Reaktion #463969

ord-22250e18af714492982e35ec314fc18a

Reaktionsgleichung

O=C(O)CC(O)(CC(=O)O)C(=O)O
citric acid
CCN(C(C)C)C(C)C
DIEA
Cl
HCl
CC(C)(C)OC(=O)N[C@@H](CC(=O)OCc1ccccc1)C(=O)ON1C(=O)CCC1=O
Boc-Asp(OBzl)-OSu
NCc1cccc(C(=O)O)c1
title compound
Ausbeute 92.0%
NCc1cccc(C(=O)O)c1
3-Aminomethylbenzoic acid
Ausbeute 92.0%

Lösungsmittel

Reaktionsbedingungen

Temperatur
5°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONwas added
  2. 2
    FiltrationThe solids were then collected by filtration
  3. 3
    Waschenwashed with ice cold water (200 ml) and ice cold ethyl ether (100 ml)
  4. 4
    Sonstigedried under reduced pressure

Vorschrift

circle-solid.HCl (Mamb; 13.08 g, 70.0 mmol) was dissolved in 120 ml DMF and DIEA (24.32 ml, 140 mmol) was added, changing the pH from 4 to 7.5. The white suspension was stirred for 30 min at room temperature before a solution of Boc-Asp(OBzl)-OSu (29.40 g, 70.0 mmol) in DMF (50 ml) was added. The mixture was allowed to stir 24 hr, during which time it turned to a gold solution. The solution was added to 5% citric acid (2000 ml) and cooled to 5° C. for 3 hr. The solids were then collected by filtration, washed with ice cold water (200 ml) and ice cold ethyl ether (100 ml), and dried under reduced pressure to give the title compound as a colorless solid (29.62 g, 92%); MP=149-151° C.; DCI-MS: [M+NH4 ]=474.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US06022523uspto-grants-2000_02