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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 732717Erstellt: 25. Oktober 2026

1-(2,3-Dihydro-1,4-benzodioxin-5-yl)ethanone → 4-(Methoxycarbonyl)phenyl(3s,4s)-3-({[1-(2,3-dihydro-1,4-benzodioxin-5-yl)ethyl]amino}methyl)-4-phenylpyrrolidine-1-carboxylate

https://huagongshe.com/reaction/732717

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-(2,3-Dihydro-1,4-benzodioxin-5-yl)ethanoneHCID 21268052—
EduktHCID 68911676HCID 68911676—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt4-(Methoxycarbonyl)phenyl(3s,4s)-3-({[1-(2,3-dihydro-1,4-benzodioxin-5-yl)ethyl]amino}methyl)-4-phenylpyrrolidine-1-carboxylateHCID 6891388239,6%

Reaktionsschritte

A 2.0 ml THF solution of 253 mg of 4-(methoxycarbonyl)phenyl(3S,4S)-3-(aminomethyl)-4-phenylpyrrolidine-1-carboxylate and 144 mg of 5-acetylbenzodioxane was mixed with 0.12 ml of a boron trifluoride diethyl ether complex at 0° C. and stirred overnight at room temperature. The reaction solution was concentrated under a reduced pressure, and the thus obtained residue was purified by a silica gel chromatography (chloroform-methanol) to obtain 146 mg of 4-(methoxycarbonyl)phenyl(3S,4S)-3-({[1-(2,3-dihydro-1,4-benzodioxin-5-yl)ethyl]amino}methyl)-4-phenylpyrrolidine-1-carboxylate as a colorless amorphous substance. EP: 517.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07585886B2
Quelldatensatzuspto-grants-2009_09
ORD IDord-a44eee1b2f0a4449b79e7922510b92ad
Quellennotizuspto-grants-2009_09