Reaktion #2383771

ord-b97275aca5914982822d5965746a0bd5

Reaktionsgleichung

ClCCl
methylene chloride
CCN(C(C)C)C(C)C
diisopropylethylamine
CSCCNCCSC
bis-(2-methylthioethyl)-amine
COC(=O)CBr
bromoacetic acid methyl ester
COC(=O)CN(CCSC)CCSC
N,N-bis-(2-methylthioethyl)-glycine methyl ester

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONis added in drops under a cover-gas atmosphere
  2. 2
    Waschenwashed twice with saturated sodium bicarbonate solution
  3. 3
    TrocknenThe organic phase is dried with sodium sulfate
  4. 4
    Einengenconcentrated by evaporation
  5. 5
    Sonstigethe residue is purified by chromatography with the mobile solvent system of methylene chloride/methanol

Vorschrift

165 mg of bis-(2-methylthioethyl)-amine (Example 8b) is dissolved in 20 ml of acetonitrile and mixed with 174 μl of diisopropylethylamine. 92.7 μl of bromoacetic acid methyl ester, dissolved in 20 ml of acetonitrile, is added in drops under a cover-gas atmosphere, and the batch is stirred for 18 hours at room temperature. The acetonitrile is drawn off, the residue is taken up with methylene chloride and washed twice with saturated sodium bicarbonate solution. The organic phase is dried with sodium sulfate and concentrated by evaporation, and the residue is purified by chromatography with the mobile solvent system of methylene chloride/methanol: Yield 183 mg=77% of theory.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06488909B1uspto-grants-2002_12