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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17424Erstellt: 23. Oktober 2026

Dimethylamine → Benzyl N-[3-(dimethylcarbamoyl)propyl]carbamate

https://huagongshe.com/de/reaction/17424

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDimethylamineHCID 674—
Edukt4-(((Benzyloxy)carbonyl)amino)butanoic acidHCID 21184—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1-(Dimethylaminopropyl)-3-ethylcarbodiimide 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochlorideHCID 86630846—
LösungsmittelDimethylformamideHCID 6228—
ProduktBenzyl N-[3-(dimethylcarbamoyl)propyl]carbamateHCID 1675435582,5%

Reaktionsschritte

4-(Benzyloxycarbonylamino)butyric acid (0.74 g, 3.12 mmol) was dissolved in N,N-dimethylformamide, then 1-(dimethylaminopropyl)-3-ethylcarbodiimide 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (0.60 g, 3.13 mmol), 1-hydroxybenzotriazole (0.48 g, 3.13 mmol) and dimethylamine (2.0 M tetrahydrofuran solution, 2.40 ml, 4.80 mmol) were added, followed by stirring at room temperature for 3 days. The reaction liquid was concentrated under reduced pressure, diluted with ethyl acetate, washed with water, and dried over anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure, and the resulting residue was purified by silica gel column chromatography (dichloromethane:methanol=70:1 to 40:1) to obtain a yellow solid (0.68 g, 82%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737166B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-3c82f86e57194445b5a85b886244c1a5
Quellennotizuspto-grants-2010_06