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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 563283Erstellt: 24. Oktober 2026

Potassium Carbonate → (2R,3R)-2-(4-Cyanonaphthalen-1-ylamino)-3-hydroxybutanoic acid

https://huagongshe.com/de/reaction/563283

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPotassium CarbonateHCID 11430—
EduktD-AllothreonineHCID 90624—
Edukt1-Cyano-4-fluoronaphthaleneHCID 2736734—
LösungsmittelDimethyl SulfoxideHCID 679—
Produkt(2R,3R)-2-(4-Cyanonaphthalen-1-ylamino)-3-hydroxybutanoic acidHCID 6700624976%

Reaktionsbedingungen

Temperatur80 °C

Reaktionsschritte

To a suspension of D-allo-threonine (2.09 g, 17.53 mmol) and K2CO3 (4.04 g, 29.21 mmol) in DMSO (40 mL) was added 4-fluoro-1-naphthonitrile (CAS 13916-99-9, 2.50 g, 14.61 mmol) at room temperature. The reaction mixture was heated to 80° C. and stirred for 89 h. The reaction mixture was allowed to cool to room temperature, quenched with H2O (150 mL) and extracted with EtOAc (3×100 mL). The aqueous layer was then acidified with solid citric acid and extracted with EtOAc (2×100 mL). The later organic extracts were combined, washed with H2O (3×100 mL), dried (Na2SO4), filtered and concentrated under reduced pressure to provided the title compound as a light brown solid (3.0 g, 76%): 1H NMR (400 MHz, DMSO-d6, δ in ppm) 8.46 (d, J=8.8 Hz, 1H), 7.97 (d, J=8.2 Hz, 1H), 7.90 (d, J=8.6 Hz, 1H), 7.74 (t, J=7.0 Hz, 1H), 7.62 (t, J=7.6 Hz, 1H), 6.98 (d, J=8.0 Hz, 1H), 6.57 (d, J=8.4 Hz, 1H), 4.29-4.20 (m, 1H), 4.08-3.99 (m, 1H), 1.28 (d, J=6.1 Hz, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08067448B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-c06a15746ef64c919ce0b5e98f0ca463
Quellennotizuspto-grants-2011_11