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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2407198Erstellt: 25. Oktober 2026

4-(5-Amino-6-(phenylmethyl)-2-pyrazinyl)phenol → 2-((3-Benzyl-5-(4-hydroxyphenyl)pyrazin-2-yl)amino)hexanoic acid

https://huagongshe.com/reaction/2407198

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-(5-Amino-6-(phenylmethyl)-2-pyrazinyl)phenolHCID 193743—
Edukt2-ketohexanoic acid sodium saltHCID 23669158—
KatalysatorAcetic AcidHCID 176—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthanolHCID 702—
Produkt2-((3-Benzyl-5-(4-hydroxyphenyl)pyrazin-2-yl)amino)hexanoic acidHCID 13639103446,1%

Reaktionsbedingungen

Temperatur65 °C

Reaktionsschritte

4-(5-amino-6-benzylpyrazin-2-yl)phenol (200 mg, 0.72 mmol) was mixed with 2-Ketohexanoic acid sodium salt (220 mg, 1.44 mmol) in ethanol (20 mL). Pd/C (10% Palladium in active carbon, 100 mg) was added with a few drops of acetic acid, and the reaction mixture heated to 65° C. Air was bubbled out by N2 gas, and a hydrogen balloon applied to the reaction flask. The reaction was continuously stirred for 4 hrs. After cooling down, it was filtered and the resulting solution was purified by flash chromatography (eluting solvent: 50% EtOAc in heptanes) to give the product as a yellow powder (130 mg, 46%). MS (ESI): m/z 392.2 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08809529B2
Quelldatensatzuspto-grants-2014_08
ORD IDord-47f86147d4124894872c2d05d8736a0c
Quellennotizuspto-grants-2014_08