Hydrochloric Acid → 3-[4-(5-Bromo-3,3-dimethyl-2-oxo-2,3-dihydroindol-1-ylmethoxy)phenyl]hex-4-ynoic acid

HRID 40484ノート

反応式

HRID 40484 の反応式
[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH2:11][O:12][C:13]1[CH:18]=[CH:17][C:16]([CH:19]([C:25]#[C:26][CH3:27])[CH2:20][C:21]([O:23]C)=[O:22])=[CH:15][CH:14]=1)[C:6](=[O:28])[C:5]2([CH3:30])[CH3:29].Cl.O>C1COCC1.CO>[Br:1][C:2]1[CH:3]=[C:4]2[C:8](=[CH:9][CH:10]=1)[N:7]([CH2:11][O:12][C:13]1[CH:18]=[CH:17][C:16]([CH:19]([C:25]#[C:26][CH3:27])[CH2:20][C:21]([OH:23])=[O:22])=[CH:15][CH:14]=1)[C:6](=[O:28])[C:5]2([CH3:30])[CH3:29]

参加物

5

実験手順

730 mg of methyl 3-[4-(5-bromo-3,3-dimethyl-2-oxo-2,3-dihydroindol-1-ylmethoxy)phenyl]-hex-4-ynoate were dissolved in a mixture of THF/MeOH/2N NaOH=1:1:1 (5 ml of each) and stirred at room temperature. After 1 hour, the mixture was acidified to pH 1 by addition of 2N HCl. 50 ml of water were added, the mixture was extracted three times with 50 ml each time of ethyl acetate. The combined organic phases were dried over MgSO4, then concentrated under reduced pressure and purified on silica gel with the n-heptane/ethyl acetate solvent mixture as a linear gradient of 100% n-heptane=>100% ethyl acetate. This gave 620 mg of 3-[4-(5-bromo-3,3-dimethyl-2-oxo-2,3-dihydroindol-1-ylmethoxy)phenyl]-hex-4-ynoic acid.

後処理

  1. extractionthe mixture was extracted three times with 50 ml each time of ethyl acetate
  2. dry with materialThe combined organic phases were dried over MgSO4
  3. concentrationconcentrated under reduced pressure
  4. custompurified on silica gel with the n-heptane/ethyl acetate solvent mixture as a linear gradient of 100% n-heptane=>100% ethyl acetate

出典と根拠

ORDレコード
ord-f6ccd08ef508492a833a623e6c26aacb
出典データセット
uspto-grants-2013_09
特許番号
US08530413B2

反応ノート

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