反応式
[C@@H:1]12[N:8](C)[C@@H:5]([CH2:6][CH2:7]1)[CH2:4][CH2:3][CH2:2]2.[Cl:10]C(OC(Cl)C)=O>C1(C)C=CC=CC=1>[ClH:10].[CH:5]12[NH:8][CH:1]([CH2:7][CH2:6]1)[CH2:2][CH2:3][CH2:4]2参加物
4
反応条件
- 温度
- 120 °C
実験手順
To an oven-dried, 100-mL, round-bottomed flask was added tropane (2.5 g, 19.96 mmol) followed by toluene (20 mL), and a-chloro-ethyl chloroformate (3.2 mL, 30 mmol). The flask was purged with N2 and the mixture was heated at 120° C. for 16 h. The reaction was allowed to cool to room temperature and the solvent was evaporated in vacuo. The resulting residue was dissolved in MeOH (20 mL) and heated to reflux at 85° C. for 3 h. The solvent was evaporated in vacuo and the product dried under vacuum to give 2.90 g (98% yield) of a light brown solid. MS m/z: 112.0 (M+1). 1H NMR (DMSO-d6; 400 MHz): d 1.64 (m, 4), 1.95 (m, 6), 3.92, (s, 2), 9.24 (br d, 2, J=7.3).
後処理
- customThe flask was purged with N2
- temperatureto cool to room temperature
- customthe solvent was evaporated in vacuo
- dissolutionThe resulting residue was dissolved in MeOH (20 mL)
- temperatureheated
- temperatureto reflux at 85° C. for 3 h
- customThe solvent was evaporated in vacuo
- customthe product dried under vacuum
出典と根拠
- ORDレコード
- ord-4c1975f272a748afae93468a11dfd09a
- 出典データセット
- uspto-grants-2003_06
- 特許番号
- US06583154B1
関連ノート
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