反応式
[CH2:1]([C:3]1[N:8]=[CH:7][C:6]([CH2:9]O)=[CH:5][CH:4]=1)[CH3:2].C1(P([N:25]=[N+:26]=[N-:27])(C2C=CC=CC=2)=O)C=CC=CC=1.N12CCCN=C1CCCCC2.O>C1(C)C=CC=CC=1.C(OCC)(=O)C>[CH2:1]([C:3]1[N:8]=[CH:7][C:6]([CH2:9][N:25]=[N+:26]=[N-:27])=[CH:5][CH:4]=1)[CH3:2]参加物
7
実験手順
After dissolving (6-ethyl-3-pyridyl)methanol (2.25 g, 16.4 mmol) in toluene (25 ml), diphenylphosphoryl azide (4.2 ml, 19.6 mmol) and 1,8-diazabicyclo[5.4.0]undec-7-ene (2.9 ml, 19.6 mmol) were added while stirring on ice, and the mixture was further stirred at room temperature for 18 hours. Water was added for treatment and extraction was performed with ethyl acetate. The extract was washed with brine and then dried over sodium sulfate and filtered. The filtrate was concentrated under reduced pressure and the residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate) to yield the title compound (2.2 g) as a yellow oil. (84.5% yield)
後処理
- additionwere added
- stirringthe mixture was further stirred at room temperature for 18 hours
- washThe extract was washed with brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationThe filtrate was concentrated under reduced pressure
- customthe residue was purified by silica gel column chromatography (solvent: n-hexane-ethyl acetate)
出典と根拠
- ORDレコード
- ord-6bcd0e354ba34994a837ebd5e87e3c84
- 出典データセット
- uspto-grants-2007_07
- 特許番号
- US07244730B2
関連ノート
読み込み中…