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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2423533Generated: November 1, 2026

Ammonium Acetate → HCID 59321495, compound

https://huagongshe.com/reaction/2423533

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium AcetateHCID 517165—
ReactantEthyl [(2-acetyl-4-bromophenyl)amino](oxo)acetateHCID 59321497—
SolventAcetic AcidHCID 176—
ProductHCID 59321495HCID 5932149549.3%

Reaction Steps

Ammonium acetate (400.0 mg, 5.19 mmol) was added to ethyl[(2-acetyl-4-bromophenyl)amino](oxo)acetate (163.0 mg, 518.9 μmol) in acetic acid (5.2 mL) at room temperature and the reaction was heated at reflux for 19 hours. The reaction mixture was concentrated, then water was added, and the solution was extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate, filtered, and concentrated. The residue was purified by silica gel chromatography eluting with 2:3 ethyl acetate:hexanes to give 75.5 mg (49%) of ethyl 6-bromo-4-methyl-2-quinazolinecarboxylate as a solid. 1H NMR (400 MHz, d6-DMSO): δ 8.63 (d, J=2 Hz, 1H), 8.21 (dd, J=9, 2 Hz, 1H), 8.07 (d, J=9 Hz, 1H), 4.41 (q, J=7 Hz, 2H), 2.97 (s, 3H), 1.35 (t, J=7 Hz, 3H). ESI-LCMS m/z 295 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07960552B2
Source datasetuspto-grants-2011_06
ORD IDord-a4f4a14886514799bed8c0f4e266fc68
Source noteuspto-grants-2011_06