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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 252845Generated: October 25, 2026

Ethyl Acetate → 4-Acetamido-N-(2-amino-5-(benzo[d]oxazol-2-yl)phenyl)benzamide

https://huagongshe.com/reaction/252845

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
Reactant4-Acetamidobenzoyl chlorideHCID 7010341—
Reactant4-(Benzo[d]oxazol-2-yl)benzene-1,2-diamineHCID 14637897—
SolventPyridineHCID 1049—
SolventAcetonitrileHCID 6342—
Product4-Acetamido-N-(2-amino-5-(benzo[d]oxazol-2-yl)phenyl)benzamideHCID 597367261%

Reaction Steps

To a stirred suspension of 227 (350 mg, 1.55 mmol) in acetonitrile (20 mL) and pyridine (2 ml) was added 4-acetamidobenzoyl chloride (307 mg, 1.55 mmol) in acetonitrile (5 ml) at 0° C. The solution was warmed up to room temperature and stirred for 4 hours. The reaction mixture was concentrated under reduced pressure and the residue was purified by flash chromatography on silica gel, eluents hexane-EtOAc (1:3), then EtOAc (100%), to afford 228 as a beige solid (5 mg, 1% yield). 1H NMR: (DMSO) δ (ppm): 10.22 (s, 1H), 9.62 (s, 1H), 8.05 (d, J=2.4 Hz, 1H), 7.89 (d, J=8.4 Hz, 2H), 7.80 (1H, dd, J=2.0, 8.4 Hz, 1H), 7.68-7.73 (m, 4H), 7.33-7.35 (m, 2H), 6.91 (d, J=8.4 Hz, 1H), 5.86 (bs, 2H), 2.12 (s, 3H). MS: (calc.) 386.41; (obt.) 387.1 (MH)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07868205B2
Source datasetuspto-grants-2011_01
ORD IDord-79fc891a262542d0af8b5159917f61bc
Source noteuspto-grants-2011_01