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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 389740Generated: October 27, 2026

Ammonia → 2-Iodo-5-(4-methoxyphenyl)oxazole-4-carboxamide

https://huagongshe.com/reaction/389740

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1,4-DioxaneHCID 31275—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant2-Iodo-5-(4-methoxyphenyl)oxazole-4-carboxylic acidHCID 68520872—
ReactantHCID 178526939HCID 178526939—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
Product2-Iodo-5-(4-methoxyphenyl)oxazole-4-carboxamideHCID 6852095270.4%

Reaction Steps

To a solution 2-iodo-5-(4-methoxyphenyl)oxazole-4-carboxylic acid (0.92 g, 2.7 mmol) in DCM (20 mL) and DMF (10 mL) was added hydroxybenzotriazole monohydrate (0.44 g, 2.9 mmol) followed by 0.5M ammonia in dioxane (22 mL, 11.0 mmol) and 1-(3-(dimethylamino)propyl)-3-ethyl-carbodiimide hydrochloride (0.77 g, 4.0 mmol) and the reaction stirred at room temperature overnight. EtOAc was then added and the mixture washed with brine. The organic phase was dried over MgSO4 and the solvent removed in vacuo. The residue was purified by silica gel column chromatography using gradient of 0-50% EtOAc in DCM to afford 2-iodo-5-(4-methoxyphenyl)oxazole-4-carboxamide (0.66 g. 1.9 mmol, 70%) as a yellow solid. 1H NMR (CDCl3) 3.79 (3H, s), 5.47 (1H, br. s), 6.90 (2H, d), 6.94 (1H, br. s), 8.14 (2H, d). LCMS (1) Rt: 1.84 min; m/z (ES+) 345.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08378095B2
Source datasetuspto-grants-2013_02
ORD IDord-9d58ccd063a54dadb12097a360eba49a
Source noteuspto-grants-2013_02