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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 489985Erstellt: 24. Oktober 2026

2-Phenylglycine → tert-butyl (RS)-2-[benzyl(methyl)amino]-2-oxo-1-phenylethylcarbamate

https://huagongshe.com/de/reaction/489985

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-PhenylglycineHCID 3866—
EduktN-MethylbenzylamineHCID 7669—
Edukt2-(((Tert-butoxy)carbonyl)amino)-2-phenylacetic acidHCID 571805—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Edukt1-Hydroxybenzotriazole hydrateHCID 2796029—
LösungsmittelDichloromethaneHCID 6344—
Produkttert-butyl (RS)-2-[benzyl(methyl)amino]-2-oxo-1-phenylethylcarbamateHCID 53439138—

Reaktionsschritte

In another example of a process for preparing a compound of formula C, where R6 is methyl and R7 is benzyl, (RS)-N-tert-butoxycarbonyl-2-phenylglycine, commercially available or prepared from (RS)-2-phenylglycine using methods well known in the art, is combined with 1-hydroxybenzotriazole hydrate, commercially available N-methylbenzylamine and N-[3-(dimethylamino)propyl-N′-ethylcarbodimide hydrochloride in dichloromethane and the resulting mixture stirred for about 24 hours. The resulting mixture is subjected to an aqueous work-up similar to that described above, providing (tert-butyl (RS)-2-[benzyl(methyl)amino]-2-oxo-1-phenylethylcarbamate, which may be treated with trifluorocaetic acid and triethylsilane in dichloromethane, followed by aqueous workup to yield (RS)-N-benzyl-N-methyl-2-phenylglycinamide.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06979692B2
Quelldatensatzuspto-grants-2005_12
ORD IDord-2cefb3b74d924722af2b728a627c7fe9
Quellennotizuspto-grants-2005_12