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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 276085Erstellt: 24. Oktober 2026

Hydrochloric Acid → HCID 70007019, Verbindung

https://huagongshe.com/de/reaction/276085

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium hydrideHCID 24758—
EduktN-(Benzyloxycarbonyl)-L-serineHCID 100310—
EduktHCID 18617241HCID 18617241—
LösungsmittelMethanolHCID 887—
LösungsmittelDimethylformamideHCID 6228—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktHCID 70007019HCID 70007019—

Reaktionsbedingungen

Temperatur0 °C

Reaktionsschritte

0.448 g of 60% NaH/oil (0.27 g, 11.1 mM of NaH) was added to 40 mL of dry THF and cooled to 0° C. 1.21 g (5.08 mM of CBZ-serine was added dropwise as a dry DMF solution (10 mL) over 5 minutes. The resulting mixture was stirred at 0° C. for 1 hr. 2.00 g (5.58 mmoles) of 3-[2-(2-phenyl-4-oxazolyl)ethoxy]benzyl bromide, prepared as described in Example 22, Part B, was also added dropwise as a dry DMF solution (10 mL) over 5 minutes. The final mixture was stirred for 5 h at 0° C. and was then allowed to warm to ambient over 12 h. The reaction was quenched with 20 mL of methanol and one equivalent of HCl. After concentrating to a small volume under reduced pressure, the mixture was diluted with 200 mL EtOAc, washed with 200 mL water (2×) and 200 mL brine. The organic phase was dried over MgSO4, filtered and concentrated to a yellow, opaque oil. The product was purified using silica column chromatography, (25:5:1 CHCl3:MeOH:NH4OH>>>3:4 MeOH:EtOAc), and recrystallized from Et2O. to provide 714 mg 49.6%) of product as a white, waxy solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06353027B1
Quelldatensatzuspto-grants-2002_03
ORD IDord-febd646685e4425eba394bb7fd54bc60
Quellennotizuspto-grants-2002_03