Reaktion #51331

ord-ce944396018f4ba4b2bf5fd4ec4ee95d

Reaktionsgleichung

Nc1ccc2c(c1)OCO2
3,4-methylenedioxyaniline
COC(=O)C(C)=O
methyl pyruvate
COC(=O)[C@H](C)Nc1ccc2c(c1)OCO2
N-(3,4-methylenedioxyphenyl)alanine methyl ester
CC(C)COC(=O)[C@H](C)Nc1ccc2c(c1)OCO2
title compound
CC(C)COC(=O)[C@H](C)Nc1ccc2c(c1)OCO2
N-(3,4-methylenedioxyphenyl)alanine iso-butyl ester

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigewas prepared

Vorschrift

Following reductive amination General Procedure AA above and using 3,4-methylenedioxyaniline (Aldrich) and methyl pyruvate (Aldrich), N-(3,4-methylenedioxyphenyl)alanine methyl ester was prepared. The methyl ester was then transesterified following General Procedure AQ above and using iso-butanol to provide the title compound as an oil. The reaction was monitored by silica gel tlc (Rf=0.61 in 25% EtOAc/hexanes). Purification was by preparative plate chromatography with silica gel using 25% EtOAc/hexanes as the eluant.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06849650B2uspto-grants-2005_02