Sodium hydride → 2-Bromo-5-(4-methylpiperazin-1-YL)pyrazine

HRID 1157310Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1157310
[H-].[Na+].[CH3:3][N:4]1[CH2:9][CH2:8][NH:7][CH2:6][CH2:5]1.Br[C:11]1[C:16]([Br:17])=[N:15][CH:14]=[CH:13][N:12]=1>C1COCC1>[Br:17][C:16]1[CH:11]=[N:12][C:13]([N:7]2[CH2:8][CH2:9][N:4]([CH3:3])[CH2:5][CH2:6]2)=[CH:14][N:15]=1

Komponenten

5

Edukt 3

HCID 24758Sodium hydrideHCID 531671-MethylpiperazineHCID 138675722,3-Dibromopyrazine

Produkt 1

HCID 457877252-Bromo-5-(4-methylpiperazin-1-YL)pyrazine

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel2×

Versuchsvorschrift

To sodium hydride (0.20 g) taken in dry THF (15 ml), N-methyl piperazine (0.93 ml) was added under nitrogen at 0° C. 2,3-Dibromopyrazine (2 g) taken in 15 ml dry THF was added to the above mixture at 0° C. The reaction mixture was allowed to reflux for overnight and quenched with water (5 ml). The organic layer was removed under vacuum. The resulting crude mass was purified by column chromatography to afford 2-bromo-5-(4-methylpiperazin-1-yl)pyrazine as pure product.

Aufarbeitung

  1. additionwas added to the above mixture at 0° C
  2. temperatureto reflux for overnight
  3. customquenched with water (5 ml)
  4. customThe organic layer was removed under vacuum
  5. customThe resulting crude mass was purified by column chromatography

Quellen und Nachweise

ORD-Eintrag
ord-19fe532ae53b45c6ae9611834c4732c5
Quelldatensatz
uspto-grants-2010_10
Patentnummer
US07807671B2

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