Dimethylformamide → 1,3,3-Trimethylpiperazine-2,5-dione

HRID 1437249Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1437249
N1CCCC[CH2:2]1.C(O[C:10](=O)[CH2:11][N:12]([C:14](=[O:16])C)C)C.[CH3:18][N:19]([CH3:22])[CH:20]=[O:21]>>[CH3:18][N:19]1[CH2:22][C:14](=[O:16])[NH:12][C:11]([CH3:10])([CH3:2])[C:20]1=[O:21]

Komponenten

4

Edukt 3

HCID 6228Dimethylformamide2×HCID 8082PiperidineHCID 23090132Ethyl N-acetyl-N-methylglycinate

Produkt 1

HCID 230901071,3,3-Trimethylpiperazine-2,5-dioneAusbeute 59 %

Versuchsvorschrift

Piperidine (867 mL) was added to N-[(α,α-dimethyl-(9H-fluoren-9-ylmethoxy)carbamino] acetylsarcosine ethyl ester (743 mg) in N,N-dimethylformamide (20 mL), followed by stirring at room temperature for 1 hour. N,N-Dimethylformamide (60 mL) was added thereto. The resultant mixture was stirred at 80° C. for 14 hours, and cooled in air. The reaction solvent was evaporated under reduced pressure, and the residue was dissolved in ethyl acetate, and then to the resultant solution, hexane was added. The precipitated crystals were recovered by filtration, to thereby give the title compound (162 mg, 59%).

Aufarbeitung

  1. temperaturecooled in air
  2. customThe reaction solvent was evaporated under reduced pressure
  3. dissolutionthe residue was dissolved in ethyl acetate
  4. additionto the resultant solution, hexane was added
  5. filtrationThe precipitated crystals were recovered by filtration

Quellen und Nachweise

ORD-Eintrag
ord-34b15116a7234665bd6ee65e4339cd7a
Quelldatensatz
uspto-grants-2009_11
Patentnummer
US07622471B2

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