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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 3-(2-Pyrazinyl)-1-azabicyclo[2.2.2]oct-2-ene | HCID 15750142 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 3-Pyrazin-2-yl-1-aza-bicyclo[2.2.2]octane | HCID 15750153 | 72.7% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05260293 |
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| Source dataset | uspto-grants-1993_11 |
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| ORD ID | ord-464f9eb28bbb423dbd4cb80a7b7a597f |
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| Source note | uspto-grants-1993_11 |
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