HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1028151Generated: October 27, 2026
Pyridine → 3-Benzyl-2,5-dioxoimidazolidine 1-hexylcarboxamide
https://huagongshe.com/reaction/1028151
Participants
| Role | Name | HCID | Charge |
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| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Hexyl isocyanate | HCID 75659 | — |
| Reactant | 1-Benzylimidazolidine-2,4-dione | HCID 2735485 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-Benzyl-2,5-dioxoimidazolidine 1-hexylcarboxamide | HCID 131731408 | — |
Reaction Steps
1-Benzylimidazolidine-2,4-dione (100 mg, 0.526 mmol) and 1-isocyanatohexane (80.3 mg, 0.63 mmol) and, if required, a catalytic amount of 4-dimethylaminopyridine were dissolved in 10 ml of toluene and 0.5 ml of pyridine and stirred at 115° C. for 6 h. Then a further 80 mg of 1-isocyanatohexane were added, and the mixture was stirred at 115° C. for a further 6 h. The reaction mixture was concentrated and the residue was taken up in ethyl acetate and H2O, and the org. phases were washed twice with water, concentrated and purified by preparative HPLC (PR18, acetonitrile/water 0.1% TFA). Yield: 11.3 mg (7%), M+H+:318.14.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08735437B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-fe93801de6af459f8d4d780a3c9f400a |
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| Source note | uspto-grants-2014_05 |
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