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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1846373Generated: November 3, 2026

2-Amino-N-(4-sec-butylphenyl)benzamide → HCID 86659825, compound

https://huagongshe.com/reaction/1846373

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Amino-N-(4-sec-butylphenyl)benzamideHCID 16770037—
Reactant2,2,2-Trifluoro-N-(4-formyl-2-iodophenyl)acetamideHCID 58767071—
SolventEthanolHCID 702—
ProductHCID 86659825HCID 8665982566%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08952021B2
Source datasetuspto-grants-2015_02
ORD IDord-0dfdd8b358f44204afd113b6c4d15252
Source noteuspto-grants-2015_02