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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2088310Generated: October 29, 2026

Triethylamine → HCID 44286533, compound

https://huagongshe.com/reaction/2088310

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Methoxybenzoic acidHCID 11370—
Reactant2-Chloro-1-methylpyridinium iodideHCID 167069—
Reactant(3S)-1-azabicyclo[2.2.2]octan-3-amine dihydrochlorideHCID 12494973—
SolventWaterHCID 962—
SolventAcetonitrileHCID 6342—
ProductHCID 44286533HCID 4428653385%

Reaction Steps

1.5 ml of Acetonitrile and Triethylamine (700 uL, 5.0 mmol) was added to a flask charged with (S)-(−)-3-Aminoquinuclidine dihydrochloride (199 mg, 1.0 mmol) and o-Methoxybenzoic acid (167 mg, 1.1 mmol), followed by addition of 2-Chloro-1-methyl pyridinium iodide (383 mg, 1.5 mmol) at room temperature. After stirring overnight, about 2 ml of water was added to reaction mixture to resolve a clear solution that was subsequently injected into a Preparative HPLC instrument for purification. Desired fractions were combined and concentrated under vacuum. (S)-2-methoxy-N-(quinuclidin-3-yl)benzamide (221 mg, 85% yield) was isolated as an oil. 1H NMR (400 MHz, Methanol-D4) δ (ppm): 7.79 (dd, J=7.7 1.6 Hz, 1H), 7.51 (td, J=8.0, 1.6 Hz, 1H), 7.15 (d, J=8.5 Hz, 1H), 7.06 (t, J=7.4 Hz, 1H), 4.45 (m, 4H), 3.97 (s, 3H), 3.82 (ddd, J=11.7, 9.9, 2.0 Hz 1H), 3.37 (m, 4H), 2.37 (q, J=3.2 Hz, 1H), 2.20 (m, 1H), 2.09 (m, 2H), 1.99 (m, 1H). LCMS (ESI): m/z 261.1 (M+H [C15H20N2O]=261.15).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08435762B2
Source datasetuspto-grants-2013_05
ORD IDord-c5e1e834057043c6835719168ec5692c
Source noteuspto-grants-2013_05