7-(Dimethoxymethyl)-1,2,3,4-tetrahydro-1,8-naphthyridine → 5,6,7,8-Tetrahydro-1,8-naphthyridine-2-carbaldehyde
反応式
C[O:2][CH:3](OC)[C:4]1[N:9]=[C:8]2[NH:10][CH2:11][CH2:12][CH2:13][C:7]2=[CH:6][CH:5]=1>FC(F)(F)C(O)=O>[NH:10]1[C:8]2=[N:9][C:4]([CH:3]=[O:2])=[CH:5][CH:6]=[C:7]2[CH2:13][CH2:12][CH2:11]1参加物
3
実験手順
Dimethoxy-1,2,3,4-tetrahydropyridino[2,3-b]pyridin-7-ylmethane was dissolved in trifluoroacetic acid (14 mL) and stirred under nitrogen for 16 hrs. The mixture was quenched with saturated sodium bicarbonate, extracted with methylene chloride, dried over sodium sulfate, filtered, in vacuo and purified by flash chromatography (5% MeOH/CH2Cl2 ). EI-MS m/z 163 (M+H)+.
後処理
- customThe mixture was quenched with saturated sodium bicarbonate
- extractionextracted with methylene chloride
- dry with materialdried over sodium sulfate
- filtrationfiltered, in vacuo
- custompurified by flash chromatography (5% MeOH/CH2Cl2 )
出典と根拠
- ORDレコード
- ord-8f6e0f92abb04482939c2ad86e76e799
- 出典データセット
- uspto-grants-2003_02
- 特許番号
- US06514964B1
反応ノート
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