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

HRID 483785

반응식

HRID 483785 반응식
[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.Br[CH2:27][CH2:28][C:29]#[N:30].C(=O)([O-])[O-].[K+].[K+].CC(C)=O>C(O)C.C(OCC)C>[ClH:1].[C:29]([CH2:28][CH2:27][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:30]

참가 물질

7

실험 절차

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.

후처리

  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 The residue
  8. dissolutionwas 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

출처 및 근거

ORD 기록
ord-24c01f1ffa3547a9a68b3642dd276af2
출처 데이터셋
uspto-grants-1993_07
특허 번호
US05227379

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