HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1608817Generated: November 2, 2026
Isatoic Anhydride → 2-Amino-N-[2-(1H-imidazol-2-yl)ethyl]benzamide
https://huagongshe.com/reaction/1608817
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isatoic Anhydride | HCID 8359 | — |
| Reactant | Isohistamine | HCID 3082145 | — |
| Solvent | Isopropanol | HCID 3776 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-Amino-N-[2-(1H-imidazol-2-yl)ethyl]benzamide | HCID 20085578 | 85.8% |
Reaction Steps
Twenty grams (0.123 mol) of isatoic anhydride were slowly added to a cold (0° C.) solution of 13.5 g (0.122 mol) of 2-(2-aminoethyl)imidazole in 220 ml isopropanol, under nitrogen. The reaction mixture was gradually warmed to room temperature and allowed to react. When the reaction was complete, as indicated by thin layer chromatography, the solution was reduced to dryness under reduced pressure and the resultant residue was redissolved in an ethyl acetate/aqueous sodium bicarbonate mixture. The resulting layers were separated, the organic layer was washed with water and reduced to dryness to provide a solid. This solid was recrystallized from ethanol containing a small amount of hexane to provide 24.1 g of the desired subtitled intermediate (m.p. 180°-185° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05397798 |
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| Source dataset | uspto-grants-1995_03 |
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| ORD ID | ord-80fb02e441474e73a92b956199ece31f |
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| Source note | uspto-grants-1995_03 |
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