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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 43373Erstellt: 23. Oktober 2026

Water → (2S)-2-Methyl-1-[(6-methyl-3-pyridinyl)carbonyl]piperazine

https://huagongshe.com/de/reaction/43373

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktDiisopropylethylamineHCID 81531—
Edukt6-Methylnicotinic acidHCID 137860—
EduktMethanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
Edukt(S)-1-Boc-3-methylpiperazineHCID 7023035—
LösungsmittelDimethylformamideHCID 6228—
Produkt(2S)-2-Methyl-1-[(6-methyl-3-pyridinyl)carbonyl]piperazineHCID 591613781.394,9%

Reaktionsschritte

To a solution of 1,1-dimethylethyl (3S)-3-methyl-1-piperazinecarboxylate (1 g, 4.99 mmol) in DMF (5 ml) was added 6-methyl-3-pyridinecarboxylic acid (0.685 g, 0.340 mmol), HOBT.H2O (0.765 g, 4.99 mmol) and HBTU (1.894 g, 4.99 mmol). Finally DIPEA (2.62 ml, 14.98 mmol) was added and the reaction mixture was stirred at room temperature for 20 hours. Solvent was removed by evaporation and EtOAc was added to the residue and the solution was extracted with saturated aqueous sodium bicarbonate and sodium chloride solutions. The organic layer was evaporated to dryness and dissolved in dioxane (100 ml) and stirred with 4M HCl in dioxane (15 ml) and water (0.25 ml) overnight. The solution was evaporated to dryness and purified using an ion exchange column (SCX, Biotage) to give the title compound as an oil (1.04 g)

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08536183B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-72d4c1c2e2d642058b9a80973bd0f26e
Quellennotizuspto-grants-2013_09