Potassium Hydroxide → 2-(2-Tert-butoxycarbonylamino-pyridin4-ylmethyl)-malonic acid monoethyl ester

HRID 1789797

反応式

HRID 1789797 の反応式
[OH-].[K+].[CH2:3]([O:5][C:6](=[O:28])[CH:7]([CH2:13][C:14]1[CH:19]=[CH:18][N:17]=[C:16]([NH:20][C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH:15]=1)[C:8]([O:10]CC)=[O:9])[CH3:4]>C(O)C.C(Cl)Cl>[CH2:3]([O:5][C:6](=[O:28])[CH:7]([CH2:13][C:14]1[CH:19]=[CH:18][N:17]=[C:16]([NH:20][C:21]([O:23][C:24]([CH3:27])([CH3:26])[CH3:25])=[O:22])[CH:15]=1)[C:8]([OH:10])=[O:9])[CH3:4]

参加物

5

実験手順

A solution of KOH (0.19 g, 3.43 mmol) in ethanol (5 mL) was added to a solution of 2-(2-tert-butoxycarbonylamino-pyridin4-ylmethyl)-malonic acid diethyl ester (1.20 g, 3.27 mmol) in ethanol (5 mL) and methylene chloride (5 mL) at 0° C. The mixture was stirred for 18 h at room temperature. The mixture was concentrated under reduced pressure and water was added to the residue. The aqueous layer was washed with diethyl ether, acidified to pH 4 by 1M HCl, and extracted with methylene chloride. The organic layer was washed with water, brine and dried. After filtration and evaporation in vacuo, the crude product was purified by flash chromatography (CH3OH/CH2Cl2, 1:20) to yield 2-(2-tert-butoxycarbonylamino-pyridin4-ylmethyl)-malonic acid monoethyl ester (0.90 g, 81%).

後処理

  1. concentrationThe mixture was concentrated under reduced pressure and water
  2. additionwas added to the residue
  3. washThe aqueous layer was washed with diethyl ether
  4. extractionextracted with methylene chloride
  5. washThe organic layer was washed with water, brine
  6. customdried
  7. filtrationAfter filtration and evaporation in vacuo
  8. customthe crude product was purified by flash chromatography (CH3OH/CH2Cl2, 1:20)

出典と根拠

ORDレコード
ord-d245cc3b73f8448fb111e6ba4a53d5dd
出典データセット
uspto-grants-2006_07
特許番号
US07071175B1

関連ノート

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