HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium hydride → 5-[1-(3-Bromo-phenyl)-1H-imidazol-4-yl]-3-methyl-[1,2,4]oxadiazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 1-(3-Bromo-phenyl)-1H-imidazole-4-carboxylic acid ethyl ester | HCID 16128754 | — |
| Reactant | HCID 178465666 | HCID 178465666 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-[1-(3-Bromo-phenyl)-1H-imidazol-4-yl]-3-methyl-[1,2,4]oxadiazole | HCID 16128506 | 35% |
Reaction Steps
To a suspension of NaH (1.30 g, 32.64 mmol, 60% in mineral oil) in THF (15 mL) under nitrogen atmosphere was added N-hydroxy-acetamidine (2.62 g, 35.4 mmol) and stirred for 1 h at room temperature. The bromo ester 3 (8 g, 27.2 mmol) in THF (2 mL) was added and refluxed for 12 h. The reaction mixture was quenched by adding brine, extracted with ethylacetate (100 mL) and dried over anhydrous Na2SO4. The organic layer was concentrated under reduced pressure and purified by flash chromatography using 25% ethylacetate in hexane as mobile phase to furnish 4 (2.8 g, 35%) as pale yellow solid, mp=200.1-202.4° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858649B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-7d095b7ed0d04e27ae4723f3d4a3b101 |
| Source note | uspto-grants-2010_12 |