Hydrochloric Acid → 4-[4,4-Bis(4-fluorophenyl)butyl]-2-piperazinemethanol
反応式
[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]=1参加物
実験手順
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).
後処理
- temperaturerefluxed for 2 hours
- extractionthe product was extracted twice with 1,1'-oxybisethane
- customThe aqueous phase was separated
- extractionThe product was extracted with trichloromethane
- customThe extract was dried
- filtrationfiltered
- customevaporated
- customThe residue was purified by column-chromatography over silica gel using
- additiona mixture of trichloromethane and methanol (85:15 by volume)
- customThe pure fractions were collected
- customthe eluent was evaporated
出典と根拠
- ORDレコード
- ord-d0945cbf0d6f4484adc377c2d8f76bb2
- 出典データセット
- uspto-grants-1988_08
- 特許番号
- US04766125
反応ノート
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