HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546636Generated: November 1, 2026
3-Aminopyridine → HCID 57626022, compound
https://huagongshe.com/reaction/546636
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Aminopyridine | HCID 10009 | — |
| Reactant | 3-(4-tert-butylphenyl)-5,5-dimethyl-1-[(2-thioxo-2H-[1,2,4]oxadiazolo[2,3-a]pyridin-7-yl)methyl]imidazolidine-2,4-dione | HCID 57625975 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57626022 | HCID 57626022 | 56.3% |
Reaction Steps
To a solution of 200 mg of 3-(4-tert-butylphenyl)-5,5-dimethyl-1-[(2-thioxo-2H-[1,2,4]oxadiazolo[2,3-a]pyridin-7-yl)methyl]imidazolidine-2,4-dione obtained in stage b) of Example 9 in 4 mL of dioxane are added 53 mg of 3-aminopyridine. The reaction mixture is heated by microwave at 130° C. for 20 minutes and concentrated under reduced pressure. The residue is purified by chromatography on a column of silica, eluting with a mixture of dichloromethane and methanol (98/2 by volume) to give 129 mg of 1-(4-{[3-(4-tert-butylphenyl)-5,5-dimethyl-2,4-dioxoimidazolidin-1-yl]methyl}pyridin-2-yl)-3-pyridin-3-ylurea, the characteristics of which are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07935819B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-68a72957ff804a58832e71d92b87cc37 |
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| Source note | uspto-grants-2011_05 |
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