4-[3-(Methylsulfanyl)phenyl]-1-propylpiperidin-4-ol → 4-[3-(Methylsulfanyl)phenyl]-1-propyl-1,2,3,6-tetrahydro-pyridine

HRID 2280367노트

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HRID 2280367 반응식
[CH3:1][S:2][C:3]1[CH:4]=[C:5]([C:9]2(O)[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][CH3:17])[CH2:11][CH2:10]2)[CH:6]=[CH:7][CH:8]=1>FC(F)(F)C(O)=O>[CH3:1][S:2][C:3]1[CH:4]=[C:5]([C:9]2[CH2:14][CH2:13][N:12]([CH2:15][CH2:16][CH3:17])[CH2:11][CH:10]=2)[CH:6]=[CH:7][CH:8]=1

참가 물질

3

실험 절차

4-(3-Methylsulfanyl-phenyl)-1-propyl-piperidin-4-ol (1) (100 mg, 0.38 mmol) was dissolved in 2 mL of trifluoroacetic acid (TFA) in a 50 mL flask while stirring in a nitrogen atmosphere. The reaction mixture was heated to reflux on an isomantle. After 15 minutes the reaction mixture was cooled to room temperature. The TFA was removed by distillation under reduced pressure. The remaining brown oil was dissolved in diethyl ether, washed 3 times with water and once with brine. The aqueous layers and brine layer were collected, basified with Na2CO3 and extracted with diethyl ether twice. The organic layers were collected, dried on MgSO4, filtered and the solvent was evaporated under reduced pressure using a rotavapor. Yield: 103 mg (111%). GCMS (EI): m/z 247 (M+), 218 (M−29); GC (100-320° C., 15° C./min): 7.6 min.

후처리

  1. temperatureThe reaction mixture was heated
  2. temperatureto reflux on an isomantle
  3. customThe TFA was removed by distillation under reduced pressure
  4. dissolutionThe remaining brown oil was dissolved in diethyl ether
  5. washwashed 3 times with water
  6. customThe aqueous layers and brine layer were collected
  7. extractionextracted with diethyl ether twice
  8. customThe organic layers were collected
  9. customdried on MgSO4
  10. filtrationfiltered
  11. customthe solvent was evaporated under reduced pressure
  12. customGC (100-320° C., 15° C./min)
  13. custom7.6 min.

출처 및 근거

ORD 기록
ord-18dd3df15804462e86125706e3c70c57
출처 데이터셋
uspto-grants-2015_09
특허 번호
US09139525B2

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