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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1921809Generated: October 30, 2026

Ammonia → 5-Bromofuran-3-carboxamide

https://huagongshe.com/reaction/1921809

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
Reactant5-Bromofuran-3-carboxylic acidHCID 13333560—
SolventDimethylformamideHCID 6228—
Product5-Bromofuran-3-carboxamideHCID 1082149479%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 5-bromo-furan-3-carboxylic acid (0.364 g, 1.92 mmol), 3-hydroxybenzotriazole hydrate (0.28 g, 2.11 mmol), 1-ethyl-3-(3′-dimethylaminopropyl)carbodiimide (0.40 g, 2.11 mmol) in DMF (11 mL) is stirred at room temperature for 2 hours. The reaction mixture is then cooled to 0° C. and aq. NH3 (0.22 mL) is added. The mixture is stirred at room temperature for an additional 5 hours, then the solvent is removed in vacuo and the residue dissolved in EtOAc, washed with 1N NaOH, and 1N HCl. The organic layers are combined, dried over MgSO4 and concentrated to afford the title compound (0.288 g, 79%). HPLC (254 nm): Rt 2.17 min (85.3%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08173656B2
Source datasetuspto-grants-2012_05
ORD IDord-e24461adca0249f5aed30aee20eec9f9
Source noteuspto-grants-2012_05