HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 546601Generated: October 31, 2026
N-Methylethylamine → HCID 67198477, compound
https://huagongshe.com/reaction/546601
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Methylethylamine | HCID 12219 | — |
| 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 67198477 | HCID 67198477 | — |
Reaction Steps
A solution of 100 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 2 mL of dioxane and 24 μl of N-ethyl-N-methylamine is heated by microwave at 130° C. for 15 minutes. The reaction mixture is concentrated under reduced pressure and the residue is purified by chromatography on a column of silica, eluting with a mixture of petroleum ether and ethyl acetate (gradient 40/60 to 0/100 by volume) followed by HPLC (gradient: water/acetonitrile containing 0.1% formic acid) to give 12 mg of 3-(4-{[3-(4-tert-butylphenyl)-5,5-dimethyl-2,4-dioxo-imidazolidin-1-yl]methyl}pyridin-2-yl)-1-ethyl-1-methylurea, the characteristics of which are as follows:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07935819B2 |
|---|
| Source dataset | uspto-grants-2011_05 |
|---|
| ORD ID | ord-66a12051a13241d88c83eaf364b04b26 |
|---|
| Source note | uspto-grants-2011_05 |
|---|