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

HRID 1250975

반응식

HRID 1250975 반응식
[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]

참가 물질

6

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-11d68de30dd44b44ae1a211a73b53cb8
출처 데이터셋
uspto-grants-2002_01
특허 번호
US06340746B1

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