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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 267082Generated: October 26, 2026

Triethylamine → N-Methoxy-N-methyl-1-(2-naphthylmethyl)-1H-imidazol-5-ylacetamide

https://huagongshe.com/reaction/267082

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant3-hydroxy-1,2,3-benzotriazin-4(3H)-oneHCID 73026—
ReactantSodium BicarbonateHCID 516892—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-(2-naphthylmethyl)-1H-imidazol-5-ylacetic acid hydrochlorideHCID 70206205—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductN-Methoxy-N-methyl-1-(2-naphthylmethyl)-1H-imidazol-5-ylacetamideHCID 86751125—

Reaction Steps

To a solution of 1-(2-naphthylmethyl)-1H-imidazol-5-ylacetic acid hydrochloride (prepared in Example 4, 0.819 mg, 2.70 mmol) in dimethylformamide (15 ml) was added sequentially N, O-dimethylhydroxylamine hydrochloride (293 mg, 3.0 mmol), 3-hydroxy-1,2,3-benzotriazin-4(3H)-one (HOOBT, 489 mg, 3.0 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (EDC, 575 mg, 3.0 mmol) and triethylamine (1.67 ml, 12.0 mmol) and the resulting mixture stirred at room temperature for 18 h. Saturated aq. sodium bicarbonate (30 ml) and water (30 ml) were added and the mixture was extracted with methylene chloride (2×50 ml). The combined organic extracts were washed with brine (50 ml) and the solvent evaporated in vacuo. The residue was purified by flash chromatography (2-4% methanol/methylene chloride gradient elution) to provide the title compound as an oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05652257
Source datasetuspto-grants-1997_07
ORD IDord-b1467f2bd5694d53a51470721eae605e
Source noteuspto-grants-1997_07