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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1379050Erstellt: 23. Oktober 2026

Ethyl Acetate → 2-[(2-bromo)acetyl]amino-3-(1H-indol-3-yl)1-[N-(2-methoxybenzyl)acetylamino]propane

https://huagongshe.com/de/reaction/1379050

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktBromoacetyl bromideHCID 61147—
EduktDiisopropylethylamineHCID 81531—
Edukt2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propaneHCID 22508955—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt2-[(2-bromo)acetyl]amino-3-(1H-indol-3-yl)1-[N-(2-methoxybenzyl)acetylamino]propaneHCID 69736949—

Reaktionsschritte

To a stirring solution of 2-amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane (7.51 g, 21.369 mmoles) in anhydrous tetrahydrofuran (100 ml) under a nitrogen atmosphere at 0° C. was added diisopropylethylamine (4.1 ml, 23.537 mmoles) and bromoacetyl bromide (2.05 ml, 23.530 mmoles). After 2 hours, ethyl acetate was added and the reaction mixture washed with water twice, 1.0N hydrochloric acid (2×), saturated sodium bicarbonate solution (2×), and brine. The organic layer was dried over anhydrous sodium sulfate, filtered, and concentrated to a tan foam on a rotary evaporator. In this manner the 2-[(2-bromo)acetyl]amino-3-(1H-indol-3-yl)-1-[N-(2-methoxybenzyl)acetylamino]propane was obtained in quantitative yield. No further purification was necessary.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05670499
Quelldatensatzuspto-grants-1997_09
ORD IDord-808277e1f054413d966db4e1c92d4e86
Quellennotizuspto-grants-1997_09