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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(2-Nitroimidazol-1-yl)acetic acid | HCID 327544 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Bis-(1H-imidazol-2-YL)-methanone | HCID 5250894 | — |
| Reactant | 3-Methylbut-2-en-1-amine hydrochloride | HCID 18326564 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane methanol | HCID 21226129 | — |
| Product | N-(3-methyl-2-butenyl)-2-(2-nitro-1H-imidazol-1-yl)acetamide | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05656254 |
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| Source dataset | uspto-grants-1997_08 |
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| ORD ID | ord-57e0c8e841d84c0da62bba5682501fe1 |
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| Source note | uspto-grants-1997_08 |
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