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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588337Generated: October 29, 2026

Potassium Carbonate → (3R)-N-(4'-Nitrobiphenyl-4-yl)quinuclidine-3-carboxamide hydrochloride

https://huagongshe.com/reaction/588337

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant4-Amino-4'-nitrobiphenylHCID 14593—
Reactant1,4-DioxaneHCID 31275—
Reactant(3R)-Quinuclidine-3-carbonyl chloride hydrochlorideHCID 57462844—
SolventDimethylformamideHCID 6228—
Product(3R)-N-(4'-Nitrobiphenyl-4-yl)quinuclidine-3-carboxamide hydrochlorideHCID 67427704—

Reaction Conditions

Temperature100 °C

Reaction Steps

480 mg (3.50 mmol) of potassium carbonate are added to a mixture, prepared under argon, of 490 mg (2.33 mmol) of (3R)-quinuclidine-3-carbonyl chloride hydrochloride (Example 5A) and 250 mg (1.17 mmol) of 4-amino-4′-nitrobiphenyl in 11 ml of a 10:1 mixture of dioxane and DMF. The reaction mixture is stirred at 100° C. for 18 h and then concentrated. The residue is suspended in methanol and filtered. The filtration residue is washed with water, mixed with 20 ml of a 3:1 mixture of acetonitrile and 1 N hydrochloric acid, again concentrated and dried under high vacuum. The above filtrate is purified by preparative HPLC. The product fractions are concentrated, taken up in 5 ml of a 3:1 mixture of acetonitrile and 1 N hydrochloric acid, again concentrated and dried under high vacuum. 291 mg (61.7% of theory) of the title compound are obtained from the filtration residue, and a further 65 mg (12.4% of theory) are obtained from the filtrate, in this way.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09227964B2
Source datasetuspto-grants-2016_01
ORD IDord-be71419077a1481da47f58a334ff99db
Source noteuspto-grants-2016_01