Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 3-(3-Chloropyrazinyl)-1-azabicyclo[2.2.2]octan-3-ol | HCID 10331840 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | HCID 10039179 | HCID 10039179 | 12% |
Reaction Steps
To a solution of 40 ml of butanol that had reacted with 0.5 g of Na (0.022 mol) was added 0.78 g of (7) (0.033 mol). The reaction was heated to 60° C. for 1.5 h and the cooled reaction treated with 6 ml of 5 N HCl. The butanol was azeotroped off with water, the residue made basic with saturated aqueous K2CO3, and the mixture extracted 3× with 25 ml of CH2Cl2. The extracts were washed with brine, dried, and the solvent evaporated to give a yellow solid that was purified by radial chromatography eluting with 5% ethanol-0.5% NH4OH-CHCl3 to give 0.55 g of (18) as a yellowish solid. Recrystallization from ether gave a white solid, mp 107°-108° C. NMR ppm (CDCl3) 1.0 (3H, t), 1.15 (1H, m), 1.35-1.6 (4H, m), 1.85 (2H, m), 2.25 (1H, m), 2.37 (1H, bs), 2.75 (1H, m), 2.82-3.0 (3H, m), 3.05 (1H, m), 3.95 (1H, s), 4.2 (1H, d), 4.45 (2H, q), 8.0 (1H, d), 8.12 (1H, d). Anal. C15H23N3O2 requires C: 64.96; H: 8.36; N: 15.15%. Found C: 65.21; H: 8.11; N: 15.25%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05182283 |
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| Source dataset | uspto-grants-1993_01 |
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| ORD ID | ord-4e7383d0b14f4713935b364db6575bf1 |
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| Source note | uspto-grants-1993_01 |
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