Potassium Carbonate → 2-[4-(2,3-Dihydro-benzo[1,4]dioxin-5-yl)-piperazin-1-yl]-propan-1-ol

HRID 51205

Reaktionsgleichung

Reaktionsgleichung von HRID 51205
[O:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[C:10]([N:11]([CH2:19][CH2:20]OS(C)(=O)=O)[CH2:12][CH2:13]OS(C)(=O)=O)[C:5]=2[O:4][CH2:3][CH2:2]1.[NH2:26][C@@H:27]([CH2:29][OH:30])[CH3:28].[Br-].[Li+].C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[O:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[C:10]([N:11]3[CH2:12][CH2:13][N:26]([CH:27]([CH3:28])[CH2:29][OH:30])[CH2:20][CH2:19]3)[C:5]=2[O:4][CH2:3][CH2:2]1

Komponenten

6

Reaktionsbedingungen

Temperatur
82 °C

Versuchsvorschrift

Dimesylate III (67.0 g, 0.17 mol), D-alaninol (14.0 g, 0.19 mol), lithium bromide (31.0 g, 0.35 mol), and potassium carbonate (74.8 g, 0.54 mol) are mixed together with acetonitrile (750 mL). The resulting suspension is refluxed (82° C.) for 27 h with monitoring by HPLC. The reaction mixture is cooled, filtered, and insoluble residue washed with acetonitrile. Mother liquor is concentrated to a small volume, filtered through 200 cm3 of silica gel, and eluted with 1.5 L of MeOH 10% in EtOAc. After removing solvent on rotary evaporator, the residue is redissolved in EtOAc (200 mL). This solution is washed with water (2×50 mL), dried with MgSO4 and concentrated to produce IV as thick golden oil that slowly crystallizes upon standing; yield 29.4 g (63%) and purity 88.3 area % (LC-MS). Melting point=91-92° C. 1H NMR (CDCl3) δ6.78 (t, J=7.5 Hz, 1H), 6.55 (m, 2H), 4.29 (m, 4H), 3.45 (dd, J=11, 5 Hz, 1H), 3.38 (t, J=11 Hz, 1H), 3.10 (br m, 4H), 2.86 (m, 3H), 2.63 (m, 2H), 0.96 (d, J=7.5 Hz, 3H).

Aufarbeitung

  1. temperatureThe reaction mixture is cooled
  2. filtrationfiltered
  3. washinsoluble residue washed with acetonitrile
  4. concentrationMother liquor is concentrated to a small volume
  5. filtrationfiltered through 200 cm3 of silica gel
  6. washeluted with 1.5 L of MeOH 10% in EtOAc
  7. customAfter removing solvent
  8. customon rotary evaporator
  9. dissolutionthe residue is redissolved in EtOAc (200 mL)
  10. washThis solution is washed with water (2×50 mL)
  11. dry with materialdried with MgSO4
  12. concentrationconcentrated

Quellen und Nachweise

ORD-Eintrag
ord-cbc164384c784410b134c01dbf34ef39
Quelldatensatz
uspto-grants-2004_03
Patentnummer
US06713626B2

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