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Bromide ion → 3-[4-[1-(4-Fluorophenyl)-4-piperazinyl]butyl]-4-thiazolidinone

HRID 484127
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 484127
Br[CH2:2][CH2:3][CH2:4][CH2:5][N:6]1[C:10](=[O:11])[CH2:9][S:8][CH2:7]1.[F:12][C:13]1[CH:18]=[CH:17][C:16]([N:19]2[CH2:24][CH2:23][NH:22][CH2:21][CH2:20]2)=[CH:15][CH:14]=1.C([O-])([O-])=O.[K+].[K+].[Br-]>[Na+].[I-].CO.CC#N>[F:12][C:13]1[CH:14]=[CH:15][C:16]([N:19]2[CH2:24][CH2:23][N:22]([CH2:2][CH2:3][CH2:4][CH2:5][N:6]3[C:10](=[O:11])[CH2:9][S:8][CH2:7]3)[CH2:21][CH2:20]2)=[CH:17][CH:18]=1
KomponentenReaktionsbedingungenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 4

HCID 259Bromide ionHCID 11430Potassium CarbonateHCID 752601-(4-Fluorophenyl)piperazineHCID 108475053-(4-Bromobutyl)-4-thiazolidinone

Produkt 1

HCID 107593943-[4-[1-(4-Fluorophenyl)-4-piperazinyl]butyl]-4-thiazolidinoneAusbeute 69,2 %

Reagenzien, Katalysatoren, Lösungsmittel 3

HCID 5238
Sodium Iodide
Katalysator
HCID 887MethanolLösungsmittel
HCID 6342AcetonitrileLösungsmittel

Reaktionsbedingungen

Temperatur
100 °C

Versuchsvorschrift

A mixture of 3-(4-bromobutyl)-4-thiazolidinone (4.01 g), 1-(4-fluorophenyl)piperazine (3.35 g), K2CO3 (4.64 g), NaI (150 mg) and CH3CN (150 ml) was heated at 100° C. (bath temperature) under N2 for 18 h. TLC analysis (silica gel, 8% MeOH/CHCL3) showed one major product at Rf =0.36, and the absence of starting bromide. The reaction mixture was cooled to room temperature and concentrated in vacuo to an oil which was taken up in EtOAc. The mixture was filtered to remove the precipitate and the filtrate concentrated in vacuo to an amber oil which solidified under vacuum. The solid (5.86 g) was dissolved in CHCl3 and flash chromatographed (silica gel) and thereafter recrystallized from hexane/CH2Cl2 to yield in two crops 3.93 g of white crystals, mp 83°-85° C. TLC analysis showed a trace of slower moving impurity. Recrystallization from hexane/CH2Cl2 afforded 3.1 g of white needles which were still slightly impure by TLC. The material was again flash chromatographed (silica gel) and recrystallized from hexane/CH2Cl2 to give 2.67 g of pure product, mp 84°-85° C.

Aufarbeitung

  1. temperatureThe reaction mixture was cooled to room temperature
  2. concentrationconcentrated in vacuo to an oil which
  3. filtrationThe mixture was filtered
  4. customto remove the precipitate
  5. concentrationthe filtrate concentrated in vacuo to an amber oil which
  6. dissolutionThe solid (5.86 g) was dissolved in CHCl3
  7. customflash chromatographed (silica gel)
  8. customrecrystallized from hexane/CH2Cl2

Quellen und Nachweise

ORD-Eintrag
ord-bfd73437482b4c6f9868805eaa31269e
Quelldatensatz
uspto-grants-1993_07
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US05229388

Notizen zur Reaktion

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