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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 560541Erstellt: 26. Oktober 2026

1,1'-Carbonyldiimidazole → (R)-ethyl 2-(3-(1-hydroxy-3-phenylpropan-2-yl)ureido)-4-methylthiazole-5-carboxylate

https://huagongshe.com/reaction/560541

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,1'-CarbonyldiimidazoleHCID 68263—
EduktEthyl 2-amino-4-methylthiazole-5-carboxylateHCID 343747—
Eduktphenylalaninol, (R)-HCID 853475—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt(R)-ethyl 2-(3-(1-hydroxy-3-phenylpropan-2-yl)ureido)-4-methylthiazole-5-carboxylateHCID 73213189—

Reaktionsschritte

To a solution of ethyl 2-amino-4-methylthiazole-5-carboxylate (1.86 g, 10.0 mmol) in tetrahydrofuran (50 mL) was added 1,1′-carbonyldiimidazole (1.95 g, 12.0 mmol) at ambient temperature. The resulting reaction mixture was stirred at ambient temperature for 17 hours, followed by the addition of (R)-(+)-2-amino-3-phenyl-1-propanol (2.00 g, 13.2 mmol). The reaction mixture was kept stirring at ambient temperature for 50 hours. The solvent was removed in vacuo. The residue was dissolved in ethyl acetate (200 mL) and washed with water and brine. The organic solution was dried over anhydrous sodium sulfate and filtered. The filtrate was concentrated in vacuo to afford the title compound in 88% (3.20 g): MS (ES+) m/z 364.4 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063084B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-0b04c58388994db6a504952ada57d2cb
Quellennotizuspto-grants-2011_11