydrochloride (21.42 g, 114.5 mmol) in tetrahydrofuran (250 mL), follow by dropwise addition of triethylamine (55.9 mL, 400.8 mmol). Stir the reaction at room temperature under nitrogen overnight. Filter the mixture, wash with tetrahydrofuran, concentrate the filtrate to a yellow oil, and partition the material between 20% isopropanol/chloroform and water. Wash the organic layer with saturated aqueous sodium bicarbonate solution, brine, dry over magnesium sulfate and concentrate. Purify by flash chromatography on silica gel (eluting with 0–1.25% methanol/chloroform) which gives 18.50 g of the title compound as a white foam, 45% yield. 1H NMR: consistent with structure. MS (ion spray) 113 (M+−1).
後処理
- customthe reaction at room temperature under nitrogen overnight
- filtrationFilter the mixture
- washwash with tetrahydrofuran
- concentrationconcentrate the filtrate to a yellow oil
- custompartition the material between 20% isopropanol/chloroform and water
- washWash the organic layer with saturated aqueous sodium bicarbonate solution, brine
- dry with materialdry over magnesium sulfate
- concentrationconcentrate
- customPurify by flash chromatography on silica gel (eluting with 0–1.25% methanol/chloroform) which
出典と根拠
- ORDレコード
- ord-0e948a608d7d414db116f88fd9c6ca3f
- 出典データセット
- uspto-grants-2006_09
- 特許番号
- US07101891B2
反応ノート
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