Triethylamine → 2-(2-Phthalimidoethylthio)pyridine

HRID 6084

反応式

HRID 6084 の反応式
C(N(CC)CC)C.[SH:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=1.Br[CH2:16][CH2:17][N:18]1[C:22](=[O:23])[C:21]2=[CH:24][CH:25]=[CH:26][CH:27]=[C:20]2[C:19]1=[O:28]>C(O)C>[C:19]1(=[O:28])[N:18]([CH2:17][CH2:16][S:8][C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][N:10]=2)[C:22](=[O:23])[C:21]2=[CH:24][CH:25]=[CH:26][CH:27]=[C:20]12

参加物

5

反応物 3

HCID 8471TriethylamineHCID 113251H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-HCID 178418616HCID 178418616、化合物

生成物 1

HCID 152314802-(2-Phthalimidoethylthio)pyridine収率 46.9%

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

Triethylamine [12.54 ml (90 mmol)] was added to a suspension of 6.67 g (60 mmol) of 2-mercaptopyridine and 15.24 g (60 mmol) of N-(2-bromoethyl)phthalimide in 200 ml of ethanol and stirred at room temperature for 24 hours. The mixture was heated under reflux for 2 hours. The solvent was distilled off, chloroform was added to the residue, and the mixture was washed with water and dried over anhydrous magnesium sulfate. The solvent was distilled off and the residue was purified by column chromatography (eluent: ethyl acetate/n-hexane=1:2) to obtain 8.00 g of the desired compound (46.9%, colorless crystals).

後処理

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 2 hours
  3. distillationThe solvent was distilled off
  4. additionchloroform was added to the residue
  5. washthe mixture was washed with water
  6. dry with materialdried over anhydrous magnesium sulfate
  7. distillationThe solvent was distilled off
  8. customthe residue was purified by column chromatography (eluent: ethyl acetate/n-hexane=1:2)

出典と根拠

ORDレコード
ord-515189e1fb57456dae58a0ec857392d2
出典データセット
uspto-grants-1993_09
特許番号
US05246948

関連ノート

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