Thionyl Chloride → 5-chloro-5-(4,6-dimethoxy-2-pyrimidinyl)furo[3,4-b]pyridine-7(5H)-one
反応式
[CH3:1][O:2][C:3]1[CH:8]=[C:7]([O:9][CH3:10])[N:6]=[C:5]([C:11]([C:13]2[C:14]([C:19]([OH:21])=[O:20])=[N:15][CH:16]=[CH:17][CH:18]=2)=O)[N:4]=1.S(Cl)([Cl:24])=O>C(Cl)(Cl)(Cl)Cl>[Cl:24][C:11]1([C:5]2[N:6]=[C:7]([O:9][CH3:10])[CH:8]=[C:3]([O:2][CH3:1])[N:4]=2)[C:13]2[C:14](=[N:15][CH:16]=[CH:17][CH:18]=2)[C:19](=[O:20])[O:21]1参加物
4
反応条件
- 温度
- 70 °C
実験手順
45.53 g of 3-[(4,6-dimethoxy-2-pyrimidinyl)carbonyl]-2-pyridinecarboxylic acid are suspended in 700 ml of carbon tetrachloride and 186.4 g of thionyl chloride added with stirring. The suspension is heated to 70° C. for 4 hrs and the reaction mixture then cooled to RT and the excess thionyl chloride and carbon tetrachloride evaporated off to give the title compound as a tan solid m.p. 146°-148° C.
後処理
- temperaturethe reaction mixture then cooled to RT
- customthe excess thionyl chloride and carbon tetrachloride evaporated off
出典と根拠
- ORDレコード
- ord-6323326f8c8d463085a4014cdd0b22a7
- 出典データセット
- uspto-grants-1996_10
- 特許番号
- US05561101
反応ノート
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