反応式
[N:1]1[CH:6]=[C:5]([C:7]([OH:9])=[O:8])[CH:4]=[C:3]([C:10]([OH:12])=[O:11])[CH:2]=1.S(Cl)([Cl:15])=O.[CH3:17]O>>[ClH:15].[CH3:17][O:8][C:7]([C:5]1[CH:6]=[N:1][CH:2]=[C:3]([C:10]([OH:12])=[O:11])[CH:4]=1)=[O:9]参加物
4
実験手順
Pyridine-3,5-dicarboxylic acid (5.00 g, 29.9 mmol) was stirred in CH3OH (100 mL), cooled in an ice bath, and treated dropwise with thionyl chloride (17.45 mL, 239.2 mmol). After 0.5 hr, the reaction mixture was refluxed for 48 hrs. Concentration to dryness gave the title compound as an off-white solid.
後処理
- temperaturecooled in an ice bath
- temperaturethe reaction mixture was refluxed for 48 hrs
- concentrationConcentration to dryness
出典と根拠
- ORDレコード
- ord-1b62a4aa5e3545ef8cc070eb914f7418
- 出典データセット
- uspto-grants-2000_10
- 特許番号
- US06127366
関連ノート
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