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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 854100Generated: October 25, 2026

Triethylamine → N-(1-Azabicyclo[2.2.2]oct-3-yl)-4-iodo-3-nitrobenzamide

https://huagongshe.com/reaction/854100

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantQuinuclidine, 3-amino-, dihydrochlorideHCID 197853—
Reactant4-Iodo-3-nitrobenzoyl chlorideHCID 58932935—
SolventDimethylformamideHCID 6228—
ProductN-(1-Azabicyclo[2.2.2]oct-3-yl)-4-iodo-3-nitrobenzamideHCID 5893294622.5%

Reaction Steps

A solution of 3.08 g (24.4 mmol) of 3-aminoquinuclidine dihydrochloride, 7.60 g (24.4 mmol) of 4-iodo-3-nitrobenzoyl chloride, 9.88 g (97.6 mmol) of triethylamine in 150 ml of DMF was stirred at room temperature overnight. The solvent was distilled off in a rotary evaporator, the residue was taken up in 200 ml of dichloromethane, and 200 ml of a saturated sodium bicarbonate solution were added. The organic phase was dried over sodium sulfate, and the solvent was distilled off in vacuo. 2.20 g (22.5%) of the desired title compound were obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07256288B2
Source datasetuspto-grants-2007_08
ORD IDord-19bae567823a440c9d3c24ed90770633
Source noteuspto-grants-2007_08