HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-amino-N-(4-chlorophenyl)benzamide → HCID 67454597, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-amino-N-(4-chlorophenyl)benzamide | HCID 670472 | — |
| Reactant | 3-Nitro-p-tolualdehyde | HCID 1798998 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67454597 | HCID 67454597 | 63.8% |
Reaction Steps
4-methyl-3-nitrobenzaldehyde (0.270 g, 1.60 mmol) and anhydrous CuCl2 (0.435 g, 3.20 mmol) were added to a solution of 2-amino-N-(4-chlorophenyl)benzamide (0.400 g, 1.60 mmol) in anhydrous EtOH (10 mL). After heating at reflux temperature for 3 hours, the reaction mixture was concentrated in vacuo. The residue was dissolved in EtOAc, washed with H2O, then brine, dried (Na2SO4), filtered, and concentrated in vacuo. Purification by flash chromatography on silica gel, eluting with 5% to 60% EtOAc in heptane, afforded 3-(4-chlorophenyl)-2-(4-methyl-3-nitrophenyl)quinazolin-4(3H)-one (0.400 g, 63%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952021B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-6628f6b1e7ff4c889da635c4434396aa |
| Source note | uspto-grants-2015_02 |