Ethanol → (-)-trans-1(2-Cyanoethyl)-4-(4-fluorophenyl)-3-(3,4-methylenedioxyphenoxymethyl)-piperidine hydrochloride

HRID 467064

反応式

HRID 467064 の反応式
[ClH:1].[F:2][C:3]1[CH:8]=[CH:7][C:6]([C@@H:9]2[CH2:14][CH2:13][NH:12][CH2:11][C@H:10]2[CH2:15][O:16][C:17]2[CH:22]=[CH:21][C:20]3[O:23][CH2:24][O:25][C:19]=3[CH:18]=2)=[CH:5][CH:4]=1.C(O)C.Br[CH2:30][CH2:31][C:32]#[N:33].C(=O)([O-])[O-].[K+].[K+]>C(OCC)C.CC(C)=O>[ClH:1].[C:32]([CH2:31][CH2:30][N:12]1[CH2:13][CH2:14][C@@H:9]([C:6]2[CH:7]=[CH:8][C:3]([F:2])=[CH:4][CH:5]=2)[C@H:10]([CH2:15][O:16][C:17]2[CH:22]=[CH:21][C:20]3[O:23][CH2:24][O:25][C:19]=3[CH:18]=2)[CH2:11]1)#[N:33]

参加物

7

実験手順

1 g of (-)-trans-4-(4-fluorophenyl)-3-(3,4-methylene dioxyphenoxymethyl)-piperidine hydrochloride in 50 ml 99 9% ethanol was mixed with 3-bromopropionitrile (7 ml) and 2 g potassium carbonate. The mixture was refluxed for 70 h. After cooling 25 ml acetone and 25 ml diethylether were added, the precipitate filtered off, and the filtrate evaporated in vacuo. The residue was extracted with 1N NaOH/ether, the ether layer dried (MgSO4) and evaporated to dryness. The residue was dissolved in acetone and excess conc. HCl was added. Subsequent evaporation gave a hard glass, which was purified on a silica gel column using 99.5% ethanol as eluent. The title compound was isolated, and its structure confirmed by the IR and NMR data. M.p. 156° C.

後処理

  1. temperatureThe mixture was refluxed for 70 h
  2. additionwere added
  3. filtrationthe precipitate filtered off
  4. customthe filtrate evaporated in vacuo
  5. extractionThe residue was extracted with 1N NaOH/ether
  6. dry with materialthe ether layer dried (MgSO4)
  7. customevaporated to dryness
  8. dissolutionThe residue was dissolved in acetone
  9. additionexcess conc. HCl was added
  10. customSubsequent evaporation
  11. customgave a hard glass, which
  12. customwas purified on a silica gel column

出典と根拠

ORDレコード
ord-eb66a0f4ae404633a525c7dfed23e0e5
出典データセット
uspto-grants-1992_10
特許番号
US05158961

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