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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 264135Generated: October 30, 2026

Bis-(1H-imidazol-2-YL)-methanone → 2-(3-Dodecyl-[1,2,4]oxadiazol-5-yl)-2-phenyl-N-(2,4,6-trimethoxy-phenyl)-acetamide

https://huagongshe.com/reaction/264135

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactantalpha-[[(2,4,6-Trimethoxyphenyl)amino]carbonyl]benzene acetic acidHCID 10665192—
ReactantHCID 178443206HCID 178443206—
SolventTetrahydrofuranHCID 8028—
Product2-(3-Dodecyl-[1,2,4]oxadiazol-5-yl)-2-phenyl-N-(2,4,6-trimethoxy-phenyl)-acetamideHCID 1072112711%

Reaction Steps

Carbonyl dimidazole (0.28 g, 1.71 mmol) was added to a solution of α-[[(2,4,6-trimethoxyphenyl)amino]carbonyl]-benzene acetic acid (0.56 g, 1.63 mmol) in dry THF (20 mL), and the resulting mixture was stirred at room temperature for 1 hour, then N-hydroxy-tridecane imidamide (0.37 g, 1.63 mmol) was added, and the mixture stirred for 1.5 hours, concentrated in vacuo, dissolved in glacial acetic acid, and refluxed for 1.5 hours. The solution was concentrated and azeotroped with benzene (2×25 mL), dissolved in ethyl acetate, and washed with NaHCO3, water, brine, dried with MgSO4, and recrystallized from ethanol/water to yield a white solid (0.093 g, 11%). %(found): C, 69.25; H, 8.08; N, 7.68. ##STR14##

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05646170
Source datasetuspto-grants-1997_07
ORD IDord-51cfadeeb06344b2ad5745172f4bfcf8
Source noteuspto-grants-1997_07