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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1784299Erstellt: 25. Oktober 2026

Methyl 3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)-4-nitrobenzoate → Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoate

https://huagongshe.com/reaction/1784299

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)-4-nitrobenzoateHCID 67235341—
KatalysatorPalladiumHCID 23938—
LösungsmittelEthylacetate methanolHCID 21584119—
ProduktMethyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoateHCID 1196207783%

Reaktionsbedingungen

Temperatur20 °C

Reaktionsschritte

Methyl 3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)-4-nitrobenzoate (10.2 g) in solution in a mixture of ethyl acetate/methanol 3:1 (300 ml), and 10% palladium on carbon (1.02 g) are introduced into an autoclave. After stirring for 4 hours under a hydrogen atmosphere (3 bar) at a temperature of approximately 20° C., the catalyst is eliminated by filtration on celite and the filtrate is concentrated under reduced pressure at 40° C. in order to produce the expected compound in the form of an oil (7.75 g; 83% yield).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07501525B2
Quelldatensatzuspto-grants-2009_03
ORD IDord-738362d4b1254d849c6196150c37dc39
Quellennotizuspto-grants-2009_03