Reaktion #65325

ord-4e2116b390d545e9826e59ea2d6f4af5

Reaktionsgleichung

[N-]=[N+]=NC(COCc1ccccc1)CN1C(=O)c2ccccc2C1=O
2-benzyloxymethyl-2-azido-1-phthalimido-ethane
O.c1ccncc1
pyridine water
S
hydrogen sulphide
NC(COCc1ccccc1)CN1C(=O)c2ccccc2C1=O
2-Amino-2-benzyloxymethyl-1-phthalimido-ethane
Ausbeute 20.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigethe reaction flask sealed
  2. 2
    Sonstigethe reaction mixture was evaporated to dryness in vacuo
  3. 3
    SonstigeAfter evaporation from ethanol (3×25 ml)
  4. 4
    Sonstigethe resulting brown solid was purified by chromatography

Vorschrift

Into a stirred solution of 2-benzyloxymethyl-2-azido-1-phthalimido-ethane (500 mg, 1.5 mmol) in 4:1 pyridine/water (25 ml) was bubbled hydrogen sulphide, and the reaction was monitored by TLC. After 4 hours, the gas flow was stopped, and the reaction flask sealed. The intense green reaction mixture was stirred for another 17 hours. TLC indicated full conversion of the starting material. Glacial acetic acid was added to pH 7, and the reaction mixture was evaporated to dryness in vacuo. After evaporation from ethanol (3×25 ml), the resulting brown solid was purified by chromatography. Yield=20%. The structure was confirmed by NMR and IR.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05419893uspto-grants-1995_05