Reaktion #2161294

ord-4d3b58bb3c9b4aa8be38dec19f5c1a97

Reaktionsgleichung

CC(C)(C)OC(=O)Cn1nc(-c2cn(C(c3ccccc3)(c3ccccc3)c3ccccc3)cn2)cc1Cc1ccc(F)cc1
tert-butyl [5-(4-fluorobenzyl)-3-(1-trityl-1H-imidazol-4-yl)-1H-pyrazol-1-yl]acetate
O=C(O)C(F)(F)F
TFA
O=C(O)Cn1nc(-c2c[nH]cn2)cc1Cc1ccc(F)cc1
title compound
Ausbeute 83.3%
O=C(O)Cn1nc(-c2c[nH]cn2)cc1Cc1ccc(F)cc1
[5-(4-fluorobenzyl)-3-(1H-imidazol-4-yl)-1H-pyrazol-1-yl]acetic acid
Ausbeute 83.3%

Lösungsmittel

Reaktionsbedingungen

Temperatur
0°CELSIUS
Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    workup.ADDITIONAfter the addition
  2. 2
    SonstigeThe solvent was removed in vacuo
  3. 3
    Waschenthe residue was washed with Et2O (3×10 mL)
  4. 4
    Sonstigedried in oven

Vorschrift

To a solution of tert-butyl [5-(4-fluorobenzyl)-3-(1-trityl-1H-imidazol-4-yl)-1H-pyrazol-1-yl]acetate (0.5 g, 0.80 mmol) in CH2Cl2 (10 mL) was added dropwise TFA (10 mL) at 0° C. After the addition, the mixture was stirred at 0° C. for 2 hours. The solvent was removed in vacuo and the residue was washed with Et2O (3×10 mL) and dried in oven to yield the title compound (0.2 g, 80.0%) as a white solid.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US07919488B2uspto-grants-2011_04