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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 23761Erstellt: 24. Oktober 2026

Dicyclohexylcarbodiimide → (S)-5-(1-amino-2-methylpropyl)-3-methyl-1,2,4-oxadiazole

https://huagongshe.com/de/reaction/23761

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDicyclohexylcarbodiimideHCID 10868—
EduktN-HydroxyacetamidineHCID 30926—
EduktBoc-L-ValineHCID 83693—
LösungsmittelPyridineHCID 1049—
LösungsmittelDichloromethaneHCID 6344—
Produkt(S)-5-(1-amino-2-methylpropyl)-3-methyl-1,2,4-oxadiazoleHCID 29550895—

Reaktionsschritte

A solution of BOC-L-valine (4.34 g, 20.0 mmol) in dichloromethane (20 mL) was cooled to 0° C. and treated dropwise with a solution of dicyclohexylcarbodiimide (2.06 g, 10.0 mmol) in dichloromethane (5 mL). After 1 hour the white solid which had formed was removed by filtration and the filtrate concentrated under reduced pressure. The residue was dissolved in pyridine (15 mL) and treated with acetamidoxime (488 mg, 6.6 mmol) in pyridine (5 mL) and the mixture heated at reflux for 1 hour. The pyridine was evaporated under reduced pressure and the residue partitioned between ethyl acetate and water. The organic phase was washed several times with water, dried over magnesium sulfate and concentrated. The residue was chromatographed on silica gel using 10% ethyl acetate in hexanes to elute the product (0.62 g, 25%) as a white solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06852745B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-63c05ebf483642babd18bb6d0f623481
Quellennotizuspto-grants-2005_02