Potassium Carbonate → (n',n'-Dimethyl-3-aminopropyl)-2-thiazolidinone

HRID 1760149

反応式

HRID 1760149 の反応式
[S:1]1[CH2:5][CH2:4][NH:3][C:2]1=[O:6].C(=O)([O-])[O-].[K+].[K+].Cl.[CH3:14][N:15]([CH3:20])[CH2:16][CH2:17][CH2:18]Cl.C1OCCOCCOCCOCCOCCOC1>C(#N)C>[CH3:14][N:15]([CH3:20])[CH2:16][CH2:17][CH2:18][N:3]1[CH2:4][CH2:5][S:1][C:2]1=[O:6]

参加物

6

実験手順

To a solution of 2-thiazolidinone (4.15 g, 40.18 mmol) in acetonitrile (60 ml) were added potassium carbonate (13.3 g 96.2 mmol), N,N-dimethyl-3-aminopropyl chloride hydrochloride (7.63 g, 48.3 mmol), and 18-crown-6 (catalytic amount). The mixture was refluxed for 18 hours, solvent removed in vacuo, then redissolved in dichloromethane and 1 M potassium chloride (40 ml each). The aqueous phase was isolated and extracted twice with 30 ml portions of dichloromethane. The combined organic fraction was washed with saturated sodium chloride (˜50 ml), dried over sodium sulfate, filtered, and dried in vacuo. The crude product was purified via silica gel chromatography, using a 10:1 ratio of silica gel A, 200˜425 mesh, and eluting with 5% methanol in chloroform, yielding 1.15 g (15%) pure product.

後処理

  1. temperatureThe mixture was refluxed for 18 hours
  2. customsolvent removed in vacuo
  3. dissolutionredissolved in dichloromethane
  4. customThe aqueous phase was isolated
  5. extractionextracted twice with 30 ml portions of dichloromethane
  6. washThe combined organic fraction was washed with saturated sodium chloride (˜50 ml)
  7. dry with materialdried over sodium sulfate
  8. filtrationfiltered
  9. customdried in vacuo
  10. customThe crude product was purified via silica gel chromatography
  11. washeluting with 5% methanol in chloroform

出典と根拠

ORDレコード
ord-9f8a8db7b9af4582ad38538ff79a6e7d
出典データセット
uspto-grants-2005_01
特許番号
US06841536B2

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