反応式
S(Cl)(Cl)=O.[CH3:5][O:6][C:7](=[O:16])[C:8]1[CH:13]=[C:12]([Cl:14])[CH:11]=[C:10](Cl)[N:9]=1>>[Cl:14][C:12]1[CH:13]=[C:8]([C:7]([O:6][CH3:5])=[O:16])[N:9]=[C:10]([C:7]([O:6][CH3:5])=[O:16])[CH:11]=1参加物
3
反応条件
- 温度
- 80 °C
実験手順
N-Ethyl-4-pyridone-2,6-dicarboxylic acid, prepared in Step A of Example 36, was treated with thionyl chloride and heated at 80° C. as described in the literature. The excess thionyl chloride was removed under reduced pressure and the remaining residue was cooled to 0° C. The product was slowly poured into cold methanol with vigorous stirring. The solvent was then removed in vacuo and the crude product was purified by silica gel column chromatography. Two products were isolated: the higher Rf product was 4,6-dichloropicolinic acid methyl ester while the lower Rf product was the title compound.
後処理
- customThe excess thionyl chloride was removed under reduced pressure
- temperaturethe remaining residue was cooled to 0° C
- additionThe product was slowly poured into cold methanol with vigorous stirring
- customThe solvent was then removed in vacuo
- customthe crude product was purified by silica gel column chromatography
- customTwo products were isolated
出典と根拠
- ORDレコード
- ord-5df0936f1d814e19b61d9d9b3a76914c
- 出典データセット
- uspto-grants-1999_10
- 特許番号
- US05972975
関連ノート
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