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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 714961Generated: November 4, 2026

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

https://huagongshe.com/reaction/714961

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 numberUS09187465B2
Source datasetuspto-grants-2015_11
ORD IDord-865a38e484584049b3a2d52f4802a249
Source noteuspto-grants-2015_11