反応式
C(OC([CH:6]1[C:11](=[O:12])[CH2:10][CH2:9][N:8]([N:13]2[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]2)[C:7]1=[O:19])=O)C>C(O)(=O)C>[N:8]1([N:13]2[CH2:18][CH2:17][CH2:16][CH2:15][CH2:14]2)[CH2:9][CH2:10][C:11](=[O:12])[CH2:6][C:7]1=[O:19]参加物
3
実験手順
The oil from step 3 was dissolved in 10% acetic acid (250 ml) and the solution boiled under reflux for one hour. The cooled reaction mixture was evaporated, and the residue purified by flash chromatography (CH2Cl2: acetone 9:1-1:1) to give 4.00 g (36%) of the title compound as a semi-solid.
後処理
- temperatureunder reflux for one hour
- customThe cooled reaction mixture
- customwas evaporated
- customthe residue purified by flash chromatography (CH2Cl2: acetone 9:1-1:1)
出典と根拠
- ORDレコード
- ord-62d2233258984e9c83d1c3131e64da14
- 出典データセット
- uspto-grants-2011_01
- 特許番号
- US07875626B2
関連ノート
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