反応式
[CH2:1]([C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([C:15]([OH:17])=[O:16])[CH:13]=2)[CH:8]=[CH:7][N:6]=1)[CH2:2][CH2:3][CH3:4].S(=O)(=O)(O)O.[CH3:23]O>>[CH2:1]([C:5]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([C:15]([O:17][CH3:23])=[O:16])[CH:13]=2)[CH:8]=[CH:7][N:6]=1)[CH2:2][CH2:3][CH3:4]参加物
4
実験手順
A solution of 1-butylisoquinoline-7-carboxylic acid (325 mg, 1.41 mmol) in methanol (25 mL) containing concentrated sulfuric acid (800 μL) was refluxed overnight. The reaction mixture was then concentrated under reduced pressure, diluted with methylene chloride, washed with water, and saturated sodium chloride. The organic layer was then dried (sodium sulfate), filtered, and concentrated to yield methyl 1-butylisoquinoline-7-carboxylate (350 mg): ESI MS m/z 244 [M+H]+;
後処理
- temperaturewas refluxed overnight
- concentrationThe reaction mixture was then concentrated under reduced pressure
- additiondiluted with methylene chloride
- washwashed with water, and saturated sodium chloride
- dry with materialThe organic layer was then dried (sodium sulfate)
- filtrationfiltered
- concentrationconcentrated
出典と根拠
- ORDレコード
- ord-7a3169cd7e464668803ed69980273ac8
- 出典データセット
- uspto-grants-2010_06
- 特許番号
- US07727997B2
関連ノート
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