HuagongsheHuagongshe Chemistry Print Report · For research reference only
Tetrahydrofuran → 7-(1-Azabicyclo[2.2.2]oct-3-yloxy)-1-benzofuran-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | HCID 66893251 | HCID 66893251 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 7-(1-Azabicyclo[2.2.2]oct-3-yloxy)-1-benzofuran-5-amine | HCID 66893005 | 40.4% |
Reaction Steps
3-[(5-Nitro-1-benzofuran-7-yl)oxy]quinuclidine (1.38 g, 4.79 mmol; obtained in Step 1) was dissolved in ethanol:THF (100 mL: 25 mL) and Raney-nickel (slurry in ethanol; 6 mL) and hydrazine (891 μL, 0.18 mmol) were added. The mixture was stirred at room temperature for 3 h and then filtered through Celite and the solvent was removed in vacuo. The crude product was purified by flash chromatography [eluent: DCM:methanol (6:1) and chloroform:MeOH:triethylamine (9:1:0.1)] to give 7-(1-azabicyclo[2.2.2]oct-3-yloxy)-1-benzofuran-5-amine (500 mg; 40%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07820675B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-c8e156baf1fc4c3f8b04b6029dab228e |
| Source note | uspto-grants-2010_10 |