Reaktion #1885191

ord-71735b5095e643d59cd8034892c96aae

Reaktionsgleichung

CC(C)(C)OC(=O)CNC(=O)c1ncccc1O
[(3-hydroxy-pyridine-2-carbonyl)-amino]-acetic acid tert-butyl ester
O=C(O)C(F)(F)F
TFA
O=C(O)CNC(=O)c1ncccc1O
desired compound
Ausbeute 99.0%
O=C(O)CNC(=O)c1ncccc1O
[(3-Hydroxy-pyridine-2-carbonyl)-amino]-acetic acid
Ausbeute 99.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Einengenthen concentrated under reduced pressure

Vorschrift

To a solution of [(3-hydroxy-pyridine-2-carbonyl)-amino]-acetic acid tert-butyl ester, 29, (0.070 g, 0.277 mmol) in CH2Cl2 (4 mL) is added TFA (1 mL). The resulting solution is stirred for 5 hours then concentrated under reduced pressure to afford 0.054 g (99% yield) of the desired compound as a colorless solid. 1H NMR (400 MHz, MeOD) δ ppm 8.09 (1 H, d, J=3.3 Hz), 7.36-7.59 (2 H, m), 4.08 (2 H, s). HPLC-MS: m/z 197 [M+H]+.

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08343952B2uspto-grants-2013_01