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Piperazine → 5-Methyl-2-(piperazin-1-yl)-1,3-benzoxazole

HRID 1267265
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Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 1267265
[CH3:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8](S)=[N:7][C:6]=2[CH:11]=1.P(Cl)(Cl)(Cl)(Cl)Cl.[NH:18]1[CH2:23][CH2:22][NH:21][CH2:20][CH2:19]1>C1(C)C=CC=CC=1>[CH3:1][C:2]1[CH:3]=[CH:4][C:5]2[O:9][C:8]([N:18]3[CH2:23][CH2:22][NH:21][CH2:20][CH2:19]3)=[N:7][C:6]=2[CH:11]=1
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

5

Edukt 3

HCID 4837PiperazineHCID 24819Phosphorus pentachlorideHCID 178423563HCID 178423563, Verbindung

Produkt 1

HCID 225582065-Methyl-2-(piperazin-1-yl)-1,3-benzoxazole

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 1140TolueneLösungsmittel

Versuchsvorschrift

A 100 mg portion of 5-methyl-2-mercaptobenzoxazole was suspended in 20 ml of anhydrous toluene, and the suspension was mixed with 150 mg of phosphorus pentachloride and heated under reflux for 1 hour. The reaction solution was cooled in an ice bath and, with stirring, 500 mg of piperazine was added thereto. After 30 minutes of stirring, the ice bath was removed to carry out 1 hour of stirring at room temperature, the reaction solution was mixed with saturated sodium bicarbonate aqueous solution, and then the water layer was washed with ethyl acetate and concentrated under a reduced pressure. Thereafter, the thus obtained mixture was purified by an LH-20 gel column chromatography (chloroform:methanol=1:1) to obtain the title compound (40 mg) in white color.

Aufarbeitung

  1. temperatureheated
  2. temperatureunder reflux for 1 hour
  3. temperatureThe reaction solution was cooled in an ice bath
  4. stirringAfter 30 minutes of stirring
  5. customthe ice bath was removed
  6. stirringof stirring at room temperature
  7. additionthe reaction solution was mixed with saturated sodium bicarbonate aqueous solution
  8. washthe water layer was washed with ethyl acetate
  9. concentrationconcentrated under a reduced pressure
  10. customThereafter, the thus obtained mixture was purified by an LH-20 gel column chromatography (chloroform:methanol=1:1)

Quellen und Nachweise

ORD-Eintrag
ord-cbd8d5427ef44a749f18bbfcb998df83
Quelldatensatz
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US06552057B2

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