HCID 69060787、化合物 → Ethyl 1-ethyl-6-hydroxy-1H-indole-3-acetate
反応式
[CH2:1]([O:3][C:4](=[O:26])[C:5]([C:7]1[C:15]2[C:10](=[CH:11][C:12]([O:16]CC3C=CC=CC=3)=[CH:13][CH:14]=2)[N:9]([CH2:24][CH3:25])[CH:8]=1)=O)[CH3:2]>O1CCOCC1>[CH2:1]([O:3][C:4](=[O:26])[CH2:5][C:7]1[C:15]2[C:10](=[CH:11][C:12]([OH:16])=[CH:13][CH:14]=2)[N:9]([CH2:24][CH3:25])[CH:8]=1)[CH3:2]参加物
実験手順
(6-Benzyloxy-1-ethyl-1H-indol-3-yl)-oxo-acetic acid ethyl ester (0.843 g, 2.40 mmol) is dissolved in anhydrous dioxane (10 mL) then purged and back filled with nitrogen a few times. Palladium on carbon (10%) (0.200 g, 20% by wt.) is added and the reaction followed by heating to reflux. Slow addition of a saturated solution of sodium hypophosphite is initiated and the reaction is monitored by TLC. After the starting material is completely consumed, the reaction is allowed to cool to room temperature, diluted with dichloromethane and celite added. The mixture is filtered through a plug of celite and the two phases are separated. The organic layer is washed with water and brine, dried over sodium sulfate, then concentrated. The residue is further purified using flash column chromatography. The (1-Ethyl-6-hydroxy-1H-indol-3-yl)-acetic acid ethyl ester (0.564 g, 2.28 mmol) is formed in 95% yield.
後処理
- customthen purged
- additionback filled with nitrogen a few times
- additionPalladium on carbon (10%) (0.200 g, 20% by wt.) is added
- temperatureby heating to reflux
- additionaddition of a saturated solution of sodium hypophosphite
- customAfter the starting material is completely consumed
- additiondiluted with dichloromethane and celite
- additionadded
- filtrationThe mixture is filtered through a plug of celite
- customthe two phases are separated
- washThe organic layer is washed with water and brine
- dry with materialdried over sodium sulfate
- concentrationconcentrated
- customThe residue is further purified
出典と根拠
- ORDレコード
- ord-3b9ec87dfb274e3286f675ec5c7b3c5c
- 出典データセット
- uspto-grants-2009_05
- 特許番号
- US07528160B2
反応ノート
読み込み中…