反応式
[CH3:1][C:2]1[CH:11]=[C:10](O)[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1.COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:22])=CC=1.C(OCC)(=O)C.O>O1CCCC1>[CH3:1][C:2]1[CH:11]=[C:10]([SH:22])[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[N:3]=1参加物
反応条件
- 温度
- 50 °C
実験手順
A stirred suspension of 2-methylquinolin-4-ol (5.10 g, 32.0 mmol, 1.0 eq.) in tetrahydrofuran (51 mL) was heated to 50° C., and 6.5 g of Lawesson's Reagent (6.5 g, 16.0 mmol, 0.5 eq.) was added in one portion. The reaction was heated to 80° C. and stirred at that temperature for 6 hours. The reaction was poured into a hot biphasic solution of ethyl acetate (200 mL) and water (200 mL) and was vigorously stirred. A viscous orange gel precipitated from the solution. The water/ethyl acetate solution was decanted into a separating funnel and the organic layer isolated. The aqueous layer was extracted with ethyl acetate (4×200 ml), and the combined extracts were dried over magnesium sulfate. The solution was filtered and concentrated in vacuo. The resulting orange gel was purified by flash chromatography (50% EtOAc:50% petroleum ether→100% EtOAc) to yield 5a as a yellow solid (1.70 g, 30%).
後処理
- temperatureThe reaction was heated to 80° C.
- stirringwas vigorously stirred
- customA viscous orange gel precipitated from the solution
- customThe water/ethyl acetate solution was decanted into a separating funnel
- customthe organic layer isolated
- extractionThe aqueous layer was extracted with ethyl acetate (4×200 ml)
- dry with materialthe combined extracts were dried over magnesium sulfate
- filtrationThe solution was filtered
- concentrationconcentrated in vacuo
- customThe resulting orange gel was purified by flash chromatography (50% EtOAc:50% petroleum ether→100% EtOAc)
出典と根拠
- ORDレコード
- ord-8f7d3a7daea74eebb0d3c6d03ff421ef
- 出典データセット
- uspto-grants-2010_08
- 特許番号
- US07786139B2
関連ノート
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