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Water → 4-[2-(2-Pyrimidinylamino)ethoxy]benzaldehyde

HRID 2119911
ノート
印刷プレビュー

反応式

HRID 2119911 の反応式
[H-].[Na+].[N:3]1[CH:8]=[CH:7][CH:6]=[N:5][C:4]=1[NH:9][CH2:10][CH2:11][OH:12].F[C:14]1[CH:21]=[CH:20][C:17]([CH:18]=[O:19])=[CH:16][CH:15]=1.O>CN(C=O)C>[N:3]1[CH:8]=[CH:7][CH:6]=[N:5][C:4]=1[NH:9][CH2:10][CH2:11][O:12][C:14]1[CH:21]=[CH:20][C:17]([CH:18]=[O:19])=[CH:16][CH:15]=1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 962WaterHCID 24758Sodium hydrideHCID 680234-FluorobenzaldehydeHCID 5727142-(Pyrimidin-2-ylamino)ethanol

生成物 1

HCID 100146614-[2-(2-Pyrimidinylamino)ethoxy]benzaldehyde

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
80 °C

実験手順

Sodium hydride (1.2 g; 60% dispersion in oil) was added portionwise to a stirred solution of 2-(2-pyrimidinyl amino)ethanol (4 g) in DMF (140 ml) under an atmosphere of nitrogen. After the vigorous reaction had subsided 4-fluorobenzaldehyde (5.35 g) was added and the solution heated to 80° C. for 20 hours. After cooling the mixture was added to water (500 ml) and extracted with diethyl ether (3×300 ml). The organic extracts were washed with brine (2×200 ml), dried (MgSO4), filtered and evaporated to dryness. Chromatography of the residue on silica gel in 2% methanol in dichloromethane afforded the title compound, which was used in the next stage without further purification.

後処理

  1. customAfter the vigorous reaction
  2. additionwas added
  3. temperatureAfter cooling the mixture
  4. extractionextracted with diethyl ether (3×300 ml)
  5. washThe organic extracts were washed with brine (2×200 ml)
  6. dry with materialdried (MgSO4)
  7. filtrationfiltered
  8. customevaporated to dryness

出典と根拠

ORDレコード
ord-7383a4a712fd4002a2559ac4d0f2a248
出典データセット
uspto-grants-2004_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06686475B2

反応ノート

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