反応式
[CH2:1]([C:3]1[N:4]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:5]2[C:10]([C:11](=O)[N:12]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH3:2].COC1C=CC(P2(SP(C3C=CC(OC)=CC=3)(=S)S2)=[S:29])=CC=1>C1(C)C=CC=CC=1>[CH2:1]([C:3]1[N:4]([C:14]2[CH:19]=[CH:18][CH:17]=[CH:16][CH:15]=2)[C:5]2[C:10]([C:11](=[S:29])[N:12]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2)[CH3:2]参加物
4
実験手順
1.50 g (5.99 mmol) 2-ethyl-1-phenyl-1H-quinazolin-4-one and 2.42 g (5.99 mmol) Lawesson's reagent (C14H14O2P2S4, Fluka) were suspended in 40 ml toluene and boiled for 1 h. After evaporation the crude mixture was purified by column chromatography on silica gel, eluent dichloromethane/acetone 95/5.
後処理
- customAfter evaporation the crude mixture
- customwas purified by column chromatography on silica gel, eluent dichloromethane/acetone 95/5
出典と根拠
- ORDレコード
- ord-551f6864684842a4b28a5737d7b2c144
- 出典データセット
- uspto-grants-2011_11
- 特許番号
- US08058431B2
関連ノート
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