Water → HCID 131716563, 화합물

HRID 2051212노트

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HRID 2051212 반응식
[OH:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]2[CH:14]=[CH:13][N:12]=[CH:11][CH:10]=2)=[CH:4][CH:3]=1.[C:15](=[O:18])([O-:17])[O-:16].[K+].[K+].Cl[CH2:22][CH2:23][CH2:24][N:25]([CH2:30][CH2:31][CH2:32][CH3:33])[CH2:26][CH2:27][CH2:28][CH3:29].[OH2:34]>CS(C)=O>[C:2]([OH:1])(=[O:34])[C:15]([OH:17])=[O:18].[C:15]([OH:16])(=[O:18])[C:2]([OH:1])=[O:34].[CH2:30]([N:25]([CH2:26][CH2:27][CH2:28][CH3:29])[CH2:24][CH2:23][CH2:22][O:1][C:2]1[CH:3]=[CH:4][C:5]([S:8][C:9]2[CH:14]=[CH:13][N:12]=[CH:11][CH:10]=2)=[CH:6][CH:7]=1)[CH2:31][CH2:32][CH3:33]

참가 물질

6

실험 절차

A solution of 0.014 mol of 4-(4-hydroxy-phenylthio)pyridine and 3 g of finely crushed anhydrous potassium carbonate in 50 ml of dimethylsulphoxide was placed under stirring for 30 min. To this medium 0.016 mol of 1-chloro-3-(di-n-butylamino)propane was added and the stirring was maintained at room-temperature for 24 hours. The reaction medium was poured into water and extracted with ethyl ether. The organic phase was washed with water, dried on sodium sulphate and filtered. After the solvent was evaporated off, an oil was provided which was purified by chromatography on a silica column (eluent:methanol). The required compound in free base form so obtained was then transformed into an oxalate by adding an ethereal solution of oxalic acid.

후처리

  1. temperaturethe stirring was maintained at room-temperature for 24 hours
  2. extractionextracted with ethyl ether
  3. washThe organic phase was washed with water
  4. customdried on sodium sulphate
  5. filtrationfiltered
  6. customAfter the solvent was evaporated off
  7. customan oil was provided which
  8. customwas purified by chromatography on a silica column (eluent:methanol)

출처 및 근거

ORD 기록
ord-994493ffdbeb4b758d4332ef7be9e506
출처 데이터셋
uspto-grants-1991_05
특허 번호
US05017579

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