Nitrogen mustard hydrochloride → 2-(4-Methylpiperazin-1-yl)-1,3-thiazole-5-carbaldehyde

HRID 336834

Reaktionsgleichung

Reaktionsgleichung von HRID 336834
[NH2:1][C:2]1[S:3][C:4]([CH:7]=[O:8])=[CH:5][N:6]=1.C([O-])([O-])=O.[K+].[K+].Cl.Cl[CH2:17][CH2:18][N:19]([CH2:21][CH2:22]Cl)[CH3:20]>CN(C=O)C>[CH3:20][N:19]1[CH2:21][CH2:22][N:1]([C:2]2[S:3][C:4]([CH:7]=[O:8])=[CH:5][N:6]=2)[CH2:17][CH2:18]1

Komponenten

5

Edukt 3

HCID 5935Nitrogen mustard hydrochlorideHCID 11430Potassium CarbonateHCID 27377982-Amino-1,3-thiazole-5-carbaldehyde

Produkt 1

HCID 14902342-(4-Methylpiperazin-1-yl)-1,3-thiazole-5-carbaldehydeAusbeute 50,9 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Reaktionsbedingungen

Temperatur
90 °C

Versuchsvorschrift

In a 25 ml flask are added 0.5 g of 2-aminothiazole-5-carboxaldehyde, 1.35 g of K2CO3 in 5 ml of DMF. After dissolution, 0.901 g of 2-chloro-N-(2-chloroethyl)-N-methylethanamine hydrochloride are added. The mixture is left at room temperature for 1 h then heated to 90° C. for 5 h. Next, the mixture is evaporated, dissolved in 100 ml of water, and the aqueous phase is extracted three times with ethyl acetate. The organic phases are combined, washed with sodium chloride saturated solution, dried over sodium sulfate, filtered, and evaporated to yield 420 mg (50%) of 2-(4-methylpiperazin-1-yl)thiazole-5-carboxaldehyde.

Aufarbeitung

  1. additionare added
  2. customNext, the mixture is evaporated
  3. dissolutiondissolved in 100 ml of water
  4. extractionthe aqueous phase is extracted three times with ethyl acetate
  5. washwashed with sodium chloride saturated solution
  6. dry with materialdried over sodium sulfate
  7. filtrationfiltered
  8. customevaporated

Quellen und Nachweise

ORD-Eintrag
ord-39af4352341447feae9be1a7f75ba4c3
Quelldatensatz
uspto-grants-2014_11
Patentnummer
US08889711B2

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