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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161999Generated: October 28, 2026

Tetrahydrofuran → 7-(1-Azabicyclo[2.2.2]oct-3-yloxy)-1-benzofuran-5-amine

https://huagongshe.com/reaction/1161999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
ReactantHydrazineHCID 9321—
ReactantHCID 66893251HCID 66893251—
CatalystNickelHCID 935—
SolventEthanolHCID 702—
Product7-(1-Azabicyclo[2.2.2]oct-3-yloxy)-1-benzofuran-5-amineHCID 6689300540.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07820675B2
Source datasetuspto-grants-2010_10
ORD IDord-c8e156baf1fc4c3f8b04b6029dab228e
Source noteuspto-grants-2010_10