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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13400Generated: October 29, 2026

Dimethylformamide → t-Butyl 2-(4-amino-2-((2'-fluorobiphenyl-4-yl)oxy)-5-nitrophenyl)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/13400

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantPotassium CarbonateHCID 11430—
Reactant4-(2-Fluorophenyl)phenolHCID 345419—
Reactantt-Butyl 2-(4-amino-2-fluoro-5-nitrophenyl)pyrrolidine-1-carboxylateHCID 23145290—
SolventEthyl AcetateHCID 8857—
Productt-Butyl 2-(4-amino-2-((2'-fluorobiphenyl-4-yl)oxy)-5-nitrophenyl)pyrrolidine-1-carboxylateHCID 23145747—

Reaction Conditions

Temperature80 °C

Reaction Steps

200 mg of 2′-fluorobiphenyl-4-ol and 184 mg of potassium carbonate were added to an N,N-dimethylformamide (3 ml) solution of 288 mg of t-butyl 2-(4-amino-2-fluoro-5-nitrophenyl)pyrrolidine-1-carboxylate, and the reaction liquid was stirred overnight at 80° C. The reaction liquid was diluted with ethyl acetate, washed with water and saturated saline in order, and dried with anhydrous magnesium sulfate. The solvent was evaporated away, and the resulting residue was purified through silica gel column chromatography (developing solvent: hexane/ethyl acetate=5/1) to obtain the entitled compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728025B2
Source datasetuspto-grants-2010_06
ORD IDord-88334f19c84844df8c80809518875144
Source noteuspto-grants-2010_06