Ethyl diazoacetate → HCID 90177064、化合物
反応式
[CH:1]([C:3]1[CH:12]=[CH:11][C:10]2[CH2:9][CH2:8][CH2:7][CH2:6][C:5]=2[N:4]=1)=[CH2:2].[N+](=[CH:15][C:16]([O:18][CH2:19][CH3:20])=[O:17])=[N-]>C1(C)C=CC=CC=1>[N:4]1[C:5]2[CH2:6][CH2:7][CH2:8][CH2:9][C:10]=2[CH:11]=[CH:12][C:3]=1[CH:1]1[CH2:2][CH:15]1[C:16]([O:18][CH2:19][CH3:20])=[O:17]参加物
4
実験手順
A solution of 2 (1.6 g, 10 mmol) in toluene (50 ml) was treated with ethyl diazoacetate (1.7 g, 15 mmol) and stirred at reflux overnight. The mixture was concentrated and the residue was purified by gradient elution on silica gel (0 to 10% EtOAc in hexanes) to afford the title compound as a pale yellow oil. LRMS m/z (M+H) 246.2 found, 246.2 required.
後処理
- temperatureat reflux overnight
- concentrationThe mixture was concentrated
- customthe residue was purified by gradient elution on silica gel (0 to 10% EtOAc in hexanes)
出典と根拠
- ORDレコード
- ord-17ff61d70c34477b905a9fae1e64a74a
- 出典データセット
- uspto-grants-2016_03
- 特許番号
- US09273033B2
反応ノート
読み込み中…