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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25692Erstellt: 23. Oktober 2026

Diisopropylethylamine → benzyl (1S)-2-[(3,3-diethoxypropyl)amino]-1-methyl-2-oxoethylcarbamate

https://huagongshe.com/de/reaction/25692

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1-Amino-3,3-diethoxypropaneHCID 521029—
EduktN-carbobenzyloxyalanineHCID 736104—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
EduktHCID 178418300HCID 178418300—
LösungsmittelTetrahydrofuranHCID 8028—
Produktbenzyl (1S)-2-[(3,3-diethoxypropyl)amino]-1-methyl-2-oxoethylcarbamateHCID 5906585785%

Reaktionsschritte

By using an analogous procedure to that described for Reference Example 13, carbobenzyloxy-L-alanine (2 g, 8.99 mmol), hydroxybenzotriazole (1.2 g, 8.99 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.72 g, 8.99 mmol), 1-amino-3,3-diethoxypropane (1.25 g, 8.53 mmol) and N,N-diisopropylethylamine (1.56 ml, 8.99 mmol) were reacted in anhydrous tetrahydrofuran (40 ml) at room temperature for 16 h, to provide benzyl (1S)-2-[(3,3-diethoxypropyl)amino]-1-methyl-2-oxoethylcarbamate (2.55 g, 85%) as a pale yellow solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858591B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-4c22e671e5fc4c8db74fcd3b242ad080
Quellennotizuspto-grants-2005_02