反応式
[C:1]([S:4][CH:5]1[CH2:10][CH2:9][N:8](C(OC(C)(C)C)=O)[CH2:7][CH2:6]1)(=[O:3])[CH3:2].C(OCC)(=O)C.[ClH:24]>C(OCC)(=O)C>[ClH:24].[C:1]([S:4][CH:5]1[CH2:10][CH2:9][NH:8][CH2:7][CH2:6]1)(=[O:3])[CH3:2]参加物
4
反応条件
- 温度
- 50 °C
実験手順
In 45 ml of ethyl acetate were dissolved 1.25 g (4.82 mmol) of 4-(acetylthio)-1-(tert-butoxycarbonyl)piperdine as described in Reference example 11, and 12.0 ml (48.2 mmol) of a 4N hydrogen chloride-ethyl acetate solution were added to the solution, followed by stirring of the resulting mixture at 50° C. for 4 hours. After cooling, the precipitated solid was collected by filtration and washed with hexane to obtain 885 mg (yield: 94%) of the desired compound as a slightly yellow powder.
後処理
- additionwere added to the solution
- temperatureAfter cooling
- filtrationthe precipitated solid was collected by filtration
- washwashed with hexane
出典と根拠
- ORDレコード
- ord-6c1c4656a7cd48f4adc4a61e0e02642c
- 出典データセット
- uspto-grants-2001_10
- 特許番号
- US06306880B1
関連ノート
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