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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389728Generated: October 29, 2026

Ammonia → 5-(4-Methoxyphenyl)-2-phenyloxazole-4-carboxamide

https://huagongshe.com/reaction/389728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1,4-DioxaneHCID 31275—
ReactantCarbodiimideHCID 160435—
Reactant5-(4-Methoxyphenyl)-2-phenyloxazole-4-carboxylic acidHCID 20120402—
Reactant5-(4-Methoxyphenyl)-2-(thiophen-2-yl)oxazole-4-carboxylic acidHCID 29281463—
ReactantHCID 178526939HCID 178526939—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product5-(4-Methoxyphenyl)-2-phenyloxazole-4-carboxamideHCID 5958743127%

Reaction Steps

To a solution of 5-(4-methoxyphenyl)-2-phenyloxazole-4-carboxylic acid (prepared according to the method described for 5-(4-methoxyphenyl)-2-(thiophen-2-yl)oxazole-4-carboxylic acid in Example M-1, 0.032 g, 0.11 mmol) and hydroxybenzotriazole monohydrate (0.02 g, 0.13 mmol) in DCM (2 mL) and DMF (1 mL) was added 0.5M ammonia in dioxane (1 mL, 0.5 mmol), followed by PS-carbodiimide resin. The resulting mixture was stirred at room temperature overnight. The mixture was passed through a MP-CO3 resin cartridge and the solvent removed in vacuo. The residue was purified by preparative HPLC to afford 5-(4-methoxyphenyl)-2-phenyloxazole-4-carboxamide (0.008 g, 0.03 mmol, 27%) as a white solid. 1H NMR (DMSO) δ 3.85 (3H, s), 7.10 (2H, d), 7.60 (3H, m), 7.66 (1H, br. s), 7.78 (1H, br. s), 8.14 (2H, m), 8.37 (2H, d). LCMS (2) Rt: 3.16 min; m/z (ES+) 295.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378095B2
Source datasetuspto-grants-2013_02
ORD IDord-8ab78547a8c34ef5901e28c81e11d08d
Source noteuspto-grants-2013_02