Reaktion #2840

ord-0a8a7f7391de4560854070e9af7b0eeb

Reaktionsgleichung

CCN=C=NCCCN(C)C.Cl
1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride
C[C@H](C(=O)OC(C)(C)C)C(N)(N)C(=O)O
(S)-Boc-Diaminobutyric acid
CCN(CC)CC
triethylamine
O.On1nnc2ccccc21
1-hydroxybenzotriazole hydrate
CC(C)(C)OC(=O)N[C@H]1CCNC1=O
title compound
Ausbeute 85.2%
CC(C)(C)OC(=O)N[C@H]1CCNC1=O
(2-Oxo-pyrrolidin-3-(S)-yl)-carbamic acid tert-butyl ester
Ausbeute 85.2%

Lösungsmittel

Reaktionsbedingungen

Temperatur
60°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    FiltrationAfter this time, the solution is filtered
  2. 2
    Einengenthe collected liquid is concentrated
  3. 3
    SonstigeThe crude product is purified by column chromatography
  4. 4
    Wascheneluting with a gradient of 1% MeOH/CH2Cl2 to 3% MeOH/CH2Cl2

Vorschrift

(S)-Boc-Diaminobutyric acid (25 g, 115 mmol), triethylamine (35 g, 344 mmol), and 1-hydroxybenzotriazole hydrate (19.3 g, 143 mmol) are dissolved in 300 mL of THF. 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (27.4 g, 143 mmol) is added to the solution. The solution is heated at 60° C. over 15 min. A white precipitate forms and the solution is kept at 60° C. for 4 h. After this time, the solution is filtered and the collected liquid is concentrated. The crude product is purified by column chromatography eluting with a gradient of 1% MeOH/CH2Cl2 to 3% MeOH/CH2Cl2 to afford the title compound (19.6 g, 98 mmol) as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05731315uspto-grants-1998_03