Diethyl Malonate → HCID 53978298、化合物

HRID 1789881ノート

反応式

HRID 1789881 の反応式
[C:1]([O:9][CH2:10][CH3:11])(=[O:8])[CH2:2][C:3]([O:5][CH2:6][CH3:7])=[O:4].[H-].[Na+].[C:14]([O:18][C:19](=[O:30])[NH:20][C:21]1[C:26]([Cl:27])=[CH:25][C:24]([CH2:28]Br)=[CH:23][N:22]=1)([CH3:17])([CH3:16])[CH3:15].[NH4+].[Cl-]>CN(C=O)C.O.C(Cl)Cl>[CH2:10]([O:9][C:1](=[O:8])[CH:2]([CH2:28][C:24]1[CH:23]=[N:22][C:21]([NH:20][C:19]([O:18][C:14]([CH3:17])([CH3:16])[CH3:15])=[O:30])=[C:26]([Cl:27])[CH:25]=1)[C:3]([O:5][CH2:6][CH3:7])=[O:4])[CH3:11]

参加物

7

実験手順

Diethyl malonate (1.87 ml, 12.31 mmol) was added to a suspension of NaH (0.54 g, 12.31 mmol, 55%) in dry DMF (15 ml) at −8° C. This mixture was stirred for 15 min. before it was added dropwise to a solution of (5-bromomethyl-3-chloro-pyridin-2-yl)-carbamic acid tert-butyl ester (3.30 g, 10.26 mmol) in dry DMF (50 ml) at 0° C. The resulting solution was stirred for 40 minutes at 0° C., then NH4Cl (5 ml, sat.) was added carefully. Stirring at room temperature overnight and concentration under reduced pressure gave a residue, which was dissolved in water/CH2Cl2. The aqueous layer was extracted with CH1Cl2 and the combined organic extracts were dried, filtered and concentrated under reduced pressure. Flash chromatography (1% MeOH in CH2Cl2) gave 2-(6-tert-butoxycarbonylamino-5-chloro-pyridin-3-ylmethyl)-malonic acid diethyl ester (2.45, 60%) as a sticky clear oil.

後処理

  1. stirringThe resulting solution was stirred for 40 minutes at 0° C.
  2. stirringStirring at room temperature overnight
  3. concentrationconcentration under reduced pressure
  4. customgave a residue, which
  5. extractionThe aqueous layer was extracted with CH1Cl2
  6. customthe combined organic extracts were dried
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure

出典と根拠

ORDレコード
ord-f8bd0dd4478c4b95809d11c933abc152
出典データセット
uspto-grants-2006_07
特許番号
US07071175B1

反応ノート

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