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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 274241Erstellt: 24. Oktober 2026

Water → ethyl 2-[2-(Boc-L-alanyl)aminothiazol-4-yl]glyoxylate

https://huagongshe.com/de/reaction/274241

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
EduktTert-butoxycarbonylalanineHCID 85082—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
EduktEthyl 2-(2-Amino-4-thiazolyl)-2-oxoacetateHCID 4356513—
Katalysator4-(Dimethylamino)pyridineHCID 14284—
LösungsmittelDimethylformamideHCID 6228—
Produktethyl 2-[2-(Boc-L-alanyl)aminothiazol-4-yl]glyoxylateHCID 1865916171,4%

Reaktionsschritte

Ethyl 2-(2-aminothiazol-4-yl)glyoxylate (4.0 g) and Boc-L-alanine (5.67 g) were dissolved in 40 ml of N,N-dimethylformamide (hereafter abbreviated as DMF), and thereto was added 1-ethyl-3-(3'-dimethylaminopropyl)carbodiimide hydrochloride (5.74 g) under ice-cooling followed by addition of 4-dimethylaminopyridine (0.4 g). The mixture was stirred at room temperature for 5 hours. Water (400 ml) was added thereto, and the mixture was extracted twice with ethyl acetate (300 ml). The ethyl acetate layer was washed with 10% aqueous solution of citric acid (200 ml), saturated aqueous solution of sodium bicarbonate (200 ml) and saturated brine (200 ml) in this order, and dried over anhydrous sodium sulfate. The ethyl acetate was distilled off under reduced pressure, and the residue was subjected to silica gel column chromatography eluted with benzene-ethyl acetate. The object fraction was concentrated to give 5.30 g of ethyl 2-[2-(Boc-L-alanyl)aminothiazol-4-yl]glyoxylate.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05389625
Quelldatensatzuspto-grants-1995_02
ORD IDord-f36417eb0f2945ac991ee10e1df38efd
Quellennotizuspto-grants-1995_02