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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 55776Generated: October 25, 2026

Hydrochloric Acid → 2-(1-Azabicyclo[2.2.2]oct-3-yl)-N-(8-nitro-2-naphthyl)acetamide hydrochloride

https://huagongshe.com/reaction/55776

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
Reactant8-Nitro-2-naphthalenamineHCID 604707—
Reactant2-(Quinuclidin-3-yl)acetic acid hydrochlorideHCID 23024147—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDimethylformamideHCID 6228—
Product2-(1-Azabicyclo[2.2.2]oct-3-yl)-N-(8-nitro-2-naphthyl)acetamide hydrochlorideHCID 17979821—

Reaction Steps

200 mg (0.97 mmol) of 1-azabicyclo[2.2.2]oct-3-ylacetic acid hydrochloride are heated under reflux in 2 ml (27.42 mol) of thionyl chloride for 2 h. The mixture is then freed of excess thionyl chloride in vacuo, and the residue is taken up in 4 ml of DMF. 0.54 ml (3.89 mmol) of triethylamine, 59.4 mg (0.4 mmol) of DMAP and 183.0 mg (0.97 mmol) of 8-nitro-2-naphthylamine are added to this solution. After reaction overnight and purification by preparative HPLC, the resulting product fractions are mixed with 1 M hydrochloric acid and concentrated in vacuo. Recrystallization, of the residue from isopropanol and drying under high vacuum result in 59 mg (15% of theory) of the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09433614B2
Source datasetuspto-grants-2016_09
ORD IDord-6cec85f52d064144a707cce7c3bf4a26
Source noteuspto-grants-2016_09