Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1359360Generated: November 1, 2026

Triethylamine → (3R)-3-[2-Benzyl-6-(3,3-ethylenedioxypyrrolidine-1-yl]-3-pyridyl]ethynyl-3-quinuclidinol

https://huagongshe.com/reaction/1359360

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant(3R)-3-ethynyl-1-azabicyclo[2.2.2]octan-3-olHCID 946095—
Reactant2-Benzyl-3-iodo-6-(3,3-ethylenedioxypyrrolidin-1-yl)pyridineHCID 21942286—
CatalystHCID 178418397HCID 178418397—
SolventMethanolHCID 887—
Product(3R)-3-[2-Benzyl-6-(3,3-ethylenedioxypyrrolidine-1-yl]-3-pyridyl]ethynyl-3-quinuclidinolHCID 5907779688.5%

Reaction Steps

A mixture of 3.0 g of 2-benzyl-3-iodo-6-(3,3-ethylenedioxypyrrolidine-1-yl)pyridine, 1.07 g of (3R)-3-ethynyl-3-quinuclidinol, 82 mg of tetrakis(triphenylphosphine)palladium (0), 68 mg of cuprous iodide, 2.0 ml of triethylamine and 7 ml of methanol was stirred at room temperature overnight in a nitrogen atmosphere. The reaction solution was partitioned between aqueous dilute ammonia-ethyl acetate, washed with washed with water, dried over anhydrous magnesium sulfate and then concentrated. 10 ml of tetrahydrofuran was added to the residue to dissolve under heating, and to the mixture was added 15 ml of ethyl acetate. The mixture was filtered through 10 g of NH-silica gel, washed with ethyl acetate, and concentrated. The residue was crystallized from ethyl acetate, to give 2.79 g of the target compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06599917B1
Source datasetuspto-grants-2003_07
ORD IDord-2d088844882042ffb72b6f09a20e2993
Source noteuspto-grants-2003_07