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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588343Generated: October 29, 2026

Potassium Carbonate → [(4'-{[(3R)-1-Azabicyclo[2.2.2]oct-3-ylcarbonyl]amino}biphenyl-4-yl)amino](oxo)acetic acid hydrochloride

https://huagongshe.com/reaction/588343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
Reactant[(4'-Aminobiphenyl-4-yl)amino](oxo)acetic acidHCID 293247—
Reactant(3R)-Quinuclidine-3-carbonyl chloride hydrochlorideHCID 57462844—
SolventDimethylformamideHCID 6228—
Product[(4'-{[(3R)-1-Azabicyclo[2.2.2]oct-3-ylcarbonyl]amino}biphenyl-4-yl)amino](oxo)acetic acid hydrochlorideHCID 11453179—

Reaction Steps

300 mg (2.14 mmol) of potassium carbonate are added to a mixture, prepared under argon, of 300 mg (1.43 mmol) of (3R)-quinuclidine-3-carbonyl chloride hydrochloride (Example 5A) and 180 mg (0.71 mmol) of [(4′-aminobiphenyl-4-yl)amino](oxo)acetic acid [CAS Registry No. 100872-66-0] in 11 ml of a 10:1 mixture of dioxane and DMF. After 18 h at 100° C., the reaction mixture is concentrated in vacuo, and the residue is dissolved in water and acetonitrile and purified by preparative HPLC. The concentrated product fractions are mixed with 5 ml of a 2:1 mixture of acetonitrile and 1 N hydrochloric acid and again concentrated. Drying under high vacuum results in 64 mg (20.3% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227964B2
Source datasetuspto-grants-2016_01
ORD IDord-88a9f0a27f29438ab59333498b44a76a
Source noteuspto-grants-2016_01