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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2256786Generated: November 1, 2026

2-(2-Nitroimidazol-1-yl)acetic acid → N-(3-methyl-2-butenyl)-2-(2-nitro-1H-imidazol-1-yl)acetamide

https://huagongshe.com/reaction/2256786

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(2-Nitroimidazol-1-yl)acetic acidHCID 327544—
ReactantSodium BicarbonateHCID 516892—
ReactantBis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
Reactant3-Methylbut-2-en-1-amine hydrochlorideHCID 18326564—
SolventDimethylformamideHCID 6228—
SolventDichloromethane methanolHCID 21226129—
ProductN-(3-methyl-2-butenyl)-2-(2-nitro-1H-imidazol-1-yl)acetamideHCID 18929154—

Reaction Steps

2-(2-Nitro-1H-imidazol-1-yl)acetic acid (8.6 g, 50 mmol) was dissolved in DMF (50 mL). Carbonyl diimidazole [CDI] (8.7 g, 60 mmol) was added to the solution in small portions. The reaction mixture was stirred under N2 for 15 min. 3,3-Dimethylallylamine hydrochloride was suspended in DMF (50 mL) and stirred with NaHCO3 (4.2 g, 50 mmol). This suspension was added to the CDI and 2-(2-nitro-1H-imidazol-1-yl)acetic acid in DMF solution. The mixture was stirred under N2 atmosphere at room temperature overnight. TLC (silica gel, 10% methanol-dichloromethane) showed one spot with Rf =0.5, indicating completion of the reaction. DMF was evaporated on a rotary evaporator and the residue was triturated with ice-water (125 mL) and filtered. The solid was washed with cold water (3×50 mL) and dried in vacuum to give a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05656254
Source datasetuspto-grants-1997_08
ORD IDord-57e0c8e841d84c0da62bba5682501fe1
Source noteuspto-grants-1997_08