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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088322Generated: November 2, 2026

Sodium Hydroxide → HCID 59331187, compound

https://huagongshe.com/reaction/2088322

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
Reactant4-Iodobenzoyl chlorideHCID 74373—
ReactantDiisopropylethylamineHCID 81531—
Reactant(3S)-1-azabicyclo[2.2.2]octan-3-amine dihydrochlorideHCID 12494973—
SolventDimethylformamideHCID 6228—
ProductHCID 59331187HCID 5933118764.2%

Reaction Steps

N,N′-Diisopropylethylamine (1.05 ml, 6.03 mmol) was added to a flask charged with DMF solution mixture of (S)-(−)-3-Aminoquinuclidine dihydrochloride (400 mg, 2.01 mmol) and 4-Iodobenzoyl chloride (616 mg, 2.31 mmol). The clear yellow solution was stirred for 3 hours. The reaction mixture was worked up by addition of 1N sodium hydroxide aqueous solution and extracted twice with ethyl acetate, combined organic layer was washed with saturated brine solution, dried over sodium sulfate, filtered, and concentrated to crude clear oil. The crude oil was purified via preparative HPLC to obtain pure product of (S)-4-iodo-N-(quinuclidin-3-yl)benzamide, (460 mg, 64% yield). 1H NMR (400 MHz, Methanol-D4) δ (ppm): 7.85 (d, J=8 Hz, 2H), 7.60 (d, J=8 Hz, 2H), 4.12 (m, 1H), 3.31 (m, 1H), 2.99 (m, 1H), 2.84 (m, 4H), 2.02 (m, 1H), 1.90 (m, 1H), 1.78 (m, 2H), 1.54 (m, 1H). C14H17IN2O=356.04 LCMS (M+H): m/z 357

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08435762B2
Source datasetuspto-grants-2013_05
ORD IDord-84da32e7f652409fb03d04d1fba25ace
Source noteuspto-grants-2013_05