Reaktion #1771997

ord-f0376a1639c644708f3c137ceedadfa1

Reaktionsgleichung

CCC[C@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)O
Fmoc-norvaline
O=S(Cl)Cl
thionyl chloride
CO
methanol
CCC[C@H](NC(=O)OCC1c2ccccc2-c2ccccc21)C(=O)OC
Fmoc-norVal-OMe

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe completion of the reaction (Rf=0.85)
  2. 2
    EinengenThe reaction mixture was concentrated
  3. 3
    workup.DISSOLUTIONthe remaining residue was dissolved in ethylacetate
  4. 4
    WaschenThe organic layer was washed with several 200 ml portions of saturated sodium bicarbonate
  5. 5
    SonstigeThe organic layer was dried
  6. 6
    Filtrationfiltered
  7. 7
    Einengenconcentrated

Vorschrift

To a chilled solution of the commercially available Fmoc-norvaline (25 g, 73.75 mmol) in anhydrous methanol (469 ml) was added thionyl chloride (53.76 ml, 737.5 mmol) over one hour. TLC in ethylacetate taken an hour later confirmed the completion of the reaction (Rf=0.85). The reaction mixture was concentrated and the remaining residue was dissolved in ethylacetate. The organic layer was washed with several 200 ml portions of saturated sodium bicarbonate followed by brine. The organic layer was dried, filtered and concentrated to afford Fmoc-norVal-OMe) as a white solid (26.03 g) in quantitative yield. NMR δ ppm (CD3OD): 7.7 (m, 2H), 7.6 (m, 2H), 7.4 (m, 2H), 7.3 (m, 2H), 4.3 (m, 2H), 4.1 (m, 2H), 3.7 (s, 3H), 1.7 (m, 1H), 1.6 (m, 1H), 1.4 (m, 2H), 0.95 (t, 3H).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE043298E1uspto-grants-2012_04