HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Benzyl-5-(4-fluorophenyl)-2,5-diazabicyclo[2.2.2]octane → 2-(4-Fluorophenyl)-2,5-diazabicyclo[2.2.2]octane, hydrochoride salt
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Benzyl-5-(4-fluorophenyl)-2,5-diazabicyclo[2.2.2]octane | HCID 9900822 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Product | 2-(4-Fluorophenyl)-2,5-diazabicyclo[2.2.2]octane, hydrochoride salt | HCID 131723788 | 100% |
Reaction Steps
2-Benzyl-5-(4-fluoro-phenyl)-2,5-diaza-bicyclo[2.2.2]octane (1.1 g, 3.71 mmol) was dissolved in 1N hydrochloric acid/methanol (60 mL) and under nitrogen 10% palladium on carbon (0.50 g) was added. The reaction was hydrogenated at 1 atmosphere for 2 hours. The reaction was filtered through Celite and concentrated to yield 2-(4-Fluoro-phenyl)-2,5-diaza-bicyclo[2.2.2]octane, hydrochoride salt (0.90 g, 100%) as an off white solid which had the following properties: Mp. 154-156° C.; 1H NMR CDCl3 δ: 9.74 (brd s, 1H), 9.67 (brd s, 1H), 7.00 (t, J=9.1 Hz, 2H), 6.68-6.61 (m, 2H), 4.07 (s, 1H), 3.70 (brd s, 1H), 3.63 (d, J=11.2 Hz, 1H), 3.29 (d, J=10.8 Hz, 1H), 3.23 (brd s, 2H), 2.19-2.04 (m, 1H), 1.95-1.83 (m, 1H), 1.81-1.64 (m, 2H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06552015B2 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-61798fe8dc1245bab0f779f399728686 |
| Source note | uspto-grants-2003_04 |