Aluminium lithium hydride → 1-[2-(2-Fluorophenoxy)-ethyl]-4-[3-(3,4,5-trimethoxyphenyl)propyl]-piperazine dihydrochloride

HRID 1928548

Reaktionsgleichung

Reaktionsgleichung von HRID 1928548
[ClH:1].[F:2][C:3]1[CH:33]=[CH:32][CH:31]=[CH:30][C:4]=1[O:5][CH2:6][CH2:7][N:8]1[CH2:13][CH2:12][N:11]([C:14](=O)[CH2:15][CH2:16][C:17]2[CH:22]=[C:21]([O:23][CH3:24])[C:20]([O:25][CH3:26])=[C:19]([O:27][CH3:28])[CH:18]=2)[CH2:10][CH2:9]1.[H-].[H-].[H-].[H-].[Li+].[Al+3]>C1COCC1>[ClH:1].[ClH:1].[F:2][C:3]1[CH:33]=[CH:32][CH:31]=[CH:30][C:4]=1[O:5][CH2:6][CH2:7][N:8]1[CH2:13][CH2:12][N:11]([CH2:14][CH2:15][CH2:16][C:17]2[CH:22]=[C:21]([O:23][CH3:24])[C:20]([O:25][CH3:26])=[C:19]([O:27][CH3:28])[CH:18]=2)[CH2:10][CH2:9]1

Komponenten

4

Versuchsvorschrift

To a solution of 1-{4-[2-(2-fluorophenoxy)ethyl]piperazin-1-yl}-3-(3,4,5-trimethoxyphenyl)-propan-1-one hydrochloride (0.2 g, 0.41 mmol) in THF (50 mL) was added LiAlH4 (0.2 g, 5 mmol). The reaction mixture was stirred under N2 for a day, cooled with an ice bath, and quenched with water (0.2 mL) and 10N NaOH aqueous solution (0.2 mL). The solid was filtered and the filtrate was concentrated to dryness. The residue was treated with ether and 2N HCl in ether (2 mL). The white solid was filtered and dried under vacuum to yield the title compound (0.18 g, 87%).

Aufarbeitung

  1. temperaturecooled with an ice bath
  2. customquenched with water (0.2 mL) and 10N NaOH aqueous solution (0.2 mL)
  3. filtrationThe solid was filtered
  4. concentrationthe filtrate was concentrated to dryness
  5. additionThe residue was treated with ether and 2N HCl in ether (2 mL)
  6. filtrationThe white solid was filtered
  7. customdried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-51b4db710de04d45974849d18197797c
Quelldatensatz
uspto-grants-2012_05
Patentnummer
US08183374B2

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