HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-3-methoxybenzamide → HCID 135471356, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-3-methoxybenzamide | HCID 18536571 | — |
| Reactant | 8-hydroxy-2-(4-nitrophenyl)-3H-quinazolin-4-one | HCID 135492389 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 135471356 | HCID 135471356 | — |
Reaction Steps
8-Hydroxy-2-(4'-nitrophenyl)quinazolin-4-[3 H]-one, prepared from 3-methoxy-2-aminobenzamide as in Example 5, (50 mg, 0.18 mmol) was suspended in methanol (20 ml) with palladium-carbon catalyst (20 mg) and the reaction vessel was placed under the atmosphere of hydrogen at ambient temperature and pressure. The reaction mixture changed from a yellow suspension to a clear, colourless solution, whereupon the catalyst was removed by filtration through Celite™. The solvent was removed under vacuum to leave a cream pale brown solid, which was recystallised from aq. methanol (25.7 mg, 0.1 mmol, 57%), m.p. >230° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06156739 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-b5d0445d9d5d4bbc9eef6286afa462be |
| Source note | uspto-grants-2000_12 |