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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 560914Erstellt: 25. Oktober 2026

(2S)-3-Phenylpropane-1,2-diamine → HCID 178428030, Verbindung

https://huagongshe.com/reaction/560914

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt(2S)-3-Phenylpropane-1,2-diamineHCID 12699301—
EduktTrimethylaluminumHCID 16682925—
EduktEthyl 5-(3-(4-fluorobenzyl)-2-oxoimidazolidin-1-yl)-3-methylthiophene-2-carboxylateHCID 58031706—
LösungsmittelTolueneHCID 1140—
ProduktHCID 178428030HCID 17842803029%

Reaktionsschritte

To a stirred solution of (S)-3-phenylpropane-1,2-diamine (0.37 g, 2.48 mmol) in toluene (20 mL) at 0° C. under nitrogen atmosphere was added dropwise trimethylaluminum (1.24 mL of 2.0 M solution in toluene, 2.48 mmol). When the fuming ceased, ethyl 5-(3-(4-fluorobenzyl)-2-oxoimidazolidin-1-yl)-3-methylthiophene-2-carboxylate (0.60 g, 1.66 mmol) in toluene (5 mL) was added slowly. The resulting mixture was stirred at reflux for 18 h, cooled to ambient temperature and partitioned between ethyl acetate (75 mL) and water (50 mL). The aqueous layer was extracted with ethyl acetate (3×75 mL), and the combined organic layer was dried over sodium sulfate, filtered and concentrated in vacuo. The residue was purified by column chromatography eluted with dichloromethane/methanol/triethyl amine (9/1/0.1) to afford the title compound as brown viscous oil in 29% yield (0.06 g): MS (ES+) m/z 449.2 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08063084B2
Quelldatensatzuspto-grants-2011_11
ORD IDord-3b2f6c1820a643cfa8e117e9cdbe91d6
Quellennotizuspto-grants-2011_11