HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 1-Azabicyclo[2.2.2]octan-3-ol, 3-(3-methoxypyrazinyl)-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 3-(3-Chloropyrazinyl)-1-azabicyclo[2.2.2]octan-3-ol | HCID 10331840 | — |
| Product | 1-Azabicyclo[2.2.2]octan-3-ol, 3-(3-methoxypyrazinyl)- | HCID 10354053 | — |
Reaction Steps
To a solution of 40 ml of methanol that had reacted with 0.5 g of Na (0.022 mol) was added 0.5 g of (7) (0.0021 mol). The reaction was heated to reflux for 1 h followed by evaporation of the solvent. The residue was treated with ice-water and extracted 3× with 25 ml of CH2Cl2. The extracts were dried and evaporated to give a yellow solid that was recrystallized from ethyl acetate to give (8), 0.12 g, mp 130°-131° C. NMR ppm (CDCl3) 1.15 (1H, m), 1.45 (2H, m), 2.25 (1H, m), 2.38 (1H, m), 2.7-3.15 (5H, m), 3.9 (1H, bs), 4.05 (3H, s), 4.3 (1H, d), 8.05 (1H, d), 8.15 (1H, d). Anal. C12H17N3O2 requires C: 61.26; H: 7.28; N: 17.86%. Found C: 61.02; H: 7.45; N: 17.95%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05182283 |
| Source dataset | uspto-grants-1993_01 |
| ORD ID | ord-b0aee7f0c0df49878816efd4235e738e |
| Source note | uspto-grants-1993_01 |