HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2075204Generated: October 27, 2026
Potassium Acetate → Ethyl 1-(3-fluoro-4-(5-(pyridin-2-ylmethyl)benzofuran-2-yl)benzyl)azetidine-3-carboxylate
https://huagongshe.com/reaction/2075204
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Acetate | HCID 517044 | — |
| Reactant | 5-(Pyridin-2-ylmethyl)benzofuran-2-ylboronic acid | HCID 58415277 | — |
| Reactant | Ethyl 1-(4-bromo-3-fluorobenzyl)azetidine-3-carboxylate | HCID 58415312 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Ethyl 1-(3-fluoro-4-(5-(pyridin-2-ylmethyl)benzofuran-2-yl)benzyl)azetidine-3-carboxylate | HCID 58415388 | — |
Reaction Steps
In a sealed flask, a mixture of 5-(pyridin-2-ylmethyl)benzofuran-2-ylboronic acid (214 mg, 846 μmol) and potassium acetate (166 mg, 1691 μmol) was set under argon, treated with bis{di(tbutyl)phenyl}palladium(II) dichloride (32 mg, 51 μmol), followed by a solution of ethyl 1-(4-bromo-3-fluorobenzyl)azetidine-3-carboxylate (267 mg, 846 μmol) in EtOH (5 mL). The resulting suspension was degassed again and heated to 80° C. for 2.5 h. The mixture was cooled to ˜10° C. and dropwise treated with H2O (15 mL). The mixture was extracted 2× with EtOAc. The combined organic layers were dried over MgSO4 and evaporated. Purification by flash chromatography (DCM to DCM/MeOH=4:1) gave ethyl 1-((3-fluoro-4-(5-(pyridin-2-ylmethyl)benzofuran-2-yl)phenyl)methyl)azetidine-3-carboxylate as a yellow foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07919519B2 |
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| Source dataset | uspto-grants-2011_04 |
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| ORD ID | ord-25e570b33dd842729abf47b41be0c8ff |
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| Source note | uspto-grants-2011_04 |
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