HCID 69060787、化合物 → Ethyl 1-ethyl-6-hydroxy-1H-indole-3-acetate

HRID 490761ノート

反応式

HRID 490761 の反応式
[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

3

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

  1. customthen purged
  2. additionback filled with nitrogen a few times
  3. additionPalladium on carbon (10%) (0.200 g, 20% by wt.) is added
  4. temperatureby heating to reflux
  5. additionaddition of a saturated solution of sodium hypophosphite
  6. customAfter the starting material is completely consumed
  7. additiondiluted with dichloromethane and celite
  8. additionadded
  9. filtrationThe mixture is filtered through a plug of celite
  10. customthe two phases are separated
  11. washThe organic layer is washed with water and brine
  12. dry with materialdried over sodium sulfate
  13. concentrationconcentrated
  14. 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

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