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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 722191Generated: October 29, 2026

Diisopropylethylamine → Methyl 4'-{[(3S)-1-azabicyclo[2.2.2]oct-3-ylcarbonyl]amino}-1,1'-biphenyl-4-carboxylate

https://huagongshe.com/reaction/722191

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4'-Aminobiphenyl-4-carboxylic acid methyl esterHCID 737635—
Reactant(3R)-1-azabicyclo[2.2.2]octane-3-carbonyl chlorideHCID 11672746—
SolventDichloromethaneHCID 6344—
SolventTetrahydrofuranHCID 8028—
ProductMethyl 4'-{[(3S)-1-azabicyclo[2.2.2]oct-3-ylcarbonyl]amino}-1,1'-biphenyl-4-carboxylateHCID 69617735—

Reaction Steps

679 mg (3.91 mmol) of (3R)-1-azabicyclo[2.2.2]octane-3-carbonyl chloride, 846 mg (3.73 mmol) methyl 4′-amino-1,1′-biphenyl-4-carboxylate, 963 mg (7.45 mmol) of N,N-diisopropylethylamine and 227 mg (1.86 mmol) of 4-N,N-dimethylaminopyridine are dissolved in 5 ml of THF and stirred at RT overnight and then at 50° C. overnight once again. The reaction mixture is taken up in dichloromethane and water, and the aqueous phase is extracted three times with dichloromethane. The crude product is purified by chromatography on silica gel 60 (mobile phase: dichloromethane/triethylamine 100:1→dichloromethane/methanol/triethylamine 50:50:1). The solvent is removed under reduced pressure. The product is taken up in 1N sodium hydroxide solution and extracted a total of three times with ethyl acetate. The organic phase is dried over magnesium sulfate and freed of solvent under reduced pressure. Finally, the last residues of solvent are removed under high vacuum. 50 mg (4% of theory) of the title compound are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07138410B2
Source datasetuspto-grants-2006_11
ORD IDord-cfce49b6ad004828a2490b8e6a3334b6
Source noteuspto-grants-2006_11