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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 730832Generated: October 25, 2026

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

https://huagongshe.com/reaction/730832

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantGlycine methyl ester hydrochlorideHCID 122755—
ReactantCarbodiimideHCID 160435—
ReactantHOAtHCID 181649—
Reactant(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanoic acidHCID 2756111—
SolventDichloromethaneHCID 6344—
ProductMethyl N-{[(9H-fluoren-9-ylmethyl)oxy]carbonyl}-D-norleucylglycinateHCID 67401200—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07582761B2
Source datasetuspto-grants-2009_09
ORD IDord-82221a597aeb4b0184ba9efcc11632d3
Source noteuspto-grants-2009_09