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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 730832Erstellt: 25. Oktober 2026

Diisopropylethylamine → Methyl N-{[(9H-fluoren-9-ylmethyl)oxy]carbonyl}-D-norleucylglycinate

https://huagongshe.com/reaction/730832

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktGlycine methyl ester hydrochlorideHCID 122755—
EduktCarbodiimideHCID 160435—
EduktHOAtHCID 181649—
Edukt(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanoic acidHCID 2756111—
LösungsmittelDichloromethaneHCID 6344—
ProduktMethyl N-{[(9H-fluoren-9-ylmethyl)oxy]carbonyl}-D-norleucylglycinateHCID 67401200—

Reaktionsschritte

A mixture of fmoc-D-Nle-OH (10 g, 28.3 mmol, Novabiochem) and PS-carbodiimide (33 g, 42.45 mmol, 1.28 mmol/g, Argonaut Technologies Inc.) in dichloromethane (250 mL) was stirred at room temperature for 0.5 h. Then, glycine methyl ester hydrochloride (5.3 g, 42.45 mmol, Aldrich), HOAt (3.8 g, 28.3 mmol, Perseptive Biosystems) and diisopropylethylamine (16 mL, 84.9 mmol, Aldrich) were added and the mixture was stirred at room temperature for 16 h. The mixture was filtered and the resin was washed with dichloromethane (2×70 mL). The filtrate was concentrated in vacuo and the residue was purified by column chromatography, eluting with EtOAc/hexane (1:2) to give the title compound as a yellow solid. MS (ESI, positive ion) m/z: 425 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07582761B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-82221a597aeb4b0184ba9efcc11632d3
Quellennotizuspto-grants-2009_09