Hydrochloric Acid → 4-[4,4-Bis(4-fluorophenyl)butyl]-2-piperazinemethanol

HRID 35331노트

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HRID 35331 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:23]2[CH:28]=[CH:27][C:26]([F:29])=[CH:25][CH:24]=2)[CH2:9][CH2:10][CH2:11][N:12]2[CH2:17][CH2:16][N:15]3C(C)(C)[O:19][CH2:20][CH:14]3[CH2:13]2)=[CH:4][CH:3]=1.Cl>O>[F:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([C:23]2[CH:24]=[CH:25][C:26]([F:29])=[CH:27][CH:28]=2)[CH2:9][CH2:10][CH2:11][N:12]2[CH2:17][CH2:16][NH:15][CH:14]([CH2:20][OH:19])[CH2:13]2)=[CH:4][CH:3]=1

참가 물질

4

실험 절차

A mixture of 34 parts of 7-[4,4-bis(4-fluorophenyl)butyl]hexahydro-3,3-dimethyl-1H-oxazolo[3,4-a]pyrazine and 272 parts of a hydrochloric acid solution 0.5N in water was stirred and refluxed for 2 hours. The reaction mixture was cooled to room temperature and the product was extracted twice with 1,1'-oxybisethane. The aqueous phase was separated, alkalized and salted out with sodium carbonate. The product was extracted with trichloromethane. The extract was dried, filtered and evaporated. The residue was purified by column-chromatography over silica gel using a mixture of trichloromethane and methanol (85:15 by volume), saturated with ammonia as eluent. The pure fractions were collected and the eluent was evaporated, yielding 17.0 parts of 4-[4,4-bis(4-fluorophenyl)butyl]-2-piperazinemethanol as an oily residue (intermediate 100).

후처리

  1. temperaturerefluxed for 2 hours
  2. extractionthe product was extracted twice with 1,1'-oxybisethane
  3. customThe aqueous phase was separated
  4. extractionThe product was extracted with trichloromethane
  5. customThe extract was dried
  6. filtrationfiltered
  7. customevaporated
  8. customThe residue was purified by column-chromatography over silica gel using
  9. additiona mixture of trichloromethane and methanol (85:15 by volume)
  10. customThe pure fractions were collected
  11. customthe eluent was evaporated

출처 및 근거

ORD 기록
ord-d0945cbf0d6f4484adc377c2d8f76bb2
출처 데이터셋
uspto-grants-1988_08
특허 번호
US04766125

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