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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 25696Erstellt: 23. Oktober 2026

Diisopropylethylamine → benzyl (3S)-3-{[(benzyloxy)carbonyl]amino}-4-[(3,3-diethoxypropyl)amino]-4-oxobutanoate

https://huagongshe.com/de/reaction/25696

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1-Amino-3,3-diethoxypropaneHCID 521029—
Edukt1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
EduktN-(Benzyloxycarbonyl)aspartic acidHCID 2723942—
EduktHCID 178418300HCID 178418300—
LösungsmittelTetrahydrofuranHCID 8028—
Produktbenzyl (3S)-3-{[(benzyloxy)carbonyl]amino}-4-[(3,3-diethoxypropyl)amino]-4-oxobutanoateHCID 59065876100%

Reaktionsschritte

By using an analogous procedure to that described for Reference Example 13, benzyloxycarbonyl-L-aspartic acid [1-benzyl ester (2 g, 5.6 mmol), hydroxybenzotriazole (756 mg, 5.6 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (1.07 g, 5.6 mmol), 1-amino-3,3-diethoxypropane (784 mg, 5.3 mmol) and N,N-diisopropylethylamine (0.986 mL, 5.6 mmol) were reacted in anhydrous tetrahydrofuran (30 ml) at room temperature for 16 hours, to provide benzyl (3S)-3-{[(benzyloxy)carbonyl]amino}-4-[(3,3-diethoxypropyl)amino]-4-oxobutanoate (2.81 g, 100%) as a pale yellow waxy solid.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06858591B2
Quelldatensatzuspto-grants-2005_02
ORD IDord-d96b4e3070854d9da39bcc7490a10a3a
Quellennotizuspto-grants-2005_02