Reaktion #628686

Reaktionsgleichung

LiOH

water

EtOH

1-(3-Chlorophenyl)-5-oxo-4,5-dihydro-1H-[1,2,4]triazole-3-carboxylic acid

HCTU

(R)-3-[N-(5′-Chloro-2′-fluorobiphenyl-4-ylmethyl)hydrazino]-2-hydroxypropionic acid ethyl ester

DIPEA

DMF

→

title compound

Ausbeute 46.6%

(R)-3-{N-(5′-Chloro-2′-fluorobiphenyl-4-ylmethyl)-N′-[1-(3-chlorophenyl)-5-oxo-4,5-dihydro-1H-[1,2,4]triazole-3-carbonyl]hydrazino}-2-hydroxypropionic Acid

Ausbeute 46.6%

Reaktionsbedingungen

Aufarbeitung

1. 1
   workup.STIRRINGthe resulting mixture was stirred at room temperature for 15 minutes
2. 2
   SonstigeThe mixture was evaporated under reduced pressure
3. 3
   workup.STIRRINGThe resulting mixture was stirred at room temperature for 1 hour
4. 4
   Sonstigeevaporated under reduced pressure
5. 5
   SonstigeThe residue was purified by reverse phase preparative HPLC

Vorschrift

1-(3-Chlorophenyl)-5-oxo-4,5-dihydro-1H-[1,2,4]triazole-3-carboxylic acid (75.8 mg, 316 μmol) and HCTU (131 mg, 316 μmol) were combined in DMF (1.3 mL, 17.2 mmol). and stirred at room temperature for 15 minutes. (R)-3-[N-(5′-Chloro-2′-fluorobiphenyl-4-ylmethyl)hydrazino]-2-hydroxypropionic acid ethyl ester (105 mg, 287 μmol) and DIPEA (150 mL, 862 μmol) were added, and the resulting mixture was stirred at room temperature for 15 minutes. The mixture was evaporated under reduced pressure. The residue was dissolved in EtOH (1.0 mL, 17.2 mmol) and a solution of 1 M LiOH in water (1.4 mL, 1.4 mmol) was added. The resulting mixture was stirred at room temperature for 1 hour, then evaporated under reduced pressure. The residue was purified by reverse phase preparative HPLC to yield the title compound (75 mg, purity 100%) as a TFA salt. MS m/z [M+H]+ calc'd for C25H20Cl2FN5O5, 560.08. found 559.6.

Quelle