Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1H-1,2,4-Triazole | HCID 9257 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Bromo-7-acetoxy-3-(3,4,5-trimethoxybenzoyl)-6-methoxybenzofuran | HCID 24786560 | — |
| Solvent | Toluene | HCID 1140 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 11524689 | HCID 11524689 | — |
Reaction Steps
To a solution of 1,2,4-triazole(22 mg, 0.32 mmol) in dry tetrahydrofuran (2 mL) was added sodium hydride (60%, 24 mg, 0.60 mmol) and resulting suspension was treated with a solution of 2-bromo-7-acetoxy-3-(3,4,5-trimethoxybenzoyl)-6-methoxy-benzo[b]furan (50 mg, 0.10 mmol) in dry toluene (2 mL). The mixture was stirred at reflux for 6 hours (tlc), quenched with saturated ammonium chloride solution, extracted with dichloromethane (10 mL), dried over magnesium sulphate and the solvent distilled under vacuum. The crude residue was purified by PTLC (eluent=ethyl acetate: 1% triethylamine) to give the title compound as a yellow solid; (22 mg, 50%); 1H NMR (300 MHz, CDCl3) δ 8.64(bs, 1H), 8.06(bs, 1H), 7.10(d, 1H, J=8.60 Hz), 7.05(s, 2H, benzoyl Hs), 6.98(d, 1H, J=8.65 Hz), 3.98(s, 3H, OMe), 3.89(s, 3H, OMe), 3.77(s, 6H, 2×OMe).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08278290B2 |
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| Source dataset | uspto-grants-2012_10 |
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| ORD ID | ord-7239404e972844b78528531c835ea2e0 |
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| Source note | uspto-grants-2012_10 |
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