HuagongsheHuagongshe Chemistry Print Report · For research reference only
Imidazole → HCID 59138482, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Imidazole | HCID 795 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 59138491 | HCID 59138491 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 59138482 | HCID 59138482 | 19.3% |
Reaction Steps
To a stirred suspension of 2-bromomethyl-3-(3,4,5-tri-methoxy-benzoyl)-6-methoxy-7-acetoxy-benzo[b]furan (Example 33) (35 mg, 0.071 mmol) and potassium carbonate (20 mg, 0.15 mmol) in dry acetonitrile (1.5 mL) was added imidazole (19 mg, 0.28 mmol) and the reaction mixture was stirred for overnight (tlc). The solvent was distilled under vacuum and the crude was taken in ethyl acetate, filleted and purified over silica gel plate to afford the title compound as a light yellow solid (6 mg, 19%). 1H NMR (300 MHz, CDCl3) δ—7.66(s, 1H), 7.19(s, 1H), 7.09(s, 2H, benzoyl Hs), 7.07(s, 1H), 6.85(d, J=8.63 Hz, 1H), 6.74(d, J=8.63 Hz, 1H), 5.37(s, 2H), 4.00(s, 3H, OMe), 3.95(s, 3H, OMe), 3.79(s, 6H, 2×OMe).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08198466B2 |
| Source dataset | uspto-grants-2012_06 |
| ORD ID | ord-1fa77b9b98a94d1591b6d7973a5808de |
| Source note | uspto-grants-2012_06 |