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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 256871Generated: October 30, 2026

3-(2-Pyrazinyl)-1-azabicyclo[2.2.2]oct-2-ene → 3-Pyrazin-2-yl-1-aza-bicyclo[2.2.2]octane

https://huagongshe.com/reaction/256871

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(2-Pyrazinyl)-1-azabicyclo[2.2.2]oct-2-eneHCID 15750142—
SolventEthanolHCID 702—
Product3-Pyrazin-2-yl-1-aza-bicyclo[2.2.2]octaneHCID 1575015372.7%

Reaction Steps

A solution of 3-(2-pyrazinyl)-1-azabicyclo [2.2.2]-oct-2-ene (75 mg, 0.4 mmol), in ethanol (20 ml), was hydrogenated over 10% pd/C (75 mg) in a Parr apparatus. After 1.5 h the catalyst was removed by filtration through hyflo and the solvent removed under reduced pressure. Chromatography of the residue through alumina eluting with dichloromethane/methanol (95:5) gave 3-(2-pyrazinyl)-1-azabicyclo [2.2.2]octane (55 mg) as a pale yellow oil. The hydrochloride salt was prepared, m.p. 203°-205° C. (isopropyl alcohol/ether); (Found C, 55.23; H, 7.15; N, 17.86 C11H15N3. HCl. 0.75 H2O requires C, 55.23; H, 7.32: N, 17.57%); m/e 189 (M+ for free base); δ (360 MHz, D2O) 1.70-1.85 (2H, m, CH2); 2.10-2.30 (2H, m, CH2); 2.40-2.48 (1H, m, CH-bridgehead); 3.28-4.04 (7H, m, 3×CH2 and CH); 8.52 (1H, m, pyrazine-H); 8.63 (2H, m, pyrazine-H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05260293
Source datasetuspto-grants-1993_11
ORD IDord-464f9eb28bbb423dbd4cb80a7b7a597f
Source noteuspto-grants-1993_11