Potassium Iodide → 3-[1-(3-Diethylaminopropyl)-4-piperidyl]-1,2-benzisoxazole difumarate

HRID 223574Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 223574
[NH:1]1[CH2:6][CH2:5][CH:4]([C:7]2[C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=3[O:9][N:8]=2)[CH2:3][CH2:2]1.[CH2:16]([N:18]([CH2:23][CH3:24])[CH2:19][CH2:20][CH2:21]Cl)[CH3:17].[I-].[K+].C(=O)(O)[O-].[Na+].[C:32]([OH:39])(=[O:38])/[CH:33]=[CH:34]/[C:35]([OH:37])=[O:36]>C(O)CCC.C(#N)C>[C:32]([OH:39])(=[O:38])/[CH:33]=[CH:34]/[C:35]([OH:37])=[O:36].[C:32]([OH:39])(=[O:38])/[CH:33]=[CH:34]/[C:35]([OH:37])=[O:36].[CH2:16]([N:18]([CH2:23][CH3:24])[CH2:19][CH2:20][CH2:21][N:1]1[CH2:2][CH2:3][CH:4]([C:7]2[C:11]3[CH:12]=[CH:13][CH:14]=[CH:15][C:10]=3[O:9][N:8]=2)[CH2:5][CH2:6]1)[CH3:17]

Komponenten

8

Versuchsvorschrift

A suspension of 4.0 g of 3-(4-piperidyl)-1,2-benzisoxazole, 3.2 g of 3-diethylaminopropyl chloride, 3.0 g of potassium iodide and 5.0 g of sodium bicarbonate in 100 ml of butanol was heated under reflux for 2 hrs, cooled to room temperature and filtered. The filitrate was washed with water and extracted with ether (3 times). The ether extracts were dried over anhydrous sodium sulfate, filtered and evaporated to give an oil. The oil was dissolved in 10 ml of acetonitrile and 4.2 g of fumaric acid was added. The mixture was stirred for 2 hrs, filtered and the filter cake was recrystallized three times from ethanol-ether to give 2.8 g (26%) of product, mp 174°-176°.

Aufarbeitung

  1. temperaturewas heated
  2. temperatureunder reflux for 2 hrs
  3. filtrationfiltered
  4. washThe filitrate was washed with water
  5. extractionextracted with ether (3 times)
  6. dry with materialThe ether extracts were dried over anhydrous sodium sulfate
  7. filtrationfiltered
  8. customevaporated
  9. customto give an oil
  10. filtrationfiltered
  11. customthe filter cake was recrystallized three times from ethanol-ether

Quellen und Nachweise

ORD-Eintrag
ord-2f0101fb514c4242b53bbb821d81edc7
Quelldatensatz
uspto-grants-1982_10
Patentnummer
US04355037

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