HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Amino-N-(4-sec-butylphenyl)benzamide → HCID 86659825, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Amino-N-(4-sec-butylphenyl)benzamide | HCID 16770037 | — |
| Reactant | 2,2,2-Trifluoro-N-(4-formyl-2-iodophenyl)acetamide | HCID 58767071 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86659825 | HCID 86659825 | 66% |
Reaction Steps
2-amino-N-(4-sec-butylphenyl)benzamide (0.275 g, 1.00 mmol) and anhydrous CuCl2 (0.275 g, 2.00 mmol) were added to a solution of 2,2,2-trifluoro-N-(4-formyl-2-iodophenyl)acetamide in anhydrous EtOH (15 mL) and heated to reflux temperature for 3 hours. After concentrating 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 10% to 60% EtOAc in heptane, afforded N-(4-(3-(4-sec-butylphenyl)-4-oxo-3,4-dihydroquinazolin-2-yl)-2-iodophenyl)-2,2,2-trifluoroacetamide (0.390 g, 66%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08952021B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-0dfdd8b358f44204afd113b6c4d15252 |
| Source note | uspto-grants-2015_02 |