HCID 22734278、化合物 → HCID 22734005、化合物
反応式
Cl[C:2]1[CH:3]=[N:4][CH:5]=[C:6](Cl)[C:7]=1[CH2:8][C:9]([C:11]1[C:20]2[O:19][CH2:18][CH2:17][O:16][C:15]=2[C:14]([O:21][CH3:22])=[CH:13][CH:12]=1)=[O:10].[H][H]>CN(C=O)C.[C].[Pd]>[CH3:22][O:21][C:14]1[C:15]2[O:16][CH2:17][CH2:18][O:19][C:20]=2[C:11]([C:9](=[O:10])[CH2:8][C:7]2[CH:6]=[CH:5][N:4]=[CH:3][CH:2]=2)=[CH:12][CH:13]=1参加物
実験手順
Compound 178 (1.1 g) obtained in Example 178 was dissolved in DMF (10 ml), mixed with palladium carbon (containing 50% water) (0.2 g), and stirred at room temperature for 24 hours in a hydrogen atmosphere. The reaction solution was filtered with Celite. The filtrate was mixed with saturated sodium bicarbonate water and extracted with ethyl acetate. The organic layer was washed with a saturated aqueous sodium chloride solution, dried over magnesium sulfate anhydride, and evaporated under reduced pressure for removing the solvent. The residue was purified by silica gel column chromatography (ethyl acetate) to give 2,3-dihydro-5-methoxy-8-[1-oxo-2-(4-pyridyl)ethyl]-1,4-benzodioxine (0.36 g, 41%) as colorless crystals. The thus-obtained compound was dissolved in ethyl acetate and mixed with a saturated hydrochloric acid ethyl acetate solution. The precipitated crystals were filtered and washed with ethyl acetate to give Compound 179 as colorless crystals.
後処理
- filtrationThe reaction solution was filtered with Celite
- additionThe filtrate was mixed with saturated sodium bicarbonate water
- extractionextracted with ethyl acetate
- washThe organic layer was washed with a saturated aqueous sodium chloride solution
- dry with materialdried over magnesium sulfate anhydride
- customevaporated under reduced pressure
- customfor removing the solvent
- customThe residue was purified by silica gel column chromatography (ethyl acetate)
出典と根拠
- ORDレコード
- ord-b5be4b16c4454f7facb6aaa58c2bf1f4
- 出典データセット
- uspto-grants-2004_04
- 特許番号
- US06716987B1
反応ノート
読み込み中…