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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1006323Erstellt: 25. Oktober 2026

2-Methoxybenzylamine → (2S)-2-[(2-methoxybenzylamino)methyl]pyrrolidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/1006323

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-MethoxybenzylamineHCID 81292—
EduktDiisopropylethylamineHCID 81531—
Edukt(S)-2-(Toluene-4-sulfonyloxymethyl)-pyrrolidine-1-carboxylic acid benzyl esterHCID 10960094—
Lösungsmittel1,3-Dimethyl-2-imidazolidinoneHCID 6661—
Produkt(2S)-2-[(2-methoxybenzylamino)methyl]pyrrolidine-1-carboxylic acid benzyl esterHCID 69745936—

Reaktionsbedingungen

Temperatur93 °C

Reaktionsschritte

A mixture of (2S)-2-(4-methylphenylsulfonyloxymethyl)pyrrolidine-1-carboxylic acid benzyl ester (26.2 g), 2-methoxybenzylamine (44 ml) and N,N-diisopropylethylamine (17.6 ml) in 1,3-dimethyl-2-imidazolidinone (393 ml) was stirred at 93° C. for 7 hours. The mixture was poured into ice-water and extracted with ethyl acetate. The extract was washed with brine, dried over magnesium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel using a mixed solvent of dichloromethane and methanol (20:1). The fractions containing the objective compound were collected and evaporated under reduced pressure to give a syrup of (2S)-2-[(2-methoxybenzylamino)methyl]pyrrolidine-1-carboxylic acid benzyl ester (15.7 g).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06787543B2
Quelldatensatzuspto-grants-2004_09
ORD IDord-52ca477d039e4fe1837ebf825f68823b
Quellennotizuspto-grants-2004_09