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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 73909Erstellt: 24. Oktober 2026

Triethylamine → {[2-(Tert-butoxycarbonyl-methyl-amino)acetyl]-methyl-amino}-acetic acid ethyl ester

https://huagongshe.com/de/reaction/73909

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktIsobutyl chloroformateHCID 62365—
EduktGlycine, N-[(1,1-dimethylethoxy)carbonyl]-N-methyl-HCID 83692—
EduktEthyl N-methylaminoacetate hydrochlorideHCID 171173—
LösungsmittelDichloromethaneHCID 6344—
Produkt{[2-(Tert-butoxycarbonyl-methyl-amino)acetyl]-methyl-amino}-acetic acid ethyl esterHCID 57470192—

Reaktionsschritte

To a stirred solution of (tert-butoxycarbonyl-methyl-amino)-acetic acid (37 g, 0.2 mol) and Et3N (60.6 g, 0.6 mol) in CH2Cl2 (300 mL) was added isobutyl chloroformate (27.3 g, 0.2 mmol) dropwise at −20° C. under argon. After stirring for 0.5 h, methylamino-acetic acid ethyl ester hydrochloride (30.5 g, 129 mmol) was added dropwise at −20° C. The mixture was allowed to warm to room temperature (c.a. 1 h) and quenched with water (500 mL). The organic layer was separated, washed with 10% citric acid solution, dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (petroleum ether/EtOAc 1:1) to give {[2-(tert-butoxycarbonyl-methyl-amino)-acetyl]-methyl-amino}-acetic acid ethyl ester (12.5 g, 22

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829204B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-4f98014265354558a01cdb1b0fffcff1
Quellennotizuspto-grants-2014_09